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S. Holter · SciRah

Researcher profile · Semantic Scholar

S. Holter

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S. Holter — researcher profile on SciRah

h-index: 30
Works: 111
Citations: 4,290

Most-cited papers

Genomics-Driven Precision Medicine for Advanced Pancreatic Cancer: Early Results from the COMPASS Trial
K. Aung, S. Fischer, R. Denroche, G. Jang +30 more
2017Clinical Cancer Research530 citations Open access
Semantic Scholar
Overall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers
T. Golan, Z. Kanji, R. Epelbaum, N. Devaud +10 more
2014British Journal of Cancer412 citations Open access
Semantic Scholar
Germline BRCA Mutations in a Large Clinic-Based Cohort of Patients With Pancreatic Adenocarcinoma.
S. Holter, A. Borgida, A. Dodd, R. Grant +7 more
2015Journal of Clinical Oncology369 citations Open access
Semantic Scholar
Prevalence of Germline Mutations in Cancer Predisposition Genes in Patients with Pancreatic Cancer
R. Grant, Iris Selander, Ashton A. Connor, S. Selvarajah +6 more
2014Gastroenterology288 citations Open access
Semantic Scholar
The PREMM1,2,6 Model Predicts Risk of MLH1, MSH2, and MSH6 Germline Mutations Based on Cancer History
F. Kastrinos, E. Steyerberg, Rowena C Mercado, J. Balmaña +10 more
2010Gastroenterology203 citations Open access
Semantic Scholar
Screening for Pancreatic Cancer in a High-Risk Cohort: An Eight-Year Experience
W. Al-Sukhni, A. Borgida, H. Rothenmund, S. Holter +8 more
2012Journal of Gastrointestinal Surgery149 citations
Semantic Scholar
Genomic Features and Classification of Homologous Recombination Deficient Pancreatic Ductal Adenocarcinoma.
T. Golan, G. O'Kane, R. Denroche, M. Raitses-Gurevich +24 more
2021Gastroenterology141 citations
Semantic Scholar
Identification of Individuals at Risk for Lynch Syndrome Using Targeted Evaluations and Genetic Testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer Joint Practice Guideline
S. Weissman, R. Burt, J. Church, S. Erdman +9 more
2012Journal of Genetic Counseling141 citations Open access
Semantic Scholar
Analysis of the Gene Coding for the BRCA2-Interacting Protein PALB2 in Familial and Sporadic Pancreatic Cancer
M. Tischkowitz, N. Sabbaghian, N. Hamel, A. Borgida +8 more
2009Gastroenterology139 citations Open access
Semantic Scholar
Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases.
Kandelaria M. Rumilla, Karen V. Schowalter, N. Lindor, Brittany C. Thomas +14 more
2011Journal of Molecular Diagnostics115 citations Open access
Semantic Scholar
Overall Survival and Clinical Characteristics of BRCA-Associated Cholangiocarcinoma: A Multicenter Retrospective Study.
T. Golan, M. Raitses-Gurevich, R. Kelley, A. Bocobo +10 more
2017The Oncologist111 citations Open access
Semantic Scholar
The Histomorphology of Lynch Syndrome–associated Ovarian Carcinomas: Toward a Subtype-specific Screening Strategy
M. Chui, P. Ryan, J. Radigan, Sarah E. Ferguson +14 more
2014American Journal of Surgical Pathology110 citations
Semantic Scholar
Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer.
Sean C. Skeldon, K. Semotiuk, M. Aronson, S. Holter +15 more
2013European Urology109 citations
Semantic Scholar
Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation‐positive patients with endometrial cancer encountered in the context of familial gastrointestinal cancer registries
P. Ryan, Anna Marie Mulligan, M. Aronson, S. Ferguson +9 more
2012Cancer78 citations Open access
Semantic Scholar
The Gastrointestinal Phenotype of Germline Biallelic Mismatch Repair Gene Mutations
C. Durno, S. Holter, P. Sherman, S. Gallinger
2010American Journal of Gastroenterology77 citations
Semantic Scholar
BRCA1 and BRCA2 mutations sensitize to chemotherapy in patient-derived pancreatic cancer xenografts
I. Lohse, Alexander Borgida, P. Cao, M. Cheung +9 more
2015British Journal of Cancer74 citations Open access
Semantic Scholar
