Wayne W Grody

Title(s)Professor, Pathology and Laboratory Medicine
SchoolMedicine
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    Other Positions
    Title(s)Professor, Human Genetics

    Title(s)Professor, Pediatrics


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    CYSTIC FIBROSIS MUTATION SCREENING AND COUNSELING
    NIH R01HD029337Sep 30, 1991 - Aug 31, 1995
    Role: Principal Investigator
    GENE TRANSFER OF HUMAN ARGINASE
    NIH K08HD000831Feb 1, 1988 - Jan 31, 1991
    Role: Principal Investigator

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Stewardship of patient genomic data: A policy statement of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2022 03; 24(3):509-511. Best RG, Khushf G, Rabin-Havt SS, Clayton EW, Grebe TA, Hagenkord J, Topper S, Fivecoat J, Chen M, Grody WW, ACMG Social, Ethical and Legal Issues Committee. Electronic address: documents@acmg.net. PMID: 35253644.
      View in: PubMed   Mentions:
    2. Response to Biesecker et al. Am J Hum Genet. 2021 09 02; 108(9):1807-1808. Hamosh A, Amberger JS, Bocchini CA, Bodurtha J, Bult CJ, Chute CG, Cutting GR, Dietz HC, Firth HV, Gibbs RA, Grody WW, Haendel MA, Lupski JR, Posey JE, Robinson PN, Schriml LM, Scott AF, Sobreira NL, Valle D, Wu N, Rasmussen SA. PMID: 34478655; PMCID: PMC8456153.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    3. Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome. J Mol Med (Berl). 2021 11; 99(11):1623-1638. Zhao Y, Wang LK, Eskin A, Kang X, Fajardo VM, Mehta Z, Pineles S, Schmidt RJ, Nagiel A, Satou G, Garg M, Federman M, Reardon LC, Lee SL, Biniwale R, Grody WW, Halnon N, Khanlou N, Quintero-Rivera F, Alejos JC, Nakano A, Fishbein GA, Van Arsdell GS, Nelson SF, Touma M. PMID: 34387706; PMCID: PMC8541947.
      View in: PubMed   Mentions:    Fields:    
    4. Central 22q11.2 deletion (LCR22 B-D) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome. Am J Med Genet A. 2021 10; 185(10):3042-3047. Lin I, Afshar Y, Goldstein J, Grossman J, Grody WW, Quintero-Rivera F. PMID: 34196458.
      View in: PubMed   Mentions: 1     Fields:    
    5. Addendum: American College of Medical Genetics consensus statement on factor V Leiden mutation testing. Genet Med. 2021 Dec; 23(12):2463. Bhatt S, Taylor AK, Lozano R, Grody WW, Griffin JH, ACMG Professional Practice and Guidelines Committee. PMID: 33674767.
      View in: PubMed   Mentions:    Fields:    
    6. Memories of Gene Herbek, MD. Arch Pathol Lab Med. 2021 03 01; 145(3):262-263. Gardner JM, Grody WW. PMID: 33238007.
      View in: PubMed   Mentions:
    7. Gene-environment regulation of chamber-specific maturation during hypoxemic perinatal circulatory transition. J Mol Med (Berl). 2020 07; 98(7):1009-1020. Zhao Y, Kang X, Barsegian A, He J, Guzman A, Lau RP, Biniwale R, Wadhra M, Reemtsen B, Garg M, Halnon N, Quintero-Rivera F, Grody WW, UCLA Congenital Heart Defects BioCore Faculty, Van Arsdell G, Nelson SF, Touma M. PMID: 32533200; PMCID: PMC7843236.
      View in: PubMed   Mentions:    Fields:    Translation:AnimalsCells
    8. Electric Field-Induced Release and Measurement (EFIRM): Characterization and Technical Validation of a Novel Liquid Biopsy Platform in Plasma and Saliva. J Mol Diagn. 2020 08; 22(8):1050-1062. Tu M, Cheng J, Chen YL, Jea WC, Chen WL, Chen CJ, Ho CL, Huang WL, Lin CC, Su WC, Ye Q, Deignan J, Grody W, Li F, Chia D, Wei F, Liao W, Wong DTW, Strom CM. PMID: 32497715; PMCID: PMC7416077.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    9. CFTR variant testing: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2020 08; 22(8):1288-1295. Deignan JL, Astbury C, Cutting GR, Del Gaudio D, Gregg AR, Grody WW, Monaghan KG, Richards S, ACMG Laboratory Quality Assurance Committee. PMID: 32404922; PMCID: PMC8268680.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    10. Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndrome. Mol Genet Metab Rep. 2020 Jun; 23:100582. Yazdani S, Badjatiya A, Dorrani N, Lee H, Grody WW, Nelson SF, Dipple KM. PMID: 32280589; PMCID: PMC7138921.
      View in: PubMed   Mentions: 1  
    11. International perspectives on the implementation of reproductive carrier screening. Prenat Diagn. 2020 02; 40(3):301-310. Delatycki MB, Alkuraya F, Archibald A, Castellani C, Cornel M, Grody WW, Henneman L, Ioannides AS, Kirk E, Laing N, Lucassen A, Massie J, Schuurmans J, Thong MK, van Langen I, Zlotogora J. PMID: 31774570.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    12. A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders. Hum Mutat. 2020 02; 41(2):487-501. Ngo KJ, Rexach JE, Lee H, Petty LE, Perlman S, Valera JM, Deignan JL, Mao Y, Aker M, Posey JE, Jhangiani SN, Coban-Akdemir ZH, Boerwinkle E, Muzny D, Nelson AB, Hassin-Baer S, Poke G, Neas K, Geschwind MD, Grody WW, Gibbs R, Geschwind DH, Lupski JR, Below JE, Nelson SF, Fogel BL. PMID: 31692161; PMCID: PMC7182470.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    13. Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centers. Mol Genet Genomic Med. 2020 01; 8(1):e1026. Eno CC, Barton SK, Dorrani N, Cederbaum SD, Deignan JL, Grody WW. PMID: 31701651; PMCID: PMC6978271.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    14. The transformation of medical genetics by clinical genomics: hubris meets humility. Genet Med. 2019 09; 21(9):1916-1926. Grody WW. PMID: 30842646.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    15. Generalized Cytokine Increase in the Setting of a Multisystem Clinical Disorder and Carcinoid Syndrome Associated with a Novel NLRP12 Variant. Dig Dis Sci. 2019 08; 64(8):2140-2146. Jacob N, Dasharathy SS, Bui V, Benhammou JN, Grody WW, Singh RR, Pisegna JR. PMID: 30788684; PMCID: PMC6707534.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    16. Home use of a compact, 12‑lead ECG recording system for newborns. J Electrocardiol. 2019 Mar - Apr; 53:89-94. Lin HJ, Lan YT, Silka MJ, Halnon NJ, Villa-Lopez E, Arenas N, Escobedo F, Montoya R, Valdez S, Rajabi Shishvan O, Sedano S, Marr EH, Lauzon M, Moosa AS, Ko KJ, Shoji EC, Clark AM, Smith LM, Criley JM, Grody WW, Chen YI, Taylor KD, Guo X, Soyata T, Rotter JI, Chien T, Chou P, Chang RK. PMID: 30716528; PMCID: PMC6458066.
      View in: PubMed   Mentions:    Fields:    Translation:HumansPHPublic Health
    17. Response to Biesecker and Harrison. Genet Med. 2018 12; 20(12):1689-1690. Richards CS, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL, ACMG/AMP Interpretation of Sequence Variants Work Group 2015. PMID: 29543230.
      View in: PubMed   Mentions: 2     Fields:    
    18. Electric Field-Induced Release and Measurement Liquid Biopsy for Noninvasive Early Lung Cancer Assessment. J Mol Diagn. 2018 11; 20(6):738-742. Wei F, Strom CM, Cheng J, Lin CC, Hsu CY, Soo Hoo GW, Chia D, Kim Y, Li F, Elashoff D, Grognan T, Tu M, Liao W, Xian R, Grody WW, Su WC, Wong DTW. PMID: 30309763; PMCID: PMC6198245.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCTClinical Trials
    19. Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis. Am J Med Genet A. 2018 12; 176(12):2829-2834. Datkhaeva I, Arboleda VA, Senaratne TN, Nikpour G, Meyerson C, Geng Y, Afshar Y, Scibetta E, Goldstein J, Quintero-Rivera F, Crandall BF, Grody WW, Deignan J, Janzen C. PMID: 30244526.
