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Anja Wagner

Showing results (121-130 of 174) with videos related to

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Journal of Medical Genetics|December 15, 2012
Pancreatic cancer risk in Peutz-Jeghers syndrome patients: a large cohort study and implications for surveillanceSusanne E Korsse, Femme Harinck, Margot G F van Lier, et al.
Familial Cancer|November 28, 2019
'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultationsNiki M Medendorp, Marij A Hillen, Pomme E A van Maarschalkerweerd, et al.
Human Mutation|April 14, 2025
Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius SyndromeHannie Douben, Marianne Hoogeveen-Westerveld, Mark Nellist, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Journal of Medical Genetics|February 7, 2014
Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repairEva A L Wielders, Jan Hettinger, Rob Dekker, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 19, 2010
Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequencesChantal R M Lammens, Neil K Aaronson, Anja Wagner, et al.
Molecular Genetics & Genomic Medicine|November 16, 2022
Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumorsIrma van de Beek, Iris E Glykofridis, Anja Wagner, et al.
Pancreas|November 16, 2016
Prevalence and Progression of Pancreatic Cystic Precursor Lesions Differ Between Groups at High Risk of Developing Pancreatic CancerIngrid C A W Konings, Femme Harinck, Jan-Werner Poley, et al.
BMC Research Notes|June 27, 2015
Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control studyThomas P Potjer, Nienke van der Stoep, Jeanine J Houwing-Duistermaat, et al.
European Journal of Cancer (Oxford, England : 1990)|July 17, 2013
The development of a clinical screening instrument for tumour predisposition syndromes in childhood cancer patientsSaskia M J Hopman, Johannes H M Merks, Corianne A J M de Borgie, et al.
Pageof 18

Showing results (121-130 of 174) with videos related to

Sort By:
Pageof 18
Journal of Medical Genetics|December 15, 2012
Pancreatic cancer risk in Peutz-Jeghers syndrome patients: a large cohort study and implications for surveillanceSusanne E Korsse, Femme Harinck, Margot G F van Lier, et al.
Familial Cancer|November 28, 2019
'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultationsNiki M Medendorp, Marij A Hillen, Pomme E A van Maarschalkerweerd, et al.
Human Mutation|April 14, 2025
Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius SyndromeHannie Douben, Marianne Hoogeveen-Westerveld, Mark Nellist, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Journal of Medical Genetics|February 7, 2014
Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repairEva A L Wielders, Jan Hettinger, Rob Dekker, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 19, 2010
Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequencesChantal R M Lammens, Neil K Aaronson, Anja Wagner, et al.
Molecular Genetics & Genomic Medicine|November 16, 2022
Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumorsIrma van de Beek, Iris E Glykofridis, Anja Wagner, et al.
Pancreas|November 16, 2016
Prevalence and Progression of Pancreatic Cystic Precursor Lesions Differ Between Groups at High Risk of Developing Pancreatic CancerIngrid C A W Konings, Femme Harinck, Jan-Werner Poley, et al.
BMC Research Notes|June 27, 2015
Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control studyThomas P Potjer, Nienke van der Stoep, Jeanine J Houwing-Duistermaat, et al.
European Journal of Cancer (Oxford, England : 1990)|July 17, 2013
The development of a clinical screening instrument for tumour predisposition syndromes in childhood cancer patientsSaskia M J Hopman, Johannes H M Merks, Corianne A J M de Borgie, et al.
Pageof 18