Sher Alam Khan - Concepedia

Author

Sher Alam Khan

Kohat University of Science and Technology ORCID

Also Known As

S A Khan, S Khan, S. Khan, S.A. Khan, Sana Farrukh Khan, Shakeeba Khan, Sher A Khan, Sher A. Khan, Sher Alam Khan, Sher Khan

Publications

611

Citations

H-Index

Concepts

All Affiliations

Kohat University of Science and Technology Quaid-i-Azam University Gyeongsang National University Universität Ulm University of Würzburg

About

Sher Alam Khan is an author at Kohat University of Science and Technology specializing in genetics, neurogenetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	41
2	Molecular Genetics	2	2	41
3	Health Sciences	1	1	28
4	Public Health	1	1	13
5	Molecular Medicine	1	1	13

Sher Alam Khan

Publications

198

Citations

H-Index

Page 1

	Year	Citations
Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations Asia Parveen, Sher Alam Khan, Muhammad Usman Mirza, International Journal of Molecular Sciences	2019	32
Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families. Asmat Ullah, Muhammad Umair, Maryam Yousaf, PubMed	2017	31
The Role of Drosophila Cytidine Monophosphate-Sialic Acid Synthetase in the Nervous System R. Islam, Michiko Nakamura, Hilary Scott, Journal of Neuroscience	2013	29
Biallelic variants in <i>WARS1</i> cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function Sheng‐Jia Lin, Barbara Vona, Hillary M. Porter, Human Mutation GeneticsMolecular GeneticsDisease Gene IdentificationMendelian DisorderCritical Exon	2022	28
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families Julia Doll, Barbara Vona, Linda Schnapp, Genes	2020	16
A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family Anwar Khan, Noor Muhammad, Abdul Aziz, BMC Medical Genetics	2017	15
Novel sequence variants in the <i>MKKS</i> gene cause Bardet‐Biedl syndrome with intra‐ and inter‐familial variable phenotypes Asmat Ullah, Maryam Khalid, Muhammad Umair, Congenital Anomalies Family MembersGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2017	13
A novel mutation in the <i>HPGD</i> gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family Anwar Khan, Noor Muhammad, Sher Alam Khan Annals of Human Genetics	2017	13
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family Sher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, BMC Medical Genetics	2020	11
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet–Biedl Syndrome Hamed Nawaz, Mujahid, Sher Alam Khan Genes	2023	10

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