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Author Details

Steven A McCarroll
1984
280
99
PMIDPaper TitleJournal TitlePublished Year
37527660Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer.2023
36416236LPAR1 and aberrantly expressed LPAR3 differentially promote the migration and proliferation of malignant peripheral nerve sheath tumor cells.GLIA2023
37677047Genetic Profiling and Genome-Scale Dropout Screening to Identify Therapeutic Targets in Mouse Models of Malignant Peripheral Nerve Sheath Tumor.2023
37824615A marmoset brain cell census reveals regional specialization of cellular identities.Sci Adv2023
37904944Sibling chimerism among microglia in marmosets.2023
38092918Conserved and divergent gene regulatory programs of the mammalian neocortex.Nature2023
37333244Hidden protein-altering variants influence diverse human phenotypes.2023
36640364Astrocytic cell adhesion genes linked to schizophrenia correlate with synaptic programs in neurons.2023
37328102Inhibition of Erb-B2 Receptor Tyrosine Kinase 3 and Associated Regulatory Pathways Potently Impairs Malignant Peripheral Nerve Sheath Tumor Proliferation and Survival.Am J Pathol2023
36563689Small-molecule screen reveals pathways that regulate C4 secretion in stem cell-derived astrocytes.Stem Cell Reports2023
37066152Comparative single cell epigenomic analysis of gene regulatory programs in the rodent and primate neocortex.bioRxiv2023
36796362Natural variation in gene expression and viral susceptibility revealed by neural progenitor cell villages.2023
37534135Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cells.2023
35101235The RASopathies: Biology, genetics and therapeutic options.2022
35396580Mapping genomic loci implicates genes and synaptic biology in schizophrenia.Nature2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
35523590Developmental, neurochemical, and behavioral analyses of ErbB4 Cyt-1 knockout mice.Journal of Neurochemistry2022
35835769Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractions.Scientific Reports2022
35760976The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.Nat Commun2022
35981533Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing.Am J Hum Genet2022
36384944Ascertaining cells' synaptic connections and RNA expression simultaneously with barcoded rabies virus libraries.Nature Communications2022
36446800Brain single cell transcriptomic profiles in episodic memory phenotypes associated with temporal lobe epilepsy.npj Genomic Medicine2022
35319013Author Correction: Comparative cellular analysis of motor cortex in human, marmoset and mouse.Nature2022
35038582Suppression of Fli-1 protects against pericyte loss and cognitive deficits in Alzheimer's disease.Mol Ther2022
35176222Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation.Cell Stem Cell2022
34530870R-Ras subfamily proteins elicit distinct physiologic effects and phosphoproteome alterations in neurofibromin-null MPNST cells.Cell Communication and Signaling2021
33707600Establishment and genomic characterization of a sporadic malignant peripheral nerve sheath tumor cell line.Scientific Reports2021
33545059Human DDK rescues stalled forks and counteracts checkpoint inhibition at unfired origins to complete DNA replication.Molecular Cell2021
34111428The Role of R-Ras Proteins in Normal and Pathologic Migration and Morphologic Change.American Journal of Pathology2021
34161264Early role for a Na<sup>+</sup>,K<sup>+</sup>-ATPase (<i>ATP1A3</i>) in brain development.Proc Natl Acad Sci U S A2021
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
34197733Anterior thalamic dysfunction underlies cognitive deficits in a subset of neuropsychiatric disease models.Neuron2021
33501449Protein-coding repeat polymorphisms strongly shape diverse human phenotypes.2021
33353966Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice.Nature Neuroscience2021
34515675Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells.Journal of Visualized Experiments2021
34616062Comparative cellular analysis of motor cortex in human, marmoset and mouse.Nature2021
34554798Protein-coding repeat polymorphisms strongly shape diverse human phenotypes.Science2021
34489608Prognostic value of polygenic risk scores for adults with psychosis.Nat Med2021
34883504Publicly Available hiPSC Lines with Extreme Polygenic Risk Scores for Modeling Schizophrenia.Complex Psychiatry2021
34417660Single cell analysis of DNA in more than 10,000 individual sperm from men with abnormal reproductive outcomes.2021
33409501Single-cell RNA sequencing reveals compromised immune microenvironment in precursor stages of multiple myeloma.Nat Cancer2020
31784742Salinomycin targets the genome of radioresistant cells in glioblastomas.Neuro-Oncology2020
31882186Serum pro-BDNF levels correlate with phospho-tau staining in Alzheimer's disease.Neurobiology of Aging2020
31932770Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.Nat Neurosci2020
31928904Differential excitatory vs inhibitory SCN expression at single cell level regulates brain sodium channel function in neurodevelopmental disorders.Eur J Paediatr Neurol2020
32494014Insights into variation in meiosis from 31,228 human sperm genomes.Nature2020
32581364Chromosomal alterations among age-related haematopoietic clones in Japan.Nature2020
32581363Monogenic and polygenic inheritance become instruments for clonal selection.Nature2020
33236004Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer.Res Sq2020
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Massachusetts General Hospital
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Brigham and Women's Hospital
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Massachusetts General Hospital
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University of North Carolina at Chapel Hill
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Karolinska Institutet
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Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
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Massachusetts General Hospital and Harvard Medical School
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Vanderbilt University Medical Center
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Broad Institute of MIT and Harvard
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University of Iceland
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Karolinska Institutet
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Regeneron Pharmaceuticals Inc.
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