Author

Michael Escamilla

Texas Tech University Health Sciences CenterORCID 0000-0002-1325-542XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Ayman H. FanousiD· 2 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

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Ayman H. FanousORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

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

𝕏 PostBluesky

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

𝕏 PostBluesky