Bilaketaren emaitzak - Rogier A. Oldenburg
- Erakusten 1 - 18 emaitzak -- 18
-
1
-
2
Adrenal Medullary Hyperplasia Is a Precursor Lesion for Pheochromocytoma in MEN2 Syndrome nork Esther Korpershoek, Bart‐Jeroen Petri, Edward P. Post, Casper H.J. van Eijck, Rogier A. Oldenburg, Eric J.T. Belt, Wouter W. de Herder, Ronald R. de Krijger, Winand N.M. Dinjens
Argitaratua 2014Artigo -
3
Comparative Genomic Hybridization Profiles in Human BRCA1 and BRCA2 Breast Tumors Highlight Differential Sets of Genomic Aberrations nork Erik H. van Beers, Tibor van Welsem, Lodewyk F.A. Wessels, Yunlei Li, Rogier A. Oldenburg, Peter Devilee, Cees J. Cornelisse, Senno Verhoef, Frans B.L. Hogervorst, Laura J. vanʼt Veer, Petra M. Nederlof
Argitaratua 2005Artigo -
4
Paraganglioma and pheochromocytoma upon maternal transmission of SDHDmutations nork Jean‐Pierre Bayley, Rogier A. Oldenburg, Jennifer Nuk, Attje S. Hoekstra, Conny A. van der Meer, Esther Korpershoek, Barbara McGillivray, Eleonora P.M. Corssmit, Winand N.M. Dinjens, Ronald R. de Krijger, Peter Devilee, Jeroen C. Jansen, Frederik J. Hes
Argitaratua 2014Artigo -
5
Treatment of inoperable or metastatic paragangliomas and pheochromocytomas with peptide receptor radionuclide therapy using 177Lu-DOTATATE nork Wouter T. Zandee, Richard A. Feelders, Daan A. Smit Duijzentkunst, Johannes Hofland, R.M. Metselaar, Rogier A. Oldenburg, Anne van Linge, Boen L.R. Kam, Jaap J.M. Teunissen, Esther Korpershoek, Johanna M. Hendriks, Huda Abusaris, Cleo Slagter, Gaston J H Franssen, Tessa Brabander, Wouter W. de Herder
Argitaratua 2019Artigo -
6
Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study nork Karin van der Tuin, Arjen R. Mensenkamp, Carli M.J. Tops, Eleonora P.M. Corssmit, Winand N.M. Dinjens, Anouk N van de Horst-Schrivers, Jeroen C. Jansen, Mirjam M. de Jong, Henricus P. M. Kunst, Benno Küsters, Edward M. Leter, Hans Morreau, B.M.P. van Nesselrooij, Rogier A. Oldenburg, Liesbeth Spruijt, Frederik J. Hes, Henri Timmers
Argitaratua 2017Artigo -
7
Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis nork Esther Korpershoek, Djamailys Koffy, Bert H.J. Eussen, Lindsey Oudijk, Thomas Papathomas, Francien H. van Nederveen, Eric J.T. Belt, Gaston J H Franssen, David F. Restuccia, Niels M. G. Krol, Rob B. van der Luijt, Richard A. Feelders, Rogier A. Oldenburg, Wilfred F. J. van IJcken, Annelies de Klein, Wouter W. de Herder, Ronald R. de Krijger, Winand N.M. Dinjens
Argitaratua 2015Artigo -
8
Expanding the Spectrum of<i>FOXC1</i>and<i>PITX2</i>Mutations and Copy Number Changes in Patients with Anterior Segment Malformations nork Barbara D′haene, Françoise Meire, Ilse Claerhout, Hester Y. Kroes, Astrid S. Plomp, Yvonne Arens, Thomy de Ravel, Ingele Casteels, Sarah De Jaegere, Sally Hooghe, Wim Wuyts, Jenneke van den Ende, Françoise Roulez, Hermine E. Veenstra‐Knol, Rogier A. Oldenburg, Jacques C. Giltay, Johanna B. G. M. Verheij, Jan-Tjeerd de Faber, Björn Menten, Anne De Paepe, Philippe Kestelyn, Bart P. Leroy, Elfride De Baere
