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Author Details

Rui Chen
Stanford University
2010
31
20
Emma Lundberg (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
35717667Analysis of the global origin, evolution and transmission dynamics of the emerging novel variant IBDV (A2dB1b): The accumulation of critical aa-residue mutations and commercial trade contributes to the emergence and transmission of novel variants.Transbound Emerg Dis2022
35671065Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy.Circ Genom Precis Med2022
35717667Analysis of the global origin, evolution and transmission dynamics of the emerging novel variant IBDV (A2dB1b): The accumulation of critical aa-residue mutations and commercial trade contributes to the emergence and transmission of novel variants.Transbound Emerg Dis2022
35671065Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy.Circ Genom Precis Med2022
33785037Circulating exosomal mRNA profiling identifies novel signatures for the detection of prostate cancer.Mol Cancer2021
33785037Circulating exosomal mRNA profiling identifies novel signatures for the detection of prostate cancer.Mol Cancer2021
32285405Online Databases and Non-coding RNAs in Cardiovascular Diseases.Adv Exp Med Biol2020
32285405Online Databases and Non-coding RNAs in Cardiovascular Diseases.Adv Exp Med Biol2020
29616851Distinct transcriptomic and exomic abnormalities within myelodysplastic syndrome marrow cells.Leuk Lymphoma2018
30397358Longitudinal personal DNA methylome dynamics in a human with a chronic condition.Nat Med2018
29616851Distinct transcriptomic and exomic abnormalities within myelodysplastic syndrome marrow cells.Leuk Lymphoma2018
30397358Longitudinal personal DNA methylome dynamics in a human with a chronic condition.Nat Med2018
28126021De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease.Genome Med2017
28362264Small-Magnitude Effect Sizes in Epigenetic End Points are Important in Children's Environmental Health Studies: The Children's Environmental Health and Disease Prevention Research Center's Epigenetics Working Group.Environ Health Perspect2017
28126021De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease.Genome Med2017
28362264Small-Magnitude Effect Sizes in Epigenetic End Points are Important in Children's Environmental Health Studies: The Children's Environmental Health and Disease Prevention Research Center's Epigenetics Working Group.Environ Health Perspect2017
25762417Whole-Exome Enrichment with the Agilent SureSelect Human All Exon Platform.Cold Spring Harb Protoc2015
25762419Whole-Exome Enrichment with the Roche NimbleGen SeqCap EZ Exome Library SR Platform.Cold Spring Harb Protoc2015
25762418Whole-Exome Enrichment with the Illumina TruSeq Exome Enrichment Platform.Cold Spring Harb Protoc2015
25762417Whole-Exome Enrichment with the Agilent SureSelect Human All Exon Platform.Cold Spring Harb Protoc2015
26030479RNA Sequencing Analysis Detection of a Novel Pathway of Endothelial Dysfunction in Pulmonary Arterial Hypertension.Am J Respir Crit Care Med2015
26030479RNA Sequencing Analysis Detection of a Novel Pathway of Endothelial Dysfunction in Pulmonary Arterial Hypertension.Am J Respir Crit Care Med2015
25762419Whole-Exome Enrichment with the Roche NimbleGen SeqCap EZ Exome Library SR Platform.Cold Spring Harb Protoc2015
25762418Whole-Exome Enrichment with the Illumina TruSeq Exome Enrichment Platform.Cold Spring Harb Protoc2015
24111759Distinct splice variants and pathway enrichment in the cell-line models of aggressive human breast cancer subtypes.J Proteome Res2014
24456465Toward more transparent and reproducible omics studies through a common metadata checklist and data publications.OMICS2014
24111759Distinct splice variants and pathway enrichment in the cell-line models of aggressive human breast cancer subtypes.J Proteome Res2014
24651605Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway.Genet Med2014
24561555Whole-genome haplotyping using long reads and statistical methods.Nat Biotechnol2014
