Wayne W. Grody - Publications

University of California, Los Angeles, Los Angeles, CA 
Molecular Biology, Microbiology Biology, Genetics

209 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.72
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  0.72
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  0.72
2016 Grody WW. Where to Draw the Boundaries for Prenatal Carrier Screening. Jama. 316: 717-9. PMID 27533155 DOI: 10.1001/jama.2016.10888  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2014 Grody WW, Vilain E, Nelson SF. Interpreting whole-genome sequencing. Jama. 312: 296. PMID 25027151 DOI: 10.1001/jama.2014.6602  0.72
2014 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. Molecular Therapy : the Journal of the American Society of Gene Therapy. 22: 1792-802. PMID 24888478 DOI: 10.1038/mt.2014.99  0.72
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  0.72
2014 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. Clinical Lymphoma, Myeloma & Leukemia. 14: e137-40. PMID 24637131 DOI: 10.1016/j.clml.2014.02.005  0.72
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  0.72
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  0.72
2013 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. Journal of Personalized Medicine. 3: 40-69. PMID 24624293 DOI: 10.3390/jpm3010040  0.36
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  0.72
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  0.72
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  0.72
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  0.72
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: 10.1038/gim.2013.47  0.72
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  0.72
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  0.72
2013 Ong FS, Grody WW, Das K. Molecular testing: Regulatory issues Molecular Genetic Pathology: Second Edition. 2147483647: 1091-1108. DOI: 10.1007/978-1-4614-4800-6-44  0.72
2013 Naeim F, Nagesh Rao P, Song S, Grody WW. Atlas of Hematopathology Atlas of Hematopathology 0.72
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  0.72
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  0.72
2012 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. Molecular Therapy : the Journal of the American Society of Gene Therapy. 20: 1844-51. PMID 22760543 DOI: 10.1038/mt.2012.129  0.72
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  0.72
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  0.72
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  0.72
2012 Grody WW. Response to metcalfe and archibald Genetics in Medicine. 14: 351. DOI: 10.1038/gim.2012.1  0.72
2011 Grody WW. Expanded carrier screening and the law of unintended consequences: from cystic fibrosis to fragile X. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 996-7. PMID 22134443 DOI: 10.1097/GIM.0b013e31823c49a2  0.72
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  0.72
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  0.72
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  0.72
2010 Grody WW, Getzug T. Colchicine's other indication--effect of FDA action. The New England Journal of Medicine. 363: 2267-8. PMID 21121853 DOI: 10.1056/NEJMc1009918  0.72
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  0.72
2010 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. 5: e10763. PMID 20505827 DOI: 10.1371/journal.pone.0010763  0.72
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  0.72
2010 Grody WW, Howell RR. The fate of newborn screening blood spots. Pediatric Research. 67: 237. PMID 20154576 DOI: 10.1203/PDR.0b013e3181d00a48  0.72
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  0.72
2010 Grody WW. Foreword Molecular Diagnostics. DOI: 10.1016/B978-0-12-369428-7.00039-2  0.72
2010 Grody WW. Regulatory Issues in Molecular Diagnostics Molecular Diagnostics. 121-124. DOI: 10.1016/B978-0-12-369428-7.00012-4  0.72
2010 ten Bosch JR, Grody WW. Next-Generation Sequencing in Molecular Diagnostics Molecular Diagnostics. 59-67. DOI: 10.1016/B978-0-12-369428-7.00006-9  0.72
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  0.72
