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Grody Wayne

Title(s)Professor, Pathology and Laboratory Medicine
Phone(310) 825-5648
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    Other Positions
    Title(s)Professor, Human Genetics

    Title(s)Professor, Pediatrics

    Title(s)Director, Orphan Disease Testing Center

    Title(s)Chief, Molecular Pathology

    Title(s)Chief, Molecular Pathology Cytogenetics and Orphan Disease


    Collapse Research 
    Collapse Research Activities and Funding
    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

    Collapse Bibliographic 
    Collapse Publications
    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.
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    1. 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. International perspectives on the implementation of reproductive carrier screening. Prenat Diagn. 2019 Nov 27. PMID: 31774570.
      View in: PubMed
    2. Eno CC, Barton SK, Dorrani N, Cederbaum SD, Deignan JL, Grody WW. Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centers. Mol Genet Genomic Med. 2019 Nov 07; e1026. PMID: 31701651.
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    3. 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. A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders. Hum Mutat. 2019 Nov 06. PMID: 31692161.
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    4. Grody WW. The transformation of medical genetics by clinical genomics: hubris meets humility. Genet Med. 2019 Sep; 21(9):1916-1926. PMID: 30842646.
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    5. Jacob N, Dasharathy SS, Bui V, Benhammou JN, Grody WW, Singh RR, Pisegna JR. Generalized Cytokine Increase in the Setting of a Multisystem Clinical Disorder and Carcinoid Syndrome Associated with a Novel NLRP12 Variant. Dig Dis Sci. 2019 Aug; 64(8):2140-2146. PMID: 30788684.
      View in: PubMed
    6. 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. Home use of a compact, 12-lead ECG recording system for newborns. J Electrocardiol. 2019 Mar - Apr; 53:89-94. PMID: 30716528.
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    7. 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. Response to Biesecker and Harrison. Genet Med. 2018 12; 20(12):1689-1690. PMID: 29543230.
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    8. 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. Electric Field-Induced Release and Measurement Liquid Biopsy for Noninvasive Early Lung Cancer Assessment. J Mol Diagn. 2018 11; 20(6):738-742. PMID: 30309763.
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    9. 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. 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. PMID: 30244526.
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    10. Kansal R, Grody WW, Zhou J, Dong L, Li X. The Value of T-Cell Receptor ? (TRG) Clonality Evaluation by Next-Generation Sequencing in Clinical Hematolymphoid Tissues: A Descriptive Study of 41 Cases From a Single Institution. Am J Clin Pathol. 2018 Jul 05. PMID: 29982316.
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    11. 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. 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). PMID: 28933790.
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    12. 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. The Case for Laboratory Developed Procedures: Quality and Positive Impact on Patient Care. Acad Pathol. 2017 Jan-Dec; 4:2374289517708309. PMID: 28815200.
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    13. 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. CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med. 2017 05; 19(5):606. PMID: 28492529.
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    14. Mullegama SV, Jensik P, Li C, Dorrani N, Kantarci S, Blumberg B, Grody WW, Strom SP. 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. PMID: 28588821.
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    15. 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. Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. J Womens Health (Larchmt). 2017 07; 26(7):755-761. PMID: 28388340.
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    16. 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. 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. PMID: 28350513.
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    17. 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. 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. PMID: 28165284.
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    18. 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. 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. PMID: 28185757.
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    19. 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. 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. PMID: 28165299.
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    20. 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. Molecular Biomarkers for the Evaluation of Colorectal Cancer. Am J Clin Pathol. 2017 Feb 03. PMID: 28165529.
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    21. Grody WW. Prenatal Carrier Screening-Reply. JAMA. 2016 12 27; 316(24):2676-2677. PMID: 28027361.
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    22. Benhammou JN, Phan J, Lee H, Ghassemi K, Parsons W, Grody WW, Pisegna JR. 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. PMID: 28012096.
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    23. 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. Missense-depleted regions in population exomes implicate ras superfamily nucleotide-binding protein alteration in patients with brain malformation. NPJ Genom Med. 2016; 1. PMID: 28868155.
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    24. Grody WW. Where to Draw the Boundaries for Prenatal Carrier Screening. JAMA. 2016 Aug 16; 316(7):717-9. PMID: 27533155.
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    25. Grody WW. The next generation of cancer management. Cancer Biol Med. 2016 Mar; 13(1):1-2. PMID: 27144057.
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    26. Mooney KL, Choy W, Woodard J, Xian RR, Deal TM, Kendle RF, Said J, Grody W, Yang I. Primary central nervous system gamma delta cytotoxic T-cell lymphoma. J Clin Neurosci. 2016 Apr; 26:138-40. PMID: 26804925.
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    27. Deignan JL, Grody WW. Molecular Diagnosis of Cystic Fibrosis. Curr Protoc Hum Genet. 2016 Jan 01; 88:Unit 9.28. PMID: 26724724.
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    28. 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. 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. PMID: 26542077.
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    29. 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. 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. PMID: 25944381.
