| Year |
Citation |
Score |
| 2023 |
Deignan JL, Gregg AR, Grody WW, Guo MH, Kearney H, Monaghan KG, Raraigh KS, Taylor J, Zepeda-Mendoza CJ, Ziats C. Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100867. PMID 37310422 DOI: 10.1016/j.gim.2023.100867 |
0.635 |
|
| 2020 |
Deignan JL, Astbury C, Cutting GR, Del Gaudio D, Gregg AR, Grody WW, Monaghan KG, Richards S. CFTR variant testing: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32404922 DOI: 10.1038/S41436-020-0822-5 |
0.693 |
|
| 2020 |
Yazdani S, Badjatiya A, Dorrani N, Lee H, Grody WW, Nelson SF, Dipple KM. Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndrome. Molecular Genetics and Metabolism Reports. 23: 100582. PMID 32280589 DOI: 10.1016/J.Ymgmr.2020.100582 |
0.377 |
|
| 2019 |
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, et al. International perspectives on the implementation of reproductive carrier screening. Prenatal Diagnosis. PMID 31774570 DOI: 10.1002/Pd.5611 |
0.309 |
|
| 2019 |
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. Molecular Genetics & Genomic Medicine. e1026. PMID 31701651 DOI: 10.1002/Mgg3.1026 |
0.674 |
|
| 2019 |
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, ... ... Grody WW, et al. A Diagnostic Ceiling for Exome Sequencing in Cerebellar Ataxia and Related Neurological Disorders. Human Mutation. PMID 31692161 DOI: 10.1002/Humu.23946 |
0.701 |
|
| 2019 |
Grody WW. The transformation of medical genetics by clinical genomics: hubris meets humility. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30842646 DOI: 10.1038/S41436-019-0450-0 |
0.417 |
|
| 2018 |
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. American Journal of Medical Genetics. Part A. PMID 30244526 DOI: 10.1002/Ajmg.A.40533 |
0.682 |
|
| 2017 |
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, et al. Is it time to retire fragile X testing as a first-tier test for developmental delay, intellectual disability, and autism spectrum disorder? Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28933790 DOI: 10.1038/Gim.2017.146 |
0.643 |
|
| 2017 |
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. Clinical Case Reports. 5: 833-840. PMID 28588821 DOI: 10.1002/Ccr3.904 |
0.385 |
|
| 2017 |
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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 19: 606. PMID 28492529 DOI: 10.1038/Gim.2017.18 |
0.326 |
|
| 2017 |
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, et al. Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. Journal of Women's Health (2002). PMID 28388340 DOI: 10.1089/Jwh.2016.6098 |
0.326 |
|
| 2017 |
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, et al. 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. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. JCO2016719807. PMID 28165299 DOI: 10.1200/Jco.2016.71.9807 |
0.342 |
|
| 2016 |
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 Genomic Medicine. 1. PMID 28868155 DOI: 10.1038/Npjgenmed.2016.36 |
0.368 |
|
| 2016 |
Grody WW. The next generation of cancer management. Cancer Biology & Medicine. 13: 1-2. PMID 27144057 DOI: 10.28092/J.Issn.2095-3941.2016.0027 |
0.35 |
|
| 2016 |
Deignan JL, Grody WW. Molecular Diagnosis of Cystic Fibrosis. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. 88: Unit 9.28. PMID 26724724 DOI: 10.1002/0471142905.Hg0928S88 |
0.693 |
|
| 2015 |
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, ... ... Grody WW, et al. An infant with MLH3 variants, FOXG1-duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing study. Genes, Chromosomes & Cancer. PMID 26542077 DOI: 10.1002/Gcc.22319 |
0.669 |
|
| 2015 |
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, ... ... Grody WW, et al. DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies. European Journal of Human Genetics : Ejhg. PMID 25944381 DOI: 10.1038/Ejhg.2015.71 |
0.653 |
|
| 2015 |
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. Molecular Oncology. PMID 25817443 DOI: 10.1016/J.Molonc.2015.01.009 |