      View in: PubMed   Mentions: 7  Translation:Humans
    20. The Value of T-Cell Receptor γ (TRG) Clonality Evaluation by Next-Generation Sequencing in Clinical Hematolymphoid Tissues. Am J Clin Pathol. 2018 Jul 31; 150(3):193-223. Kansal R, Grody WW, Zhou J, Dong L, Li X. PMID: 29982316.
      View in: PubMed   Mentions: 3     Fields:    
    21. Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder? Genet Med. 2017 12; 19(12). Mullegama SV, Klein SD, Nguyen DC, Kim A, Signer R, Fox M, Dorrani N, Hendershot A, Mardach R, Suddath R, Dipple K, Vilain E, Wong DA, Deignan JL, D Cederbaum S, Grody WW, Martinez-Agosto JA. PMID: 28933790.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    22. The Case for Laboratory Developed Procedures: Quality and Positive Impact on Patient Care. Acad Pathol. 2017 Jan-Dec; 4:2374289517708309. Kaul KL, Sabatini LM, Tsongalis GJ, Caliendo AM, Olsen RJ, Ashwood ER, Bale S, Benirschke R, Carlow D, Funke BH, Grody WW, Hayden RT, Hegde M, Lyon E, Murata K, Pessin M, Press RD, Thomson RB. PMID: 28815200; PMCID: PMC5528950.
      View in: PubMed   Mentions: 3  
    23. CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med. 2017 05; 19(5):606. Green RC, Berg JS, Grody WW, Kalia SS, Korf BR, Martin CL, McGuire AL, Nussbaum RL, O'Daniel JM, Ormond KE, Rehm HL, Watson MS, Williams MS, Biesecker LG. PMID: 28492529.
      View in: PubMed   Mentions: 11     Fields:    
    24. Coupling clinical exome sequencing with functional characterization studies to diagnose a patient with familial Mediterranean fever and MED13L haploinsufficiency syndromes. Clin Case Rep. 2017 06; 5(6):833-840. Mullegama SV, Jensik P, Li C, Dorrani N, UCLA Clinical Genomics Center, Kantarci S, Blumberg B, Grody WW, Strom SP. PMID: 28588821; PMCID: PMC5458005.
      View in: PubMed   Mentions: 2  
    25. Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. J Womens Health (Larchmt). 2017 07; 26(7):755-761. Allyse M, Aypar U, Bonhomme N, Darilek S, Dougherty M, Farrell R, Grody W, Highsmith WE, Michie M, Nunes M, Otto L, Pabst R, Palomaki G, Runke C, Sharp RR, Skotko B, Stoll K, Wick M. PMID: 28388340.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    26. Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline Summary From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and American Society of Clinical Oncology. J Oncol Pract. 2017 05; 13(5):333-337. Sepulveda AR, Hamilton SR, Allegra CJ, Grody W, Cushman-Vokoun AM, Funkhouser WK, Kopetz SE, Lieu C, Lindor NM, Minsky BD, Monzon FA, Sargent DJ, Singh VM, Willis J, Clark J, Colasacco C, Rumble RB, Temple-Smolkin R, Ventura CB, Nowak JA. PMID: 28350513.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    27. Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and American Society of Clinical Oncology. J Mol Diagn. 2017 03; 19(2):187-225. Sepulveda AR, Hamilton SR, Allegra CJ, Grody W, Cushman-Vokoun AM, Funkhouser WK, Kopetz SE, Lieu C, Lindor NM, Minsky BD, Monzon FA, Sargent DJ, Singh VM, Willis J, Clark J, Colasacco C, Rumble RB, Temple-Smolkin R, Ventura CB, Nowak JA. PMID: 28185757; PMCID: PMC5971222.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    28. Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and American Society of Clinical Oncology. Arch Pathol Lab Med. 2017 May; 141(5):625-657. Sepulveda AR, Hamilton SR, Allegra CJ, Grody W, Cushman-Vokoun AM, Funkhouser WK, Kopetz SE, Lieu C, Lindor NM, Minsky BD, Monzon FA, Sargent DJ, Singh VM, Willis J, Clark J, Colasacco C, Bryan Rumble R, Temple-Smolkin R, B Ventura C, Nowak JA. PMID: 28165284.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    29. Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecular Pathology, and the American Society of Clinical Oncology. J Clin Oncol. 2017 May 01; 35(13):1453-1486. Sepulveda AR, Hamilton SR, Allegra CJ, Grody W, Cushman-Vokoun AM, Funkhouser WK, Kopetz SE, Lieu C, Lindor NM, Minsky BD, Monzon FA, Sargent DJ, Singh VM, Willis J, Clark J, Colasacco C, Rumble RB, Temple-Smolkin R, Ventura CB, Nowak JA. PMID: 28165299.
      View in: PubMed   Mentions: 77     Fields:    Translation:Humans
    30. Molecular Biomarkers for the Evaluation of Colorectal Cancer. Am J Clin Pathol. 2017 03; 147(3):221-260. Sepulveda AR, Hamilton SR, Allegra CJ, Grody W, Cushman-Vokoun AM, Funkhouser WK, Kopetz SE, Lieu C, Lindor NM, Minsky BD, Monzon FA, Sargent DJ, Singh VM, Willis J, Clark J, Colasacco C, Rumble RB, Temple-Smolkin R, Ventura CB, Nowak JA. PMID: 28165529; PMCID: PMC7263311.
      View in: PubMed   Mentions: 2     Fields:    
    31. Prenatal Carrier Screening-Reply. JAMA. 2016 12 27; 316(24):2676-2677. Grody WW. PMID: 28027361.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    32. A Sodium Channel Myotonia Presenting with Intermittent Dysphagia as a Manifestation of a Rare SCN4A Variant. J Mol Neurosci. 2017 Mar; 61(3):312-314. Benhammou JN, Phan J, Lee H, Ghassemi K, Parsons W, Grody WW, Pisegna JR. PMID: 28012096; PMCID: PMC5346050.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    33. Missense-depleted regions in population exomes implicate ras superfamily nucleotide-binding protein alteration in patients with brain malformation. NPJ Genom Med. 2016; 1. Ge X, Gong H, Dumas K, Litwin J, Phillips JJ, Waisfisz Q, Weiss MM, Hendriks Y, Stuurman KE, Nelson SF, Grody WW, Lee H, Kwok PY, Shieh JT. PMID: 28868155; PMCID: PMC5576364.
      View in: PubMed   Mentions: 16  
    34. Where to Draw the Boundaries for Prenatal Carrier Screening. JAMA. 2016 Aug 16; 316(7):717-9. Grody WW. PMID: 27533155.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    35. The next generation of cancer management. Cancer Biol Med. 2016 Mar; 13(1):1-2. Grody WW. PMID: 27144057; PMCID: PMC4850118.
      View in: PubMed   Mentions:
    36. Primary central nervous system gamma delta cytotoxic T-cell lymphoma. J Clin Neurosci. 2016 Apr; 26:138-40. Mooney KL, Choy W, Woodard J, Xian RR, Deal TM, Kendle RF, Said J, Grody W, Yang I. PMID: 26804925.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    37. Molecular Diagnosis of Cystic Fibrosis. Curr Protoc Hum Genet. 2016 Jan 01; 88:9.28.1-9.28.6. Deignan JL, Grody WW. PMID: 26724724.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    38. An infant with MLH3 variants, FOXG1-duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing study. Genes Chromosomes Cancer. 2016 Feb; 55(2):131-42. Kansal R, Li X, Shen J, Samuel D, Laningham F, Lee H, Panigrahi GB, Shuen A, Kantarci S, Dorrani N, Reiss J, Shintaku P, Deignan JL, Strom SP, Pearson CE, Vilain E, Grody WW. PMID: 26542077.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    39. DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. Eur J Hum Genet. 2015 Nov; 23(11):1473-81. Ji J, Lee H, Argiropoulos B, Dorrani N, Mann J, Martinez-Agosto JA, Gomez-Ospina N, Gallant N, Bernstein JA, Hudgins L, Slattery L, Isidor B, Le Caignec C, David A, Obersztyn E, Wisniowiecka-Kowalnik B, Fox M, Deignan JL, Vilain E, Hendricks E, Horton Harr M, Noon SE, Jackson JR, Wilkens A, Mirzaa G, Salamon N, Abramson J, Zackai EH, Krantz I, Innes AM, Nelson SF, Grody WW, Quintero-Rivera F. PMID: 25944381; PMCID: PMC4613469.
