Fine mapping of the uterine leiomyoma locus on 1q43 close to a lncRNA in the RGS7-FH interval

Yazar: Aissani, Brahim, Zhang, Kui, Mensenkamp, Arjen R, Menko, Fred H, Wiener, Howard W
Yayımlandı Endocr Relat Cancer (2015)

Direct Interaction with Rab11a Targets the Epithelial Ca(2+) Channels TRPV5 and TRPV6 to the Plasma Membrane

Yazar: van de Graaf, Stan F. J., Chang, Qing, Mensenkamp, Arjen R., Hoenderop, Joost G. J., Bindels, René J. M.
Baskı/Yayın Bilgisi 2006

DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct

Yazar: Sie, Aisha S, Spruijt, Liesbeth, van Zelst-Stams, Wendy AG, Mensenkamp, Arjen R, Ligtenberg, Marjolijn J, Brunner, Han G, Prins, Judith B, Hoogerbrugge, Nicoline
Baskı/Yayın Bilgisi 2012

High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling

Yazar: Sie, Aisha S., Spruijt, Liesbeth, van Zelst-Stams, Wendy A. G., Mensenkamp, Arjen R., Ligtenberg, Marjolijn J. L., Brunner, Han G., Prins, Judith B., Hoogerbrugge, Nicoline
Yayımlandı J Genet Couns (2015)

Calbindin-D(28K) dynamically controls TRPV5-mediated Ca(2+) transport

Yazar: Lambers, Tim T, Mahieu, Frank, Oancea, Elena, Hoofd, Louis, de Lange, Frank, Mensenkamp, Arjen R, Voets, Thomas, Nilius, Bernd, Clapham, David E, Hoenderop, Joost G, Bindels, René J
Baskı/Yayın Bilgisi 2006

Evaluation of yield and experiences of age‐related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch sy...

Yazar: Vos, Janet R., Fakkert, Ingrid E., Spruijt, Liesbeth, Willems, Riki W., Langenveld, Sera, Mensenkamp, Arjen R., Leter, Edward M., Nagtegaal, Iris D., Ligtenberg, Marjolijn J. L., Hoogerbrugge, Nicoline
Yayımlandı Int J Cancer (2020)

Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity

Yazar: Houlleberghs, Hellen, Goverde, Anne, Lusseveld, Jarnick, Dekker, Marleen, Bruno, Marco J., Menko, Fred H., Mensenkamp, Arjen R., Spaander, Manon C. W., Wagner, Anja, Hofstra, Robert M. W., te Riele, Hein
Yayımlandı PLoS Genet (2017)

Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance

Yazar: van Spaendonck-Zwarts, Karin Y., Badeloe, Sadhanna, Oosting, Sjoukje F., Hovenga, Sjoerd, Semmelink, Harry J. F., van Moorselaar, R. Jeroen A., van Waesberghe, Jan Hein, Mensenkamp, Arjen R., Menko, Fred H.
Baskı/Yayın Bilgisi 2011

TINF2 is a haploinsufficient tumor suppressor that limits telomere length

Yazar: Schmutz, Isabelle, Mensenkamp, Arjen R, Takai, Kaori K, Haadsma, Maaike, Spruijt, Liesbeth, de Voer, Richarda M, Choo, Seunga Sara, Lorbeer, Franziska K, van Grinsven, Emma J, Hockemeyer, Dirk, Jongmans, Marjolijn CJ, de Lange, Titia
Yayımlandı eLife (2020)

The Endoplasmic Reticulum Coat Protein II Transport Machinery Coordinates Cellular Lipid Secretion and Cholesterol Biosynthesis

Yazar: Fryer, Lee G. D., Jones, Bethan, Duncan, Emma J., Hutchison, Claire E., Ozkan, Tozen, Williams, Paul A., Alder, Olivia, Nieuwdorp, Max, Townley, Anna K., Mensenkamp, Arjen R., Stephens, David J., Dallinga-Thie, Geesje M., Shoulders, Carol C.
Baskı/Yayın Bilgisi 2014

The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype

Yazar: Kwok, Chau-To, Vogelaar, Ingrid P, van Zelst-Stams, Wendy A, Mensenkamp, Arjen R, Ligtenberg, Marjolijn J, Rapkins, Robert W, Ward, Robyn L, Chun, Nicolette, Ford, James M, Ladabaum, Uri, McKinnon, Wendy C, Greenblatt, Marc S, Hitchins, Megan P
Baskı/Yayın Bilgisi 2014

Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer

Yazar: Elsayed, Fadwa A, Kets, C Marleen, Ruano, Dina, van den Akker, Brendy, Mensenkamp, Arjen R, Schrumpf, Melanie, Nielsen, Maartje, Wijnen, Juul T, Tops, Carli M, Ligtenberg, Marjolijn J, Vasen, Hans FA, Hes, Frederik J, Morreau, Hans, van Wezel, Tom
Yayımlandı Eur J Hum Genet (2015)

The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?

