Sanne W. Bajwa -  ten Broeke
Sanne W. Bajwa - ten Broeke
University Medical Center Groningen
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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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