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 · 314 citations

Medicine, Cardiology, Physiology +14

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 · 173 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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 · 80 citations · Full text

Medicine, Genetics, Molecular Genetics +11

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

Veterinary Medicine, Veterinary Epidemiology, Veterinary Parasitology +10

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 · 54 citations

Life Sciences, Dermatology, Genetics +15