Farooq Ahmad

Clinical Genetics of Polydactyly: An Updated Review

Muhammad Umair, Farooq Ahmad, Muhammad Bilal et al. · Frontiers in Genetics · 2018 · 119 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Biallelic variants in four genes underlying recessive osteogenesis imperfecta

Amir Hayat, Shabir Hussain, Muhammad Bilal et al. · European Journal of Medical Genetics · 2020 · 41 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3

Muhammad Umair, Bader Alhaddad, Afzal Rafique et al. · Pediatric Research · 2017 · 33 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous families

Muhammad Umair, Annum Hassan, Abid Jan et al. · Journal of Human Genetics · 2015 · 32 citations

Medicine, Genetics, Molecular Genetics +11

Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families.

Asmat Ullah, Muhammad Umair, Maryam Yousaf et al. · PubMed · 2017 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16