Charles P. Venditti - Publications

Affiliations: 
Biochemistry and Molecular Biology The George Washington University, Washington, DC, United States 
Area:
Molecular Biology, Genetics, Medicine and Surgery

74 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 Kang HR, Gjorgjieva M, Smith SN, Brooks ED, Chen Z, Burgess SM, Chandler RJ, Waskowicz LR, Grady KM, Li S, Mithieux G, Venditti CP, Rajas F, Koeberl DD. Pathogenesis of Hepatic Tumors following Gene Therapy in Murine and Canine Models of Glycogen Storage Disease. Molecular Therapy. Methods & Clinical Development. 15: 383-391. PMID 31890731 DOI: 10.1016/j.omtm.2019.10.016  0.96
2019 Chandler RJ, Venditti CP. Gene Therapy for Methylmalonic Acidemia: Past, Present, and Future. Human Gene Therapy. PMID 31303064 DOI: 10.1089/hum.2019.113  0.96
2018 Manoli I, Sysol JR, Epping MW, Li L, Wang C, Sloan JL, Pass A, Gagné J, Ktena YP, Li L, Trivedi NS, Ouattara B, Zerfas PM, Hoffmann V, Abu-Asab M, ... ... Venditti CP, et al. FGF21 underlies a hormetic response to metabolic stress in methylmalonic acidemia. Jci Insight. 3. PMID 30518688 DOI: 10.1172/jci.insight.124351  0.96
2018 An D, Schneller JL, Frassetto A, Liang S, Zhu X, Park JS, Theisen M, Hong SJ, Zhou J, Rajendran R, Levy B, Howell R, Besin G, Presnyak V, Sabnis S, ... ... Venditti CP, et al. Systemic Messenger RNA Therapy as a Treatment for Methylmalonic Acidemia. Cell Reports. 24: 2520. PMID 30157442 DOI: 10.1016/j.celrep.2018.08.049  0.96
2017 An D, Schneller JL, Frassetto A, Liang S, Zhu X, Park JS, Theisen M, Hong SJ, Zhou J, Rajendran R, Levy B, Howell R, Besin G, Presnyak V, Sabnis S, ... ... Venditti CP, et al. Systemic Messenger RNA Therapy as a Treatment for Methylmalonic Acidemia. Cell Reports. 21: 3548-3558. PMID 29262333 DOI: 10.1016/j.celrep.2017.11.081  0.96
2017 Chandler RJ, Sands M, Venditti CP. rAAV integration and genotoxicity: insights from animal models. Human Gene Therapy. PMID 28293963 DOI: 10.1089/hum.2017.009  0.96
2016 Chandler RJ, Venditti CP. Gene Therapy for Metabolic Diseases. Translational Science of Rare Diseases. 1: 73-89. PMID 27853673 DOI: 10.3233/TRD-160007  0.96
2016 Chandler RJ, Williams IM, Gibson AL, Davidson CD, Incao AA, Hubbard BT, Porter FD, Pavan WJ, Venditti CP. Systemic AAV9 gene therapy improves the lifespan of mice with Niemann-Pick disease, type C1. Human Molecular Genetics. PMID 27798114 DOI: 10.1093/hmg/ddw367  0.96
2016 Lerin C, Goldfine AB, Boes T, Liu M, Kasif S, Dreyfuss JM, De Sousa-Coelho AL, Daher G, Manoli I, Sysol JR, Isganaitis E, Jessen N, Goodyear LJ, Beebe K, Gall W, ... Venditti CP, et al. Defects in muscle branched-chain amino acid oxidation contribute to impaired lipid metabolism. Molecular Metabolism. 5: 926-36. PMID 27689005 DOI: 10.1016/j.molmet.2016.08.001  0.32
2016 Fraser JL, Venditti CP. Methylmalonic and propionic acidemias: clinical management update. Current Opinion in Pediatrics. PMID 27653704 DOI: 10.1097/MOP.0000000000000422  0.92
2016 Manoli I, Myles JG, Sloan JL, Shchelochkov OA, Venditti CP. Response to Cunningham et al. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26963280 DOI: 10.1038/gim.2016.12  0.92
2016 Chandler RJ, LaFave MC, Varshney GK, Burgess SM, Venditti CP. Genotoxicity in Mice Following AAV Gene Delivery: A Safety Concern for Human Gene Therapy? Molecular Therapy : the Journal of the American Society of Gene Therapy. 24: 198-201. PMID 26906613 DOI: 10.1038/mt.2016.17  0.92