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    30. Cherukuri DP, Deignan JL, Das K, Grody WW, Herschman H. 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. PMID: 25817443.
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    31. 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. 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. PMID: 25741868.
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    32. 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. 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. PMID: 25728775.
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    33. 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. Clinical exome sequencing for genetic identification of rare Mendelian disorders. JAMA. 2014 Nov 12; 312(18):1880-7. PMID: 25326637.
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    34. 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. Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia. JAMA Neurol. 2014 Oct; 71(10):1237-46. PMID: 25133958.
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    35. 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. College of American Pathologists' laboratory standards for next-generation sequencing clinical tests. Arch Pathol Lab Med. 2015 Apr; 139(4):481-93. PMID: 25152313.
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    36. Grody WW, Vilain E, Nelson SF. Interpreting whole-genome sequencing. JAMA. 2014 Jul 16; 312(3):296. PMID: 25027151.
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    37. Hu C, Kasten J, Park H, Bhargava R, Tai DS, Grody WW, Nguyen QG, Hauschka SD, Cederbaum SD, Lipshutz GS. Myocyte-mediated arginase expression controls hyperargininemia but not hyperammonemia in arginase-deficient mice. Mol Ther. 2014 Oct; 22(10):1792-802. PMID: 24888478.
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    38. 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. 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. PMID: 24886118.
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    39. Loh JC, Cassarino DS, Grody WW, Chiu MW, Pinter-Brown LC. 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. PMID: 24637131.
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    40. Strom SP, Lee H, Das K, Vilain E, Nelson SF, Grody WW, Deignan JL. Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory. Genet Med. 2014 Jul; 16(7):510-5. PMID: 24406459.
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    41. Grody WW, Thompson BH, Hudgins L. Whole-exome/genome sequencing and genomics. Pediatrics. 2013 Dec; 132(Suppl 3):S211-5. PMID: 24298129.
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    42. Massie J, Castellani C, Grody WW. Carrier screening for cystic fibrosis in the new era of medications that restore CFTR function. Lancet. 2014 Mar 08; 383(9920):923-5. PMID: 23992917.
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    43. 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. Lethal phenotype in conditional late-onset arginase 1 deficiency in the mouse. Mol Genet Metab. 2013 Nov; 110(3):222-30. PMID: 23920045.
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    44. Kalman LV, Lubin IM, Barker S, du Sart D, Elles R, Grody WW, Pazzagli M, Richards S, Schrijver I, Zehnbauer B. 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. PMID: 23808472.
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    45. 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. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med. 2013 Jul; 15(7):565-74. PMID: 23788249.
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    46. Grody WW, Thompson BH, Gregg AR, Bean LH, Monaghan KG, Schneider A, Lebo RV. ACMG position statement on prenatal/preconception expanded carrier screening. Genet Med. 2013 Jun; 15(6):482-3. PMID: 23619275.
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    47. Palmer CG, Boudreault P, Baldwin EE, Fox M, Deignan JL, Kobayashi Y, Sininger Y, Grody W, Sinsheimer JS. Deaf genetic testing and psychological well-being in deaf adults. J Genet Couns. 2013 Aug; 22(4):492-507. PMID: 23430402.
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    48. 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. AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouse. Gene Ther. 2013 Aug; 20(8):785-96. PMID: 23388701.
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    49. Bavisetty S, Grody WW, Yazdani S. Emergence of pediatric rare diseases: Review of present policies and opportunities for improvement. Rare Dis. 2013; 1:e23579. PMID: 25002987.
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    50. Ong FS, Kuo JZ, Wu WC, Cheng CY, Blackwell WL, Taylor BL, Grody WW, Rotter JI, Lai CC, Wong TY. Personalized Medicine in Ophthalmology: From Pharmacogenetic Biomarkers to Therapeutic and Dosage Optimization. J Pers Med. 2013; 3(1):40-69. PMID: 24624293.
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    51. 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. 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. PMID: 23038988.
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    52. 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. 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. PMID: 22918138.
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    53. 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. Human Variome Project country nodes: documenting genetic information within a country. Hum Mutat. 2012 Nov; 33(11):1513-9. PMID: 22753370.
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    54. Lee EK, Hu C, Bhargava R, Rozengurt N, Stout D, Grody WW, Cederbaum SD, Lipshutz GS. Long-term survival of the juvenile lethal arginase-deficient mouse with AAV gene therapy. Mol Ther. 2012 Oct; 20(10):1844-51. PMID: 22760543.
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    55. Ong FS, Das K, Wang J, Vakil H, Kuo JZ, Blackwell WL, Lim SW, Goodarzi MO, Bernstein KE, Rotter JI, Grody WW. Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing. Expert Rev Mol Diagn. 2012 Jul; 12(6):593-602. PMID: 22845480.
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    56. Arboleda VA, Lee H, Sánchez FJ, Délot EC, Sandberg DE, Grody WW, Nelson SF, Vilain E. Targeted massively parallel sequencing provides comprehensive genetic diagnosis for patients with disorders of sex development. Clin Genet. 2013 Jan; 83(1):35-43. PMID: 22435390.
