Search details
1.
Genomic Features and Classification of Homologous Recombination Deficient Pancreatic Ductal Adenocarcinoma.
Gastroenterology
; 160(6): 2119-2132.e9, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33524400
2.
Is Biannual Surveillance for Pancreatic Cancer Sufficient in Individuals With Genetic Syndromes or Familial Pancreatic Cancer?
J Natl Compr Canc Netw
; 20(6): 663-673.e12, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35714671
3.
Brief family history questionnaire to screen for Lynch syndrome in women with newly diagnosed non-serous, non-mucinous ovarian cancers.
Int J Gynecol Cancer
; 32(7): 891-898, 2022 07 04.
Article
in English
| MEDLINE | ID: mdl-35012974
4.
Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study.
J Med Genet
; 58(4): 275-283, 2021 04.
Article
in English
| MEDLINE | ID: mdl-32581083
5.
Risk assessment and genetic counseling for Lynch syndrome - Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
J Genet Couns
; 31(3): 568-583, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35001450
6.
A region-based gene association study combined with a leave-one-out sensitivity analysis identifies SMG1 as a pancreatic cancer susceptibility gene.
PLoS Genet
; 15(8): e1008344, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31469826
7.
Clinical and genomic characterisation of mismatch repair deficient pancreatic adenocarcinoma.
Gut
; 70(10): 1894-1903, 2021 10.
Article
in English
| MEDLINE | ID: mdl-32933947
8.
Maximizing cancer prevention through genetic navigation for Lynch syndrome detection in women with newly diagnosed endometrial and nonserous/nonmucinous epithelial ovarian cancer.
Cancer
; 127(17): 3082-3091, 2021 09 01.
Article
in English
| MEDLINE | ID: mdl-33983630
9.
Understanding the clinical implication of mismatch repair deficiency in endometrioid endometrial cancer through a prospective study.
Gynecol Oncol
; 161(1): 221-227, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33478752
10.
Performance characteristics of screening strategies to identify Lynch syndrome in women with ovarian cancer.
Cancer
; 126(22): 4886-4894, 2020 11 15.
Article
in English
| MEDLINE | ID: mdl-32809219
11.
Tumor site discordance in mismatch repair deficiency in synchronous endometrial and ovarian cancers.
Int J Gynecol Cancer
; 30(12): 1951-1958, 2020 12.
Article
in English
| MEDLINE | ID: mdl-33082239
12.
The impact of health anxiety on perceptions of personal and children's health in parents with Lynch syndrome.
J Genet Couns
; 28(3): 495-506, 2019 06.
Article
in English
| MEDLINE | ID: mdl-30638287
13.
Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study.
Hered Cancer Clin Pract
; 17: 16, 2019.
Article
in English
| MEDLINE | ID: mdl-31391872
14.
Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome.
Hered Cancer Clin Pract
; 17: 24, 2019.
Article
in English
| MEDLINE | ID: mdl-31423292
15.
Comparison of Practice Guidelines, BRCAPRO, and Genetic Counselor Estimates to Identify Germline BRCA1 and BRCA2 Mutations in Pancreatic Cancer.
J Genet Couns
; 27(4): 988-995, 2018 08.
Article
in English
| MEDLINE | ID: mdl-29441441
16.
Overall Survival and Clinical Characteristics of BRCA-Associated Cholangiocarcinoma: A Multicenter Retrospective Study.
Oncologist
; 22(7): 804-810, 2017 07.
Article
in English
| MEDLINE | ID: mdl-28487467
17.
Genetic testing for Lynch syndrome in the province of Ontario.
Cancer
; 122(11): 1672-9, 2016 06 01.
Article
in English
| MEDLINE | ID: mdl-27019099
18.
Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.
Gastroenterology
; 148(3): 556-64, 2015 Mar.
Article
in English
| MEDLINE | ID: mdl-25479140
19.
Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium.
Am J Gastroenterol
; 111(2): 275-84, 2016 Feb.
Article
in English
| MEDLINE | ID: mdl-26729549
20.
PMS2 monoallelic mutation carriers: the known unknown.
Genet Med
; 18(1): 13-9, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-25856668