Steven Andrew Mccarroll


Ontology type: schema:Person     


Person Info

NAME

Steven Andrew

SURNAME

Mccarroll

Publications in SciGraph latest 50 shown

  • 2022-10-24 Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p in NATURE GENETICS
  • 2022-07-14 Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractions in SCIENTIFIC REPORTS
  • 2022-06-27 The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia in NATURE COMMUNICATIONS
  • 2022-04-08 Rare coding variants in ten genes confer substantial risk for schizophrenia in NATURE
  • 2021-12-15 Author Correction: Schizophrenia risk from complex variation of complement component 4 in NATURE
  • 2021-10-06 A multimodal cell census and atlas of the mammalian primary motor cortex in NATURE
  • 2021-09-06 Prognostic value of polygenic risk scores for adults with psychosis in NATURE MEDICINE
  • 2021-08-20 Single cell analysis of DNA in more than 10,000 individual sperm from men with abnormal reproductive outcomes in JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
  • 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
  • 2021-01-22 Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder in MOLECULAR PSYCHIATRY
  • 2020-12-22 Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice in NATURE NEUROSCIENCE
  • 2020-11-24 Author Correction: Innovations present in the primate interneuron repertoire in NATURE
  • 2020-09-30 Innovations present in the primate interneuron repertoire in NATURE
  • 2020-06-24 Chromosomal alterations among age-related haematopoietic clones in Japan in NATURE
  • 2020-06-24 Monogenic and polygenic inheritance become instruments for clonal selection in NATURE
  • 2020-06-03 Insights into variation in meiosis from 31,228 human sperm genomes in NATURE
  • 2020-04-27 Single-cell RNA sequencing reveals compromised immune microenvironment in precursor stages of multiple myeloma in NATURE CANCER
  • 2020-04-01 Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries in NATURE COMMUNICATIONS
  • 2020-01-13 Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations in NATURE NEUROSCIENCE
  • 2019-11-20 Genetic predisposition to mosaic Y chromosome loss in blood in NATURE
  • 2019-11-18 Comparative genetic architectures of schizophrenia in East Asian and European populations in NATURE GENETICS
  • 2019-10-07 Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry in MOLECULAR PSYCHIATRY
  • 2019-09-17 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis in TRANSLATIONAL PSYCHIATRY
  • 2019-06-03 Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection in NATURE GENETICS
  • 2019-04-16 Multi-platform discovery of haplotype-resolved structural variation in human genomes in NATURE COMMUNICATIONS
  • 2019-02-04 The genomics of major psychiatric disorders in a large pedigree from Northern Sweden in TRANSLATIONAL PSYCHIATRY
  • 2018-08-23 Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries in NATURE COMMUNICATIONS
  • 2018-07-11 Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations in NATURE
  • 2018-07-04 Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries in NATURE COMMUNICATIONS
  • 2018-05-16 A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica in NATURE COMMUNICATIONS
  • 2018-05-02 Using Droplet Digital PCR to Analyze Allele-Specific RNA Expression in DIGITAL PCR
  • 2018-05-02 Analyzing Copy Number Variation with Droplet Digital PCR in DIGITAL PCR
  • 2018-04-26 An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder in NATURE GENETICS
  • 2018-04-12 Polygenic risk for schizophrenia and measured domains of cognition in individuals with psychosis and controls in TRANSLATIONAL PSYCHIATRY
  • 2018-04-09 Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types in NATURE GENETICS
  • 2018-04-09 Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights in NATURE GENETICS
  • 2018-03-16 Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium in NATURE NEUROSCIENCE
  • 2018-02-26 Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection in NATURE GENETICS
  • 2017-11-28 Whole genome sequencing in psychiatric disorders: the WGSPD consortium in NATURE NEUROSCIENCE
  • 2017-10-24 Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study in TRANSLATIONAL PSYCHIATRY
  • 2017-10-24 Adaptive combination of Bayes factors as a powerful method for the joint analysis of rare and common variants in SCIENTIFIC REPORTS
  • 2017-04-26 Cell diversity and network dynamics in photosensitive human brain organoids in NATURE
  • 2017-04-26 Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations in NATURE
  • 2017-02-06 A molecular census of arcuate hypothalamus and median eminence cell types in NATURE NEUROSCIENCE
  • 2017-01-10 Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder in TRANSLATIONAL PSYCHIATRY
  • 2016-11-21 Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects in NATURE GENETICS
  • 2016-10-03 Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia in NATURE NEUROSCIENCE
  • 2016-10-03 Ultra-rare disruptive and damaging mutations influence educational attainment in the general population in NATURE NEUROSCIENCE
  • 2016-08-17 Analysis of protein-coding genetic variation in 60,706 humans in NATURE
  • 2016-07-26 Functional analysis of rare variants found in schizophrenia implicates a critical role for GIT1–PAK3 signaling in neuroplasticity in MOLECULAR PSYCHIATRY
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