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    57. 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. Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med. 2012 Apr; 14(4):405-10. PMID: 22422049.
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    58. Dry S, Grody WW, Papagni P. 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. PMID: 22338046.
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    59. Ong FS, Deignan JL, Kuo JZ, Bernstein KE, Rotter JI, Grody WW, Das K. Clinical utility of pharmacogenetic biomarkers in cardiovascular therapeutics: a challenge for clinical implementation. Pharmacogenomics. 2012 Mar; 13(4):465-75. PMID: 22380001.
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    60. 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. 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. PMID: 22281937.
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    61. Grody WW. Expanded carrier screening and the law of unintended consequences: from cystic fibrosis to fragile X. Genet Med. 2011 Dec; 13(12):996-7. PMID: 22134443.
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    62. 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. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study. Genet Med. 2011 Nov; 13(11):913-20. PMID: 22005709.
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    63. Ong FS, Grody WW, Deignan JL. Privacy and data management in the era of massively parallel next-generation sequencing. Expert Rev Mol Diagn. 2011 Jun; 11(5):457-9. PMID: 21707452.
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    64. Zadeh N, Getzug T, Grody WW. Diagnosis and management of familial Mediterranean fever: integrating medical genetics in a dedicated interdisciplinary clinic. Genet Med. 2011 Mar; 13(3):263-9. PMID: 21317656.
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    65. Deignan JL, Grody WW. Ordering genetic tests and interpreting the results. Adv Otorhinolaryngol. 2011; 70:18-24. PMID: 21358180.
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    66. Grody WW, Getzug T. Colchicine's other indication--effect of FDA action. N Engl J Med. 2010 Dec 02; 363(23):2267-8. PMID: 21121853.
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    67. Quintero-Rivera F, Deignan JL, Peredo J, Grody WW, Crandall B, Sims M, Cederbaum SD. 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. PMID: 20817516.
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    68. Bender L, Silverman LM, Dinulos MB, Nickel J, Grody WW. Direct-to-consumer genotyping: are we ready for a brave new world? Clin Chem. 2010 Jul; 56(7):1056-60. PMID: 20511451.
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    69. Wehling-Henricks M, Jordan MC, Gotoh T, Grody WW, Roos KP, Tidball JG. Arginine metabolism by macrophages promotes cardiac and muscle fibrosis in mdx muscular dystrophy. PLoS One. 2010 May 21; 5(5):e10763. PMID: 20505827.
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    70. Boudreault P, Baldwin EE, Fox M, Dutton L, Tullis L, Linden J, Kobayashi Y, Zhou J, Sinsheimer JS, Sininger Y, Grody WW, Palmer CG. 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. PMID: 20488870.
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    71. 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. Benchmarks for cystic fibrosis carrier screening: a European consensus document. J Cyst Fibros. 2010 May; 9(3):165-78. PMID: 20363197.
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    72. Grody WW, Howell RR. The fate of newborn screening blood spots. Pediatr Res. 2010 Mar; 67(3):237. PMID: 20154576.
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    73. Grody WW. Genetics in Hollywood: from real to reel. Clin Genet. 2010 Feb; 77(2):106-11. PMID: 20096067.
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    74. 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. Development and characterization of reference materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 genetic testing. J Mol Diagn. 2009 Nov; 11(6):553-61. PMID: 19767587.
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    75. Rosove MH, Grody WW. Should we be applying warfarin pharmacogenetics to clinical practice? No, not now. Ann Intern Med. 2009 Aug 18; 151(4):270-3, W95. PMID: 19687493.
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    76. Palmer CG, Martinez A, Fox M, Zhou J, Shapiro N, Sininger Y, Grody WW, Schimmenti LA. 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. PMID: 19449415.
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    77. Gau CL, Rosenblatt RA, Cerullo V, Lay FD, Dow AC, Livesay J, Brunetti-Pierri N, Lee B, Cederbaum SD, Grody WW, Lipshutz GS. 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. PMID: 19367256.
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    78. Grody WW. Cystic fibrosis testing comes of age. J Mol Diagn. 2009 May; 11(3):173-5. PMID: 19359497.
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    79. Pullarkat ST, Pullarkat V, Kroft SH, Wilson CS, Ahsanuddin AN, Mann KP, Thein M, Grody WW, Brynes RK. Systemic mastocytosis associated with t(8;21)(q22;q22) acute myeloid leukemia. J Hematop. 2009 Mar; 2(1):27-33. PMID: 19669220.
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    80. ten Bosch JR, Grody WW. Keeping up with the next generation: massively parallel sequencing in clinical diagnostics. J Mol Diagn. 2008 Nov; 10(6):484-92. PMID: 18832462.
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    81. Mumenthaler SM, Rozengurt N, Livesay JC, Sabaghian A, Cederbaum SD, Grody WW. Disruption of arginase II alters prostate tumor formation in TRAMP mice. Prostate. 2008 Oct 01; 68(14):1561-9. PMID: 18663728.
