| Year |
Citation |
Score |
| 2018 |
Motulsky AG. A German-Jewish refugee in Vichy France 1939-1941. Arno Motulsky's memoir of life in the internment camps at St. Cyprien and Gurs. American Journal of Medical Genetics. Part A. PMID 29697901 DOI: 10.1002/Ajmg.A.38701 |
0.42 |
|
| 2016 |
Motulsky AG, King MC. The Great Adventure of an American Human Geneticist. Annual Review of Genomics and Human Genetics. PMID 27147253 DOI: 10.1146/Annurev-Genom-083115-022528 |
0.426 |
|
| 2016 |
Giblett ER, Coleman DH, Pirzio-Biroli G, Donohue DM, Motulsky AG, Finch CA. Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia. Blood. 127: 1375. PMID 26989183 DOI: 10.1182/Blood-2016-01-692863 |
0.353 |
|
| 2015 |
Gallego CJ, Burt A, Sundaresan AS, Ye Z, Shaw C, Crosslin DR, Crane PK, Fullerton SM, Hansen K, Carrell D, Kuivaniemi H, Derr K, de Andrade M, McCarty CA, Kitchner TE, ... ... Motulsky AG, et al. Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network. American Journal of Human Genetics. PMID 26365338 DOI: 10.1016/J.Ajhg.2015.08.008 |
0.361 |
|
| 2015 |
Kim DS, Burt AA, Ranchalis JE, Vuletic S, Vaisar T, Li WF, Rosenthal EA, Dong W, Eintracht JF, Motulsky AG, Brunzell JD, Albers JJ, Furlong CE, Jarvik GP. PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity. Journal of Lipid Research. 56: 1351-62. PMID 26009633 DOI: 10.1194/Jlr.P058032 |
0.387 |
|
| 2015 |
Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS, Bennett JT, Crosslin DR, Ranchalis J, Jones KL, Rosenthal EA, ... ... Motulsky AG, et al. Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Research. 25: 305-15. PMID 25637381 DOI: 10.1101/Gr.183483.114 |
0.39 |
|
| 2014 |
Deeb SS, Motulsky AG. Genetics of Color Vision Defects Reference Module in Biomedical Research. DOI: 10.1016/B978-0-12-801238-3.05605-1 |
0.322 |
|
| 2013 |
Rosenthal EA, Ranchalis J, Crosslin DR, Burt A, Brunzell JD, Motulsky AG, Nickerson DA, Wijsman EM, Jarvik GP. Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia. American Journal of Human Genetics. 93: 1035-45. PMID 24268658 DOI: 10.1016/J.Ajhg.2013.10.019 |
0.449 |
|
| 2013 |
Dorschner MO, Amendola LM, Turner EH, Robertson PD, Shirts BH, Gallego CJ, Bennett RL, Jones KL, Tokita MJ, Bennett JT, Kim JH, Rosenthal EA, Kim DS, Tabor HK, ... ... Motulsky AG, et al. Actionable, pathogenic incidental findings in 1,000 participants' exomes. American Journal of Human Genetics. 93: 631-40. PMID 24055113 DOI: 10.1016/J.Ajhg.2013.08.006 |
0.4 |
|
| 2013 |
Anderson CA, Beresford SA, McLerran D, Lampe JW, Deeb S, Feng Z, Motulsky AG. Response of serum and red blood cell folate concentrations to folic acid supplementation depends on methylenetetrahydrofolate reductase C677T genotype: results from a crossover trial. Molecular Nutrition & Food Research. 57: 637-44. PMID 23456769 DOI: 10.1002/Mnfr.201200108 |
0.351 |
|
| 2013 |
Deeb SS, Motulsky AG. Color Vision Defects Emery and Rimoin's Principles and Practice of Medical Genetics. 1-17. DOI: 10.1016/B978-0-12-383834-6.00142-7 |
0.203 |
|
| 2011 |
Pierce SB, Spurrell CH, Mandell JB, Lee MK, Zeligson S, Bereman MS, Stray SM, Fokstuen S, MacCoss MJ, Levy-Lahad E, King MC, Motulsky AG. Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria. Proceedings of the National Academy of Sciences of the United States of America. 108: 18313-7. PMID 22042873 DOI: 10.1073/Pnas.1115888108 |
0.37 |
|
| 2011 |
Wynshaw-Boris A, Risch N, Motulsky A. Charles Joseph Epstein, M.D., 1933-2011, in memoriam American Journal of Human Genetics. 88: 684-688. PMID 21805720 DOI: 10.1016/J.Ajhg.2011.05.016 |
0.402 |
|
| 2011 |
Rosenthal EA, Ronald J, Rothstein J, Rajagopalan R, Ranchalis J, Wolfbauer G, Albers JJ, Brunzell JD, Motulsky AG, Rieder MJ, Nickerson DA, Wijsman EM, Jarvik GP. Linkage and association of phospholipid transfer protein activity to LASS4. Journal of Lipid Research. 52: 1837-46. PMID 21757428 DOI: 10.1194/Jlr.P016576 |
0.404 |
|
| 2011 |
Motulsky A, Epstein CJ. 2010 Victor A. McKusick Leadership Award introduction and address. American Journal of Human Genetics. 88: 269-72. PMID 21516616 DOI: 10.1016/J.Ajhg.2011.01.012 |
0.489 |
|
| 2011 |
Bookman EB, Langehorne AA, Eckfeldt JH, Glass KC, Jarvik GP, Klag M, Koski G, Motulsky A, Wilfond B, Manolio TA, Fabsitz RR, Luepker RV. Comment on "Multidimensional results reporting to participants in genomic studies: getting it right". Science Translational Medicine. 3: 70le1. PMID 21325615 DOI: 10.1126/Scitranslmed.3001516 |
0.385 |
|
| 2010 |
Wijsman EM, Rothstein JH, Igo RP, Brunzell JD, Motulsky AG, Jarvik GP. Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families. Human Genetics. 127: 705-19. PMID 20383777 DOI: 10.1007/S00439-010-0819-2 |
0.413 |
|
| 2010 |
Jarvik GP, Rajagopalan R, Rosenthal EA, Wolfbauer G, McKinstry L, Vaze A, Brunzell J, Motulsky AG, Nickerson DA, Heagerty PJ, Wijsman EM, Albers JJ. Genetic and nongenetic sources of variation in phospholipid transfer protein activity. Journal of Lipid Research. 51: 983-90. PMID 19965587 DOI: 10.1194/Jlr.M000125 |
0.371 |
|
| 2010 |
Bamshad M, Motulsky AG. Health consequences of ecogenetic variation Evolution in Health and Disease. DOI: 10.1093/acprof:oso/9780199207466.003.0004 |
0.216 |
|
| 2010 |
Motulsky AG, Dean M. Linkage analysis for monogenic traits Vogel and Motulsky's Human Genetics: Problems and Approaches (Fourth Edition). 211-241. DOI: 10.1007/978-3-540-37654-5_7 |
0.28 |
|
| 2010 |
Motulsky AG. Formal genetics of humans: Modes of inheritance Vogel and Motulsky's Human Genetics: Problems and Approaches (Fourth Edition). 165-209. DOI: 10.1007/978-3-540-37654-5_6 |
0.307 |
|
| 2010 |
Motulsky AG. History of human genetics Vogel and Motulsky's Human Genetics: Problems and Approaches (Fourth Edition). 13-29. DOI: 10.1007/978-3-540-37654-5_2 |
0.354 |
|
| 2010 |
Speicher MR, Antonarakis SE, Motulsky AG. Preface Vogel and Motulsky's Human Genetics: Problems and Approaches (Fourth Edition). vii-viii. DOI: 10.1007/978-3-540-37654-5 |
0.168 |
|
| 2009 |
Ozdemir V, Motulsky AG, Kolker E, Godard B. Genome-environment interactions and prospective technology assessment: evolution from pharmacogenomics to nutrigenomics and ecogenomics. Omics : a Journal of Integrative Biology. 13: 1-6. PMID 19290807 DOI: 10.1089/Omi.2009.0013 |
0.351 |
|
| 2008 |
Jarvik GP, Brunzell JD, Motulsky AG. Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia. Journal of the American College of Cardiology. 52: 1554-6. PMID 19007591 DOI: 10.1016/J.Jacc.2008.08.012 |
0.411 |
|
| 2007 |
Gurwitz D, Motulsky AG. 'Drug reactions, enzymes, and biochemical genetics': 50 years later. Pharmacogenomics. 8: 1479-84. PMID 18034611 DOI: 10.2217/14622416.8.11.1479 |
0.419 |
|
| 2007 |
Anderson CA, Beresford SA, Lampe J, Knopp RH, Motulsky AG. Enhancing recruitment of healthy African American volunteers in a city with a small African American community: results from a dietary supplement crossover trial. Ethnicity & Disease. 17: 555-9. PMID 17985513 |
0.206 |
|
| 2006 |
Zambon A, Brown BG, Hokanson JE, Motulsky AG, Brunzell JD. Genetically determined apo B levels and peak LDL density predict angiographic response to intensive lipid-lowering therapy. Journal of Internal Medicine. 259: 401-9. PMID 16594908 DOI: 10.1111/J.1365-2796.2006.01626.X |
0.404 |
|
| 2006 |
Bookman EB, Langehorne AA, Eckfeldt JH, Glass KC, Jarvik GP, Klag M, Koski G, Motulsky A, Wilfond B, Manolio TA, Fabsitz RR, Luepker RV. Reporting genetic results in research studies: summary and recommendations of an NHLBI working group. American Journal of Medical Genetics. Part A. 140: 1033-40. PMID 16575896 DOI: 10.1002/Ajmg.A.31195 |
0.44 |
|
| 2006 |
Motulsky AG, Qi M. Pharmacogenetics, pharmacogenomics and ecogenetics. Journal of Zhejiang University. Science. B. 7: 169-70. PMID 16421980 DOI: 10.1631/Jzus.2006.B0169 |
0.409 |
|
| 2006 |
Motulsky AG. Genetics of complex diseases. Journal of Zhejiang University. Science. B. 7: 167-8. PMID 16421979 DOI: 10.1631/Jzus.2006.B0167 |
0.419 |
|
| 2006 |
Motulsky AG. Perspectives in human genetics: Introduction American Journal of Human Genetics. 79: 193. DOI: 10.1086/505886 |
0.412 |
|
| 2006 |
Omenn GS, Motulsky AG. Ecogenetics: Historical Perspectives Gene-Environment Interactions: Fundamentals of Ecogenetics. 7-16. DOI: 10.1002/0471758043.ch2 |
0.194 |
|
| 2006 |
Motulsky AG. Foreword Gene-Environment Interactions: Fundamentals of Ecogenetics. ix-x. DOI: 10.1002/0471758043 |
0.266 |
|
| 2005 |
Need AC, Motulsky AG, Goldstein DB. Priorities and standards in pharmacogenetic research. Nature Genetics. 37: 671-81. PMID 15990888 DOI: 10.1038/Ng1593 |
0.396 |
|
| 2005 |
Gagnon F, Jarvik GP, Badzioch MD, Motulsky AG, Brunzell JD, Wijsman EM. Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia. Human Genetics. 117: 494-505. PMID 15959807 DOI: 10.1007/S00439-005-1338-4 |
0.391 |
|
| 2005 |
Anderson CA, Jorgensen AL, Deeb S, McLerran D, Beresford SA, Motulsky AG. Equal proportion of adult male and female homozygous for the 677C --> T mutation in the methylenetetrahydrofolate reductase polymorphism. American Journal of Medical Genetics. Part A. 134: 97-9. PMID 15704130 DOI: 10.1002/Ajmg.A.30391 |