2010 Grody WW, Nakamura RM, Kiechle FL, Strom Dr. CC. Molecular Diagnostics Molecular Diagnostics 0.72
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  0.72
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  0.72
2009 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. Journal of Hematopathology. 2: 27-33. PMID 19669220 DOI: 10.1007/s12308-009-0023-2  0.72
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  0.72
2009 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. Molecular Therapy : the Journal of the American Society of Gene Therapy. 17: 1155-63. PMID 19367256 DOI: 10.1038/mt.2009.65  0.72
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  0.72
2009 Grody WW. Quality Assurance of Molecular Assays Cell and Tissue Based Molecular Pathology. 10-16. DOI: 10.1016/B978-044306901-7.50007-9  0.72
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  0.72
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  0.72
2008 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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 10: 517-24. PMID 18580690 DOI: 10.1097/GIM.0b013e31817708fa  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2008 Naeim F, Rao PN, Grody WW. Non-Neoplastic and Borderline Lymphocytic Disorders Hematopathology. 455-476. DOI: 10.1016/B978-0-12-370607-2.00019-3  0.72
2008 Song S, Grody WW, Naeim F. Hodgkin Lymphoma Hematopathology. 441-454. DOI: 10.1016/B978-0-12-370607-2.00018-1  0.72
2008 Naeim F, Rao PN, Song S, Grody WW. Mature T-Cell and NK-Cell Neoplasms Hematopathology. 397-440. DOI: 10.1016/B978-0-12-370607-2.00017-X  0.72
2008 Naeim F, Rao PN, Grody WW. Plasma Cell Myeloma and Related Disorders Hematopathology. 373-396. DOI: 10.1016/B978-0-12-370607-2.00016-8  0.72
2008 Naeim F, Rao PN, Grody WW. Mature B-Cell Neoplasms Hematopathology. 297-372. DOI: 10.1016/B978-0-12-370607-2.00015-6  0.72
2008 Naeim F, Rao PN, Grody WW. Lymphoid Malignancies of Non-Precursor Cells: General Considerations Hematopathology. 287-296. DOI: 10.1016/B978-0-12-370607-2.00014-4  0.72
2008 Naeim F, Rao PN, Grody WW. The Neoplasms of Precursor Lymphoblasts Hematopathology. 257-277. DOI: 10.1016/B978-0-12-370607-2.00012-0  0.72
2008 Naeim F, Rao PN, Grody WW. Chronic Myeloproliferative Diseases Hematopathology. 155-189. DOI: 10.1016/B978-0-12-370607-2.00009-0  0.72
2008 Naeim F, Rao PN, Grody WW. Myelodysplastic Syndromes Hematopathology. 129-154. DOI: 10.1016/B978-0-12-370607-2.00008-9  0.72
2008 Naeim F, Rao PN, Grody WW. Bone Marrow Aplasia Hematopathology. 115-127. DOI: 10.1016/B978-0-12-370607-2.00007-7  0.72
2008 Grody WW, Rao PN, Naeim F. Principles of Molecular Techniques Hematopathology. 65-79. DOI: 10.1016/B978-0-12-370607-2.00004-1  0.72
2008 Naeim F, Rao PN, Grody WW. Hematopathology Hematopathology 0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2007 Kern RM, Yang Z, Kim PS, Grody WW, Iyer RK, Cederbaum SD. Arginase induction by sodium phenylbutyrate in mouse tissues and human cell lines. Molecular Genetics and Metabolism. 90: 37-41. PMID 16935537 DOI: 10.1016/j.ymgme.2006.07.002  0.72
2006 Elshimali YI, Grody WW. The clinical significance of circulating tumor cells in the peripheral blood. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 15: 187-94. PMID 17122646 DOI: 10.1097/01.pdm.0000213463.98763.b9  0.72
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  0.72
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  0.72
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  0.72
2005 Palmer CG, Martinez A, Sininger Y, Shapiro N, Grody WW, Schimmenti LA. Prelingual siblings of children with GJB2 hearing loss: issues to consider. Archives of Otolaryngology--Head & Neck Surgery. 131: 1020-2. PMID 16301377 DOI: 10.1001/archotol.131.11.1020  0.72
2005 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, ... ... Grody WW, et al. Developing a sustainable process to provide quality control materials for genetic testing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 7: 534-49. PMID 16247292 DOI: 10.1097/01.GIM.0000183043.94406.81  0.72
