Steven A McCarroll
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Biology
Steven A McCarroll's Degrees
- Bachelors Biology Stanford University
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(Suggest an Edit or Addition)Steven A McCarroll's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Finding the missing heritability of complex diseases (2009) (7749)
- An integrated map of genetic variation from 1,092 human genomes (2012) (7565)
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
- Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets (2015) (5020)
- A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Mutational heterogeneity in cancer and the search for new cancer-associated genes (2013) (2852)
- Mutational heterogeneity in cancer and the search for new cancer genes (2013) (2691)
- Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. (2014) (2344)
- Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans (2003) (2118)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
- An integrated map of structural variation in 2,504 human genomes (2015) (1800)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
- Schizophrenia risk from complex variation of complement component 4 (2016) (1724)
- Genome-wide detection and characterization of positive selection in human populations (2007) (1558)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (2008) (1506)
- Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
- De novo mutations in schizophrenia implicate synaptic networks (2014) (1454)
- A polygenic burden of rare disruptive mutations in schizophrenia (2014) (1371)
- Mapping and sequencing of structural variation from eight human genomes (2008) (1195)
- Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
- A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes (2012) (1127)
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) (1125)
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (1124)
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (2009) (1100)
- Mapping copy number variation by population scale genome sequencing (2010) (1057)
- Single‐Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell‐State Changes (2019) (1004)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Integrated detection and population-genetic analysis of SNPs and copy number variation (2008) (980)
- Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain (2018) (929)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
- Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. (2015) (858)
- Comprehensive Classification of Retinal Bipolar Neurons by Single-Cell Transcriptomics (2016) (856)
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs (2008) (838)
- Copy number variation: new insights in genome diversity. (2006) (832)
- Cell diversity and network dynamics in photosensitive human brain organoids (2017) (789)
- Common deletion polymorphisms in the human genome (2006) (754)
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) (736)
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
- Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease (2008) (674)
- Whole-genome sequence variation, population structure and demographic history of the Dutch population (2014) (650)
- Copy-number variation and association studies of human disease (2007) (626)
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types (2017) (578)
- A Molecular Census of Arcuate Hypothalamus and Median Eminence Cell Types (2017) (522)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) (510)
- Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation (2012) (497)
- Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. (2012) (496)
- Comparing genomic expression patterns across species identifies shared transcriptional profile in aging (2004) (455)
- De Novo Copy Number Variants Identify New Genes and Loci in Isolated, Sporadic Tetralogy of Fallot (2009) (403)
- Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA. (2015) (394)
- A structural variation reference for medical and population genetics (2020) (394)
- Analysis of copy number variations at 15 schizophrenia-associated loci (2014) (387)
- Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1. (2014) (384)
- Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia (2016) (381)
- Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders (2016) (363)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) (361)
- Quantifying prion disease penetrance using large population control cohorts (2016) (352)
- Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations (2017) (347)
- Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome. (2006) (340)
- Discovery and genotyping of genome structural polymorphism by sequencing on a population scale (2011) (334)
- Large multi-allelic copy number variations in humans (2015) (332)
