Fereydoun Hormozdiari

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Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

S. Cenk SahinalpSenior Investigator, Cancer Data Science Lab, National Cancer Institute, NIHnih.gov üzerinde doğrulanmış e-posta adresine sahip
Evan EichlerProfessor of Genome Sciences, University of Washingtongs.washington.edu üzerinde doğrulanmış e-posta adresine sahip
Can AlkanBilkent University, Ankara, Turkeycs.bilkent.edu.tr üzerinde doğrulanmış e-posta adresine sahip
Iman HajirasoulihaAssociate Professor, Weill Cornell Medicine of Cornell University, New York Citymed.cornell.edu üzerinde doğrulanmış e-posta adresine sahip
Faraz HachAssistant Professor at University of British Columbiaubc.ca üzerinde doğrulanmış e-posta adresine sahip
Phuong DaoGooglegoogle.com üzerinde doğrulanmış e-posta adresine sahip
Sohrab ShahMemorial Sloan Kettering Cancer Centermskcc.org üzerinde doğrulanmış e-posta adresine sahip
Farhad HormozdiariResearch Scientist at Google Healthgoogle.com üzerinde doğrulanmış e-posta adresine sahip
Jacob KitzmanAssociate Professorumich.edu üzerinde doğrulanmış e-posta adresine sahip
Alexander SchönhuthProfessor, Faculty for Technology, Bielefeld Universitycebitec.uni-bielefeld.de üzerinde doğrulanmış e-posta adresine sahip
Raheleh Salarics.stanford.edu üzerinde doğrulanmış e-posta adresine sahip
Michael BrudnoProfessor of Computer Science, University of Toronto; Chief Data Scientist, UHNcs.toronto.edu üzerinde doğrulanmış e-posta adresine sahip
Martin EsterDistinguished Professor of Computer Science, Simon Fraser Universitycs.sfu.ca üzerinde doğrulanmış e-posta adresine sahip
Natasa Przulj, PhD, FBCS, MAEICREA Research Professor at Barcelona Supercomputing Center; Professor, Computer Science, UCLbsc.es üzerinde doğrulanmış e-posta adresine sahip

Takip et

Fereydoun Hormozdiari

Associate Professor at University of California - Davis

ucdavis.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

Computational Biology Algorithms Machine Learning Genomics Cancer Systems Biology


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	16333	2015
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8978	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8588	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	2557	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	1318	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	996	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	983	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	885	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	846	2019
Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014	739	2014
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	739	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	652	2022
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	630	2011
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	575	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	468	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	427	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	413	2015
High-resolution comparative analysis of great ape genomes ZN Kronenberg, IT Fiddes, D Gordon, S Murali, S Cantsilieris, ... Science 360 (6393), eaar6343, 2018	389	2018
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	388	2009
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	376	2017

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