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Kelly A Frazer

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 24

Top Venues

Nature communications

Nature genetics

Blood

PLoS genetics

University of California San Diego Health Sciences

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of California San Diego Health Sciences

United States

Professor

Publications

Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, null null, Hiroko Matsui, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease. Nature communications 14 (1) (2023)
Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, null null, Hiroko Matsui, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease. Nature communications 14 (1) (2023)
Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, null null, Hiroko Matsui, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease. Nature communications 14 (1) (2023)
Jennifer P Nguyen, Timothy D Arthur, Kyohei Fujita, Bianca M Salgado, Margaret K R Donovan, null null, Hiroko Matsui, Ji Hyun Kim, Agnieszka D'Antonio-Chronowska, Matteo D'Antonio, Kelly A Frazer
eQTL mapping in fetal-like pancreatic progenitor cells reveals early developmental insights into diabetes risk. Nature communications 14 (1) (2023)
Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, null null, Hiroko Matsui, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease. Nature communications 14 (1) (2023)
Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, null null, Hiroko Matsui, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
Author Correction: Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease. Nature communications 14 (1) (2023)
Matteo D'Antonio, Jennifer P Nguyen, Timothy D Arthur, Hiroko Matsui, Margaret K R Donovan, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms. PLoS computational biology 18 (2) (2022)
Jian Yan, Yunjiang Qiu, André M Ribeiro Dos Santos, Yimeng Yin, Yang Eric Li, Nick Vinckier, Naoki Nariai, Paola Benaglio, Anugraha Raman, Xiaoyu Li, Shicai Fan, Joshua Chiou, Fulin Chen, Kelly A Frazer, Kyle J Gaulton, Bjoern Gaertner, Jussi Taipale, Bing Ren
Systematic analysis of binding of transcription factors to noncoding variants. Nature 591 (7848) (2021)
Pooja Biswas, Adda L Villanueva, Angel Soto-Hermida, Jacque L Duncan, Hiroko Matsui, Shyamanga Borooah, Berzhan Kurmanov, Gabriele Richard, Shahid Y Khan, Kari Branham, Bonnie Huang, John Suk, Benjamin Bakall, Jeffrey Louis Goldberg, Luis Gabriel, Naheed W Khan, Pongali B Raghavendra, Jason Zhou, Sindhu Devalaraja, Andrew Huynh, Akhila N Alapati, Qais Zawaydeh, Richard G Weleber, John R Heckenlively, James Fielding Hejtmancik, Sheikh Riazuddin, Paul A Sieving, S Amer Riazuddin, Kelly A Frazer, Radha Ayyagari
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis. PLoS genetics 17 (10) (2021)
Matteo D'Antonio, null null, Timothy D Arthur, Jennifer P Nguyen, Hiroko Matsui, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
Insights into genetic factors contributing to variability in SARS-CoV-2 susceptibility and COVID-19 disease severity. medRxiv : the preprint server for health sciences (2021)
Marc Jan Bonder, Craig Smail, Michael J Gloudemans, Laure Frésard, David Jakubosky, Matteo D'Antonio, Xin Li, Nicole M Ferraro, Ivan Carcamo-Orive, Bogdan Mirauta, Daniel D Seaton, Na Cai, Dara Vakili, Danilo Horta, Chunli Zhao, Diane B Zastrow, Devon E Bonner, null null, null null, null null, null null, Matthew T Wheeler, Helena Kilpinen, Joshua W Knowles, Erin N Smith, Kelly A Frazer, Stephen B Montgomery, Oliver Stegle
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. Nature genetics 53 (3) (2021)
David Jakubosky, Matteo D'Antonio, Marc Jan Bonder, Craig Smail, Margaret K R Donovan, William W Young Greenwald, Hiroko Matsui, null null, Agnieszka D'Antonio-Chronowska, Oliver Stegle, Erin N Smith, Stephen B Montgomery, Christopher DeBoever, Kelly A Frazer
Properties of structural variants and short tandem repeats associated with gene expression and complex traits. Nature communications 11 (1) (2020)
