Iltaf Ahmed

Mutations in MBOAT7 , Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

Anide Johansen, Rasim Özgür Rosti, Damir Musaev et al. · The American Journal of Human Genetics · 2016 · 90 citations · Full text

Intellectual Disability Accompanied, Mendelian Disorder, Genetic Disorder +8

Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment

Iltaf Ahmed, Rebecca Buchert, Mi Zhou et al. · Human Molecular Genetics · 2015 · 58 citations · Full text

Mutations in the histamine<i>N</i>-methyltransferase gene,<i>HNMT</i>, are associated with nonsyndromic autosomal recessive intellectual disability

Abolfazl Heidari, Chanakan Tongsook, Reza Najafipour et al. · Human Molecular Genetics · 2015 · 33 citations · Full text

Histone Modifications, Genetic Testing, Epigenetic Change +16

Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder

Iltaf Ahmed, Kirti Mittal, Taimoor I. Sheikh et al. · Human Genetics · 2014 · 32 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +6

Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability

Nasim Vasli, Iltaf Ahmed, Kirti Mittal et al. · Psychiatric Genetics · 2015 · 27 citations

Exome Sequencing, Genetics, Genetic Epidemiology +27