0.651 |
|
| 2015 |
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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 405-24. PMID 25741868 DOI: 10.1038/Gim.2015.30 |
0.436 |
|
| 2015 |
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, et al. De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay. American Journal of Human Genetics. 96: 498-506. PMID 25728775 DOI: 10.1016/J.Ajhg.2015.01.017 |
0.66 |
|
| 2015 |
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, et al. College of American Pathologists' laboratory standards for next-generation sequencing clinical tests. Archives of Pathology & Laboratory Medicine. 139: 481-93. PMID 25152313 DOI: 10.5858/Arpa.2014-0250-Cp |
0.341 |
|
| 2014 |
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, ... ... Grody WW, et al. Clinical exome sequencing for genetic identification of rare Mendelian disorders. Jama. 312: 1880-7. PMID 25326637 DOI: 10.1001/Jama.2014.14604 |
0.701 |
|
| 2014 |
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 Neurology. 71: 1237-46. PMID 25133958 DOI: 10.1001/Jamaneurol.2014.1944 |
0.706 |
|
| 2014 |
Grody WW, Vilain E, Nelson SF. Interpreting whole-genome sequencing. Jama. 312: 296. PMID 25027151 DOI: 10.1001/Jama.2014.6602 |
0.357 |
|
| 2014 |
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 Medical Genetics. 15: 49. PMID 24886118 DOI: 10.1186/1471-2350-15-49 |
0.679 |
|
| 2014 |
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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 510-5. PMID 24406459 DOI: 10.1038/Gim.2013.183 |
0.692 |
|
| 2014 |
Massie J, Castellani C, Grody WW. Carrier screening for cystic fibrosis in the new era of medications that restore CFTR function. Lancet (London, England). 383: 923-5. PMID 23992917 DOI: 10.1016/S0140-6736(13)61092-2 |
0.332 |
|
| 2014 |
Sepulveda AR, Hamilton SR, Grody W. Molecular testing guidelines for selection of colorectal cancer patients for targeted and conventional therapies. Journal of Clinical Oncology. 32: 600-600. DOI: 10.1200/Jco.2014.32.3_Suppl.600 |
0.325 |
|
| 2013 |
Grody WW, Thompson BH, Hudgins L. Whole-exome/genome sequencing and genomics. Pediatrics. 132: S211-5. PMID 24298129 DOI: 10.1542/Peds.2013-1032E |
0.367 |
|
| 2013 |
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. Molecular Genetics and Metabolism. 110: 222-30. PMID 23920045 DOI: 10.1016/J.Ymgme.2013.06.020 |
0.308 |
|
| 2013 |
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. Archives of Pathology & Laboratory Medicine. 137: 983-8. PMID 23808472 DOI: 10.5858/Arpa.2012-0311-Ra |
0.35 |
|
| 2013 |
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 Genetics in Medicine. 15: 565-574. PMID 23788249 DOI: 10.1038/Gim.2013.73 |
0.369 |
|
| 2013 |
Grody WW, Thompson BH, Gregg AR, Bean LH, Monaghan KG, Schneider A, Lebo RV. ACMG position statement on prenatal/preconception expanded carrier screening. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 482-3. PMID 23619275 DOI: 10.1097/01.Ogx.0000441141.05679.2C |
0.339 |
|
| 2013 |
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. Journal of Genetic Counseling. 22: 492-507. PMID 23430402 DOI: 10.1007/S10897-013-9573-7 |
0.666 |
|
| 2013 |
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. Clinical Genetics. 84: 55-9. PMID 23038988 DOI: 10.1111/Cge.12029 |
0.685 |
|
| 2013 |
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. Clinical Genetics. 83: 35-43. PMID 22435390 DOI: 10.1111/J.1399-0004.2012.01879.X |
0.415 |
|
| 2013 |
Grody WW, Deignan JL. Diagnostic Molecular Genetics Emery and Rimoin's Principles and Practice of Medical Genetics. 1-31. DOI: 10.1016/B978-0-12-383834-6.00030-6 |
0.648 |
|
| 2012 |
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, et al. Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology. The Journal of Molecular Diagnostics : Jmd. 14: 525-40. PMID 22918138 DOI: 10.1016/J.Jmoldx.2012.04.006 |
0.356 |
|
| 2012 |
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 Review of Molecular Diagnostics. 12: 593-602. PMID 22845480 DOI: 10.1586/Erm.12.59 |
