Works matching AU Meijers, Hanne

Results: 61
    1

    Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumors.

    Published in:
    Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 2, p. 1, doi. 10.1002/mgg3.2098
    By:
    • van de Beek, Irma;
    • Glykofridis, Iris E.;
    • Wagner, Anja;
    • den Toom, Dorine T.;
    • Bongers, Ernie M. H. F.;
    • van Leenders, Geert J. L. H.;
    • Johannesma, Paul C.;
    • Meijers‐Heijboer, Hanne E. J.;
    • Wolthuis, Rob M. F.;
    • van Steensel, Maurice A. M.;
    • Dubbink, Hendrikus J.;
    • Houweling, Arjan C.
    Publication type:
    Article
    2
    3
    4

    Loss of FLCN-FNIP1/2 induces a non-canonical interferon response in human renal tubular epithelial cells.

    Published in:
    eLife, 2021, p. 1, doi. 10.7554/eLife.61630
    By:
    • Glykofridis, Iris E.;
    • Knol, Jaco C.;
    • Balk, Jesper A.;
    • Westland, Denise;
    • Pham, Thang V.;
    • Piersma, Sander R.;
    • Lougheed, Sinéad M.;
    • Derakhshan, Sepide;
    • Veen, Puck;
    • Rooimans, Martin A.;
    • van Mil, Saskia E.;
    • Böttger, Franziska;
    • Poddighe, Pino J.;
    • van de Beek, Irma;
    • Drost, Jarno;
    • Zwartkruis, Fried J. T.;
    • de Menezes, Renee X.;
    • Meijers-Heijboer, Hanne E. J.;
    • Houweling, Arjan C.;
    • Jimenez, Connie R.
    Publication type:
    Article
    5
    6

    Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients.

    Published in:
    Journal of Pathology, 2000, v. 192, n. 3, p. 328, doi. 10.1002/1096-9896(2000)9999:9999<::AID-PATH701>3.0.CO;2-2
    By:
    • de Leeuw, Wiljo J. F.;
    • Dierssen, JanWillem;
    • Vasen, Hans F. A.;
    • Wijnen, Juul Th.;
    • Kenter, Gemma G.;
    • Meijers-Heijboer, Hanne;
    • Brocker-Vriends, Annette;
    • Stormorken, Astrid;
    • Moller, Pal;
    • Menko, Fred;
    • Cornelisse, Cees J.;
    • Morreau, Hans
    Publication type:
    Article
    7

    Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.

    Published in:
    Oncogene, 2000, v. 19, n. 36, p. 4170, doi. 10.1038/sj.onc.1203735
    By:
    • Rahman, Nazneen;
    • Teare, M Dawn;
    • Seal, Sheila;
    • Renard, Helene;
    • Mangion, Jon;
    • Cour, Chantal;
    • Thompson, Deborah;
    • Shugart, Yin;
    • Eccles, Diana;
    • Devilee, Peter;
    • Meijers, Hanne;
    • Nathanson, Katherine L;
    • Neuhausen, Susan L;
    • Weber, Barbara;
    • Chang-Claude, Jenny;
    • Easton, Douglas F;
    • Goldgar, David;
    • Stratton, Michael R
    Publication type:
    Article
    8

    PRDM10 directs FLCN expression in a novel disorder overlapping with Birt–Hogg–Dubé syndrome and familial lipomatosis.

    Published in:
    Human Molecular Genetics, 2023, v. 32, n. 7, p. 1223, doi. 10.1093/hmg/ddac288
    By:
    • van de Beek, Irma;
    • Glykofridis, Iris E;
    • Oosterwijk, Jan C;
    • Akker, Peter C van den;
    • Diercks, Gilles F H;
    • Bolling, Maria C;
    • Waisfisz, Quinten;
    • Mensenkamp, Arjen R;
    • Balk, Jesper A;
    • Zwart, Rob;
    • Postma, Alex V;
    • Meijers-Heijboer, Hanne E J;
    • Moorselaar, R Jeroen A van;
    • Wolthuis, Rob M F;
    • Houweling, Arjan C
    Publication type:
    Article
    9

    Mutant BRCA1 alleles transmission: Different approaches and different biases.

