Arno G. Motulsky, M.D.

Medical Genetics University of Washington, Seattle, Seattle, WA 
"Arno Motulsky"

Motulsky was recognized for his decades of contributions to genetic medicine and as a founder of the field of pharmacogenetics.

Mean distance: 15.85 (cluster 11)
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Giblett ER, Coleman DH, Pirzio-Biroli G, et al. (2016) Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia. Blood. 127: 1375
Gallego CJ, Burt A, Sundaresan AS, et al. (2015) Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network. American Journal of Human Genetics
Kim DS, Burt AA, Ranchalis JE, et al. (2015) PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity. Journal of Lipid Research. 56: 1351-62
Amendola LM, Dorschner MO, Robertson PD, et al. (2015) Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Research. 25: 305-15
Deeb SS, Motulsky AG. (2014) Genetics of Color Vision Defects Reference Module in Biomedical Research
Rosenthal EA, Ranchalis J, Crosslin DR, et al. (2013) Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia. American Journal of Human Genetics. 93: 1035-45
Dorschner MO, Amendola LM, Turner EH, et al. (2013) Actionable, pathogenic incidental findings in 1,000 participants' exomes. American Journal of Human Genetics. 93: 631-40
Anderson CA, Beresford SA, McLerran D, et al. (2013) 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
Deeb SS, Motulsky AG. (2013) Color Vision Defects Emery and Rimoin's Principles and Practice of Medical Genetics. 1-17
Pierce SB, Spurrell CH, Mandell JB, et al. (2011) 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
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