Valeed Khan

Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability.

S. Gabriel, J. Vincent, M. Rafiq, 2014, American journal of human genetics.

Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability

D. Nickerson, S. Leal, M. Bamshad, 2018, Human Genetics.

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

A. Noor, J. Vincent, M. Rafiq, 2017, Molecular Psychiatry.

Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability

D. Nickerson, S. Leal, M. Bamshad, 2018, Human Genetics.

Genomic Characterization of SARS-CoV2 from Peshawar Pakistan Using Next-Generation Sequencing

S. A. Haider, N. Bibi, Johar Ali, 2022, Current microbiology.

Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice

C. Lelliott, B. Yalcin, Jacob O Day, 2022, PLoS genetics.

Exome sequencing identifies novel and known mutations in families with intellectual disability

J. Vincent, M. Ansar, R. Harripaul, 2021, BMC Medical Genomics.

Exome sequencing identifies novel and known mutations in families with intellectual disability

J. Vincent, M. Ansar, R. Harripaul, 2021, BMC medical genomics.

Carbon Stock Availability in Forests of the Zabarwan Mountain Range in Kashmir Himalaya

F. Bashir, Shiekh Marifatul Haq, Umer Yaqoob, 2022, Proceedings of the National Academy of Sciences, India Section B: Biological Sciences.

The use of multiplex ARMS-PCR for mutational analysis of beta-globin gene in consanguineous population of KP Pakistan

R. Pervaiz, S. Shams, Valeed Khan, 2023, Arab Gulf Journal of Scientific Research.