2016 Brooks BP, Thompson AH, Sloan JL, Manoli I, Carrillo-Carrasco N, Zein WM, Venditti CP. Ophthalmic Manifestations and Long-Term Visual Outcomes in Patients with Cobalamin C Deficiency. Ophthalmology. PMID 26825575 DOI: 10.1016/j.ophtha.2015.10.041  0.92
2016 Harrington EA, Sloan JL, Manoli I, Chandler RJ, Schneider M, McGuire PJ, Calcedo R, Wilson JM, Venditti CP. Neutralizing Antibodies against AAV Capsids in Patients with mut Methylmalonic Acidemia (MMA). Human Gene Therapy. PMID 26790480 DOI: 10.1089/hum.2015.092  0.92
2015 Caterino M, Chandler RJ, Sloan JL, Dorko K, Cusmano-Ozog K, Ingenito L, Strom SC, Imperlini E, Scolamiero E, Venditti CP, Ruoppolo M. The proteome of methylmalonic acidemia (MMA): the elucidation of altered pathways in patient livers. Molecular Biosystems. PMID 26672496 DOI: 10.1039/c5mb00736d  0.92
2015 Manoli I, Myles JG, Sloan JL, Carrillo-Carrasco N, Morava E, Strauss KA, Morton H, Venditti CP. A critical reappraisal of dietary practices in methylmalonic acidemia raises concerns about the safety of medical foods. Part 2: cobalamin C deficiency. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26270766 DOI: 10.1038/gim.2015.107  0.92
2015 Manoli I, Myles JG, Sloan JL, Shchelochkov OA, Venditti CP. A critical reappraisal of dietary practices in methylmalonic acidemia raises concerns about the safety of medical foods. Part 1: isolated methylmalonic acidemias. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26270765 DOI: 10.1038/gim.2015.102  0.92
2015 Ktena YP, Ramstad T, Baker EH, Sloan JL, Mannes AJ, Manoli I, Venditti CP. Propofol administration in patients with methylmalonic acidemia and intracellular cobalamin metabolism disorders: a review of theoretical concerns and clinical experiences in 28 patients. Journal of Inherited Metabolic Disease. PMID 25985870 DOI: 10.1007/s10545-015-9816-x  0.92
2015 Ktena YP, Paul SM, Hauser NS, Sloan JL, Gropman A, Manoli I, Venditti CP. Delineating the spectrum of impairments, disabilities, and rehabilitation needs in methylmalonic acidemia (MMA). American Journal of Medical Genetics. Part A. PMID 25959030 DOI: 10.1002/ajmg.a.37127  0.92
2015 Sloan JL, Manoli I, Venditti CP. Liver or combined liver-kidney transplantation for patients with isolated methylmalonic acidemia: who and when? The Journal of Pediatrics. 166: 1346-50. PMID 25882873 DOI: 10.1016/j.jpeds.2015.03.026  0.92
2015 Chandler RJ, LaFave MC, Varshney GK, Trivedi NS, Carrillo-Carrasco N, Senac JS, Wu W, Hoffmann V, Elkahloun AG, Burgess SM, Venditti CP. Vector design influences hepatic genotoxicity after adeno-associated virus gene therapy. The Journal of Clinical Investigation. 125: 870-80. PMID 25607839 DOI: 10.1172/JCI79213  0.96
2015 Raval DB, Merideth M, Sloan JL, Braverman NE, Conway RL, Manoli I, Venditti CP. Methylmalonic acidemia (MMA) in pregnancy: a case series and literature review. Journal of Inherited Metabolic Disease. PMID 25567501 DOI: 10.1007/s10545-014-9802-8  0.92
2015 Baker EH, Sloan JL, Hauser NS, Gropman AL, Adams DR, Toro C, Manoli I, Venditti CP. MRI characteristics of globus pallidus infarcts in isolated methylmalonic acidemia. Ajnr. American Journal of Neuroradiology. 36: 194-201. PMID 25190203 DOI: 10.3174/ajnr.A4087  0.92
2014 Vernon HJ, Sperati CJ, King JD, Poretti A, Miller NR, Sloan JL, Cameron AM, Myers D, Venditti CP, Valle D. A detailed analysis of methylmalonic acid kinetics during hemodialysis and after combined liver/kidney transplantation in a patient with mut (0) methylmalonic acidemia. Journal of Inherited Metabolic Disease. 37: 899-907. PMID 24961826 DOI: 10.1007/s10545-014-9730-7  0.92