    Published in:
    International Journal of Cancer, 2005, v. 113, n. 1, p. 166, doi. 10.1002/ijc.20541
    By:
    • de la Hoya, Miguel;
    • Meijers-Heijboer, Hanne;
    • Fernández, Juan Manuel;
    • Díez, Orland;
    • Osorio, Ana;
    • Alonso, Carmen;
    • van Leeuwen, Inge;
    • Díaz-Rubio, Eduardo;
    • Cornelisse, Cees;
    • Benítez, Javier;
    • Devilee, Peter;
    • Caldés, Trinidad
    Publication type:
    Article
    10
    11

    Prophylactic Mastectomy in BRCA1/2 Mutation Carriers and Women at Risk of Hereditary Breast Cancer: Long-Term Experiences at the Rotterdam Family Cancer Clinic.

    Published in:
    Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2007, v. 14, n. 12, p. 3335, doi. 10.1245/s10434-007-9449-x
    By:
    • Heemskerk-Gerritsen, Bernadette;
    • Brekelmans, Cecile;
    • Menke-Pluymers, Marian;
    • Geel, Albert;
    • Tilanus-Linthorst, Madeleine;
    • Bartels, Carina;
    • Tan, Murly;
    • Meijers-Heijboer, Hanne;
    • Klijn, Jan;
    • Seynaeve, Caroline
    Publication type:
    Article
    12
    13

    Low-penetrance susceptibility to breast cancer due to CHEK2<sup>*</sup>1100delC in noncarriers of BRCA1 or BRCA2 mutations.

    Published in:
    Nature Genetics, 2002, v. 31, n. 1, p. 55
    By:
    • Meijers-Heijboer, Hanne;
    • van den Ouweland, Ans;
    • Klijn, Jan;
    • Wasielewski, Marijke;
    • de Snoo, Anja;
    • Oldenburg, Rogier;
    • Hollestelle, Antoinette;
    • Houben, Mark;
    • Crepin, Ellen;
    • van Veghel-Plandsoen, Monique;
    • Elstrodt, Fons;
    • van Duijn, Cornelia;
    • Bartels, Carina;
    • Meijers, Carel;
    • Schutte, Mieke;
    • McGuffog, Lesley;
    • Thompson, Deborah;
    • Easton, Douglas F.;
    • Sodha, Nayanta
    Publication type:
    Article
    14

    Familial endometrial cancer in female carriers of MSH6 germline mutations.

    Published in:
    Nature Genetics, 1999, v. 23, n. 2, p. 142, doi. 10.1038/13773
    By:
    • Wijnen, Juul;
    • Leeuw, Wiljo de;
    • Vasen, Hans;
    • Klift, Heleen van der;
    • Møller, Pål;
    • Stormorken, Astrid;
    • Meijers-Heijboer, Hanne;
    • Lindhout, Dick;
    • Menko, Fred;
    • Vossen, Sandra;
    • Möslein, Gabriela;
    • Tops, Carli;
    • Bröcker-Vriends, Annette;
    • Wu, Ying;
    • Hofstra, Robert;
    • Sijmons, Rolf;
    • Cornelisse, Cees;
    • Morreau, Hans;
    • Fodde, Riccardo
    Publication type:
    Article
    15

    MSH2 genomic deletions are a frequent cause of HNPCC.

    Published in:
    Nature Genetics, 1998, v. 20, n. 4, p. 326, doi. 10.1038/3795
    By:
    • Wijnen, Juul;
    • van der Klift, Heleen;
    • Vasen, Hans;
    • Khan, P. Meera;
    • Menko, Fred;
    • Tops, Carli;
    • Meijers Heijboer, Hanne;
    • Lindhout, Dick;
    • Møller, Pål;
    • Fodde, Ricardo
    Publication type:
    Article
    16

    Renal imaging in 199 Dutch patients with Birt-Hogg-Dubé syndrome: Screening compliance and outcome.

    Published in:
    PLoS ONE, 2019, v. 14, n. 3, p. 1, doi. 10.1371/journal.pone.0212952
    By:
    • Johannesma, Paul C.;
    • van de Beek, Irma;
    • van der Wel, Tijmen J. W. T.;
    • Reinhard, Rinze;
    • Rozendaal, Lawrence;
    • Starink, Theo M.;
    • van Waesberghe, Jan Hein T. M.;
    • Horenblas, Simon;
    • Gille, Hans J. J. P.;
    • Jonker, Marianne A.;
    • Meijers-Heijboer, Hanne E. J.;
    • Postmus, Pieter E.;
    • Houweling, Arjan C.;
    • van Moorselaar, Jeroen R. A.
    Publication type:
    Article
    17
    18
    19
    20
    21
    22
    23
    24

    A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.