      View in: PubMed   Mentions: 41     Fields:    Translation:Humans
    40. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015 May; 17(5):405-24. Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL, ACMG Laboratory Quality Assurance Committee. PMID: 25741868; PMCID: PMC4544753.
      View in: PubMed   Mentions: 5104     Fields:    Translation:Humans
    41. Instability of a dinucleotide repeat in the 3'-untranslated region (UTR) of the microsomal prostaglandin E synthase-1 (mPGES-1) gene in microsatellite instability-high (MSI-H) colorectal carcinoma. Mol Oncol. 2015 Aug; 9(7):1252-8. Cherukuri DP, Deignan JL, Das K, Grody WW, Herschman H. PMID: 25817443; PMCID: PMC4523444.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    42. De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay. Am J Hum Genet. 2015 Mar 05; 96(3):498-506. Arboleda VA, Lee H, Dorrani N, Zadeh N, Willis M, Macmurdo CF, Manning MA, Kwan A, Hudgins L, Barthelemy F, Miceli MC, Quintero-Rivera F, Kantarci S, Strom SP, Deignan JL, UCLA Clinical Genomics Center, Grody WW, Vilain E, Nelson SF. PMID: 25728775; PMCID: PMC4375619.
      View in: PubMed   Mentions: 41     Fields:    Translation:HumansCells
    43. Clinical exome sequencing for genetic identification of rare Mendelian disorders. JAMA. 2014 Nov 12; 312(18):1880-7. Lee H, Deignan JL, Dorrani N, Strom SP, Kantarci S, Quintero-Rivera F, Das K, Toy T, Harry B, Yourshaw M, Fox M, Fogel BL, Martinez-Agosto JA, Wong DA, Chang VY, Shieh PB, Palmer CG, Dipple KM, Grody WW, Vilain E, Nelson SF. PMID: 25326637; PMCID: PMC4278636.
      View in: PubMed   Mentions: 360     Fields:    Translation:Humans
    44. Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia. JAMA Neurol. 2014 Oct; 71(10):1237-46. Fogel BL, Lee H, Deignan JL, Strom SP, Kantarci S, Wang X, Quintero-Rivera F, Vilain E, Grody WW, Perlman S, Geschwind DH, Nelson SF. PMID: 25133958; PMCID: PMC4324730.
      View in: PubMed   Mentions: 92     Fields:    Translation:Humans
    45. College of American Pathologists' laboratory standards for next-generation sequencing clinical tests. Arch Pathol Lab Med. 2015 Apr; 139(4):481-93. Aziz N, Zhao Q, Bry L, Driscoll DK, Funke B, Gibson JS, Grody WW, Hegde MR, Hoeltge GA, Leonard DG, Merker JD, Nagarajan R, Palicki LA, Robetorye RS, Schrijver I, Weck KE, Voelkerding KV. PMID: 25152313.
      View in: PubMed   Mentions: 101     Fields:    Translation:Humans
    46. Interpreting whole-genome sequencing. JAMA. 2014 Jul 16; 312(3):296. Grody WW, Vilain E, Nelson SF. PMID: 25027151.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    47. Myocyte-mediated arginase expression controls hyperargininemia but not hyperammonemia in arginase-deficient mice. Mol Ther. 2014 Oct; 22(10):1792-802. Hu C, Kasten J, Park H, Bhargava R, Tai DS, Grody WW, Nguyen QG, Hauschka SD, Cederbaum SD, Lipshutz GS. PMID: 24888478; PMCID: PMC4428413.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimalsCells
    48. De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing. BMC Med Genet. 2014 May 01; 15:49. Strom SP, Lozano R, Lee H, Dorrani N, Mann J, O'Lague PF, Mans N, Deignan JL, Vilain E, Nelson SF, Grody WW, Quintero-Rivera F. PMID: 24886118; PMCID: PMC4072606.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    49. A case of mycosis fungoides transmitted from donor to recipient, and review of literature of T-cell malignancies after transplantation. Clin Lymphoma Myeloma Leuk. 2014 Aug; 14(4):e137-40. Loh JC, Cassarino DS, Grody WW, Chiu MW, Pinter-Brown LC. PMID: 24637131.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    50. Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory. Genet Med. 2014 Jul; 16(7):510-5. Strom SP, Lee H, Das K, Vilain E, Nelson SF, Grody WW, Deignan JL. PMID: 24406459; PMCID: PMC4079763.
      View in: PubMed   Mentions: 51     Fields:    Translation:Humans
    51. Whole-exome/genome sequencing and genomics. Pediatrics. 2013 Dec; 132(Suppl 3):S211-5. Grody WW, Thompson BH, Hudgins L. PMID: 24298129.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    52. Carrier screening for cystic fibrosis in the new era of medications that restore CFTR function. Lancet. 2014 Mar 08; 383(9920):923-5. Massie J, Castellani C, Grody WW. PMID: 23992917.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    53. Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouse. Mol Genet Metab. 2013 Nov; 110(3):222-30. Kasten J, Hu C, Bhargava R, Park H, Tai D, Byrne JA, Marescau B, De Deyn PP, Schlichting L, Grody WW, Cederbaum SD, Lipshutz GS. PMID: 23920045; PMCID: PMC3800271.
      View in: PubMed   Mentions: 16     Fields:    Translation:Animals
    54. Current landscape and new paradigms of proficiency testing and external quality assessment for molecular genetics. Arch Pathol Lab Med. 2013 Jul; 137(7):983-8. Kalman LV, Lubin IM, Barker S, du Sart D, Elles R, Grody WW, Pazzagli M, Richards S, Schrijver I, Zehnbauer B. PMID: 23808472; PMCID: PMC4684176.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    55. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med. 2013 Jul; 15(7):565-74. Green RC, Berg JS, Grody WW, Kalia SS, Korf BR, Martin CL, McGuire AL, Nussbaum RL, O'Daniel JM, Ormond KE, Rehm HL, Watson MS, Williams MS, Biesecker LG, American College of Medical Genetics and Genomics. PMID: 23788249; PMCID: PMC3727274.
      View in: PubMed   Mentions: 920     Fields:    Translation:Humans
    56. ACMG position statement on prenatal/preconception expanded carrier screening. Genet Med. 2013 Jun; 15(6):482-3. Grody WW, Thompson BH, Gregg AR, Bean LH, Monaghan KG, Schneider A, Lebo RV. PMID: 23619275.
      View in: PubMed   Mentions: 72     Fields:    Translation:Humans
    57. Deaf genetic testing and psychological well-being in deaf adults. J Genet Couns. 2013 Aug; 22(4):492-507. Palmer CG, Boudreault P, Baldwin EE, Fox M, Deignan JL, Kobayashi Y, Sininger Y, Grody W, Sinsheimer JS. PMID: 23430402; PMCID: PMC3701749.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    58. AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouse. Gene Ther. 2013 Aug; 20(8):785-96. Lee EK, Hu C, Bhargava R, Ponnusamy R, Park H, Novicoff S, Rozengurt N, Marescau B, De Deyn P, Stout D, Schlichting L, Grody WW, Cederbaum SD, Lipshutz GS. PMID: 23388701; PMCID: PMC3679314.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimalsCells
    59. Emergence of pediatric rare diseases: Review of present policies and opportunities for improvement. Rare Dis. 2013; 1:e23579. Bavisetty S, Grody WW, Yazdani S. PMID: 25002987; PMCID: PMC3932940.
      View in: PubMed   Mentions: 11  
    60. Personalized Medicine in Ophthalmology: From Pharmacogenetic Biomarkers to Therapeutic and Dosage Optimization. J Pers Med. 2013; 3(1):40-69. Ong FS, Kuo JZ, Wu WC, Cheng CY, Blackwell WL, Taylor BL, Grody WW, Rotter JI, Lai CC, Wong TY. PMID: 24624293; PMCID: PMC3947950.
      View in: PubMed   Mentions: 5  
    61. The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA. Clin Genet. 2013 Jul; 84(1):55-9. Ong FS, Vakil H, Xue Y, Kuo JZ, Shah KH, Lee RB, Bernstein KE, Rimoin DL, Getzug T, Das K, Deignan JL, Rotter JI, Grody WW. PMID: 23038988; PMCID: PMC3570680.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    62. Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology. J Mol Diagn. 2012 Nov; 14(6):525-40. Schrijver I, Aziz N, Farkas DH, Furtado M, Gonzalez AF, Greiner TC, Grody WW, Hambuch T, Kalman L, Kant JA, Klein RD, Leonard DG, Lubin IM, Mao R, Nagan N, Pratt VM, Sobel ME, Voelkerding KV, Gibson JS. PMID: 22918138; PMCID: PMC6504171.
