Skip to Main Content
CKG
Home
Home
Home
TKG
Author details
Breadcrumb
Author Details
Full Name
Kelly A Frazer
Affiliation
University of California, USA Institute for Genomic Medicine
ORCID
Career Start Year
1967
Papers
159
H Index
59
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36854752
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease.
Nat Commun
2023
37848026
Single-nucleotide variants within heart enhancers increase binding affinity and disrupt heart development.
Dev Cell
2023
37903777
eQTL mapping in fetal-like pancreatic progenitor cells reveals early developmental insights into diabetes risk.
Nat Commun
2023
37474502
Author Correction: Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease.
Nat Commun
2023
36854752
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease.
Nat Commun
2023
37492100
The human pangenome reference anticipates equitable and fundamental genomic insights.
Cell Genom
2023
37292794
Analysis of regulatory network modules in hundreds of human stem cell lines reveals complex epigenetic and genetic factors contribute to pluripotency state differences between subpopulations.
bioRxiv
2023
37492100
The human pangenome reference anticipates equitable and fundamental genomic insights.
Cell Genom
2023
37903777
eQTL mapping in fetal-like pancreatic progenitor cells reveals early developmental insights into diabetes risk.
Nat Commun
2023
37848026
Single-nucleotide variants within heart enhancers increase binding affinity and disrupt heart development.
Dev Cell
2023
37292794
Analysis of regulatory network modules in hundreds of human stem cell lines reveals complex epigenetic and genetic factors contribute to pluripotency state differences between subpopulations.
bioRxiv
2023
37474502
Author Correction: Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease.
Nat Commun
2023
35226669
In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms.
PLoS Comput Biol
2022
36108770
Systems genomics in age-related macular degeneration.
Exp Eye Res
2022
35705058
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues.
Cell Rep
2022
35603230
Ultra-Sharp Nanowire Arrays Natively Permeate, Record, and Stimulate Intracellular Activity in Neuronal and Cardiac Networks.
Adv Funct Mater
2022
36778047
Type 1 diabetes risk genes mediate pancreatic beta cell survival in response to proinflammatory cytokines.
Cell Genom
2022
35226669
In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms.
PLoS Comput Biol
2022
35705058
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues.
Cell Rep
2022
35603230
Ultra-Sharp Nanowire Arrays Natively Permeate, Record, and Stimulate Intracellular Activity in Neuronal and Cardiac Networks.
Adv Funct Mater
2022
36778047
Type 1 diabetes risk genes mediate pancreatic beta cell survival in response to proinflammatory cytokines.
Cell Genom
2022
36108770
Systems genomics in age-related macular degeneration.
Exp Eye Res
2022
33252167
Detection and validation of novel mutations in MERTK in a simplex case of retinal degeneration using WGS and hiPSC-RPEs model.
Hum Mutat
2021
34013287
Insights into genetic factors contributing to variability in SARS-CoV-2 susceptibility and COVID-19 disease severity.
medRxiv
2021
34040254
Enhancer release and retargeting activates disease-susceptibility genes.
Nature
2021
33505025
Systematic analysis of binding of transcription factors to noncoding variants.
Nature
2021
33373444
Genomics Links Inflammation With Neurocognitive Impairment in Children Living With Human Immunodeficiency Virus Type-1.
J Infect Dis
2021
33252167
Detection and validation of novel mutations in MERTK in a simplex case of retinal degeneration using WGS and hiPSC-RPEs model.
Hum Mutat
2021
34662339
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.
PLoS Genet
2021
33505025
Systematic analysis of binding of transcription factors to noncoding variants.
Nature
2021
34662339
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.
PLoS Genet
2021
34040254
Enhancer release and retargeting activates disease-susceptibility genes.
Nature
2021
34013287
Insights into genetic factors contributing to variability in SARS-CoV-2 susceptibility and COVID-19 disease severity.
medRxiv
2021
33373444
Genomics Links Inflammation With Neurocognitive Impairment in Children Living With Human Immunodeficiency Virus Type-1.
J Infect Dis
2021
31582554
Fibrinogen gamma gene <i>rs2066865</i> and risk of cancer-related venous thromboembolism.
Haematologica
2020
32075962
Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants.
Nat Commun
2020
32312984
Author Correction: Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells.
Nat Commun
2020
31582554
Fibrinogen gamma gene <i>rs2066865</i> and risk of cancer-related venous thromboembolism.
Haematologica
2020
31992716
Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells.
Nat Commun
2020
32442913
Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program.
Stem Cell Res
2020
33659414
<i>In vitro</i> Differentiation of Human iPSC-derived Cardiovascular Progenitor Cells (iPSC-CVPCs).
Bio Protoc
2020
32873812
Author Correction: Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants.
Nat Commun
2020
32522985
Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats.
Nat Commun
2020
32888420
Revealing Instability: Genetic Variation Underlies Variability in mESC Pluripotency.
Cell Stem Cell
2020
33659414
<i>In vitro</i> Differentiation of Human iPSC-derived Cardiovascular Progenitor Cells (iPSC-CVPCs).
Bio Protoc
2020
31992716
Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells.
Nat Commun
2020
32075962
Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants.
Nat Commun
2020
32888420
Revealing Instability: Genetic Variation Underlies Variability in mESC Pluripotency.
Cell Stem Cell
2020
32873812
Author Correction: Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants.
Nat Commun
2020
32312984
Author Correction: Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells.
