Author

Hamed Kazemi

University of ArizonaORCID 0000-0001-5820-2324Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-genome sequencing· 2 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Ayman H. FanousiD· 3 shared Silviu‐Alin BacanuiD· 3 shared Vladimir I. VladimiroviD· 3 shared Célia Barreto CarvalhoiD· 2 shared Helena MedeirosiD· 2 shared John Drake· 2 shared Michele T. PatoiD· 2 shared Alejandro Zuniga· 1 shared

Activity by Year

2026-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Ayman H. FanousORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 22, 2026

Genomic and transcriptomic insights into antipsychotic-induced changes in total cholesterol and body mass index in a multi-ancestry cohort of the US veterans

Hamed Kazemi, John E. Drake, Silviu‐Alin Bacanu…·Ayman H. Fanous

The paper conducts a GWAS on antipsychotic-induced changes in total cholesterol and BMI in a multi-ancestry cohort, identifying genetic loci and pathways associated with these metabolic effects.

DOI 10.64898/2026.07.20.26358275

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineGenomic psychiatry :Peer-reviewedJun 16, 2026

Multiplex Portuguese Families as a Lens into rare mutations and the Shared Genetic Architecture of Schizophrenia, Mood Disorders, and Autism Spectrum Disorders

Carlos N. Pato, Michele T. Pato, Jennifer Mulle…·Ayman H. Fanous

This study analyzes 173 multiplex Portuguese families to identify rare genetic variants associated with schizophrenia, mood disorders, and autism, finding a CHD2 mutation linked to diverse mental illness phenotypes.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJun 1, 2026

Gene-Set Based Rare Variant Association Analysis of Whole Genome Sequencing Data in the Portuguese Island Collection for Schizophrenia and Bipolar Disorder

Hamed Kazemi, John Drake, Tim Bigdeli…·Ayman H. Fanous

The paper performs rare variant association analysis using whole-genome sequencing data from the Portuguese Island Collection to identify shared genetic pathways in schizophrenia and bipolar disorder.

DOI 10.64898/2026.05.28.26354351

humanwhole-genome sequencing

𝕏 PostBluesky