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Grody Wayne

TitleProfessor
InstitutionUniversity of California Los Angeles
DepartmentPathology and Laboratory Medicine
Address200 UCLA Med Plaza Suite 265
Los Angeles CA 90095
Phone(310) 825-5648
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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

    Collapse Bibliographic 
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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.
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    1. Kansal R, Grody W, 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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    2. Richards CS, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody W, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL. Response to Biesecker and Harrison. Genet Med. 2018 Mar 15. PMID: 29543230.
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    3. 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 W, 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 Dec; 19(12). PMID: 28933790.
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    4. Kaul KL, Sabatini LM, Tsongalis GJ, Caliendo AM, Olsen RJ, Ashwood ER, Bale S, Benirschke R, Carlow D, Funke BH, Grody W, 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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    5. Green RC, Berg JS, Grody W, 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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    6. Mullegama SV, Jensik P, Li C, Dorrani N, Kantarci S, Blumberg B, Grody W, 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 Jun; 5(6):833-840. PMID: 28588821.
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    7. 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 Jul; 26(7):755-761. PMID: 28388340.
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    8. 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 May; 13(5):333-337. PMID: 28350513.
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    9. 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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    10. 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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    11. 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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    12. 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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    13. Grody W. Prenatal Carrier Screening-Reply. JAMA. 2016 12 27; 316(24):2676-2677. PMID: 28027361.
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    14. Benhammou JN, Phan J, Lee H, Ghassemi K, Parsons W, Grody W, 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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    15. Ge X, Gong H, Dumas K, Litwin J, Phillips JJ, Waisfisz Q, Weiss MM, Hendriks Y, Stuurman KE, Nelson SF, Grody W, 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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    16. Grody W. Where to Draw the Boundaries for Prenatal Carrier Screening. JAMA. 2016 Aug 16; 316(7):717-9. PMID: 27533155.
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    17. Grody W. The next generation of cancer management. Cancer Biol Med. 2016 Mar; 13(1):1-2. PMID: 27144057; PMCID: PMC4850118.
    18. 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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    19. Deignan JL, Grody W. Molecular Diagnosis of Cystic Fibrosis. Curr Protoc Hum Genet. 2016 Jan 01; 88:Unit 9.28. PMID: 26724724.
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    20. 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 W. 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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    21. 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 W, 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; PMCID: PMC4613469 [Available on 10/01/16].
    22. Cherukuri DP, Deignan JL, Das K, Grody W, 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; PMCID: PMC4523444.
    23. Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody W, 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; PMCID: PMC4544753.
    24. 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 W, 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; PMCID: PMC4375619.
    25. 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 W, Vilain E, Nelson SF. Clinical exome sequencing for genetic identification of rare Mendelian disorders. JAMA. 2014 Nov 12; 312(18):1880-7. PMID: 25326637; PMCID: PMC4278636.
    26. Fogel BL, Lee H, Deignan JL, Strom SP, Kantarci S, Wang X, Quintero-Rivera F, Vilain E, Grody W, 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; PMCID: PMC4324730.
    27. Aziz N, Zhao Q, Bry L, Driscoll DK, Funke B, Gibson JS, Grody W, 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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    28. Grody W, Vilain E, Nelson SF. Interpreting whole-genome sequencing. JAMA. 2014 Jul 16; 312(3):296. PMID: 25027151.
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    29. Hu C, Kasten J, Park H, Bhargava R, Tai DS, Grody W, 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; PMCID: PMC4428413.
    30. Strom SP, Lozano R, Lee H, Dorrani N, Mann J, O'Lague PF, Mans N, Deignan JL, Vilain E, Nelson SF, Grody W, 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; PMCID: PMC4072606.
    31. Loh JC, Cassarino DS, Grody W, 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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    32. Strom SP, Lee H, Das K, Vilain E, Nelson SF, Grody W, 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; PMCID: PMC4079763.
    33. Grody W, Thompson BH, Hudgins L. Whole-exome/genome sequencing and genomics. Pediatrics. 2013 Dec; 132(Suppl 3):S211-5. PMID: 24298129.
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    34. Massie J, Castellani C, Grody W. 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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    35. Kasten J, Hu C, Bhargava R, Park H, Tai D, Byrne JA, Marescau B, De Deyn PP, Schlichting L, Grody W, 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; PMCID: PMC3800271.
    36. Kalman LV, Lubin IM, Barker S, du Sart D, Elles R, Grody W, 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; PMCID: PMC4684176.
    37. Green RC, Berg JS, Grody W, 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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    38. Grody W, 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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    39. 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; PMCID: PMC3701749.
    40. Bavisetty S, Grody W, Yazdani S. Emergence of pediatric rare diseases: Review of present policies and opportunities for improvement. Rare Dis. 2013; 1:e23579. PMID: 25002987; PMCID: PMC3932940.
