Asma Gul

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 6

Top Venues

BMC medical genetics

Congenital anomalies

American journal of medical genetics. Part A

The journal of gene medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Shazia Khan, Muhammad Umair, Safdar Abbas, Uroba Ali, Gohar Zaman, Muhammad Ansar, Rongrong Wang, Xue Zhang, Henry Houlden, Gaurav V Harlalka, Asma Gul
Overlapping neurological phenotypes in two extended consanguineous families with novel variants in the CNTNAP1 and ADGRG1 genes. The journal of gene medicine (2023)
Ayesha Zaka, Shaheen Shahzad, Hadi Zahid Rao, Sadia Kanwal, Asma Gul, Sulman Basit
An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation. American journal of medical genetics. Part A 185 (10) (2021)
Abida Akbar, Muneeba Bint-E-Farrakh, Andrew H Crosby, Asma Gul, Gaurav V Harlalka
Variants in NIPAL4 and ALOXE3 cause autosomal recessive congenital ichthyosis in Pakistani families. Congenital anomalies 60 (5) (2020)
Shazia Khan, Lettie E Rawlins, Gaurav V Harlalka, Muhammad Umair, Asmat Ullah, Shaheen Shahzad, Muhammad Javed, Emma L Baple, Andrew H Crosby, Wasim Ahmad, Asma Gul
Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families. BMC medical genetics 20 (1) (2019)
Abida Akbar, Claire Prince, Chloe Payne, James Fasham, Wasim Ahmad, Emma L Baple, Andrew H Crosby, Gaurav V Harlalka, Asma Gul
Novel nonsense variants in SLURP1 and DSG1 cause palmoplantar keratoderma in Pakistani families. BMC medical genetics 20 (1) (2019)
Shazia Khan, Siying Lin, Gaurav V Harlalka, Asmat Ullah, Khadim Shah, Sumbul Khalid, Sarmad Mehmood, Muhammad Jawad Hassan, Wasim Ahmad, Jay E Self, Andrew H Crosby, Emma L Baple, Asma Gul
BBS5 and INPP5E mutations associated with ciliopathy disorders in families from Pakistan. Annals of human genetics 83 (6) (2019)

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Publication Activity (10 Years)

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Asma Gul