- Comparative genetic architectures of schizophrenia in East Asian and European populations (2018) (329)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2016) (327)
- The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay (2014) (317)
- Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
- Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences (2016) (263)
- Increased neutrophil extracellular trap formation promotes thrombosis in myeloproliferative neoplasms (2018) (255)
- Understanding Anasazi culture change through agent-based modeling (2000) (243)
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
- Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes (2007) (217)
- Differential relationship of DNA replication timing to different forms of human mutation and variation. (2012) (217)
- zCall: a rare variant caller for array-based genotyping: Genetics and population analysis (2012) (209)
- Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
- An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder (2018) (194)
- A multimodal cell census and atlas of the mammalian primary motor cortex (2020) (190)
- Single-Tissue and Cross-Tissue Heritability of Gene Expression Via Identity-by-Descent in Related or Unrelated Individuals (2011) (189)
- Extending genome-wide association studies to copy-number variation. (2008) (178)
- Comparative cellular analysis of motor cortex in human, marmoset and mouse (2021) (177)
- Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals (2019) (176)
- Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia (2015) (164)
- Insights about clonal hematopoiesis from 8,342 mosaic chromosomal alterations (2018) (157)
- Characterization of Bipolar Disorder Patient-Specific Induced Pluripotent Stem Cells from a Family Reveals Neurodevelopmental and mRNA Expression Abnormalities (2014) (154)
- Copy number variation in bipolar disorder (2015) (154)
- Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function (2010) (154)
- Rare coding variants in ten genes confer substantial risk for schizophrenia (2022) (154)
- The Genetic Landscape of Diamond-Blackfan Anemia (2018) (151)
- Single-cell RNA sequencing reveals compromised immune microenvironment in precursor stages of multiple myeloma (2018) (148)
- Innovations present in the primate interneuron repertoire (2020) (140)
- Genetic Variation in Human DNA Replication Timing (2014) (139)
- DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage (2006) (138)
- Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder (2017) (136)
- Genetic predisposition to mosaic Y chromosome loss in blood (2019) (131)
- Evidence that duplications of 22q11.2 protect against schizophrenia (2013) (130)
- Exome Aggregation Consortium (2016) (125)
- Genetically Distinct Parallel Pathways in the Entopeduncular Nucleus for Limbic and Sensorimotor Output of the Basal Ganglia (2017) (122)
- Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
- Structural forms of the human amylase locus and their relationships to SNPs, haplotypes, and obesity (2015) (118)
- Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) (116)
- Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions (2018) (116)
- Structural haplotypes and recent evolution of the human 17q21.31 region (2012) (115)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (115)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
- Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice (2020) (100)
- The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
- Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans (2011) (95)
- Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations (2019) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Evidence of Common Genetic Overlap Between Schizophrenia and Cognition (2015) (92)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (89)
- Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. (2011) (88)
- Finding the missing heritability of complex (2009) (87)
- SnapShot-Seq: A Method for Extracting Genome-Wide, In Vivo mRNA Dynamics from a Single Total RNA Sample (2014) (86)
- Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease (2009) (86)
- Evaluating drug targets through human loss-of-function genetic variation (2019) (86)
- CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 (2013) (83)
- Genome-scale neurogenetics: methodology and meaning (2014) (81)
- Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for Neurobiology (2013) (80)
- Ultra-rare disruptive and damaging mutations influence educational attainment in the general population (2016) (79)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) (78)
- Monogenic and polygenic inheritance become instruments for clonal selection (2019) (78)
- Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis (2011) (76)