Yazar: Teixeira, Natalia, van der Hout, Annemieke, Oosterwijk, Jan C., Vos, Janet R., Devilee, Peter, van Engelen, Klaartje, Meijers-Heijboer, Hanne, van der Luijt, Rob B., Kriege, Mieke, Mensenkamp, Arjen R., Rookus, Matti A., van Roozendaal, Kees E., Mourits, Marian J. E., de Bock, Geertruida H.
Yayımlandı Eur J Hum Genet (2018)

Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer

Yazar: de Voer, Richarda M., Hahn, Marc-Manuel, Mensenkamp, Arjen R., Hoischen, Alexander, Gilissen, Christian, Henkes, Arjen, Spruijt, Liesbeth, van Zelst-Stams, Wendy A., Marleen Kets, C., Verwiel, Eugene T., Nagtegaal, Iris D., Schackert, Hans K., van Kessel, Ad Geurts, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L., Kuiper, Roland P.
Yayımlandı Sci Rep (2015)

Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas

Yazar: Weren, Robbert D.A., Mensenkamp, Arjen R., Simons, Michiel, Eijkelenboom, Astrid, Sie, Aisha S., Ouchene, Hicham, van Asseldonk, Monique, Gomez‐Garcia, Encarna B., Blok, Marinus J., de Hullu, Joanne A., Nelen, Marcel R., Hoischen, Alexander, Bulten, Johan, Tops, Bastiaan B.J., Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L.
Yayımlandı Hum Mutat (2016)

Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands

Yazar: Dommering, Charlotte J., Henneman, Lidewij, van der Hout, Annemarie H., Jonker, Marianne A., Tops, Carli M. J., van den Ouweland, Ans M. W., van der Luijt, Rob B., Mensenkamp, Arjen R., Hogervorst, Frans B. L., Redeker, Egbert J. W., de Die-Smulders, Christine E. M., Moll, Annette C., Meijers-Heijboer, Hanne
Yayımlandı Fam Cancer (2016)

Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition

Yazar: Vos, Janet R, Fakkert, Ingrid E, de Hullu, Joanne A, van Altena, Anne M, Sie, Aisha S, Ouchene, Hicham, Willems, Riki W, Nagtegaal, Iris D, Jongmans, Marjolijn C J, Mensenkamp, Arjen R, Woldringh, Gwendolyn H, Bulten, Johan, Leter, Edward M, Kets, C Marleen, Simons, Michiel, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline
Yayımlandı J Natl Cancer Inst (2019)

Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility

Yazar: de Voer, Richarda M., Hahn, Marc-Manuel, Weren, Robbert D. A., Mensenkamp, Arjen R., Gilissen, Christian, van Zelst-Stams, Wendy A., Spruijt, Liesbeth, Kets, C. Marleen, Zhang, Junxiao, Venselaar, Hanka, Vreede, Lilian, Schubert, Nil, Tychon, Marloes, Derks, Ronny, Schackert, Hans K., Geurts van Kessel, Ad, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J. L., Kuiper, Roland P.
Yayımlandı PLoS Genet (2016)

Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders

Yazar: Pfundt, Rolph, del Rosario, Marisol, Vissers, Lisenka E.L.M., Kwint, Michael P., Janssen, Irene M., de Leeuw, Nicole, Yntema, Helger G., Nelen, Marcel R., Lugtenberg, Dorien, Kamsteeg, Erik-Jan, Wieskamp, Nienke, Stegmann, Alexander P.A., Stevens, Servi J.C., Rodenburg, Richard J.T., Simons, Annet, Mensenkamp, Arjen R., Rinne, Tuula, Gilissen, Christian, Scheffer, Hans, Veltman, Joris A., Hehir-Kwa, Jayne Y.
Yayımlandı Genet Med (2017)

An evaluation of the challenges to developing tumor BRCA1 and BRCA2 testing methodologies for clinical practice

Yazar: Ellison, Gillian, Ahdesmäki, Miika, Luke, Sally, Waring, Paul M., Wallace, Andrew, Wright, Ronnie, Röthlisberger, Benno, Ludin, Katja, Merkelbach‐Bruse, Sabine, Heydt, Carina, Ligtenberg, Marjolijn J.L., Mensenkamp, Arjen R., de Castro, David Gonzalez, Jones, Thomas, Vivancos, Ana, Kondrashova, Olga, Pauwels, Patrick, Weyn, Christine, Hahnen, Eric, Hauke, Jan, Soong, Richie, Lai, Zhongwu, Dougherty, Brian, Carr, T. Hedley, Johnson, Justin, Mills, John, Barrett, J. Carl
Yayımlandı Hum Mutat (2017)