Author

Sohail Aziz Paracha

Khyber Medical UniversityORCID 0000-0002-2616-1705Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Abbas TafakhoriiD· 1 shared Alexandre ReymondiD· 1 shared Francesca MattioliiD· 1 shared Hafiz Muhammad Azhar BaigiD· 1 shared Hossein DarvishiD· 1 shared Marjan ChapiiD· 1 shared Muhammad AnsariD· 1 shared Saghar Ghasemi FirouzabadiiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abbas TafakhoriORCID

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1 paper

Recent·Most cited

Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedNov 11, 2021

Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

Francesca Mattioli, Hossein Darvish, Sohail Aziz Paracha…·Muhammad Ansar

The paper identifies biallelic truncation variants in ATP9A as a cause of a novel autosomal recessive neurodevelopmental disorder in two consanguineous families.

29 citations

humanstatistical model

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