2014 Zsengellér ZK, Aljinovic N, Teot LA, Korson M, Rodig N, Sloan JL, Venditti CP, Berry GT, Rosen S. Methylmalonic acidemia: a megamitochondrial disorder affecting the kidney. Pediatric Nephrology (Berlin, Germany). 29: 2139-46. PMID 24865477 DOI: 10.1007/s00467-014-2847-y  0.92
2014 Trakadis YJ, Alfares A, Bodamer OA, Buyukavci M, Christodoulou J, Connor P, Glamuzina E, Gonzalez-Fernandez F, Bibi H, Echenne B, Manoli I, Mitchell J, Nordwall M, Prasad C, Scaglia F, ... ... Venditti CP, et al. Update on transcobalamin deficiency: clinical presentation, treatment and outcome. Journal of Inherited Metabolic Disease. 37: 461-73. PMID 24305960 DOI: 10.1007/s10545-013-9664-5  0.92
2014 Watkins D, Venditti CP, Rosenblatt DS. Vitamins: Cobalamin and Folate Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease: Fifth Edition. 521-529. DOI: 10.1016/B978-0-12-410529-4.00047-4  0.92
2013 Chandler RJ, Tarasenko TN, Cusmano-Ozog K, Sun Q, Sutton VR, Venditti CP, McGuire PJ. Liver-directed adeno-associated virus serotype 8 gene transfer rescues a lethal murine model of citrullinemia type 1. Gene Therapy. 20: 1188-91. PMID 24131980 DOI: 10.1038/gt.2013.53  0.92
2013 Yu HC, Sloan JL, Scharer G, Brebner A, Quintana AM, Achilly NP, Manoli I, Coughlin CR, Geiger EA, Schneck U, Watkins D, Suormala T, Van Hove JL, Fowler B, Baumgartner MR, ... ... Venditti CP, et al. An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1. American Journal of Human Genetics. 93: 506-14. PMID 24011988 DOI: 10.1016/j.ajhg.2013.07.022  0.92
2013 Tanpaiboon P, Venditti CP. Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C disease: Response to letter "Disappearance of congenital noncompaction in hereditary cobalamin-C-deficiency 2.5 years after birth" by J. Finsterer and Claudia Stöllberger, DOI 10.1007/s10545-013-9612-4. Journal of Inherited Metabolic Disease. 36: 1085. PMID 23974651 DOI: 10.1007/s10545-013-9644-9  0.92
2013 Manoli I, Sysol JR, Li L, Houillier P, Garone C, Wang C, Zerfas PM, Cusmano-Ozog K, Young S, Trivedi NS, Cheng J, Sloan JL, Chandler RJ, Abu-Asab M, Tsokos M, ... ... Venditti CP, et al. Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia. Proceedings of the National Academy of Sciences of the United States of America. 110: 13552-7. PMID 23898205 DOI: 10.1073/pnas.1302764110  0.92
2013 Camp KM, Lloyd-Puryear MA, Yao L, Groft SC, Parisi MA, Mulberg A, Gopal-Srivastava R, Cederbaum S, Enns GM, Ershow AG, Frazier DM, Gohagan J, Harding C, Howell RR, Regan K, ... ... Venditti C, et al. Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolism. Molecular Genetics and Metabolism. 109: 319-28. PMID 23806236 DOI: 10.1016/j.ymgme.2013.05.008  0.92
2013 Kruszka PS, Manoli I, Sloan JL, Kopp JB, Venditti CP. Renal growth in isolated methylmalonic acidemia. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 990-6. PMID 23639900 DOI: 10.1038/gim.2013.42  0.92
2012 Chandler RJ, Venditti CP. Pre-clinical efficacy and dosing of an AAV8 vector expressing human methylmalonyl-CoA mutase in a murine model of methylmalonic acidemia (MMA). Molecular Genetics and Metabolism. 107: 617-9. PMID 23046887 DOI: 10.1016/j.ymgme.2012.09.019  0.92
2012 O'Shea CJ, Sloan JL, Wiggs EA, Pao M, Gropman A, Baker EH, Manoli I, Venditti CP, Snow J. Neurocognitive phenotype of isolated methylmalonic acidemia. Pediatrics. 129: e1541-51. PMID 22614770 DOI: 10.1542/peds.2011-1715  0.92