Argitaratua 2010Artigo -
9
Aggressive Cardiovascular Phenotype of Aneurysms-Osteoarthritis Syndrome Caused by Pathogenic SMAD3 Variants nork Denise van der Linde, Ingrid M.B.H. van de Laar, Aida M. Bertoli‐Avella, Rogier A. Oldenburg, Jos A. Bekkers, Francesco Mattace‐Raso, Anton H. van den Meiracker, Adriaan Moelker, Fop van Kooten, Ingrid M.E. Frohn-Mulder, Janneke Timmermans, Els Moltzer, Jan M. Cobben, Lut Van Laer, Bart Loeys, Julie De Backer, Paul Coucke, Anne De Paepe, Yvonne Hilhorst‐Hofstee, Marja W. Wessels, Jolien W. Roos‐Hesselink
Argitaratua 2012Artigo -
10
A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example nork Leila Mohammadi, Maaike P.G. Vreeswijk, Rogier A. Oldenburg, Ans van den Ouweland, Jan C. Oosterwijk, Annemarie H. van der Hout, Nicoline Hoogerbrugge, Marjolijn J. L. Ligtenberg, Margreet G.E.M. Ausems, Rob B. van der Luijt, Charlotte J. Dommering, Gilles Thomas, Senno Verhoef, Frans B.L. Hogervorst, Theo A. van Os, E. Gómez, Marinus J. Blok, Juul Wijnen, Quinta Helmer, Peter Devilee, Christi J. van Asperen, Hans C. van Houwelingen
Argitaratua 2009Artigo -
11
<i>Lamin A/C</i> -Related Cardiac Disease nork Edgar T. Hoorntje, Ilse A. E. Bollen, Daniela Q.C.M. Barge‐Schaapveld, Florence H. van Tienen, Gerard J. te Meerman, Joeri A. Jansweijer, Anthonie J. van Essen, Paul G.A. Volders, Alina A. Constantinescu, Peter C. van den Akker, Karin Y. van Spaendonck‐Zwarts, Rogier A. Oldenburg, Carlo Marcelis, Jasper J. van der Smagt, Eric A. M. Hennekam, Aryan Vink, Marianne Bootsma, Emmelien Aten, Arthur A.M. Wilde, Arthur van den Wijngaard, Jos L. V. Broers, Jan D.H. Jongbloed, Jolanda van der Velden, Maarten P. van den Berg, J. Peter van Tintelen
Argitaratua 2017Artigo -
12
Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations nork Hanne Meijers‐Heijboer, Ans van den Ouweland, Jan G.M. Klijn, Marijke Wasielewski, Anja de Snoo, Rogier A. Oldenburg, Antoinette Hollestelle, M.P.W.A. Houben, Ellen Crepin, Monique van Veghel‐Plandsoen, Fons Elstrodt, Cornelia M. van Duijn, Carina C. M. Bartels, Carel Meijers, Mieke Schutte, Lesley McGuffog, Deborah J. Thompson, Douglas F. Easton, Nayanta Sodha, Sheila Seal, Rita Barfoot, Jon Mangion, Jenny Chang‐Claude, Diana Eccles, Rosalind A. Eeles, D. Gareth Evans, Richard S. Houlston, Victoria Murday, Steven A. Narod, T. Peretz, Julian Peto, Catherine Phelan, Hong Xiang Zhang, Csilla I. Szabo, Peter Devilee, David E. Goldgar, P. Andrew Futreal, Katherine L. Nathanson, Barbara L. Weber, Nazneen Rahman, Michael R. Stratton
Argitaratua 2002Artigo -
13
