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Author Details

Laura J Scott
1998
118
64
PMIDPaper TitleJournal TitlePublished Year
37425837Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health.medRxiv2023
37662416Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies.bioRxiv2023
34099189Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.Biol Psychiatry2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
35589964ACE2 expression in adipose tissue is associated with cardio-metabolic risk factors and cell type composition-implications for COVID-19.Int J Obes (Lond)2022
35410376Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia.Nat Genet2022
36055244Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.Am J Hum Genet2022
35981533Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing.Am J Hum Genet2022
34586374The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study.JAMA Psychiatry2021
34002096Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.Nat Genet2021
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
33730541A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank.Am J Hum Genet2021
34038741Genetic effects on liver chromatin accessibility identify disease regulatory variants.Am J Hum Genet2021
33720349Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.Genetics2021
34682540Cabbage and Sauerkraut Consumption in Adolescence and Adulthood and Breast Cancer Risk among US-Resident Polish Migrant Women.Int J Environ Res Public Health2021
34855821Prediction of suicidal ideation risk in a prospective cohort study of medical interns.PLoS ONE2021
32999275Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D.Nat Commun2020
31736264Heritability of the Fibromyalgia Phenotype Varies by Age.Arthritis and Rheumatology2020
31659322Genomic prediction of depression risk and resilience under stress.Nature Human Behaviour2020
31980570Ancestry-agnostic estimation of DNA sample contamination from sequence reads.Genome Res2020
32817962ACE2 expression in adipose tissue is associated with COVID-19 cardio-metabolic risk factors and cell type composition.medRxiv2020
32915782Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences.PLoS Genet2020
31358974New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders.Nat Hum Behav2019
31686056Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.Nature2019
31564431Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits.Am J Hum Genet2019
30298564Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes.Genetic Epidemiology2019
31164008GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.Am J Psychiatry2019
31118516Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.Nature2019
31367044Exome sequencing of Finnish isolates enhances rare-variant association power.Nature2019
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
30218074Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.Nat Commun2018
29141982A Partial Loss-of-Function Variant in <i>AKT2</i> Is Associated With Reduced Insulin-Mediated Glucose Uptake in Multiple Insulin-Sensitive Tissues: A Genotype-Based Callback Positron Emission Tomography Study.Diabetes2018
29659628Interactions between genetic variation and cellular environment in skeletal muscle gene expression.PLoS One2018
29279374Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.Proc Natl Acad Sci U S A2018
28193859Genetic regulatory signatures underlying islet gene expression and type 2 diabetes.Proc Natl Acad Sci U S A2017
28684635A Type 2 Diabetes-Associated Functional Regulatory Variant in a Pancreatic Islet Enhancer at the <i>ADCY5</i> Locus.Diabetes2017
28724990Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.Nat Commun2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
28632202Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.Transl Psychiatry2017
28369632Differential expression analysis for RNAseq using Poisson mixed models.Nucleic Acids Research2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
29116125Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.Nat Commun2017
28257690Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.Am J Hum Genet2017
27548312A reference panel of 64,976 haplotypes for genotype imputation.Nat Genet2016
27120077Exome Sequencing of Familial Bipolar Disorder.JAMA Psychiatry2016
27398621The genetic architecture of type 2 diabetes.Nature2016
27353450The genetic regulatory signature of type 2 diabetes in human skeletal muscle.Nat Commun2016
26363037An efficient resampling method for calibrating single and gene-based rare variant association analysis in case-control studies.Biostatistics2016
27571263Next-generation genotype imputation service and methods.Nat Genet2016
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