2012 Schreiber J, Chapman KA, Summar ML, Ah Mew N, Sutton VR, MacLeod E, Stagni K, Ueda K, Franks J, Island E, Matern D, Peña L, Smith B, Urv T, Venditti C, et al. Neurologic considerations in propionic acidemia. Molecular Genetics and Metabolism. 105: 10-5. PMID 22078457 DOI: 10.1016/j.ymgme.2011.10.003  0.92
2012 Chapman KA, Gropman A, MacLeod E, Stagni K, Summar ML, Ueda K, Ah Mew N, Franks J, Island E, Matern D, Pena L, Smith B, Sutton VR, Urv T, Venditti C, et al. Acute management of propionic acidemia. Molecular Genetics and Metabolism. 105: 16-25. PMID 22000903 DOI: 10.1016/j.ymgme.2011.09.026  0.92
2012 Pena L, Franks J, Chapman KA, Gropman A, Ah Mew N, Chakrapani A, Island E, MacLeod E, Matern D, Smith B, Stagni K, Sutton VR, Ueda K, Urv T, Venditti C, et al. Natural history of propionic acidemia. Molecular Genetics and Metabolism. 105: 5-9. PMID 21986446 DOI: 10.1016/j.ymgme.2011.09.022  0.92
2012 Sutton VR, Chapman KA, Gropman AL, MacLeod E, Stagni K, Summar ML, Ueda K, Ah Mew N, Franks J, Island E, Matern D, Peña L, Smith B, Urv T, Venditti C, et al. Chronic management and health supervision of individuals with propionic acidemia. Molecular Genetics and Metabolism. 105: 26-33. PMID 21963082 DOI: 10.1016/j.ymgme.2011.08.034  0.92
2012 Sénac JS, Chandler RJ, Sysol JR, Li L, Venditti CP. Gene therapy in a murine model of methylmalonic acidemia using rAAV9-mediated gene delivery. Gene Therapy. 19: 385-91. PMID 21776024 DOI: 10.1038/gt.2011.108  0.92
2012 Carrillo-Carrasco N, Chandler RJ, Venditti CP. Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management. Journal of Inherited Metabolic Disease. 35: 91-102. PMID 21748409 DOI: 10.1007/s10545-011-9364-y  0.92
2012 Carrillo-Carrasco N, Venditti CP. Combined methylmalonic acidemia and homocystinuria, cblC type. II. Complications, pathophysiology, and outcomes. Journal of Inherited Metabolic Disease. 35: 103-14. PMID 21748408 DOI: 10.1007/s10545-011-9365-x  0.92
2011 Sloan JL, Johnston JJ, Manoli I, Chandler RJ, Krause C, Carrillo-Carrasco N, Chandrasekaran SD, Sysol JR, O'Brien K, Hauser NS, Sapp JC, Dorward HM, Huizing M, Barshop BA, ... ... Venditti CP, et al. Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria. Nature Genetics. 43: 883-6. PMID 21841779 DOI: 10.1038/ng.908  0.92
2011 Chandler RJ, Venditti CP. A barrel of monkeys: scAAV8 gene therapy for hemophilia in nonhuman primates. Molecular Therapy : the Journal of the American Society of Gene Therapy. 19: 826-7. PMID 21532610 DOI: 10.1038/mt.2011.73  0.92
2011 Hauser NS, Manoli I, Graf JC, Sloan J, Venditti CP. Variable dietary management of methylmalonic acidemia: metabolic and energetic correlations. The American Journal of Clinical Nutrition. 93: 47-56. PMID 21048060 DOI: 10.3945/ajcn.110.004341  0.92
2011 Chandler RJ, Chandrasekaran S, Carrillo-Carrasco N, Senac JS, Hofherr SE, Barry MA, Venditti CP. Adeno-associated virus serotype 8 gene transfer rescues a neonatal lethal murine model of propionic acidemia. Human Gene Therapy. 22: 477-81. PMID 20950151 DOI: 10.1089/hum.2010.164  0.92
2010 Chandler RJ, Venditti CP. Long-term Rescue of a Lethal Murine Model of Methylmalonic Acidemia Using Adeno associated Viral Gene Therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 18: 11-16. PMID 28178549 DOI: 10.1038/mt.2009.247  0.96
2010 Carrillo-Carrasco N, Chandler RJ, Chandrasekaran S, Venditti CP. Liver-directed recombinant adeno-associated viral gene delivery rescues a lethal mouse model of methylmalonic acidemia and provides long-term phenotypic correction. Human Gene Therapy. 21: 1147-54. PMID 20486773 DOI: 10.1089/hum.2010.008  0.92
