A.H.M. Mahbubul Huq

A unique mutation in the vitamin D receptor gene in three Japanese patients with vitamin D-dependent rickets type II: utility of single-strand conformation polymorphism analysis for heterozygous carrier detection.

Takahiko Saijo, Masaaki Ito, Eiji Takeda et al. · PubMed · 1991 · 196 citations

Medicine, Genetics, Molecular Genetics +15

Association of Reelin gene polymorphisms with autism

Fatema Serajee, Hailang Zhong, A.H.M. Mahbubul Huq · Genomics · 2005 · 124 citations

Life Sciences, Genetics, Molecular Genetics +9

Association of tryptophan 2,3 dioxygenase gene polymorphism with autism

Rafiqun Nabi, Fatema Serajee, Diane C. Chugani et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2003 · 77 citations

Life Sciences, Genetics, Molecular Genetics +17

X-Linked Glycerol Kinase Deficiency in the Mouse Leads to Growth Retardation, Altered Fat Metabolism, Autonomous Glucocorticoid Secretion and Neonatal Death

A.H.M. Mahbubul Huq, Rhonda S. Lovell, C N Ou et al. · Human Molecular Genetics · 1997 · 65 citations · Full text

Life Sciences, Biochemistry, Genetics +17

Encephalopathies with <i>KCNC1</i> variants: genotype‐phenotype‐functional correlations

Jillian M. Cameron, Snezana Maljevic, Umesh Nair et al. · Annals of Clinical and Translational Neurology · 2019 · 63 citations · Full text

Life Sciences, Genetics, Neuroscience +17