David S. Sinasac

The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

Keiko Kobayashi, David S. Sinasac, Mikio Iijima et al. · Nature Genetics · 1999 · 409 citations

Mitochondrial Biogenesis, Mitochondrial Function, Genetic Disorder +9

Genetic architecture of complex traits: Large phenotypic effects and pervasive epistasis

Haifeng Shao, Lindsay C. Burrage, David S. Sinasac et al. · Proceedings of the National Academy of Sciences · 2008 · 266 citations · Full text

Phenotypic Variation, Genetics, Genetic Foundation +18

Mice With a Deletion in the Gene for CCAAT/Enhancer-Binding Protein β Are Protected Against Diet-Induced Obesity

Carrie A. Millward, Jason D. Heaney, David S. Sinasac et al. · Diabetes · 2006 · 105 citations · Full text

Nutrition, Immunology, Caloric Restriction +18

Citrin/Mitochondrial Glycerol-3-phosphate Dehydrogenase Double Knock-out Mice Recapitulate Features of Human Citrin Deficiency

Takeyori Saheki, Mikio Iijima, Meng Xian Li et al. · Journal of Biological Chemistry · 2007 · 82 citations · Full text

<i>Slc25a13</i>-Knockout Mice Harbor Metabolic Deficits but Fail To Display Hallmarks of Adult-Onset Type II Citrullinemia

David S. Sinasac, Mitsuaki Moriyama, Md. Abdul Jalil et al. · Molecular and Cellular Biology · 2003 · 80 citations · Full text

Metabolic Disorder, Genetics, Immunology +22