Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors
Mensenkamp, Arjen R, Vogelaar, Ingrid P, van Zelst–Stams, Wendy A.G, Goossens, Monique, Ouchene, Hicham, Hendriks–Cornelissen, Sandra J.B, Kwint, Michael P, Hoogerbrugge, Nicoline, Nagtegaal, Iris D, Ligtenberg, Marjolijn J.L
Published in Gastroenterology (New York, N.Y. 1943) (01.03.2014)
Published in Gastroenterology (New York, N.Y. 1943) (01.03.2014)
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Journal Article
Familial gastric cancer: detection of a hereditary cause helps to understand its etiology
Vogelaar, Ingrid P, van der Post, Rachel S, Bisseling, Tanya M, van Krieken, J Han Jm, Ligtenberg, Marjolijn Jl, Hoogerbrugge, Nicoline
Published in Hereditary cancer in clinical practice (12.12.2012)
Published in Hereditary cancer in clinical practice (12.12.2012)
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Journal Article
Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1
van der Post, Rachel S, Vogelaar, Ingrid P, Manders, Peggy, van der Kolk, Lizet E, Cats, Annemieke, van Hest, Liselotte P, Sijmons, Rolf, Aalfs, Cora M, Ausems, Margreet G.E.M, Gómez García, Encarna B, Wagner, Anja, Hes, Frederik J, Arts, Neeltje, Mensenkamp, Arjen R, van Krieken, J. Han, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L
Published in Gastroenterology (New York, N.Y. 1943) (01.10.2015)
Published in Gastroenterology (New York, N.Y. 1943) (01.10.2015)
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Journal Article
Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility
Weren, Robbert D A, van der Post, Rachel S, Vogelaar, Ingrid P, van Krieken, J Han, Spruijt, Liesbeth, Lubinski, Jan, Jakubowska, Anna, Teodorczyk, Urszula, Aalfs, Cora M, van Hest, Liselotte P, Oliveira, Carla, Kamping, Eveline J, Schackert, Hans K, Ranzani, Guglielmina N, Gómez García, Encarna B, Hes, Frederik J, Holinski-Feder, Elke, Genuardi, Maurizio, Ausems, Margreet G E M, Sijmons, Rolf H, Wagner, Anja, van der Kolk, Lizet E, Cats, Annemieke, Bjørnevoll, Inga, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J L
Published in Journal of medical genetics (01.10.2018)
Published in Journal of medical genetics (01.10.2018)
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Journal Article
Large Cancer Pedigree Involving Multiple Cancer Genes including Likely Digenic MSH2 and MSH6 Lynch Syndrome (LS) and an Instance of Recombinational Rescue from LS
Vogelaar, Ingrid P, Greer, Stephanie, Wang, Fan, Shin, GiWon, Lau, Billy, Hu, Yajing, Haraldsdottir, Sigurdis, Alvarez, Rocio, Hazelett, Dennis, Nguyen, Peter, Aguirre, Francesca P, Guindi, Maha, Hendifar, Andrew, Balcom, Jessica, Leininger, Anna, Fairbank, Beth, Ji, Hanlee, Hitchins, Megan P
Published in Cancers (30.12.2022)
Published in Cancers (30.12.2022)
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Journal Article
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing
Vogelaar, Ingrid P, van der Post, Rachel S, van Krieken, J Han Jm, Spruijt, Liesbeth, van Zelst-Stams, Wendy Ag, Kets, C Marleen, Lubinski, Jan, Jakubowska, Anna, Teodorczyk, Urszula, Aalfs, Cora M, van Hest, Liselotte P, Pinheiro, Hugo, Oliveira, Carla, Jhangiani, Shalini N, Muzny, Donna M, Gibbs, Richard A, Lupski, James R, de Ligt, Joep, Vissers, Lisenka E L M, Hoischen, Alexander, Gilissen, Christian, van de Vorst, Maartje, Goeman, Jelle J, Schackert, Hans K, Ranzani, Guglielmina N, Molinaro, Valeria, Gómez García, Encarna B, Hes, Frederik J, Holinski-Feder, Elke, Genuardi, Maurizio, Ausems, Margreet G E M, Sijmons, Rolf H, Wagner, Anja, van der Kolk, Lizet E, Bjørnevoll, Inga, Høberg-Vetti, Hildegunn, van Kessel, Ad Geurts, Kuiper, Roland P, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline
Published in European journal of human genetics : EJHG (01.11.2017)
Published in European journal of human genetics : EJHG (01.11.2017)
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Journal Article
Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts
Vogelaar, Ingrid P, Figueiredo, Joana, van Rooij, Iris A L M, Simões-Correia, Joana, van der Post, Rachel S, Melo, Soraia, Seruca, Raquel, Carels, Carine E L, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline
Published in Human molecular genetics (01.03.2013)
Published in Human molecular genetics (01.03.2013)
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Journal Article
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
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
Published in European journal of human genetics : EJHG (01.05.2014)
Published in European journal of human genetics : EJHG (01.05.2014)
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Journal Article
Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements
Phylipsen, Marion, Chaibunruang, Attawut, Vogelaar, Ingrid P., Balak, Jeetindra R. A., Schaap, Rianne A. C., Ariyurek, Yavuz, Fucharoen, Supan, den Dunnen, Johan T., Giordano, Piero C., Bakker, Egbert, Harteveld, Cornelis L.
