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Sanne W. Bajwa -  ten Broeke
Sanne W. Bajwa - ten Broeke
University Medical Center Groningen
Verified email at umcg.nl
Title
Cited by
Cited by
Year
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
M Dominguez-Valentin, JR Sampson, TT Seppälä, SW Ten Broeke, ...
Genetics in Medicine 22 (1), 15-25, 2020
4622020
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk
SW Ten Broeke, RM Brohet, CM Tops, HM van der Klift, ME Velthuizen, ...
J Clin Oncol 33 (4), 319-325, 2015
2192015
Cancer risks for PMS2-associated Lynch syndrome
SW Ten Broeke, HM van der Klift, CMJ Tops, S Aretz, I Bernstein, ...
Journal of Clinical Oncology 36 (29), 2961, 2018
1802018
Mutational signature analysis reveals NTHL1 deficiency to cause a multi-tumor phenotype
JE Grolleman, RM De Voer, FA Elsayed, M Nielsen, RDA Weren, C Palles, ...
Cancer cell 35 (2), 256-266. e5, 2019
1502019
The shared frameshift mutation landscape of microsatellite-unstable cancers suggests immunoediting during tumor evolution
A Ballhausen, MJ Przybilla, M Jendrusch, S Haupt, E Pfaffendorf, ...
Nature communications 11 (1), 4740, 2020
942020
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome
HM van der Klift, AR Mensenkamp, M Drost, EC Bik, YJ Vos, HJJP Gille, ...
Human mutation 37 (11), 1162-1179, 2016
632016
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
AK Win, JG Dowty, JC Reece, G Lee, AS Templeton, JP Plazzer, ...
The Lancet Oncology 22 (7), 1014-1022, 2021
572021
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
TT Seppälä, A Ahadova, M Dominguez-Valentin, F Macrae, DG Evans, ...
Hereditary cancer in clinical practice 17, 1-8, 2019
562019
The “unnatural” history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance
A Ahadova, TT Seppälä, C Engel, R Gallon, J Burn, E Holinski‐Feder, ...
International journal of cancer 148 (4), 800-811, 2021
532021
Molecular background of colorectal tumors from patients with Lynch syndrome associated with germline variants in PMS2
SW Ten Broeke, TC van Bavel, AML Jansen, E Gómez-García, FJ Hes, ...
Gastroenterology 155 (3), 844-851, 2018
492018
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
M Dominguez-Valentin, EJ Crosbie, C Engel, S Aretz, F Macrae, I Winship, ...
Genetics in Medicine 23 (4), 705-712, 2021
332021
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
M Dominguez-Valentin, TT Seppälä, JR Sampson, F Macrae, I Winship, ...
Hereditary cancer in clinical practice 17, 1-6, 2019
332019
A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects
IHM Van der Linde, YL Hiemstra, R Bökenkamp, AM van Mil, ...
Netherlands Heart Journal 25, 675-681, 2017
262017
Constitutional mismatch repair deficiency in a healthy child: on the spot diagnosis?
M Suerink, TP Potjer, AB Versluijs, SW Ten Broeke, CM Tops, K Wimmer, ...
Clinical genetics 93 (1), 134-137, 2018
232018
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome
M Suerink, M Rodríguez-Girondo, HM van der Klift, C Colas, L Brugieres, ...
Genetics in Medicine 21 (12), 2706-2712, 2019
212019
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
M Suerink, HM Van Der Klift, SW Ten Broeke, OM Dekkers, I Bernstein, ...
Genetics in Medicine 18 (4), 405-409, 2016
212016
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
P Møller, T Seppälä, JG Dowty, S Haupt, M Dominguez-Valentin, L Sunde, ...
Hereditary cancer in clinical practice 20 (1), 36, 2022
202022
Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders
JR Stolz, KM Foote, HE Veenstra-Knol, R Pfundt, SW Ten Broeke, ...
The American Journal of Human Genetics 108 (9), 1692-1709, 2021
202021
The diverse molecular profiles of lynch syndrome-associated colorectal cancers are (highly) dependent on underlying germline mismatch repair mutations
NC Helderman, SW Bajwa-ten Broeke, H Morreau, M Suerink, D Terlouw, ...
Critical Reviews in Oncology/Hematology 163, 103338, 2021
142021
Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum
M Dominguez‐Valentin, JR Sampson, P Møller, TT Seppälä, ...
International Journal of Cancer 148 (2), 512-513, 2021
142021
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