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Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

American journal of human genetics, 2013-10, Vol.93 (4), p.631-640

2013

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Joint Linkage and Association Analysis with Exome Sequence Data Implicates SLC25A40 in Hypertriglyceridemia

American journal of human genetics, 2013-12, Vol.93 (6), p.1035-1045

2013

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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, 2018-06, Vol.176 (6), p.1289-1295

Motulsky, Arno G.

2018

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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, 2013-04, Vol.57 (4), p.637-644

2013

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Cardiovascular disease mortality in familial forms of hypertriglyceridemia : A 20-year prospective study

Circulation (New York, N.Y.), 2000-06, Vol.101 (24), p.2777-2782

2000

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Genetic and nongenetic sources of variation in phospholipid transfer protein activity[S]

Journal of lipid research, 2010-05, Vol.51 (5), p.983-990

2010

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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, 2003-07, Vol.23 (7), p.1289-1294

2003

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Linkage and association of phospholipid transfer protein activity to LASS4

Journal of lipid research, 2011-10, Vol.52 (10), p.1837-1846

2011

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Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (45), p.18313-18317

2011

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Frequent Detection of Familial Hypercholesterolemia Mutations in Familial Combined Hyperlipidemia

Journal of the American College of Cardiology, 2008-11, Vol.52 (19), p.1554-1556

2008

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Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia

Blood, 2016-03, Vol.127 (11), p.1375-1375

2016

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Priorities and standards in pharmacogenetic research

Nature genetics, 2005-07, Vol.37 (7), p.671-681

2005

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A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

JAMA : the journal of the American Medical Association, 1995-10, Vol.274 (13), p.1049

1995

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‘Drug reactions, enzymes, and biochemical genetics ’: 50 years later

Pharmacogenomics, 2007-11, Vol.8 (11), p.1479-1484

2007

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PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity

Journal of lipid research, 2015-07, Vol.56 (7), p.1351-1362

2015

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Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia

Journal of lipid research, 2003-11, Vol.44 (11), p.2161-2168

2003

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Lipoprotein and apolipoprotein abnormalities in familial combined hyperlipidemia: a 20-year prospective study

Atherosclerosis, 2001-12, Vol.159 (2), p.471-481

2001

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PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity1[S]

Journal of lipid research, 2015-07, Vol.56 (7), p.1351-1362

2015

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Hereditary hemochromatosis: gene discovery and its implications for population-based screening

JAMA : the journal of the American Medical Association, 1998-07, Vol.280 (2), p.172

1998

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Human genetics. Mapping human history

Science (American Association for the Advancement of Science), 2002-12, Vol.298 (5602), p.2342-2343

2002

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Genetics of complex diseases

Journal of Zhejiang University. B. Science, 2006-02, Vol.7 (2), p.167-168

Motulsky, Arno G

2006

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Preventing coronary heart disease: B vitamins and homocysteine

Circulation (New York, N.Y.), 1998-02, Vol.97 (5), p.421-424

1998

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Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families

Human genetics, 2010-06, Vol.127 (6), p.705-719

2010

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Mapping Human History

Science (American Association for the Advancement of Science), 2002-12, Vol.298 (5602), p.2342-2343

2002

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Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors

Journal of genetic counseling, 2002-04, Vol.11 (2), p.97-119

2002

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Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes

Joint Linkage and Association Analysis with Exome Sequence Data Implicates SLC25A40 in Hypertriglyceridemia

A German‐Jewish refugee in Vichy France 1939–1941. Arno Motulsky's memoir of life in the internment camps at St. Cyprien and Gurs

Response of serum and red blood cell folate concentrations to folic acid supplementation depends on methylenetetrahydrofolate reductase C677T genotype: Results from a crossover trial

Cardiovascular disease mortality in familial forms of hypertriglyceridemia : A 20-year prospective study

Genetic and nongenetic sources of variation in phospholipid transfer protein activity[S]

Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia

Linkage and association of phospholipid transfer protein activity to LASS4

Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria

Frequent Detection of Familial Hypercholesterolemia Mutations in Familial Combined Hyperlipidemia

Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia

Priorities and standards in pharmacogenetic research

A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

‘Drug reactions, enzymes, and biochemical genetics ’: 50 years later

PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity

Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia

Lipoprotein and apolipoprotein abnormalities in familial combined hyperlipidemia: a 20-year prospective study

PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity1[S]

Hereditary hemochromatosis: gene discovery and its implications for population-based screening

Human genetics. Mapping human history

Genetics of complex diseases

Preventing coronary heart disease: B vitamins and homocysteine

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families

Mapping Human History

Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors

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