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analy... nork Francien H. van Nederveen, José Gaal, Judith Favier, Esther Korpershoek, Rogier A. Oldenburg, Elly MCA de Bruyn, Hein F.B.M. Sleddens, Pieter Derkx, Julie Rivière, Hilde Dannenberg, Bart‐Jeroen Petri, Paul Komminoth, Karel Pacák, Wim C.J. Hop, Patrick J. Pollard, Massimo Mannelli, Jean‐Pierre Bayley, Aurel Perren, Stephan Niemann, A.A.J. Verhofstad, Adriaan P. de Bruı̈ne, Eamonn R. Maher, Frédérique Tissier, Tchao Méatchi, Cécile Badoual, Jérôme Bertherat, Laurence Amar, Despoina Alataki, Eric Van Marck, Francesco Ferraù, Jerney François, Wouter W. de Herder, Mark-Paul FM Vrancken Peeters, Anne van Linge, Jacques W.M. Lenders, Anne‐Paule Gimenez‐Roqueplo, Ronald R. de Krijger, Winand N.M. Dinjens
Argitaratua 2009Artigo -
14
A genome wide linkage search for breast cancer susceptibility genes nork Paula Smith, Lesley McGuffog, Douglas F. Easton, Graham J. Mann, Gulietta M. Pupo, Beth Newman, Georgia Chenevix‐Trench, Csilla I. Szabo, Melissa C. Southey, Hélène Renard, Fabrice Odefrey, Henry T. Lynch, Dominique Stoppa‐Lyonnet, Fergus Couch, John L. Hopper, Graham G. Giles, Margaret McCredie, Saundra S. Buys, Irene L. Andrulis, Ruby T. Senie, David E. Goldgar, Rogier A. Oldenburg, Karin Kroeze‐Jansema, Jaco Kraan, Hanne Meijers‐Heijboer, Jan G.M. Klijn, Christi J. van Asperen, Inge van Leeuwen, Hans F. A. Vasen, Cees J. Cornelisse, Peter Devilee, Linda Baskcomb, Sheila Seal, Rita Barfoot, Jon Mangion, Anita Hall, Sarah Edkins, Elizabeth Rapley, Richard Wooster, Jenny Chang‐Claude, Diana Eccles, D. Gareth Evans, P. Andrew Futreal, Katherine L. Nathanson, Barbara L. Weber, Nazneen Rahman, Michael R. Stratton
Argitaratua 2006Artigo -
15
Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium nork Deborah J. Thompson, Csilla I. Szabo, Jon Mangion, Rogier A. Oldenburg, Fabrice Odefrey, Sheila Seal, Rita Barfoot, Karin Kroeze‐Jansema, M. Dawn Teare, Nazneen Rahman, Hélène Renard, Graham J. Mann, John L. Hopper, Saundra S. Buys, Irene L. Andrulis, Ruby T. Senie, Mary B. Daly, Dee W. West, Elaine A. Ostrander, Ken Offit, Tamar Peretz, Ana Osório, Javier Benı́tez, Katherine L. Nathanson, Olga M. Sinilnikova, Edith Oláh, Yves‐Jean Bignon, Pablo Ruíz-Flores, Michael D. Badzioch, Hans F. A. Vasen, P. Andrew Futreal, Catherine M. Phelan, Steven A. Narod, Henry T. Lynch, Bruce A.J. Ponder, Rosalind A. Eeles, Hanne Meijers‐Heijboer, Dominique Stoppa‐Lyonnet, Fergus J. Couch, Diana Eccles, D. Gareth Evans, Jenny Chang‐Claude, Gilbert Lenoir, Barbara Weber, Peter Devilee, Douglas F. Easton, David E. Goldgar, Michael R. Stratton
Argitaratua 2002Artigo -
16
