239 Papers
559 Citations
Elad Ziv is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Medicine & Breast cancer. The author has an hindex of 62, co-authored 186 publications. Previous affiliations of Elad Ziv include University of California, Berkeley & New Mexico State University.
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Papers
Creating ethnicity-specific reference intervals for lab tests from EHR data
TL;DR: It is shown that for two lab tests, serum creatinine level and hemoglobin A1C, SIRE-specific reference intervals are more predictive for need for dialysis and development type 2 diabetes than existing reference intervals.
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Polygenic risk score for ulcerative colitis predicts immune checkpoint inhibitor-mediated colitis
Pooja Middha,Rohit Thummalapalli,Michael J Betti,Lydia Yao,Zoe Quandt,Karmugi Balaratnam,Cosmin Adrian Bejan,Eduardo Cardenas,Christina J Falcon,David M Faleck,Matthew A. Gubens,Scott Huntsman,Douglas B. Johnson,Linda Kachuri,Khaleeq Khan,Min Li,Christine M. Lovly,Megan Hollister Murray,Devalben Patel,Kristin Werking,Yaomin Xu,L. Zhan,Justin M. Balko,Geoffrey Liu,Melinda C. Aldrich,Adam J. Schoenfeld,Elad Ziv +26 more
TL;DR: A polygenic risk score for ulcerative colitis (PRSUC) predicts immune checkpoint inhibitor-mediated colitis in cancer patients, identifying those at risk and potentially improving patient outcomes, with a meta-analysis showing a significant association between PRSUC and all-grade and severe IMC.
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Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies
Taylor B. Cavazos,Linda Kachuri,Rebecca E. Graff,Jovia L. Nierenberg,Khanh K. Thai,Stacey E. Alexeeff,Stephen K. Van Den Eeden,Douglas A. Corley,Lawrence H. Kushi,Thomas J. Hoffmann,Elad Ziv,Laurie A. Habel,Eric Jorgenson,Lori C. Sakoda,John S. Witte +14 more
TL;DR: The authors conducted a pan-cancer, whole-exome sequencing study of individuals drawn from two large multi-ancestry populations (6429 cases, 165,853 controls).
Gene expression in African Americans and Latinos reveals ancestry-specific patterns of genetic architecture
Angel C.Y. Mak,Linda Kachuri,Donglei Hu,Celeste Eng,Scott Huntsman,Jennifer R. Elhawary,Namrata Gupta,Stacey Gabriel,Shujie Xiao,Hongsheng Gui,Kevin L. Keys,Kevin L. Keys,Akinyemi Oni-Orisan,Sam S. Oh,Max A. Seibold,Jose R. Rodriguez-Santana,Michael A. LeNoir,L. Keoki Williams,Luisa N. Borrell,Christopher R. Gignoux,Noah Zaitlen,Esteban G. Burchard,Elad Ziv +22 more
TL;DR: This paper explored the role of genetic ancestry in shaping the genetic architecture of whole blood gene expression using whole genome and RNA sequencing data from 2,733 African American and Hispanic/Latino children.
Expression quantitative trait loci of genes predicting outcome are associated with survival of multiple myeloma patients
Angelica Macauda,Angelica Macauda,Chiara Piredda,Alyssa I. Clay-Gilmour,Juan Sainz,Gabriele Buda,Mirosław Markiewicz,Torben Barington,Elad Ziv,Michelle A.T. Hildebrandt,Alem A. Belachew,Judit Várkonyi,Witold Prejzner,Agnieszka Druzd-Sitek,John J. Spinelli,John J. Spinelli,Niels Frost Andersen,Jonathan N. Hofmann,Marek Dudziński,Joaquin Martinez-Lopez,Elżbieta Iskierka-Jażdżewska,Roger L. Milne,Roger L. Milne,Roger L. Milne,Grzegorz Mazur,Graham G. Giles,Graham G. Giles,Graham G. Giles,Lene Hyldahl Ebbesen,Marcin Rymko,Krzysztof Jamroziak,Edyta Subocz,Rui Manuel Reis,Ramón García-Sanz,Anna Suska,Eva Haastrup,Daria Zawirska,Norbert Grzasko,Norbert Grzasko,Annette Juul Vangsted,Charles Dumontet,Marcin Kruszewski,Magdalena Dutka,Nicola J. Camp,Rosalie G. Waller,Waldemar Tomczak,Matteo Pelosini,Małgorzata Raźny,Herlander Marques,Niels Abildgaard,Marzena Wątek,Artur Jurczyszyn,Elizabeth E. Brown,Sonja I. Berndt,Aleksandra Butrym,Celine M. Vachon,Aaron D. Norman,Susan L. Slager,Federica Gemignani,Federico Canzian,Daniele Campa +60 more
TL;DR: An association study to test whether eQTLs of genes reported to be associated with prognosis ofMM patients are directly associated with measures of adverse outcome found biologically a plausible association between a SNP in TBRG4 and OS of MM patients.
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