Saadullah Khan

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 5

Top Venues

Annals of human genetics

Human mutation

BMC medical genetics

Journal of clinical laboratory analysis

Kohat University of Science and Technology

Quaid-i-Azam University (PHD)

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

Affiliation History

Kohat University of Science and Technology Mar 11o 2013

Pakistan

Assistant Professor :: Biotechnology& Genetic Engneering

Education History

Quaid-i-Azam University

Pakistan

PHD :: Department of Biochemistry

Publications

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, Gaurav 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)
Fozia Fozia, Khadim Shah, Rubina Nazli, Sher Alam Khan, Ijaz Ahmad, Noor Mohammad, Saadullah Khan, Amal Alotaibi
Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family. Journal of clinical laboratory analysis (2021)
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)
Hadia Gul, Abdul Haleem Shah, Ricardo Harripaul, Anna Mikhailov, Kamalben Prajapati, Ejazullah Khan, Farman Ullah, Muhammad Zubair, Muhammad Zeeshan Ali, Ayesha Haleem Shah, Said Salman, Saadullah Khan, John B Vincent, Muzammil Ahmad Khan
Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations. Annals of human genetics 83 (4) (2019)
Anwar Kamal Khan, Noor Muhammad, Sher Alam Khan, Waheed Ullah, Abdul Nasir, Sibtain Afzal, Khushnooda Ramzan, Sulman Basit, Saadullah Khan
A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family. Annals of human genetics 82 (3) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Saadullah Khan