Common Variants at the 19p13.1 and <i>ZNF365</i> Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers nork Fergus J. Couch, Mia M. Gaudet, Antonis C. Antoniou, Susan J. Ramus, Karoline Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaohong Chen, Xianshu Wang, Tomas Kirchhoff, Lesley McGuffog, Daniel Barrowdale, Andrew Lee, Sue Healey, Olga M. Sinilnikova, Irene L. Andrulis, Hilmi Özçelik, Anna Marie Mulligan, Mads Thomassen, Anne‐Marie Gerdes, Uffe Birk Jensen, Anne‐Bine Skytte, Torben A. Kruse, Maria A. Caligo, Anna von Wachenfeldt, Gisela Barbany, Niklas Loman, Maria Soller, Hans Ehrencrona, Per Karlsson, Katherine L. Nathanson, Timothy R. Rebbeck, Susan M. Domchek, Anna Jakubowska, Jan Lubiński, Katarzyna Jaworska, Katarzyna Durda, Elżbieta Złowocka, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Cezary Cybulski, Bohdan Górski, Ana Osório, M. Durán, María‐Isabel Tejada, Javier Benı́tez, Ute Hamann, Frans B.L. Hogervorst, Theo A. van Os, Flora E. van Leeuwen, Hanne Meijers‐Heijboer, Juul Wijnen, Marinus J. Blok, Marleen Kets, Maartje J. Hooning, Rogier A. Oldenburg, Margreet G.E.M. Ausems, Susan Peock, Debra Frost, Steve D. Ellis, Radka Platte, Elena Fineberg, D. Gareth Evans, Chris Jacobs, Rosalind A. Eeles, Julian Adlard, Rosemarie Davidson, Diana Eccles, Trevor Cole, Jackie Cook, Joan Paterson, Carole Brewer, Fiona Douglas, Shirley V. Hodgson, Patrick J. Morrison, Lisa Walker, Mary Porteous, Esther M. John, Lucy Side, Betsy Bove, Andrew K. Godwin, Dominique Stoppa‐Lyonnet, Marion Fassy-Colcombet, Laurent Castéra, François Cornelis, Sylvie Mazoyer, Mélanie Léoné, Nadia Boutry‐Kryza, Brigitte Bressac–de Paillerets, Olivier Caron, Pascal Pujol, Isabelle Coupier, Capucine Delnatte, Linda Akloul, Henry T. Lynch, Carrie Snyder, Saundra S. Buys, Mary B. Daly, Mary Beth Terry
Argitaratua 2012Artigo -
17
Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers nork Elizabeth Page, Elizabeth Bancroft, Mark N. Brook, Melissa Assel, Mona Hassan Al Battat, Sarah Thomas, Natalie Taylor, Anthony Chamberlain, Jennifer Pope, Holly Ní Raghallaigh, D. Gareth Evans, Jeanette Rothwell, Lovise Mæhle, Eli Marie Grindedal, Paul A. James, Lyon Mascarenhas, Joanne McKinley, Lucy Side, Tessy Thomas, Christi J. van Asperen, Hans F. A. Vasen, Lambertus A. Kiemeney, Janneke Ringelberg, Thomas D. Jensen, Palle Jørn Sloth Osther, Brian T. Helfand, Elena Genova, Rogier A. Oldenburg, Cezary Cybulski, Dominika Wokołorczyk, Kai‐Ren Ong, Camilla Huber, Jimmy Lam, Louise Taylor, Mónica Salinas, Lídia Feliubadaló, Jan C. Oosterwijk, Wendy van Zelst-Stams, Jackie Cook, Derek J. Rosario, Susan M. Domchek, Jacquelyn M. Powers, Saundra S. Buys, Karen O’Toole, Margreet G.E.M. Ausems, Rita K. Schmutzler, Kerstin Rhiem, Louise Izatt, Vishakha Tripathi, Manuel R. Teixeira, Marta Cardoso, William D. Foulkes, Armen Aprikian, Heleen van Randeraad, Rosemarie Davidson, Mark Longmuir, Mariëlle Ruijs, Apollonia T.J.M. Helderman van den Enden, Muriel A. Adank, Rachel Williams, Lesley Andrews, Declan G. Murphy, Dorothy Halliday, Lisa