24561555Whole-genome haplotyping using long reads and statistical methods.Nat Biotechnol2014
24651605Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway.Genet Med2014
24456465Toward more transparent and reproducible omics studies through a common metadata checklist and data publications.OMICS2014
23184638Promise of personalized omics to precision medicine.Wiley Interdiscip Rev Syst Biol Med2013
27447251Toward More Transparent and Reproducible Omics Studies Through a Common Metadata Checklist and Data Publications.Big Data2013
24264604Specific plasma autoantibody reactivity in myelodysplastic syndromes.Sci Rep2013
23830146Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.J Allergy Clin Immunol2013
23184638Promise of personalized omics to precision medicine.Wiley Interdiscip Rev Syst Biol Med2013
23259914A chromosome-centric human proteome project (C-HPP) to characterize the sets of proteins encoded in chromosome 17.J Proteome Res2013
23547016Exome sequencing by targeted enrichment.Curr Protoc Mol Biol2013
27447251Toward More Transparent and Reproducible Omics Studies Through a Common Metadata Checklist and Data Publications.Big Data2013
24264604Specific plasma autoantibody reactivity in myelodysplastic syndromes.Sci Rep2013
23830146Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.J Allergy Clin Immunol2013
23547016Exome sequencing by targeted enrichment.Curr Protoc Mol Biol2013
23259914A chromosome-centric human proteome project (C-HPP) to characterize the sets of proteins encoded in chromosome 17.J Proteome Res2013
22398612The Chromosome-Centric Human Proteome Project for cataloging proteins encoded in the genome.Nat Biotechnol2012
22398614Detecting and annotating genetic variations using the HugeSeq pipeline.Nat Biotechnol2012
22398612The Chromosome-Centric Human Proteome Project for cataloging proteins encoded in the genome.Nat Biotechnol2012
22424236Personal omics profiling reveals dynamic molecular and medical phenotypes.Cell2012
22517884Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.Sci Transl Med2012
22858243Systems biology: personalized medicine for the future?Curr Opin Pharmacol2012
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Collaborators

Michael Snyder
Stanford University
Co-authored papers 27
Hogune Im
Genome Opinion Inc.
Co-authored papers 10
George I Mias
Michigan State University
Co-authored papers 7
William S Hancock
Northeastern University
Co-authored papers 5
Gilbert S Omenn
and School of Public Health, University of Michigan ann arbor
Co-authored papers 5
Euan A Ashley
Stanford University
Co-authored papers 4
Rong Chen
Co-authored papers 4
Mark Gerstein
Yale University
Co-authored papers 4
Atul J Butte
Bakar Computational Health Sciences Institute, University of California san francisco
Co-authored papers 4
Lihua Jiang
Stanford University
Co-authored papers 3
Frederick E Dewey
Co-authored papers 3
Ghia Euskirchen
Co-authored papers 3
Mathias Uhl??n
KTH Royal Institute of Technology
Co-authored papers 2
Brynn H Voy
Co-authored papers 2
Sanjay Joshi
Co-authored papers 2
Peter Uetz
Center for the Study of Biological Complexity, Virginia Commonwealth University
Co-authored papers 2
Larry Smarr
Co-authored papers 2
Sanjeeva Srivastava
Indian Institute of Technology Bombay
Co-authored papers 2
Imre Janko
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Larissa Stanberry
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Seul-Ki Jeong
Seul-Ki Jeong Neurology Clinic
Co-authored papers 2
Kenneth Verheggen
Co-authored papers 2
Isaac S Kohane
Harvard Medical School
Co-authored papers 2
Natali Kolker
Co-authored papers 2
Geoffrey Fox
Co-authored papers 2
Robert L Grossman
University of Chicago
Co-authored papers 2
Mara H Hutz
Co-authored papers 2
Young-Ki Paik
College of Life Sciences and Biotechnology, Yonsei University
Co-authored papers 2
Courtney MacNealy-Koch
Co-authored papers 2
Joseph W Kemnitz
Co-authored papers 2
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