Anand Srivastava

X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

Juha Kere, Anand Srivastava, Outi Montonen et al. · Nature Genetics · 1996 · 753 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

Patrick Tarpey, F. Lucy Raymond, Lam Son Nguyen et al. · Nature Genetics · 2007 · 284 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7

Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor

Patrick Tarpey, F. Lucy Raymond, Sarah O’Meara et al. · The American Journal of Human Genetics · 2007 · 223 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8

Linear aggregation of proteins on the membrane as a prelude to membrane remodeling

Mijo Simunovic, Anand Srivastava, Gregory A. Voth · Proceedings of the National Academy of Sciences · 2013 · 165 citations · Full text

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

Lam Son Nguyen, Lachlan A. Jolly, Cheryl Shoubridge et al. · Molecular Psychiatry · 2011 · 123 citations · Full text

Immunogenetics, Immunology, Transcriptome Profiling +8