Fereydoun Hormozdiari

Citované v

	Všetky	Od 2019
Citácie	50926	26459
h-index	44	37
i10-index	63	56

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55 článkov

1 článok

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Na základe mandátov na financovanie

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S. Cenk SahinalpSenior Investigator, Cancer Data Science Lab, National Cancer Institute, NIHOverená e-mailová adresa na: nih.gov
Evan EichlerProfessor of Genome Sciences, University of WashingtonOverená e-mailová adresa na: gs.washington.edu
Can AlkanBilkent University, Ankara, TurkeyOverená e-mailová adresa na: cs.bilkent.edu.tr
Iman HajirasoulihaAssociate Professor, Weill Cornell Medicine of Cornell University, New York CityOverená e-mailová adresa na: med.cornell.edu
Faraz HachAssistant Professor at University of British ColumbiaOverená e-mailová adresa na: ubc.ca
Phuong DaoGoogleOverená e-mailová adresa na: google.com
Sohrab ShahMemorial Sloan Kettering Cancer CenterOverená e-mailová adresa na: mskcc.org
Farhad HormozdiariResearch Scientist at Google HealthOverená e-mailová adresa na: google.com
Jacob KitzmanAssociate ProfessorOverená e-mailová adresa na: umich.edu
Alexander SchönhuthProfessor, Faculty for Technology, Bielefeld UniversityOverená e-mailová adresa na: cebitec.uni-bielefeld.de
Raheleh SalariOverená e-mailová adresa na: cs.stanford.edu
Michael BrudnoProfessor of Computer Science, University of Toronto; Chief Data Scientist, UHNOverená e-mailová adresa na: cs.toronto.edu
Martin EsterDistinguished Professor of Computer Science, Simon Fraser UniversityOverená e-mailová adresa na: cs.sfu.ca
Natasa Przulj, PhD, FBCS, MAEICREA Research Professor at Barcelona Supercomputing Center; Professor, Computer Science, UCLOverená e-mailová adresa na: bsc.es

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Fereydoun Hormozdiari

Associate Professor at University of California - Davis

Overená e-mailová adresa na: ucdavis.edu - Domovská stránka

Computational Biology Algorithms Machine Learning Genomics Cancer Systems Biology


Názov Zoradiť podľa citácií Zoradiť podľa roka Zoradiť podľa názvu	Citované v Citované v	Rok
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	15962	2015
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8919	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8540	2012
An integrated map of structural variation in 2,504 human genomes PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75-81, 2015	2503	2015
Mapping copy number variation by population-scale genome sequencing RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ... Nature 470 (7332), 59-65, 2011	1312	2011
Great ape genetic diversity and population history J Prado-Martinez, PH Sudmant, JM Kidd, H Li, JL Kelley, ... Nature 499 (7459), 471-475, 2013	974	2013
Personalized copy number and segmental duplication maps using next-generation sequencing C Alkan, JM Kidd, T Marques-Bonet, G Aksay, F Antonacci, F Hormozdiari, ... Nature genetics 41 (10), 1061-1067, 2009	972	2009
Resolving the complexity of the human genome using single-molecule sequencing MJP Chaisson, J Huddleston, MY Dennis, PH Sudmant, M Malig, ... Nature 517 (7536), 608-611, 2015	874	2015
Multi-platform discovery of haplotype-resolved structural variation in human genomes MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ... Nature communications 10 (1), 1784, 2019	823	2019
Demographic history and rare allele sharing among human populations S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ... Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011	733	2011
Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014	731	2014
deFuse: an algorithm for gene fusion discovery in tumor RNA-Seq data A McPherson, F Hormozdiari, A Zayed, R Giuliany, G Ha, MGF Sun, ... PLoS computational biology 7 (5), e1001138, 2011	625	2011
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios M Byrska-Bishop, US Evani, X Zhao, AO Basile, HJ Abel, AA Regier, ... Cell 185 (18), 3426-3440. e19, 2022	593	2022
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ... Nature genetics 49 (4), 515-526, 2017	566	2017
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini Nature communications 5 (1), 3934, 2014	460	2014
Integrative annotation of variants from 1092 humans: application to cancer genomics E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ... Science 342 (6154), 1235587, 2013	425	2013
Global diversity, population stratification, and selection of human copy-number variation PH Sudmant, S Mallick, BJ Nelson, F Hormozdiari, N Krumm, ... Science 349 (6253), aab3761, 2015	410	2015
Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes F Hormozdiari, C Alkan, EE Eichler, SC Sahinalp Genome research 19 (7), 1270-1278, 2009	387	2009
High-resolution comparative analysis of great ape genomes ZN Kronenberg, IT Fiddes, D Gordon, S Murali, S Cantsilieris, ... Science 360 (6393), eaar6343, 2018	385	2018
Genomic patterns of de novo mutation in simplex autism TN Turner, BP Coe, DE Dickel, K Hoekzema, BJ Nelson, MC Zody, ... Cell 171 (3), 710-722. e12, 2017	371	2017

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