Fuli Yu

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Cristian CoarfaAssociate Professor in Molecular and Cellular Biology, Baylor College of MedicineVerifisert e-postadresse på bcm.edu
Aleksandar MilosavljevicProfessor, Henry and Emma Meyer Chair in Molecular Genetics, Baylor College of MedicineVerifisert e-postadresse på bcm.edu
R. Alan HarrisAssistant Professor, HGSC, Department of Molecular and Human Genetics, Baylor College of MedicineVerifisert e-postadresse på bcm.edu
Uday S. EvaniSenior Data Scientist at New York Genome CenterVerifisert e-postadresse på nygenome.org
Danny ChallisBayer Crop ScienceVerifisert e-postadresse på bayer.com
Zhuoyi HuangIllumina, Baylor College of Medicine, Astronomical Observatory of Rome, Astronomical Observatory ofVerifisert e-postadresse på bcm.edu
Adam EnglishSpiral GeneticsVerifisert e-postadresse på spiralgenetics.com
Andrew CarrollGoogleVerifisert e-postadresse på google.com
Xiaoming LiuAssociate Professor, College of Public Health, University of South FloridaVerifisert e-postadresse på usf.edu
Laura ClarkeHealth Informatics EastVerifisert e-postadresse på healthinnovationeast.co.uk
Paul FlicekThe Jackson Laboratory, University of CambridgeVerifisert e-postadresse på jax.org
Lynn JordeProfessor and Chair, Department of Human Genetics, University of Utah School of MedicineVerifisert e-postadresse på genetics.utah.edu
Jinchuan XingRutgers, the State University of New JerseyVerifisert e-postadresse på biology.rutgers.edu
Simon WhiteStaff Bioinformatics Scientist at HelixVerifisert e-postadresse på helix.com
James LupskiBaylor College of MedicineVerifisert e-postadresse på bcm.edu
George WeinstockDirector of Microbial Genomics, Professor, Jackson LaboratoryVerifisert e-postadresse på jax.org
Yufeng ShenAssociate Professor, Columbia UniversityVerifisert e-postadresse på cumc.columbia.edu
Stephen SchaffnerSenior Computational Biologist, Broad InstituteVerifisert e-postadresse på broadinstitute.org
Alon KeinanAssociate Professor of Computational Biology, Cornell UniversityVerifisert e-postadresse på cornell.edu
Gabor T MarthProfessor of Human Genetics, University of UtahVerifisert e-postadresse på genetics.utah.edu

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Fuli Yu

Baylor College of Medicine

Verifisert e-postadresse på bcm.edu - Startside

Population and Medical Genomics Bioinformatics Big Data Cloud Clinical Genomics


Tittel Sorter etter sitater Sorter etter år Sorter etter tittel	Sitert av Sitert av	År
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	15880	2015
A haplotype map of the human genome hapmap	10697*	2005
A map of human genome variation from population scale sequencing DM Altshuler, ES Lander, L Ambrogio, T Bloom, K Cibulskis, TJ Fennell, ... Nature 467 (7319), 1061-1073, 2010	8902*	2010
An integrated map of genetic variation from 1,092 human genomes 1000G Nature 491, 1, 2012	8547*	2012
The international HapMap project RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ... Nature Publishing Group, 2003	6402	2003
Integrating common and rare genetic variation in diverse human populations International HapMap 3 Consortium Nature 467 (7311), 52, 2010	3249	2010
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	2492	2015
Genome-wide detection and characterization of positive selection in human populations PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ... Nature 449 (7164), 913-918, 2007	2296	2007
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	735	2011
Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay P Hardenbol, F Yu, J Belmont, J MacKenzie, C Bruckner, T Brundage, ... Genome research 15 (2), 269-275, 2005	499	2005
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	458	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
The 1000 Genomes Project: data management and community access L Clarke, X Zheng-Bradley, R Smith, E Kulesha, C Xiao, I Toneva, ... Nature methods 9 (5), 459-462, 2012	369	2012
A genomewide admixture map for Latino populations AL Price, N Patterson, F Yu, DR Cox, A Waliszewska, GJ McDonald, ... The American Journal of Human Genetics 80 (6), 1024-1036, 2007	344	2007
An integrative variant analysis suite for whole exome next-generation sequencing data D Challis, J Yu, US Evani, AR Jackson, S Paithankar, C Coarfa, ... BMC bioinformatics 13, 1-12, 2012	326	2012
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline JG Reid, A Carroll, N Veeraraghavan, M Dahdouli, A Sundquist, A English, ... BMC bioinformatics 15, 1-11, 2014	258	2014
The functional spectrum of low-frequency coding variation GT Marth, F Yu, AR Indap, K Garimella, S Gravel, WF Leong, ... Genome biology 12, 1-17, 2011	244	2011
A SNP discovery method to assess variant allele probability from next-generation resequencing data Y Shen, Z Wan, C Coarfa, R Drabek, L Chen, EA Ostrowski, Y Liu, ... Genome research 20 (2), 273-280, 2010	234	2010
Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes D Liang, DS Cram, HU Tan, S Linpeng, Y Liu, H Sun, Y Zhang, F Tian, ... Genetics in Medicine 21 (9), 1998-2006, 2019	221	2019
Whole-genome sequence–based analysis of high-density lipoprotein cholesterol Nature genetics 45 (8), 899-901, 2013	148	2013

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