Detalhe da pesquisa
1.
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells.
Nature
; 586(7831): 769-775, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057200
2.
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.
Am J Hum Genet
; 107(3): 432-444, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32758450
3.
Mutational landscape and clinical outcome of patients with de novo acute myeloid leukemia and rearrangements involving 11q23/KMT2A.
Proc Natl Acad Sci U S A
; 117(42): 26340-26346, 2020 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33020282
4.
Assessing thyroid cancer risk using polygenic risk scores.
Proc Natl Acad Sci U S A
; 117(11): 5997-6002, 2020 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32132206
5.
Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.
Int J Cancer
; 148(12): 2935-2946, 2021 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33527407
6.
Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses.
Gastroenterology
; 158(5): 1300-1312.e20, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31884074
7.
Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patients.
Gynecol Oncol
; 160(1): 161-168, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33393477
8.
Variants in LRRC34 reveal distinct mechanisms for predisposition to papillary thyroid carcinoma.
J Med Genet
; 57(8): 519-527, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32051256
9.
Adiposity, metabolites, and colorectal cancer risk: Mendelian randomization study.
BMC Med
; 18(1): 396, 2020 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33327948
10.
Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome.
J Med Genet
; 56(7): 462-470, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30877237
11.
MYH9 binds to lncRNA gene PTCSC2 and regulates FOXE1 in the 9q22 thyroid cancer risk locus.
Proc Natl Acad Sci U S A
; 114(3): 474-479, 2017 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28049826
12.
Identification of NRAS isoform 2 overexpression as a mechanism facilitating BRAF inhibitor resistance in malignant melanoma.
Proc Natl Acad Sci U S A
; 114(36): 9629-9634, 2017 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28827320
13.
Fine mapping of 14q13 reveals novel variants associated with different histological subtypes of papillary thyroid carcinoma.
Int J Cancer
; 144(3): 503-512, 2019 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30350351
14.
Response to Li and Hopper.
Am J Hum Genet
; 108(3): 527-529, 2021 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33667396
15.
PD-1 Blockade in Tumors with Mismatch-Repair Deficiency.
N Engl J Med
; 372(26): 2509-20, 2015 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26028255
16.
The role of SMAD3 in the genetic predisposition to papillary thyroid carcinoma.
Genet Med
; 20(9): 927-935, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29300379
17.
MicroRNA-3151 inactivates TP53 in BRAF-mutated human malignancies.
Proc Natl Acad Sci U S A
; 112(49): E6744-51, 2015 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26582795
18.
Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer.
Proc Natl Acad Sci U S A
; 112(19): 6128-33, 2015 May 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25918370
19.
Immunoglobulin transcript sequence and somatic hypermutation computation from unselected RNA-seq reads in chronic lymphocytic leukemia.
Proc Natl Acad Sci U S A
; 112(14): 4322-7, 2015 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25787252
20.
Frequent PIK3CA Mutations in Colorectal and Endometrial Tumors With 2 or More Somatic Mutations in Mismatch Repair Genes.
Gastroenterology
; 151(3): 440-447.e1, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27302833