0.329 |
|
| 2004 |
Badzioch MD, Igo RP, Gagnon F, Brunzell JD, Krauss RM, Motulsky AG, Wijsman EM, Jarvik GP. Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 1942-50. PMID 15331429 DOI: 10.1161/01.Atv.0000143499.09575.93 |
0.373 |
|
| 2004 |
Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, ... Motulsky AG, et al. X-linked high myopia associated with cone dysfunction. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 897-908. PMID 15197065 DOI: 10.1001/Archopht.122.6.897 |
0.406 |
|
| 2004 |
Motulsky AG. Introductory Speech for Joan Marks American Journal of Human Genetics. 74: 393-394. DOI: 10.1086/381719 |
0.446 |
|
| 2003 |
Gagnon F, Jarvik GP, Motulsky AG, Deeb SS, Brunzell JD, Wijsman EM. Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment. Human Genetics. 113: 522-33. PMID 14569462 DOI: 10.1007/S00439-003-1006-5 |
0.398 |
|
| 2003 |
MOTULSKY A, ROHN RJ. Tietze's syndrome; cause of chest pain and chest wall swelling. Journal of the American Medical Association. 152: 504-6. PMID 13044558 DOI: 10.1001/Jama.1953.03690060020007 |
0.335 |
|
| 2003 |
Austin MA, Edwards KL, Monks SA, Koprowicz KM, Brunzell JD, Motulsky AG, Mahaney MC, Hixson JE. Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia. Journal of Lipid Research. 44: 2161-8. PMID 12923221 DOI: 10.1194/Jlr.M300272-Jlr200 |
0.409 |
|
| 2003 |
Ayyobi AF, McGladdery SH, McNeely MJ, Austin MA, Motulsky AG, Brunzell JD. Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 1289-94. PMID 12750118 DOI: 10.1161/01.Atv.0000077220.44620.9B |
0.361 |
|
| 2003 |
Imperatore G, Pinsky LE, Motulsky A, Reyes M, Bradley LA, Burke W. Hereditary hemochromatosis: Perspectives of public health, medical genetics, and primary care Genetics in Medicine. 5: 1-8. PMID 12544469 DOI: 10.1097/00125817-200301000-00001 |
0.405 |
|
| 2002 |
Bennett RL, Motulsky AG, Bittles AH. Letter to the Editor: Reply to Becker and Morgan. Journal of Genetic Counseling. 11: 427-8. PMID 26142135 DOI: 10.1023/A:1016802017314 |
0.302 |
|
| 2002 |
Bennett RL, Motulsky AG, Bittles A, Hudgins L, Uhrich S, Doyle DL, Silvey K, Scott CR, Cheng E, McGillivray B, Steiner RD, Olson D. Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 11: 97-119. PMID 26141656 DOI: 10.1023/A:1014593404915 |
0.428 |
|
| 2002 |
Motulsky A, Motuslky A. From pharmacogenetics and ecogenetics to pharmacogenomics. Medicina Nei Secoli. 14: 683-705. PMID 14650398 |
0.322 |
|
| 2002 |
King MC, Motulsky AG. Human genetics. Mapping human history. Science (New York, N.Y.). 298: 2342-3. PMID 12493903 DOI: 10.1126/Science.1080373 |
0.438 |
|
| 2002 |
Motulsky AG. 2001 William Allan Award Address. Introductory speech for Charles J. Epstein. American Journal of Human Genetics. 70: 297-9. PMID 11753823 DOI: 10.1086/338916 |
0.299 |
|
| 2002 |
Cordero JF, Hamerton JL, King MC, Motulsky AG, Pelias MZ, Reilly PR, Salomon J, Schull WJ, Spielman RS, Ward RH, Weitkamp LR, Worton RG. Response to allegations against James V. Neel in Darkness in El Dorado, by Patrick Tierney American Journal of Human Genetics. 70: 1-10. PMID 11715114 DOI: 10.1086/338147 |
0.451 |
|
| 2002 |
Becker SM, Morgan LM, Bennett RL, Motulsky AG, Bittles AH. Consanguinity and congenital birth defects [2] (multiple letters) Journal of Genetic Counseling. 11: 423-428. DOI: 10.1023/A:1016897816405 |
0.214 |
|
| 2001 |
McNeely MJ, Edwards KL, Marcovina SM, Brunzell JD, Motulsky AG, Austin MA. Lipoprotein and apolipoprotein abnormalities in familial combined hyperlipidemia: a 20-year prospective study. Atherosclerosis. 159: 471-81. PMID 11730829 DOI: 10.1016/S0021-9150(01)00528-7 |
0.379 |
|
| 2001 |
Kim H, Marcovina SM, Edwards KL, McKnight B, Bradley CM, McNeely MJ, Psaty BM, Motulsky AG, Austin MA. Lipoprotein(a) as a risk factor for maternal cardiovascular disease mortality in kindreds with familial combined hyperlipidemia or familial hypertriglyceridemia. Clinical Genetics. 60: 188-97. PMID 11595020 DOI: 10.1034/J.1399-0004.2001.600304.X |
0.355 |
|
| 2001 |
Hayashi T, Yamaguchi T, Kitahara K, Sharpe LT, Jägle H, Yamade S, Ueyama H, Motulsky AG, Deeb SS. The importance of gene order in expression of the red and green visual pigment genes and in color vision Color Research and Application. 26: S79-S83. DOI: 10.1002/1520-6378(2001)26:1+<::Aid-Col18>3.0.Co;2-4 |
0.359 |
|
| 2000 |
Weber W, Nash DJ, Motulsky AG, Henneberg M, Crawford MH, Martin SK, Goldsmid JM, Spedini G, Glidewell S, Schanfield MS. Phylogenetic relationships of human populations in sub-Saharan Africa. Human Biology. 72: 753-72. PMID 11126723 |
0.311 |
|
| 2000 |
Motulsky AG, Beutler E. Population screening in hereditary hemochromatosis. Annual Review of Public Health. 21: 65-79. PMID 10884946 DOI: 10.1146/Annurev.Publhealth.21.1.65 |
0.372 |
|
| 2000 |
Austin MA, McKnight B, Edwards KL, Bradley CM, McNeely MJ, Psaty BM, Brunzell JD, Motulsky AG. Cardiovascular disease mortality in familial forms of hypertriglyceridemia: A 20-year prospective study. Circulation. 101: 2777-82. PMID 10859281 DOI: 10.1161/01.Cir.101.24.2777 |
0.358 |
|
| 2000 |
Motulsky AG. 1999 ASHG Award for Excellence in Education. Some future directions in medical genetics. American Journal of Human Genetics. 66: 1190-1. PMID 10836910 DOI: 10.1086/302837 |
0.415 |
|
| 2000 |
Austin M, McKnight B, Edwards K, Bradley C, McNeely M, Psaty B, Brunzell J, Motulsky A. Twenty-year cardiovascular disease mortality in the familial forms of hypertriglyceridemia Atherosclerosis. 151: 161. DOI: 10.1016/S0021-9150(00)80730-3 |
0.35 |
|
| 1999 |
Bennett RL, Hudgins L, Smith CO, Motulsky AG. Inconsistencies in genetic counseling and screening for consanguineous couples and their offspring: the need for practice guidelines. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 1: 286-92. PMID 11258630 DOI: 10.1097/00125817-199909000-00007 |
0.389 |
|
| 1999 |
Edwards KL, Mahaney MC, Motulsky AG, Austin MA. Pleiotropic genetic effects on LDL size, plasma triglyceride, and HDL cholesterol in families. Arteriosclerosis, Thrombosis, and Vascular Biology. 19: 2456-64. PMID 10521376 DOI: 10.1161/01.Atv.19.10.2456 |
0.414 |
|
| 1999 |
Motulsky AG. If I had a gene test, what would I have and who would I tell? Lancet. 354: SI35-7. PMID 10437855 DOI: 10.1016/S0140-6736(99)90436-1 |
0.338 |
|
| 1999 |
Crognale MA, Teller DY, Yamaguchi T, Motulsky AG, Deeb SS. Analysis of red/green color discrimination in subjects with a single X-linked photopigment gene. Vision Research. 39: 707-19. PMID 10341958 DOI: 10.1016/S0042-6989(98)00140-0 |
0.384 |
|
| 1999 |
Hayashi T, Motulsky AG, Deeb SS. Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype. Nature Genetics. 22: 90-3. PMID 10319869 DOI: 10.1038/8798 |
0.364 |
|
| 1998 |
Crognale MA, Teller DY, Motulsky AG, Deeb SS. Severity of color vision defects: electroretinographic (ERG), molecular and behavioral studies. Vision Research. 38: 3377-85. PMID 9893852 DOI: 10.1016/S0042-6989(97)00425-2 |
0.377 |
|
| 1998 |
Burke W, Thomson E, Khoury MJ, McDonnell SM, Press N, Adams PC, Barton JC, Beutler E, Brittenham G, Buchanan A, Clayton EW, Cogswell ME, Meslin EM, Motulsky AG, Powell LW, et al. Hereditary hemochromatosis: gene discovery and its implications for population-based screening. Jama. 280: 172-8. PMID 9669792 DOI: 10.1001/Jama.280.2.172 |
0.45 |
|
| 1998 |
Omenn GS, Beresford SA, Motulsky AG. Preventing coronary heart disease: B vitamins and homocysteine. Circulation. 97: 421-4. PMID 9490234 |
0.22 |
|
| 1998 |
Wijsman EM, Brunzell JD, Jarvik GP, Austin MA, Motulsky AG, Deeb SS. Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex. Arteriosclerosis, Thrombosis, and Vascular Biology. 18: 215-26. PMID 9484986 DOI: 10.1161/01.Atv.18.2.215 |
0.429 |
|
| 1998 |
James P, Glomset J, Brown MS, Schaefer EJ, Friedman J, Kontula K, Marckmann P, Auwerx J, Sorensen T, Gustafsson JA, Astrup A, Motulsky AG, Pedersen J, Norum K, Angelin B, et al. Discussion: Molecular basis of the hepatic control of cholesterol metabolism Nutrition Reviews. 56: S54-S75. |
0.22 |
|
| 1997 |
Spiegler GE, Motulsky AG. Genetic screening of adolescents [5] (multiple letters) New England Journal of Medicine. 337: 639-640. PMID 9280838 DOI: 10.1056/NEJM199708283370915 |
0.271 |
|
| 1997 |
Yamaguchi T, Motulsky AG, Deeb SS. Visual pigment gene structure and expression in human retinae. Human Molecular Genetics. 6: 981-90. PMID 9215665 DOI: 10.1093/Hmg/6.7.981 |
0.37 |
|
| 1997 |
Motulsky AG. Screening for genetic diseases. The New England Journal of Medicine. 336: 1314-6. PMID 9113938 DOI: 10.1056/Nejm199705013361810 |
0.425 |
|
| 1996 |
Epstein CJ, Motulsky AG. Werner syndrome: entering the helicase era. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 18: 1025-7. PMID 8976161 DOI: 10.1002/Bies.950181214 |
0.532 |
|
| 1996 |
Beutler E, McKusick VA, Motulsky AG, Scriver CR, Hutchinson F. Mutation nomenclature: nicknames, systematic names, and unique identifiers. Human Mutation. 8: 203-6. PMID 8889577 DOI: 10.1002/(Sici)1098-1004(1996)8:3<203::Aid-Humu1>3.0.Co;2-A |
