Seva Kashin

发表

An integrated map of structural variation in 2,504 human genomes

Gabor T. Marth, Hugo Y. K. Lam, Miriam K. Konkel, 2015, Nature.

Evolution of genes and genomes on the Drosophila phylogeny

Melanie A. Huntley, Sonja J. Prohaska, Albert J. Vilella, 2007, Nature.

The GTEx Consortium atlas of genetic regulatory effects across human tissues

Christopher D. Brown, Benjamin J. Strober, Stephane E. Castel, 2019, Science.

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

R. Handsaker, S. Mccarroll, K. Eggan, 2017, Nature.

A Quantitative Proteome Map of the Human Body

Christopher D. Brown, Katherine H. Huang, Christopher M. Lee, 2019, Cell.

Large multi-allelic copy number variations in humans

R. Handsaker, S. Mccarroll, Seva Kashin, 2015, Nature Genetics.

The GTEx Consortium atlas of genetic regulatory effects across human tissues

Christopher D. Brown, Katherine H. Huang, Jared L. Nedzel, 2019, Science.

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

Ryan L. Collins, Ryan M. Layer, Jeffrey D. Mandell, 2018, Nature Genetics.

Insights into dispersed duplications and complex structural mutations from whole genome sequencing 706 families

Christopher W. Whelan, R. Handsaker, D. MacArthur, 2020, bioRxiv.

Biological insights from the whole genome analysis of human embryonic stem cells

R. Handsaker, D. MacArthur, S. Mccarroll, 2020, bioRxiv.

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

Ryan L. Collins, Ryan M. Layer, Gabor T. Marth, 2017, bioRxiv.

Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences

Maria Cerezo, Paul Flicek, Yaniv Erlich, 2016, Nature Genetics.

Chromosomal phase improves aneuploidy detection in non-invasive prenatal testing at low fetal DNA fractions

Christopher W. Whelan, R. Handsaker, S. Mccarroll, 2022, Scientific Reports.

A marmoset brain cell census reveals persistent influence of developmental origin on neurons

Fenna M. Krienen, S. Mccarroll, Melissa Goldman, 2022, bioRxiv.

Ascertaining cells’ synaptic connections and RNA expression simultaneously with barcoded rabies virus libraries

S. Mccarroll, B. Sabatini, J. Nemesh, 2022, Nature Communications.

Genetic effects on gene expression across human tissues

Nicola J. Rinaldi, Ian C. McDowell, Christopher D. Brown, 2017, Nature.

Structural forms of the human amylase locus and their relationships to SNPs, haplotypes, and obesity

Andres Metspalu, Christian Fuchsberger, Mark I McCarthy, 2015, Nature Genetics.

The impact of rare variation on gene expression across tissues

Gao Wang, Mary Goldman, Brian Craft, 2016, Nature.

Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease

Christopher D. Brown, Katherine H. Huang, Christopher M. Lee, 2021, Cell.

Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation

R. Handsaker, D. MacArthur, S. Mccarroll, 2022, Cell stem cell.

A Quantitative Proteome Map of the Human Body

Christopher D. Brown, Katherine H. Huang, Christopher M. Lee, 2019, Cell.

Ascertaining cells’ synaptic connections and RNA expression simultaneously with massively barcoded rabies virus libraries

S. Mccarroll, B. Sabatini, J. Nemesh, 2021, bioRxiv.

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics

Nicola J. Rinaldi, Ian C. McDowell, Christopher D. Brown, 2018, Nature Communications.

A marmoset brain cell census reveals influence of developmental origin and functional class on neuronal identity

Fenna M. Krienen, Edwatrd S. Boyden, S. Mccarroll, 2023, bioRxiv.

Long non-coding RNA gene regulation and trait associations across human tissues

Ellen, Christopher D. Brown, Benjamin J. Strober, 2019, bioRxiv.

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics

Mary Goldman, Brian Craft, Jingchun Zhu, 2016, Nature Communications.

Exploring the Phenotypic Consequences of Tissue Specific Gene Exploring the Phenotypic Consequences of Tissue Specific Gene Expression Variation Inferred from GWAS Summary Statistics Expression Variation Inferred from GWAS Summary Statistics

Ian C. McDowell, Christopher D. Brown, Eun Yong Kang, 2021 .

Structural forms of the human amylase locus and their relationships to SNPs, haplotypes, and obesity

R. Handsaker, S. Mccarroll, D. Altshuler, 2015, Nature Genetics.

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

Ryan L. Collins, Ryan M. Layer, Gabor T. Marth, 2018, Nature Genetics.

A marmoset brain cell census reveals regional specialization of cellular identities

Fenna M. Krienen, S. Mccarroll, Melissa Goldman, 2023, Science advances.

A concerted neuron–astrocyte program declines in ageing and schizophrenia

R. Handsaker, S. Mccarroll, Melissa Goldman, 2024, Nature.

A vast resource of allelic expression data spanning human tissues

Christopher M. Lee, Benjamin J. Strober, Jared L. Nedzel, 2019, Genome Biology.