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One or more keywords matched the following items that are connected to McCarroll, Steven
Item TypeName
Academic Article Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes.
Academic Article Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease.
Academic Article Mapping and sequencing of structural variation from eight human genomes.
Academic Article Genome-wide detection and characterization of positive selection in human populations.
Academic Article Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease.
Academic Article Copy number variation: new insights in genome diversity.
Academic Article Discovery and genotyping of genome structural polymorphism by sequencing on a population scale.
Academic Article Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.
Academic Article New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
Academic Article Using population admixture to help complete maps of the human genome.
Academic Article Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
Academic Article Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
Academic Article Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
Academic Article Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
Academic Article Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
Academic Article Mapping copy number variation by population-scale genome sequencing.
Academic Article Finding the missing heritability of complex diseases.
Academic Article Common deletion polymorphisms in the human genome.
Academic Article Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
Academic Article A genome-wide association search for type 2 diabetes genes in African Americans.
Academic Article Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
Academic Article A systematic survey of loss-of-function variants in human protein-coding genes.
Academic Article Differential relationship of DNA replication timing to different forms of human mutation and variation.
Academic Article Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
Academic Article Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Academic Article Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Academic Article Copy number variation and human genome maps.
Academic Article Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection.
Academic Article Mapping duplicated sequences.
Academic Article Integrated detection and population-genetic analysis of SNPs and copy number variation.
Academic Article Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
Academic Article Extending genome-wide association studies to copy-number variation.
Academic Article Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Concept Genome-Wide Association Study
Concept Genome
Concept Genome, Human
Academic Article Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Academic Article Mutational heterogeneity in cancer and the search for new cancer-associated genes.
Academic Article Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.
Academic Article The genomic psychiatry cohort: partners in discovery.
Academic Article Random replication of the inactive X chromosome.
Academic Article Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes.
Academic Article Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Academic Article Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Academic Article Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.
Academic Article Genetics. Our fallen genomes.
Academic Article Progress in the genetics of polygenic brain disorders: significant new challenges for neurobiology.
Academic Article SnapShot-Seq: a method for extracting genome-wide, in vivo mRNA dynamics from a single total RNA sample.
Academic Article A polygenic burden of rare disruptive mutations in schizophrenia.
Academic Article Genome-scale neurogenetics: methodology and meaning.
Academic Article Copy number variation in schizophrenia in Sweden.
Academic Article Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.
Academic Article De novo CNVs in bipolar affective disorder and schizophrenia.
Academic Article Genetic variation in human DNA replication timing.
Academic Article Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.
Academic Article Genetic studies of body mass index yield new insights for obesity biology.
Academic Article Large multiallelic copy number variations in humans.
Academic Article Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets.
Academic Article Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity.
Academic Article Complex and multi-allelic copy number variation in human disease.
Academic Article Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
Academic Article An integrated map of structural variation in 2,504 human genomes.
Academic Article New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.
Academic Article Exome arrays capture polygenic rare variant contributions to schizophrenia.
Academic Article Polygenic risk for type 2 diabetes mellitus among individuals with psychosis and their relatives.
Academic Article Common alleles contribute to schizophrenia in CNV carriers.
Academic Article Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.
Grant Accurate analysis of genome structural variation using large-scale sequence data
Grant Development of a Software Pipeline for Sequence Data
Grant 2/3-Whole Genome Sequencing for Schizophrenia and Bipolar Disorder in the GPC
Grant Population-Based Approaches to Genome Structure and Structural Variation
Academic Article A reference panel of 64,976 haplotypes for genotype imputation.
Academic Article Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
Academic Article Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.
Academic Article Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.
Academic Article A molecular census of arcuate hypothalamus and median eminence cell types.
Academic Article Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.
Academic Article Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Academic Article Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia.
Academic Article Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.
Grant Neural-immune mechanisms and synaptic connectivity in psychiatric illness
Academic Article Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.
Academic Article Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Academic Article Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.
Academic Article Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Academic Article Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Academic Article Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Academic Article Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
Academic Article An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.
Academic Article A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica.
Academic Article Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Academic Article Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Academic Article Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.
Academic Article Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions.
Academic Article Multi-platform discovery of haplotype-resolved structural variation in human genomes.
Academic Article The genomics of major psychiatric disorders in a large pedigree from Northern Sweden.
Academic Article Genome-wide association study identifies 30 loci associated with bipolar disorder.
Academic Article NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.
Academic Article Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
Academic Article Comparative genetic architectures of schizophrenia in East Asian and European populations.
Academic Article Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
Academic Article Insights into variation in meiosis from 31,228 human sperm genomes.
Academic Article Chromosomal alterations among age-related haematopoietic clones in Japan.
Grant Multi-allelic forms of human genome structural variation
Academic Article Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.
Academic Article Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Academic Article Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection.
Academic Article Prognostic value of polygenic risk scores for adults with psychosis.
Academic Article Protein-coding repeat polymorphisms strongly shape diverse human phenotypes.
Search Criteria
  • Genome
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.