0.329 |
|
| 1996 |
Ross G, Erickson R, Knorr D, Motulsky AG, Parkman R, Samulski J, Straus SE, Smith BR. Gene therapy in the United States: a five-year status report. Human Gene Therapy. 7: 1781-90. PMID 8886849 DOI: 10.1089/Hum.1996.7.14-1781 |
0.33 |
|
| 1996 |
Deeb SS, Motulsky AG. Molecular genetics of human color vision. Behavior Genetics. 26: 195-207. PMID 8754247 DOI: 10.1007/Bf02359380 |
0.431 |
|
| 1996 |
Jonsen AR, Durfy SJ, Burke W, Motulsky AG. The advent of the "unpatients'. Nature Medicine. 2: 622-4. PMID 8640544 DOI: 10.1038/Nm0696-622 |
0.325 |
|
| 1996 |
Bostom AG, Appel LJ, Grunwald HW, Rosner F, Beresford SAA, Motulsky AG, Omenn GS, Boushey CJ. Folic acid fortification of food [1] Journal of the American Medical Association. 275: 681-683. PMID 8594257 DOI: 10.1001/jama.275.9.681 |
0.173 |
|
| 1996 |
Motulsky AG. Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid. American Journal of Human Genetics. 58: 17-20. PMID 8554053 |
0.218 |
|
| 1996 |
Motulsky AG. Genes and molecules in human health and disease Trends in Genetics. 12: 374-375. DOI: 10.1016/S0168-9525(96)80025-4 |
0.363 |
|
| 1996 |
Yamaguchi T, Motulsky AG, Deeb SS. Relationship between structure of the X-chromosome linked color vision genes and their levels of expression in human retinae Investigative Ophthalmology and Visual Science. 37: S337. |
0.251 |
|
| 1995 |
Walters LB, Wivel NA, Capron AM, Chase GA, DeLeon PA, Doi RH, Dronamraju KR, Erickson RP, Ginsburg D, Meyers AS, Miller AD, Motulsky AG, Parkman R, Ross GS, Saha BK, et al. Recombinant DNA Advisory Committee. Minutes of meeting September 12-13, 1994 Human Gene Therapy. 6: 481-525. PMID 11644708 |
0.197 |
|
| 1995 |
Deeb SS, Alvarez A, Malkki M, Motulsky AG. Molecular patterns and sequence polymorphisms in the red and green visual pigment genes of Japanese men. Human Genetics. 95: 501-6. PMID 7759069 DOI: 10.1007/Bf00223860 |
0.388 |
|
| 1995 |
Motulsky AG. Jewish diseases and origins. Nature Genetics. 9: 99-101. PMID 7719352 DOI: 10.1038/Ng0295-99 |
0.351 |
|
| 1995 |
Boushey CJ, Beresford SA, Omenn GS, Motulsky AG. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes. Jama. 274: 1049-57. PMID 7563456 DOI: 10.1001/Jama.1995.03530130055028 |
0.358 |
|
| 1995 |
Motulsky AG. Exploding the Gene Myth The Journal of Nervous and Mental Disease. 183: 274-275. DOI: 10.1097/00005053-199504000-00019 |
0.235 |
|
| 1995 |
Brinckerhoff CE, Capron AM, Chase GA, DeLeon PA, Doi RH, Erickson RP, Glorioso JC, Haselkorn R, Meyers AS, Miller AD, Motulsky AG, Parkman R, Ross GS, Saha BK, Samulski RJ, et al. Department of Health and Human Services, National Institutes of Health, Recombinant DNA Advisory Committee. Minutes of Meeting, December 1-2, 1994 Human Gene Therapy. 6: 1065-1124. |
0.21 |
|
| 1994 |
Deeb SS, Jorgensen AL, Battisti L, Iwasaki L, Motulsky AG. Sequence divergence of the red and green visual pigments in great apes and humans. Proceedings of the National Academy of Sciences of the United States of America. 91: 7262-6. PMID 8041777 DOI: 10.1073/Pnas.91.15.7262 |
0.376 |
|
| 1994 |
Jarvik GP, Brunzell JD, Austin MA, Krauss RM, Motulsky AG, Wijsman E. Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype. Arteriosclerosis and Thrombosis : a Journal of Vascular Biology / American Heart Association. 14: 1687-94. PMID 7947591 DOI: 10.1161/01.Atv.14.11.1687 |
0.451 |
|
| 1994 |
Motulsky AG. Predictive genetic diagnosis. American Journal of Human Genetics. 55: 603-5. PMID 7942837 |
0.308 |
|
| 1994 |
Buc NL, Capron AM, Carmen IH, Chase GA, DeLeon PA, Doi RH, Dronamraju KR, Geiduschek EP, Haselkorn R, Hirano SS, Krogstad DJ, Miller AD, Motulsky AG, Parkman R, Post LE, et al. Minutes of the September 9–10, 1993 Recombinant DNA Advisory Committee Meeting Human Gene Therapy. 5: 645-660. DOI: 10.1089/Hum.1994.5.5-645 |
0.31 |
|
| 1994 |
Motulsky AG. A human geneticist's odyssey Nature. 369: 111-112. DOI: 10.1038/369111B0 |
0.424 |
|
| 1994 |
Motulsky AG, Robbins FC, Murray TH. Introduction: The New Genetics and Health Care International Journal of Technology Assessment in Health Care. 10: 525-526. DOI: 10.1017/S0266462300008138 |
0.617 |
|
| 1994 |
Motulsky AG. “Humangenetik und Neuropsychiatrie in Meiner Zeit (1932-1978) Jahre der Entscheidung.” By Gerhard Koch. Verlag Palm & Enke, Erlangen und Jena, 1993, 501 pp American Journal of Medical Genetics. 50: 309-309. DOI: 10.1002/Ajmg.1320500322 |
0.304 |
|
| 1994 |
Buc NL, Capron AM, Carmen IH, Chase GA, DeLEon PA, Doi RH, Dronamraju KR, Geiduschek EP, Haselkorn R, Hirano SS, Krogstad DJ, Miller AD, Motulsky AG, Parkman R, Post LE, et al. Regulatory issues: Department of Health and Human Services National Institutes of Health recombinant DNA advisory committee. Minutes of meeting Human Gene Therapy. 5: 645-660. |
0.211 |
|
| 1994 |
Brinckerhoff CE, Buc NL, Carmen IH, Chase GA, DeLeon PA, Dronamraju KR, Geiduschek EP, Grossman M, Haselkorn R, Hirano SS, Krogstad DJ, Leventhal BG, Meyers AS, Miller AD, Motulsky AG, et al. Regulatory issues: Department of Health and Human Services, Public Health Services, National Institutes of Health, Recombinant DNA Advisory Committee: Minutes of meeting, March 1-2 1993 Human Gene Therapy. 5: 97-131. |
0.203 |
|
| 1993 |
Motulsky AG. Genetics by nation. Science (New York, N.Y.). 259: 1476-7. PMID 17801287 DOI: 10.1126/Science.259.5100.1476 |
0.439 |
|
| 1993 |
Nazar-Stewart V, Motulsky AG, Eaton DL, White E, Hornung SK, Leng ZT, Stapleton P, Weiss NS. The glutathione S-transferase mu polymorphism as a marker for susceptibility to lung carcinoma. Cancer Research. 53: 2313-8. PMID 8485718 |
0.225 |
|
| 1993 |
Caskey CT, Motulsky AG, McLendon WW. Molecular genetics and medicine. A call for papers. Archives of Pathology & Laboratory Medicine. 117: 32. PMID 8418757 DOI: 10.1001/Jama.1992.03490220085034 |
0.412 |
|
| 1993 |
Sanocki E, Lindsey DT, Winderickx J, Teller DY, Deeb SS, Motulsky AG. Serine/alanine amino acid polymorphism of the L and M cone pigments: effects on Rayleigh matches among deuteranopes, protanopes and color normal observers. Vision Research. 33: 2139-52. PMID 8266655 DOI: 10.1016/0042-6989(93)90012-L |
0.344 |
|
| 1993 |
Winderickx J, Battisti L, Hibiya Y, Motulsky AG, Deeb SS. Haplotype diversity in the human red and green opsin genes: evidence for frequent sequence exchange in exon 3. Human Molecular Genetics. 2: 1413-21. PMID 8242064 |
0.268 |
|
| 1993 |
Jarvik GP, Wijsman E, Little RE, Albers JJ, Motulsky AG, Brunzell JD. Host and environmental effects on plasma apolipoprotein B. International Journal of Clinical & Laboratory Research. 23: 215-20. PMID 8123878 DOI: 10.1007/Bf02592312 |
0.333 |
|
| 1993 |
Caskey CT, Motulsky AG, Mclendon WW. The American Medical Association Scientific Journals 1993 Theme Issues on Molecular Genetics and Medicine: Call for Papers Archives of Dermatology. 129: 99-100. DOI: 10.1001/Archderm.1993.01680220111026 |
0.412 |
|
| 1992 |
Jørgensen AL, Philip J, Raskind WH, Matsushita M, Christensen B, Dreyer V, Motulsky AG. Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency. American Journal of Human Genetics. 51: 291-8. PMID 1642230 |
0.262 |
|
| 1992 |
Motulsky AG. Nutrition and genetic susceptibility to common diseases. The American Journal of Clinical Nutrition. 55: 1244S-1245S. PMID 1590264 DOI: 10.1093/Ajcn/55.6.1244S |
0.426 |
|
| 1992 |
Winderickx J, Lindsey DT, Sanocki E, Teller DY, Motulsky AG, Deeb SS. Polymorphism in red photopigment underlies variation in colour matching. Nature. 356: 431-3. PMID 1557123 DOI: 10.1038/356431A0 |
0.393 |
|
| 1992 |
Heckbert SR, Weiss NS, Hornung SK, Eaton DL, Motulsky AG. Glutathione S-transferase and epoxide hydrolase activity in human leukocytes in relation to risk of lung cancer and other smoking-related cancers. Journal of the National Cancer Institute. 84: 414-22. PMID 1538419 DOI: 10.1093/Jnci/84.6.414 |
0.327 |
|
| 1992 |
Caskey CT, Motulsky AG, McLendon WW. Molecular genetics and medicine. A call for papers. Jama. 268: 3241. PMID 1433767 DOI: 10.1001/jama.1992.03490220085034 |
0.328 |
|
| 1992 |
Deeb SS, Lindsey DT, Hibiya Y, Sanocki E, Winderickx J, Teller DY, Motulsky AG. Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies. American Journal of Human Genetics. 51: 687-700. PMID 1415215 |
0.285 |
|
| 1992 |
Winderickx J, Battisti L, Motulsky AG, Deeb SS. Selective expression of human X chromosome-linked green opsin genes. Proceedings of the National Academy of Sciences of the United States of America. 89: 9710-4. PMID 1409688 DOI: 10.1073/Pnas.89.20.9710 |
0.372 |
|
| 1992 |
Deeb SS, Failor RA, Brown BG, Brunzell JD, Albers JJ, Motulsky AG, Wijsman E. Association of apolipoprotein B gene variants with plasma apoB and low density lipoprotein (LDL) cholesterol levels. Human Genetics. 88: 463-70. PMID 1346774 DOI: 10.1007/Bf00215683 |
0.381 |
|
| 1992 |
Winderickx J, Sanocki E, Lindsey DT, Teller DY, Motulsky AG, Deeb SS. Defective colour vision associated with a missense mutation in the human green visual pigment gene. Nature Genetics. 1: 251-6. PMID 1302020 DOI: 10.1038/Ng0792-251 |