      View in: PubMed   Mentions: 55     Fields:    Translation:Humans
    63. Human Variome Project country nodes: documenting genetic information within a country. Hum Mutat. 2012 Nov; 33(11):1513-9. Patrinos GP, Smith TD, Howard H, Al-Mulla F, Chouchane L, Hadjisavvas A, Hamed SA, Li XT, Marafie M, Ramesar RS, Ramos FJ, de Ravel T, El-Ruby MO, Shrestha TR, Sobrido MJ, Tadmouri G, Witsch-Baumgartner M, Zilfalil BA, Auerbach AD, Carpenter K, Cutting GR, Dung VC, Grody W, Hasler J, Jorde L, Kaput J, Macek M, Matsubara Y, Padilla C, Robinson H, Rojas-Martinez A, Taylor GR, Vihinen M, Weber T, Burn J, Qi M, Cotton RG, Rimoin D, International Confederation of Countries Advisory Council. PMID: 22753370.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    64. Long-term survival of the juvenile lethal arginase-deficient mouse with AAV gene therapy. Mol Ther. 2012 Oct; 20(10):1844-51. Lee EK, Hu C, Bhargava R, Rozengurt N, Stout D, Grody WW, Cederbaum SD, Lipshutz GS. PMID: 22760543; PMCID: PMC3464644.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    65. Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing. Expert Rev Mol Diagn. 2012 Jul; 12(6):593-602. Ong FS, Das K, Wang J, Vakil H, Kuo JZ, Blackwell WL, Lim SW, Goodarzi MO, Bernstein KE, Rotter JI, Grody WW. PMID: 22845480; PMCID: PMC3495985.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    66. Targeted massively parallel sequencing provides comprehensive genetic diagnosis for patients with disorders of sex development. Clin Genet. 2013 Jan; 83(1):35-43. Arboleda VA, Lee H, Sánchez FJ, Délot EC, Sandberg DE, Grody WW, Nelson SF, Vilain E. PMID: 22435390; PMCID: PMC4052834.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    67. Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med. 2012 Apr; 14(4):405-10. Green RC, Berg JS, Berry GT, Biesecker LG, Dimmock DP, Evans JP, Grody WW, Hegde MR, Kalia S, Korf BR, Krantz I, McGuire AL, Miller DT, Murray MF, Nussbaum RL, Plon SE, Rehm HL, Jacob HJ. PMID: 22422049; PMCID: PMC3763716.
      View in: PubMed   Mentions: 87     Fields:    Translation:Humans
    68. Stuck between a scalpel and a rock, or molecular pathology and legal-ethical issues in use of tissues for clinical care and research: what must a pathologist know? Am J Clin Pathol. 2012 Mar; 137(3):346-55. Dry S, Grody WW, Papagni P. PMID: 22338046.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    69. Clinical utility of pharmacogenetic biomarkers in cardiovascular therapeutics: a challenge for clinical implementation. Pharmacogenomics. 2012 Mar; 13(4):465-75. Ong FS, Deignan JL, Kuo JZ, Bernstein KE, Rotter JI, Grody WW, Das K. PMID: 22380001; PMCID: PMC3306231.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    70. DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study. Genet Med. 2012 Mar; 14(3):296-305. Palomaki GE, Deciu C, Kloza EM, Lambert-Messerlian GM, Haddow JE, Neveux LM, Ehrich M, van den Boom D, Bombard AT, Grody WW, Nelson SF, Canick JA. PMID: 22281937; PMCID: PMC3938175.
      View in: PubMed   Mentions: 131     Fields:    Translation:HumansCellsCTClinical Trials
    71. Expanded carrier screening and the law of unintended consequences: from cystic fibrosis to fragile X. Genet Med. 2011 Dec; 13(12):996-7. Grody WW. PMID: 22134443.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    72. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study. Genet Med. 2011 Nov; 13(11):913-20. Palomaki GE, Kloza EM, Lambert-Messerlian GM, Haddow JE, Neveux LM, Ehrich M, van den Boom D, Bombard AT, Deciu C, Grody WW, Nelson SF, Canick JA. PMID: 22005709.
      View in: PubMed   Mentions: 186     Fields:    Translation:HumansCTClinical Trials
    73. Privacy and data management in the era of massively parallel next-generation sequencing. Expert Rev Mol Diagn. 2011 Jun; 11(5):457-9. Ong FS, Grody WW, Deignan JL. PMID: 21707452; PMCID: PMC3130532.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    74. Diagnosis and management of familial Mediterranean fever: integrating medical genetics in a dedicated interdisciplinary clinic. Genet Med. 2011 Mar; 13(3):263-9. Zadeh N, Getzug T, Grody WW. PMID: 21317656.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    75. Ordering genetic tests and interpreting the results. Adv Otorhinolaryngol. 2011; 70:18-24. Deignan JL, Grody WW. PMID: 21358180.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    76. Colchicine's other indication--effect of FDA action. N Engl J Med. 2010 Dec 02; 363(23):2267-8. Grody WW, Getzug T. PMID: 21121853.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    77. An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: implications for the prenatal diagnosis of ornithine transcarbamylase deficiency. Mol Genet Metab. 2010 Dec; 101(4):413-6. Quintero-Rivera F, Deignan JL, Peredo J, Grody WW, Crandall B, Sims M, Cederbaum SD. PMID: 20817516.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    78. Direct-to-consumer genotyping: are we ready for a brave new world? Clin Chem. 2010 Jul; 56(7):1056-60. Bender L, Silverman LM, Dinulos MB, Nickel J, Grody WW. PMID: 20511451.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    79. Arginine metabolism by macrophages promotes cardiac and muscle fibrosis in mdx muscular dystrophy. PLoS One. 2010 May 21; 5(5):e10763. Wehling-Henricks M, Jordan MC, Gotoh T, Grody WW, Roos KP, Tidball JG. PMID: 20505827; PMCID: PMC2874011.
      View in: PubMed   Mentions: 52     Fields:    Translation:AnimalsCells
    80. Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study. J Deaf Stud Deaf Educ. 2010; 15(3):209-27. Boudreault P, Baldwin EE, Fox M, Dutton L, Tullis L, Linden J, Kobayashi Y, Zhou J, Sinsheimer JS, Sininger Y, Grody WW, Palmer CG. PMID: 20488870; PMCID: PMC2902357.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    81. Benchmarks for cystic fibrosis carrier screening: a European consensus document. J Cyst Fibros. 2010 May; 9(3):165-78. Castellani C, Macek M, Cassiman JJ, Duff A, Massie J, ten Kate LP, Barton D, Cutting G, Dallapiccola B, Dequeker E, Girodon E, Grody W, Highsmith EW, Kääriäinen H, Kruip S, Morris M, Pignatti PF, Pypops U, Schwarz M, Soller M, Stuhrman M, Cuppens H. PMID: 20363197.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansPHPublic Health
    82. The fate of newborn screening blood spots. Pediatr Res. 2010 Mar; 67(3):237. Grody WW, Howell RR. PMID: 20154576.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansPHPublic Health
    83. Genetics in Hollywood: from real to reel. Clin Genet. 2010 Feb; 77(2):106-11. Grody WW. PMID: 20096067.
      View in: PubMed   Mentions:    Fields:    
    84. Development and characterization of reference materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 genetic testing. J Mol Diagn. 2009 Nov; 11(6):553-61. Barker SD, Bale S, Booker J, Buller A, Das S, Friedman K, Godwin AK, Grody WW, Highsmith E, Kant JA, Lyon E, Mao R, Monaghan KG, Payne DA, Pratt VM, Schrijver I, Shrimpton AE, Spector E, Telatar M, Toji L, Weck K, Zehnbauer B, Kalman LV. PMID: 19767587; PMCID: PMC2765754.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    85. Should we be applying warfarin pharmacogenetics to clinical practice? No, not now. Ann Intern Med. 2009 Aug 18; 151(4):270-3, W95. Rosove MH, Grody WW. PMID: 19687493.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    86. A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants. Am J Med Genet A. 2009 Jun; 149A(6):1169-82. Palmer CG, Martinez A, Fox M, Zhou J, Shapiro N, Sininger Y, Grody WW, Schimmenti LA. PMID: 19449415; PMCID: PMC2866144.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    87. Short-term correction of arginase deficiency in a neonatal murine model with a helper-dependent adenoviral vector. Mol Ther. 2009 Jul; 17(7):1155-63. Gau CL, Rosenblatt RA, Cerullo V, Lay FD, Dow AC, Livesay J, Brunetti-Pierri N, Lee B, Cederbaum SD, Grody WW, Lipshutz GS. PMID: 19367256; PMCID: PMC2835205.