- De novo CNVs in bipolar affective disorder and schizophrenia (2014) (72)
- Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations (2018) (72)
- Chromosomal alterations among age-related haematopoietic clones in Japan (2020) (70)
- Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network. (2013) (70)
- The effect of LRRK2 loss-of-function variants in humans (2020) (69)
- Using population admixture to help complete maps of the human genome (2013) (68)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2017) (68)
- Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder (2015) (68)
- Evolution of cellular diversity in primary motor cortex of human, marmoset monkey, and mouse (2020) (66)
- A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica (2018) (66)
- Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry (2019) (65)
- Common alleles contribute to schizophrenia in CNV carriers (2015) (65)
- Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection (2021) (61)
- The genomic psychiatry cohort: Partners in discovery (2013) (61)
- Random replication of the inactive X chromosome (2014) (60)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. (2015) (58)
- Thy-1 Is a Component Common to Multiple Populations of Synaptic Vesicles (1998) (55)
- Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (2016) (53)
- A Rapid Molecular Approach for Chromosomal Phasing (2015) (53)
- Recurring exon deletions in the haptoglobin (HP) gene associate with lower blood cholesterol levels (2016) (52)
- Exome arrays capture polygenic rare variant contributions to schizophrenia (2016) (51)
- Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection (2016) (50)
- Insights about variation in meiosis from 31,228 human sperm genomes (2019) (50)
- Identification of Transcriptional Regulatory Elements in Chemosensory Receptor Genes by Probabilistic Segmentation (2005) (50)
- Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders. (2014) (47)
- Complex and multi-allelic copy number variation in human disease (2015) (46)
- Copy-number analysis goes more than skin deep (2008) (44)
- A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes (2017) (43)
- Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes. (2013) (43)
- Polygenic risk for schizophrenia and measured domains of cognition in individuals with psychosis and controls (2018) (42)
- Innovations in Primate Interneuron Repertoire (2019) (40)
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types (2018) (39)
- Mapping genetic effects on cellular phenotypes with “cell villages” (2020) (38)
- Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases (2018) (36)
- Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia (2015) (34)
- Implication of LRRC4C and DPP6 in neurodevelopmental disorders (2017) (33)
- Protein-coding repeat polymorphisms strongly shape diverse human phenotypes (2021) (32)
- A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
- Clonal hematopoiesis and blood-cancer risk. (2015) (31)
- Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia (2018) (31)
- Protein-coding repeat polymorphisms strongly shape diverse human phenotypes (2021) (31)
- Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes (2008) (31)
- Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease (2018) (31)
- Analyzing Copy Number Variation with Droplet Digital PCR. (2018) (29)
- Functional analysis of rare variants found in schizophrenia implicates a critical role for GIT1–PAK3 signaling in neuroplasticity (2017) (29)
- A Single-Cell Atlas of Cell Types, States, and Other Transcriptional Patterns from Nine Regions of the Adult Mouse Brain (2018) (28)
- Copy number variation and human genome maps (2010) (26)
- Erratum: Common alleles contribute to schizophrenia in CNV carriers (2015) (26)
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Prognostic value of polygenic risk scores for adults with psychosis (2021) (24)
- Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study (2017) (23)
- Exploring the variation within (2012) (22)
- Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
- Polygenic risk for type 2 diabetes mellitus among individuals with psychosis and their relatives. (2016) (22)
- Regulatory variants explain much more heritability than coding variants across 11 common diseases (2014) (22)
- Narrow-sense heritability estimation of complex traits using identity-by-descent information (2017) (22)
- No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia (2014) (21)
- Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2019) (20)
- Publicly available hiPSC lines with extreme polygenic risk scores for modeling schizophrenia (2020) (18)
- Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia (2017) (17)
- Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families (2017) (16)
- Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (16)
- Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (2016) (16)
- Anterior thalamic dysfunction underlies cognitive deficits in a subset of neuropsychiatric disease models (2021) (16)
- Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
- Human DDK rescues stalled forks and counteracts checkpoint inhibition at unfired origins to complete DNA replication. (2021) (14)
- The genomics of major psychiatric disorders in a large pedigree from Northern Sweden (2019) (14)
- Early role for a Na+,K+-ATPase (ATP1A3) in brain development (2021) (14)
- The Genetic Landscape of Diamond-Blackfan Anemia. (2019) (14)
- Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (2017) (13)
- Corrigendum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia (Molecular Psychiatry (2017) 22 (1502-1508) DOI: 10.1038/mp.2016.97) (2018) (13)
- CUB and Sushi Multiple Domains 1 (CSMD1) opposes the complement cascade in neural tissues (2020) (13)
- CNV analysis in a large schizophrenia sample implicates deletions at 16 p 12 . 1 and SLC 1 A 1 and duplications at 1 p 36 . 33 and CGNL 1 (2014) (13)
- New insights into the biological basis of genomic disorders (2006) (13)
- Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010) (13)
- NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis (2019) (13)
- On the level: IRGM gene function is all about expression (2009) (12)
- The effects of common structural variants on 3D chromatin structure (2020) (12)
- Insights into variation in meiosis from 31,228 human sperm genomes (2020) (11)
- A haplotype map of the human genome The International HapMap Consortium (2005) (10)
- Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (10)
- Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation (2022) (9)
- Complex cell-state changes revealed by single cell RNA sequencing of 76,149 microglia throughout the mouse lifespan and in the injured brain (2018) (9)
- Using Droplet Digital PCR to Analyze Allele-Specific RNA Expression. (2018) (8)
- Our Fallen Genomes (2013) (8)
- Differential excitatory vs inhibitory SCN expression at single cell level regulates brain sodium channel function in neurodevelopmental disorders. (2019) (8)
- The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia (2021) (8)
- Efficient generation of lower induced motor neurons by coupling Ngn2 expression with developmental cues (2022) (8)
- Erratum: Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1 (Cell Stem Cell (2014) 14 (781795)) (2014) (7)
- Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer (2020) (7)
- Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants (2017) (7)
- Of Rats and Men (2013) (7)
- Common variants of NRXN1, LRP1B and RORA are associated with increased ventricular volumes in psychosis - GWAS findings from the B-SNIP deep phenotyping study (2017) (7)
- Schizophrenia risk conferred by protein-coding de novo mutations (2018) (7)
- Biological insights from the whole genome analysis of human embryonic stem cells (2020) (6)
- Mapping duplicated sequences (2009) (6)
- Single-nucleus sequencing reveals enriched expression of genetic risk factors in Extratelencephalic Neurons sensitive to degeneration in ALS (2021) (6)
- Absolute quantification and degradation evaluation of SARS-CoV-2 RNA by droplet digital PCR (2020) (5)
- Natural variation in gene expression and Zika virus susceptibility revealed by villages of neural progenitor cells (2021) (5)
- Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p (2022) (4)
- Ascertaining cells’ synaptic connections and RNA expression simultaneously with massively barcoded rabies virus libraries (2021) (4)
- Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations (2020) (4)
- WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene (2019) (4)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (3)
- Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (3)
- Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses (2019) (3)
- Higher genetic risk of schizophrenia is associated with lower cognitive performance in healthy individuals (2017) (3)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (3)
- Ascertaining cells’ synaptic connections and RNA expression simultaneously with barcoded rabies virus libraries (2022) (2)
- Small-molecule screen reveals pathways that regulate C4 secretion in stem cell-derived astrocytes (2022) (2)
- Natural variation in gene expression and viral susceptibility revealed by neural progenitor cell villages. (2023) (2)
- Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing. (2022) (2)
- Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions (2022) (2)
- Extraction of Nuclei from Brain Tissue v1 (2020) (2)
- The genomic landscape of clonal hematopoiesis in Japan (2019) (2)