0.378 |
|
| 1992 |
Burke W, Motulsky AG. Molecular Genetics of Hypertension Monographs in Human Genetics. 14: 228-236. DOI: 10.1159/000421516 |
0.411 |
|
| 1992 |
Motulsky AG. Genetic Variation and Disorders in Peoples of African Origin.James E. Bowman , Robert F. Murray, Jr. The Quarterly Review of Biology. 67: 84-84. DOI: 10.1086/417524 |
0.279 |
|
| 1991 |
Motulsky AG. Pharmacogenetics and ecogenetics in 1991. Pharmacogenetics. 1: 2-3. PMID 1844819 |
0.21 |
|
| 1990 |
Jørgensen AL, Deeb SS, Motulsky AG. Molecular genetics of X chromosome-linked color vision among populations of African and Japanese ancestry: high frequency of a shortened red pigment gene among Afro-Americans. Proceedings of the National Academy of Sciences of the United States of America. 87: 6512-6. PMID 2395857 DOI: 10.1073/Pnas.87.17.6512 |
0.404 |
|
| 1990 |
Bierman EL, Motulsky AG, Ross R, White JG. Arteriosclerosis: the first 10 years. Arteriosclerosis (Dallas, Tex.). 10: 959-60. PMID 2244861 |
0.186 |
|
| 1990 |
Motulsky AG. Allelic Association of Human Dopamine D2 Receptor Gene in Alcoholism Jama: the Journal of the American Medical Association. 264: 1807-1808. PMID 1976139 DOI: 10.1001/jama.1990.03450140027014 |
0.225 |
|
| 1990 |
Costa LG, McDonald BE, Murphy SD, Omenn GS, Richter RJ, Motulsky AG, Furlong CE. Serum paraoxonase and its influence on paraoxon and chlorpyrifos-oxon toxicity in rats. Toxicology and Applied Pharmacology. 103: 66-76. PMID 1690462 DOI: 10.1016/0041-008X(90)90263-T |
0.328 |
|
| 1990 |
Motulsky AG. Proceed With Caution: Predicting Genetic Risks in the Recombinant DNA Era Jama: the Journal of the American Medical Association. 263: 2257. DOI: 10.1001/jama.1990.03440160119052 |
0.28 |
|
| 1989 |
Drummond-Borg M, Deeb SS, Motulsky AG. Molecular patterns of X chromosome-linked color vision genes among 134 men of European ancestry. Proceedings of the National Academy of Sciences of the United States of America. 86: 983-7. PMID 2915991 DOI: 10.1073/Pnas.86.3.983 |
0.379 |
|
| 1989 |
Motulsky AG. Medical genetics. Jama. 261: 2855-6. PMID 2775348 DOI: 10.1001/jama.1989.03420190131041 |
0.303 |
|
| 1989 |
Motulsky AG. Metabolic polymorphisms and the role of infectious diseases in human evolution. 1960. Human Biology. 61: 835-69; discussion 8. PMID 2699603 |
0.258 |
|
| 1989 |
Motulsky AG. Societal problems in human and medical genetics. Genome / National Research Council Canada = Gã©Nome / Conseil National De Recherches Canada. 31: 870-5. PMID 2698844 DOI: 10.1139/G89-153 |
0.445 |
|
| 1989 |
Motulsky AG. Genetic aspects of familial hypercholesterolemia and its diagnosis. Arteriosclerosis (Dallas, Tex.). 9: I3-7. PMID 2563220 |
0.351 |
|
| 1989 |
Furlong CE, Richter RJ, Seidel SL, Costa LG, Motulsky AG. Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesterase. Analytical Biochemistry. 180: 242-7. PMID 2479288 DOI: 10.1016/0003-2697(89)90424-7 |
0.359 |
|
| 1989 |
Motulsky AG. Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes Jama: the Journal of the American Medical Association. 261: 3177. DOI: 10.1001/Jama.1989.03420210127033 |
0.387 |
|
| 1989 |
Motulsky AG. Update to 'Metabolic polymorphisms and the role of infectious diseases in human evolution' Human Biology. 61: 870-877. |
0.258 |
|
| 1988 |
Motulsky AG. Human genetic individuality and risk assessment. Basic Life Sciences. 43: 7-9. PMID 3365225 |
0.309 |
|
| 1988 |
Childs B, Motulsky AG. Recombinant DNA analysis of multifactorial disease. Progress in Medical Genetics. 7: 180-94. PMID 3277254 |
0.234 |
|
| 1988 |
Motulsky AG. Normal and abnormal color-vision genes. American Journal of Human Genetics. 42: 405-7. PMID 3258123 |
0.254 |
|
| 1988 |
Thompson EA, Deeb S, Walker D, Motulsky AG. The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes. American Journal of Human Genetics. 42: 113-24. PMID 2892394 |
0.318 |
|
| 1988 |
Drummond-Borg M, Deeb S, Motulsky AG. Molecular basis of abnormal red-green color vision: a family with three types of color vision defects. American Journal of Human Genetics. 43: 675-83. PMID 2847528 |
0.286 |
|
| 1988 |
Furlong CE, Richter RJ, Seidel SL, Motulsky AG. Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon. American Journal of Human Genetics. 43: 230-8. PMID 2458038 |
0.295 |
|
| 1988 |
Motulsky AG. The Statue Within: An Autobiography Jama: the Journal of the American Medical Association. 260: 1299. DOI: 10.1001/jama.1988.03410090133050 |
0.171 |
|
| 1987 |
Motulsky AG. Genetics and environment in "alcoholism". Progress in Clinical and Biological Research. 241: 327-9. PMID 3615522 |
0.27 |
|
| 1987 |
Motulsky AG. Human genetic variation and nutrition. The American Journal of Clinical Nutrition. 45: 1108-13. PMID 3578105 DOI: 10.1093/Ajcn/45.5.1108 |
0.433 |
|
| 1987 |
Murray JC, Buetow KH, Donovan M, Hornung S, Motulsky AG, Disteche C, Dyer K, Swisshelm K, Anderson J, Giblett E. Linkage disequilibrium of plasminogen polymorphisms and assignment of the gene to human chromosome 6q26-6q27. American Journal of Human Genetics. 40: 338-50. PMID 2883890 |
0.259 |
|
| 1987 |
Motulsky AG, Burke W, Billings PR, Ward RH. Hypertension and the genetics of red cell membrane abnormalities. Ciba Foundation Symposium. 130: 150-66. PMID 2450724 |
0.315 |
|
| 1986 |
Motulsky AG. The 1985 Nobel Prize in physiology or medicine. Science (New York, N.Y.). 231: 126-9. PMID 3510453 |
0.198 |
|
| 1986 |
Deeb SS, Disteche C, Motulsky AG, Lebo RV, Kan YW. Chromosomal localization of the human apolipoprotein B gene and detection of homologous RNA in monkey intestine. Proceedings of the National Academy of Sciences of the United States of America. 83: 419-22. PMID 3455779 DOI: 10.1073/Pnas.83.2.419 |
0.344 |
|
| 1986 |
Deeb S, Failor A, Brown BG, Brunzell JD, Albers JJ, Motulsky AG. Molecular genetics of apolipoproteins and coronary heart disease. Cold Spring Harbor Symposia On Quantitative Biology. 51: 403-9. PMID 2884066 DOI: 10.1101/Sqb.1986.051.01.048 |
0.467 |
|
| 1986 |
MOTULSKY AG. Modern medical genetics Journal of Heredity. 77: 139-139. DOI: 10.1093/oxfordjournals.jhered.a110194 |
0.304 |
|
| 1985 |
Burke W, Motulsky AG. Hypertension: some unanswered questions. Jama. 253: 2260-1. PMID 3974121 DOI: 10.1001/Jama.1985.03350390102037 |
0.333 |
|
| 1985 |
Deeb SS, Motulsky AG, Albers JJ. A partial cDNA clone for human apolipoprotein B. Proceedings of the National Academy of Sciences of the United States of America. 82: 4983-6. PMID 3860836 DOI: 10.1073/Pnas.82.15.4983 |
0.334 |
|
| 1984 |
Brunzell JD, Motulsky AG. Status of "familial combined hyperlipidemia". Progress in Clinical and Biological Research. 147: 403-5. PMID 6739492 |
0.233 |
|
| 1984 |
ten Kate LP, Boman H, Daiger SP, Motulsky AG. Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: assortative mating for lifestyle and risk factors? The American Journal of Cardiology. 53: 399-403. PMID 6695767 DOI: 10.1016/0002-9149(84)90001-8 |
0.353 |
|
| 1984 |
Motulsky AG. Genetic engineering, medicine and medical genetics. Biomedicine & Pharmacotherapy = Biomã©Decine & Pharmacothã©Rapie. 38: 185-6. PMID 6594166 |
0.358 |
|
| 1984 |
Motulsky AG. The 'new genetics' in blood and cardiovascular research: applications to prevention and treatment. Circulation. 70: III26-30. PMID 6593138 |
0.348 |
|
| 1984 |
Motulsky AG. Genetic epidemiology. Genetic Epidemiology. 1: 143-4. PMID 6544236 DOI: 10.1002/gepi.1370010205 |
0.352 |
|
| 1984 |
Miller M, Opheim KE, Raisys VA, Motulsky AG. Theophylline metabolism: variation and genetics. Clinical Pharmacology and Therapeutics. 35: 170-82. PMID 6362955 DOI: 10.1038/Clpt.1984.23 |
0.401 |
|
| 1984 |
Motulsky AG. Genetic research in coronary heart disease. Progress in Clinical and Biological Research. 147: 541-8. PMID 6330756 |
0.304 |
|
| 1984 |
Murray JC, Mills KA, Demopulos CM, Hornung S, Motulsky AG. Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus. Proceedings of the National Academy of Sciences of the United States of America. 81: 3486-90. PMID 6328518 DOI: 10.1073/Pnas.81.11.3486 |
0.39 |
|
| 1984 |
Ortigoza-Ferado J, Richter RJ, Hornung SK, Motulsky AG, Furlong CE. Paraoxon hydrolysis in human serum mediated by a genetically variable arylesterase and albumin. American Journal of Human Genetics. 36: 295-305. PMID 6324579 |
0.329 |
|
| 1983 |
Guntheroth WG, Motulsky AG. Inherited primary disorders of cardiac rhythm and conduction. Progress in Medical Genetics. 5: 381-402. PMID 6344144 |
0.211 |
|
| 1983 |
Motulsky AG. Impact of genetic manipulation on society and medicine. Science (New York, N.Y.). 219: 135-40. PMID 6336852 DOI: 10.1126/Science.6336852 |
0.454 |
|
| 1983 |
Murray JC, Demopulos CM, Lawn RM, Motulsky AG. Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia. Proceedings of the National Academy of Sciences of the United States of America. 80: 5951-5. PMID 6310605 |
0.318 |
|
| 1983 |
Mueller RF, Hornung S, Furlong CE, Anderson J, Giblett ER, Motulsky AG. Plasma paraoxonase polymorphism: a new enzyme assay, population, family, biochemical, and linkage studies. American Journal of Human Genetics. 35: 393-408. PMID 6305189 |