    41. Ong FS, Kuo JZ, Wu WC, Cheng CY, Blackwell WL, Taylor BL, Grody W, 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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    42. Schrijver I, Aziz N, Farkas DH, Furtado M, Gonzalez AF, Greiner TC, Grody W, 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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    43. 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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    44. Lee EK, Hu C, Bhargava R, Rozengurt N, Stout D, Grody W, 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; PMCID: PMC3464644.
    45. Ong FS, Das K, Wang J, Vakil H, Kuo JZ, Blackwell WL, Lim SW, Goodarzi MO, Bernstein KE, Rotter JI, Grody W. Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing. Expert Rev Mol Diagn. 2012 Jul; 12(6):593-602. PMID: 22845480; PMCID: PMC3495985.
    46. Green RC, Berg JS, Berry GT, Biesecker LG, Dimmock DP, Evans JP, Grody W, 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; PMCID: PMC3763716.
    47. Dry S, Grody W, 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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    48. Ong FS, Deignan JL, Kuo JZ, Bernstein KE, Rotter JI, Grody W, Das K. Clinical utility of pharmacogenetic biomarkers in cardiovascular therapeutics: a challenge for clinical implementation. Pharmacogenomics. 2012 Mar; 13(4):465-75. PMID: 22380001; PMCID: PMC3306231.
    49. Palomaki GE, Deciu C, Kloza EM, Lambert-Messerlian GM, Haddow JE, Neveux LM, Ehrich M, van den Boom D, Bombard AT, Grody W, 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; PMCID: PMC3938175.
    50. Grody W. 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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    51. Palomaki GE, Kloza EM, Lambert-Messerlian GM, Haddow JE, Neveux LM, Ehrich M, van den Boom D, Bombard AT, Deciu C, Grody W, 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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    52. Ong FS, Grody W, 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; PMCID: PMC3130532.
    53. Zadeh N, Getzug T, Grody W. 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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    54. Deignan JL, Grody W. Ordering genetic tests and interpreting the results. Adv Otorhinolaryngol. 2011; 70:18-24. PMID: 21358180.
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    55. Grody W, 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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    56. Quintero-Rivera F, Deignan JL, Peredo J, Grody W, 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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    57. Bender L, Silverman LM, Dinulos MB, Nickel J, Grody W. 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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    58. Wehling-Henricks M, Jordan MC, Gotoh T, Grody W, 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; PMCID: PMC2874011.
    59. Boudreault P, Baldwin EE, Fox M, Dutton L, Tullis L, Linden J, Kobayashi Y, Zhou J, Sinsheimer JS, Sininger Y, Grody W, 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; PMCID: PMC2902357.
    60. 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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    61. Grody W, Howell RR. The fate of newborn screening blood spots. Pediatr Res. 2010 Mar; 67(3):237. PMID: 20154576.
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    62. Grody W. Genetics in Hollywood: from real to reel. Clin Genet. 2010 Feb; 77(2):106-11. PMID: 20096067.
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    63. Barker SD, Bale S, Booker J, Buller A, Das S, Friedman K, Godwin AK, Grody W, 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; PMCID: PMC2765754.
    64. Rosove MH, Grody W. 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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    65. Palmer CG, Martinez A, Fox M, Zhou J, Shapiro N, Sininger Y, Grody W, 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; PMCID: PMC2866144.
    66. Gau CL, Rosenblatt RA, Cerullo V, Lay FD, Dow AC, Livesay J, Brunetti-Pierri N, Lee B, Cederbaum SD, Grody W, 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; PMCID: PMC2835205.
    67. Grody W. Cystic fibrosis testing comes of age. J Mol Diagn. 2009 May; 11(3):173-5. PMID: 19359497; PMCID: PMC2671332.
    68. Pullarkat ST, Pullarkat V, Kroft SH, Wilson CS, Ahsanuddin AN, Mann KP, Thein M, Grody W, Brynes RK. Systemic mastocytosis associated with t(8;21)(q22;q22) acute myeloid leukemia. J Hematop. 2009 Mar; 2(1):27-33. PMID: 19669220; PMCID: PMC2713498.
    69. ten Bosch JR, Grody W. Keeping up with the next generation: massively parallel sequencing in clinical diagnostics. J Mol Diagn. 2008 Nov; 10(6):484-92. PMID: 18832462; PMCID: PMC2570630.
    70. Mumenthaler SM, Rozengurt N, Livesay JC, Sabaghian A, Cederbaum SD, Grody W. 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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    71. Schimmenti LA, Martinez A, Telatar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody W, 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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    72. Grody W, Richards CS. New quality assurance standards for rare disease testing. Genet Med. 2008 May; 10(5):320-4. PMID: 18496029.
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    73. Richards CS, Bale S, Bellissimo DB, Das S, Grody W, 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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    74. Mumenthaler SM, Yu H, Tze S, Cederbaum SD, Pegg AE, Seligson DB, Grody W. Expression of arginase II in prostate cancer. Int J Oncol. 2008 Feb; 32(2):357-65. PMID: 18202758.