      View in: PubMed   Mentions: 22     Fields:    Translation:AnimalsCells
    88. Cystic fibrosis testing comes of age. J Mol Diagn. 2009 May; 11(3):173-5. Grody WW. PMID: 19359497; PMCID: PMC2671332.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    89. Systemic mastocytosis associated with t(8;21)(q22;q22) acute myeloid leukemia. J Hematop. 2009 Mar; 2(1):27-33. Pullarkat ST, Pullarkat V, Kroft SH, Wilson CS, Ahsanuddin AN, Mann KP, Thein M, Grody WW, Brynes RK. PMID: 19669220; PMCID: PMC2713498.
      View in: PubMed   Mentions: 5  
    90. Keeping up with the next generation: massively parallel sequencing in clinical diagnostics. J Mol Diagn. 2008 Nov; 10(6):484-92. ten Bosch JR, Grody WW. PMID: 18832462; PMCID: PMC2570630.
      View in: PubMed   Mentions: 64     Fields:    Translation:HumansCells
    91. Disruption of arginase II alters prostate tumor formation in TRAMP mice. Prostate. 2008 Oct 01; 68(14):1561-9. Mumenthaler SM, Rozengurt N, Livesay JC, Sabaghian A, Cederbaum SD, Grody WW. PMID: 18663728.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    92. Infant hearing loss and connexin testing in a diverse population. Genet Med. 2008 Jul; 10(7):517-24. Schimmenti LA, Martinez A, Telatar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody WW, Palmer CG. PMID: 18580690.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    93. New quality assurance standards for rare disease testing. Genet Med. 2008 May; 10(5):320-4. Grody WW, Richards CS. PMID: 18496029.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    94. ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007. Genet Med. 2008 Apr; 10(4):294-300. Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE, Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee. PMID: 18414213.
      View in: PubMed   Mentions: 313     Fields:    Translation:HumansCells
    95. Expression of arginase II in prostate cancer. Int J Oncol. 2008 Feb; 32(2):357-65. Mumenthaler SM, Yu H, Tze S, Cederbaum SD, Pegg AE, Seligson DB, Grody WW. PMID: 18202758.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    96. Increased plasma and tissue guanidino compounds in a mouse model of hyperargininemia. Mol Genet Metab. 2008 Feb; 93(2):172-8. Deignan JL, Marescau B, Livesay JC, Iyer RK, De Deyn PP, Cederbaum SD, Grody WW. PMID: 17997338.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimals
    97. The Cystic Fibrosis mutation "arms race": when less is more. Genet Med. 2007 Nov; 9(11):739-44. Grody WW, Cutting GR, Watson MS. PMID: 18007142.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    98. Contrasting features of urea cycle disorders in human patients and knockout mouse models. Mol Genet Metab. 2008 Jan; 93(1):7-14. Deignan JL, Cederbaum SD, Grody WW. PMID: 17933574; PMCID: PMC2692509.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansAnimals
    99. Ethnic differences in parental perceptions of genetic testing for deaf infants. J Genet Couns. 2008 Feb; 17(1):129-38. Palmer CG, Martinez A, Fox M, Sininger Y, Grody WW, Schimmenti LA. PMID: 17952575.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    100. Polyamine homeostasis in arginase knockout mice. Am J Physiol Cell Physiol. 2007 Oct; 293(4):C1296-301. Deignan JL, Livesay JC, Shantz LM, Pegg AE, O'Brien WE, Iyer RK, Cederbaum SD, Grody WW. PMID: 17686999.
      View in: PubMed   Mentions: 9  Translation:Animals
    101. Sharing GJB2/GJB6 genetic test information with family members. J Genet Couns. 2007 Jun; 16(3):313-24. Blase T, Martinez A, Grody WW, Schimmenti L, Palmer CG. PMID: 17318457.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    102. Testing and reporting ACMG cystic fibrosis mutation panel results. Genet Test. 2007; 11(1):11-31. Lebo RV, Grody WW. PMID: 17394390.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    103. Variable penetrance and expressivity of the splice altering 5T sequence in the cystic fibrosis gene. Genet Test. 2007; 11(1):32-44. Lebo RV, Grody WW. PMID: 17394391.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    104. The clinical significance of circulating tumor cells in the peripheral blood. Diagn Mol Pathol. 2006 Dec; 15(4):187-94. Elshimali YI, Grody WW. PMID: 17122646.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    105. Arginase induction by sodium phenylbutyrate in mouse tissues and human cell lines. Mol Genet Metab. 2007 Jan; 90(1):37-41. Kern RM, Yang Z, Kim PS, Grody WW, Iyer RK, Cederbaum SD. PMID: 16935537.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimalsCells
    106. Ornithine deficiency in the arginase double knockout mouse. Mol Genet Metab. 2006 Sep-Oct; 89(1-2):87-96. Deignan JL, Livesay JC, Yoo PK, Goodman SI, O'Brien WE, Iyer RK, Cederbaum SD, Grody WW. PMID: 16753325.
      View in: PubMed   Mentions: 26     Fields:    Translation:AnimalsCells
    107. Microelectronic array system for molecular diagnostic genotyping: Nanogen NanoChip 400 and molecular biology workstation. Expert Rev Mol Diagn. 2006 May; 6(3):287-94. Keen-Kim D, Grody WW, Richards CS. PMID: 16706733.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    108. Monitoring standards for molecular genetic testing in the United Kingdom, the Netherlands, and Ireland. Genet Test. 2006; 10(3):147-56. Ramsden SC, Deans Z, Robinson DO, Mountford R, Sistermans EA, Grody WW, McQuaid S, Patton SJ, Stenhouse SA. PMID: 17020464.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    109. Prelingual siblings of children with GJB2 hearing loss: issues to consider. Arch Otolaryngol Head Neck Surg. 2005 Nov; 131(11):1020-2. Palmer CG, Martinez A, Sininger Y, Shapiro N, Grody WW, Schimmenti LA. PMID: 16301377.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    110. Technical standards and guidelines: molecular genetic testing for ultra-rare disorders. Genet Med. 2005 Oct; 7(8):571-83. Maddalena A, Bale S, Das S, Grody W, Richards S, ACMG Laboratory Quality Assurance Committee. PMID: 16247296.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    111. Developing a sustainable process to provide quality control materials for genetic testing. Genet Med. 2005 Oct; 7(8):534-49. Chen B, O' Connell CD, Boone DJ, Amos JA, Beck JC, Chan MM, Farkas DH, Lebo RV, Richards CS, Roa BB, Silverman LM, Barton DE, Bejjani BA, Belloni DR, Bernacki SH, Caggana M, Charache P, Dequeker E, Ferreira-Gonzalez A, Friedman KJ, Greene CL, Grody WW, Highsmith WE, Hinkel CS, Kalman LV, Lubin IM, Lyon E, Payne DA, Pratt VM, Rohlfs E, Rundell CA, Schneider E, Willey AM, Williams LO, Willey JC, Winn-Deen ES, Wolff DJ. PMID: 16247292.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    112. Technical standards and guidelines: venous thromboembolism (Factor V Leiden and prothrombin 20210G >A testing): a disease-specific supplement to the standards and guidelines for clinical genetics laboratories. Genet Med. 2005 Jul-Aug; 7(6):444-53. Spector EB, Grody WW, Matteson CJ, Palomaki GE, Bellissimo DB, Wolff DJ, Bradley LA, Prior TW, Feldman G, Popovich BW, Watson MS, Richards CS. PMID: 16024978.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    113. Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation tests. Genet Med. 2005 May-Jun; 7(5):317-27. Ogino S, Flodman P, Wilson RB, Gold B, Grody WW. PMID: 15915083.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansPHPublic Health
    114. A novel method for creating artificial mutant samples for performance evaluation and quality control in clinical molecular genetics. J Mol Diagn. 2005 May; 7(2):247-51. Jarvis M, Iyer RK, Williams LO, Noll WW, Thomas K, Telatar M, Grody WW. PMID: 15858148; PMCID: PMC1867527.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    115. Genetic testing as part of the early hearing detection and intervention (EHDI) process. Genet Med. 2004 Nov-Dec; 6(6):521-5. Schimmenti LA, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Palmer CG. PMID: 15545749.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansPHPublic Health
    116. Cystic fibrosis mutation analysis: how many is enough? Genet Med. 2004 Sep-Oct; 6(5):456-8. Tsongalis GJ, Belloni DR, Grody WW. PMID: 15371913.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    117. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. Genet Med. 2004 Sep-Oct; 6(5):387-91. Watson MS, Cutting GR, Desnick RJ, Driscoll DA, Klinger K, Mennuti M, Palomaki GE, Popovich BW, Pratt VM, Rohlfs EM, Strom CM, Richards CS, Witt DR, Grody WW. PMID: 15371902; PMCID: PMC3110945.
