Sher Alam Khan (Sher A Khan)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 10

Top Topics

Mitochondrial Dna

Intellectual Disability

Hepatitis C Virus

Top Venues

BMC medical genetics

International journal of dermatology

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

Publications

Niamatullah Khan, Khadim Shah, Fozia Fozia, Sher Alam Khan, Nazif Muhammad, Abdul Nasir, Ijaz Ahmad, Zia U Rehman, Abid Jan, Noor Muhammad, Saadullah Khan
Biallelic mutations in FLG, TGM1, and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin. International journal of dermatology (2023)
Hamed Nawaz, null Mujahid, Sher Alam Khan, Farhana Bibi, Ahmed Waqas, Abdul Bari, null Fardous, Niamatullah Khan, Nazif Muhammad, Amjad Khan, Sohail Aziz Paracha, Qamre Alam, Mohammad Azhar Kamal, Misbahuddin M Rafeeq, Noor Muhammad, Fayaz Ul Haq, Shazia Khan, Arif Mahmood, Saadullah Khan, Muhammad Umair
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome. Genes 14 (5) (2023)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Sheng-Jia Lin, Barbara Vona, Hillary M Porter, Mahmoud Izadi, Kevin Huang, Yves Lacassie, Jill Anne Rosenfeld, Saadullah Khan, Cassidy Petree, Tayyiba Akbar Ali, Nazif Muhammad, Sher Alam Khan, Noor Muhammad, Pengfei Liu, Marie-Louise Haymon, Franz Rüschendorf, Il-Keun Kong, Linda Schnapp, Natasha Shur, Lynn P Chorich, Lawrence C Layman, Thomas Haaf, Ehsan Pourkarimi, Hyung-Goo Kim, Guarav K Varshney
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function. Human mutation 43 (10) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Sher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, Hina Bashir, Niamat Khan, Noor Muhammad, Rüstem Yilmaz, Saadullah Khan, Naveed Wasif
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family. BMC medical genetics 21 (1) (2020)
Julia Doll, Barbara Vona, Linda Schnapp, Franz Rüschendorf, Imran Khan, Saadullah Khan, Noor Muhammad, Sher Alam Khan, Hamed Nawaz, Ajmal Khan, Naseer Ahmad, Susanne M Kolb, Laura Kuehlewein, Jonathan D J Labonne, Lawrence C Layman, Michaela A H Hofrichter, Tabea Röder, Marcus Dittrich, Tobias Müller, Tyler D Graves, Il-Keun Kong, Indrajit Nanda, Hyung-Goo Kim, Thomas Haaf
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families. Genes 11 (11) (2020)