0.312 |
|
| 2012 |
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, et al. Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 405-10. PMID 22422049 DOI: 10.1038/Gim.2012.21 |
0.373 |
|
| 2012 |
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. 13: 465-75. PMID 22380001 DOI: 10.2217/Pgs.12.2 |
0.65 |
|
| 2012 |
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? American Journal of Clinical Pathology. 137: 346-55. PMID 22338046 DOI: 10.1309/Ajcps26Ukhnyceav |
0.32 |
|
| 2011 |
Ong FS, Grody WW, Deignan JL. Privacy and data management in the era of massively parallel next-generation sequencing. Expert Review of Molecular Diagnostics. 11: 457-9. PMID 21707452 DOI: 10.1586/Erm.11.34 |
0.691 |
|
| 2011 |
Deignan JL, Grody WW. Ordering genetic tests and interpreting the results. Advances in Oto-Rhino-Laryngology. 70: 18-24. PMID 21358180 DOI: 10.1159/000322466 |
0.7 |
|
| 2011 |
Zadeh N, Getzug T, Grody WW. Diagnosis and management of familial Mediterranean fever: integrating medical genetics in a dedicated interdisciplinary clinic. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 263-9. PMID 21317656 DOI: 10.1097/Gim.0B013E31820E27B1 |
0.352 |
|
| 2010 |
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. Molecular Genetics and Metabolism. 101: 413-6. PMID 20817516 DOI: 10.1016/J.Ymgme.2010.08.008 |
0.678 |
|
| 2010 |
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. Journal of Deaf Studies and Deaf Education. 15: 209-27. PMID 20488870 DOI: 10.1093/Deafed/Enq012 |
0.31 |
|
| 2010 |
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, et al. Benchmarks for cystic fibrosis carrier screening: a European consensus document. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 9: 165-78. PMID 20363197 DOI: 10.1016/J.Jcf.2010.02.005 |
0.312 |
|
| 2010 |
Grody WW. Genetics in Hollywood: from real to reel. Clinical Genetics. 77: 106-11. PMID 20096067 DOI: 10.1111/J.1399-0004.2009.01343.X |
0.314 |
|
| 2010 |
Trimble SW, Grody WW, McKelvey B, Gad-el-Hak M. The Glut of Academic Publishing: A Call for a New Culture Academic Questions. 23: 276-286. DOI: 10.1007/S12129-010-9179-6 |
0.31 |
|
| 2009 |
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, et al. Development and characterization of reference materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 genetic testing. The Journal of Molecular Diagnostics : Jmd. 11: 553-61. PMID 19767587 DOI: 10.2353/Jmoldx.2009.090078 |
0.397 |
|
| 2009 |
Rosove MH, Grody WW. Should we be applying warfarin pharmacogenetics to clinical practice? No, not now. Annals of Internal Medicine. 151: 270-3, W95. PMID 19687493 DOI: 10.7326/0003-4819-151-4-200908180-00009 |
0.311 |
|
| 2009 |
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. American Journal of Medical Genetics. Part A. 149: 1169-82. PMID 19449415 DOI: 10.1002/Ajmg.A.32853 |
0.325 |
|
| 2009 |
Grody WW. Cystic fibrosis testing comes of age. The Journal of Molecular Diagnostics : Jmd. 11: 173-5. PMID 19359497 DOI: 10.2353/Jmoldx.2009.090024 |
0.35 |
|
| 2008 |
ten Bosch JR, Grody WW. Keeping up with the next generation: massively parallel sequencing in clinical diagnostics. The Journal of Molecular Diagnostics : Jmd. 10: 484-92. PMID 18832462 DOI: 10.2353/Jmoldx.2008.080027 |
0.328 |
|
| 2008 |
Mumenthaler SM, Rozengurt N, Livesay JC, Sabaghian A, Cederbaum SD, Grody WW. Disruption of arginase II alters prostate tumor formation in TRAMP mice. The Prostate. 68: 1561-9. PMID 18663728 DOI: 10.1002/Pros.20816 |
0.597 |
|
| 2008 |
Grody WW, Richards CS. New quality assurance standards for rare disease testing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 10: 320-4. PMID 18496029 DOI: 10.1097/Gim.0B013E31817283Ba |
0.43 |
|
| 2008 |
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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 10: 294-300. PMID 18414213 DOI: 10.1097/Gim.0B013E31816B5Cae |
0.345 |
|
| 2008 |
