Asma Ali Khan

Also affiliated with COMSATS University Islamabad, Abbott (Germany), National Institutes of Health Clinical Center, Mirpur University of Science and Technology

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 5 papers. Top paper: “Issue Information”.

Issue Information

Human Mutation(2018)10.1002/humu.23568

N/A

0DataRank · unranked

0 citations

R. Donald Harvey, Tracy Dudding‐Byth, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel +135 more

Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

Genes(2020)10.3390/genes11101122

N/A

0DataRank · unranked

20 citations

Iván A. López, Cristina Fenollar‐Ferrer, Rabia Faridi, Claudio Anselmi, Asma Ali Khan +10 more

New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder

Human Genetics(2021)10.1007/s00439-021-02319-7

N/A

0DataRank · unranked

52 citations

Alessandro Rea, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, Shoujun Gu, Zunaira Munir +7 more

Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly

Communications Biology(2024)10.1038/s42003-024-06466-1

N/A

0DataRank · unranked

12 citations

Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen +17 more

Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome

Clinical Genetics(2024)10.1111/cge.14514

N/A

0DataRank · unranked

6 citations

Pamela Stratton, Noemi Salmeri, Robert J. Morell, Asma Ali Khan, Muhammad A. Usmani +4 more