- Single-cell Genomics using Droplet-based Microfluidics (2014) (2)
- Brain single cell transcriptomic profiles in episodic memory phenotypes associated with temporal lobe epilepsy (2022) (2)
- Comparative genetic architectures of schizophrenia in East Asian and European populations (2019) (2)
- Sperm-seq wet lab protocol: sperm preparation and droplet-based sequencing library generation (2020) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- Author Correction: Schizophrenia risk from complex variation of complement component 4 (2021) (2)
- Transcript expression-aware annotation improves rare variant interpretation (2020) (1)
- Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2021) (1)
- Monogenic and polygenic inheritance become instruments for clonal selection (2020) (1)
- SHARED CONTRIBUTIONS OF COMMON GENETIC VARIANTS TO RISK OF PSYCHOSIS AMONG INDIVIDUALS OF AFRICAN, LATINO, AND EUROPEAN ANCESTRY (2019) (1)
- Polygenic risk scores lack prognostic value for adults with severe mental illness (2021) (1)
- Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cells (2022) (1)
- Astrocytic cell adhesion genes linked to schizophrenia correlate with synaptic programs in neurons (2021) (1)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- A marmoset brain cell census reveals persistent influence of developmental origin on neurons (2022) (1)
- 55 LARGE META-ANALYSIS OF SCANDINAVIAN EXOME SEQUENCING STUDIES OF SCHIZOPHRENIA (2019) (1)
- Single cell analysis of DNA in more than 10,000 individual sperm from men with abnormal reproductive outcomes (2021) (1)
- M94. Genetic Analyses of Cognitive Performance in Psychotic Disorders From the Bipolar-Schizophrenia Network on Intermediate Phenotypes (B-SNIP) Consortium (2017) (1)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- STATISTICAL AND FUNCTIONAL CONVERGENCE OF COMMON AND RARE VARIANT RISK FOR AUTISM SPECTRUM DISORDERS AT CHROMOSOME 16P (2022) (1)
- The effects of common structural variants on 3D chromatin structure (2020) (1)
- Comparative transcriptomics reveals human-specific cortical features (2022) (1)
- Resource Phenotypic Landscape of Schizophrenia-Associated Genes Defines Candidates and Their Shared Functions Graphical (2019) (1)
- Author Correction: Innovations present in the primate interneuron repertoire (2020) (1)
- Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractions (2022) (0)
- 113. Genetic and Single-Cell Resolution Analyses of Brain and Schizophrenia (2017) (0)
- 169. New Technology for Learning About Genetic Effects on Brain Cells and Brain Tissue (2019) (0)
- Comparison of Mitogenomic and Mitochondrial Markers for the Phylogenetic and Evolutionary Study of Marmosets, with special focus on captive Callithrix jacchus (2022) (0)
- Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer (2020) (0)
- Ultra-Rare Protein-Altering Variants Among 4,877 Swedish Individuals with Schizophrenia (2017) (0)
- High-dimensional phenotyping to define the genetic basis of cellular morphology (2023) (0)
- Author Correction: Evaluating drug targets through human loss-of-function genetic variation (2021) (0)
- EXOME SEQUENCING IN SCHIZOPHRENIA TO MAP DISEASE VARIANTS, GENES AND NETWORKS (2012) (0)
- Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (0)
- 80. SINGLE-CELL RNA-SEQUENCING OF HUMAN BRAIN REGIONS IDENTIFIES CELL TYPES AND STATES RELEVANT TO DISEASE (2021) (0)
- Chromosomal alterations among age-related haematopoietic clones in Japan (2020) (0)
- SU68 COMMON VARIANTS OF NRXN1, LRP1B AND RORA ARE ASSOCIATED WITH INCREASED VENTRICULAR VOLUMES IN SCHIZOPHRENIA AND BIPOLAR DISORDER (2019) (0)
- A framework for the detection of de novo mutations in family-based sequencing data (2016) (0)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2020) (0)
- Role of complement C4A in developmental synaptic pruning (2018) (0)
- The Effects of Gene Regulation on Aging in Caenorhabditis elegans (2003) (2018) (0)
- Insights into dispersed duplications and complex structural mutations from whole genome sequencing 706 families (2020) (0)
- Author Correction: Transcript expression-aware annotation improves rare variant interpretation (2021) (0)
- Author Correction: Comparative cellular analysis of motor cortex in human, marmoset and mouse (2022) (0)
- Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights (2018) (0)
- Cover Image, Volume 173A, Number 2, February 2017. (2017) (0)
- Innovations present in the primate interneuron repertoire (2020) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (0)
- Evaluating drug targets through human loss-of-function genetic variation (2020) (0)
- 5:15 PM NOVEL GENETIC RISK VARIANTS FOR CLOZAPINE-ASSOCIATED NEUTROPENIA (2014) (0)
- Role for the Na+/K+ ATPase pump alpha 3 (ATP1A3) subunit in folding and lamination of the human neocortex (2020) (0)