Margaret K R Donovan, Agnieszka D'Antonio-Chronowska, Matteo D'Antonio, Kelly A Frazer
Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants. Nature communications 11 (1) (2020)
Tomoyuki Koga, Isaac A Chaim, Jorge A Benitez, Sebastian Markmiller, Alison D Parisian, Robert F Hevner, Kristen M Turner, Florian M Hessenauer, Matteo D'Antonio, Nam-Phuong D Nguyen, Shahram Saberi, Jianhui Ma, Shunichiro Miki, Antonia D Boyer, John Ravits, Kelly A Frazer, Vineet Bafna, Clark C Chen, Paul S Mischel, Gene W Yeo, Frank B Furnari
Author Correction: Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells. Nature communications 11 (1) (2020)
David Jakubosky, Erin N Smith, Matteo D'Antonio, Marc Jan Bonder, William W Young Greenwald, Agnieszka D'Antonio-Chronowska, Hiroko Matsui, null null, Oliver Stegle, Stephen B Montgomery, Christopher DeBoever, Kelly A Frazer
Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats. Nature communications 11 (1) (2020)
Margaret K R Donovan, Agnieszka D'Antonio-Chronowska, Matteo D'Antonio, Kelly A Frazer
Author Correction: Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants. Nature communications 11 (1) (2020)
Tomoyuki Koga, Isaac A Chaim, Jorge A Benitez, Sebastian Markmiller, Alison D Parisian, Robert F Hevner, Kristen M Turner, Florian M Hessenauer, Matteo D'Antonio, Nam-Phuong D Nguyen, Shahram Saberi, Jianhui Ma, Shunichiro Miki, Antonia D Boyer, John Ravits, Kelly A Frazer, Vineet Bafna, Clark C Chen, Paul S Mischel, Gene W Yeo, Frank B Furnari
Longitudinal assessment of tumor development using cancer avatars derived from genetically engineered pluripotent stem cells. Nature communications 11 (1) (2020)
Emanuela M Ghia, Laura Z Rassenti, Donna S Neuberg, Alejandro Blanco, Fouad Yousif, Erin N Smith, John D McPherson, Thomas J Hudson, null null, Olivier Harismendy, Kelly A Frazer, Thomas J Kipps
Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia. Blood 133 (25) (2019)
Matteo D'Antonio, Joaquin Reyna, David Jakubosky, Margaret Kr Donovan, Marc-Jan Bonder, Hiroko Matsui, Oliver Stegle, Naoki Nariai, Agnieszka D'Antonio-Chronowska, Kelly A Frazer
Systematic genetic analysis of the MHC region reveals mechanistic underpinnings of HLA type associations with disease. eLife 8 (2019)
Paola Benaglio, Agnieszka D'Antonio-Chronowska, Wubin Ma, Feng Yang, William W Young Greenwald, Margaret K R Donovan, Christopher DeBoever, He Li, Frauke Drees, Sanghamitra Singhal, Hiroko Matsui, Jessica van Setten, Nona Sotoodehnia, Kyle J Gaulton, Erin N Smith, Matteo D'Antonio, Michael G Rosenfeld, Kelly A Frazer
Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits. Nature genetics 51 (10) (2019)
Lori Broderick, Shawn Yost, Dong Li, Matthew D McGeough, Laela M Booshehri, Marisela Guaderrama, Susannah D Brydges, Karolina Kucharova, Niraj C Patel, Margaret Harr, Hakon H Hakonarson, Elaine Zackai, Ian G Cowell, Caroline A Austin, Boris Hügle, Corinna Gebauer, Jianguo Zhang, Xue Liu, Jian Wang, Ben A Croker, Kelly A Frazer, Christopher D Putnam, Hal M Hoffman
Mutations in topoisomerase IIβ result in a B cell immunodeficiency. Nature communications 10 (1) (2019)
Naoki Nariai, William W Greenwald, Christopher DeBoever, He Li, Kelly A Frazer
Efficient Prioritization of Multiple Causal eQTL Variants via Sparse Polygenic Modeling. Genetics 207 (4) (2017)
Kevin Gustafson, Jacque L Duncan, Pooja Biswas, Angel Soto-Hermida, Hiroko Matsui, David Jakubosky, John Suk, Amalio Telenti, Kelly A Frazer, Radha Ayyagari
Correction: Gustafson et al., Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes 2017, 8, 210. Genes 8 (10) (2017)
Bing Cui, Emanuela M Ghia, Liguang Chen, Laura Z Rassenti, Christopher DeBoever, George F Widhopf, Jian Yu, Donna S Neuberg, William G Wierda, Kanti R Rai, Neil E Kay, Jennifer R Brown, Jeffrey A Jones, John G Gribben, Kelly A Frazer, Thomas J Kipps
High-level ROR1 associates with accelerated disease progression in chronic lymphocytic leukemia. Blood 128 (25) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Kelly A Frazer