    Published in:
    Human Mutation, 2006, v. 27, n. 7, p. 654, doi. 10.1002/humu.20340
    By:
    • Hout, Annemarie H. van der;
    • Ouweland, Ans M.W. van den;
    • Luijt, Rob B. van der;
    • Gille, Hans J.P.;
    • Bodmer, Daniëlle;
    • Brüggenwirth, Hennie;
    • Mulder, Inge M.;
    • Vlies, Pieter van der;
    • Elfferich, Peter;
    • Huisman, Maarten T.;
    • Berge, Annelies M. ten;
    • Kromosoeto, Joan;
    • Jansen, Rumo P.M.;
    • Zon, Patrick H.A. van;
    • Vriesman, Thyrsa;
    • Arts, Neeltje;
    • Lange, Majella Boutmy-de;
    • Oosterwijk, Jan C.;
    • Meijers-Heijboer, Hanne;
    • Ausems, Margreet G.E.M.
    Publication type:
    Article
    25
    26
    27
    28

    High resolution SNP array profiling identifies variability in retinoblastoma genome stability.

    Published in:
    Genes, Chromosomes & Cancer, 2014, v. 53, n. 1, p. 1, doi. 10.1002/gcc.22111
    By:
    • Mol, Berber M.;
    • Massink, Maarten P. G.;
    • van der Hout, Annemarie H.;
    • Dommering, Charlotte J.;
    • Zaman, Johannes M. A.;
    • Bosscha, Machteld I.;
    • Kors, Wijnanda A.;
    • Meijers‐Heijboer, Hanne E.;
    • Kaspers, Gertjan J. L.;
    • Riele, Hein te;
    • Moll, Annette C.;
    • Cloos, Jacqueline;
    • Dorsman, Josephine C.
    Publication type:
    Article
    29
    30

    Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.

    Published in:
    Genes, Chromosomes & Cancer, 2008, v. 47, n. 11, p. 947, doi. 10.1002/gcc.20597
    By:
    • Oldenburg, Rogier A.;
    • Kroeze-Jansema, Karin H. G.;
    • Houwing-Duistermaat, Jeanine J.;
    • Bayley, Jean-Pierre;
    • Dambrot, Cheryl;
    • van Asperen, Christi J.;
    • van den Ouweland, Ans M. W.;
    • Bakker, Bert;
    • van Beers, Erik H.;
    • Nederlof, Petra M.;
    • Vasen, Hans;
    • Hoogerbrugge, Nicoline;
    • Cornelisse, Cees J.;
    • Meijers-Heijboer, Hanne;
    • Devilee, Peter
    Publication type:
    Article
    31
    32

    A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51.

    Published in:
    Nature Communications, 2015, v. 6, n. 12, p. 8829, doi. 10.1038/ncomms9829
    By:
    • Ameziane, Najim;
    • May, Patrick;
    • Haitjema, Anneke;
    • van de Vrugt, Henri J.;
    • van Rossum-Fikkert, Sari E.;
    • Ristic, Dejan;
    • Williams, Gareth J.;
    • Balk, Jesper;
    • Rockx, Davy;
    • Li, Hong;
    • Rooimans, Martin A.;
    • Oostra, Anneke B.;
    • Velleuer, Eunike;
    • Dietrich, Ralf;
    • Bleijerveld, Onno B.;
    • Maarten Altelaar, A. F.;
    • Meijers-Heijboer, Hanne;
    • Joenje, Hans;
    • Glusman, Gustavo;
    • Roach, Jared
    Publication type:
    Article
    33

    Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence.

    Published in:
    European Journal of Human Genetics, 2015, v. 23, n. 9, p. 1151, doi. 10.1038/ejhg.2014.273
    By:
    • Tan-Sindhunata, M Brigita;
    • Mathijssen, Inge B;
    • Smit, Margriet;
    • Baas, Frank;
    • de Vries, Johanna I;
    • van der Voorn, J Patrick;
    • Kluijt, Irma;
    • Hagen, Marleen A;
    • Blom, Eveline W;
    • Sistermans, Erik;
    • Meijers-Heijboer, Hanne;
    • Waisfisz, Quinten;
    • Weiss, Marjan M;
    • Groffen, Alexander J
    Publication type:
    Article
    34

    Whole-genome sequencing in health care.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, p. S1, doi. 10.1038/ejhg.2013.46
    By:
    • van El, Carla G;
    • Cornel, Martina C;
    • Borry, Pascal;
    • Hastings, Ros J;
    • Fellmann, Florence;
    • Hodgson, Shirley V;
    • Howard, Heidi C;
    • Cambon-Thomsen, Anne;
    • Knoppers, Bartha M;
    • Meijers-Heijboer, Hanne;
    • Scheffer, Hans;
    • Tranebjaerg, Lisbeth;
    • Dondorp, Wybo;
    • de Wert, Guido MWR
    Publication type:
    Article
    35

