Lynsey S. Hall

Biochemistry, Genetics and Molecular Biology · Life Sciences

40h-index11.5kcitations86works0.02yr avg
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Research Topics

Genetic Associations and Epidemiology(50), Genetics and Neurodevelopmental Disorders(17), Cognitive Abilities and Testing(14), Epigenetics and DNA Methylation(10), Birth, Development, and Health(9)

Publications77 total

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
UNC Libraries·2025Open Access
From peas to people - using quantitative traits to aid genetic discovery in depression
2024Open Access
Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability
The American Journal of Human Genetics·2023· 22 citedOpen Access
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Nature·2022· 2.6k citedOpen Access
The Genetic Architecture of Depression in Individuals of East Asian Ancestry
JAMA Psychiatry·2021· 190 citedOpen Access
Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort
Translational Psychiatry·2020· 34 citedOpen Access
Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Molecular Psychiatry·2020· 1 citedOpen Access
A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank
Nature Communications·2020· 121 citedOpen Access
Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders
Molecular Psychiatry·2020· 44 citedOpen Access
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
UNC Libraries·2020Open Access
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank
Molecular Psychiatry·2020· 206 citedOpen Access
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
Nature Neuroscience·2020· 137 citedOpen Access
Genome-wide association summary statistics of antidepressant treatment resistance meta-analysis
University of Edinburgh·2020Open Access
Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington’s Disease
Biological Psychiatry·2019· 44 citedOpen Access
A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia
Human Molecular Genetics·2019· 73 citedOpen Access
Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression
Biological Psychiatry·2019· 45 citedOpen Access
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset
Cell·2019· 519 citedOpen Access
Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns
Nature Communications·2019· 139 citedOpen Access
Genetic risk underlying psychiatric and cognitive symptoms in Huntington’s Disease
2019· 2 citedOpen Access
Novel Insight Into the Etiology of Autism Spectrum Disorder Gained by Integrating Expression Data With Genome-wide Association Statistics
Biological Psychiatry·2019· 96 citedOpen Access
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Frequent Co-authors

Toni‐Kim Clarke(33), Ian J. Deary(31), Andrew M. McIntosh(31), Mark J. Adams(29), David J. Porteous(22), Gail Davies(18), Caroline Hayward(18), David M. Howard(16), Blair H. Smith(16), Naomi R. Wray(15), Stephan Ripke(15), Enda M. Byrne(15), Tracy Air(14), Jonathan R. I. Coleman(14), Franziska Degenhardt(14), Erin C. Dunn(14), Valentina Escott‐Price(14), Andreas J. Forstner(14), Donald J. MacIntyre(14), Tim B. Bigdeli(13)