Mumenthaler SM, Yu H, Tze S, Cederbaum SD, Pegg AE, Seligson DB, Grody WW. Expression of arginase II in prostate cancer. International Journal of Oncology. 32: 357-65. PMID 18202758 DOI: 10.3892/Ijo.32.2.357 |
0.599 |
|
| 2008 |
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. Molecular Genetics and Metabolism. 93: 172-8. PMID 17997338 DOI: 10.1016/J.Ymgme.2007.09.016 |
0.645 |
|
| 2008 |
Palmer CG, Martinez A, Fox M, Sininger Y, Grody WW, Schimmenti LA. Ethnic differences in parental perceptions of genetic testing for deaf infants. Journal of Genetic Counseling. 17: 129-38. PMID 17952575 DOI: 10.1007/S10897-007-9134-Z |
0.311 |
|
| 2008 |
Deignan JL, Cederbaum SD, Grody WW. Contrasting features of urea cycle disorders in human patients and knockout mouse models. Molecular Genetics and Metabolism. 93: 7-14. PMID 17933574 DOI: 10.1016/J.Ymgme.2007.08.123 |
0.662 |
|
| 2007 |
Grody WW, Cutting GR, Watson MS. The Cystic Fibrosis mutation "arms race": when less is more. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 9: 739-44. PMID 18007142 DOI: 10.1097/Gim.0B013E318159A331 |
0.341 |
|
| 2007 |
Deignan JL, Livesay JC, Shantz LM, Pegg AE, O'Brien WE, Iyer RK, Cederbaum SD, Grody WW. Polyamine homeostasis in arginase knockout mice. American Journal of Physiology. Cell Physiology. 293: C1296-301. PMID 17686999 DOI: 10.1152/Ajpcell.00393.2006 |
0.629 |
|
| 2007 |
Lebo RV, Grody WW. Variable penetrance and expressivity of the splice altering 5T sequence in the cystic fibrosis gene. Genetic Testing. 11: 32-44. PMID 17394391 DOI: 10.1089/Gte.2006.9997 |
0.342 |
|
| 2007 |
Lebo RV, Grody WW. Testing and reporting ACMG cystic fibrosis mutation panel results. Genetic Testing. 11: 11-31. PMID 17394390 DOI: 10.1089/Gte.2006.9996 |
0.349 |
|
| 2007 |
Blase T, Martinez A, Grody WW, Schimmenti L, Palmer CGS. Sharing GJB2/GJB6 genetic test information with family members Journal of Genetic Counseling. 16: 313-324. PMID 17318457 DOI: 10.1007/S10897-006-9066-Z |
0.328 |
|
| 2006 |
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. Genetic Testing. 10: 147-56. PMID 17020464 DOI: 10.1089/Gte.2006.10.147 |
0.326 |
|
| 2006 |
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. Molecular Genetics and Metabolism. 89: 87-96. PMID 16753325 DOI: 10.1016/J.Ymgme.2006.04.007 |
0.648 |
|
| 2006 |
Keen-Kim D, Grody WW, Richards CS. Microelectronic array system for molecular diagnostic genotyping: Nanogen NanoChip 400 and molecular biology workstation. Expert Review of Molecular Diagnostics. 6: 287-94. PMID 16706733 DOI: 10.1586/14737159.6.3.287 |
0.365 |
|
| 2006 |
Orkin MB, Mumenthaler SM, Cederbaum S, Grody W. 438 ARGINASE AS A PROLIFERATIVE DETERMINANT IN PROSTATE CANCER. Journal of Investigative Medicine. 54: S155.2-S155. DOI: 10.2310/6650.2005.X0004.437 |
0.594 |
|
| 2006 |
Maddalena A, Bale S, Das S, Grody W, Richards CS. Erratum: Technical standards and guidelines: Molecular genetic testing for ultra-rare disorders (Genetics in Medicine (2005) 8, (571-583)) Genetics in Medicine. 8. DOI: 10.1097/00125817-200611000-00009 |
0.375 |
|
| 2005 |
Maddalena A, Bale S, Das S, Grody W, Richards S. Technical standards and guidelines: molecular genetic testing for ultra-rare disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 7: 571-83. PMID 16247296 DOI: 10.1097/01.Gim.0000182738.95726.Ca |
0.36 |
|
| 2005 |
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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 7: 444-53. PMID 16024978 DOI: 10.1097/01.Gim.0000172641.57755.3A |
0.351 |
|
| 2005 |
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. The Journal of Molecular Diagnostics : Jmd. 7: 247-51. PMID 15858148 DOI: 10.1016/S1525-1578(10)60551-X |
0.365 |
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| 2004 |
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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 6: 521-5. PMID 15545749 DOI: 10.1097/01.Gim.0000144187.21727.28 |
0.301 |
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| 2004 |