      View in: PubMed   Mentions: 121     Fields:    Translation:Humans
    118. Bayesian analysis for cystic fibrosis risks in prenatal and carrier screening. Genet Med. 2004 Sep-Oct; 6(5):439-49. Ogino S, Wilson RB, Gold B, Hawley P, Grody WW. PMID: 15371910.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    119. Development and integration of molecular genetic tests into clinical practice: the US experience. Expert Rev Mol Diagn. 2004 Jul; 4(4):465-77. Amos J, Grody W. PMID: 15225094.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    120. Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation. J Med Genet. 2004 May; 41(5):e70. Ogino S, Wilson RB, Grody WW. PMID: 15121798; PMCID: PMC1735756.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    121. Arginases I and II: do their functions overlap? Mol Genet Metab. 2004 Apr; 81 Suppl 1:S38-44. Cederbaum SD, Yu H, Grody WW, Kern RM, Yoo P, Iyer RK. PMID: 15050972.
      View in: PubMed   Mentions: 62     Fields:    Translation:HumansAnimalsCells
    122. Prenatal screening for cystic fibrosis: past, present and future. Expert Rev Mol Diagn. 2004 Jan; 4(1):49-62. Richards CS, Grody WW. PMID: 14711349.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    123. Quest for controls in molecular genetics. J Mol Diagn. 2003 Nov; 5(4):209-11. Grody WW. PMID: 14573778; PMCID: PMC1907341.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    124. Estimated analytic validity of HFE C282Y mutation testing in population screening: the potential value of confirmatory testing. Genet Med. 2003 Nov-Dec; 5(6):440-3. Palomaki GE, Haddow JE, Bradley LA, Richards CS, Stenzel TT, Grody WW. PMID: 14614395.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    125. Widespread expression of arginase I in mouse tissues. Biochemical and physiological implications. J Histochem Cytochem. 2003 Sep; 51(9):1151-60. Yu H, Yoo PK, Aguirre CC, Tsoa RW, Kern RM, Grody WW, Cederbaum SD, Iyer RK. PMID: 12923240.
      View in: PubMed   Mentions: 26     Fields:    Translation:Animals
    126. Alternative approaches to proficiency testing in molecular genetics. Clin Chem. 2003 May; 49(5):717-8. Richards CS, Grody WW. PMID: 12709360.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    127. Cystic fibrosis mutations in Costa Rica. Hum Biol. 2003 Apr; 75(2):179-88. Venegas PB, Novak JM, Oscar CA, Sánchez FL, Gutiérrez IG, Rivera JM, Salas JP, Montero JF, Grody WW. PMID: 12943157.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    128. Ethical issues raised by genetic testing with oligonucleotide microarrays. Mol Biotechnol. 2003 Feb; 23(2):127-38. Grody WW. PMID: 12632697.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    129. Cystic fibrosis carrier screening: issues in implementation. Genet Med. 2002 Nov-Dec; 4(6):407-9. Watson MS, Desnick RJ, Grody WW, Mennuti MT, Popovich BW, Richards CS. PMID: 12509709.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    130. Standards and guidelines for CFTR mutation testing. Genet Med. 2002 Sep-Oct; 4(5):379-91. Richards CS, Bradley LA, Amos J, Allitto B, Grody WW, Maddalena A, McGinnis MJ, Prior TW, Popovich BW, Watson MS, Palomaki GE. PMID: 12394352.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    131. Mitoxantrone/ifosfamide/etoposide salvage regimen with rituximab for in vivo purging in patients with relapsed lymphoma. Clin Lymphoma. 2002 Sep; 3(2):111-6. Emmanouilides C, Lill M, Telatar M, Rosenfelt F, Grody W, Territo M, Rosen P. PMID: 12435284.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCellsCTClinical Trials
    132. Mouse model for human arginase deficiency. Mol Cell Biol. 2002 Jul; 22(13):4491-8. Iyer RK, Yoo PK, Kern RM, Rozengurt N, Tsoa R, O'Brien WE, Yu H, Grody WW, Cederbaum SD. PMID: 12052859; PMCID: PMC133904.
      View in: PubMed   Mentions: 71     Fields:    Translation:HumansAnimals
    133. Arginase expression in mouse embryonic development. Mech Dev. 2002 Jul; 115(1-2):151-5. Yu H, Iyer RK, Yoo PK, Kern RM, Grody WW, Cederbaum SD. PMID: 12049781.
      View in: PubMed   Mentions: 5     Fields:    Translation:AnimalsCells
    134. Discordant pursuit asymmetry and esotropia in monozygous twins. Am J Ophthalmol. 2002 Jul; 134(1):143-6. Sharma P, Rosenbaum AL, Vives T, Grody WW, Demer JL. PMID: 12095832.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    135. An electrochemical detection scheme for identification of single nucleotide polymorphisms using hairpin-forming probes. Nucleic Acids Res. 2002 Jun 15; 30(12):e55. Huang TJ, Liu M, Knight LD, Grody WW, Miller JF, Ho CM. PMID: 12060693; PMCID: PMC117297.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    136. Expression of the liver form of arginase in erythrocytes. Mol Genet Metab. 2002 Jun; 76(2):100-10. Kim PS, Iyer RK, Lu KV, Yu H, Karimi A, Kern RM, Tai DK, Cederbaum SD, Grody WW. PMID: 12083807.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    137. Cloning and characterization of human agmatinase. Mol Genet Metab. 2002 Mar; 75(3):209-18. Iyer RK, Kim HK, Tsoa RW, Grody WW, Cederbaum SD. PMID: 11914032.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansAnimalsCells
    138. Molecular genetic risk screening. Annu Rev Med. 2003; 54:473-90. Grody WW. PMID: 12525682.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    139. Expression of arginase isozymes in mouse brain. J Neurosci Res. 2001 Nov 01; 66(3):406-22. Yu H, Iyer RK, Kern RM, Rodriguez WI, Grody WW, Cederbaum SD. PMID: 11746358.
      View in: PubMed   Mentions: 22     Fields:    Translation:AnimalsCells
    140. Quality control in molecular genetic testing. Nat Rev Genet. 2001 09; 2(9):717-23. Dequeker E, Ramsden S, Grody WW, Stenzel TT, Barton DE. PMID: 11533720.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    141. Detection of bcl-2/IgH rearrangements by quantitative-competitive PCR and capillary electrophoresis. Mol Diagn. 2001 Sep; 6(3):161-8. Telatar M, Grody WW, Emmanouilides C. PMID: 11571709.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    142. A multiethnic study of Delta32ccr5 and ccr2b-V64I allele distribution in four Los Angeles populations. Diagn Mol Pathol. 2001 Jun; 10(2):105-10. Iyer RK, Kim PS, Bando JM, Lu KV, Gregg JP, Grody WW. PMID: 11385319.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    143. American College of Medical Genetics consensus statement on factor V Leiden mutation testing. Genet Med. 2001 Mar-Apr; 3(2):139-48. Grody WW, Griffin JH, Taylor AK, Korf BR, Heit JA, ACMG Factor V. Leiden Working Group. PMID: 11280951; PMCID: PMC3111091.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    144. Laboratory standards and guidelines for population-based cystic fibrosis carrier screening. Genet Med. 2001 Mar-Apr; 3(2):149-54. Grody WW, Cutting GR, Klinger KW, Richards CS, Watson MS, Desnick RJ, Subcommittee on Cystic Fibrosis Screening, Accreditation of Genetic Services Committee, ACMG. Ameri. PMID: 11280952.
