Abstract 1158: Hypermutation patterns shape tumorigenesis and immunotherapy response in mismatch repair deficient glioma
Nicholas R. Fernandez, Yuan Chang, Nuno M. Nunes, Jose Rafael Dimayacyac et autres
0 citationsCancer Research
Melyssa Aronson
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246Publications signalées
9184Citations signalées
4Affiliations récentes
Institutions déclarées
Domaines associés
Genetic factors in colorectal cancerBRCA gene mutations in cancerGlioma Diagnosis and TreatmentCancer Genomics and DiagnosticsGenomics and Rare Diseases
Publications récentes
Clinicopathological Factors Associated with Gastric Signet Ring Cell Carcinoma in CDH1 Pathogenic Variant Carriers: Report from the GASTRIC Consortium
Ophir Gilad, Christine Drogan, Emma Keel, Guimin Gao et autres
0 citationsmedRxiv
Correction: The development and usability of ‘The Genetics Navigator’: a digital solution for adult and paediatric clinical genetics services
Saumeh Saeedi, Daena Hirjikaka, Marc Clausen, Stephanie Luca et autres
0 citationsEuropean Journal of Human Genetics
“Where do I go from here?” Navigating a lifelong road without a map: the care experiences of hereditary cancer patients
Carly Butkowsky, June C. Carroll, Melyssa Aronson, Jordan Sam et autres
1 citationEuropean Journal of Human Genetics
Non-invasive screening in hereditary cancer: a randomized controlled trial to test cell-free DNA-based early detection in the CHARM consortium
Kirsten M. Farncombe, Julia A. Sobotka, Melyssa Aronson, Mark Basik et autres
3 citationsEuropean Journal of Human Genetics
Patterns of hypermutation shape tumorigenesis and immunotherapy response in mismatch-repair-deficient glioma
Nicholas R. Fernandez, Yuan Chang, Nuno M. Nunes, Jose Rafael Dimayacyac et autres
6 citationsNature Genetics
Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdens
Chloe Mighton, Emma Reble, Jordan Sam, Rita Kodida et autres
0 citationsGenetics in Medicine
Hereditary diffuse gastric cancer spectrum associated with germline CTNNA1 loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls
Silvana Lobo, Alexandre Dias, Marta Ferreira, André Pinto-Oliveira et autres
8 citationsGut
Comprehensively Testing the Function of Missense Variation in the STK11 Tumour Suppressor
Daniel Zimmerman, Atina G. Coté, Warren van Loggerenberg, Marinella Gebbia et autres
0 citationsbioRxiv (Cold Spring Harbor Laboratory)
The development and usability of ‘The Genetics Navigator’: a digital solution for adult and paediatric clinical genetics services
Saumeh Saeedi, Daena Hirijkaka, Marc Clausen, Stephanie Luca et autres
2 citationsEuropean Journal of Human Genetics
Psychological impact of risk-reducing surgery for gynecologic cancer among women with Lynch syndrome
Helen Huband, Kaitlin McGarragle, Crystal Hare, Melyssa Aronson et autres
0 citationsGynecologic Oncology Reports
Canadian consensus for the assessment and testing of Lynch syndrome
Melyssa Aronson, Laura Palma, Kara Semotiuk, Jennifer Nuk et autres
4 citationsJournal of Medical Genetics
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