Yefim Anbinder

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

Hanna Mandel, Raymonde Szargel, Valentina Labay et al. · Nature Genetics · 2001 · 585 citations

Life Sciences, Genetics, Molecular Genetics +11

Vitamin E Supplementation Reduces Cardiovascular Events in a Subgroup of Middle-Aged Individuals With Both Type 2 Diabetes Mellitus and the Haptoglobin 2-2 Genotype

Uzi Milman, Shany Blum, Chen Shapira et al. · Arteriosclerosis Thrombosis and Vascular Biology · 2007 · 280 citations · Full text

Veterinary Medicine, Nutritional Sciences, Pharmacotherapy +13

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin

Eli Sprecher, Gabriele Richard, Raziel Lurie et al. · Nature Genetics · 2001 · 188 citations

Medicine, Molecular Genetics, Ophthalmology +12

The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia geneSLC19A2 of eight families

Tal Raz, Valentina Labay, Dana Baron et al. · Human Mutation · 2000 · 62 citations

Life Sciences, Genetics, Hematology +11

Haptoglobin genotype predicts development of coronary artery calcification in a prospective cohort of patients with type 1 diabetes

Melissa Simpson, Janet K. Snell‐Bergeon, Gregory L. Kinney et al. · Cardiovascular Diabetology · 2011 · 43 citations · Full text

Medicine, Cardiology, Genetics +16