Anand K. Srivastava

<i>AGTR2</i> Mutations in X-Linked Mental Retardation

Virginie Vervoort, Michael A. Beachem, Penny S. Edwards et al. · Science · 2002 · 718 citations

Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption

Mi‐Hye Lee, Kangmo Lu, Star Hazard et al. · Nature Genetics · 2001 · 685 citations · Full text

Oxysterol, Biochemistry, Lipid Nutrition +8

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Patrick Tarpey, Raffaella Smith, Erin Pleasance et al. · Nature Genetics · 2009 · 613 citations · Full text

Chromatin, Psychiatry, Genetic Disorder +11

Two Genes That Map to the STSL Locus Cause Sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 and Sterolin-2, Encoded by ABCG5 and ABCG8, Respectively

Kangmo Lu, Mi-Hye Lee, E. Starr Hazard et al. · The American Journal of Human Genetics · 2001 · 353 citations · Full text

Genetic Disorder, Medicine, Genetics +6

The Tabby phenotype is caused by mutation in a mouse homologue of the<i>EDA</i>gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

Anand K. Srivastava, Johanna Pispa, Andrew J. Hartung et al. · Proceedings of the National Academy of Sciences · 1997 · 312 citations · Full text