Kyle Kai-How Farh
Kyle Kai-How Farh
Principal Investigator, Illumina AI Lab
Verified email at illumina.com
Title
Cited by
Cited by
Year
Most mammalian mRNAs are conserved targets of microRNAs
RC Friedman, KKH Farh, CB Burge, DP Bartel
Genome research 19 (1), 92-105, 2009
79592009
MicroRNA targeting specificity in mammals: determinants beyond seed pairing
A Grimson, KKH Farh, WK Johnston, P Garrett-Engele, LP Lim, DP Bartel
Molecular cell 27 (1), 91-105, 2007
41172007
Integrative analysis of 111 reference human epigenomes
A Kundaje, W Meuleman, J Ernst, M Bilenky, A Yen, A Heravi-Moussavi, ...
Nature 518 (7539), 317-330, 2015
39912015
The widespread impact of mammalian MicroRNAs on mRNA repression and evolution
KKH Farh, A Grimson, C Jan, BP Lewis, WK Johnston, LP Lim, CB Burge, ...
Science 310 (5755), 1817-1821, 2005
17052005
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421, 2014
16132014
Genetic and epigenetic fine mapping of causal autoimmune disease variants
KKH Farh, A Marson, J Zhu, M Kleinewietfeld, WJ Housley, S Beik, ...
Nature 518 (7539), 337-343, 2015
13602015
Partitioning heritability by functional annotation using genome-wide association summary statistics
HK Finucane, B Bulik-Sullivan, A Gusev, G Trynka, Y Reshef, PR Loh, ...
Nature genetics 47 (11), 1228, 2015
11932015
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
6792018
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
6482015
Expanding the microRNA targeting code: functional sites with centered pairing
C Shin, JW Nam, KKH Farh, HR Chiang, A Shkumatava, DP Bartel
Molecular cell 38 (6), 789-802, 2010
6342010
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ...
The American Journal of Human Genetics 95 (5), 535-552, 2014
4882014
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature genetics 49 (1), 27-35, 2017
4502017
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS Genet 6 (2), e1000841, 2010
4022010
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ...
Nature genetics 48 (8), 856-866, 2016
3862016
Predicting splicing from primary sequence with deep learning
K Jaganathan, SK Panagiotopoulou, JF McRae, SF Darbandi, D Knowles, ...
Cell 176 (3), 535-548. e24, 2019
3292019
Fine-mapping inflammatory bowel disease loci to single-variant resolution
H Huang, M Fang, L Jostins, MU Mirkov, G Boucher, CA Anderson, ...
Nature 547 (7662), 173-178, 2017
3132017
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium
Science (New York, NY) 360 (6395), 2018
2802018
Genomic hallmarks and structural variation in metastatic prostate cancer
DA Quigley, HX Dang, SG Zhao, P Lloyd, R Aggarwal, JJ Alumkal, A Foye, ...
Cell 174 (3), 758-769. e9, 2018
2682018
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
2212018
Genome-wide identification and characterization of functional neuronal activity–dependent enhancers
AN Malik, T Vierbuchen, M Hemberg, AA Rubin, E Ling, CH Couch, ...
Nature neuroscience 17 (10), 1330-1339, 2014
1782014
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