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Author Details

Jared C Roach
Institute for Systems Biology
1995
76
36
PMIDPaper TitleJournal TitlePublished Year
36752514ARAX: a graph-based modular reasoning tool for translational biomedicine.Bioinformatics2023
38012377Author Correction: Lifespan-extending interventions induce consistent patterns of fatty acid oxidation in mouse livers.Commun Biol2023
37481675Lifespan-extending interventions induce consistent patterns of fatty acid oxidation in mouse livers.Commun Biol2023
36175836RTX-KG2: a system for building a semantically standardized knowledge graph for translational biomedicine.BMC Bioinformatics2022
35546635Rare variants implicate NMDA receptor signaling and cerebellar gene networks in risk for bipolar disorder.Mol Psychiatry2022
35733645Dense data enables 21st century clinical trials.Alzheimers Dement (N Y)2022
36679852Reinfection with SARS-CoV-2 and Waning Humoral Immunity: A Case Report.Vaccines (Basel)2022
35910672The Coaching for Cognition in Alzheimer's (COCOA) trial: Study design.Alzheimers Dement (N Y)2022
34295960A systems-biology clinical trial of a personalized multimodal lifestyle intervention for early Alzheimer's disease.Alzheimers Dement (N Y)2021
35237464Case Study: A Precision Medicine Approach to Multifactorial Dementia and Alzheimer's Disease.J Alzheimers Dis Parkinsonism2021
32995830Reinfection with SARS-CoV-2 and Failure of Humoral Immunity: a case report.medRxiv2020
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
30833390Genomic and molecular characterization of preterm birth.Proc Natl Acad Sci U S A2019
29691419Author Correction: A population-specific reference panel empowers genetic studies of Anabaptist populations.Sci Rep2018
30291356Author Correction: Parent-of-origin-specific signatures of de novo mutations.Nat Genet2018
29750799Population-specific genetic modification of Huntington's disease in Venezuela.PLoS Genet2018
28729679A population-specific reference panel empowers genetic studies of Anabaptist populations.Sci Rep2017
28448578Evolutionary history of Tibetans inferred from whole-genome sequencing.PLoS Genet2017
27081563Genomic architecture of inflammatory bowel disease in five families with multiple affected individuals.Hum Genome Var2016
27322544Parent-of-origin-specific signatures of de novo mutations.Nat Genet2016
25285920A gain-of-function mutation in TRPV3 causes focal palmoplantar keratoderma in a Chinese family.J Invest Dermatol2015
26299364Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.Am J Hum Genet2015
26324103Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease.Mol Psychiatry2015
26322789Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.PLoS One2015
26320893Sequence-Level Analysis of the Major European Huntington Disease Haplotype.Am J Hum Genet2015
26681308A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51.Nat Commun2015
25996915Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.PLoS One2015
25730879Rare variants in neuronal excitability genes influence risk for bipolar disorder.Proc Natl Acad Sci U S A2015
25741365Identification of copy number variants in whole-genome data using Reference Coverage Profiles.Front Genet2015
24239249Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease.Alzheimers Dement2014
25473435Whole-genome haplotyping approaches and genomic medicine.Genome Med2014
25390934Whole-genome sequencing of the world's oldest people.PLoS One2014
25362483Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes.Nat Genet2014
25091416Diffuse angiopathy in Adams-Oliver syndrome associated with truncating DOCK6 mutations.Am J Med Genet A2014
25132448Mutations in NOTCH1 cause Adams-Oliver syndrome.Am J Hum Genet2014
24837662A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.Nat Biotechnol2014
24586241Accurate and robust prediction of genetic relationship from whole-genome sequences.PLoS One2014
24667040An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.Genome Biol2014
24497848Relationship estimation from whole-genome sequence data.PLoS Genet2014
27447256Predictive Analytics In Healthcare: Medications as a Predictor of Medical Complexity.Big Data2013
22696644Paramecium bursaria chlorella virus 1 proteome reveals novel architectural and regulatory features of a giant virus.J Virol2012
21250827Design and initial characterization of the SC-200 proteomics standard mixture.OMICS2011
21855840Chromosomal haplotypes by genetic phasing of human families.Am J Hum Genet2011
21965822Kaviar: an accessible system for testing SNV novelty.Bioinformatics2011
20220176Analysis of genetic inheritance in a family quartet by whole-genome sequencing.Science2010
20445565The association between the PTPN22 1858C>T variant and type 1 diabetes depends on HLA risk and GAD65 autoantibodies.Genes Immun2010
19284633TFCat: the curated catalog of mouse and human transcription factors.Genome Biol2009
18369420Uncovering a macrophage transcriptional program by integrating evidence from motif scanning and expression dynamics.PLoS Comput Biol2008
19090620High functional diversity in Mycobacterium tuberculosis driven by genetic drift and human demography.PLoS Biol2008
18321385The Innate Immune Database (IIDB).BMC Immunol2008
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Collaborators

Leroy Hood
Center for Phenomic Health, The Buck Institute for Research on Aging
Co-authored papers 38
Gustavo Glusman
Institute for Systems Biology
Co-authored papers 32
Andrew F Siegel
University of Washington
Co-authored papers 8
Chad D Huff
University of Texas M.D. Anderson Cancer Center
Co-authored papers 7
Alan Aderem
Seattle Children's Research Institute
Co-authored papers 6
Lynn B Jorde
University of Utah School of Medicine
Co-authored papers 6
Arian F A Smit
Co-authored papers 6
Robert Hubley
Co-authored papers 5
David W Craig
University of Southern California
Co-authored papers 5
Inyoul Lee
Co-authored papers 5
Seth A Ament
Institute for Genome Sciences, University of Maryland School of Medicine
Co-authored papers 5
Nathan D Price
Institute for Systems Biology
Co-authored papers 4
Ilya Shmulevich
Institute for Systems Biology
Co-authored papers 4
Juan Caballero
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 4
Vesteinn Thorsson
Institute for Systems Biology
Co-authored papers 4
Benjamin D Solomon
Co-authored papers 4
Cory C Funk
Institute for Systems Biology
Co-authored papers 4
Nicholas J Schork
University of California San Diego
Co-authored papers 4
Howard J Edenberg
Indiana University School of Medicine
Co-authored papers 3
Christian Gilissen
Radboud University Medical Center
Co-authored papers 3
Liping Hou
Harrison International Peace Hospital
Co-authored papers 3
Stephen A Ramsey
Oregon State University
Co-authored papers 3
Elliot S Gershon
University of Chicago
Co-authored papers 3
John I Nurnberger
Stark Neurosciences Research Institute, Indiana University School of Medicine
Co-authored papers 3
Francis J McMahon
National Institute of Mental Health, National Institutes of Health
Co-authored papers 3
James R Heath
Institute of Systems Biology, University of Washington
Co-authored papers 3
Judith A Badner
Rush University Medical College
Co-authored papers 3
Hao Hu
Aerospace Center Hospital
Co-authored papers 3
Tatyana Shekhtman
University of California
Co-authored papers 3
John R Kelsoe
University of California
Co-authored papers 3
Release 1.2