0.3 |
|
| 1983 |
Motulsky AG, Murray J. Will prenatal diagnosis with selective abortion affect society's attitude toward the handicapped? Progress in Clinical and Biological Research. 128: 277-91. PMID 6227010 |
0.211 |
|
| 1982 |
ten Kate LP, Boman H, Daiger SP, Motulsky AG. Familial aggregation of coronary heart disease and its relation to known genetic risk factors. The American Journal of Cardiology. 50: 945-53. PMID 7137046 DOI: 10.1016/0002-9149(82)90400-3 |
0.396 |
|
| 1981 |
Pauli RM, Motulsky AG. Risk counselling in autosomal dominant disorders with undetermined penetrance. Journal of Medical Genetics. 18: 340-3. PMID 7328613 |
0.245 |
|
| 1981 |
Gartler SM, Hornung SK, Motulsky AG. Effect of chronologic age on induction of cystathionine synthase, uroporphyrinogen I synthase, and glucose-6-phosphate dehydrogenase activities in lymphocytes. Proceedings of the National Academy of Sciences of the United States of America. 78: 1916-9. PMID 6940198 DOI: 10.1073/Pnas.78.3.1916 |
0.358 |
|
| 1981 |
Modiano G, Battistuzzi G, Motulsky AG. Nonrandom patterns of codon usage and of nucleotide substitutions in human alpha- and beta-globin genes: an evolutionary strategy reducing the rate of mutations with drastic effects? Proceedings of the National Academy of Sciences of the United States of America. 78: 1110-4. PMID 6940129 |
0.244 |
|
| 1980 |
Motulsky AG, Fraser GR. Effects of antenatal diagnosis and selective abortion on frequencies of genetic disorders. Clinics in Obstetrics and Gynaecology. 7: 121-33. PMID 6155236 |
0.309 |
|
| 1979 |
Motulsky AG. Historical genetics. Science (New York, N.Y.). 203: 1102-3. PMID 17776042 DOI: 10.1126/Science.203.4385.1102 |
0.441 |
|
| 1979 |
Motulsky AG. Genetic doomsaying: the fears are groundless. American Medical News. 22: suppl 11. PMID 10240350 |
0.332 |
|
| 1979 |
Motulsky AG. The HLA complex and disease: some interpretations and new data in cardiomyopathy. The New England Journal of Medicine. 300: 918-9. PMID 570641 DOI: 10.1056/NEJM197904193001610 |
0.221 |
|
| 1979 |
Motulsky AG. Genetics of hemochromatosis. The New England Journal of Medicine. 301: 1291. PMID 503142 DOI: 10.1056/NEJM197912063012319 |
0.351 |
|
| 1979 |
Kurnit DM, Motulsky AG. New clinical implications of molecular genetics. Jama. 241: 1616-8. PMID 85727 DOI: 10.1001/Jama.1979.03290410048026 |
0.394 |
|
| 1979 |
Sybert VP, Motulsky AG. Renal involvement in hereditary multiple osteolysis. Lancet. 1: 52. PMID 83506 |
0.183 |
|
| 1978 |
Motulsky AG. Bioethical problems in pharmacogenetics and ecogenetics. Human Genetics. 185-92. PMID 11657363 DOI: 10.1007/978-3-642-67179-1_24 |
0.417 |
|
| 1978 |
Motulsky AG. Medical and human genetics 1977: trends and directions. American Journal of Human Genetics. 30: 123-31. PMID 655162 |
0.332 |
|
| 1978 |
Motulsky AG. Sounding board. Biased ascertainment and the natural history of diseases. The New England Journal of Medicine. 298: 1196-7. PMID 651950 DOI: 10.1056/NEJM197805252982111 |
0.246 |
|
| 1978 |
Motulsky AG. The William Allan Memorial Award presented to Victor A. McKusick at the annual meeting of the American Society of Human Genetics. American Journal of Human Genetics. 30: 101-4. PMID 350040 |
0.275 |
|
| 1978 |
Motulsky AG. Multifactorial inheritance and heritability in pharmacogenetics. Human Genetics. Supplement. 7-11. PMID 285035 |
0.361 |
|
| 1978 |
Motulsky AG. Bioethical problems in pharmacogenetics and ecogenetics. Human Genetics. Supplement. 185-92. PMID 285029 |
0.323 |
|
| 1978 |
Motulsky AG. Pharmacogenetics and ecogenetics: the problem and its scope. Human Genetics. Supplement. 1-3. PMID 285021 |
0.179 |
|
| 1978 |
Motulsky AG. Pharmacogenetics and ecogenetics. The problem and its scope Human Genetics. 45: 1-3. |
0.179 |
|
| 1977 |
Kukolich MK, Telsey A, Ott J, Motulsky AG. Sudden infant death syndrome: normal QT interval on ECGs of relatives. Pediatrics. 60: 51-4. PMID 876734 |
0.278 |
|
| 1977 |
Motulsky AG. The George M. Kober lecture: a genetical view of modern medicine. Transactions of the Association of American Physicians. 90: 76-90. PMID 565552 |
0.352 |
|
| 1977 |
Motulsky AG. Genetics of coronary heart diseases Paediatrician. 6: 366-370. |
0.302 |
|
| 1976 |
Motulsky AG. Editorial: Prenatal diagnosis and genetic counseling. The Western Journal of Medicine. 124: 410-2. PMID 1274340 DOI: 10.1007/BF00282813 |
0.337 |
|
| 1976 |
Boman H, Hermodson M, Hammond CA, Motulsky AG. Analbuminemia in an American Indian girl. Clinical Genetics. 9: 513-26. PMID 1269174 DOI: 10.1111/J.1399-0004.1976.Tb01606.X |
0.386 |
|
| 1976 |
Brunzell JD, Schrott HG, Motulsky AG, Bierman EL. Myocardial infarction in the familial forms of hypertriglyceridemia. Metabolism: Clinical and Experimental. 25: 313-20. PMID 1250165 DOI: 10.1016/0026-0495(76)90089-5 |
0.344 |
|
| 1976 |
Weinberg SK, Motulsky AG. Aberrant axillary breast tissue: A report of a family with six affected women in two generations. Clinical Genetics. 10: 325-8. PMID 991442 DOI: 10.1111/J.1399-0004.1976.Tb00056.X |
0.35 |
|
| 1976 |
Motulsky AG. Current concepts in genetics. The genetic hyperlipidemias. The New England Journal of Medicine. 294: 823-7. PMID 175274 DOI: 10.1056/Nejm197604082941507 |
0.386 |
|
| 1976 |
Motulsky AG. Book ReviewGenetics and the Law. New England Journal of Medicine. 295: 1022-1022. DOI: 10.1056/Nejm197610282951823 |
0.291 |
|
| 1976 |
Motulsky AG. Prenatal diagnosis and genetic counseling Western Journal of Medicine. 124: 410-412. |
0.337 |
|
| 1976 |
Motulsky AG. Hemoglobin and G6PD variation: model system in human genetics Clinical Genetics. 10: 367. |
0.339 |
|
| 1976 |
Motulsky AG. Ecogenetics: genetic variation in susceptibility to environmental agents | FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS Excerpta Med.,Amsterdam,I.C.S.. No.29. |
0.349 |
|
| 1975 |
Motulsky AG, Omenn GS. Special award lecture: biochemical genetics and psychiatry. Proceedings of the Annual Meeting of the American Psychopathological Association. 3-14. PMID 1242232 |
0.354 |
|
| 1975 |
Brunzell JD, Hazzard WR, Motulsky AG, Bierman EL. Evidence for diabetes mellitus and genetic forms of hypertriglyceridemia as independent entities. Metabolism: Clinical and Experimental. 24: 1115-21. PMID 1165727 DOI: 10.1016/0026-0495(75)90148-1 |
0.354 |
|
| 1975 |
Bethlenfalvay NC, Motulsky AG, Ringelhann B, Lehmann H, Humbert JR, Konotey-Ahulu FI. Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations. American Journal of Human Genetics. 27: 140-54. PMID 1124762 |
0.31 |
|
| 1974 |
Motulsky AG. Brave new world? Science (New York, N.Y.). 185: 653-63. PMID 4601914 |
0.318 |
|
| 1974 |
Omenn GS, Motulsky AG. Editorial: Pharmacogenetics and mental disease. Psychological Medicine. 4: 125-9. PMID 4597902 DOI: 10.1017/S0033291700041945 |
0.218 |
|
| 1974 |
Motulsky AG. Genetics of human hemoglobins: an overview. Annals of the New York Academy of Sciences. 241: 7-11. PMID 4530690 DOI: 10.1111/J.1749-6632.1974.Tb21862.X |
0.442 |
|
| 1974 |
Goldstein JL, Albers JJ, Schrott HG, Hazzard WR, Bierman EL, Motulsky AG. Plasma lipid levels and coronary heart disease in adult relatives of newborns with normal and elevated cord blood lipids. American Journal of Human Genetics. 26: 727-35. PMID 4440681 |
0.424 |
|
| 1974 |
Ott J, Schrott HG, Goldstein JL, Hazzard WR, Allen FH, Falk CT, Motulsky AG. Linkage studies in a large kindred with familial hypercholesterolemia. American Journal of Human Genetics. 26: 598-603. PMID 4213615 |
0.435 |
|
| 1974 |
Motulsky AG, Lenz W, Ebling FJG. Birth Defects. Proceedings of the Fourth International Conference, Vienna, Austria, 2-8 September, 1973 | INTERNATIONAL CONGRESS SERIES NO. 310 Excerpta Medica, Amsterdam. 373 p. Fl 105,-/-. |
0.199 |
|
| 1973 |
Motulsky AG. Significance of genetic diseases for population studies. Israel Journal of Medical Sciences. 9: 1410-6. PMID 4775127 |
0.33 |
|
| 1973 |
Motulsky AG. Screening for sickle cell hemoglobinopathy and thalassemia. Israel Journal of Medical Sciences. 9: 1341-9. PMID 4775114 |
0.204 |
|
| 1973 |
Goldstein JL, Schrott HG, Hazzard WR, Bierman EL, Motulsky AG. Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia. The Journal of Clinical Investigation. 52: 1544-68. PMID 4718953 DOI: 10.1172/Jci107332 |
0.547 |
|
| 1973 |
Goldstein JL, Hazzard WR, Schrott HG, Bierman EL, Motulsky AG. Hyperlipidemia in coronary heart disease. I. Lipid levels in 500 survivors of myocardial infarction. The Journal of Clinical Investigation. 52: 1533-43. PMID 4718952 DOI: 10.1172/Jci107331 |
0.505 |
|
| 1973 |
Chen SH, Giblett ER, Motulsky AG. Some red cell enzyme phenotype frequencies in Chinese. Humangenetik. 17: 341-3. PMID 4694517 DOI: 10.1007/Bf00273190 |
0.365 |
|
| 1973 |
Motulsky AG. Frequency of sickling disorders in U.S. blacks. The New England Journal of Medicine. 288: 31-3. PMID 4681897 DOI: 10.1056/Nejm197301042880108 |
0.369 |
|
| 1973 |