      View in: PubMed   Mentions: 96     Fields:    Translation:Humans
    145. Cystic fibrosis population carrier screening: here at last--are we ready? Genet Med. 2001 Mar-Apr; 3(2):87-90. Grody WW, Desnick RJ. PMID: 11280954.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    146. Ethical ramifications of genetic analysis using DNA arrays. Methods Mol Biol. 2001; 170:53-69. Grody WW. PMID: 11357689.
      View in: PubMed   Mentions: 2     Fields:    
    147. In-frame deletions of BRCA1 may define critical functional domains. Hum Genet. 2000 Oct; 107(4):385-90. Rohlfs EM, Chung CH, Yang Q, Skrzynia C, Grody WW, Graham ML, Silverman LM. PMID: 11129340.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    148. Molecular genetic testing for familial Mediterranean fever. Mol Genet Metab. 2000 Sep-Oct; 71(1-2):256-60. Telatar M, Grody WW. PMID: 11001819.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    149. Excellent tolerance of rituximab when given after mitoxantrone/cyclophosphamide: an effective and safe combination for indolent non-Hodgkin's lymphoma. Clin Lymphoma. 2000 Sep; 1(2):146-51; discussion 152-3. Emmanouilides C, Rosen P, Telatar M, Malone R, Bosserman L, Menco H, Patel R, Barstis J, Grody WW. PMID: 11707827.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    150. Cystic fibrosis: molecular diagnosis, population screening, and public policy. Arch Pathol Lab Med. 1999 Nov; 123(11):1041-6. Grody WW. PMID: 10539904.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    151. Molecular pathology: role in improving patient outcome: Overview. Arch Pathol Lab Med. 1999 Nov; 123(11):1000-1. Stass SA, Grody WW. PMID: 10539895.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    152. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Nat Genet. 1999 Nov; 23(3):271-2. Noll WW, Belloni DR, Stenzel TT, Grody WW. PMID: 10610176.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    153. Issues in implementing prenatal screening for cystic fibrosis: results of a working conference. Genet Med. 1999 May-Jun; 1(4):129-35. Haddow JE, Bradley LA, Palomaki GE, Doherty RA, Bernhardt BA, Brock DJ, Cheuvront B, Cunningham GC, Donnenfeld AE, Erickson JL, Erlich HA, Ferrie RM, FitzSimmons SC, Greene MF, Grody WW, Haddow PK, Harris H, Holmes LB, Howell RR, Katz M, Klinger KW, Kloza EM, LeFevre ML, Little S, Loeben G, McGovern M, Pyeritz RE, Rowley PT, Saiki RK, Short MP, Tabone J, Wald NJ, Wilker NL, Witt DR. PMID: 11258347.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    154. Recommended policies for uses of human tissue in research, education, and quality control. Ad Hoc Committee on Stored Tissue, College of American Pathologists. Arch Pathol Lab Med. 1999 Apr; 123(4):296-300. Grizzle W, Grody WW, Noll WW, Sobel ME, Stass SA, Trainer T, Travers H, Weedn V, Woodruff K. PMID: 10320140.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    155. Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil. Hum Biol. 1999 Apr; 71(2):189-96. Cabello GM, Moreira AF, Horovitz D, Correia P, Santa Rosa A, Llerena J, Greg J, Grody WW, Degrave WM, Fernandes O, Cabello PH. PMID: 10222642.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansPHPublic Health
    156. Report card on molecular genetic testing: room for improvement? JAMA. 1999 Mar 03; 281(9):845-7. Grody WW, Pyeritz RE. PMID: 10071008.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    157. Immunohistochemical evaluation of K-ras, p53, and HER-2/neu expression in hyperplastic, dysplastic, and carcinomatous lesions of the pancreas: evidence for multistep carcinogenesis. Hum Pathol. 1999 Feb; 30(2):123-9. Apple SK, Hecht JR, Lewin DN, Jahromi SA, Grody WW, Nieberg RK. PMID: 10029438.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    158. Molecular temporal bone pathology: III. Genotyping of the deltaF508 deletion in the DNA of patients with cystic fibrosis. Laryngoscope. 1998 Aug; 108(8 Pt 2 Suppl 88):1-3. Wackym PA, Kerner MM, Grody WW. PMID: 9707259.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    159. Diversity of cystic fibrosis mutation-screening practices. Am J Hum Genet. 1998 May; 62(5):1252-4. Grody WW, Desnick RJ, Carpenter NJ, Noll WW. PMID: 9545412; PMCID: PMC1377099.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    160. Cloning and characterization of the mouse and rat type II arginase genes. Mol Genet Metab. 1998 Mar; 63(3):168-75. Iyer RK, Bando JM, Jenkinson CP, Vockley JG, Kim PS, Kern RM, Cederbaum SD, Grody WW. PMID: 9608538.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansAnimalsCells
    161. The human arginases and arginase deficiency. J Inherit Metab Dis. 1998; 21 Suppl 1:86-100. Iyer R, Jenkinson CP, Vockley JG, Kern RM, Grody WW, Cederbaum S. PMID: 9686347.
      View in: PubMed   Mentions: 42     Fields:    Translation:HumansAnimalsCells
    162. Prevalence of the factor V-Leiden mutation in four distinct American ethnic populations. Am J Med Genet. 1997 Dec 19; 73(3):334-6. Gregg JP, Yamane AJ, Grody WW. PMID: 9415695.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    163. Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia. Neurology. 1997 Oct; 49(4):1004-9. Geschwind DH, Perlman S, Grody WW, Telatar M, Montermini L, Pandolfo M, Gatti RA. PMID: 9339680.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    164. Diagnostic molecular genetics: current applications and future technologies. Pediatr Ann. 1997 Sep; 26(9):553-61. Gregg JP, Grody WW. PMID: 9302718.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    165. Those elusive molecular diagnostics CPT codes. Diagn Mol Pathol. 1997 Jun; 6(3):131-3. Grody WW, Watson MS. PMID: 9276183.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    166. PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population. Am J Hum Genet. 1997 Apr; 60(4):935-47. Grody WW, Dunkel-Schetter C, Tatsugawa ZH, Fox MA, Fang CY, Cantor RM, Novak JM, Bass HN, Crandall BF. PMID: 9106541; PMCID: PMC1712478.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    167. Demonstration of cytoplasmic tyrosinase mRNA in tissue-cultured cells by reverse transcription (RT) in situ polymerase chain reaction (PCR) and RT PCR in situ hybridization. Diagn Mol Pathol. 1997 Feb; 6(1):26-33. Li PX, Cheng L, Wen DR, Wissmann PB, Cheng J, Grody WW, Cochran AJ. PMID: 9028734.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    168. Donor origin of a posttransplant liver allograft malignancy identified by fluorescence in situ hybridization for the Y chromosome and DNA genotyping. Transplantation. 1997 Jan 15; 63(1):80-4. Donovan JA, Simmons FA, Esrason KT, Jamehdor M, Busuttil RW, Novak JM, Grody WW. PMID: 9000665.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    169. Attitudes toward genetic carrier screening for cystic fibrosis among pregnant women: the role of health beliefs and avoidant coping style. Womens Health. 1997; 3(1):31-51. Fang CY, Dunkel-Schetter C, Tatsugawa ZH, Fox MA, Bass HN, Crandall BF, Grody WW. PMID: 9106369.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    170. Cloning and characterization of the human type II arginase gene. Genomics. 1996 Dec 01; 38(2):118-23. Vockley JG, Jenkinson CP, Shukla H, Kern RM, Grody WW, Cederbaum SD. PMID: 8954792.
      View in: PubMed   Mentions: 51     Fields:    Translation:HumansAnimalsCells
    171. Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapy. Somat Cell Mol Genet. 1996 Nov; 22(6):489-98. Wissmann PB, Goodman BK, Vockley JG, Kern RM, Cederbaum SD, Grody WW. PMID: 9131018.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    172. Loss of function mutations in conserved regions of the human arginase I gene. Biochem Mol Med. 1996 Oct; 59(1):44-51. Vockley JG, Goodman BK, Tabor DE, Kern RM, Jenkinson CP, Grody WW, Cederbaum SD. PMID: 8902193.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansAnimalsCells
    173. Update on informed consent for stored tissue research. Diagn Mol Pathol. 1996 Jun; 5(2):79-80. Grody WW, Sobel ME. PMID: 8727093.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    174. Comparative properties of arginases. Comp Biochem Physiol B Biochem Mol Biol. 1996 May; 114(1):107-32. Jenkinson CP, Grody WW, Cederbaum SD. PMID: 8759304.
