Genetic & Genomic MedicinemedRxivPreprint
Rare coding variation implicates thirteen genes in bipolar disorder across 232,536 individuals from global populations
DOI 10.64898/2026.09.30.26364416
Author
Felecia E. Cerrato
Broad InstituteORCID 0000-0002-9086-7710Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2018-2026 · peak 6/yrCo-Author Collaboration Network
10 top collaborators · 45 mutual co-author linksFocal author (center)Selected co-authorORCID co-authorUnlinked name
Curved chords = mutual co-authorship13 papers
Recent·Most cited
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A founder population reveals genetic variation with major effect on serious mental illness
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Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
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Genome-wide association study of school grades identifies a genetic overlap between language ability, psychopathology and creativity
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Ultra-rare constrained missense variants in the epilepsies: Shared and specific enrichment patterns in neuronal gene-sets
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The paper analyzes ultra-rare variants in epilepsy patients to identify gene-set enrichment patterns and differential impacts in neuronal gene categories.
18 citations - GeneticsMolecular PsychiatryPeer-reviewed
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
Till F. M. Andlauer, Jose Guzman Parra, Fabian Streit…·Claudia Giambartolomei
The paper examines common genetic variants' contribution to bipolar disorder risk in multiplex families and finds higher polygenic risk scores in affected individuals compared to controls and unaffected family members.
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The genetics of the mood disorder spectrum: genome-wide association analyses of over 185,000 cases and 439,000 controls
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This study identifies 73 genome-wide significant loci for mood disorders, revealing shared and distinct genetic factors between major depressive disorder and bipolar disorder.
199 citationstop 5% - GeneticsThe American Journal of Human GeneticsPeer-reviewed
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297 citationstop 1% - GeneticsNature GeneticsPeer-reviewed
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The paper investigates polygenic associations between ADHD and literacy/language abilities, finding that genetic confounding with educational attainment masks ADHD-specific reading impairments.
27 citations - GeneticsbioRxivPreprint
Schizophrenia risk conferred by protein-coding de novo mutations
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6 citations - GeneticsNature GeneticsPeer-reviewed✦ In-depth digest
Discovery Of The First Genome-Wide Significant Risk Loci For ADHD
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