2010 Murphy GE, Lowekamp BC, Zerfas PM, Chandler RJ, Narasimha R, Venditti CP, Subramaniam S. Ion-abrasion scanning electron microscopy reveals distorted liver mitochondrial morphology in murine methylmalonic acidemia. Journal of Structural Biology. 171: 125-32. PMID 20399866 DOI: 10.1016/j.jsb.2010.04.005  0.92
2010 Chandler RJ, Venditti CP. Long-term rescue of a lethal murine model of methylmalonic acidemia using adeno-associated viral gene therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 18: 11-6. PMID 19861951 DOI: 10.1038/mt.2009.247  0.92
2010 Carrillo-Carrasco N, Venditti CP. Hydroxocobalamin for cobalamin C: Which dosage? by V. Wiwanitkit Journal of Inherited Metabolic Disease. 33: 455. DOI: 10.1007/s10545-010-9092-8  0.92
2009 Carrillo-Carrasco N, Sloan J, Valle D, Hamosh A, Venditti CP. Hydroxocobalamin dose escalation improves metabolic control in cblC. Journal of Inherited Metabolic Disease. 32: 728-31. PMID 19821145 DOI: 10.1007/s10545-009-1257-y  0.92
2009 Bassim CW, Wright JT, Guadagnini JP, Muralidharan R, Sloan J, Domingo DL, Venditti CP, Hart TC. Enamel defects and salivary methylmalonate in methylmalonic acidemia. Oral Diseases. 15: 196-205. PMID 19143946 DOI: 10.1111/j.1601-0825.2008.01509.x  0.92
2009 Chandler RJ, Zerfas PM, Shanske S, Sloan J, Hoffmann V, DiMauro S, Venditti CP. Mitochondrial dysfunction in mut methylmalonic acidemia. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 23: 1252-61. PMID 19088183 DOI: 10.1096/fj.08-121848  0.92
2008 Buccafusca R, Venditti CP, Kenyon LC, Johanson RA, Van Bockstaele E, Ren J, Pagliardini S, Minarcik J, Golden JA, Coady MJ, Greer JJ, Berry GT. Characterization of the null murine sodium/myo-inositol cotransporter 1 (Smit1 or Slc5a3) phenotype: myo-inositol rescue is independent of expression of its cognate mitochondrial ribosomal protein subunit 6 (Mrps6) gene and of phosphatidylinositol levels in neonatal brain. Molecular Genetics and Metabolism. 95: 81-95. PMID 18675571 DOI: 10.1016/j.ymgme.2008.05.008  0.92
2008 Chandler RJ, Venditti CP. Adenovirus-mediated gene delivery rescues a neonatal lethal murine model of mut(0) methylmalonic acidemia. Human Gene Therapy. 19: 53-60. PMID 18052792 DOI: 10.1089/hum.2007.0118  0.92
2008 Venditti CP. Increased C3-Carnitine in a healthy premature infant: Commentary Clinical Chemistry. 54: 1917-1918. DOI: 10.1373/clinchem.2008.113449  0.92
2007 Chandler RJ, Sloan J, Fu H, Tsai M, Stabler S, Allen R, Kaestner KH, Kazazian HH, Venditti CP. Metabolic phenotype of methylmalonic acidemia in mice and humans: the role of skeletal muscle. Bmc Medical Genetics. 8: 64. PMID 17937813 DOI: 10.1186/1471-2350-8-64  0.92
2007 Chandler RJ, Tsai MS, Dorko K, Sloan J, Korson M, Freeman R, Strom S, Venditti CP. Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes. Bmc Medical Genetics. 8: 24. PMID 17470278 DOI: 10.1186/1471-2350-8-24  0.92
2006 Chandler RJ, Aswani V, Tsai MS, Falk M, Wehrli N, Stabler S, Allen R, Sedensky M, Kazazian HH, Venditti CP. Propionyl-CoA and adenosylcobalamin metabolism in Caenorhabditis elegans: evidence for a role of methylmalonyl-CoA epimerase in intermediary metabolism. Molecular Genetics and Metabolism. 89: 64-73. PMID 16843692 DOI: 10.1016/j.ymgme.2006.06.001  0.92
2005 Chandler RJ, Venditti CP. Genetic and genomic systems to study methylmalonic acidemia. Molecular Genetics and Metabolism. 86: 34-43. PMID 16182581 DOI: 10.1016/j.ymgme.2005.07.020  0.92
