Anand K. Srivastava

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

Virginie Vervoort, Michael A. Beachem, Penny S. Edwards et al. · Science · 2002 · 719 citations

Natural Sciences, Physics, Biophotonics +16

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 · 688 citations · Full text

Life Sciences, Genetics, Molecular Biology +11

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 · 617 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

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 · 358 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

Life Sciences, Genetics, Molecular Genetics +13