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  0.72
2005 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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 7: 317-27. PMID 15915083 DOI: 10.1097/01.GIM.0000162871.68167.8A  0.72
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  0.72
2005 Grody WW. Molecular testing for heritable disease Journal of Clinical Ligand Assay. 28: 50-53.  0.72
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  0.72
2004 Tsongalis GJ, Belloni DR, Grody WW. Cystic fibrosis mutation analysis: how many is enough? Genetics in Medicine : Official Journal of the American College of Medical Genetics. 6: 456-8. PMID 15371913 DOI: 10.1097/01.GIM.0000139542.56994.67  0.72
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  0.72
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  0.72
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  0.72
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  0.72
2003 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. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 5: 440-3. PMID 14614395 DOI: 10.1097/01.GIM.0000096500.66084.85  0.72
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  0.72
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  0.72
2003 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. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 51: 1151-60. PMID 12923240  0.72
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  0.72
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  0.72
2003 Grody WW. Molecular genetic risk screening. Annual Review of Medicine. 54: 473-90. PMID 12525682 DOI: 10.1146/annurev.med.54.101601.152127  0.72
2003 Grody WW, Telatar M. Multiplex SNP analysis: Screening Factor V R506Q (Leiden) mutations American Biotechnology Laboratory. 21: 34-47.  0.72
2002 Watson MS, Desnick RJ, Grody WW, Mennuti MT, Popovich BW, Richards CS. Cystic fibrosis carrier screening: issues in implementation. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 4: 407-9. PMID 12509709 DOI: 10.1097/00125817-200211000-00001  0.72
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  0.72
2002 Sharma P, Rosenbaum AL, Vives T, Grody WW, Demer JL. Discordant pursuit asymmetry and esotropia in monozygous twins. American Journal of Ophthalmology. 134: 143-6. PMID 12095832 DOI: 10.1016/S0002-9394(02)01405-8  0.72
2002 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. Molecular Genetics and Metabolism. 76: 100-10. PMID 12083807 DOI: 10.1016/S1096-7192(02)00034-3  0.72
2002 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 Research. 30: e55. PMID 12060693  0.72
2002 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. Molecular and Cellular Biology. 22: 4491-8. PMID 12052859 DOI: 10.1128/MCB.22.13.4491-4498.2002  0.72
2002 Yu H, Iyer RK, Yoo PK, Kern RM, Grody WW, Cederbaum SD. Arginase expression in mouse embryonic development. Mechanisms of Development. 115: 151-5. PMID 12049781 DOI: 10.1016/S0925-4773(02)00089-8  0.72
2002 Iyer RK, Kim HK, Tsoa RW, Grody WW, Cederbaum SD. Cloning and characterization of human agmatinase. Molecular Genetics and Metabolism. 75: 209-18. PMID 11914032 DOI: 10.1006/mgme.2001.3277  0.72
2001 Yu H, Iyer RK, Kern RM, Rodriguez WI, Grody WW, Cederbaum SD. Expression of arginase isozymes in mouse brain. Journal of Neuroscience Research. 66: 406-22. PMID 11746358 DOI: 10.1002/jnr.1233  0.72
2001 Telatar M, Grody WW, Emmanouilides C. Detection of bcl-2/IgH rearrangements by quantitative-competitive PCR and capillary electrophoresis Molecular Diagnosis. 6: 161-168. PMID 11571709 DOI: 10.1054/modi.2001.26056  0.72
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  0.72
2001 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. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 10: 105-10. PMID 11385319 DOI: 10.1097/00019606-200106000-00006  0.72
2001 Grody WW. Ethical ramifications of genetic analysis using DNA arrays Methods in Molecular Biology (Clifton, N.J.). 170: 53-69. PMID 11357689  0.72
2001 Grody WW, Desnick RJ. Cystic fibrosis population carrier screening: Here at last - Are we ready? Genetics in Medicine. 3: 87-90. PMID 11280954  0.72
