Author

Fatima Khan

Aga Khan UniversityPrimary ORCID profile (0000-0002-8026-4238 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Same name, identified by ORCID

Fatima KhaniD1 paper · Columbia University Irving Medical Center

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alba Sanchis‐JuaniD· 1 shared Alfred Ngombo· 1 shared Alice GalviniD· 1 shared Alistair T. PagnamentaiD· 1 shared Amal Al Tenaiji· 1 shared Amina A AbubakariD· 1 shared Amir SzeinbergiD· 1 shared Angelika SeitziD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alba Sanchis‐JuanORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 6, 2026

NeuroDev: etiology and experience of neurodevelopmental disorders in Kenya and South Africa

Patricia Kipkemoi, Emily O’Heir, Mutaz Amin…·Elise Robinson

The paper presents genetic and phenotypic data from 521 children with neurodevelopmental disorders in Kenya and South Africa, highlighting high genetic diagnosis rates linked to environmental risk factors.

1 citation

humanwhole-exome sequencing

Genetic & Genomic MedicineHuman MutationPeer-reviewedApr 13, 2021

Clinical, neuroimaging and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability

Sonja Neuser, Barbara Brechmann, Gali Heimer…·Darius Ebrahimi‐Fakhari

The paper describes the clinical, neuroimaging, and molecular features of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability, providing variant interpretation guidelines and carrier frequency estimates.

32 citations

humanstatistical model