Clinical and genomic characterisation of mismatch repair deficient pancreatic adenocarcinoma
R. Grant, R. Denroche, G. Jang, Klaudia M. Nowak +20 more
2020Gut68 citations
Semantic Scholar
PMS2 monoallelic mutation carriers: the known unknown
M. Goodenberger, Brittany C. Thomas, D. Riegert-Johnson, C. Boland +26 more
2015Genetics in Medicine61 citations Open access
Semantic Scholar
Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioning
C. Maheu, A. Vodermaier, H. Rothenmund, S. Gallinger +5 more
2010Familial Cancer59 citations
Semantic Scholar
Lack of evidence for germline RNF43 mutations in patients with serrated polyposis syndrome from a large multinational study
D. Buchanan, M. Clendenning, Zhuo-Er Li, J. Stewart +13 more
2016Gut58 citations
Semantic Scholar
Candidate DNA Repair Susceptibility Genes Identified by Exome Sequencing in High-Risk Pancreatic Cancer
A. L. Smith, N. Alirezaie, Ashton A. Connor, M. Chan-Seng-Yue +18 more
2015Cancer Letters52 citations Open access
Semantic Scholar
Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium
M. Aronson, S. Gallinger, Z. Cohen, S. Cohen +29 more
2016American Journal of Gastroenterology45 citations
Semantic Scholar
Whole genome and transcriptome profiling in advanced pancreatic cancer patients on the COMPASS trial
Jennifer J. Knox, G. Jang, R. Grant, Amy Zhang +40 more
2025Nature Communications38 citations Open access
Semantic Scholar
Exome sequencing identifies nonsegregating nonsense ATM and PALB2 variants in familial pancreatic cancer
R. Grant, W. Al-Sukhni, A. Borgida, S. Holter +9 more
2013Human Genomics37 citations Open access
Semantic Scholar
Moderators of cancer‐related distress and worry after a pancreatic cancer genetic counseling and screening intervention
Stacey L. Hart, Lindsey A. Torbit, Cassandra J. Crangle, M. Esplen +6 more
2012Psycho-Oncology35 citations
Semantic Scholar
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
S. Holter, M. Hall, H. Hampel, K. Jasperson +8 more
2022Journal of Genetic Counseling29 citations Open access
Semantic Scholar
Identification of germline genomic copy number variation in familial pancreatic cancer
W. Al-Sukhni, Sarah Joe, A. C. Lionel, N. Zwingerman +14 more
2012Human Genetics29 citations Open access
Semantic Scholar
How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry
L. Keogh, Douglass Fisher, S. Sheinfeld Gorin, S. Schully +13 more
2014Journal of Community Genetics28 citations Open access
Semantic Scholar
A Preclinical Trial and Molecularly Annotated Patient Cohort Identify Predictive Biomarkers in Homologous Recombination–deficient Pancreatic Cancer
Yi-Fan Wang, J. Park, Alain Pacis, R. Denroche +32 more
2020Clinical Cancer Research26 citations Open access
Semantic Scholar
Examining intrafamilial communication of colorectal cancer risk status to family members and kin responses to colonoscopy: a qualitative study
Kaitlin M. McGarragle, C. Hare, S. Holter, D. Facey +3 more
2019Hereditary Cancer in Clinical Practice25 citations Open access
Semantic Scholar
Reflex Testing for Germline BRCA1, BRCA2, PALB2, and ATM Mutations in Pancreatic Cancer: Mutation Prevalence and Clinical Outcomes From Two Canadian Research Registries.
Alyssa L. Smith, Cavin Wong, A. Cuggia, A. Borgida +24 more
2018JCO Precision Oncology24 citations Open access
Semantic Scholar
Understanding the clinical implication of mismatch repair deficiency in endometrioid endometrial cancer through a prospective study.
S. Kim, A. Tone, R. Kim, M. Cesari +18 more
2021Gynecologic Oncology22 citations
Semantic Scholar
DNA Mismatch Repair Status Predicts Need for Future Colorectal Surgery for Metachronous Neoplasms in Young Individuals Undergoing Colorectal Cancer Resection
M. Aronson, S. Holter, K. Semotiuk, L. Winter +4 more
2015Diseases of the Colon & Rectum22 citations
Semantic Scholar
Exome and Genome Sequencing in Adults with Undiagnosed Disease: A Prospective Cohort Study