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    75. Deignan JL, Marescau B, Livesay JC, Iyer RK, De Deyn PP, Cederbaum SD, Grody W. 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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    76. Grody W, 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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    77. Deignan JL, Cederbaum SD, Grody W. Contrasting features of urea cycle disorders in human patients and knockout mouse models. Mol Genet Metab. 2008 Jan; 93(1):7-14. PMID: 17933574; PMCID: PMC2692509.
    78. Palmer CG, Martinez A, Fox M, Sininger Y, Grody W, 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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    79. Deignan JL, Livesay JC, Shantz LM, Pegg AE, O'Brien WE, Iyer RK, Cederbaum SD, Grody W. Polyamine homeostasis in arginase knockout mice. Am J Physiol Cell Physiol. 2007 Oct; 293(4):C1296-301. PMID: 17686999.
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    80. Blase T, Martinez A, Grody W, 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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    81. Lebo RV, Grody W. Testing and reporting ACMG cystic fibrosis mutation panel results. Genet Test. 2007; 11(1):11-31. PMID: 17394390.
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    82. Lebo RV, Grody W. 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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    83. Elshimali YI, Grody W. 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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    84. Deignan JL, Livesay JC, Yoo PK, Goodman SI, O'Brien WE, Iyer RK, Cederbaum SD, Grody W. 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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    85. Keen-Kim D, Grody W, 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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    86. Ramsden SC, Deans Z, Robinson DO, Mountford R, Sistermans EA, Grody W, 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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    87. Palmer CG, Martinez A, Sininger Y, Shapiro N, Grody W, 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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    88. 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 W, 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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    89. 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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    90. Spector EB, Grody W, 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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    91. Jarvis M, Iyer RK, Williams LO, Noll WW, Thomas K, Telatar M, Grody W. 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; PMCID: PMC1867527.
    92. Ogino S, Flodman P, Wilson RB, Gold B, Grody W. 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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    93. Schimmenti LA, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody W, 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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    94. Ogino S, Wilson RB, Gold B, Hawley P, Grody W. 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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    95. 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 W. 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; PMCID: PMC3110945.
    96. Tsongalis GJ, Belloni DR, Grody W. Cystic fibrosis mutation analysis: how many is enough? Genet Med. 2004 Sep-Oct; 6(5):456-8. PMID: 15371913.
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    97. 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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    98. Cederbaum SD, Yu H, Grody W, 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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    99. Richards CS, Grody W. 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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    100. Palomaki GE, Haddow JE, Bradley LA, Richards CS, Stenzel TT, Grody W. 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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    101. Grody W. Quest for controls in molecular genetics. J Mol Diagn. 2003 Nov; 5(4):209-11. PMID: 14573778; PMCID: PMC1907341.
    102. Yu H, Yoo PK, Aguirre CC, Tsoa RW, Kern RM, Grody W, 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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    103. Richards CS, Grody W. Alternative approaches to proficiency testing in molecular genetics. Clin Chem. 2003 May; 49(5):717-8. PMID: 12709360.
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    104. Venegas PB, Novak JM, Oscar CA, Sánchez FL, Gutiérrez IG, Rivera JM, Salas JP, Montero JF, Grody W. Cystic fibrosis mutations in Costa Rica. Hum Biol. 2003 Apr; 75(2):179-88. PMID: 12943157.
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    105. Grody W. Ethical issues raised by genetic testing with oligonucleotide microarrays. Mol Biotechnol. 2003 Feb; 23(2):127-38. PMID: 12632697.
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    106. Watson MS, Desnick RJ, Grody W, 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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    107. 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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    108. Richards CS, Bradley LA, Amos J, Allitto B, Grody W, 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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    109. Sharma P, Rosenbaum AL, Vives T, Grody W, 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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    110. Yu H, Iyer RK, Yoo PK, Kern RM, Grody W, Cederbaum SD. Arginase expression in mouse embryonic development. Mech Dev. 2002 Jul; 115(1-2):151-5. PMID: 12049781.
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    111. Iyer RK, Yoo PK, Kern RM, Rozengurt N, Tsoa R, O'Brien WE, Yu H, Grody W, Cederbaum SD. Mouse model for human arginase deficiency. Mol Cell Biol. 2002 Jul; 22(13):4491-8. PMID: 12052859; PMCID: PMC133904.
    112. Huang TJ, Liu M, Knight LD, Grody W, 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; PMCID: PMC117297.
    113. Kim PS, Iyer RK, Lu KV, Yu H, Karimi A, Kern RM, Tai DK, Cederbaum SD, Grody W. Expression of the liver form of arginase in erythrocytes. Mol Genet Metab. 2002 Jun; 76(2):100-10. PMID: 12083807.
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    114. Iyer RK, Kim HK, Tsoa RW, Grody W, Cederbaum SD. Cloning and characterization of human agmatinase. Mol Genet Metab. 2002 Mar; 75(3):209-18. PMID: 11914032.
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    115. Grody W. Molecular genetic risk screening. Annu Rev Med. 2003; 54:473-90. PMID: 12525682.
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