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Author Details

Arno G Motulsky
University of Washington
1949
285
67
PMIDPaper TitleJournal TitlePublished Year
29697901A German-Jewish refugee in Vichy France 1939-1941. Arno Motulsky's memoir of life in the internment camps at St. Cyprien and Gurs.Am J Med Genet A2018
26989183Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia.Blood2016
27147253The Great Adventure of an American Human Geneticist.Annu Rev Genomics Hum Genet2016
25637381Actionable exomic incidental findings in 6503 participants: challenges of variant classification.Genome Res2015
26365338Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.Am J Hum Genet2015
26009633PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity.J Lipid Res2015
23456769Response of serum and red blood cell folate concentrations to folic acid supplementation depends on methylenetetrahydrofolate reductase C677T genotype: results from a crossover trial.Mol Nutr Food Res2013
24268658Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.Am J Hum Genet2013
24055113Actionable, pathogenic incidental findings in 1,000 participants' exomes.Am J Hum Genet2013
21325615Comment on "Multidimensional results reporting to participants in genomic studies: getting it right".Sci Transl Med2011
22042873Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria.Proc Natl Acad Sci U S A2011
21805720Charles Joseph Epstein, M.D., 1933â¿¿2011, in memoriam.Am J Hum Genet2011
215166162010 Victor A. McKusick Leadership Award introduction and address.Am J Hum Genet2011
21757428Linkage and association of phospholipid transfer protein activity to LASS4.J Lipid Res2011
19965587Genetic and nongenetic sources of variation in phospholipid transfer protein activity.J Lipid Res2010
20383777Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.Hum Genet2010
19290807Genome-environment interactions and prospective technology assessment: evolution from pharmacogenomics to nutrigenomics and ecogenomics.OMICS2009
19007591Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia.J Am Coll Cardiol2008
18034611'Drug reactions, enzymes, and biochemical genetics': 50 years later.Pharmacogenomics2007
17985513Enhancing recruitment of healthy African American volunteers in a city with a small African American community: results from a dietary supplement crossover trial.Ethn Dis2007
16575896Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.Am J Med Genet A2006
16421980Pharmacogenetics, pharmacogenomics and ecogenetics.J Zhejiang Univ Sci B2006
16421979Genetics of complex diseases.J Zhejiang Univ Sci B2006
16594908Genetically determined apo B levels and peak LDL density predict angiographic response to intensive lipid-lowering therapy.J Intern Med2006
15704130Equal proportion of adult male and female homozygous for the 677C --> T mutation in the methylenetetrahydrofolate reductase polymorphism.Am J Med Genet A2005
15959807Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia.Hum Genet2005
15990888Priorities and standards in pharmacogenetic research.Nat Genet2005
15331429Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan.Arterioscler Thromb Vasc Biol2004
15197065X-linked high myopia associated with cone dysfunction.Arch Ophthalmol2004
12544469Hereditary hemochromatosis: perspectives of public health, medical genetics, and primary care.Genet Med2003
12923221Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia.J Lipid Res2003
14569462Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment.Hum Genet2003
12750118Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia.Arterioscler Thromb Vasc Biol2003
117538232001 William Allan Award Address. Introductory speech for Charles J. Epstein.Am J Hum Genet2002
26142135Letter to the Editor: Reply to Becker and Morgan.J Genet Couns2002
26141656Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors.J Genet Couns2002
12493903Human genetics. Mapping human history.Science2002
11595020Lipoprotein(a) as a risk factor for maternal cardiovascular disease mortality in kindreds with familial combined hyperlipidemia or familial hypertriglyceridemia.Clin Genet2001
11730829Lipoprotein and apolipoprotein abnormalities in familial combined hyperlipidemia: a 20-year prospective study.Atherosclerosis2001
11126723Phylogenetic relationships of human populations in sub-Saharan Africa.Hum Biol2000
10859281Cardiovascular disease mortality in familial forms of hypertriglyceridemia: A 20-year prospective study.Circulation2000
10884946Population screening in hereditary hemochromatosis.Annu Rev Public Health2000
108369101999 ASHG Award for Excellence in Education. Some future directions in medical genetics.Am J Hum Genet2000
10521376Pleiotropic genetic effects on LDL size, plasma triglyceride, and HDL cholesterol in families.Arterioscler Thromb Vasc Biol1999
11258630Inconsistencies in genetic counseling and screening for consanguineous couples and their offspring: the need for practice guidelines.Genet Med1999
10319869Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.Nat Genet1999
10437855If I had a gene test, what would I have and who would I tell?Lancet1999
10341958Analysis of red/green color discrimination in subjects with a single X-linked photopigment gene.Vision Res1999
9669792Hereditary hemochromatosis: gene discovery and its implications for population-based screening.JAMA1998
9484986Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex.Arterioscler Thromb Vasc Biol1998
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Collaborators

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University of Washington Medical Center
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