Ogino S, Wilson RB, Gold B, Hawley P, Grody WW. Bayesian analysis for cystic fibrosis risks in prenatal and carrier screening. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 6: 439-49. PMID 15371910 DOI: 10.1097/01.Gim.0000139511.83336.8F |
0.344 |
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| 2004 |
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 Genetics in Medicine. 6: 387-391. PMID 15371902 DOI: 10.1097/01.Gim.0000139506.11694.7C |
0.333 |
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| 2004 |
Amos J, Grody W. Development and integration of molecular genetic tests into clinical practice: the US experience. Expert Review of Molecular Diagnostics. 4: 465-77. PMID 15225094 DOI: 10.1586/14737159.4.4.465 |
0.401 |
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| 2004 |
Ogino S, Wilson RB, Grody WW. Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR mutation. Journal of Medical Genetics. 41: e70. PMID 15121798 DOI: 10.1136/Jmg.2003.015065 |
0.342 |
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| 2004 |
Cederbaum SD, Yu H, Grody WW, Kern RM, Yoo P, Iyer RK. Arginases I and II: do their functions overlap? Molecular Genetics and Metabolism. 81: S38-44. PMID 15050972 DOI: 10.1016/J.Ymgme.2003.10.012 |
0.322 |
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| 2004 |
Richards CS, Grody WW. Prenatal screening for cystic fibrosis: past, present and future. Expert Review of Molecular Diagnostics. 4: 49-62. PMID 14711349 DOI: 10.1586/14737159.4.1.49 |
0.395 |
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| 2003 |
Grody WW. Quest for controls in molecular genetics. The Journal of Molecular Diagnostics : Jmd. 5: 209-11. PMID 14573778 DOI: 10.1016/S1525-1578(10)60475-8 |
0.399 |
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| 2003 |
Venegas PB, Novak JM, Oscar CA, Sánchez FL, Gutiérrez IG, Rivera JM, Salas JP, Montero JF, Grody WW. Cystic fibrosis mutations in Costa Rica. Human Biology. 75: 179-88. PMID 12943157 DOI: 10.1353/Hub.2003.0039 |
0.332 |
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| 2003 |
Richards CS, Grody WW. Alternative approaches to proficiency testing in molecular genetics. Clinical Chemistry. 49: 717-8. PMID 12709360 DOI: 10.1373/49.5.717 |
0.39 |
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| 2003 |
Grody WW. Ethical issues raised by genetic testing with oligonucleotide microarrays. Molecular Biotechnology. 23: 127-38. PMID 12632697 DOI: 10.1385/Mb:23:2:127 |
0.407 |
|
| 2003 |
Grody WW. Molecular genetic risk screening. Annual Review of Medicine. 54: 473-90. PMID 12525682 DOI: 10.1146/Annurev.Med.54.101601.152127 |
0.374 |
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| 2002 |
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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 4: 379-91. PMID 12394352 DOI: 10.1097/00125817-200209000-00010 |
0.357 |
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| 2002 |
Richards CS, Bradley LA, Amos J, Allitto B, Grody WW, Maddalena A, McGinnis MJ, Prior TW, Popovich BW, Watson MS. Erratum: Standards and guidelines for CFTR mutation testing (Genetics in Medicine (2002) 4 (379-391)) Genetics in Medicine. 4. DOI: 10.1097/00125817-200211000-00013 |
0.368 |
|
| 2001 |
Dequeker E, Ramsden S, Grody WW, Stenzel TT, Barton DE. Quality control in molecular genetic testing Nature Reviews Genetics. 2: 717-723. PMID 11533720 DOI: 10.1038/35088588 |
0.337 |
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| 2001 |
Grody WW, Cutting GR, Klinger KW, Richards CS, Watson MS, Desnick RJ. Laboratory standards and guidelines for population-based cystic fibrosis carrier screening Genetics in Medicine. 3: 149-154. PMID 11280952 DOI: 10.1097/00125817-200103000-00010 |
0.386 |
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| 2001 |
Grody WW, Griffin JH, Taylor AK, Korf BR, Heit JA. American College of Medical Genetics Consensus Statement on Factor V Leiden Mutation Testing Genetics in Medicine. 3: 139-148. PMID 11280951 DOI: 10.1097/00125817-200103000-00009 |
