Author

Ma’n H. Zawati

McGill UniversityORCID 0000-0002-8905-6259Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Mayada ElsabbaghiD· 2 shared Ada J. S. Chan· 1 shared Adrien E. E. DuboisiD· 1 shared Afiqah YusufiD· 1 shared Alan Charles EvansiD· 1 shared Alana Iaboni· 1 shared Aline LefebvreiD· 1 shared Annabel Rutherford· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersNeuroscience

Mayada ElsabbaghORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintSep 8, 2026

Heterogeneity of Brain Dynamics in Genetic and Psychiatric Conditions

Adrien E. E. Dubois, Sarah Lippé, Charles-Olivier Martin…·Guillaume Dumas

The paper analyzes EEG data from 4,812 individuals to identify shared and distinct neurophysiological signatures across psychiatric conditions and rare genetic variants.

DOI 10.64898/2026.09.01.748394

humanelectronic health records

Genetic & Genomic MedicinemedRxivPreprintMay 5, 2022

Genomic architecture of autism spectrum disorder from comprehensive whole-genome sequence annotation

Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan…·Evdokia A. Anagnostou

This study identifies 135 ASD-associated protein-coding genes using whole-genome sequencing data from 11,312 individuals and exome sequencing from over 18,000 trios, with a false discovery rate of 80%.

3 citations

humanwhole-genome sequencing