Fereydoun Hormozdiari

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Cenk SahinalpSenior Investigator, Cancer Data Science Lab, National Cancer Institute, NIHPotvrđena adresa e-pošte na nih.gov
Evan EichlerProfessor of Genome Sciences, University of WashingtonPotvrđena adresa e-pošte na gs.washington.edu
Can AlkanBilkent University, Ankara, TurkeyPotvrđena adresa e-pošte na cs.bilkent.edu.tr
Iman HajirasoulihaAssociate Professor, Weill Cornell Medicine of Cornell University, New York CityPotvrđena adresa e-pošte na med.cornell.edu
Faraz HachAssistant Professor at University of British ColumbiaPotvrđena adresa e-pošte na ubc.ca
The Phuong DaoMemorial Sloan Kettering Cancer CenterPotvrđena adresa e-pošte na mskcc.org
Sohrab ShahMemorial Sloan Kettering Cancer CenterPotvrđena adresa e-pošte na mskcc.org
Farhad HormozdiariResearch Scientist at Google HealthPotvrđena adresa e-pošte na google.com
Jacob KitzmanAssociate ProfessorPotvrđena adresa e-pošte na umich.edu
Alexander SchönhuthSenior Researcher, Centrum Wiskunde & Informatica, AmsterdamPotvrđena adresa e-pošte na cwi.nl
Raheleh SalariNatera IncPotvrđena adresa e-pošte na natera.com
Michael BrudnoProfessor of Computer Science, University of Toronto; Chief Data Scientist, UHNPotvrđena adresa e-pošte na cs.toronto.edu
Natasa Przulj, PhD, FBCS, MAEICREA Research Professor at Barcelona Supercomputing Center; Professor, Computer Science, UCLPotvrđena adresa e-pošte na bsc.es
Martin EsterDistinguished Professor of Computer Science, Simon Fraser UniversityPotvrđena adresa e-pošte na cs.sfu.ca

Prati

Fereydoun Hormozdiari

Associate Professor at University of California - Davis

Potvrđena adresa e-pošte na ucdavis.edu - Početna stranica

Computational Biology Algorithms Human Genomics


Naslov Poredaj po navodima Poredaj po godini Poredaj po naslovu	Citirano Citirano	Godina
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	11877	2015
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	8274	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	7824	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	1998	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	1181	2011
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	927	2009
Great ape genetic diversity and population history J Prado-Martinez, PH Sudmant, JM Kidd, H Li, JL Kelley, ... Nature 499 (7459), 471-475, 2013	838	2013
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	748	2015
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	654	2011
Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014	652	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	587	2011
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	579	2019
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	424	2017
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	401	2013
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	381	2014
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	379	2009
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	349	2015
mrsFAST: a cache-oblivious algorithm for short-read mapping F Hach, F Hormozdiari, C Alkan, F Hormozdiari, I Birol, EE Eichler, ... Nature methods 7 (8), 576-577, 2010	328	2010
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	278	2017
Genome sequencing of autism-affected families reveals disruption of putative noncoding regulatory DNA TN Turner, F Hormozdiari, MH Duyzend, SA McClymont, PW Hook, ... The American Journal of Human Genetics 98 (1), 58-74, 2016	276	2016

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