Detalhe da pesquisa
1.
Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma.
Blood
; 141(11): 1293-1307, 2023 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35977101
2.
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
Am J Hum Genet
; 106(2): 264-271, 2020 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32004448
3.
Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma.
Hum Mutat
; 43(10): 1396-1407, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35762214
4.
Rare germline variants in known melanoma susceptibility genes in familial melanoma.
Hum Mol Genet
; 26(24): 4886-4895, 2017 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29036293
5.
Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.
Br J Haematol
; 181(3): 372-377, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29693246
6.
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Hum Genet
; 135(11): 1241-1249, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27449771
7.
Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family.
Hum Genet
; 134(7): 775-87, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25939664
8.
GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas.
Sci Data
; 10(1): 25, 2023 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36635305
9.
DNA methylation age in paired tumor and adjacent normal breast tissue in Chinese women with breast cancer.
Clin Epigenetics
; 15(1): 55, 2023 03 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36991516
10.
GSTM1 and GSTT1 copy numbers and mRNA expression in lung cancer.
Mol Carcinog
; 51 Suppl 1: E142-50, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22392686
11.
Integrated Analysis of Coexpression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma.
J Invest Dermatol
; 142(9): 2464-2475.e5, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35181301
12.
Rare Germline Variants in Chordoma-Related Genes and Chordoma Susceptibility.
Cancers (Basel)
; 13(11)2021 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34070849
13.
Using whole-exome sequencing and protein interaction networks to prioritize candidate genes for germline cutaneous melanoma susceptibility.
Sci Rep
; 10(1): 17198, 2020 10 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057211
14.
XAF1 as a modifier of p53 function and cancer susceptibility.
Sci Adv
; 6(26): eaba3231, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32637605
15.
Whole-Exome Sequencing of Nasopharyngeal Carcinoma Families Reveals Novel Variants Potentially Involved in Nasopharyngeal Carcinoma.
Sci Rep
; 9(1): 9916, 2019 07 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31289279
16.
Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer.
J Natl Cancer Inst
; 109(11)2017 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29059430
17.
Rare inactivating PDE11A variants associated with testicular germ cell tumors.
Endocr Relat Cancer
; 22(6): 909-17, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26459559
18.
Germline TP53 variants and susceptibility to osteosarcoma.
J Natl Cancer Inst
; 107(7)2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25896519
19.
A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.
Cancer Discov
; 5(9): 920-31, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26084801