Detalhe da pesquisa
1.
Advancing gastric cancer precision medicine with novel genomic screens.
J Pathol
; 259(4): 359-361, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36541926
2.
Exome sequencing of affected duos and trios uncovers PRUNE2 as a novel prostate cancer predisposition gene.
Br J Cancer
; 128(6): 1077-1085, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36564567
3.
Promotores' perspectives on the virtual adaptation of a hereditary breast cancer education program.
J Genet Couns
; 32(6): 1226-1231, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37747056
4.
Cancer health disparities in racial/ethnic minorities in the United States.
Br J Cancer
; 124(2): 315-332, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32901135
5.
Haplotype analysis of the internationally distributed BRCA1 c.3331_3334delCAAG founder mutation reveals a common ancestral origin in Iberia.
Breast Cancer Res
; 22(1): 108, 2020 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33087180
6.
Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas.
Breast Cancer Res
; 21(1): 3, 2019 01 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30642363
7.
Racial/ethnic differences in survival among gastric cancer patients in california.
Cancer Causes Control
; 30(7): 687-696, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31102083
8.
Progress and future challenges in aging and diversity research in the United States.
Alzheimers Dement
; 15(7): 995-1003, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30240574
9.
Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer.
Gastroenterology
; 152(5): 983-986.e6, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28024868
10.
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
PLoS Genet
; 11(3): e1004925, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25781923
11.
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk.
Hum Mol Genet
; 24(5): 1478-92, 2015 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25378557
12.
The dual pandemic of COVID-19 and systemic inequities in US Latino communities.
Cancer
; 127(10): 1548-1550, 2021 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33405237
13.
Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development.
J Pathol
; 236(2): 155-64, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25712196
14.
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
Nat Genet
; 39(8): 984-8, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17618284
15.
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk.
Hum Genet
; 134(2): 231-45, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25487306
16.
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13.
Hum Mol Genet
; 21(4): 934-46, 2012 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22076443
17.
Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.
Gastroenterology
; 144(1): 53-5, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22999960
18.
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
PLoS Genet
; 7(6): e1002105, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21655089
19.
Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals.
Gut
; 62(6): 871-81, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22490517
20.
Assessment of Patient-Derived Xenograft Growth and Antitumor Activity: The NCI PDXNet Consensus Recommendations.
Mol Cancer Ther
; 2024 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38641411