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Authors whose works are in public domain in at least one jurisdiction

List of works by Benjamin M. Neale

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Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts

scientific article published on 18 May 2020
The Weighting is the Hardest Part: On the Behavior of the Likelihood Ratio Test and the Score Test Under a Data-Driven Weighting Scheme in Sequenced Samples

scientific article
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

scientific article published on 14 October 2020
Author Correction: A global overview of pleiotropy and genetic architecture in complex traits

scientific article published on 01 March 2020
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology

scientific article published on 21 December 2018
Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci

scholarly article published in Nature Genetics
Large-scale meta-analysis highlights the hypothalamic-pituitary-gonadal axis in the genetic regulation of menstrual cycle length

scientific article published on 01 December 2018
Human demographic history impacts genetic risk prediction across diverse populations

Genetic markers of ADHD-related variations in intracranial volume

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

scientific article published on 8 April 2022
Advanced Paternal Age and Early Onset of Schizophrenia in Sporadic Cases: Not Confounded by Parental Polygenic Risk for Schizophrenia

scientific article published on 07 February 2019
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

scientific article published in June 2021
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality

scientific article published on 04 January 2019
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 23 January 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

scientific article published on 01 December 2018
Mapping and characterization of structural variation in 17,795 human genomes

scientific article published on 27 May 2020
GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size

scientific article published on 17 February 2020
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

scientific article published on 01 April 2020
Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

article published in 2018
Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Publisher Correction: Multi-trait analysis of genome-wide association summary statistics using MTAG

scientific article published on 01 July 2019
Author Correction: Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection

scientific article published on 01 August 2019
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations

scientific article published on 01 October 2020
EXPLORING GENETIC VARIATION THAT INFLUENCES BRAIN METHYLATION IN ATTENTION-DEFICIT/HYPERACTIVITY DISORDER (ADHD)

scholarly article
Reply to Cipriani et al.

scientific article
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

scientific article
The genetic architecture of sporadic and multiple consecutive miscarriage

scientific article published on 25 November 2020
T58EVALUATION OF POLYGENIC RISK SCORE PERFORMANCE IN AN ADMIXED BRAZILIAN COHORT

scholarly article
Recent advances in understanding of attention deficit hyperactivity disorder (ADHD): how genetics are shaping our conceptualization of this disorder

scientific article published on 05 December 2019
SA122STRUCTURAL VARIATIONS OF SCHIZOPHRENIA RISK GENE COMPLEMENT COMPONENT 4 (C4) AND BRAIN MRI PHENOTYPES

scientific article published on 26 July 2019
Common body mass index-associated variants confer risk of extreme obesity

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

scientific article published on 21 October 2019
A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

article
33 INVESTIGATING RARE PATHOGENIC/LIKELY PATHOGENIC EXONIC VARIATION IN 3,987 BIPOLAR PATIENTS

scholarly article
Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder

Genome-wide association study identifies new locus associated with OCD

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

Erratum

scholarly article published in Genetic Epidemiology
The Manifestation Of Genetic Risk For Attention Deficit Hyperactivity Disorder In Females And Males In The General Population

scholarly article
Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

scientific article published on 05 December 2019
Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

scientific article published in December 2015
Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics

scientific article published on 21 May 2020
Unfolding The Genetic Basis of ADHD

scholarly article
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

Human genetic analyses of organelles highlight the nucleus in age-related trait heritability

scientific article published in 2021
Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics

scientific article published on 01 June 2020
An open resource of structural variation for medical and population genetics

scientific article

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