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  0.72
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  0.72
2001 Palmer CGS, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Schimmenti LA. Genetic testing and the early hearing detection and intervention process Volta Review. 103: 371-390.  0.72
2000 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 Clinical Lymphoma. 1: 146-151. PMID 11707827  0.72
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  0.72
1999 Grody WW. Cystic fibrosis: Molecular diagnosis, population screening, and public policy Archives of Pathology and Laboratory Medicine. 123: 1041-1046. PMID 10539904  0.72
1999 Stass SA, Grody WW. Molecular pathology: Role in improving patient outcome Archives of Pathology and Laboratory Medicine. 123: 1000-1001. PMID 10539895  0.72
1999 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 Archives of Pathology and Laboratory Medicine. 123: 296-300. PMID 10320140  0.72
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  0.72
1999 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. Human Pathology. 30: 123-9. PMID 10029438 DOI: 10.1016/S0046-8177(99)90265-4  0.72
1998 Wackym PA, Kerner MM, Grody WW. Molecular temporal bone pathology: IV. Analysis of DNA template length using mitochondrial PCR primers Laryngoscope. 108: 4-7. PMID 9707260  0.72
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  0.72
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  0.72
1998 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. Molecular Genetics and Metabolism. 63: 168-75. PMID 9608538 DOI: 10.1006/mgme.1997.2669  0.72
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  0.72
1998 Apple SK, Alzona MC, Jahromi SA, Grody WW. Can different thyroid tumor types be distinguished by polymerase chain reaction-based K-ras mutation detection? Molecular Diagnosis. 3: 143-148. DOI: 10.1016/S1084-8592(98)80032-5  0.72
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  0.72
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  0.72
1997 Gregg JP, Grody WW. Diagnostic molecular genetics: Current applications and future technologies Pediatric Annals. 26: 553-561. PMID 9302718  0.72
1997 Grody WW, Watson MS. Those elusive molecular diagnostics CPT codes Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 6: 131-133. PMID 9276183  0.72
1997 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. American Journal of Human Genetics. 60: 935-47. PMID 9106541  0.72
1997 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. Women's Health (Hillsdale, N.J.). 3: 31-51. PMID 9106369  0.72
1997 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 Diagnostic Molecular Pathology. 6: 26-33. PMID 9028734 DOI: 10.1097/00019606-199702000-00005  0.72
1997 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. 63: 80-84. PMID 9000665 DOI: 10.1097/00007890-199701150-00015  0.72
1997 Sazama K, Caplan A, Cataldo N, Farkas DH, Fox M, Grody WW. Roundtable: Ethical dilemmas in genetic testing Laboratory Medicine. 28: 311-315.  0.72
1996 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. Somatic Cell and Molecular Genetics. 22: 489-98. PMID 9131018  0.72
1996 Vockley JG, Jenkinson CP, Shukla H, Kern RM, Grody WW, Cederbaum SD. Cloning and characterization of the human type II arginase gene. Genomics. 38: 118-23. PMID 8954792 DOI: 10.1006/geno.1996.0606  0.72
1996 Lovell MA, Grody WW. Molecular pathology 1995. Birth of an association [meeting report] Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 5: 1-2. PMID 8919538  0.72
1996 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. Biochemical and Molecular Medicine. 59: 44-51. PMID 8902193 DOI: 10.1006/bmme.1996.0063  0.72
1996 Jenkinson CP, Grody WW, Cederbaum SD. Comparative properties of arginases Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology. 114: 107-132. PMID 8759304 DOI: 10.1016/0305-0491(95)02138-8  0.72
1996 Grody WW, Sobel ME. Update on informed consent for stored tissue research Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 5: 79-80. PMID 8727093  0.72
