Yoel Gofin
Tel Aviv University
18 Papers
11 Citations
Yoel Gofin is an academic researcher from Tel Aviv University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 2, co-authored 3 publications.
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Papers
The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models
Joel Rozowsky,Jorg Drenkow,Yucheng T. Yang,Gamze Gursoy,Timur R. Galeev,Beatrice Borsari,Charles B. Epstein,Kun Xiong,Jinrui Xu,Jiahao Gao,Kai Yu,Ana Berthel,Zhanlin Chen,Fabio C. P. Navarro,Jason Liu,Maxwell S Sun,James C. Wright,Justin Chang,Christopher J. F. Cameron,Noam Shoresh,Elizabeth Gaskell,Jessika Adrian,Sergey Aganezov,François Aguet,Gabriela Balderrama-Gutierrez,Samridhi Banskota,G. Corona,Sora Chee,Surya B. Chhetri,Gabriel Conte Cortez Martins,Cassidy Danyko,Carrie A. Davis,Daniel Farid,Nina Farrell,Idan Gabdank,Yoel Gofin,David U. Gorkin,Mengting Gu,Vivian C. Hecht,Benjamin C. Hitz,Robbyn Issner,Melanie Kirsche,Xiangmeng Kong,Bonita R Lam,Shantao Li,Bian Li,Tianxiao Li,Xiqi Li,Khine Lin,Ruibang Luo,Mark Mackiewicz,Jill Moore,Jonathan M. Mudge,Nicholas C Nelson,Chad Nusbaum,Ioann O. Popov,Henry Pratt,Yunjiang Qiu,Srividya Ramakrishnan,Joe Raymond,Leonidas Salichos,Alexandra Scavelli,Jacob Schreiber,Fritz J. Sedlazeck,Lei-Hoon See,Rachel M. Sherman,Xu Shi,Minyi Shi,Cricket A. Sloan,J. Seth Strattan,Zhenqi Tan,Forrest Y. Tanaka,Anna Vlasova,Jun Wang,Jonathan D. Werner,Brian A. Williams,Min Xu,Chengfei Yan,Lu Yu,Chris Zaleski,Jing Zhang,Kristin G. Ardlie,J. M. Cherry,Eric M. Mendenhall,William Noble,Zhiping Weng,Morgan E. Levine,Alexander Dobin,Barbara J. Wold,Ali Mortazavi,Bing Ren,Jesse Gillis,Richard M. Myers,Michael Snyder,Jyoti S. Choudhary,Aleksandar Milosavljević,Michael C. Schatz,Roderic Guigó,Bradley E. Bernstein,Thomas R. Gingeras,Mark Gerstein +100 more
TL;DR: The EN-TEx dataset as mentioned in this paper contains 1,635 open-access datasets from four donors (∼30 tissues × ∼15 assays) mapped to matched, diploid genomes with long read phasing and structural variants, instantiating a catalog of >1 million allele-specific loci.
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Underlying genetic etiologies of congenital diaphragmatic hernia
TL;DR: Patients should be counseled about the possible genetic causes of the CDH, and the genetic testing modalities available to them, in accordance with generally accepted guidelines for pretest counseling in the prenatal setting.
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Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency
Yoel Gofin,Tianyun Wang,Madelyn A. Gillentine,Tiana M. Scott,A. M. Berry,Mahshid S. Azamian,Casie A. Genetti,Pankaj B. Agrawal,Jonathan Picker,Monica H. Wojcik,Mauricio R. Delgado,Sally Ann Lynch,Stephen W. Scherer,Jennifer L. Howe,Carlos A. Bacino,Stephanie P. DiTroia,Grace E. VanNoy,Anne H. O’Donnell-Luria,Seema R. Lalani,William D. Graf,Jill A. Rosenfeld,Evan E. Eichler,Rachel K. Earl,Daryl A. Scott +23 more
TL;DR: It is suggested that PAX5 haploinsufficiency causes a neurodevelopmental disorder whose cardinal features include DD, variable ID, and/or ASD.
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•Journal Article
A model for assessing the gap between physician residency demand and present status.
TL;DR: The suggested model, based on a survey of demand and current or projected future needs, can be used to assess gaps and plan early interventions and the decline in selection of surgical professions and the increasing workload as a consideration for residency choice should be given attention.
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Therapeutic Drug Monitoring Increases Drug Retention of Anti-Tumor Necrosis Factor Alpha Agents in Pediatric Patients With Crohn's Disease.
TL;DR: TDM-based treatment enables longer drug retention time, reflecting better utilization of anti-TNFα agents, with several additional favorable outcomes.
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