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Monogenic and polygenic inheritance become instruments for clonal selection

Nature (London), 2020-08, Vol.584 (7819), p.136-141

2020

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Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets

Cell, 2015-05, Vol.161 (5), p.1202-1214

2015

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Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Neuron (Cambridge, Mass.), 2015-06, Vol.86 (5), p.1203-1214

2015

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Single-Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell-State Changes

Immunity (Cambridge, Mass.), 2019-01, Vol.50 (1), p.253-271.e6

2019

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Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice

Nature neuroscience, 2021-02, Vol.24 (2), p.214-224

2021

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Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain

Cell, 2018-08, Vol.174 (4), p.1015-1030.e16

2018

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Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for Neurobiology

Neuron (Cambridge, Mass.), 2013-10, Vol.80 (3), p.578-587

2013

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Differential Relationship of DNA Replication Timing to Different Forms of Human Mutation and Variation

American journal of human genetics, 2012-12, Vol.91 (6), p.1033-1040

2012

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Schizophrenia risk from complex variation of complement component 4

Nature (London), 2016-02, Vol.530 (7589), p.177-183

2016

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Cell diversity and network dynamics in photosensitive human brain organoids

Nature (London), 2017-05, Vol.545 (7652), p.48-53

2017

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Comprehensive Classification of Retinal Bipolar Neurons by Single-Cell Transcriptomics

Cell, 2016-08, Vol.166 (5), p.1308-1323.e30

2016

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Chromosomal alterations among age-related haematopoietic clones in Japan

Nature (London), 2020-08, Vol.584 (7819), p.130-135

2020

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Genetic Variation in Human DNA Replication Timing

Cell, 2014-11, Vol.159 (5), p.1015-1026

2014

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Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

Science (American Association for the Advancement of Science), 2021-09, Vol.373 (6562), p.1499-1505

2021

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Copy-number variation and association studies of human disease

Nature genetics, 2007-07, Vol.39 (7 Suppl), p.S37-S42

2007

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Extending genome-wide association studies to copy-number variation

Human molecular genetics, 2008-10, Vol.17 (R2), p.R135-R142

McCarroll, Steven A

2008

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Genetic predisposition to mosaic Y chromosome loss in blood

Nature (London), 2019-11, Vol.575 (7784), p.652-657

2019

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Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals

PLoS genetics, 2011-02, Vol.7 (2), p.e1001317-e1001317

2011

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Genetically Distinct Parallel Pathways in the Entopeduncular Nucleus for Limbic and Sensorimotor Output of the Basal Ganglia

Neuron (Cambridge, Mass.), 2017-04, Vol.94 (1), p.138-152.e5

2017

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Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

Nature genetics, 2011-03, Vol.43 (3), p.269-276

2011

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Random replication of the inactive X chromosome

Genome research, 2014-01, Vol.24 (1), p.64-69

2014

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An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Nature genetics, 2018-04, Vol.50 (5), p.727-736

2018

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Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations

Nature (London), 2017-05, Vol.545 (7653), p.229-233

2017

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Large multiallelic copy number variations in humans

Nature genetics, 2015-03, Vol.47 (3), p.296-303

2015

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Insights into variation in meiosis from 31,228 human sperm genomes

Nature (London), 2020-07, Vol.583 (7815), p.259-264

2020

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Monogenic and polygenic inheritance become instruments for clonal selection

Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Single-Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell-State Changes

Overexpression of schizophrenia susceptibility factor human complement C4A promotes excessive synaptic loss and behavioral changes in mice

Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain

Progress in the Genetics of Polygenic Brain Disorders: Significant New Challenges for Neurobiology

Differential Relationship of DNA Replication Timing to Different Forms of Human Mutation and Variation

Schizophrenia risk from complex variation of complement component 4

Cell diversity and network dynamics in photosensitive human brain organoids

Comprehensive Classification of Retinal Bipolar Neurons by Single-Cell Transcriptomics

Chromosomal alterations among age-related haematopoietic clones in Japan

Genetic Variation in Human DNA Replication Timing

Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

Copy-number variation and association studies of human disease

Extending genome-wide association studies to copy-number variation

Genetic predisposition to mosaic Y chromosome loss in blood

Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals

Genetically Distinct Parallel Pathways in the Entopeduncular Nucleus for Limbic and Sensorimotor Output of the Basal Ganglia

Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

Random replication of the inactive X chromosome

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations

Large multiallelic copy number variations in humans

Insights into variation in meiosis from 31,228 human sperm genomes

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