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    82. Schimmenti LA, Martinez A, Telatar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody WW, Palmer CG. Infant hearing loss and connexin testing in a diverse population. Genet Med. 2008 Jul; 10(7):517-24. PMID: 18580690.
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    83. Grody WW, Richards CS. New quality assurance standards for rare disease testing. Genet Med. 2008 May; 10(5):320-4. PMID: 18496029.
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    84. Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE. ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007. Genet Med. 2008 Apr; 10(4):294-300. PMID: 18414213.
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    85. Mumenthaler SM, Yu H, Tze S, Cederbaum SD, Pegg AE, Seligson DB, Grody WW. Expression of arginase II in prostate cancer. Int J Oncol. 2008 Feb; 32(2):357-65. PMID: 18202758.
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    86. Deignan JL, Marescau B, Livesay JC, Iyer RK, De Deyn PP, Cederbaum SD, Grody WW. Increased plasma and tissue guanidino compounds in a mouse model of hyperargininemia. Mol Genet Metab. 2008 Feb; 93(2):172-8. PMID: 17997338.
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    87. Grody WW, Cutting GR, Watson MS. The Cystic Fibrosis mutation "arms race": when less is more. Genet Med. 2007 Nov; 9(11):739-44. PMID: 18007142.
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    88. Deignan JL, Cederbaum SD, Grody WW. Contrasting features of urea cycle disorders in human patients and knockout mouse models. Mol Genet Metab. 2008 Jan; 93(1):7-14. PMID: 17933574.
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    89. Palmer CG, Martinez A, Fox M, Sininger Y, Grody WW, Schimmenti LA. Ethnic differences in parental perceptions of genetic testing for deaf infants. J Genet Couns. 2008 Feb; 17(1):129-38. PMID: 17952575.
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    90. Deignan JL, Livesay JC, Shantz LM, Pegg AE, O'Brien WE, Iyer RK, Cederbaum SD, Grody WW. Polyamine homeostasis in arginase knockout mice. Am J Physiol Cell Physiol. 2007 Oct; 293(4):C1296-301. PMID: 17686999.
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    91. Blase T, Martinez A, Grody WW, Schimmenti L, Palmer CG. Sharing GJB2/GJB6 genetic test information with family members. J Genet Couns. 2007 Jun; 16(3):313-24. PMID: 17318457.
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    92. Lebo RV, Grody WW. Testing and reporting ACMG cystic fibrosis mutation panel results. Genet Test. 2007; 11(1):11-31. PMID: 17394390.
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    93. Lebo RV, Grody WW. Variable penetrance and expressivity of the splice altering 5T sequence in the cystic fibrosis gene. Genet Test. 2007; 11(1):32-44. PMID: 17394391.
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    94. Elshimali YI, Grody WW. The clinical significance of circulating tumor cells in the peripheral blood. Diagn Mol Pathol. 2006 Dec; 15(4):187-94. PMID: 17122646.
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    95. Kern RM, Yang Z, Kim PS, Grody WW, Iyer RK, Cederbaum SD. Arginase induction by sodium phenylbutyrate in mouse tissues and human cell lines. Mol Genet Metab. 2007 Jan; 90(1):37-41. PMID: 16935537.
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    96. Deignan JL, Livesay JC, Yoo PK, Goodman SI, O'Brien WE, Iyer RK, Cederbaum SD, Grody WW. Ornithine deficiency in the arginase double knockout mouse. Mol Genet Metab. 2006 Sep-Oct; 89(1-2):87-96. PMID: 16753325.
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    97. Keen-Kim D, Grody WW, Richards CS. Microelectronic array system for molecular diagnostic genotyping: Nanogen NanoChip 400 and molecular biology workstation. Expert Rev Mol Diagn. 2006 May; 6(3):287-94. PMID: 16706733.
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    98. Ramsden SC, Deans Z, Robinson DO, Mountford R, Sistermans EA, Grody WW, McQuaid S, Patton SJ, Stenhouse SA. Monitoring standards for molecular genetic testing in the United Kingdom, the Netherlands, and Ireland. Genet Test. 2006; 10(3):147-56. PMID: 17020464.
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    99. Palmer CG, Martinez A, Sininger Y, Shapiro N, Grody WW, Schimmenti LA. Prelingual siblings of children with GJB2 hearing loss: issues to consider. Arch Otolaryngol Head Neck Surg. 2005 Nov; 131(11):1020-2. PMID: 16301377.
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    100. 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. Developing a sustainable process to provide quality control materials for genetic testing. Genet Med. 2005 Oct; 7(8):534-49. PMID: 16247292.
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    101. Maddalena A, Bale S, Das S, Grody W, Richards S. Technical standards and guidelines: molecular genetic testing for ultra-rare disorders. Genet Med. 2005 Oct; 7(8):571-83. PMID: 16247296.
