Mapping the human DC lineage through the integration of high-dimensional techniques
Dutertre, Charles-Antoine, See, Peter, Chen, Jinmiao, Günther, Patrick, McGovern, Naomi, Irac, Sergio Erdal, Gunawan, Merry, Beyer, Marc, Händler, Kristian, Duan, Kaibo, Sumatoh, Hermi Rizal Bin, Ruffin, Nicolas, Jouve, Mabel, Gea-Mallorquí, Ester, Hennekam, Raoul C. M., Lim, Tony, Yip, Chan Chung, Wen, Ming, Malleret, Benoit, Low, Ivy, Shadan, Nurhidaya Binte, Fen, Charlene Foong Shu, Tay, Alicia, Lum, Josephine, Zolezzi, Francesca, Larbi, Anis, Poidinger, Michael, Chan, Jerry K. Y., Chen, Qingfeng, Rénia, Laurent, Haniffa, Muzlifah, Benaroch, Philippe, Schlitzer, Andreas, Schultze, Joachim L., Newell, Evan W., Ginhoux, Florent
Published in Science (American Association for the Advancement of Science) (09.06.2017)
Published in Science (American Association for the Advancement of Science) (09.06.2017)
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A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
Rutsch, Frank, MacDougall, Mary, Lu, Changming, Buers, Insa, Mamaeva, Olga, Nitschke, Yvonne, Rice, Gillian I., Erlandsen, Heidi, Kehl, Hans Gerd, Thiele, Holger, Nürnberg, Peter, Höhne, Wolfgang, Crow, Yanick J., Feigenbaum, Annette, Hennekam, Raoul C.
Published in American journal of human genetics (05.02.2015)
Published in American journal of human genetics (05.02.2015)
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Risk of subsequent primary neoplasms in survivors of adolescent and young adult cancer (Teenage and Young Adult Cancer Survivor Study): a population-based, cohort study
Bright, Chloe J, Reulen, Raoul C, Winter, David L, Stark, Daniel P, McCabe, Martin G, Edgar, Angela B, Frobisher, Clare, Hawkins, Michael M
Published in The lancet oncology (01.04.2019)
Published in The lancet oncology (01.04.2019)
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Etiology of non-immune hydrops fetalis: An update
Bellini, Carlo, Donarini, Gloria, Paladini, Dario, Calevo, Maria Grazia, Bellini, Tommaso, Ramenghi, Luca A, Hennekam, Raoul C
Published in American journal of medical genetics. Part A (01.05.2015)
Published in American journal of medical genetics. Part A (01.05.2015)
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Journal Article
Long-term Risks of Subsequent Primary Neoplasms Among Survivors of Childhood Cancer
Reulen, Raoul C, Frobisher, Clare, Winter, David L, Kelly, Julie, Lancashire, Emma R, Stiller, Charles A, Pritchard-Jones, Kathryn, Jenkinson, Helen C, Hawkins, Michael M, British Childhood Cancer Survivor Study Steering Group, for the
Published in JAMA : the journal of the American Medical Association (08.06.2011)
Published in JAMA : the journal of the American Medical Association (08.06.2011)
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Journal Article
Long-term Cause-Specific Mortality Among Survivors of Childhood Cancer
Reulen, Raoul C, Winter, David L, Frobisher, Clare, Lancashire, Emma R, Stiller, Charles A, Jenney, Meriel E, Skinner, Roderick, Stevens, Michael C, Hawkins, Michael M, British Childhood Cancer Survivor Study Steering Group, for the
Published in JAMA : the journal of the American Medical Association (14.07.2010)
Published in JAMA : the journal of the American Medical Association (14.07.2010)
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Cantú Syndrome Is Caused by Mutations in ABCC9
van Bon, Bregje W.M., Gilissen, Christian, Grange, Dorothy K., Hennekam, Raoul C.M., Kayserili, Hülya, Engels, Hartmut, Reutter, Heiko, Ostergaard, John R., Morava, Eva, Tsiakas, Konstantinos, Isidor, Bertrand, Le Merrer, Martine, Eser, Metin, Wieskamp, Nienke, de Vries, Petra, Steehouwer, Marloes, Veltman, Joris A., Robertson, Stephen P., Brunner, Han G., de Vries, Bert B.A., Hoischen, Alexander
Published in American journal of human genetics (08.06.2012)
Published in American journal of human genetics (08.06.2012)
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Journal Article
Non-immune hydrops fetalis: A short review of etiology and pathophysiology
Bellini, Carlo, Hennekam, Raoul CM
Published in American journal of medical genetics. Part A (01.03.2012)
Published in American journal of medical genetics. Part A (01.03.2012)
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Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups
Maas, Saskia M., Vansenne, Fleur, Kadouch, Daniel J. M., Ibrahim, Abdulla, Bliek, Jet, Hopman, Saskia, Mannens, Marcel M., Merks, Johannes H. M., Maher, Eamonn R., Hennekam, Raoul C.
