Author

Christopher P. Morley

SUNY Upstate Medical UniversityORCID 0000-0003-0185-7148Unclaimed 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:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:synaptic & neural circuits· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ayman H. FanousiD· 3 shared Carlos N. PatoiD· 3 shared Helena MedeirosiD· 3 shared James A. KnowlesiD· 3 shared Michele T. PatoiD· 3 shared Christina M. HultmaniD· 2 shared Dolores MalaspinaiD· 2 shared Douglas S. LehreriD· 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

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

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

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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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