Muhammad Farooq

Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

Shahid Mahmood Baig, Alexandra Koschak, Andreas Lieb et al. · Nature Neuroscience · 2010 · 313 citations

Congenital Deafness, Channelopathies, Human Channelopathy +5

A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function

Muhammad Sajid Hussain, Shahid Mahmood Baig, Sascha Neumann et al. · The American Journal of Human Genetics · 2012 · 171 citations · Full text

Developmental Biology, Genetic Disorder, Autophagy +8

A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis

Atsushi Fujimoto, Muhammad Farooq, Hiroki Fujikawa et al. · Journal of Investigative Dermatology · 2012 · 79 citations

Developmental Biology, Genetics, Missense Mutation +5

Sero-epidemiology of peste des petits ruminants (PPR) in Pakistan

Aamer Bin Zahur, Aman Ullah, Manzoor Hussain et al. · Preventive Veterinary Medicine · 2011 · 65 citations

Peste Des, Animal Science, Livestock Health +2

Acrodermatitis Continua of Hallopeau Is a Clinical Phenotype of DITRA: Evidence that It Is a Variant of Pustular Psoriasis

Ossama Abbas, Salam Itani, Samer Ghosn et al. · Dermatology · 2013 · 53 citations