Tahir N Khan
6PUBLICATIONS
52CO-AUTHORS
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Publications (6)
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|Sep 04, 2025
Exome sequencing in a Pakistani male infertility cohort: perspective on molecular diagnosis, genetic heterogeneity, and diagnostic yield.Dapeng Zhou, Ambrin Fatima, Afrasiab Ahmed
|Aug 27, 2025
Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz-Jeghers Syndrome.Tahir N Khan, Chunyu Liu, Kai Lee Yap
|May 21, 2024
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN.Tehseen Ullah Khan Afridi, Ambrin Fatima, Humayoon Shafique Satti
|Feb 28, 2023
Regulatory de novo mutations underlying intellectual disability.Matias G De Vas, Fanny Boulet, Shweta S Joshi
|Nov 05, 2022
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy.Laura J Grange, John J Reynolds, Farid Ullah
|Sep 21, 2020
Candidate variants in TUB are associated with familial tremor.M Reza Sailani, Fereshteh Jahanbani, Charles W Abbott
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Frequent Collaborators
3 joint publications
Erica E Davis
2 joint publications
Humayoon Shafique Satti
2 joint publications
Tehseen Ullah Khan Afridi
2 joint publications
David Parry
1 joint publications
Muhammad Tariq
1 joint publications
John J Reynolds
1 joint publications
Robert F Shearer
1 joint publications
Ryan M Baxley
1 joint publications
Antony W Oliver
1 joint publications
Sophie L Cooke
