Arjen R Mensenkamp

ResearcherID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 19

Top Venues

Journal of medical genetics

Cancers

JNCI cancer spectrum

International journal of cancer

This page only lists publications with an associated author ORCID identifier.

Publications

Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, Arjen R Mensenkamp, Hilde Brems, Robin de Putter, Violetta C Anastasiadou, Marie-Charlotte Villy, Arne Jahn, Verena Steinke-Lange, Margherita Baldassarri, Arvids Irmejs, Mirjam M de Jong, Thera P Links, Edward M Leter, Daniëlle G M Bosch, Hildegunn Høberg Vetti, Marianne Tveit Haavind, Kjersti Jørgensen, Lovise Mæhle, Ana Blatnik, Joan Brunet, Esther Darder, Emma Tham, Nicoline Hoogerbrugge, Janet R Vos
Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS). Cancers 16 (5) (2024)
Snežana Hinić, Rachel S van der Post, Lilian Vreede, Janneke Schuurs-Hoeijmakers, Saskia Koene, Erik A M Jansen, Franziska Bervoets-Metge, Arjen R Mensenkamp, Nicoline Hoogerbrugge, Marjolijn J L Ligtenberg, Richarda M de Voer
The genomic landscape of breast and non-breast cancers from individuals with germline CHEK2 deficiency. JNCI cancer spectrum 8 (4) (2024)
Stephanie A Schubert, Dina Ruano, Sebastien M Joruiz, Jordy Stroosma, Nikolina Glavak, Anna Montali, Lia M Pinto, Mar Rodríguez-Girondo, Daniela Q C M Barge-Schaapveld, Maartje Nielsen, Bernadette P M van Nesselrooij, Arjen R Mensenkamp, Monique E van Leerdam, Thomas H Sharp, Hans Morreau, Jean-Christophe Bourdon, Noel F C C de Miranda, J Tom van Wezel
Germline variant affecting p53β isoforms predisposes to familial cancer. Nature communications 15 (1) (2024)
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, Arjen R Mensenkamp, Hilde Brems, Robin de Putter, Violetta C Anastasiadou, Marie-Charlotte Villy, Arne Jahn, Verena Steinke-Lange, Margherita Baldassarri, Arvids Irmejs, Mirjam M de Jong, Thera P Links, Edward M Leter, Daniëlle G M Bosch, Hildegunn Høberg Vetti, Marianne Tveit Haavind, Kjersti Jørgensen, Lovise Mæhle, Ana Blatnik, Joan Brunet, Esther Darder, Emma Tham, Nicoline Hoogerbrugge, Janet R Vos
Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS). Cancers 16 (5) (2024)
Snežana Hinić, Rachel S van der Post, Lilian Vreede, Janneke Schuurs-Hoeijmakers, Saskia Koene, Erik A M Jansen, Franziska Bervoets-Metge, Arjen R Mensenkamp, Nicoline Hoogerbrugge, Marjolijn J L Ligtenberg, Richarda M de Voer
The genomic landscape of breast and non-breast cancers from individuals with germline CHEK2 deficiency. JNCI cancer spectrum 8 (4) (2024)
Ane J Schei-Andersen, Linda A J Hendricks, Rachel S van der Post, Arjen R Mensenkamp, Jolanda Schieving, null null, Janneke H M Schuurs-Hoeijmakers, Nicoline Hoogerbrugge, Janet R Vos
Histopathological phenotyping of cancers in PTEN Hamartoma Tumor Syndrome for improved recognition: A single-center study. International journal of cancer (2024)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Taco W Kuijpers, Andrica C H de Vries, Ester M van Leeuwen, A Ton A M Ermens, Saskia de Pont, Desirée E C Smith, Mirjam M C Wamelink, Arjen R Mensenkamp, Marcel R Nelen, Hana Lango Allen, Steven T Pals, Berna H B Beverloo, Hidde H Huidekoper, Anja Wagner
Megalobastic anemia, infantile leukemia, and immunodeficiency caused by a novel homozygous mutation in the DHFR gene. Blood advances 6 (22) (2022)
Inge M M Lakeman, Mar D M Rodríguez-Girondo, Andrew J Lee, Nandi Celosse, Merel E Braspenning, Klaartje van Engelen, Irma van de Beek, Annemiek H van der Hout, Encarna B Gómez García, Arjen R Mensenkamp, Margreet G E M Ausems, Maartje J Hooning, Muriel A Adank, Antoinette Hollestelle, Marjanka K Schmidt, Christi J van Asperen, Peter Devilee
Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases. Journal of medical genetics (2022)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Mariangela Sabatella, Tuomo Mantere, Esmé Waanders, Kornelia Neveling, Arjen R Mensenkamp, Freerk van Dijk, Jayne Y Hehir-Kwa, Ronnie Derks, Michael Kwint, Luke O'Gorman, Madalena Tropa Martins, Corrie Em Gidding, Maarten H Lequin, Benno Küsters, Pieter Wesseling, Marcel Nelen, Jacklyn A Biegel, Alexander Hoischen, Marjolijn C Jongmans, Roland P Kuiper
Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors. The Journal of pathology 255 (2) (2021)
Isabelle Schmutz, Arjen R Mensenkamp, Kaori K Takai, Maaike Haadsma, Liesbeth Spruijt, Richarda M de Voer, Seunga Sara Choo, Franziska K Lorbeer, Emma J van Grinsven, Dirk Hockemeyer, Marjolijn Cj Jongmans, Titia de Lange
TINF2 is a haploinsufficient tumor suppressor that limits telomere length. eLife 9 (2020)
Janet R Vos, Ingrid E Fakkert, Liesbeth Spruijt, Riki W Willems, Sera Langenveld, Arjen R Mensenkamp, Edward M Leter, Iris D Nagtegaal, Marjolijn J L Ligtenberg, Nicoline Hoogerbrugge, null null
Evaluation of yield and experiences of age-related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch syndrome. International journal of cancer 147 (8) (2020)
Cindy Chau, Remco van Doorn, Natasha M van Poppelen, Nienke van der Stoep, Arjen R Mensenkamp, Rolf H Sijmons, Barbara W van Paassen, Ans M W van den Ouweland, Nicole C Naus, Annemieke H van der Hout, Thomas P Potjer, Fonnet E Bleeker, Marijke R Wevers, Liselotte P van Hest, Marjolijn C J Jongmans, Marina Marinkovic, Jaco C Bleeker, Martine J Jager, Gregorius P M Luyten, Maartje Nielsen
Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines. Cancers 11 (8) (2019)
Kristy Lee, Kate Krempely, Maegan E Roberts, Michael J Anderson, Fátima Carneiro, Elizabeth Chao, Katherine Dixon, Joana Figueiredo, Rajarshi Ghosh, David Huntsman, Pardeep Kaurah, Chimene Kesserwan, Tyler Landrith, Shuwei Li, Arjen R Mensenkamp, Carla Oliveira, Carolina Pardo, Tina Pesaran, Matthew Richardson, Thomas P Slavin, Amanda B Spurdle, Mackenzie Trapp, Leora Witkowski, Charles S Yi, Liying Zhang, Sharon E Plon, Kasmintan A Schrader, Rachid Karam
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants. Human mutation 39 (11) (2019)
Natalia Teixeira, Annemieke van der Hout, Jan C Oosterwijk, Janet R Vos, null null, Peter Devilee, Klaartje van Engelen, Hanne Meijers-Heijboer, Rob B van der Luijt, Mieke Kriege, Arjen R Mensenkamp, Matti A Rookus, Kees E van Roozendaal, Marian J E Mourits, Geertruida H de Bock
The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position? European journal of human genetics : EJHG 26 (6) (2018)
Hellen Houlleberghs, Anne Goverde, Jarnick Lusseveld, Marleen Dekker, Marco J Bruno, Fred H Menko, Arjen R Mensenkamp, Manon C W Spaander, Anja Wagner, Robert M W Hofstra, Hein Te Riele
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity. PLoS genetics 13 (5) (2017)
Rolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, Michael P Kwint, Irene M Janssen, Nicole de Leeuw, Helger G Yntema, Marcel R Nelen, Dorien Lugtenberg, Erik-Jan Kamsteeg, Nienke Wieskamp, Alexander P A Stegmann, Servi J C Stevens, Richard J T Rodenburg, Annet Simons, Arjen R Mensenkamp, Tuula Rinne, Christian Gilissen, Hans Scheffer, Joris A Veltman, Jayne Y Hehir-Kwa
Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders. Genetics in medicine : official journal of the American College of Medical Genetics 19 (6) (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Arjen R Mensenkamp