Webinars
As part of the ERN GENTURIS e-training programme, each of our webinars provides either a general overview of a genturis-related topic or an in-depth look at one of the genturis diseases from a specific healthcare perspective. An important goal of our webinar series is to cover each genturis from several perspectives in order to create a comprehensive overview of the currently available knowledge for every genturis.
All our webinars include at least one speaker that is a member of ERN GENTURIS. The target audience for the webinars consists of clinicians, genetic counsellors, clinical scientists and other genetics health professionals. The webinars last approximately 30-40 minutes, and viewers have the opportunity to send questions on the subject area, which will be addressed in a question & answer session afterwards. Webinars are usually held on Wednesday afternoons.
Date |
Time |
Speaker |
Title |
Registration* |
---|---|---|---|---|
12-03-2025 | 16:00-17:00 CET | Richarda de Voer | Genetic cancer predisposition in adolescents and young adults | register |
* Please pay attention to the technical requirements provided with the access link. In case of access problems related to hospital firewalls, please use your private computer and internet connection.
The previous webinars listed below are subdivided into the following categories:
Thematic group 3: Hereditary breast and ovarian cancer syndrome (HBOC)
Thematic group 4: Other rare – predominantly malignant – genturis
Date |
Speaker |
Title |
View** |
---|---|---|---|
07-06-2023 | Gareth Evans | New ERN GENTURIS NF1 guidelines and update on NF2 and SCHWN nomenclature | view |
27-01-2022 | Sirkku Peltonen & Pierre Wolkenstein | Cutaneous neurofibromas | view |
28-10-2020 | Gareth Evans | Neurocutaneous tumour syndromes | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
07-06-2023 | Gareth Evans | New ERN GENTURIS NF1 guidelines and update on NF2 and SCHWN nomenclature | view |
07-12-2021 | Eric Legius | Legius syndrome and its link with Neurofibromatosis type 1 | view |
10-11-2021 | Rianne Oostenbrink | NF1 from the pediatric perspective | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
13-03-2024 | Verena Steinke-Lange | Hereditary tumour syndromes for gastroenterologists | view |
08-03-2023 | Richarda de Voer | Genetics of (new) colorectal cancer & polyposis syndromes | view |
25-01-2023 | Stefan Aretz | Genetics 30 years after the discovery of APC | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
20-11-2024 | Marjolijn Ligtenberg | Molecular profiles of noncanonical malignancies from patients with Lynch syndrome or a BRCA1/2 pathogenic variant may generate putative options for personalized treatment. | view |
09-11-2023 | Monique van Leerdam | Lynch syndrome – the gastroenterologist’s perspective | view |
06-09-2023 | Elke Holinski-Feder | Lynch syndrome update | view |
13-10-2021 | Iosune Baraibar | Update in therapeutic options for Lynch-associated colorectal cancer patients | view |
30-09-2020 | Elke Holinski-Feder | HNPCC related tumour risk syndromes – pathomechanisms and clinical implications | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
09-04-2024 | Lenka Foretova | Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS) – not so infrequent disease | view |
25-10-2023 | Anja Wagner & Esther Korpershoek | Peutz-Jeghers syndrome – the clinical genetic perspective | view |
22-03-2023 | Marco Vitellaro | Familial adenomatous polyposis - the surgeon's perspective | view |
06-02-2023 | Chella van der Post | Hereditary gastrointestinal cancer – the pathologist's perspective | view |
13-01-2021 | Stefan Aretz | Gastrointestinal polyposis syndromes | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
14-02-2024 | Nicoline Hoogerbrugge | PTEN hamartoma tumour syndrome (PHTS, Cowden syndrome): update on cancer risks and yield of surveillance | view |
06-02-2023 | Chella van der Post | Hereditary gastrointestinal cancer – the pathologist's perspective | view |
21-10-2021 | Jolanda Schieving | PTEN hamartoma tumour syndrome in childhood | view |
09-12-2020 | Nicoline Hoogerbrugge | Recognising PTEN hamartoma tumour syndrome for early cancer detection | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
27-03-2024 | Thomas van Overeem Hansen | TP53 variant classification | view |
31-03-2021 | Yvonne Brandberg | Psychological aspects on the TP53 related cancer syndromes | view |
14-10-2020 | Thierry Frebourg | Li-Fraumeni and heritable TP53-related cancer syndromes | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
25-09-2024 | Marianne Geilswijk | ERN GENTURIS guideline on Birt-Hogg-Dubé syndrome diagnosis, surveillance and management | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
24-06-2024 | Barbara Perić | Familal melanoma - the surgeon’s perspective | view |
28-02-2024 | Remco van Doorn | Familial melanoma - the dermatologist's perspective | view |
09-03-2022 | Karin Wadt | Genetic predisposition to melanoma | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
22-01-2025 | Katharina Wimmer & Chrystelle Colas | ERN GENTURIS guideline on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management | view |
26-05-2021 | Chrystelle Colas | Constitutional Mismatch Repair Deficiency (CMMRD) Syndrome | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
22-11-2023 | Carla Oliveira | CTNNA1 germline variants: genotype-phenotype associations | view |
06-02-2023 | Chella van der Post | Hereditary gastrointestinal cancer – the pathologist's perspective | view |
24-05-2022 | Fátima Carneiro | Pathology of CDH1-related diffuse gastric cancer | view |
11-05-2021 | Tanya Bisseling | A personal history about hereditary diffuse gastric cancer | view |
25-11-2020 | Carla Oliveira | Hereditary Gastric Cancer | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
28-10-2020 | Gareth Evans | Neurocutaneous tumour syndromes (including Gorlin) | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
06-12-2023 | Eamonn Maher | Hereditary Leiomyomatosis and Renal Cell Cancer | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
22-06-2023 | Marieke de Laat | von Hippel-Lindau disease - the endocrinologist’s perspective | view |
17-03-2021 | Eamonn Maher | Von Hippel-Lindau disease: from clinic to gene and back | view |
Date |
Speaker |
Title |
View** |
---|---|---|---|
11-11-2020 | Evelin Schröck | Pheochromocytoma/ paraganglioma – benefit of combined germline and tumour testing for PPGL patients | view |
** A recording of each webinar will be made available within a week after broadcast. Please pay attention to the technical requirements provided with the access link. In case of access problems related to hospital firewalls, please use your private PC and internet connection.
Updated on 7-2-2024