Detalhe da pesquisa
1.
Organoid Modeling of the Tumor Immune Microenvironment.
Cell
; 175(7): 1972-1988.e16, 2018 12 13.
Artigo
Inglês
| MEDLINE | ID: mdl-30550791
2.
The status of the human gene catalogue.
Nature
; 622(7981): 41-47, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-37794265
3.
Molecular profiling of a real-world breast cancer cohort with genetically inferred ancestries reveals actionable tumor biology differences between European ancestry and African ancestry patient populations.
Breast Cancer Res
; 25(1): 58, 2023 05 25.
Artigo
Inglês
| MEDLINE | ID: mdl-37231433
4.
Integrated genomic characterization of ERBB2/HER2 alterations in invasive breast carcinoma: a focus on unusual FISH groups.
Mod Pathol
; 33(8): 1546-1556, 2020 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32161378
5.
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort.
Lancet Oncol
; 19(6): 785-798, 2018 06.
Artigo
Inglês
| MEDLINE | ID: mdl-29753700
6.
Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data.
Bioinformatics
; 33(8): 1147-1153, 2017 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-28035032
7.
Discovery and functional characterization of a neomorphic PTEN mutation.
Proc Natl Acad Sci U S A
; 112(45): 13976-81, 2015 Nov 10.
Artigo
Inglês
| MEDLINE | ID: mdl-26504226
8.
Nucleosome regulatory dynamics in response to TGFß.
Nucleic Acids Res
; 42(11): 6921-34, 2014 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-24771338
9.
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Nat Genet
; 39(2): 207-11, 2007 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-17200669
10.
Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation.
Am J Hum Genet
; 91(4): 660-71, 2012 Oct 05.
Artigo
Inglês
| MEDLINE | ID: mdl-23040495
11.
Imputation of race and ethnicity categories using genetic ancestry from real-world genomic testing data.
Pac Symp Biocomput
; 29: 433-445, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38160297
12.
Session Introduction: Overcoming health disparities in precision medicine.
Pac Symp Biocomput
; 29: 322-326, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38160289
13.
The transcriptomes of two heritable cell types illuminate the circuit governing their differentiation.
PLoS Genet
; 6(8): e1001070, 2010 Aug 19.
Artigo
Inglês
| MEDLINE | ID: mdl-20808890
14.
Session Introduction: Overcoming health disparities in precision medicine.
Pac Symp Biocomput
; 28: 181-185, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36540975
15.
A deep-learning-based RNA-seq germline variant caller.
Bioinform Adv
; 3(1): vbad062, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37416509
16.
The status of the human gene catalogue.
ArXiv
; 2023 Mar 24.
Artigo
Inglês
| MEDLINE | ID: mdl-36994150
17.
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding.
Genome Res
; 19(9): 1527-41, 2009 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-19546169
18.
Genomics for the world.
Nature
; 475(7355): 163-5, 2011 Jul 13.
Artigo
Inglês
| MEDLINE | ID: mdl-21753830
19.
A new expectation-maximization statistical test for case-control association studies considering rare variants obtained by high-throughput sequencing.
Hum Hered
; 71(2): 113-25, 2011.
Artigo
Inglês
| MEDLINE | ID: mdl-21734402
20.
Racial and Ethnic Differences in Genomic Profiling of Early Onset Colorectal Cancer.
J Natl Cancer Inst
; 114(5): 775-778, 2022 05 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35134211