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    102. Spector EB, Grody WW, Matteson CJ, Palomaki GE, Bellissimo DB, Wolff DJ, Bradley LA, Prior TW, Feldman G, Popovich BW, Watson MS, Richards CS. 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. PMID: 16024978.
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    103. Jarvis M, Iyer RK, Williams LO, Noll WW, Thomas K, Telatar M, Grody WW. 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. PMID: 15858148.
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    104. Ogino S, Flodman P, Wilson RB, Gold B, Grody WW. Risk calculations for cystic fibrosis in neonatal screening by immunoreactive trypsinogen and CFTR mutation tests. Genet Med. 2005 May-Jun; 7(5):317-27. PMID: 15915083.
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    105. Schimmenti LA, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Palmer CG. Genetic testing as part of the early hearing detection and intervention (EHDI) process. Genet Med. 2004 Nov-Dec; 6(6):521-5. PMID: 15545749.
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    106. Ogino S, Wilson RB, Gold B, Hawley P, Grody WW. Bayesian analysis for cystic fibrosis risks in prenatal and carrier screening. Genet Med. 2004 Sep-Oct; 6(5):439-49. PMID: 15371910.
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    107. 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. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. Genet Med. 2004 Sep-Oct; 6(5):387-91. PMID: 15371902.
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    108. Tsongalis GJ, Belloni DR, Grody WW. Cystic fibrosis mutation analysis: how many is enough? Genet Med. 2004 Sep-Oct; 6(5):456-8. PMID: 15371913.
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    109. Amos J, Grody W. Development and integration of molecular genetic tests into clinical practice: the US experience. Expert Rev Mol Diagn. 2004 Jul; 4(4):465-77. PMID: 15225094.
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    110. Ogino S, Wilson RB, Grody WW. 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. PMID: 15121798.
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    111. Cederbaum SD, Yu H, Grody WW, Kern RM, Yoo P, Iyer RK. Arginases I and II: do their functions overlap? Mol Genet Metab. 2004 Apr; 81 Suppl 1:S38-44. PMID: 15050972.
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    112. Richards CS, Grody WW. Prenatal screening for cystic fibrosis: past, present and future. Expert Rev Mol Diagn. 2004 Jan; 4(1):49-62. PMID: 14711349.
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    113. Palomaki GE, Haddow JE, Bradley LA, Richards CS, Stenzel TT, Grody WW. 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. PMID: 14614395.
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    114. Grody WW. Quest for controls in molecular genetics. J Mol Diagn. 2003 Nov; 5(4):209-11. PMID: 14573778.
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    115. Yu H, Yoo PK, Aguirre CC, Tsoa RW, Kern RM, Grody WW, Cederbaum SD, Iyer RK. Widespread expression of arginase I in mouse tissues. Biochemical and physiological implications. J Histochem Cytochem. 2003 Sep; 51(9):1151-60. PMID: 12923240.
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    116. Richards CS, Grody WW. Alternative approaches to proficiency testing in molecular genetics. Clin Chem. 2003 May; 49(5):717-8. PMID: 12709360.
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    117. Venegas PB, Novak JM, Oscar CA, Sánchez FL, Gutiérrez IG, Rivera JM, Salas JP, Montero JF, Grody WW. Cystic fibrosis mutations in Costa Rica. Hum Biol. 2003 Apr; 75(2):179-88. PMID: 12943157.
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    118. Grody WW. Ethical issues raised by genetic testing with oligonucleotide microarrays. Mol Biotechnol. 2003 Feb; 23(2):127-38. PMID: 12632697.
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    119. Watson MS, Desnick RJ, Grody WW, Mennuti MT, Popovich BW, Richards CS. Cystic fibrosis carrier screening: issues in implementation. Genet Med. 2002 Nov-Dec; 4(6):407-9. PMID: 12509709.
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    120. Emmanouilides C, Lill M, Telatar M, Rosenfelt F, Grody W, Territo M, Rosen P. Mitoxantrone/ifosfamide/etoposide salvage regimen with rituximab for in vivo purging in patients with relapsed lymphoma. Clin Lymphoma. 2002 Sep; 3(2):111-6. PMID: 12435284.
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    121. Richards CS, Bradley LA, Amos J, Allitto B, Grody WW, Maddalena A, McGinnis MJ, Prior TW, Popovich BW, Watson MS, Palomaki GE. Standards and guidelines for CFTR mutation testing. Genet Med. 2002 Sep-Oct; 4(5):379-91. PMID: 12394352.
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    122. Sharma P, Rosenbaum AL, Vives T, Grody WW, Demer JL. Discordant pursuit asymmetry and esotropia in monozygous twins. Am J Ophthalmol. 2002 Jul; 134(1):143-6. PMID: 12095832.
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    123. Yu H, Iyer RK, Yoo PK, Kern RM, Grody WW, Cederbaum SD. Arginase expression in mouse embryonic development. Mech Dev. 2002 Jul; 115(1-2):151-5. PMID: 12049781.