Walker, Annelie Liljegren, Stefan Carlsson, Ashraf Azzabi, Irene Jobson, Catherine Morton, Kylie Shackleton, Katie Snape, Helen Hanson, Marion Harris, Marc Tischkowitz, Amy Taylor, Judy Kirk, Rachel Susman, Rakefet Chen‐Shtoyerman, Allan D. Spigelman, Nicholas Pachter, Munaza Ahmed, Teresa Ramón y Cajal, Janez Žgajnar, Carole Brewer, Neus Gadea, Angela F. Brady, Theo van Os, David Gallagher, Oskar T. Johannsson, Alan Donaldson, Julian Barwell, Nicola Nicolai, Eitan Friedman, Elias Obeid, Lynn Greenhalgh, Vedang Murthy, Lucia Copáková, Sibel Saya, John McGrath, Peter Cooke
Argitaratua 2019Artigo -
18
Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study nork Elizabeth Bancroft, Elizabeth Page, Elena Castro, Hans Lilja, Andrew J. Vickers, Daniel D. Sjoberg, Melissa Assel, Christopher S. Foster, Gillian Mitchell, Kate Drew, Lovise Mæhle, Karol Axcrona, D. Gareth Evans, Barbara Bulman, Diana Eccles, Donna McBride, Nicholas van As, Hans F. A. Vasen, Lambertus A. Kiemeney, Janneke Ringelberg, Cezary Cybulski, Dominika Wokołorczyk, Christina G. Selkirk, Peter J. Hulick, Anders Bojesen, Anne‐Bine Skytte, Jimmy Lam, Louise Taylor, Rogier A. Oldenburg, R.G.H.M. Cremers, Gerald W. Verhaegh, Wendy A. van Zelst-Stams, Jan C. Oosterwijk, Ignacio Blanco, Mónica Salinas, Jackie Cook, Derek J. Rosario, Saundra Buys, Tom Conner, Margreet G.E.M. Ausems, Kai‐ren Ong, Jonathan Hoffman, Susan M. Domchek, Jacquelyn Powers, Manuel R. Teixeira, Sofia Maia, William D. Foulkes, Nassim Taherian, Mariëlle Ruijs, Apollonia T. Helderman-van den Enden, Louise Izatt, Rosemarie Davidson, Muriel A. Adank, Lisa Walker, Rita K. Schmutzler, Kathy Tucker, Judy Kirk, Shirley Hodgson, Marion Harris, Fiona Douglas, Geoffrey J. Lindeman, Janez Žgajnar, Marc Tischkowitz, Virginia E. Clowes, Rachel Susman, Teresa Ramón y Cajal, Nicholas Patcher, Neus Gadea, Allan D. Spigelman, Theo van Os, Annelie Liljegren, Lucy Side, Carole Brewer, Angela F. Brady, Alan Donaldson, Vigdís Stefànsdóttir, Eitan Friedman, Rakefet Chen‐Shtoyerman, David J. Amor, Lucia Copáková, Julian Barwell, Veda N. Giri, Vedang Murthy, Nicola Nicolai, Soo‐Hwang Teo, Lynn Greenhalgh, Sara S. Strom, Alex Henderson, John McGrath, David Gallagher, Neil K. Aaronson, Audrey Ardern‐Jones, Chris Bangma, David Dearnaley, Philandra Costello, Jórunn E. Eyfjörd, Jeanette Rothwell, Alison Falconer, Henrik Grönberg, Freddie C. Hamdy
Argitaratua 2014Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Biology
Gene
Genetics
Medicine
Mutation
Internal medicine
Germline mutation
Cancer
Breast cancer
Cancer research
Oncology
Pathology
Pheochromocytoma
Endocrinology
Paraganglioma
Phenotype
Germline
Penetrance
Proband
SDHD
BRCA2 Protein
Context (archaeology)
Gene expression
Genetic linkage
Genetic testing
Genome
Genotype
Gynecology
Ovarian cancer
Paleontology