Hazzard WR, Goldstein JL, Schrott MG, Motulsky AG, Bierman EL. Hyperlipidemia in coronary heart disease. 3. Evaluation of lipoprotein phenotypes of 156 genetically defined survivors of myocardial infarction. The Journal of Clinical Investigation. 52: 1569-77. PMID 4352458 DOI: 10.1172/Jci107333 |
0.551 |
|
| 1973 |
Cohen PT, Omenn GS, Motulsky AG, Chen SH, Giblett ER. Restricted variation in the glycolytic enzymes of human brain and erythrocytes. Nature: New Biology. 241: 229-33. PMID 4266990 DOI: 10.1038/Newbio241229A0 |
0.355 |
|
| 1972 |
Schrott HG, Goldstein JL, Hazzard WR, McGoodwin MM, Motulsky AG. Familial hypercholesterolemia in a large indred. Evidence for a monogenic mechanism. Annals of Internal Medicine. 76: 711-20. PMID 5025321 DOI: 10.7326/0003-4819-76-5-711 |
0.484 |
|
| 1972 |
Lisker R, Linares C, Motulsky AG. Glucose-6-phosphate dehydrogenase Mexico. A new variant with enzyme deficiency, abnormal mobility, and absence of hemolysis. The Journal of Laboratory and Clinical Medicine. 79: 788-93. PMID 5018742 |
0.245 |
|
| 1972 |
Motulsky AG. Hemolysis in glucose-6-phosphate dehydrogenase deficiency. Federation Proceedings. 31: 1286-92. PMID 4556779 |
0.21 |
|
| 1972 |
Omenn GS, Motulsky AG. A biochemical and genetic approach to alcoholism. Annals of the New York Academy of Sciences. 197: 16-23. PMID 4504589 DOI: 10.1111/J.1749-6632.1972.Tb28112.X |
0.372 |
|
| 1972 |
Goldstein JL, Hazzard WR, Schrott HG, Bierman EL, Motulsky AG. Genetics of hyperlipidemia in coronary heart disease. Transactions of the Association of American Physicians. 85: 120-38. PMID 4349620 |
0.469 |
|
| 1972 |
Veltkamp JJ, Mayo O, Motulsky AG, Fraser GR. Blood coagulation factors I, II, V, VII, VIII, IX, X, XI and XII in twins Human Heredity. 22: 102-117. DOI: 10.1159/000152477 |
0.336 |
|
| 1971 |
Omenn GS, Motulsky AG. Brain, genetics, and behavior. Science (New York, N.Y.). 173: 1255-6. PMID 17775224 DOI: 10.1126/Science.173.4003.1255 |
0.373 |
|
| 1971 |
Murray RF, Motulsky AG. Developmental variation in the isoenzymes of human liver and gastric alchhol dehydrogenase. Science (New York, N.Y.). 171: 71-3. PMID 5538702 DOI: 10.1126/Science.171.3966.71 |
0.326 |
|
| 1971 |
Yoshida A, Beutler E, Motulsky AG. Human glucose-6-phosphate dehydrogenase variants. Bulletin of the World Health Organization. 45: 243-53. PMID 5316621 |
0.245 |
|
| 1971 |
Schultz AL, Motulsky AG. Medical genetics and adoption. Child Welfare. 50: 4-17. PMID 5170811 |
0.303 |
|
| 1971 |
Beutler E, Boggs DR, Heller P, Maurer A, Motulsky AG, Sheehy TW. Hazards of indiscriminate screening for sickling. The New England Journal of Medicine. 285: 1485-6. PMID 5122899 DOI: 10.1056/NEJM197112232852612 |
0.19 |
|
| 1971 |
Motulsky AG, Fraser GR, Felsenstein J. Public health and long-term genetic implications of intrauterine diagnosis and selective abortion. Birth Defects Original Article Series. 7: 22-32. PMID 5120222 |
0.282 |
|
| 1971 |
Motulsky AG. The William Allan Memorial Award Lecture. Human and medical genetics: a scientific discipline and an expanding horizon. American Journal of Human Genetics. 23: 107-23. PMID 5092477 |
0.283 |
|
| 1971 |
Motulsky AG, Yoshida A, Stamatoyannopoulos G. Variants of glucose-6-phosphate dehydrogenase. Annals of the New York Academy of Sciences. 179: 636-43. PMID 4936780 DOI: 10.1111/J.1749-6632.1971.Tb46939.X |
0.335 |
|
| 1971 |
Motulsky AG. Genetic Aspects of Hemoglobins and Red Cell Enzymes. Annals of Internal Medicine. 74: 844. DOI: 10.7326/0003-4819-74-5-844_2 |
0.387 |
|
| 1971 |
Robert F M, Motulsky AG. Developmental variation in the isoenzymes of human liver and gastric alcohol dehydrogenase Science. 171: 71-73. |
0.212 |
|
| 1970 |
Detter JC, Stamatoyannopoulos G, Giblett ER, Motulsky AG. Adenosine deaminase: racial distribution and report of a new phenotype. Journal of Medical Genetics. 7: 356-7. PMID 5501699 |
0.227 |
|
| 1970 |
Motulsky AG. General remarks on genetic factors in anesthesia. Humangenetik. 9: 246-8. PMID 5451688 DOI: 10.1007/Bf00279235 |
0.412 |
|
| 1970 |
Huehns ER, Hecht F, Yoshida A, Stamatoyannopoulos G, Hartman J, Motulsky AG. Hemoglobin-Seattle (alpha-2 beta-2 76-Glu): an unstable hemoglobin causing chronic hemolytic anemia. Blood. 36: 209-18. PMID 5427455 |
0.199 |
|
| 1970 |
Gelehrter T, Motulsky AG, Omenn GS. Genetic control mechanisms in man and other mammals. Science (New York, N.Y.). 169: 791-2. PMID 4393493 DOI: 10.1126/Science.169.3947.791 |
0.414 |
|
| 1970 |
HUEHNS ER, HECHT F, YOSHIDA A, STAMATOYANNOPOULOS G, HARTMAN J, MOTULSKY AG. Hemoglobin-Seattle (α2Aβ276 Glu): An Unstable Hemoglobin Causing Chronic Hemolytic Anemia Blood. 36: 209-218. DOI: 10.1182/Blood.V36.2.209.209 |
0.322 |
|
| 1969 |
Yoshida A, Motulsky AG. A pseudocholinesterase variant (E Cynthiana) associated with elevated plasma enzyme activity. American Journal of Human Genetics. 21: 486-98. PMID 5822291 |
0.226 |
|
| 1969 |
Brimhall B, Jones RT, Baur EW, Motulsky AG. Structural characterization of hemoglobin Tacoma. Biochemistry. 8: 2125-9. PMID 5785231 DOI: 10.1021/Bi00833A051 |
0.309 |
|
| 1969 |
Thuline HC, Hodgkin WE, Fraser GR, Motulsky AG. Genetics of protan and deutan color-vision anomalies: an instructive family. American Journal of Human Genetics. 21: 581-92. PMID 5365760 |
0.332 |
|
| 1969 |
Stamatoyannopoulos G, Papayannopoulou T, Fessas P, Motulsky AG. The beta-delta thalassemias. Annals of the New York Academy of Sciences. 165: 25-36. PMID 5260150 DOI: 10.1111/j.1749-6632.1969.tb27773.x |
0.18 |
|
| 1969 |
Fraser GR, Steinberg AG, Defaranas B, Mayo O, Stamatoyannopoulos G, Motulsky AG. Gene frequencies at loci determining blood-group and serum-protein polymorphisms in two villages of northwestern Greece. American Journal of Human Genetics. 21: 46-60. PMID 4974136 |
0.262 |
|
| 1969 |
Motulsky AG. Drugs and genes. Annals of Internal Medicine. 70: 1269-72. PMID 4182785 DOI: 10.7326/0003-4819-70-6-1269 |
0.334 |
|
| 1969 |
Yoshida A, Stamatoyannopoulos G, Motulsky AG. BIOCHEMICAL GENETICS OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIATION Annals of the New York Academy of Sciences. 155: 868-879. DOI: 10.1111/J.1749-6632.1969.Tb50309.X |
0.409 |
|
| 1968 |
Motulsky AG. Human genetics, society, ad medicine. The Journal of Heredity. 59: 329-36. PMID 5713932 |
0.302 |
|
| 1968 |
Hook EB, Stamatoyannopoulos G, Yoshida A, Motulsky AG. Glucose-6-phosphate dehydrogenase Madrona: a slow electrophoretic glucose-6-phosphate dehydrogenase variant with kinetic characteristics similar to those of normal type. The Journal of Laboratory and Clinical Medicine. 72: 404-9. PMID 5674071 DOI: 10.5555/Uri:Pii:0022214368901625 |
0.356 |
|
| 1968 |
Azevedo E, Kirkman HN, Morrow AC, Motulsky AG. Variants of red cell glucose-6-phosphate dehydrogenase among Asiatic Indians. Annals of Human Genetics. 31: 373-9. PMID 5673160 DOI: 10.1111/J.1469-1809.1968.Tb00569.X |
0.347 |
|
| 1968 |
Epstein CJ, Graham CB, Hodgkin WE, Hecht F, Motulsky AG. Hereditary dysplasia of bone with kyphoscoliosis, contractures, and abnormally shaped ears. The Journal of Pediatrics. 73: 379-86. PMID 5667420 DOI: 10.1016/S0022-3476(68)80115-5 |
0.538 |
|
| 1968 |
Hall JG, Motulsky AG. Production of foetal haemoglobin in marrow cultures of human adults. Nature. 217: 569-71. PMID 5641113 DOI: 10.1038/217569A0 |
0.316 |
|
| 1968 |
Motulsky AG. Genetics and environmental health. Archives of Environmental Health. 16: 75-6. PMID 5638229 |
0.306 |
|
| 1968 |
Jones RT, Brimhall B, Huehns ER, Motulsky AG. Structural characterization of hemoglobin-N-Seattle. Biochimica Et Biophysica Acta. 154: 278-83. PMID 5637049 DOI: 10.1016/0005-2795(68)90041-X |
0.319 |
|
| 1968 |
Motulsky AG. Crohn's disease and G-6-PD deficiency. The New England Journal of Medicine. 278: 281-2. PMID 5635469 |
0.21 |
|
| 1968 |
Motulsky AG, Morrow A. Atypical cholinesterase gene E1a: rarity in Negroes and most Orientals. Science (New York, N.Y.). 159: 202-3. PMID 5634910 DOI: 10.1126/Science.159.3811.202 |
0.377 |
|
| 1968 |
Motulsky AG, Stamatoyannopoulos G. Drugs, anesthesia and abnormal hemoglobins. Annals of the New York Academy of Sciences. 151: 807-21. PMID 5263689 DOI: 10.1111/J.1749-6632.1968.Tb48264.X |
0.315 |
|
| 1968 |
Rosenzweig AI, Heywood JD, Motulsky AG, Finch CA. Hemoglobin H as an acquired defect of alpha-chain synthesis. Report of two cases. Acta Haematologica. 39: 91-101. PMID 4968785 |
0.198 |
|
| 1968 |
Motulsky AG. Vernon M. American Journal of Human Genetics. 20: 287-8. PMID 4873803 |
0.171 |
|
| 1967 |
Lisker R, Motulsky AG. Computer simulation of evolutionary trends in an X linked trait. Application to glucose-6-phosphate dehydrogenase deficiency in man. Acta Genetica Et Statistica Medica. 17: 465-74. PMID 6072880 |
0.236 |
|
| 1967 |
Sparkes RS, Motulsky AG. The Turner syndrome with isochromosome X and Hashimoto's thyroiditis. Annals of Internal Medicine. 67: 132-44. PMID 6071743 DOI: 10.7326/0003-4819-67-1-132 |
0.339 |
|
| 1967 |
Thuline HC, Morrow AC, Norby DE, Motulsky AG. Autosomal phosphogluconic dehydrogenase polymorphism in the cat (Felis catus L.). Science (New York, N.Y.). 157: 431-2. PMID 6028025 DOI: 10.1126/Science.157.3787.431 |