Salma Shickh, Mariana Guitierrez Salazar, Kathleen-Rose Zakoor, C. Lázaro +33 more
2020Journal of Medical Genetics21 citations Open access
Semantic Scholar
Performance characteristics of screening strategies to identify Lynch syndrome in women with ovarian cancer
S. Kim, A. Tone, R. Kim, M. Cesari +18 more
2020Cancer19 citations Open access
Semantic Scholar
A region-based gene association study combined with a leave-one-out sensitivity analysis identifies SMG1 as a pancreatic cancer susceptibility gene
Cavin Wong, Fei Chen, N. Alirezaie, Yi-Fan Wang +19 more
2019PLoS Genetics18 citations Open access
Semantic Scholar
Additional germline findings from a tumor profiling program
N. Stjepanovic, T. Stockley, Philippe Bédard, J. McCuaig +14 more
2018BMC Medical Genomics17 citations Open access
Semantic Scholar
Physician trust moderates the relationship between intolerance of uncertainty and cancer worry interference among women with Lynch syndrome
Lindsey A. Torbit, Jenna J. Albiani, M. Aronson, S. Holter +3 more
2016Journal of behavioral medicine16 citations
Semantic Scholar
Evaluating Colonoscopy Screening Intervals in Patients with Lynch Syndrome from a Large Canadian Registry.
M. Aronson, R. Gryfe, Yun-Hee Choi, K. Semotiuk +5 more
2023Journal of the National Cancer Institute15 citations
Semantic Scholar
An integrative DNA sequencing and methylation panel to assess mismatch repair deficiency.
L. Oldfield, Tian-Tian Li, Alicia Tone, M. Aronson +11 more
2020Journal of Molecular Diagnostics15 citations Open access
Semantic Scholar
Hepatic adenomas caused by somatic HNF1A mutations in children with biallelic mismatch repair gene mutations.
S. Holter, A. Pollett, G. Zogopoulos, Hyeja Kim +7 more
2011Gastroenterology14 citations Open access
Semantic Scholar
Genetic testing for Lynch syndrome in the province of Ontario
Marina Wang, S. AlDubayan, Ashton A. Connor, Beatrix Wong +11 more
2016Cancer13 citations Open access
Semantic Scholar
Benefits of platinum-based chemotherapy (Pt-chemo) in pancreatic adenocarcinoma (PC) associated with BRCA mutations: A translational case series.
O. Faluyi, B. Tran, Z. Kanji, S. Moore +5 more
201212 citations
Semantic Scholar
Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome
Kaitlin M. McGarragle, M. Aronson, K. Semotiuk, S. Holter +4 more
2019Hereditary Cancer in Clinical Practice11 citations Open access
Semantic Scholar
Overall survival of patients with pancreatic adenocarcinoma and BRCA1 or BRCA2 germline mutation.
K. Aung, S. Holter, A. Borgida, Ashton A. Connor +5 more
201610 citations
Semantic Scholar
Germline BRCA2 variants in advanced pancreatic acinar cell carcinoma: A case report and review of literature
C. Lee, S. Holter, A. Borgida, A. Dodd +12 more
2022World Journal of Gastroenterology9 citations Open access
Semantic Scholar
Maximizing cancer prevention through genetic navigation for Lynch syndrome detection in women with newly diagnosed endometrial and nonserous/nonmucinous epithelial ovarian cancer
S. Kim, A. Tone, R. Kim, M. Cesari +18 more
2021Cancer9 citations Open access
Semantic Scholar
Platinum-based chemotherapy (Pt-chemo) in pancreatic adenocarcinoma (PC) associated with BRCA mutations: A translational case series.
B. Tran, S. Moore, G. Zogopoulos, A. Borgida +3 more
2012Journal of Clinical Oncology9 citations
Semantic Scholar
Is Biannual Surveillance for Pancreatic Cancer Sufficient in Individuals With Genetic Syndromes or Familial Pancreatic Cancer?
Yi-Fan Wang, A. Cuggia, Yen-I Chen, J. Parent +19 more
2022The Journal of the National Comprehensive Cancer Network8 citations
Semantic Scholar
Hereditary colorectal cancer registries in Canada: report from the Colorectal Cancer Association of Canada consensus meeting; Montreal, Quebec; October 28, 2011.
H. Rothenmund, H. Singh, B. Candas, B. N. Chodirker +11 more
2013Current Oncology6 citations Open access
Semantic Scholar

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