Published in Human mutation (01.01.2012)
Published in Human mutation (01.01.2012)
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Journal Article
Thalassemia in Western Australia: 11 novel deletions characterized by Multiplex Ligation-dependent Probe Amplification
Phylipsen, Marion, Prior, John F., Lim, Erna, Lingam, Neela, Vogelaar, Ingrid P., Giordano, Piero C., Finlayson, Jill, Harteveld, Cornelis L.
Published in Blood cells, molecules, & diseases (15.03.2010)
Published in Blood cells, molecules, & diseases (15.03.2010)
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Journal Article
Methylated SEPTIN9 plasma test for colorectal cancer detection may be applicable to Lynch syndrome
Hitchins, Megan P, Vogelaar, Ingrid P, Brennan, Kevin, Haraldsdottir, Sigurdis, Zhou, Nianmin, Martin, Brock, Alvarez, Rocio, Yuan, Xiaopu, Kim, Sungjin, Guindi, Maha, Hendifar, Andrew E, Kalady, Matthew F, DeVecchio, Jennifer, Church, James M, de la Chapelle, Albert, Hampel, Heather, Pearlman, Rachel, Christensen, Maria, Snyder, Carrie, Lanspa, Stephen J, Haile, Robert W, Lynch, Henry T
Published in BMJ open gastroenterology (01.01.2019)
Published in BMJ open gastroenterology (01.01.2019)
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Journal Article
Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation
Vogelaar, Ingrid P., van der Post, Rachel S., van de Vosse, Esther, van Krieken, J. Han J. M., Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J. L., Gómez García, Encarna
Published in Familial cancer (01.03.2015)
Published in Familial cancer (01.03.2015)
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Journal Article
Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect
Vogelaar, Ingrid P., Ligtenberg, Marjolijn J. L., van der Post, Rachel S., de Voer, Richarda M., Kets, C. Marleen, Jansen, Trees J. G., Jacobs, Liesbeth, Schreibelt, Gerty, de Vries, I. Jolanda M., Netea, Mihai G., Hoogerbrugge, Nicoline
Published in Familial cancer (01.04.2016)
Published in Familial cancer (01.04.2016)
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Journal Article
Germline MUTYH gene mutations are not frequently found in unselected patients with papillary breast carcinoma
Boesaard, Ewout P, Vogelaar, Ingrid P, Bult, Peter, Wauters, Carla Ap, van Krieken, J Han Jm, Ligtenberg, Marjolijn Jl, van der Post, Rachel S, Hoogerbrugge, Nicoline
Published in Hereditary cancer in clinical practice (12.12.2014)
Published in Hereditary cancer in clinical practice (12.12.2014)
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Journal Article
A new alpha(0)-thalassemia deletion found in a Dutch family (--(AW))
Phylipsen, Marion, Vogelaar, Ingrid P, Schaap, Rianne A C, Arkesteijn, Sandra G J, Boxma, George L, van Helden, Willem C H, Wildschut, Irene C M, de Bruin-Roest, Andrea C, Giordano, Piero C, Harteveld, Cornelis L
Published in Blood cells, molecules, & diseases (15.08.2010)
Published in Blood cells, molecules, & diseases (15.08.2010)
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Journal Article
Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers
van der Post, Rachel S, Vogelaar, Ingrid P, Carneiro, Fátima, Guilford, Parry, Huntsman, David, Hoogerbrugge, Nicoline, Caldas, Carlos, Schreiber, Karen E Chelcun, Hardwick, Richard H, Ausems, Margreet G E M, Bardram, Linda, Benusiglio, Patrick R, Bisseling, Tanya M, Blair, Vanessa, Bleiker, Eveline, Boussioutas, Alex, Cats, Annemieke, Coit, Daniel, DeGregorio, Lynn, Figueiredo, Joana, Ford, James M, Heijkoop, Esther, Hermens, Rosella, Humar, Bostjan, Kaurah, Pardeep, Keller, Gisella, Lai, Jennifer, Ligtenberg, Marjolijn J L, O'Donovan, Maria, Oliveira, Carla, Pinheiro, Hugo, Ragunath, Krish, Rasenberg, Esther, Richardson, Susan, Roviello, Franco, Schackert, Hans, Seruca, Raquel, Taylor, Amy, ter Huurne, Anouk, Tischkowitz, Marc, Joe, Sheena Tjon A, van Dijck, Benjamin, van Grieken, Nicole C T, van Hillegersberg, Richard, van Sandick, Johanna W, Vehof, Rianne, van Krieken, J Han, Fitzgerald, Rebecca C
Published in Journal of Medical Genetics (01.06.2015)
Published in Journal of Medical Genetics (01.06.2015)
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Journal Article
Book Review
Large Cancer Pedigree Involving Multiple Cancer Genes including Likely Digenic IMSH2/I and IMSH6/I Lynch Syndrome and an Instance of Recombinational Rescue from LS
Vogelaar, Ingrid P, Greer, Stephanie, Wang, Fan, Shin, GiWon, Lau, Billy, Hu, Yajing, Haraldsdottir, Sigurdis, Alvarez, Rocio, Hazelett, Dennis, Nguyen, Peter, Aguirre, Francesca P, Guindi, Maha, Hendifar, Andrew, Balcom, Jessica, Leininger, Anna, Fairbank, Beth, Ji, Hanlee, Hitchins, Megan P
Published in Cancers (01.12.2022)
Published in Cancers (01.12.2022)
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Journal Article
Fine-tiling array CGH to improve diagnostics for [alpha]- and [beta]-thalassemia rearrangements
Phylipsen, Marion, Chaibunruang, Attawut, Vogelaar, Ingrid P, Balak, Jeetindra R A, Schaap, Rianne A C, Ariyurek, Yavuz, Fucharoen, Supan, den Dunnen, Johan T, Giordano, Piero C, Bakker, Egbert, Harteveld, Cornelis L
Published in Human mutation (01.01.2012)
Published in Human mutation (01.01.2012)
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Journal Article
A new α0-thalassemia deletion found in a Dutch family (--AW)
Phylipsen, Marion, Vogelaar, Ingrid P., Schaap, Rianne A.C., Arkesteijn, Sandra G.J., Boxma, George L., van Helden, Willem C.H., Wildschut, Irene C.M., de Bruin-Roest, Andrea C., Giordano, Piero C., Harteveld, Cornelis L.
Published in Blood cells, molecules, & diseases (01.08.2010)
Published in Blood cells, molecules, & diseases (01.08.2010)
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Journal Article
A new α 0-thalassemia deletion found in a Dutch family (-- AW)
Phylipsen, Marion, Vogelaar, Ingrid P., Schaap, Rianne A.C., Arkesteijn, Sandra G.J., Boxma, George L., van Helden, Willem C.H., Wildschut, Irene C.M., de Bruin-Roest, Andrea C., Giordano, Piero C., Harteveld, Cornelis L.
Published in Blood cells, molecules, & diseases (2010)
Published in Blood cells, molecules, & diseases (2010)
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