0.384 |
|
| 1967 |
Comings DE, Skubi KB, Van Eyes J, Motulsky AG. Familial multifocal fibrosclerosis. Findings suggesting that retroperitoneal fibrosis, mediastinal fibrosis, sclerosing cholangitis, Riedel's thyroiditis, and pseudotumor of the orbit may be different manifestations of a single disease. Annals of Internal Medicine. 66: 884-92. PMID 6025229 DOI: 10.7326/0003-4819-66-5-884 |
0.359 |
|
| 1967 |
Fialkow PJ, Giblett ER, Motulsky AG. Measurable linkage between ocular albinism and Xg. American Journal of Human Genetics. 19: 63-9. PMID 6019304 |
0.218 |
|
| 1967 |
Stamatoyannopoulos G, Papayannopoulou T, Bakopoulos C, Motulsky AG. Detection of glucose-6-phosphate dehydrogenase deficient heterozygotes. Blood. 29: 87-101. PMID 6017611 DOI: 10.1182/Blood.V29.1.87.87 |
0.38 |
|
| 1967 |
Yoshida A, Stamatoyannopoulos G, Motulsky AG. Negro variant of glucose-6-phosphate dehydrogenase deficiency (A-) in man. Science (New York, N.Y.). 155: 97-9. PMID 6015571 DOI: 10.1126/Science.155.3758.97 |
0.367 |
|
| 1967 |
Steinmuller D, Motulsky AG. Treatment of hereditary spherocytosis in Peromyscus by radiation and allogeneic bone marrow transplantation. Blood. 29: 320-30. PMID 5335711 DOI: 10.1097/00007890-196709000-00023 |
0.371 |
|
| 1967 |
Motulsky AG. Biochemical genetics in medicine. Acta Paediatrica Scandinavica. Suppl 172:156+. PMID 4860134 DOI: 10.1111/J.1651-2227.1967.Tb15291.X |
0.429 |
|
| 1966 |
Motulsky AG. Biochemical genetics in medicine. The Alabama Journal of Medical Sciences. 3: 359-69. PMID 5978166 |
0.352 |
|
| 1966 |
Hecht F, Motulsky AG, Lemire RJ, Shepard TE. Predominance of hemoglobin Gower 1 in early human embryonic development. Science (New York, N.Y.). 152: 91-2. PMID 5948690 DOI: 10.1126/Science.152.3718.91 |
0.335 |
|
| 1966 |
Stamatoyannopoulos G, Panayotopoulos A, Motulsky AG. The distribution of glucose-6-phosphate dehydrogenase deficiency in Greece. American Journal of Human Genetics. 18: 296-308. PMID 5944422 |
0.206 |
|
| 1966 |
Comings DE, Motulsky AG. Absence of cis delta chain synthesis in (sigma beta) thalassemia (F-thalassemia). Blood. 28: 54-69. PMID 5944262 |
0.184 |
|
| 1966 |
Stamatoyannopoulos G, Papayannopoulou T, Bakopoulos C, Motulsky AG. Methemoglobin reduction and the inactive X hypothesis. American Journal of Human Genetics. 18: 417-23. PMID 5927285 |
0.186 |
|
| 1966 |
Anderson R, Motulsky AG. Adverse effects of raised environment temperature on the expression of hereditary spherocytosis in deer mice. Blood. 28: 365-76. PMID 5918469 DOI: 10.1182/Blood.V28.3.365.365 |
0.354 |
|
| 1966 |
Motulsky AG, Stamatoyannopoulos G. Clinical implications of glucose-6-phosphate dehydrogenase deficiency. Annals of Internal Medicine. 65: 1329-34. PMID 5333234 DOI: 10.7326/0003-4819-65-6-1329 |
0.334 |
|
| 1966 |
Motulsky AG, Vandepitte J, Fraser GR. Population genetic studies in the Congo. I. Glucose-6-phosphate dehydrogenase deficiency, hemoglobin S, and malaria. American Journal of Human Genetics. 18: 514-37. PMID 5333143 |
0.301 |
|
| 1966 |
Epstein CJ, Martin GM, Schultz AL, Motulsky AG. Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine. 45: 177-221. PMID 5327241 DOI: 10.1097/00005792-196605000-00001 |
0.527 |
|
| 1966 |
Fraser GR, Giblett ER, Motulsky AG. Population genetic studies in the Congo. 3. Blood groups (ABO, MNSs, Rh, Jsa). American Journal of Human Genetics. 18: 546-52. PMID 4959344 |
0.304 |
|
| 1966 |
COMINGS DE, MOTULSKY AG. Absence of Cis Delta Chain Synthesis in (δ β) Thalassemia (F-thalassemia) Blood. 28: 54-69. DOI: 10.1182/Blood.V28.1.54.54 |
0.355 |
|
| 1966 |
Hecht F, Motulsky AG, Lemira RJ, Shepard TE. Predominance of hemoglobin Gower 1 in early human embryonic life The Journal of Pediatrics. 69: 974. DOI: 10.1016/S0022-3476(66)80568-1 |
0.332 |
|
| 1966 |
Baur EW, Motulsky AG. Hemoglobin tacoma ? A ?-chain variant Human Genetics. 1: 621-634. DOI: 10.1007/BF00281050 |
0.225 |
|
| 1965 |
MOTULSKY AG. THE GENETICS OF ABNORMAL DRUG RESPONSES. Annals of the New York Academy of Sciences. 123: 167-77. PMID 14329199 DOI: 10.1111/J.1749-6632.1965.Tb12254.X |
0.398 |
|
| 1965 |
FRASER GR, GIBLETT ER, LEE TC, MOTULSKY AG. BLOOD AND SERUM GROUPS IN TAIWAN. Journal of Medical Genetics. 2: 21-3. PMID 14296919 |
0.214 |
|
| 1965 |
MOTULSKY AG, LEE TC, FRASER GR. GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY, THALASSAEMIA, AND ABNORMAL HAEMOGLOBINS IN TAIWAN. Journal of Medical Genetics. 2: 18-20. PMID 14296917 |
0.222 |
|
| 1965 |
HODGKIN W, GIBLETT ER, LEVINE H, BAUER W, MOTULSKY AG. COMPLETE PSEUDOCHOLINESTERASE DEFICIENCY: GENETIC AND IMMUNOLOGIC CHARACTERIZATION. The Journal of Clinical Investigation. 44: 486-93. PMID 14271308 DOI: 10.1172/Jci105162 |
0.444 |
|
| 1965 |
Lewis KB, Bruce RA, Baum D, Motulsky AG. The upper limb-cardiovascular syndrome. An autosomal dominant genetic effect on embryogenesis. Jama. 193: 1080-6. PMID 5896868 DOI: 10.1001/Jama.1965.03090130008002 |
0.385 |
|
| 1965 |
Baur EW, Motulsky AG. Hemoglobin tacoma--a beta-chain variant associated with increased hb A2. Humangenetik. 1: 621-34. PMID 5869485 DOI: 10.1007/Bf00281050 |
0.364 |
|
| 1965 |
Epstein CJ, Martin GM, Motulsky AG. Werner's syndrome; caricature of aging. A genetic model for the study of degenerative diseases. Transactions of the Association of American Physicians. 78: 73-81. PMID 5864984 |
0.514 |
|
| 1965 |
Epstein CJ, Motulsky AG. Evolutionary origins of human proteins. Progress in Medical Genetics. 4: 85-127. PMID 5319298 |
0.444 |
|
| 1965 |
Fialkow PJ, Browder JA, Sparkes RS, Motulsky AG. Mental retardation in methemoglobinemia due to diaphorase deficiency. The New England Journal of Medicine. 273: 840-5. PMID 4378489 DOI: 10.1056/Nejm196510142731602 |
0.368 |
|
| 1965 |
Fialkow PJ, Hecht F, Uchida IA, Motulsky AG. Increased frequency of thyroid autoantibodies in mothers of patients with Down's syndrome. Lancet. 2: 868-70. PMID 4158240 |
0.217 |
|
| 1964 |
MOTULSKY AG. CURRENT CONCEPTS OF THE GENETICS OF THE THALASSEMIAS. Cold Spring Harbor Symposia On Quantitative Biology. 29: 399-413. PMID 14278485 DOI: 10.1101/Sqb.1964.029.01.042 |
0.416 |
|
| 1964 |
HUEHNS ER, DANCE N, BEAVEN GH, HECHT F, MOTULSKY AG. HUMAN EMBRYONIC HEMOGLOBINS. Cold Spring Harbor Symposia On Quantitative Biology. 29: 327-31. PMID 14278479 DOI: 10.1101/Sqb.1964.029.01.035 |
0.339 |
|
| 1964 |
FRASER GR, GIBLETT ER, STRANSKY E, MOTULSKY AG. BLOOD GROUPS IN THE PHILIPPINES. Journal of Medical Genetics. 1: 107-9. PMID 14234104 |
0.205 |
|
| 1964 |
MOTULSKY AG, STRANSKY E, FRASER GR. GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G6PD) DEFICIENCY, THALASSAEMIA, AND ABNORMAL HAEMOGLOBINS IN THE PHILIPPINES. Journal of Medical Genetics. 1: 102-6. PMID 14234103 |
0.222 |
|
| 1964 |
MOTULSKY AG, HECHT F. GENETIC PROGNOSIS AND COUNSELING. American Journal of Obstetrics and Gynecology. 90: SUPPL:1227-41. PMID 14231697 DOI: 10.1016/0002-9378(64)90843-9 |
0.458 |
|
| 1964 |
FRASER GR, STAMATOYANNOPOULOS G, KATTAMIS C, LOUKOPOULOS D, DEFARANAS B, KITSOS C, ZANNOS-MARIOLEA L, CHOREMIS C, FESSAS P, MOTULSKY AG. THALASSEMIAS, ABNORMAL HEMOGLOBINS AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN THE ARTA AREA OF GREECE: DIAGNOSTIC AND GENETIC ASPECTS OF COMPLETE VILLAGE STUDIES. Annals of the New York Academy of Sciences. 119: 415-35. PMID 14219423 DOI: 10.1111/J.1749-6632.1965.Tb54044.X |
0.408 |
|
| 1964 |
HUEHNS ER, DANCE N, BEAVEN GH, KEIL JV, HECHT F, MOTULSKY AG. HUMAN EMBRYONIC HAEMOGLOBINS. Nature. 201: 1095-7. PMID 14152781 DOI: 10.1038/2011095A0 |
0.335 |
|
| 1964 |
MOTULSKY AG. PHARMACOGENETICS. Progress in Medical Genetics. 23: 49-74. PMID 14110077 |
0.21 |
|
| 1964 |
MOTULSKY AG. HEREDITARY RED CELL TRAITS AND MALARIA. The American Journal of Tropical Medicine and Hygiene. 13: SUPPL147-58. PMID 14106725 |
0.251 |
|
| 1964 |
HUEHNS ER, HECHT F, KEIL JV, MOTULSKY AG. DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME. Proceedings of the National Academy of Sciences of the United States of America. 51: 89-97. PMID 14104609 DOI: 10.1073/Pnas.51.1.89 |
0.338 |
|
| 1963 |
HECHT F, BRYANT JS, MOTULSKY AG, GIBLETT ER. THE NO. 17-18 (E) TRISOMY SYNDROME. STUDIES ON CYTOGENETICS, DERMATOGLYPHICS, PATERNAL AGE, AND LINKAGE. The Journal of Pediatrics. 63: 605-21. PMID 14074419 DOI: 10.1016/S0022-3476(63)80371-6 |
0.379 |
|
| 1963 |
PRIEST JH, BRYANT J, MOTULSKY AG. DOWN'S SYNDROME: TRISOMY AND A DE-NOVO TRANSLOCATION IN A FAMILY. Lancet. 2: 411-2. PMID 14044305 |
0.254 |
|
| 1963 |
SPARKES RS, MOTULSKY AG. Hashimoto's disease in Turner's syndrome with isochromosome X. Lancet. 1: 947. PMID 13989924 |
0.237 |
|
| 1962 |
MOTULSKY AG. Medical genetics in the Pacific area. Eugenics Quarterly. 9: 1-4. PMID 14476613 |
0.295 |
|
| 1962 |
MOTULSKY AG. Controller genes in synthesis of human haemoglobin. Nature. 194: 607-9. PMID 14476612 DOI: 10.1038/194607B0 |
0.375 |
|
| 1962 |