Nat Commun
2020
1 - 50 of 318
Column Actions
Search
Recommended Authors
Marta Gut
Universitat de Barcelona (UB)
Career Start Year
2010
Number of shared co-authors
22
Martin Kircher
Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin
Career Start Year
2008
Number of shared co-authors
12
Mark J Cowley
Children's Cancer Institute, Lowy Cancer Research Centre
Career Start Year
2006
Number of shared co-authors
9
Alison Meynert
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year
2006
Number of shared co-authors
7
Ali Torkamani
Scripps Science Institute
Career Start Year
2005
Number of shared co-authors
20
James G D Prendergast
The Roslin Institute, The University of Edinburgh
Career Start Year
2005
Number of shared co-authors
11
Praveen F Cherukuri
Sanford School of Medicine, University of South Dakota
Career Start Year
2005
Number of shared co-authors
8
Alicia Hawes
Regeneron Pharmaceuticals Inc.
Career Start Year
2004
Number of shared co-authors
80
David W Craig
University of Southern California
Career Start Year
2004
Number of shared co-authors
22
Yufeng Shen
Columbia University
Career Start Year
2002
Number of shared co-authors
26
Paul Scheet
University of Texas M.D. Anderson Cancer Center
Career Start Year
2001
Number of shared co-authors
32
Kai Wang
University of Pennsylvania
Career Start Year
2001
Number of shared co-authors
35
Jan O Korbel
European Bioinformatics Institute (EMBL-EBI)
Career Start Year
2001
Number of shared co-authors
46
Martin S Taylor
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year
2000
Number of shared co-authors
23
Nancy F Hansen
National Human Genome Research Institute, National Institutes of Health
Career Start Year
2000
Number of shared co-authors
45
Shawn Levy
HudsonAlpha Institute for Biotechnology
Career Start Year
1999
Number of shared co-authors
20
Eric E Schadt
Icahn School of Medicine at Mount Sinai
Career Start Year
1998
Number of shared co-authors
65
Sarah J Wheelan
National Human Genome Research Institute, National Institutes of Health
Career Start Year
1998
Number of shared co-authors
16
Michael O Dorschner
University of Washington
Career Start Year
1997
Number of shared co-authors
33
Colin A Semple
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year
1997
Number of shared co-authors
8
Sean McGrath
Harvard T.H. Chan School of Public Health
Career Start Year
1996
Number of shared co-authors
10
John V Pearson
QIMR Berghofer Medical Research Institute
Career Start Year
1996
Number of shared co-authors
7
Jay Shendure
University of Washington
Career Start Year
1996
Number of shared co-authors
33
Unnur Thorsteinsdottir
University of Iceland
Career Start Year
1995
Number of shared co-authors
74
Robert S Fulton
McDonnell Genome Institute, Washington University School of Medicine
Career Start Year
1994
Number of shared co-authors
72
Kimberly F Doheny
Center for Inherited Disease Research, Johns Hopkins School of Medicine
Career Start Year
1993
Number of shared co-authors
48
Francisco M De La Vega
Stanford University School of Medicine
Career Start Year
1991
Number of shared co-authors
19
Gustavo Glusman
Institute for Systems Biology
Career Start Year
1988
Number of shared co-authors
35
Steven E Scherer
Baylor College of Medicine
Career Start Year
1987
Number of shared co-authors
74
Deborah A Nickerson
University of Washington
Career Start Year
1976
Number of shared co-authors
75
row(s) 1 - 30 of 30
Collaborators
Olivier Harismendy
University of California
Co-authored papers
29
Erin N Smith
Department of Pediatrics and Rady's Children's Hospital, University of California
Co-authored papers
28
David R Cox
Rinat (Pfizer Inc.)
Co-authored papers
21
Kristen Jepsen
Institute for Genomic Medicine, University of California San Diego
Co-authored papers
16
Eric J Topol
Universidade Federal de Sao Paulo
Co-authored papers
13
David A Hinds
23andMe Inc.
Co-authored papers
12
Christopher DeBoever
Stanford University
Co-authored papers
12
Edward M Rubin
Co-authored papers
10
Naoki Nariai
Co-authored papers
9
Richard B Schwab
Department of Medicine and Moores Cancer Center, University of California San Diego
Co-authored papers
9
Dennis G Ballinger
Memorial Sloan-Kettering Cancer Center
Co-authored papers
9
Vineet Bafna
University of California San Diego
Co-authored papers
8
Sarah S Murray
University of California San Diego Health System
Co-authored papers
8
Radha Ayyagari
Shiley Eye Institute, University of California San Diego
Co-authored papers
8
Karen Messer
Herbert Wertheim School of Public Health, University of California San Diego
Co-authored papers
8
Paola Benaglio
Co-authored papers
8
Thomas J Kipps
University of California San Diego
Co-authored papers
6
Thomas J Hudson
Ontario Institute for Cancer Research
Co-authored papers
6
Laura Z Rassenti
University of California San Diego
Co-authored papers
6
Mark J Daly
Massachusetts General Hospital
Co-authored papers
6
Inna Dubchak
Lawrence Berkeley National Laboratory
Co-authored papers
6
Nicholas J Schork
University of California San Diego
Co-authored papers
6
Frank B Furnari
University of California San Diego
Co-authored papers
5
Nila Patil
Co-authored papers
5
Bing Ren
Center for Epigenomics, University of California San Diego
Co-authored papers
5
Frits R Rosendaal
Co-authored papers
5
Joshua Chiou
Co-authored papers
4
Lei Bao
Moores Cancer Center, university of california san diego Health System
Co-authored papers
4
Amalio Telenti
Vir Biotechnology Inc.
Co-authored papers
4
Jacque L Duncan
University of California san francisco
Co-authored papers
4
1 - 30