Kai Ye

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Michael WendlAssociate Professor, Washington UniversityCorreu electrònic verificat a wustl.edu
Beifang NiuResearch professor at Computer Network Information Center of Chinese Academy of Sciences (CNIC)Correu electrònic verificat a cnic.cn
Michael D McLellanThe Genome Institute at Washington University School of MedicineCorreu electrònic verificat a wustl.edu
Matthew WyczalkowskiWashington University in St. LouisCorreu electrònic verificat a wustl.edu
Xie MingchaoWashington University in St LouisCorreu electrònic verificat a genome.wustl.edu
Li Guo 郭立Principal Investigator, Peking University IAASCorreu electrònic verificat a pku-iaas.edu.cn
Zemin NingThe Wellcome Trust Sanger InstituteCorreu electrònic verificat a sanger.ac.uk
Peng JiaXi'an Jiaotong UniversityCorreu electrònic verificat a xjtu.edu.cn
Xiaofei Yang - 杨晓飞Xi'an Jiaotong UniversityCorreu electrònic verificat a xjtu.edu.cn
P. Eline SlagboomProfessor Molecular Epidemiology, Leiden University Medical CenterCorreu electrònic verificat a lumc.nl
Joshua McMichaelBusiness and Technical Analyst IICorreu electrònic verificat a genome.wustl.edu
Ben RaphaelProfessor of Computer Science, Princeton UniversityCorreu electrònic verificat a princeton.edu
Quan LongUniversity of CalgaryCorreu electrònic verificat a ucalgary.ca
Jiadong LinXi'an Jiaotong UniversityCorreu electrònic verificat a stu.xjtu.edu.cn
Chris MillerAssociate Professor, Washington University in St LouisCorreu electrònic verificat a wustl.edu
Richard K. Wilson, Ph.D.Nationwide Children's Hospital; Ohio State UniversityCorreu electrònic verificat a NationwideChildrens.org
TJ LeyProfessor of Medicine and Genetics, Washington University School of MedicineCorreu electrònic verificat a wustl.edu
Fabio VandinUniversity of PadovaCorreu electrònic verificat a unipd.it
Cyriac KandothUniversity of PennsylvaniaCorreu electrònic verificat a pennmedicine.upenn.edu
Paul I W de BakkerVertex PharmaceuticalsCorreu electrònic verificat a vrtx.com

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Kai Ye

Xi'an Jiaotong University

Correu electrònic verificat a xjtu.edu.cn - Pàgina d'inici

bioinformatics pharmacology cancer


Títol Ordena per cites Ordena per any Ordena per títol	Citada per Citada per	Any
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	16629	2015
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010	9061	2010
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8642	2012
Integrated genomic characterization of endometrial carcinoma DA Levine, ... Nature 497 (7447), 67-73, 2013	5347	2013
Mutational landscape and significance across 12 major cancer types C Kandoth, MD McLellan, F Vandin, K Ye, B Niu, C Lu, M Xie, Q Zhang, ... Nature 502 (7471), 333-339, 2013	5027	2013
Comprehensive molecular profiling of lung adenocarcinoma Cancer Genome Atlas Research Network Nature 511 (7511), 543, 2014	4970*	2014
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	2579	2015
Pan-cancer analysis of whole genomes Nature 578 (7793), 82-93, 2020	2360	2020
Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads K Ye, MH Schulz, Q Long, R Apweiler, Z Ning Bioinformatics 25 (21), 2865-2871, 2009	2325	2009
A comprehensive catalogue of somatic mutations from a human cancer genome ED Pleasance, RK Cheetham, PJ Stephens, DJ McBride, SJ Humphray, ... Nature 463 (7278), 191-196, 2010	2076	2010
A systematic survey of loss-of-function variants in human protein-coding genes DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ... Science 335 (6070), 823-828, 2012	1428	2012
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	1333	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	851	2019
MSIsensor: microsatellite instability detection using paired tumor-normal sequence data B Niu, K Ye, Q Zhang, C Lu, M Xie, MD McLellan, MC Wendl, L Ding Bioinformatics 30 (7), 1015-1016, 2014	757	2014
Whole-genome sequence variation, population structure and demographic history of the Dutch population Nature genetics 46 (8), 818-825, 2014	748	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	747	2011
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing I Cortés-Ciriano, JJK Lee, R Xi, D Jain, YL Jung, L Yang, D Gordenin, ... Nature genetics 52 (3), 331-341, 2020	648	2020
Haplotype-resolved diverse human genomes and integrated analysis of structural variation P Ebert, PA Audano, Q Zhu, B Rodriguez-Martin, D Porubsky, MJ Bonder, ... Science 372 (6537), eabf7117, 2021	571	2021
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	477	2014
Genome-wide patterns and properties of de novo mutations in humans LC Francioli, PP Polak, A Koren, A Menelaou, S Chun, I Renkens, ... Nature genetics 47 (7), 822-826, 2015	426	2015

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