A.M.W. van den Ouweland

Author

Also Known As

A M W VAN DEN OUWELAND, A M W van den Ouweland, A M van den Ouweland, A. M. W. van den Ouweland, A.M.W van den Ouweland, A.M.W. Van Den Ouweland, A.M.W. Van den Ouweland, A.M.W. van den Ouweland, Ans M W van den Ouweland, J L Boessenkool-Pape

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Erasmus University Rotterdam Radboud University Nijmegen University of Groningen Erasmus MC Cancer Institute

About

A.M.W. van den Ouweland is an author at Erasmus MC specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	626
2	Natural Sciences	1	1	30
3	Public Health	1	1	46
4	Social Sciences	1	1	24
5	Cell Biology	1	1	211

A.M.W. van den Ouweland

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Inflammatory processes in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex Karin Boer, Floor E. Jansen, Mark Nellist, Epilepsy Research Tuberous Sclerosis ComplexNeuro-oncologyCortical TubersInflammatory ProcessesMedicine	2007	211
Survival in Hereditary Breast Cancer Associated With Germline Mutations of <i>BRCA2</i> L.C. Verhoog, Cecile T.M. Brekelmans, Caroline Seynaeve, Journal of Clinical Oncology	1999	176
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11 Yuan Wu, Peter Heutink, Bert B.A. de Vries, Human Molecular Genetics	1994	162
A prospective 10 year follow up study of patients with neurofibromatosis type 1 Marjon H. Cnossen, Arja de Goede-Bolder, K M van den Broek, Archives of Disease in Childhood	1998	114
A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands Rick van Minkelen, Yolande van Bever, Joan N. R. Kromosoeto, Clinical Genetics Neurological DisorderDiagnosisPathologyDisease Gene IdentificationDermatology	2013	91
Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapy Caroline Seynaeve, L.C. Verhoog, L.M.C van de Bosch, European Journal of Cancer Tumour RecurrenceSurgical OncologyBreast OncologyMedicineCancer Recurrence	2004	91
<i>CHEK2</i>*1100delC homozygosity is associated with a high breast cancer risk in women Muriel A. Adank, Marianne A. Jonker, Irma Kluijt, Journal of Medical Genetics	2011	79
Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families L.C. Verhoog, A.M.W. van den Ouweland, E. Berns, European Journal of Cancer Breast OncologySomatic VariantDistinct Brca1/brca2 MutationsTumor HeterogeneityMedicine	2001	78
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study Lieske H. Schrijver, Antonis C Antoniou, Håkan Olsson, American Journal of Obstetrics and Gynecology	2021	56
The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data Gert R. Dohle, HJ Veeze, Shelley E. Overbeek, Human Reproduction	1999	53

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