      View in: PubMed   Mentions: 136     Fields:    Translation:HumansAnimalsCells
    175. Molecular pathology 1995. Birth of an association [meeting report]. Diagn Mol Pathol. 1996 Mar; 5(1):1-2. Lovell MA, Grody WW. PMID: 8919538.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    176. Polymerase chain reaction-based K-ras mutation detection of pancreatic adenocarcinoma in routine cytology smears. Am J Clin Pathol. 1996 Mar; 105(3):321-6. Apple SK, Hecht JR, Novak JM, Nieberg RK, Rosenthal DL, Grody WW. PMID: 8602613.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    177. Molecular pathology, informed consent, and the paraffin block. Diagn Mol Pathol. 1995 Sep; 4(3):155-7. Grody WW. PMID: 7493133.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    178. Minimal or no cancer in radical prostatectomy specimens. Report of 13 cases of the "vanishing cancer phenomenon". Am J Surg Pathol. 1995 Sep; 19(9):1002-9. Goldstein NS, Bégin LR, Grody WW, Novak JM, Qian J, Bostwick DG. PMID: 7661273.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    179. Education and testing strategy for large-scale cystic fibrosis carrier screening. J Genet Couns. 1994 Dec; 3(4):279-89. Tatsugawa ZH, Fox MA, Fang CY, Novak JM, Cantor RM, Bass HN, Dunkel-Schetter C, Crandall BF, Grody WW. PMID: 24234134.
      View in: PubMed   Mentions: 1     Fields:    
    180. Proficiency testing in diagnostic molecular pathology. Diagn Mol Pathol. 1994 Dec; 3(4):221-3. Grody WW. PMID: 7866631.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    181. A de novo deletion in FMR1 in a patient with developmental delay. Hum Mol Genet. 1994 Sep; 3(9):1705-6. Gu Y, Lugenbeel KA, Vockley JG, Grody WW, Nelson DL. PMID: 7530551.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    182. The coming era of cancer genetic screening. Diagn Mol Pathol. 1994 Sep; 3(3):145-6. Grody WW. PMID: 7981888.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    183. Tumor necrosis factor-alpha plays a central role in interleukin-2-induced pulmonary vascular leak and lymphocyte accumulation. Cell Immunol. 1994 Aug; 157(1):170-80. Dubinett SM, Huang M, Lichtenstein A, McBride WH, Wang J, Markovitz G, Kelley D, Grody WW, Mintz LE, Dhanani S. PMID: 8039244.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    184. Functional and molecular analysis of liver arginase promoter sequences from man and Macaca fascicularis. Somat Cell Mol Genet. 1994 Jul; 20(4):313-25. Goodman BK, Klein D, Tabor DE, Vockley JG, Cederbaum SD, Grody WW. PMID: 7974006.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    185. DMP News and Comment. Diagn Mol Pathol. 1994 Jun; 3(2):71-3. Grody WW. PMID: 8061890.
      View in: PubMed   Mentions:    Fields:    
    186. Menstrual cycle and gonadal steroid effects on symptomatic hyperammonaemia of urea-cycle-based and idiopathic aetiologies. J Inherit Metab Dis. 1994; 17(5):566-74. Grody WW, Chang RJ, Panagiotis NM, Matz D, Cederbaum SD. PMID: 7837763.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    187. Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia. Hum Mutat. 1994; 4(2):150-4. Vockley JG, Tabor DE, Kern RM, Goodman BK, Wissmann PB, Kang DS, Grody WW, Cederbaum SD. PMID: 7981719.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    188. PCR-based cystic fibrosis (CF) carrier screening in a first-year medical student biochemistry laboratory. Am J Hum Genet. 1993 Dec; 53(6):1352-5. Grody WW, Kronquist KE, Lee EU, Edmond J, Rome LH. PMID: 8250051; PMCID: PMC1682492.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    189. Molecular genetics. Introduction. Arch Pathol Lab Med. 1993 May; 117(5):470-2. Grody WW. PMID: 8489333.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    190. Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme. Hum Genet. 1993 Mar; 91(1):1-5. Grody WW, Kern RM, Klein D, Dodson AE, Wissman PB, Barsky SH, Cederbaum SD. PMID: 8454280.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    191. In situ regulation of pulmonary macrophage TNF-alpha mRNA expression by IL2. Chest. 1993 Feb; 103(2 Suppl):91S-94S. Dubinett SM, Huang M, Dhanani S, Kelley D, Lichtenstein A, Grody WW, Mintz LE. PMID: 8428548.
      View in: PubMed   Mentions:    Fields:    Translation:AnimalsCells
    192. Pitfalls of restriction endonuclease digestion for direct detection of point mutations. Clin Chem. 1992 Jul; 38(7):1392-4. Klein D, Grody WW, Tabor DE, Cederbaum SD. PMID: 1320472.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    193. Molecular genetic study of human arginase deficiency. Am J Hum Genet. 1992 Jun; 50(6):1281-90. Grody WW, Klein D, Dodson AE, Kern RM, Wissmann PB, Goodman BK, Bassand P, Marescau B, Kang SS, Leonard JV, et al. PMID: 1598908; PMCID: PMC1682550.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    194. AIDS and the heart: Review and consideration of pathogenetic mechanisms. Cardiovasc Pathol. 1992 Jan-Mar; 1(1):53-64. Lewis W, Grody WW. PMID: 25990037.
      View in: PubMed   Mentions: 2     Fields:    
    195. Effect of an adjacent base on detection of a point mutation by restriction enzyme digestion. Somat Cell Mol Genet. 1991 Jul; 17(4):369-75. Klein D, Dodson AE, Tabor DE, Cederbaum SD, Grody WW. PMID: 1887333.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    196. Rapid diagnosis of Legionella infection by a nonisotopic in situ hybridization method. Am J Clin Pathol. 1991 May; 95(5):719-24. Fain JS, Bryan RN, Cheng L, Lewin KJ, Porter DD, Grody WW. PMID: 2024627.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    197. Infection of the heart by the human immunodeficiency virus. Am J Cardiol. 1990 Jul 15; 66(2):203-6. Grody WW, Cheng L, Lewis W. PMID: 2371952.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansCells
    198. Genetic linkage group (ARG1-D6S33-MYB) on chromosome 6q containing the arginase-1 and MYB genes. Cytogenet Cell Genet. 1990; 54(1-2):95-6. Nguyen J, Charmley P, Grody WW, Cederbaum SD, King MC, Gatti RA. PMID: 1979025.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    199. Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysis. J Clin Invest. 1989 Feb; 83(2):602-9. Grody WW, Argyle C, Kern RM, Dizikes GJ, Spector EB, Strickland AD, Klein D, Cederbaum SD. PMID: 2913054; PMCID: PMC303720.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    200. Detection of human immunodeficiency virus (HIV) infection in formalin-fixed, paraffin-embedded tissues by DNA amplification. Nucleic Acids Res. 1988 Aug 25; 16(16):8191. Lai-Goldman M, Lai E, Grody WW. PMID: 3419916; PMCID: PMC338535.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    201. Human arginase isozymes. Isozymes Curr Top Biol Med Res. 1987; 13:181-214. Grody WW, Dizikes GJ, Cederbaum SD. PMID: 3583682.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    202. A PvuII RFLP for the human liver arginase (ARG1) gene. Nucleic Acids Res. 1986 Dec 09; 14(23):9544. Kidd JR, Dizikes GJ, Grody WW, Cederbaum SD, Kidd KK. PMID: 2879271; PMCID: PMC311993.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    203. Isolation of human liver arginase cDNA and demonstration of nonhomology between the two human arginase genes. Biochem Biophys Res Commun. 1986 Nov 26; 141(1):53-9. Dizikes GJ, Grody WW, Kern RM, Cederbaum SD. PMID: 3801008.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    204. Pathologic evaluation of thymic hyperplasia in myasthenia gravis and Lambert-Eaton myasthenic syndrome. Arch Pathol Lab Med. 1986 Sep; 110(9):843-6. Grody WW, Jobst S, Keesey J, Herrmann C, Naeim F. PMID: 3755894.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    205. The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23. Am J Hum Genet. 1986 Aug; 39(2):186-93. Sparkes RS, Dizikes GJ, Klisak I, Grody WW, Mohandas T, Heinzmann C, Zollman S, Lusis AJ, Cederbaum SD. PMID: 3752085; PMCID: PMC1683935.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
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