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Wayne W Grody

Title(s)Professor, Pathology and Laboratory Medicine
SchoolMedicine
Address760 Westwood Plaza A3-251
Los Angeles CA 90024
Phone55648
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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/NICHD R01HD029337Sep 30, 1991 - Aug 31, 1995
    Role: Principal Investigator
    GENE TRANSFER OF HUMAN ARGINASE
    NIH/NICHD 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. Gene-environment regulation of chamber-specific maturation during hypoxemic perinatal circulatory transition. J Mol Med (Berl). 2020 Jul; 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, Van Arsdell G, Nelson SF, Touma M. PMID: 32533200.
      View in: PubMed   Mentions:    Fields:    
    2. 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 Aug; 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.
      View in: PubMed   Mentions: 2     Fields:    
    3. CFTR variant testing: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2020 Aug; 22(8):1288-1295. Deignan JL, Astbury C, Cutting GR, Del Gaudio D, Gregg AR, Grody WW, Monaghan KG, Richards S. PMID: 32404922.
      View in: PubMed   Mentions:    Fields:    
    4. 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.
      View in: PubMed   Mentions:
    5. 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.
      View in: PubMed   Mentions: 3     Fields:    
    6. 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.
      View in: PubMed   Mentions: 1     Fields:    
    7. 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:    Fields:    Translation:Humans
    8. 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.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    9. 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.
      View in: PubMed   Mentions:    Fields:    Translation:HumansPHPublic Health
    10. 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. PMID: 29543230.
      View in: PubMed   Mentions:    Fields:    
    11. 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.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCTClinical Trials
    12. Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis. . 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:
    13. The Value of T-Cell Receptor ? (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:    
    14. 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: 1     Fields:    Translation:Humans
    15. 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: 10     Fields:    
    16. 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, Kantarci S, Blumberg B, Grody WW, Strom SP. PMID: 28588821.
      View in: PubMed   Mentions:
    17. 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
    18. 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
    19. 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.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    20. 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: 10     Fields:    Translation:Humans
    21. 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: 52     Fields:    Translation:Humans
    22. Prenatal Carrier Screening-Reply. JAMA. 2016 12 27; 316(24):2676-2677. Grody WW. PMID: 28027361.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    23. 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.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    24. 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.
      View in: PubMed   Mentions:
    25. 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: 5     Fields:    Translation:Humans
    26. 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
    27. 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
    28. 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: 1     Fields:    Translation:Humans
    29. 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.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    30. 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. PMID: 25741868.
      View in: PubMed   Mentions: 3307     Fields:    Translation:Humans
    31. 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.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    32. 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, Grody WW, Vilain E, Nelson SF. PMID: 25728775.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    33. 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.
      View in: PubMed   Mentions: 289     Fields:    Translation:Humans
    34. 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.
      View in: PubMed   Mentions: 75     Fields:    Translation:Humans
    35. 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: 86     Fields:    Translation:Humans
    36. 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
    37. 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.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimalsCells
    38. 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
    39. 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.
      View in: PubMed   Mentions: 42     Fields:    Translation:Humans
    40. 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: 12     Fields:    Translation:Humans
    41. 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
    42. 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.
      View in: PubMed   Mentions: 14     Fields:    Translation:Animals
    43. 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.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    44. 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. PMID: 23788249.
      View in: PubMed   Mentions: 826     Fields:    Translation:Humans
    45. 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: 51     Fields:    Translation:Humans
    46. 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.
      View in: PubMed   Mentions:
    47. 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.
      View in: PubMed   Mentions: 49     Fields:    Translation:Humans
    48. 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. PMID: 22753370.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    49. 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.
      View in: PubMed   Mentions: 19     Fields:    Translation:AnimalsCells
    50. 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.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    51. 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.
      View in: PubMed   Mentions: 84     Fields:    Translation:Humans
    52. 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.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    53. 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
    54. 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.
      View in: PubMed   Mentions: 118     Fields:    Translation:HumansCellsCTClinical Trials
    55. 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
    56. 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: 164     Fields:    Translation:HumansCTClinical Trials
    57. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    58. 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: 9     Fields:    Translation:Humans
    59. 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
    60. 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
    61. 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.
      View in: PubMed   Mentions: 38     Fields:    Translation:AnimalsCells
    62. 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: 20     Fields:    Translation:HumansPHPublic Health
    63. Genetics in Hollywood: from real to reel. Clin Genet. 2010 Feb; 77(2):106-11. Grody WW. PMID: 20096067.
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    64. 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.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    65. 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.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    66. 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.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    67. Cystic fibrosis testing comes of age. J Mol Diagn. 2009 May; 11(3):173-5. Grody WW. PMID: 19359497.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    68. 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.
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    69. 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.
      View in: PubMed   Mentions: 60     Fields:    Translation:HumansCells
    70. 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
    71. 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
    72. 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
    73. 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. PMID: 18414213.
      View in: PubMed   Mentions: 281     Fields:    Translation:HumansCells
    74. 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: 17     Fields:    Translation:HumansCells
    75. 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: 12     Fields:    Translation:HumansAnimals
    76. 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
    77. 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.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansAnimals
    78. 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: 9     Fields:    Translation:Humans
    79. Polyamine homeostasis in arginase knockout mice. . 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.
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    80. 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: 7     Fields:    Translation:Humans
    81. 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: 3     Fields:    Translation:HumansCells
    82. 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: 23     Fields:    Translation:AnimalsCells
    83. 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: 3     Fields:    Translation:HumansCells
    84. 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
    85. 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: 13     Fields:    Translation:Humans
    86. 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. PMID: 16247296.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    87. 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
    88. 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
    89. 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.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    90. 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: 6     Fields:    Translation:HumansPHPublic Health
    91. 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.
      View in: PubMed   Mentions: 108     Fields:    Translation:Humans
    92. 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
    93. 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
    94. 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: 59     Fields:    Translation:HumansAnimalsCells
    95. 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
    96. Quest for controls in molecular genetics. J Mol Diagn. 2003 Nov; 5(4):209-11. Grody WW. PMID: 14573778.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    97. 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
    98. 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: 25     Fields:    Translation:Animals
    99. 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
    100. 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
    101. 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: 5     Fields:    Translation:Humans
    102. 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
    103. 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
    104. 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
    105. 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.
      View in: PubMed   Mentions: 68     Fields:    Translation:HumansAnimals
    106. 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
    107. 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.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    108. 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
    109. 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: 19     Fields:    Translation:HumansAnimalsCells
    110. Molecular genetic risk screening. Annu Rev Med. 2003; 54:473-90. Grody WW. PMID: 12525682.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
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