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    124. Iyer RK, Yoo PK, Kern RM, Rozengurt N, Tsoa R, O'Brien WE, Yu H, Grody WW, Cederbaum SD. Mouse model for human arginase deficiency. Mol Cell Biol. 2002 Jul; 22(13):4491-8. PMID: 12052859.
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    125. Huang TJ, Liu M, Knight LD, Grody WW, Miller JF, Ho CM. An electrochemical detection scheme for identification of single nucleotide polymorphisms using hairpin-forming probes. Nucleic Acids Res. 2002 Jun 15; 30(12):e55. PMID: 12060693.
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    126. Kim PS, Iyer RK, Lu KV, Yu H, Karimi A, Kern RM, Tai DK, Cederbaum SD, Grody WW. Expression of the liver form of arginase in erythrocytes. Mol Genet Metab. 2002 Jun; 76(2):100-10. PMID: 12083807.
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    127. Iyer RK, Kim HK, Tsoa RW, Grody WW, Cederbaum SD. Cloning and characterization of human agmatinase. Mol Genet Metab. 2002 Mar; 75(3):209-18. PMID: 11914032.
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    128. Grody WW. Molecular genetic risk screening. Annu Rev Med. 2003; 54:473-90. PMID: 12525682.
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    129. Yu H, Iyer RK, Kern RM, Rodriguez WI, Grody WW, Cederbaum SD. Expression of arginase isozymes in mouse brain. J Neurosci Res. 2001 Nov 01; 66(3):406-22. PMID: 11746358.
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    130. Telatar M, Grody WW, Emmanouilides C. Detection of bcl-2/IgH rearrangements by quantitative-competitive PCR and capillary electrophoresis. Mol Diagn. 2001 Sep; 6(3):161-8. PMID: 11571709.
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    131. Dequeker E, Ramsden S, Grody WW, Stenzel TT, Barton DE. Quality control in molecular genetic testing. Nat Rev Genet. 2001 09; 2(9):717-23. PMID: 11533720.
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    132. Iyer RK, Kim PS, Bando JM, Lu KV, Gregg JP, Grody WW. A multiethnic study of Delta32ccr5 and ccr2b-V64I allele distribution in four Los Angeles populations. Diagn Mol Pathol. 2001 Jun; 10(2):105-10. PMID: 11385319.
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    133. Grody WW, Cutting GR, Klinger KW, Richards CS, Watson MS, Desnick RJ. Laboratory standards and guidelines for population-based cystic fibrosis carrier screening. Genet Med. 2001 Mar-Apr; 3(2):149-54. PMID: 11280952.
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    134. Grody WW, Griffin JH, Taylor AK, Korf BR, Heit JA. American College of Medical Genetics consensus statement on factor V Leiden mutation testing. Genet Med. 2001 Mar-Apr; 3(2):139-48. PMID: 11280951.
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    135. Grody WW, Desnick RJ. Cystic fibrosis population carrier screening: here at last--are we ready? Genet Med. 2001 Mar-Apr; 3(2):87-90. PMID: 11280954.
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    136. Grody WW. Ethical ramifications of genetic analysis using DNA arrays. Methods Mol Biol. 2001; 170:53-69. PMID: 11357689.
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    137. Rohlfs EM, Chung CH, Yang Q, Skrzynia C, Grody WW, Graham ML, Silverman LM. In-frame deletions of BRCA1 may define critical functional domains. Hum Genet. 2000 Oct; 107(4):385-90. PMID: 11129340.
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    138. Telatar M, Grody WW. Molecular genetic testing for familial Mediterranean fever. Mol Genet Metab. 2000 Sep-Oct; 71(1-2):256-60. PMID: 11001819.
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    139. Emmanouilides C, Rosen P, Telatar M, Malone R, Bosserman L, Menco H, Patel R, Barstis J, Grody WW. 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. PMID: 11707827.
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    140. Noll WW, Belloni DR, Stenzel TT, Grody WW. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Nat Genet. 1999 Nov; 23(3):271-2. PMID: 10610176.
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    141. Stass SA, Grody WW. Molecular pathology: role in improving patient outcome: Overview. Arch Pathol Lab Med. 1999 Nov; 123(11):1000-1. PMID: 10539895.
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    142. Grody WW. Cystic fibrosis: molecular diagnosis, population screening, and public policy. Arch Pathol Lab Med. 1999 Nov; 123(11):1041-6. PMID: 10539904.
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    143. 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. Issues in implementing prenatal screening for cystic fibrosis: results of a working conference. Genet Med. 1999 May-Jun; 1(4):129-35. PMID: 11258347.
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    144. Cabello GM, Moreira AF, Horovitz D, Correia P, Santa Rosa A, Llerena J, Greg J, Grody WW, Degrave WM, Fernandes O, Cabello PH. Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil. Hum Biol. 1999 Apr; 71(2):189-96. PMID: 10222642.
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    145. Grizzle W, Grody WW, Noll WW, Sobel ME, Stass SA, Trainer T, Travers H, Weedn V, Woodruff K. 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. PMID: 10320140.