0.329 |
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| 2000 |
Rohlfs EM, Chung CH, Yang Q, Skrzynia C, Grody WW, Graham ML, Silverman LM. In-frame deletions of BRCA1 may define critical functional domains. Human Genetics. 107: 385-90. PMID 11129340 DOI: 10.1007/S004390000372 |
0.314 |
|
| 2000 |
Telatar M, Grody WW. Molecular genetic testing for familial Mediterranean fever Molecular Genetics and Metabolism. 71: 256-260. PMID 11001819 DOI: 10.1006/Mgme.2000.3047 |
0.331 |
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| 1999 |
Grody WW. Cystic fibrosis: Molecular diagnosis, population screening, and public policy Archives of Pathology and Laboratory Medicine. 123: 1041-1046. PMID 10539904 DOI: 10.1043/0003-9985(1999)123<1041:Cf>2.0.Co;2 |
0.386 |
|
| 1999 |
Grody WW, Pyeritz RE. Report card on molecular genetic testing: Room for improvement? Journal of the American Medical Association. 281: 845-847. PMID 10071008 DOI: 10.1001/Jama.281.9.845 |
0.347 |
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| 1998 |
Wackym PA, Kerner MM, Grody WW. Molecular temporal bone pathology: III. Genotyping of the ΔF508 deletion in the DNA of patients with cystic fibrosis Laryngoscope. 108: 1-3. PMID 9707259 DOI: 10.1097/00005537-199808001-00001 |
0.363 |
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| 1998 |
Iyer R, Jenkinson CP, Vockley JG, Kern RM, Grody WW, Cederbaum S. The human arginases and arginase deficiency. Journal of Inherited Metabolic Disease. 21: 86-100. PMID 9686347 DOI: 10.1023/A:1005313809037 |
0.309 |
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| 1998 |
Grody WW, Desnick RJ, Carpenter NJ, Noll WW. Diversity of cystic fibrosis mutation-screening practices [2] American Journal of Human Genetics. 62: 1252-1254. PMID 9545412 DOI: 10.1086/301842 |
0.35 |
|
| 1997 |
Gregg JP, Yamane AJ, Grody WW. Prevalence of the factor V-Leiden mutation in four distinct American ethnic populations American Journal of Medical Genetics. 73: 334-336. PMID 9415695 DOI: 10.1002/(Sici)1096-8628(19971219)73:3<334::Aid-Ajmg20>3.0.Co;2-J |
0.307 |
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| 1997 |
Geschwind DH, Perlman S, Grody WW, Milhan Telatar P, Laura Montermini P, Pandolfo M, Gatti RA. Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia Neurology. 49: 1004-1009. PMID 9339680 DOI: 10.1212/Wnl.49.4.1004 |
0.312 |
|
| 1997 |
Gregg JP, Grody WW. Diagnostic molecular genetics: Current applications and future technologies Pediatric Annals. 26: 553-561. PMID 9302718 DOI: 10.3928/0090-4481-19970901-11 |
0.307 |
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| 1994 |
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. Journal of Genetic Counseling. 3: 279-89. PMID 24234134 DOI: 10.1007/Bf01412373 |
0.349 |
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| 1994 |
Kerner MM, Wackym PA, Popper P, Tabor DE, Grody WW. Cloning and sequencing of genomic DNA extracted from archival human temporal bone sections. The Laryngoscope. 104: 127-34. PMID 8302113 DOI: 10.1288/00005537-199402000-00002 |
0.303 |
|
| 1994 |
Grody WW. The coming era of cancer genetic screening Diagnostic Molecular Pathology. 3: 145-146. PMID 7981888 DOI: 10.1097/00019606-199409000-00001 |
0.307 |
|
| 1994 |
Grody WW. Proficiency testing in diagnostic molecular pathology Diagnostic Molecular Pathology. 3: 221-223. PMID 7866631 DOI: 10.1097/00019606-199412000-00001 |
0.302 |
|
| 1991 |
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. Somatic Cell and Molecular Genetics. 17: 369-75. PMID 1887333 DOI: 10.1007/Bf01233062 |
0.319 |
|
| 1991 |
Hilborne LH, Grody WW. Diagnostic applications of recombinant nucleic acid technology: Basic techniques Laboratory Medicine. 22: 849-856. DOI: 10.1093/Labmed/22.12.849 |
0.308 |
|
| 1989 |
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. The Journal of Clinical Investigation. 83: 602-9. PMID 2913054 DOI: 10.1172/Jci113923 |
0.327 |
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