    Whole-genome sequencing in health care.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 6, p. 580, doi. 10.1038/ejhg.2013.46
    By:
    • van El, Carla G;
    • Cornel, Martina C;
    • Borry, Pascal;
    • Hastings, Ros J;
    • Fellmann, Florence;
    • Hodgson, Shirley V;
    • Howard, Heidi C;
    • Cambon-Thomsen, Anne;
    • Knoppers, Bartha M;
    • Meijers-Heijboer, Hanne;
    • Scheffer, Hans;
    • Tranebjaerg, Lisbeth;
    • Dondorp, Wybo;
    • de Wert, Guido M W R
    Publication type:
    Article
    36
    37

    CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 12, p. 1560, doi. 10.1038/ejhg.2009.75
    By:
    • Van Dijk, Fleur S.;
    • Nesbitt, Isabel M.;
    • Nikkels, Peter G. J.;
    • Dalton, Ann;
    • Bongers, Ernie M. H. F.;
    • van de Kamp, Jiddeke M.;
    • Hilhorst-Hofstee, Yvonne;
    • Den Hollander, Nicolette S.;
    • Lachmeijer, Augusta M. A.;
    • Marcelis, Carlo L.;
    • Tan-Sindhunata, Gita M. B.;
    • van Rijn, Rick R.;
    • Meijers-Heijboer, Hanne;
    • Cobben, Jan M.;
    • Pals, Gerard
    Publication type:
    Article
    38
    39

    Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: A prospective analysis.

    Published in:
    International Journal of Cancer, 2015, v. 136, n. 3, p. 668, doi. 10.1002/ijc.29032
    By:
    • Heemskerk‐Gerritsen, Bernadette A.M.;
    • Rookus, Matti A.;
    • Aalfs, Cora M.;
    • Ausems, Margreet G.E.M.;
    • Collée, Johanna M.;
    • Jansen, Liesbeth;
    • Kets, C. Marleen;
    • Keymeulen, Kristien B.M.I.;
    • Koppert, Linetta B.;
    • Meijers‐Heijboer, Hanne E.J.;
    • Mooij, Thea M.;
    • Tollenaar, Rob A.E.M.;
    • Vasen, Hans F.A.;
    • HEBON;
    • Hooning, Maartje J.;
    • Seynaeve, Caroline
    Publication type:
    Article
    40

    Relevance and efficacy of breast cancer screening in BRCA1 and BRCA2 mutation carriers above 60 years: A national cohort study.

    Published in:
    International Journal of Cancer, 2014, v. 135, n. 12, p. 2940, doi. 10.1002/ijc.28941
    By:
    • Saadatmand, Sepideh;
    • Vos, Janet R.;
    • Hooning, Maartje J.;
    • Oosterwijk, Jan C.;
    • Koppert, Linetta B.;
    • de Bock, Geertruida H.;
    • Ausems, Margreet G.;
    • van Asperen, Christi J.;
    • Aalfs, Cora M.;
    • Gómez Garcia, Encarna B.;
    • Meijers‐Heijboer, Hanne;
    • Hoogerbrugge, Nicoline;
    • Piek, Marianne;
    • Seynaeve, Caroline;
    • Verhoef, Cornelis;
    • Rookus, Matti;
    • Tilanus‐Linthorst, Madeleine M.
    Publication type:
    Article
    41

    Effect of Comprehensive Oncogenetics Training Interventions for General Practitioners, Evaluated at Multiple Performance Levels.

    Published in:
    PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0122648
    By:
    • Houwink, Elisa J. F.;
    • Muijtjens, Arno M. M.;
    • van Teeffelen, Sarah R.;
    • Henneman, Lidewij;
    • Rethans, Jan Joost;
    • Jacobi, Florijn;
    • van der Jagt, Liesbeth;
    • Stirbu, Irina;
    • van Luijk, Scheltus J.;
    • Stumpel, Connie T. R. M.;
    • Meijers-Heijboer, Hanne E.;
    • van der Vleuten, Cees;
    • Cornel, Martina C.;
    • Dinant, Geert Jan
    Publication type:
    Article
    42
    43

    P4‐038: IS SORL1 AN AUTOSOMAL DOMINANT ALZHEIMER GENE?