MOTULSKY AG, ANDERSON R, SPARKES RS, HUESTIS RH. Marrow transplantation in newborn mice with hereditary spherocytosis: a model system. Transactions of the Association of American Physicians. 75: 64-72. PMID 13936283 |
0.189 |
|
| 1962 |
MOTULSKY A. WERNER'S SYNDROME: CHROMOSOMES, GENES, AND THE AGEING PROCESS The Lancet. 279: 160-161. DOI: 10.1016/S0140-6736(62)91160-1 |
0.247 |
|
| 1962 |
Motulsky AG, Gartler SM. General principles of medical genetics Disease-a-Month. 8: 1-62. DOI: 10.1016/S0011-5029(62)80013-3 |
0.302 |
|
| 1962 |
Motulsky AG. Medical Genetics 1958-1960: An Annotated Review Jama: the Journal of the American Medical Association. 181: 656. DOI: 10.1001/Jama.1962.03050330086031 |
0.414 |
|
| 1961 |
Siniscalco M, Bernini L, Latte B, Motulsky AG. Favism and thalassaemia in Sardinia and their relationship to malaria Nature. 190: 1179-1180. DOI: 10.1038/1901179A0 |
0.304 |
|
| 1961 |
Motulsky AG. Human biochemical genetics. By H. Harris. Cambridge University Press. 1959 American Journal of Physical Anthropology. 19: 220-221. DOI: 10.1002/AJPA.1330190217 |
0.307 |
|
| 1960 |
MOTULSKY AG. Metabolic polymorphisms and the role of infectious diseases in human evolution. Human Biology. 32: 28-62. PMID 14424690 |
0.258 |
|
| 1960 |
ANDERSON R, HUESTIS RR, MOTULSKY AG. Hereditary spherocytosis in the deer mouse. Its similarity to the human disease. Blood. 15: 491-504. PMID 13793441 DOI: 10.1182/Blood.V15.4.491.491 |
0.454 |
|
| 1959 |
MOTULSKY AG. Joseph Adams (1756-1818): a forgotten founder of medical genetics. Archives of Internal Medicine. 104: 490-6. PMID 14424689 |
0.305 |
|
| 1959 |
MOTULSKY AG, GARTLER SM. Consanguinity and marriage. The Practitioner. 183: 170-7. PMID 14424688 |
0.229 |
|
| 1959 |
VANARSDEL PP, MOTULSKY AG. Blood groups and secretion of blood group substances. Comparison of allergic with nonallergic persons in a Pacific Northwest college population. The Journal of Allergy. 30: 460-3. PMID 13841173 DOI: 10.1016/0021-8707(59)90024-3 |
0.329 |
|
| 1959 |
VAN ARSDEL PP, MOTULSKY AG. Frequency and hereditability of asthma and allergic rhinitis in college students. Acta Genetica Et Statistica Medica. 9: 101-14. PMID 13840956 |
0.175 |
|
| 1959 |
Motulsky AG. Annual Review of Medicine. Volume 9.David A. Rytand , William P. Creger The Quarterly Review of Biology. 34: 264-265. DOI: 10.1086/402812 |
0.19 |
|
| 1958 |
MOTULSKY AG, CASSERD F, GIBLETT ER, BROUN GO, FINCH CA. Anemia and the spleen. The New England Journal of Medicine. 259: 1215-9 concl. PMID 13622913 DOI: 10.1056/NEJM195812182592506 |
0.213 |
|
| 1958 |
MOTULSKY AG, CASSERD F, GIBLETT ER, BROUN GO, FINCH CA. Anemia and the spleen. The New England Journal of Medicine. 259: 1164-9 contd. PMID 13613484 DOI: 10.1056/Nejm195812112592405 |
0.306 |
|
| 1958 |
GIBLETT ER, CHASE J, MOTULSKY AG. Studies on anti-V, a new potentially dangerous blood group antibody. Bibliotheca Haematologica. 7: 119-22. PMID 13499241 DOI: 10.1159/000427071 |
0.312 |
|
| 1958 |
MOTULSKY AG. Chronicle of the WHO Challenge of Atomic Energy Annals of Human Genetics. 23: 73-73. DOI: 10.1111/J.1469-1809.1958.Tb01443.X |
0.282 |
|
| 1957 |
MOTULSKY AG. Drug reactions enzymes, and biochemical genetics. Journal of the American Medical Association. 165: 835-7. PMID 13462859 DOI: 10.1001/Jama.1957.72980250010016 |
0.373 |
|
| 1957 |
GIBLETT ER, CHASE J, MOTULSKY AG. Studies on anti-V; a recently discovered Rh antibody. The Journal of Laboratory and Clinical Medicine. 49: 433-9. PMID 13406376 |
0.184 |
|
| 1957 |
MOTULSKY AG. Karl Singer, 1902-1956. Blood. 12: 94-5. PMID 13382993 |
0.177 |
|
| 1956 |
MOTULSKY AG, HUESTIS RR, ANDERSON R. Hereditary spherocytosis in mouse and man. Acta Genetica Et Statistica Medica. 6: 240-5. PMID 13410485 DOI: 10.1159/000150827 |
0.356 |
|
| 1956 |
DONOHUE DM, FINCH CA, GIBLETT ER, HURTADO AV, MOTULSKY AG, REIFF RH. Quantitative aspects of erythropoiesis in man. Transactions of the Association of American Physicians. 69: 149-54. PMID 13380957 |
0.221 |
|
| 1956 |
MOTULSKY AG. Genetic and haematological significance of haemoglobin H. Nature. 178: 1055-6. PMID 13378527 DOI: 10.1038/1781055B0 |
0.38 |
|
| 1956 |
CASSERD F, FINCH CA, GIBLETT ER, HOUGHTON B, MOTULSKY AG. Studies on the pathogenesis of splenic anemia. Blood. 11: 1118-31. PMID 13373929 DOI: 10.1182/Blood.V11.12.1118.1118 |
0.346 |
|
| 1956 |
COLEMAN DH, DONOHUE DM, FINCH CA, MOTULSKY AG, REIFF RH. Erythrokinetics in pernicious anemia. Blood. 11: 807-20. PMID 13355891 DOI: 10.1182/Blood.V11.9.807.807 |
0.352 |
|
| 1956 |
VANDEPITTE J, MOTULSKY AG. Abnormal haemoglobins in the Kasai province of the Belgian Congo. Nature. 177: 757. PMID 13321956 DOI: 10.1038/177757A0 |
0.358 |
|
| 1956 |
GIBLETT ER, COLEMAN DH, PIRZIOBIROLI G, DONOHUE DM, MOTULSKY AG, FINCH CA. Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia. Blood. 11: 291-309. PMID 13304119 |
0.222 |
|
| 1956 |
MACKAY IR, ERIKSEN N, MOTULSKY AG, VOLWILER W. Cryo- and macroglobulinemia; electrophoretic, ultracentrifugal and clinical studies. The American Journal of Medicine. 20: 564-87. PMID 13302234 DOI: 10.1016/0002-9343(56)90139-5 |
0.36 |
|
| 1956 |
ROTTER R, LUTTGENS WF, PETERSON WL, STOCK AE, MOTULSKY AG. Splenic infarction in sicklemia during airplane flight: pathogenesis, hemoglobin analysis and clinical features of six cases. Annals of Internal Medicine. 44: 257-70. PMID 13292838 |
0.206 |
|
| 1955 |
THOMAS ED, MOTULSKY AG, WALTERS DH. Homozygous hemoglobin C disease; report of a case with studies on the pathophysiology and neonatal formation of hemoglobin C. The American Journal of Medicine. 18: 832-8. PMID 14361465 |
0.231 |
|
| 1955 |
DONOHUE DM, MOTULSKY AG, GIBLETT ER, PIRZIO-BIROLI G, VIRANUVATTI V, FINCH CA. The use of chromium as red-cell tag. British Journal of Haematology. 1: 249-63. PMID 13240014 DOI: 10.1111/J.1365-2141.1955.Tb05508.X |
0.313 |
|
| 1955 |
Motulsky A, Gabrio B, Burkhardt J, Finch C. Erythrocyte carbohydrate metabolism in hereditary hemolytic anemias The American Journal of Medicine. 19: 291. DOI: 10.1016/0002-9343(55)90398-3 |
0.213 |
|
| 1954 |
TERRY DW, MOTULSKY AG, RATH CE. A new hereditary hemolytic disease. The New England Journal of Medicine. 251: 365-73. PMID 13194076 DOI: 10.1056/Nejm195409022511001 |
0.349 |
|
| 1954 |
MOTULSKY AG, PAUL MH, DURRUM EL. Paper electrophoresis of abnormal hemoglobins and its clinical applications; a simple semiquantitative method for the study of the hereditary hemoglobinopathies. Blood. 9: 897-910. PMID 13189919 |
0.22 |
|
| 1954 |
MOTULSKY AG, CROSBY WH, RAPPAPORT H. Hereditary nonspherocytic hemolytic disease; a study of a singular familial hemolytic syndrome. Blood. 9: 749-72. PMID 13181939 |
0.28 |
|
| 1954 |
BRUTON OC, CROSBY WH, MOTULSKY AG. Hereditary nonspherocytic hemolytic anemia presenting as hemolytic disease of the newborn infant. Pediatrics. 13: 41-3. PMID 13133551 |
0.218 |
|
| 1954 |
MOTULSKY AG, SINGER K, CROSBY WH, SMITH V. The life span of the elliptocyte; hereditary elliptocytosis and its relationship to other familial hemolytic diseases. Blood. 9: 57-72. PMID 13115472 DOI: 10.1182/Blood.V9.1.57.57 |
0.495 |
|
| 1954 |
Terry DW, Motulsky A, Rath CE, Jeghers H. Homozygous hemoglobin C: A new hereditary hemolytic disease The American Journal of Medicine. 16: 611. DOI: 10.1016/0002-9343(54)90432-5 |
0.351 |
|
| 1954 |
Motulsky AG, Crosby WH. Experimental production of red cell autoimmunization The American Journal of Medicine. 17: 102. DOI: 10.1016/0002-9343(54)90150-3 |
0.201 |
|
| 1953 |
VAN WYK JJ, BAXTER JH, AKEROYD JH, MOTULSKY AG. The anemia of copper deficiency in dogs compared with that produced by iron deficiency. Bulletin of the Johns Hopkins Hospital. 93: 41-9. PMID 13082313 |
0.196 |
|
| 1953 |
MOTULSKY AG, ROHN RJ. The bone marrow in metastatic malignant melanoma. The Journal of Laboratory and Clinical Medicine. 41: 526-33. PMID 13045003 |
0.185 |
|
| 1952 |
MOTULSKY AG, WEINBERG S, SAPHIR O, ROSENBERG E. Lymph nodes in rheumatoid arthritis. A.M.a. Archives of Internal Medicine. 90: 660-76. PMID 12984866 |
0.167 |
|
| 1951 |
MOTULSKY AG, WEINBERG SL, SAPHIR O, ROSENBERG EF. Significance of giant follicular hyperplasia in the lymphadenopath of rheumatoid arthritis. Annals of the Rheumatic Diseases. 10: 486-7. PMID 14895100 |
0.186 |
|
| 1950 |
SINGER K, MOTULSKY AG, WILE SA. Aplastic crisis in sickle cell anemia; a study of its mechanism and its relationship to other types of hemolytic crises. The Journal of Laboratory and Clinical Medicine. 35: 721-36. PMID 15422207 DOI: 10.5555/Uri:Pii:0022214350900333 |
0.533 |
|
| 1950 |
SINGER K, MOTULSKY AG, SHANBERGE JN. Thrombotic thrombocytopenic purpura. II. Studies on the hemolytic syndrome in this disease. Blood. 5: 434-48. PMID 15414199 DOI: 10.1182/Blood.V5.5.434.434 |
0.523 |
|
| 1949 |
SINGER K, MOTULSKY AG. The developing (Coombs) test in spherocytic hemolytic anemias; its significance for the pathophysiology of spherocytosis and splenic hemolysis. The Journal of Laboratory and Clinical Medicine. 34: 768-83. PMID 18151315 DOI: 10.5555/Uri:Pii:0022214349902255 |
0.518 |
|
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