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Author Details

Kevin S Smith
Stanford University
1997
38
26
PMIDPaper TitleJournal TitlePublished Year
35298243Multiple causal variants underlie genetic associations in humans.Science2022
35298243Multiple causal variants underlie genetic associations in humans.Science2022
32483373C9orf72 suppresses systemic and neural inflammation induced by gut bacteria.Nature2020
32483373C9orf72 suppresses systemic and neural inflammation induced by gut bacteria.Nature2020
31235787Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure.Nat Commun2019
31684996Genetic regulation of gene expression and splicing during a 10-year period of human aging.Genome Biol2019
31235787Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure.Nat Commun2019
31684996Genetic regulation of gene expression and splicing during a 10-year period of human aging.Genome Biol2019
28869759p75 neurotrophin receptor interacts with and promotes BACE1 localization in endosomes aggravating amyloidogenesis.J Neurochem2018
28640241Long-read genome sequencing identifies causal structural variation in a Mendelian disease.Genet Med2018
28869759p75 neurotrophin receptor interacts with and promotes BACE1 localization in endosomes aggravating amyloidogenesis.J Neurochem2018
28640241Long-read genome sequencing identifies causal structural variation in a Mendelian disease.Genet Med2018
27799337Small RNA Sequencing in Cells and Exosomes Identifies eQTLs and 14q32 as a Region of Active Export.G3 (Bethesda)2017
28332630PML nuclear bodies contribute to the basal expression of the mTOR inhibitor DDIT4.Sci Rep2017
28394350Population- and individual-specific regulatory variation in Sardinia.Nat Genet2017
28251733Whole-transcriptome sequencing in blood provides a diagnosis of spinal muscular atrophy with progressive myoclonic epilepsy.Hum Mutat2017
27799337Small RNA Sequencing in Cells and Exosomes Identifies eQTLs and 14q32 as a Region of Active Export.G3 (Bethesda)2017
28251733Whole-transcriptome sequencing in blood provides a diagnosis of spinal muscular atrophy with progressive myoclonic epilepsy.Hum Mutat2017
28332630PML nuclear bodies contribute to the basal expression of the mTOR inhibitor DDIT4.Sci Rep2017
28394350Population- and individual-specific regulatory variation in Sardinia.Nat Genet2017
27197214Impact of the X Chromosome and sex on regulatory variation.Genome Res2016
27197214Impact of the X Chromosome and sex on regulatory variation.Genome Res2016
25711805Characterization and changes in neurotrophin receptor p75-Expressing motor neurons in SOD1(G93A) G1H mice [corrected].J Comp Neurol2015
25848752Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse.Nat Genet2015
25711805Characterization and changes in neurotrophin receptor p75-Expressing motor neurons in SOD1(G93A) G1H mice [corrected].J Comp Neurol2015
25954003Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.Science2015
25953952The landscape of genomic imprinting across diverse adult human tissues.Genome Res2015
26311362MLL leukemia induction by genome editing of human CD34+ hematopoietic cells.Blood2015
26588248Conditional Expression of E2A-HLF Induces B-Cell Precursor Death and Myeloproliferative-Like Disease in Knock-In Mice.PLoS One2015
26382029Characterization and changes in neurotrophin receptor p75-expressing motor neurons in SOD1(G⁹³A) G1H mice.J Comp Neurol2015
26382029Characterization and changes in neurotrophin receptor p75-expressing motor neurons in SOD1(G⁹³A) G1H mice.J Comp Neurol2015
26588248Conditional Expression of E2A-HLF Induces B-Cell Precursor Death and Myeloproliferative-Like Disease in Knock-In Mice.PLoS One2015
26311362MLL leukemia induction by genome editing of human CD34+ hematopoietic cells.Blood2015
25848752Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse.Nat Genet2015
25954003Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.Science2015
25953952The landscape of genomic imprinting across diverse adult human tissues.Genome Res2015
24270603Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.Nat Methods2014
25352776Non-viral gene therapy that targets motor neurons in vivo.Front Mol Neurosci2014
24270603Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.Nat Methods2014
25192044Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants.Am J Hum Genet2014
24805851Transcriptome analysis reveals differential splicing events in IPF lung tissue.PLoS One2014
24786518Allelic expression of deleterious protein-coding variants across human tissues.PLoS Genet2014
24647608Transcriptome analysis reveals differential splicing events in IPF lung tissue.PLoS One2014
25251678High-resolution transcriptome analysis with long-read RNA sequencing.PLoS One2014
25251678High-resolution transcriptome analysis with long-read RNA sequencing.PLoS One2014
25192044Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants.Am J Hum Genet2014
25352776Non-viral gene therapy that targets motor neurons in vivo.Front Mol Neurosci2014
24805851Transcriptome analysis reveals differential splicing events in IPF lung tissue.PLoS One2014
24786518Allelic expression of deleterious protein-coding variants across human tissues.PLoS Genet2014
24647608Transcriptome analysis reveals differential splicing events in IPF lung tissue.PLoS One2014
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Collaborators

Stephen B Montgomery
Stanford University
Co-authored papers 20
Xin Li
Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences
Co-authored papers 9
Kimberly R Kukurba
Co-authored papers 8
Alexis Battle
Johns Hopkins University School of Medicine
Co-authored papers 6
Zachary Zappala
Vertex Pharmaceuticals
Co-authored papers 5
Jin Billy Li
Co-authored papers 5
David A Knowles
Co-authored papers 5
Rui Zhang
Co-authored papers 5
Joe R Davis
Stanford University School of Medicine
Co-authored papers 4
Michael J Gloudemans
Co-authored papers 4
Daniel G MacArthur
Broad Institute of MIT and Harvard
Co-authored papers 4
Emily K Tsang
Co-authored papers 4
Sara Mostafavi
University of British Columbia and BC Children's Hospital
Co-authored papers 3
Konrad J Karczewski
Broad Institute of MIT and Harvard
Co-authored papers 3
Nathan S Abell
Co-authored papers 3
Taru Tukiainen
Co-authored papers 2
Francesco Cucca
University of Sassari
Co-authored papers 2
Matthew T Wheeler
Stanford University School of Medicine
Co-authored papers 2
Matti Pirinen
Co-authored papers 2
Manuel A Rivas
Stanford University School of Medicine
Co-authored papers 2
Chenwei Lin
Clinical Research Division, Fred Hutchinson Cancer Center
Co-authored papers 2
Monkol Lek
Co-authored papers 2
David Schlessinger
NIH/National Institute of Ageing
Co-authored papers 2
Daryl Waggott
Ontario Institute for Cancer Research
Co-authored papers 2
Tuuli Lappalainen
Columbia University
Co-authored papers 2
Brunilda Balliu
Co-authored papers 2
Euan A Ashley
Stanford University
Co-authored papers 2
Laure Fr??sard
Invitae Corporation
Co-authored papers 2
Serena Sanna
Co-authored papers 1
Victoria N Parikh
Stanford University
Co-authored papers 1
Release 1.2