Detalhe da pesquisa
1.
Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants.
J Med Genet
; 58(4): 264-269, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32482799
2.
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome.
Genet Med
; 21(12): 2706-2712, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204389
3.
Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriers.
Br J Cancer
; 119: 357-363, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29937543
4.
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
Hum Mutat
; 37(11): 1162-1179, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27435373
5.
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers.
Genet Med
; 18(4): 405-9, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26110232
6.
A case series of intestinal adenomatous polyposis of unidentified etiology; a late effect of irradiation?
BMC Cancer
; 16(1): 862, 2016 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27821077
7.
Yield of screening colonoscopy in first-degree relatives of patients with serrated polyposis syndrome.
J Clin Gastroenterol
; 49(5): 407-12, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-24583756
8.
Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas.
J Med Genet
; 49(6): 362-5, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22636603
9.
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
Breast Cancer Res
; 14(1): R33, 2012 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22348646
10.
CDH1-related hereditary diffuse gastric cancer syndrome: clinical variations and implications for counseling.
Int J Cancer
; 131(2): 367-76, 2012 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22020549
11.
Body weight and risk of breast cancer in BRCA1/2 mutation carriers.
Breast Cancer Res Treat
; 126(1): 193-202, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20730487
12.
Compliance with periodic surveillance for Von-Hippel-Lindau disease.
Genet Med
; 13(6): 519-27, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21415761
13.
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.
Gastroenterology
; 136(1): 131-7, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19010329
14.
Synchronous Hodgkin's lymphoma and schwannomas mimicking refractory Hodgkin's lymphoma.
Ann Hematol
; 94(9): 1593-5, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26025633
15.
A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history.
Breast Cancer Res
; 11(1): R8, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19200354
16.
A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example.
BMC Cancer
; 9: 211, 2009 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-19563646
17.
The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect.
Cancer Epidemiol Biomarkers Prev
; 28(6): 1010-1014, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30824524
18.
SNP association study in PMS2-associated Lynch syndrome.
Fam Cancer
; 17(4): 507-515, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29147930
19.
Cancer Risks for PMS2-Associated Lynch Syndrome.
J Clin Oncol
; 36(29): 2961-2968, 2018 10 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30161022
20.
Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study.
JNCI Cancer Spectr
; 2(2): pky023, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31360853