Search details
1.
Passenger Mutations in More Than 2,500 Cancer Genomes: Overall Molecular Functional Impact and Consequences.
Cell
; 180(5): 915-927.e16, 2020 03 05.
Article
in English
| MEDLINE | ID: mdl-32084333
2.
Comprehensive Characterization of Cancer Driver Genes and Mutations.
Cell
; 173(2): 371-385.e18, 2018 04 05.
Article
in English
| MEDLINE | ID: mdl-29625053
3.
Comprehensive Characterization of Cancer Driver Genes and Mutations.
Cell
; 174(4): 1034-1035, 2018 08 09.
Article
in English
| MEDLINE | ID: mdl-30096302
4.
Patterns of somatic structural variation in human cancer genomes.
Nature
; 578(7793): 112-121, 2020 02.
Article
in English
| MEDLINE | ID: mdl-32025012
5.
Author Correction: Patterns of somatic structural variation in human cancer genomes.
Nature
; 614(7948): E38, 2023 Feb.
Article
in English
| MEDLINE | ID: mdl-36697835
6.
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk.
Proc Natl Acad Sci U S A
; 118(51)2021 12 21.
Article
in English
| MEDLINE | ID: mdl-34916285
7.
CNCDatabase: a database of non-coding cancer drivers.
Nucleic Acids Res
; 49(D1): D1094-D1101, 2021 01 08.
Article
in English
| MEDLINE | ID: mdl-33095860
8.
Loss-of-function tolerance of enhancers in the human genome.
PLoS Genet
; 16(4): e1008663, 2020 04.
Article
in English
| MEDLINE | ID: mdl-32243438
9.
Role of non-coding sequence variants in cancer.
Nat Rev Genet
; 17(2): 93-108, 2016 Feb.
Article
in English
| MEDLINE | ID: mdl-26781813
10.
FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and Applications.
Am J Hum Genet
; 102(5): 920-942, 2018 05 03.
Article
in English
| MEDLINE | ID: mdl-29727691
11.
MYBL1 rearrangements and MYB amplification in breast adenoid cystic carcinomas lacking the MYB-NFIB fusion gene.
J Pathol
; 244(2): 143-150, 2018 02.
Article
in English
| MEDLINE | ID: mdl-29149504
12.
Architecture of the human regulatory network derived from ENCODE data.
Nature
; 489(7414): 91-100, 2012 Sep 06.
Article
in English
| MEDLINE | ID: mdl-22955619
13.
Cancer genomics: Hard-to-reach repairs.
Nature
; 532(7598): 181-2, 2016 Apr 14.
Article
in English
| MEDLINE | ID: mdl-27075092
14.
Mapping copy number variation by population-scale genome sequencing.
Nature
; 470(7332): 59-65, 2011 Feb 03.
Article
in English
| MEDLINE | ID: mdl-21293372
15.
LARVA: an integrative framework for large-scale analysis of recurrent variants in noncoding annotations.
Nucleic Acids Res
; 43(17): 8123-34, 2015 Sep 30.
Article
in English
| MEDLINE | ID: mdl-26304545
16.
Prediction and characterization of noncoding RNAs in C. elegans by integrating conservation, secondary structure, and high-throughput sequencing and array data.
Genome Res
; 21(2): 276-85, 2011 Feb.
Article
in English
| MEDLINE | ID: mdl-21177971
17.
Interpretation of genomic variants using a unified biological network approach.
PLoS Comput Biol
; 9(3): e1002886, 2013.
Article
in English
| MEDLINE | ID: mdl-23505346
18.
TAD hierarchy restricts poised LTR activation and loss of TAD hierarchy promotes LTR co-option in cancer.
bioRxiv
; 2024 Jun 03.
Article
in English
| MEDLINE | ID: mdl-38895201
19.
VAT: a computational framework to functionally annotate variants in personal genomes within a cloud-computing environment.
Bioinformatics
; 28(17): 2267-9, 2012 Sep 01.
Article
in English
| MEDLINE | ID: mdl-22743228
20.
Impulsivity and Risk-Taking Behavior in School-Going Adolescents.
Cureus
; 15(6): e40728, 2023 Jun.
Article
in English
| MEDLINE | ID: mdl-37485185