2004 Venditti CP, Harris MC, Huff D, Peterside I, Munson D, Weber HS, Rome J, Kaye EM, Shanske S, Sacconi S, Tay S, DiMauro S, Berry GT. Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency. Journal of Inherited Metabolic Disease. 27: 735-9. PMID 15505378 DOI: 10.1023/B:BOLI.0000045711.89888.5e  0.92
2004 Venditti CP, Hunt P, Donnenfeld A, Zackai E, Spinner NB. Mosaic paternal uniparental (iso)disomy for chromosome 20 associated with multiple anomalies. American Journal of Medical Genetics. Part A. 124: 274-9. PMID 14708100 DOI: 10.1002/ajmg.a.20430  0.92
2003 Morrissette JJ, Laufer-Cahana A, Medne L, Russell KL, Venditti CP, Kline R, Zackai EH, Spinner NB. Patient with trisomy 9p and a hypoplastic left heart with a tricentric chromosome 9. American Journal of Medical Genetics. Part A. 123: 279-84. PMID 14608650 DOI: 10.1002/ajmg.a.20293  0.92
2003 Venditti LN, Venditti CP, Berry GT, Kaplan PB, Kaye EM, Glick H, Stanley CA. Newborn screening by tandem mass spectrometry for medium-chain Acyl-CoA dehydrogenase deficiency: a cost-effectiveness analysis. Pediatrics. 112: 1005-15. PMID 14595039 DOI: 10.1542/peds.112.5.1005  0.92
2002 Venditti CP, Farmer J, Russell KL, Friedrich CA, Alter C, Canning D, Whitaker L, Mennuti MT, Driscoll DA, Zackai EH. Omodysplasia: an affected mother and son. American Journal of Medical Genetics. 111: 169-77. PMID 12210345 DOI: 10.1002/ajmg.10555  0.92
1997 Venditti CP, Seese NK, Gerhard GS, Ten Eishof AE, Chorney KA, Mowrey PN, Lacey PG, Knoll JHM, Chorney MJ. 46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis Journal of Medical Genetics. 34: 24-27. PMID 9032645  0.92
1996 Beutler E, Gelbart T, West C, Lee P, Adams M, Blackstone R, Pockros P, Kosty M, Venditti CP, Phatak PD, Seese NK, Chorney KA, Ten Elshof AE, Gerhard GS, Chorney M. Mutation analysis in hereditary hemochromatosis Blood Cells, Molecules, and Diseases. 22: 187-194. PMID 8931958 DOI: 10.1006/bcmd.1996.0027  0.92
1996 Venditti CP, Lawlor DA, Sharma P, Chorney MJ. Structure and content of the major histocompatibility complex (MHC) class I regions of the great anthropoid apes Human Immunology. 49: 71-84. PMID 8872161 DOI: 10.1016/0198-8859(96)00017-1  0.92
1996 Seese NK, Venditti CP, Chorney KA, Gerhard GS, Ma J, Hudson TJ, Phatak PD, Chorney MJ. Localization of the hemochromatosis disease gene: Linkage disequilibrium analysis using an American patient collection Blood Cells, Molecules, and Diseases. 22: 36-46. PMID 8807084 DOI: 10.1006/bcmd.1996.0006  0.92
1994 Plomin R, McClearn GE, Smith DL, Vignetti S, Chorney MJ, Chorney K, Venditti CP, Kasarda S, Thompson LA, Detterman DK. DNA markers associated with high versus low IQ: the IQ Quantitative Trait Loci (QTL) Project. Behavior Genetics. 24: 107-18. PMID 8024528 DOI: 10.1007/BF01067815  0.92
1994 Venditti CP, Harris JM, Geraghty DE, Chorney MJ. Mapping and characterization of non-HLA multigene assemblages in the human MHC class I region Genomics. 22: 257-266. PMID 7806210 DOI: 10.1006/geno.1994.1382  0.92
1993 Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, Zbar B, Robins DB, Rogan PK, Ladda RL. Clinical and molecular analyses of deletion 3p25-pter syndrome. American Journal of Medical Genetics. 46: 623-9. PMID 8103286 DOI: 10.1002/ajmg.1320460604  0.92
1992 Venditti CP, Chorney MJ. Class I gene contraction within the HLA-A subregion of the human MHC Genomics. 14: 1003-1009. PMID 1362179 DOI: 10.1016/S0888-7543(05)80123-5  0.92
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