1996 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 American Journal of Clinical Pathology. 105: 321-326. PMID 8602613  0.72
1995 Gregg JP, Grody WW. Molecular pathology and cancer genetic screening Western Journal of Medicine. 162: 449-450. PMID 7785261  0.72
1995 Goldstein NS, Begin 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' American Journal of Surgical Pathology. 19: 1002-1009. PMID 7661273  0.72
1995 Grody WW. Molecular pathology, informed consent, and the paraffin block Diagnostic Molecular Pathology. 4: 155-157. PMID 7493133  0.72
1995 Grody WW, Lovell MA. Molecular pathology 1994 Diagnostic Molecular Pathology. 4: 1.  0.72
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  0.72
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  0.72
1994 Grody WW. DMP news and comment Diagnostic Molecular Pathology. 3: 71-73. PMID 8061890  0.72
1994 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. Cellular Immunology. 157: 170-80. PMID 8039244 DOI: 10.1006/cimm.1994.1214  0.72
1994 Grody WW. The coming era of cancer genetic screening Diagnostic Molecular Pathology. 3: 145-146. PMID 7981888  0.72
1994 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. Human Mutation. 4: 150-4. PMID 7981719 DOI: 10.1002/humu.1380040210  0.72
1994 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. Somatic Cell and Molecular Genetics. 20: 313-25. PMID 7974006 DOI: 10.1007/BF02254720  0.72
1994 Grody WW. Breast and prostate cancer, 1994 American Journal of Clinical Pathology. 102. PMID 7942608  0.72
1994 Grody WW. Proficiency testing in diagnostic molecular pathology Diagnostic Molecular Pathology. 3: 221-223. PMID 7866631  0.72
1994 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 Journal of Inherited Metabolic Disease. 17: 566-574. PMID 7837763 DOI: 10.1007/BF00711592  0.72
1994 Gu Y, Lugenbeel KA, Vockley JG, Grody WW, Nelson DL. A de novo deletion in FMR1 in a patient with developmental delay Human Molecular Genetics. 3: 1705-1706. PMID 7530551 DOI: 10.1093/hmg/3.9.1705  0.72
1994 Grody WW. Integration and quality assurance of new molecular genetic technologies in clinical laboratories Clinical Chemistry. 40: 647-648.  0.72
1993 Grody WW. Molecular genetics: Introduction Archives of Pathology and Laboratory Medicine. 117: 470-472. PMID 8489333  0.72
1993 Grody WW. Molecular techniques Western Journal of Medicine. 158: 299. PMID 8460517  0.72
1993 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. Human Genetics. 91: 1-5. PMID 8454280 DOI: 10.1007/BF00230212  0.72
1993 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. 103: 91S-94S. PMID 8428548  0.72
1993 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 American Journal of Human Genetics. 53: 1352-1355. PMID 8250051  0.72
1993 Wackym PA, Popper P, Kerner MM, Grody WW. Varicella-zoster DNA in temporal bones of patients with ramsay hunt syndrome The Lancet. 342: 1555. PMID 7902926 DOI: 10.1016/S0140-6736(05)80126-6  0.72
1993 Storek J, Glaspy JA, Grody WW, Susi E, Slater ED. Adult-onset cyclic neutropenia responsive to cyclosporine therapy in a patient with ankylosing spondylitis American Journal of Hematology. 43: 139-143. PMID 7688178  0.72
1993 Beall MH, Grody WW. Cytomegalovirus DNA as a potential placental marker for fetal infection Journal of Maternal-Fetal and Neonatal Medicine. 2: 229-232. DOI: 10.3109/14767059309017239  0.72
1992 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. American Journal of Human Genetics. 50: 1281-90. PMID 1598908  0.72
1992 Klein D, Grody WW, Tabor DE, Cederbaum SD. Pitfalls of restriction endonuclease digestion for direct detection of point mutations. Clinical Chemistry. 38: 1392-4. PMID 1320472  0.72
1992 Lewis W, Grody WW. AIDS and the heart: Review and consideration of pathogenetic mechanisms Cardiovascular Pathology. 1: 53-64.  0.72
1992 Grody WW, Hilborne LH. Diagnostic applications of recombinant nucleic acid technology: Genetic diseases Laboratory Medicine. 23: 166-171.  0.72
1992 Hilborne LH, Grody WW. Diagnostic applications of recombinant nucleic acid technology: Infectious diseases Laboratory Medicine. 23: 89-94.  0.72
