关注
Joshua M Korn
Joshua M Korn
Novartis Institutes for Biomedical Research
在 alum.mit.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87692010
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
Cancer Genome Atlas Research Network Tissue source sites: Duke University ...
Nature 455 (7216), 1061-1068, 2008
74282008
Next-generation characterization of the cancer cell line encyclopedia
M Ghandi, FW Huang, J Jané-Valbuena, GV Kryukov, CC Lo, ...
Nature 569 (7757), 503-508, 2019
25042019
Association between microdeletion and microduplication at 16p11. 2 and autism
LA Weiss, Y Shen, JM Korn, DE Arking, DT Miller, R Fossdal, ...
New England Journal of Medicine 358 (7), 667-675, 2008
19522008
Rare chromosomal deletions and duplications increase risk of schizophrenia
Cardiff University O’Donovan Michael C. 5 Kirov George K. 5 Craddock Nick J ...
Nature 455 (7210), 237-241, 2008
15692008
Mapping and sequencing of structural variation from eight human genomes
JM Kidd, GM Cooper, WF Donahue, HS Hayden, N Sampas, T Graves, ...
Nature 453 (7191), 56-64, 2008
14322008
High-throughput screening using patient-derived tumor xenografts to predict clinical trial drug response
H Gao, JM Korn, S Ferretti, JE Monahan, Y Wang, M Singh, C Zhang, ...
Nature medicine 21 (11), 1318-1325, 2015
13472015
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Heart Attack Risk in Puget Sound. Schwartz Stephen M 20 26 Siscovick David S ...
Nature genetics 41 (3), 334-341, 2009
13022009
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
12862011
Integrated detection and population-genetic analysis of SNPs and copy number variation
SA McCarroll, FG Kuruvilla, JM Korn, S Cawley, J Nemesh, A Wysoker, ...
Nature genetics 40 (10), 1166-1174, 2008
11492008
The plasticity of dendritic cell responses to pathogens and their components
Q Huang, D Liu, P Majewski, LC Schulte, JM Korn, RA Young, ES Lander, ...
Science 294 (5543), 870-875, 2001
10442001
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
JM Korn, FG Kuruvilla, SA McCarroll, A Wysoker, J Nemesh, S Cawley, ...
Nature genetics 40 (10), 1253-1260, 2008
9422008
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
MA Rivas, M Beaudoin, A Gardet, C Stevens, Y Sharma, CK Zhang, ...
Nature genetics 43 (11), 1066-1073, 2011
8872011
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
7962009
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
7152011
Project DRIVE: a compendium of cancer dependencies and synthetic lethal relationships uncovered by large-scale, deep RNAi screening
ER McDonald, A De Weck, MR Schlabach, E Billy, KJ Mavrakis, ...
Cell 170 (3), 577-592. e10, 2017
6162017
An F876L mutation in androgen receptor confers genetic and phenotypic resistance to MDV3100 (enzalutamide)
M Korpal, JM Korn, X Gao, DP Rakiec, DA Ruddy, S Doshi, J Yuan, ...
Cancer discovery 3 (9), 1030-1043, 2013
6082013
Studying clonal dynamics in response to cancer therapy using high-complexity barcoding
HC Bhang, DA Ruddy, V Krishnamurthy Radhakrishna, JX Caushi, ...
Nature medicine 21 (5), 440-448, 2015
5302015
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot
SC Greenway, AC Pereira, JC Lin, SR DePalma, SJ Israel, SM Mesquita, ...
Nature genetics 41 (8), 931-935, 2009
4992009
Discovery and genotyping of genome structural polymorphism by sequencing on a population scale
RE Handsaker, JM Korn, J Nemesh, SA McCarroll
Nature genetics 43 (3), 269-276, 2011
4122011
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