Benjamin Michael Neale


Ontology type: schema:Person     


Person Info

NAME

Benjamin Michael

SURNAME

Neale

Publications in SciGraph latest 50 shown

  • 2022-10-18 Publisher Correction: SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests in NATURE GENETICS
  • 2022-09-26 Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups in NATURE GENETICS
  • 2022-09-22 SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests in NATURE GENETICS
  • 2022-09-16 Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks in NATURE COMMUNICATIONS
  • 2022-08-04 Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder in NATURE GENETICS
  • 2022-05-14 Reverend Dr. Lindon Eaves: A Career Remembrance in BEHAVIOR GENETICS
  • 2022-04-11 Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia in NATURE GENETICS
  • 2022-04-08 Rare coding variants in ten genes confer substantial risk for schizophrenia in NATURE
  • 2022-04-08 Mapping genomic loci implicates genes and synaptic biology in schizophrenia in NATURE
  • 2021-11-25 Reply to: On powerful GWAS in admixed populations in NATURE GENETICS
  • 2021-08-09 Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans in NATURE
  • 2021-05-17 Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology in NATURE GENETICS
  • 2021-04-22 Genetic analyses identify widespread sex-differential participation bias in NATURE GENETICS
  • 2021-03-05 Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder in MOLECULAR PSYCHIATRY
  • 2021-02-24 Correction to: Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality in MOLECULAR PSYCHIATRY
  • 2021-02-15 Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder in NATURE COMMUNICATIONS
  • 2021-02-03 Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans in NATURE
  • 2021-01-28 Publisher Correction: Clinical use of current polygenic risk scores may exacerbate health disparities in NATURE GENETICS
  • 2021-01-25 Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder in NATURE COMMUNICATIONS
  • 2021-01-22 Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder in MOLECULAR PSYCHIATRY
  • 2021-01-18 Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power in NATURE GENETICS
  • 2020-11-25 The genetic architecture of sporadic and multiple consecutive miscarriage in NATURE COMMUNICATIONS
  • 2020-09-28 Genome-wide association study identifies 48 common genetic variants associated with handedness in NATURE HUMAN BEHAVIOUR
  • 2020-09-25 A data-driven medication score predicts 10-year mortality among aging adults in SCIENTIFIC REPORTS
  • 2020-08-24 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale in NATURE GENETICS
  • 2020-05-27 Mapping and characterization of structural variation in 17,795 human genomes in NATURE
  • 2020-05-27 A structural variation reference for medical and population genetics in NATURE
  • 2020-05-27 The mutational constraint spectrum quantified from variation in 141,456 humans in NATURE
  • 2020-05-18 Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts in NATURE GENETICS
  • 2020-04-01 Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries in NATURE COMMUNICATIONS
  • 2020-02-17 GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size in MOLECULAR PSYCHIATRY
  • 2020-02-06 Author Correction: A global overview of pleiotropy and genetic architecture in complex traits in NATURE GENETICS
  • 2020-01-13 Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations in NATURE NEUROSCIENCE
  • 2019-12-19 Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein in NATURE NEUROSCIENCE
  • 2019-11-25 Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants in NATURE NEUROSCIENCE
  • 2019-11-25 Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein in NATURE NEUROSCIENCE
  • 2019-11-18 Comparative genetic architectures of schizophrenia in East Asian and European populations in NATURE GENETICS
  • 2019-10-21 Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation in MOLECULAR PSYCHIATRY
  • 2019-08-19 A global overview of pleiotropy and genetic architecture in complex traits in NATURE GENETICS
  • 2019-07-04 Author Correction: Linkage disequilibrium–dependent architecture of human complex traits shows action of negative selection in NATURE GENETICS
  • 2019-06-25 Author Correction: Multi-trait analysis of genome-wide association summary statistics using MTAG in NATURE GENETICS
  • 2019-06-01 Estimation of metabolic syndrome heritability in three large populations including full pedigree and genomic information in HUMAN GENETICS
  • 2019-05-30 Publisher Correction: Multi-trait analysis of genome-wide association summary statistics using MTAG in NATURE GENETICS
  • 2019-05-01 Genome-wide association study identifies 30 loci associated with bipolar disorder in NATURE GENETICS
  • 2019-04-16 Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion in HUMAN GENOMICS
  • 2019-03-29 Clinical use of current polygenic risk scores may exacerbate health disparities in NATURE GENETICS
  • 2019-02-25 Identification of common genetic risk variants for autism spectrum disorder in NATURE GENETICS
  • 2019-01-28 A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment in NATURE NEUROSCIENCE
  • 2019-01-24 Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language in TRANSLATIONAL PSYCHIATRY
  • 2019-01-04 Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality in MOLECULAR PSYCHIATRY
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