Published in American journal of medical genetics. Part A (01.09.2016)
Published in American journal of medical genetics. Part A (01.09.2016)
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Changing patterns in the epidemiology and outcomes of inflammatory bowel disease in the United Kingdom: 2000‐2018
King, Dominic, Reulen, Raoul C., Thomas, Tom, Chandan, Joht Singh, Thayakaran, Rasiah, Subramanian, Anuradhaa, Gokhale, Krishna, Bhala, Neeraj, Nirantharakumar, Krishnarajah, Adderley, Nicola J., Trudgill, Nigel
Published in Alimentary pharmacology & therapeutics (01.05.2020)
Published in Alimentary pharmacology & therapeutics (01.05.2020)
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Risk, Risk Factors, and Surveillance of Subsequent Malignant Neoplasms in Survivors of Childhood Cancer: A Review
Turcotte, Lucie M, Neglia, Joseph P, Reulen, Raoul C, Ronckers, Cecile M, van Leeuwen, Flora E, Morton, Lindsay M, Hodgson, David C, Yasui, Yutaka, Oeffinger, Kevin C, Henderson, Tara O
Published in Journal of clinical oncology (20.07.2018)
Published in Journal of clinical oncology (20.07.2018)
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Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement
Kline, Antonie D, Moss, Joanna F, Selicorni, Angelo, Bisgaard, Anne-Marie, Deardorff, Matthew A, Gillett, Peter M, Ishman, Stacey L, Kerr, Lynne M, Levin, Alex V, Mulder, Paul A, Ramos, Feliciano J, Wierzba, Jolanta, Ajmone, Paola Francesca, Axtell, David, Blagowidow, Natalie, Cereda, Anna, Costantino, Antonella, Cormier-Daire, Valerie, FitzPatrick, David, Grados, Marco, Groves, Laura, Guthrie, Whitney, Huisman, Sylvia, Kaiser, Frank J, Koekkoek, Gerritjan, Levis, Mary, Mariani, Milena, McCleery, Joseph P, Menke, Leonie A, Metrena, Amy, O'Connor, Julia, Oliver, Chris, Pie, Juan, Piening, Sigrid, Potter, Carol J, Quaglio, Ana L, Redeker, Egbert, Richman, David, Rigamonti, Claudia, Shi, Angell, Tümer, Zeynep, Van Balkom, Ingrid D C, Hennekam, Raoul C
Published in Nature reviews. Genetics (01.10.2018)
Published in Nature reviews. Genetics (01.10.2018)
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Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
Brioude, Frédéric, Kalish, Jennifer M., Mussa, Alessandro, Foster, Alison C., Bliek, Jet, Ferrero, Giovanni Battista, Boonen, Susanne E., Cole, Trevor, Baker, Robert, Bertoletti, Monica, Cocchi, Guido, Coze, Carole, De Pellegrin, Maurizio, Hussain, Khalid, Ibrahim, Abdulla, Kilby, Mark D., Krajewska-Walasek, Malgorzata, Kratz, Christian P., Ladusans, Edmund J., Lapunzina, Pablo, Le Bouc, Yves, Maas, Saskia M., Macdonald, Fiona, Õunap, Katrin, Peruzzi, Licia, Rossignol, Sylvie, Russo, Silvia, Shipster, Caroleen, Skórka, Agata, Tatton-Brown, Katrina, Tenorio, Jair, Tortora, Chiara, Grønskov, Karen, Netchine, Irène, Hennekam, Raoul C., Prawitt, Dirk, Tümer, Zeynep, Eggermann, Thomas, Mackay, Deborah J. G., Riccio, Andrea, Maher, Eamonn R.
