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Author Details

Tina Graves
McDonnell Genome Institute, Washington University
1998
86
58
Christopher Churas (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
35290762Familial long-read sequencing increases yield of de novo mutations.Am J Hum Genet2022
35962045Author Correction: Comparative and demographic analysis of orang-utan genomes.Nature2022
35444317The Human Pangenome Project: a global resource to map genomic diversity.Nature2022
35290762Familial long-read sequencing increases yield of de novo mutations.Am J Hum Genet2022
35444317The Human Pangenome Project: a global resource to map genomic diversity.Nature2022
35962045Author Correction: Comparative and demographic analysis of orang-utan genomes.Nature2022
33664263A chromosome-level genome of Astyanax mexicanus surface fish for comparing population-specific genetic differences contributing to trait evolution.Nat Commun2021
33664263A chromosome-level genome of Astyanax mexicanus surface fish for comparing population-specific genetic differences contributing to trait evolution.Nat Commun2021
33828295The structure, function and evolution of a complete human chromosome 8.Nature2021
33828295The structure, function and evolution of a complete human chromosome 8.Nature2021
33090996A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism.PLoS Genet2020
33208454Sequence analysis in <i>Bos taurus</i> reveals pervasiveness of X-Y arms races in mammalian lineages.Genome Res2020
33090996A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism.PLoS Genet2020
33335035Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility.Science2020
33335035Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility.Science2020
33208454Sequence analysis in <i>Bos taurus</i> reveals pervasiveness of X-Y arms races in mammalian lineages.Genome Res2020
30661756Characterizing the Major Structural Variant Alleles of the Human Genome.Cell2019
30559433Long-read sequence and assembly of segmental duplications.Nat Methods2019
30661756Characterizing the Major Structural Variant Alleles of the Human Genome.Cell2019
30559433Long-read sequence and assembly of segmental duplications.Nat Methods2019
29295848Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data.Genome Res2018
29880660High-resolution comparative analysis of great ape genomes.Science2018
29295848Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data.Genome Res2018
29686068Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (<i>CFH</i>) gene family.Proc Natl Acad Sci U S A2018
29880660High-resolution comparative analysis of great ape genomes.Science2018
29686068Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (<i>CFH</i>) gene family.Proc Natl Acad Sci U S A2018
27895111Discovery and genotyping of structural variation from long-read haploid genome sequence data.Genome Res2017
28864551Corrigendum: The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2.Genome Res2017
28580430The evolution and population diversity of human-specific segmental duplications.Nat Ecol Evol2017
28396521Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.Genome Res2017
27895111Discovery and genotyping of structural variation from long-read haploid genome sequence data.Genome Res2017
27852011A New Chicken Genome Assembly Provides Insight into Avian Genome Structure.G3 (Bethesda)2017
28135246Avian W and mammalian Y chromosomes convergently retained dosage-sensitive regulators.Nat Genet2017
28135246Avian W and mammalian Y chromosomes convergently retained dosage-sensitive regulators.Nat Genet2017
28396521Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.Genome Res2017
28580430The evolution and population diversity of human-specific segmental duplications.Nat Ecol Evol2017
28864551Corrigendum: The evolution of African great ape subtelomeric heterochromatin and the fusion of human chromosome 2.Genome Res2017
27852011A New Chicken Genome Assembly Provides Insight into Avian Genome Structure.G3 (Bethesda)2017
27029710A genomic case study of mixed fibrolamellar hepatocellular carcinoma.Ann Oncol2016
27029710A genomic case study of mixed fibrolamellar hepatocellular carcinoma.Ann Oncol2016
27803192Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region.Genome Res2016
27803192Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region.Genome Res2016
25338678Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity.Genes Immun2015
25338678Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity.Genes Immun2015
26377836The genome of the vervet (Chlorocebus aethiops sabaeus).Genome Res2015
26377836The genome of the vervet (Chlorocebus aethiops sabaeus).Genome Res2015
24418700Reconstructing complex regions of genomes using long-read sequencing technology.Genome Res2014
25417157Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes.Cell2014
25373144Single haplotype assembly of the human genome from a hydatidiform mole.Genome Res2014
25326701Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability.Nat Genet2014
  • 1 - 50 of 172

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Collaborators

Richard K Wilson
The Ohio State University
Co-authored papers 67
Evan E Eichler
University of Washington
Co-authored papers 45
Wesley C Warren
Institute of Informatics and Data Sciences, University of Missouri
Co-authored papers 34
Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 30
LaDeana W Hillier
University of Washington
Co-authored papers 24
Elaine R Mardis
The Ohio State University
Co-authored papers 22
Lucinda Fulton
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 20
Paul Flicek
European Bioinformatics Institute
Co-authored papers 12
Ze Cheng
University of Washington School of Medicine
Co-authored papers 10
Can Alkan
Bilkent University
Co-authored papers 10
Richard A Gibbs
Baylor College of Medicine
Co-authored papers 10
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University of California san francisco
Co-authored papers 10
Helen Skaletsky
Co-authored papers 10
Donna M Muzny
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David Haussler
Genomics Institute, University of California Santa Cruz
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Jeffrey M Kidd
University of Michigan Medical School ann arbor
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Catrina Fronick
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Chris P Ponting
The University of Edinburgh
Co-authored papers 9
Carl Baker
University of Washington School of Medicine
Co-authored papers 8
John D McPherson
Ontario Institute for Cancer Research
Co-authored papers 8
David C Page
Co-authored papers 8
George M Weinstock
The Genome Center at Washington University, Washington University School of Medicine
Co-authored papers 8
Laura G Brown
Co-authored papers 8
Webb Miller
Co-authored papers 8
Deanna M Church
Present address: Inscripta Inc.
Co-authored papers 7
Steven T Rosen
Co-authored papers 7
Michael C Zody
Broad Institute of Harvard and MIT
Co-authored papers 7
Kim C Worley
Baylor College of Medicine
Co-authored papers 7
Pieter J de Jong
Center for Genetics, Children's Hospital Oakland Research Institute
Co-authored papers 6
David C Schwartz
University of Wisconsin-Madison
Co-authored papers 6
Release 1.2