- Clonal haematopoiesis and risk of chronic liver disease (2023) (0)
- Novel Technologies for Single-Cell Resolution Whole-Transcriptome Analysis in CNS Tissue (2016) (0)
- Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (0)
- SU28 THE GENOMICS OF BIPOLAR AND SCHIZOPHRENIC DISORDERS IN A LARGE PEDIGREE FROM A NORTHERN SWEDISH ISOLATE (2019) (0)
- T13 Gwas Of Bsnip Biofactors And Biotypes As Intermediate Phenotypes For Psychosis (2017) (0)
- P167. Association of Wnt7a Pathways in Distinct Human Amygdala Cell Populations and Affective Symptoms in Bipolar Disease (2022) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- Utilising machine-learning algorithms to uncovercomplex genetic interactions in schizophrenia [Conference Abstract] (2015) (0)
- Abstract 1789: Genomic Analyses Identify New Loci and Genes in Isolated, Sporadic Congenital Heart Disease (2009) (0)
- Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (0)
- Genome-Wide Association Studies Of Smooth Pursuit Eye Movements Across Psychotic Disorders: Preliminary Findings From The B-Snip Sample (2017) (0)
- Author Correction: Innovations present in the primate interneuron repertoire (2020) (0)
- Sex-Specific Molecular Expression in the Human Brain: A Step Toward a Better Understanding of Sexually Dimorphic Mechanisms of Stress-Related Disorders (2021) (0)
- Poster #T149 LINE1 POLYMORPHIC RETROTRANSPOSITIONS IN SCHIZOPHRENIA (2014) (0)
- SA122STRUCTURAL VARIATIONS OF SCHIZOPHRENIA RISK GENE COMPLEMENT COMPONENT 4 (C4) AND BRAIN MRI PHENOTYPES (2019) (0)
- The effect of LRRK2 loss-of-function variants in humans (2020) (0)
- Genetic predisposition to mosaic Y chromosome loss in blood (2019) (0)
- 5:00 PM DOPAMINE OR GLUTAMATE: USING GENETIC COPY NUMBER VARIANT PATHWAY ANALYSIS AND TREATMENT RESISTANCE TO ADJUDICATE SCHIZOPHRENIA HYPOTHESES (2014) (0)
- Copy-number variation and association studies of human disease. Commentary (2007) (0)
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2020) (0)
- Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants (2017) (0)
- A structural variation reference for medical and population genetics (2020) (0)
- 11. Extended Association Studies of Smooth Pursuit and Antisaccade Eye Movements: Findings From the B-SNIP Study (2017) (0)
- Chapter 4. UNDERSTANDING ANASAZI CULTURE CHANGE THROUGH AGENT-BASED MODELING (2012) (0)
- Comparative cellular analysis of motor cortex in human, marmoset and mouse (2021) (0)
- Author Correction: A structural variation reference for medical and population genetics (2021) (0)
- 38. COMMON AND RARE GENETIC RISK FACTORS FOR SCHIZOPHRENIA AT CHROMOSOME 22Q INDUCE CONVERGENT, DISPERSED CHANGES IN GENE EXPRESSION (2022) (0)
- Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
- A Cell Atlas of the Human Amygdala (2021) (0)
- Key Roles of L-Type Calcium Channels CACNA1C in Dorsolateral Prefrontal Cortex Cognition (2022) (0)
- 115.3 Single-Cell Analysis of Adolescence and Other Critical Periods in Brain Development (2017) (0)
- F118CONTRIBUTIONS OF COMMON GENETIC VARIANTS TO SCHIZOPHRENIA RISK IN INDIVIDUALS WITH AFRICAN AND LATINO ANCESTRY (2019) (0)
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) (0)
- An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder (2018) (0)
- Damaging Missense De Novo Coding Mutations Contribute To Schizophrenia Risk (2017) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2020) (0)
- Single-Cell RNA Sequencin g of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell-State Changes Graphical (0)
- Genome Variation and Donor-Recipient Compatibility in Graft-Versus-Host Disease (2010) (0)
- Population Perspectives on Genome Variation and Complex Disease (2013) (0)
- Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
- VKučinskas-2001-2016 (2016) (0)
- Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
- Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2021) (0)
- SU119GENETIC OVERLAP AND CAUSALITY AMONG SCHIZOPHRENIA AND SUBSTANCE USE: FINDINGS FROM THE GENOMIC PSYCHIATRY COHORT (2019) (0)
- Genetically Distinct Parall el Pathways in the Entopeduncular Nucleus for Limbic and Sensorimotor Output of the Basal Ganglia Highlights (2017) (0)
- M87 WHOLE GENOME SEQUENCING OF MULTIPLY-AFFECTED SCHIZOPHRENIA AND BIPOLAR DISORDER FAMILIES FROM THE AZORES AND MADEIRA (2019) (0)
- Comparative single cell epigenomic analysis of gene regulatory programs in the rodent and primate neocortex (2023) (0)
- A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica (2018) (0)
- THU0002 SOLVING THE COMPLEX MHC ASSOCIATIONS IN SLE IDENTIFIES SEX-RELATED GENE EFFECTS (2020) (0)
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What Schools Are Affiliated With Steven A McCarroll?
Steven A McCarroll is affiliated with the following schools:
