Author

Marjan Chapi

Arizona State UniversityORCID 0009-0009-8938-2773Unclaimed 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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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abbas TafakhoriiD· 1 shared Akshit ModiiD· 1 shared Alexandre ReymondiD· 1 shared Beate PeteriD· 1 shared Caitlin V. RaaziD· 1 shared Francesca MattioliiD· 1 shared Hafiz Muhammad Azhar BaigiD· 1 shared Hossein DarvishiD· 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

Abbas TafakhoriORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintOct 4, 2026

Developmental Convergence Across Diverse Genetic Architectures in Childhood Apraxia of Speech

Tiffanie White, Marjan Chapi, Caitlin V. Raaz…·Beate Peter

The paper identifies multiple genetic variants associated with childhood apraxia of speech through whole-exome sequencing and functional analysis, proposing four novel candidate genes.

DOI 10.64898/2026.10.03.756424

humanwhole-exome sequencing

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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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