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    146. Grody WW, Pyeritz RE. Report card on molecular genetic testing: room for improvement? JAMA. 1999 Mar 03; 281(9):845-7. PMID: 10071008.
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    147. Apple SK, Hecht JR, Lewin DN, Jahromi SA, Grody WW, Nieberg RK. 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. PMID: 10029438.
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    148. Wackym PA, Kerner MM, Grody WW. 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. PMID: 9707259.
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    149. Grody WW, Desnick RJ, Carpenter NJ, Noll WW. Diversity of cystic fibrosis mutation-screening practices. Am J Hum Genet. 1998 May; 62(5):1252-4. PMID: 9545412.
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    150. Iyer RK, Bando JM, Jenkinson CP, Vockley JG, Kim PS, Kern RM, Cederbaum SD, Grody WW. Cloning and characterization of the mouse and rat type II arginase genes. Mol Genet Metab. 1998 Mar; 63(3):168-75. PMID: 9608538.
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    151. Iyer R, Jenkinson CP, Vockley JG, Kern RM, Grody WW, Cederbaum S. The human arginases and arginase deficiency. J Inherit Metab Dis. 1998; 21 Suppl 1:86-100. PMID: 9686347.
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    152. Gregg JP, Yamane AJ, Grody WW. Prevalence of the factor V-Leiden mutation in four distinct American ethnic populations. Am J Med Genet. 1997 Dec 19; 73(3):334-6. PMID: 9415695.
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    153. Geschwind DH, Perlman S, Grody WW, Telatar M, Montermini L, Pandolfo M, Gatti RA. Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia. Neurology. 1997 Oct; 49(4):1004-9. PMID: 9339680.
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    154. Gregg JP, Grody WW. Diagnostic molecular genetics: current applications and future technologies. Pediatr Ann. 1997 Sep; 26(9):553-61. PMID: 9302718.
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    155. Grody WW, Watson MS. Those elusive molecular diagnostics CPT codes. Diagn Mol Pathol. 1997 Jun; 6(3):131-3. PMID: 9276183.
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    156. Grody WW, Dunkel-Schetter C, Tatsugawa ZH, Fox MA, Fang CY, Cantor RM, Novak JM, Bass HN, Crandall BF. PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population. Am J Hum Genet. 1997 Apr; 60(4):935-47. PMID: 9106541.
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    157. Li PX, Cheng L, Wen DR, Wissmann PB, Cheng J, Grody WW, Cochran AJ. 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. PMID: 9028734.
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    158. Donovan JA, Simmons FA, Esrason KT, Jamehdor M, Busuttil RW, Novak JM, Grody WW. 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. PMID: 9000665.
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    159. Fang CY, Dunkel-Schetter C, Tatsugawa ZH, Fox MA, Bass HN, Crandall BF, Grody WW. 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. PMID: 9106369.
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    160. Vockley JG, Jenkinson CP, Shukla H, Kern RM, Grody WW, Cederbaum SD. Cloning and characterization of the human type II arginase gene. Genomics. 1996 Dec 01; 38(2):118-23. PMID: 8954792.
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    161. Wissmann PB, Goodman BK, Vockley JG, Kern RM, Cederbaum SD, Grody WW. 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. PMID: 9131018.
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    162. Vockley JG, Goodman BK, Tabor DE, Kern RM, Jenkinson CP, Grody WW, Cederbaum SD. Loss of function mutations in conserved regions of the human arginase I gene. Biochem Mol Med. 1996 Oct; 59(1):44-51. PMID: 8902193.
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    163. Grody WW, Sobel ME. Update on informed consent for stored tissue research. Diagn Mol Pathol. 1996 Jun; 5(2):79-80. PMID: 8727093.
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    164. Jenkinson CP, Grody WW, Cederbaum SD. Comparative properties of arginases. Comp Biochem Physiol B Biochem Mol Biol. 1996 May; 114(1):107-32. PMID: 8759304.
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    165. Lovell MA, Grody WW. Molecular pathology 1995. Birth of an association [meeting report]. Diagn Mol Pathol. 1996 Mar; 5(1):1-2. PMID: 8919538.
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    166. Apple SK, Hecht JR, Novak JM, Nieberg RK, Rosenthal DL, Grody WW. 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. PMID: 8602613.
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    167. Goldstein NS, Bégin LR, Grody WW, Novak JM, Qian J, Bostwick DG. 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. PMID: 7661273.
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    168. Grody WW. Proficiency testing in diagnostic molecular pathology. Diagn Mol Pathol. 1994 Dec; 3(4):221-3. PMID: 7866631.
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    169. Tatsugawa ZH, Fox MA, Fang CY, Novak JM, Cantor RM, Bass HN, Dunkel-Schetter C, Crandall BF, Grody WW. Education and testing strategy for large-scale cystic fibrosis carrier screening. J Genet Couns. 1994 Dec; 3(4):279-89. PMID: 24234134.