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1447, doi. 10.1016/j.jalz.2018.06.2440
    By:
    • Van der Lee, Sven J.;
    • Minderhoud, Crista;
    • van Spaendonk, Rosalina;
    • Meijers-Heijboer, Hanne;
    • Van der Flier, Wiesje M.;
    • Scheltens, Philip;
    • Holstege, Henne
    Publication type:
    Article
    44

    P2‐134: THE ADDED VALUE OF EXTREME PHENOTYPES IN ALZHEIMER'S DISEASE CASE‐CONTROL STUDIES.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P719, doi. 10.1016/j.jalz.2018.06.820
    By:
    • Tesi, Niccoló;
    • Van der Lee, Sven J.;
    • Hulsman, Marc;
    • Jansen, Iris E.;
    • Stringa, Najada;
    • van Schoor, Natasja;
    • Meijers-Heijboer, Hanne;
    • Huisman, Martijn;
    • Scheltens, Philip;
    • Reinders, Marcel JT.;
    • Van der Flier, Wiesje M.;
    • Holstege, Henne
    Publication type:
    Article
    45

    Pathology of cognitively healthy centenarians.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P257, doi. 10.1016/j.jalz.2015.07.321
    By:
    • Holstege, Henne;
    • Hoozemans, Jeroen M.M.;
    • van Woerden, Neline;
    • Wemmenhove, Elizabeth;
    • Pieterse, Karlijn;
    • Schouten, Kimja;
    • Meijers-Heijboer, Hanne;
    • Scheltens, Philip;
    • Rozemuller, Annemieke
    Publication type:
    Article
    46

    The 100-plus study: What the oldest-old can teach us.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P787, doi. 10.1016/j.jalz.2014.05.1524
    By:
    • Holstege, Henne;
    • Wemmenhove, Elizabeth;
    • Sistermans, Erik;
    • Reinders, Marcel J.T.;
    • Meijers-Heijboer, Hanne;
    • Scheltens, Philip
    Publication type:
    Article
    47

    The spectrum of mutations in UBE3A causing Angelman syndrome.

    Published in:
    Human Molecular Genetics, 1999, v. 8, n. 1, p. 129, doi. 10.1093/hmg/8.1.129
    By:
    • Fang, Ping;
    • Lev-Lehman, Efrat;
    • Tsai, Ting-Fen;
    • Matsuura, Toshinobu;
    • Benton, Claudia S.;
    • Sutcliffe, James S.;
    • Christian, Susan L.;
    • Kubota, Takeo;
    • Halley, Dicky J.;
    • Meijers-Heijboer, Hanne;
    • Langlois, Sylvie;
    • Graham Jr, John M.;
    • Beuten, Joke;
    • Willems, Patrick J.;
    • Ledbetter, David H.;
    • Beaudet, Arthur L.
    Publication type:
    Article
    48

    Fanconi anemia gene mutations are not involved in sporadic Wilms tumor.

    Published in:
    Pediatric Blood & Cancer, 2010, v. 55, n. 4, p. 742, doi. 10.1002/pbc.22588
    By:
    • Adank, Muriel A.;
    • Segers, Heidi;
    • van Mil, Saskia E.;
    • van Helsdingen, Yvette M.;
    • Ameziane, Najim;
    • van den Ouweland, Ans M.W.;
    • Wagner, Anja;
    • Meijers-Heijboer, Hanne;
    • Kool, Marcel;
    • de Kraker, Jan;
    • Waisfisz, Quinten;
    • van den Heuvel-Eibrink, Marry M.
    Publication type:
    Article
    49

    Genome-wide association analysis identifies three new breast cancer susceptibility loci.

    Published in:
    Nature Genetics, 2012, v. 44, n. 3, p. 312, doi. 10.1038/ng.1049
    By:
    • Ghoussaini, Maya;
    • Fletcher, Olivia;
    • Michailidou, Kyriaki;
    • Turnbull, Clare;
    • Schmidt, Marjanka K;
    • Dicks, Ed;
    • Dennis, Joe;
    • Wang, Qin;
    • Humphreys, Manjeet K;
    • Luccarini, Craig;
    • Baynes, Caroline;
    • Conroy, Don;
    • Maranian, Melanie;
    • Ahmed, Shahana;
    • Driver, Kristy;
    • Johnson, Nichola;
    • Orr, Nicholas;
    • dos Santos Silva, Isabel;
    • Waisfisz, Quinten;
    • Meijers-Heijboer, Hanne
    Publication type:
    Article
    50