Author

Zehra Agha

COMSATS University IslamabadORCID 0000-0003-3413-0578Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

John B. VincentiD· 2 shared Leon FrenchiD· 2 shared Muhammad AyubiD· 2 shared Nasim Vasli· 2 shared Raheel QamariD· 2 shared Ricardo HarripauliD· 2 shared A Heidari· 1 shared A Mikhailov· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

John B. VincentORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 24, 2021

Autism spectrum disorder trios from consanguineous populations are enriched for rare biallelic variants, identifying 32 new candidate genes

Ricardo Harripaul, Ansa Rabia, Nasim Vasli…·John B. Vincent

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GeneticsMolecular PsychiatryPeer-reviewedApr 11, 2017

Mapping Autosomal Recessive Intellectual Disability: Combined Microarray and Exome Sequencing Identifies 26 Novel Candidate Genes in 192 Consanguineous Families

Ricardo Harripaul, Nasim Vasli, A Mikhailov…·John B. Vincent

182 citationstop 1%

humanwhole-exome sequencing

𝕏 PostBluesky