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    170. Gu Y, Lugenbeel KA, Vockley JG, Grody WW, Nelson DL. A de novo deletion in FMR1 in a patient with developmental delay. Hum Mol Genet. 1994 Sep; 3(9):1705-6. PMID: 7530551.
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    171. Dubinett SM, Huang M, Lichtenstein A, McBride WH, Wang J, Markovitz G, Kelley D, Grody WW, Mintz LE, Dhanani S. 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. PMID: 8039244.
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    172. Goodman BK, Klein D, Tabor DE, Vockley JG, Cederbaum SD, Grody WW. Functional and molecular analysis of liver arginase promoter sequences from man and Macaca fascicularis. Somat Cell Mol Genet. 1994 Jul; 20(4):313-25. PMID: 7974006.
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    173. Vockley JG, Tabor DE, Kern RM, Goodman BK, Wissmann PB, Kang DS, Grody WW, Cederbaum SD. Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia. Hum Mutat. 1994; 4(2):150-4. PMID: 7981719.
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    174. Grody WW, Chang RJ, Panagiotis NM, Matz D, Cederbaum SD. 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. PMID: 7837763.
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    175. Grody WW, Kronquist KE, Lee EU, Edmond J, Rome LH. 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. PMID: 8250051.
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    176. Grody WW. Molecular genetics. Introduction. Arch Pathol Lab Med. 1993 May; 117(5):470-2. PMID: 8489333.
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    177. Grody WW, Kern RM, Klein D, Dodson AE, Wissman PB, Barsky SH, Cederbaum SD. Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme. Hum Genet. 1993 Mar; 91(1):1-5. PMID: 8454280.
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    178. Dubinett SM, Huang M, Dhanani S, Kelley D, Lichtenstein A, Grody WW, Mintz LE. In situ regulation of pulmonary macrophage TNF-alpha mRNA expression by IL2. Chest. 1993 Feb; 103(2 Suppl):91S-94S. PMID: 8428548.
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    179. Klein D, Grody WW, Tabor DE, Cederbaum SD. Pitfalls of restriction endonuclease digestion for direct detection of point mutations. Clin Chem. 1992 Jul; 38(7):1392-4. PMID: 1320472.
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    180. Grody WW, Klein D, Dodson AE, Kern RM, Wissmann PB, Goodman BK, Bassand P, Marescau B, Kang SS, Leonard JV. Molecular genetic study of human arginase deficiency. Am J Hum Genet. 1992 Jun; 50(6):1281-90. PMID: 1598908.
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    181. Lewis W, Grody WW. AIDS and the heart: Review and consideration of pathogenetic mechanisms. Cardiovasc Pathol. 1992 Jan-Mar; 1(1):53-64. PMID: 25990037.
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    182. Klein D, Dodson AE, Tabor DE, Cederbaum SD, Grody WW. 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. PMID: 1887333.
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    183. Fain JS, Bryan RN, Cheng L, Lewin KJ, Porter DD, Grody WW. Rapid diagnosis of Legionella infection by a nonisotopic in situ hybridization method. Am J Clin Pathol. 1991 May; 95(5):719-24. PMID: 2024627.
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    184. Grody WW, Cheng L, Lewis W. Infection of the heart by the human immunodeficiency virus. Am J Cardiol. 1990 Jul 15; 66(2):203-6. PMID: 2371952.
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    185. Nguyen J, Charmley P, Grody WW, Cederbaum SD, King MC, Gatti RA. 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. PMID: 1979025.
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    186. Grody WW, Argyle C, Kern RM, Dizikes GJ, Spector EB, Strickland AD, Klein D, Cederbaum SD. Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysis. J Clin Invest. 1989 Feb; 83(2):602-9. PMID: 2913054.
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    187. Lai-Goldman M, Lai E, Grody WW. 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. PMID: 3419916.
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    188. Grody WW, Dizikes GJ, Cederbaum SD. Human arginase isozymes. Isozymes Curr Top Biol Med Res. 1987; 13:181-214. PMID: 3583682.
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    189. Kidd JR, Dizikes GJ, Grody WW, Cederbaum SD, Kidd KK. A PvuII RFLP for the human liver arginase (ARG1) gene. Nucleic Acids Res. 1986 Dec 09; 14(23):9544. PMID: 2879271.
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    190. Dizikes GJ, Grody WW, Kern RM, Cederbaum SD. 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. PMID: 3801008.
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    191. Grody WW, Jobst S, Keesey J, Herrmann C, Naeim F. Pathologic evaluation of thymic hyperplasia in myasthenia gravis and Lambert-Eaton myasthenic syndrome. Arch Pathol Lab Med. 1986 Sep; 110(9):843-6. PMID: 3755894.
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    192. Sparkes RS, Dizikes GJ, Klisak I, Grody WW, Mohandas T, Heinzmann C, Zollman S, Lusis AJ, Cederbaum SD. The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23. Am J Hum Genet. 1986 Aug; 39(2):186-93. PMID: 3752085.
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