Detalhe da pesquisa
1.
Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma.
Nature
; 596(7872): 398-403, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34349258
2.
Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas.
Am J Hum Genet
; 110(3): 460-474, 2023 03 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36773604
3.
Molecular subclass of uterine fibroids predicts tumor shrinkage in response to ulipristal acetate.
Hum Mol Genet
; 32(7): 1063-1071, 2023 03 20.
Artigo
Inglês
| MEDLINE | ID: mdl-36048862
4.
GNAS mutation inhibits growth and induces phosphodiesterase 4D expression in colorectal cancer cell lines.
Int J Cancer
; 154(11): 1987-1998, 2024 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38319157
5.
Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5.
Gastroenterology
; 165(4): 861-873, 2023 10.
Artigo
Inglês
| MEDLINE | ID: mdl-37453564
6.
Genetic and Epigenetic Characteristics of Inflammatory Bowel Disease-Associated Colorectal Cancer.
Gastroenterology
; 161(2): 592-607, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33930428
7.
No evidence of EMAST in whole genome sequencing data from 248 colorectal cancers.
Genes Chromosomes Cancer
; 60(7): 463-473, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33527622
8.
Exome-wide somatic mutation characterization of small bowel adenocarcinoma.
PLoS Genet
; 14(3): e1007200, 2018 03.
Artigo
Inglês
| MEDLINE | ID: mdl-29522538
9.
The Contribution of Genetic Variation of Streptococcus pneumoniae to the Clinical Manifestation of Invasive Pneumococcal Disease.
Clin Infect Dis
; 68(1): 61-69, 2019 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29788414
10.
Combined Analysis of Variation in Core, Accessory and Regulatory Genome Regions Provides a Super-Resolution View into the Evolution of Bacterial Populations.
PLoS Genet
; 12(9): e1006280, 2016 09.
Artigo
Inglês
| MEDLINE | ID: mdl-27618184
11.
Towards pan-genome read alignment to improve variation calling.
BMC Genomics
; 19(Suppl 2): 87, 2018 May 09.
Artigo
Inglês
| MEDLINE | ID: mdl-29764365
12.
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.
Int J Cancer
; 142(3): 540-546, 2018 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28960316
13.
Exploration and retrieval of whole-metagenome sequencing samples.
Bioinformatics
; 30(17): 2471-9, 2014 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24845653
14.
Previously reported CCDC26 risk variant and novel germline variants in GALNT13, AR, and MYO10 associated with familial glioma in Finland.
Sci Rep
; 14(1): 11562, 2024 05 21.
Artigo
Inglês
| MEDLINE | ID: mdl-38773237
15.
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers.
Clin Epigenetics
; 15(1): 7, 2023 01 14.
Artigo
Inglês
| MEDLINE | ID: mdl-36639817
16.
Paneth cells as the origin of intestinal cancer in the context of inflammation.
Res Sq
; 2023 Jan 19.
Artigo
Inglês
| MEDLINE | ID: mdl-36711533
17.
The origin of intestinal cancer in the context of inflammation.
bioRxiv
; 2023 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37873142
18.
Fast scaffolding with small independent mixed integer programs.
Bioinformatics
; 27(23): 3259-65, 2011 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21998153
19.
Histopathologic and Molecular Characterization of Uterine Leiomyoma-like Inflammatory Myofibroblastic Tumor: Comparison to Molecular Subtypes of Uterine Leiomyoma.
Am J Surg Pathol
; 46(8): 1126-1136, 2022 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35426837
20.
Parity associates with chromosomal damage in uterine leiomyomas.
Nat Commun
; 12(1): 5448, 2021 09 14.
Artigo
Inglês
| MEDLINE | ID: mdl-34521855