1992 Grody WW, Hilborne LH. Diagnostic applications of recombinant nucleic acid technology: Neoplastic disease Laboratory Medicine. 23: 19-23.  0.72
1991 Fain JS, Bryan RN, Cheng L, Lewin KJ, Porter DD, Grody WW. Rapid diagnosis of Legionella infection by a nonisotopic in situ hybridization method. American Journal of Clinical Pathology. 95: 719-24. PMID 2024627  0.72
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  0.72
1991 Lewis W, Papoian T, Gonzalez B, Louie H, Kelly DP, Payne RM, Grody WW. Mitochondrial ultrastructural and molecular changes induced by zidovudine in rat hearts Laboratory Investigation. 65: 228-236. PMID 1715447  0.72
1991 Farrell MA, Cheng L, Cornford ME, Grody WW, Vinters HV. Cytomegalovirus and Rasmussen's encephalitis. Lancet. 337: 1551-2. PMID 1675405 DOI: 10.1016/0140-6736(91)93249-9  0.72
1991 Hilborne LH, Grody WW. Diagnostic applications of recombinant nucleic acid technology: Basic techniques Laboratory Medicine. 22: 849-856.  0.72
1990 Grody WW, Cheng L, Lewis W. Infection of the heart by the human immunodeficiency virus The American Journal of Cardiology. 66: 203-206. PMID 2371952 DOI: 10.1016/0002-9149(90)90589-S  0.72
1990 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 Cytogenetic and Genome Research. 54: 95-96. PMID 1979025 DOI: 10.1159/000132968  0.72
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  0.72
1989 Grody WW, Gatti RA, Naeim F. Diagnostic molecular pathology Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. 2: 553-568. PMID 2685810  0.72
1989 Gatti RA, Nakamura Y, Nussmeier M, Susi E, Shan W, Grody WW. Informativeness of VNTR genetic markers for detecting chimerism after bone marrow transplantation Disease Markers. 7: 105-112. PMID 2659237  0.72
1989 Grody WW. Clinical applications of DNA probes in the diagnosis of genetic disorders Clinical Laboratory Science. 2: 218-222.  0.72
1988 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 Research. 16: 8191. PMID 3419916 DOI: 10.1093/nar/16.16.8191  0.72
1988 Grody WW, Lewin KJ, Naeim F. Detection of cytomegalovirus DNA in classic and epidemic Kaposi's sarcoma by in situ hybridization. Human Pathology. 19: 524-8. PMID 2836296 DOI: 10.1016/S0046-8177(88)80198-9  0.72
1987 Grody WW, Dizikes GJ, Cederbaum SD. Human arginase isozymes Isozymes. 13: 181-214. PMID 3583682  0.72
1987 Grody WW, Cheng L, Lewin KJ. Application of in situ DNA hybridization technology to diagnostic surgical pathology. Pathology Annual. 22: 151-75. PMID 3317222  0.72
1987 Grody WW, Cheng L, Lewin KJ. In situ viral DNA hybridization in diagnostic surgical pathology. Human Pathology. 18: 535-43. PMID 3297990  0.72
1986 Dizikes GJ, Grody WW, Kern RM, Cederbaum SD. Isolation of human liver arginase cDNA and demonstration of nonhomology between the two human arginase genes. Biochemical and Biophysical Research Communications. 141: 53-9. PMID 3801008 DOI: 10.1016/S0006-291X(86)80333-3  0.72
1986 Grody WW, Jobst S, Keesey J, Herrmann C, Naeim F. Pathologic evaluation of thymic hyperplasia in myasthenia gravis and Lambert-Eaton myasthenic syndrome Archives of Pathology and Laboratory Medicine. 110: 843-846. PMID 3755894  0.72
1986 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 American Journal of Human Genetics. 39: 186-193. PMID 3752085  0.72
1986 Kidd JR, Dizikes GJ, Grody WW, Cederbaum SD, Kidd KK. A pvuII RFLP for the human liver arginase (ARG1) gene Nucleic Acids Research. 14: 9544. PMID 2879271 DOI: 10.1093/nar/14.23.9544  0.72
1985 Grody WW, Fligiel S, Naeim F. Thymus involution in the acquired immunodeficiency syndrome American Journal of Clinical Pathology. 84: 85-95. PMID 4014079  0.72
1985 Grody WW, Magidson JG, Weiss LM, Hu E, Warnke HA, Lewin KJ. Gastrointestinal lymphomas. Immunohistochemical studies on the cell of origin. The American Journal of Surgical Pathology. 9: 328-37. PMID 3911777 DOI: 10.1097/00000478-198505000-00002  0.72
1985 Grody WW, Nieberg RK, Bhuta S. Ependymoma-like tumor of the mesovarium Archives of Pathology and Laboratory Medicine. 109: 291-293. PMID 3838461  0.72
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