Author

Stephen R. Marder

University of California, Los AngelesORCID 0000-0003-0288-309XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:differential expression· 1 Research Focus:synaptic & neural circuits· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ayman H. FanousiD· 3 shared Carlos N. PatoiD· 2 shared Christina M. HultmaniD· 2 shared Christopher P. MorleyiD· 2 shared Dolores MalaspinaiD· 2 shared Douglas S. LehreriD· 2 shared Eli A. StahliD· 2 shared Evelyn J. BrometiD· 2 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Ayman H. FanousORCID

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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

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Genetic & Genomic MedicineNaturePeer-reviewedApr 8, 2022

✦ In-depth digest

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

Tarjinder Singh, Timothy Poterba, David Curtis…·David St Clair

Exomes of 24,248 schizophrenia cases and 97,322 controls implicate ultra-rare damaging variants in 10 genes, including GRIN2A and GRIA3, with odds ratios of 3 to 50.

979 citationstop 1%

humanwhole-exome sequencing

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GeneticsBiological PsychiatryPeer-reviewedDec 19, 2018

Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

Alexander W. Charney, Eli A. Stahl, Elaine Green…·Pamela B. Sklar

The study finds that rare copy number variants (CNVs) contribute to bipolar disorder risk primarily in schizoaffective disorder bipolar type cases, with differences in CNV burden and schizophrenia polygenic risk scores between subtypes.

69 citationstop 4%

humanstatistical model

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