Published in Nature reviews. Endocrinology (01.04.2018)
Published in Nature reviews. Endocrinology (01.04.2018)
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Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders
Aref-Eshghi, Erfan, Kerkhof, Jennifer, Pedro, Victor P., Barat-Houari, Mouna, Ruiz-Pallares, Nathalie, Andrau, Jean-Christophe, Lacombe, Didier, Van-Gils, Julien, Fergelot, Patricia, Dubourg, Christèle, Cormier-Daire, Valerie, Rondeau, Sophie, Lecoquierre, François, Saugier-Veber, Pascale, Nicolas, Gaël, Lesca, Gaetan, Chatron, Nicolas, Sanlaville, Damien, Vitobello, Antonio, Faivre, Laurence, Thauvin-Robinet, Christel, Laumonnier, Frederic, Raynaud, Martine, Alders, Mariëlle, Mannens, Marcel, Henneman, Peter, Hennekam, Raoul C., Velasco, Guillaume, Francastel, Claire, Ulveling, Damien, Ciolfi, Andrea, Pizzi, Simone, Tartaglia, Marco, Heide, Solveig, Héron, Delphine, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Afenjar, Alexandra, Bienvenu, Thierry, Campeau, Philippe M., Rousseau, Justine, Levy, Michael A., Brick, Lauren, Kozenko, Mariya, Balci, Tugce B., Siu, Victoria Mok, Stuart, Alan, Kadour, Mike, Masters, Jennifer, Takano, Kyoko, Kleefstra, Tjitske, de Leeuw, Nicole, Field, Michael, Shaw, Marie, Gecz, Jozef, Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Friez, Michael J., Tedder, Matt, Lee, Jennifer A., DuPont, Barbara R., Stevenson, Roger E., Skinner, Steven A., Schwartz, Charles E., Genevieve, David, Sadikovic, Bekim
Published in American journal of human genetics (05.03.2020)
Published in American journal of human genetics (05.03.2020)
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Analysis of genes differentially expressed in the cortex of mice with the Tbl1xr1Y446C/Y446C variant
Hu, Yalan, Lauffer, Peter, Jongejan, Aldo, Falize, Kim, Bruinstroop, Eveline, van Trotsenburg, Paul, Fliers, Eric, Hennekam, Raoul C., Boelen, Anita
Published in Gene (15.11.2024)
Published in Gene (15.11.2024)
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Mortality in patients with Cushing's disease more than 10 years after remission: a multicentre, multinational, retrospective cohort study
Clayton, Richard N, Prof, Jones, Peter W, Prof, Reulen, Raoul C, Prof, Stewart, Paul M, Prof, Hassan-Smith, Zaki K, PhD, Ntali, Georgia, MD, Karavitaki, Niki, PhD, Dekkers, Olaf M, Prof, Pereira, Alberto M, Prof, Bolland, Mark, PhD, Holdaway, Ian, Prof, Lindholm, Jorgen, Prof
Published in The lancet. Diabetes & endocrinology (01.07.2016)
Published in The lancet. Diabetes & endocrinology (01.07.2016)
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Long term cause specific mortality among 34489 five year survivors of childhood cancer in Great Britain: population based cohort study
Fidler, Miranda M, Reulen, Raoul C, Winter, David L, Kelly, Julie, Jenkinson, Helen C, Skinner, Rod, Frobisher, Clare, Hawkins, Michael M
Published in BMJ (Online) (01.09.2016)
Published in BMJ (Online) (01.09.2016)
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"Hypothesis: Patient with possible disturbance in programmed cell death": further insights in pathogenicity and clinical features of Fraser syndrome
Rumping, Lynne, Hennekam, Raoul C M, Alders, Mariëlle, van Haelst, Mieke M
Published in European journal of human genetics : EJHG (01.01.2023)
Published in European journal of human genetics : EJHG (01.01.2023)
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