Human Molecular Genetics, 0964-6906

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  1. 2020
  2. Demonstration of brain region-specific neuronal vulnerability in human iPSC-based model of familial Parkinson's disease

    Razvan Marius Brazdis, Julian E. Alecu, Daniel Marsch, Annika Dahms, Katrin Simmnacher, Sandra Lörentz, Anna Brendler, Yanni Schneider, Franz Marxreiter, Laurent Roybon, Beate Winner, Wei Xiang & Iryna Prots, 2020 Apr 1, In : Human Molecular Genetics. 29, 7, p. 1180-1191 12 p.

    Research output: Contribution to journalArticle

  3. Effect of rare coding variants in the CFI gene on Factor I expression levels

    Sarah de Jong, Elena B. Volokhina, Anita de Breuk, Sara C. Nilsson, Eiko K. de Jong, Nicole C.A.J. van der Kar, Bjorn Bakker, Carel B. Hoyng, Lambert P. van den Heuvel, Anna M. Blom & Anneke I. den Hollander, 2020, In : Human Molecular Genetics. 29, 14, p. 2313-2324 12 p.

    Research output: Contribution to journalArticle

  4. Prostate cancer risk SNP rs10993994 is a trans-eQTL for SNHG11 mediated through MSMB

    Mesude Bicak, Xing Wang, Xiaoni Gao, Xing Xu, Riina Minna Väänänen, Pekka Taimen, Hans Lilja, Kim Pettersson & Robert J. Klein, 2020, In : Human Molecular Genetics. 29, 10, p. 1581-1591 11 p.

    Research output: Contribution to journalArticle

  5. 2019
  6. Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis

    João Fadista, Line Skotte, Frank Geller, Jonas Bybjerg-Grauholm, Sanne Gørtz, Paul A. Romitti, Michele Caggana, Denise M. Kay, Hans Matsson, Heather A. Boyd, David M. Hougaard, Agneta Nordenskjöld, James L. Mills, Mads Melbye & Bjarke Feenstra, 2019, In : Human Molecular Genetics. 28, 2, p. 332-340 9 p.

    Research output: Contribution to journalArticle

  7. 2018
  8. A genome-wide association study of IgM antibody against phosphorylcholine: Shared genetics and phenotypic relationship to chronic lymphocytic leukemia

    Xu Chen, Stefan Gustafsson, Thomas Whitington, Yan Borné, Erik Lorentzen, Jitong Sun, Peter Almgren, Jun Su, Robert Karlsson, Jie Song, Yi Lu, Yiqiang Zhan, Sara Hägg, Per Svensson, Karin E. Smedby, Susan L. Slager, Erik Ingelsson, Cecilia M. Lindgren, Andrew P. Morris, Olle Melander & 9 others, Thomas Karlsson, Ulf de Faire, Kenneth Caidahl, Gunnar Engström, Lars Lind, Mikael C.I. Karlsson, Nancy L. Pedersen, Johan Frostegård & Patrik K.E. Magnusson, 2018 May 15, In : Human Molecular Genetics. 27, 10, p. 1809-1818 10 p.

    Research output: Contribution to journalArticle

  9. Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin

    Anke Tönjes, Markus Scholz, Jacqueline Krüger, Kerstin Krause, Dorit Schleinitz, Holger Kirsten, Claudia Gebhardt, Carola Marzi, Harald Grallert, Claes Ladenvall, Henrike Heyne, Esa Laurila, Jennifer Kriebel, Christa Meisinger, Wolfgang Rathmann, Christian Gieger, Leif Groop, Inga Prokopenko, Bo Isomaa, Frank Beutner & 9 others, Jürgen Kratzsch, Antje Fischer-Rosinsky, Andreas Pfeiffer, Knut Krohn, Joachim Spranger, Joachim Thiery, Matthias Blüher, Michael Stumvoll & Peter Kovacs, 2018 Feb 1, In : Human Molecular Genetics. 27, 3, p. 546-558

    Research output: Contribution to journalArticle

  10. Consortium-based genome-wide meta-analysis for childhood dental caries traits

    Simon Haworth, Dmitry Shungin, Justin T. Van Der Tas, Strahinja Vucic, Carolina Medina-Gomez, Victor Yakimov, Bjarke Feenstra, John R. Shaffer, Myoung Keun Lee, Marie Standl, Elisabeth Thiering, Carol Wang, Klaus Bønnelykke, Johannes Waage, Leon Eyrich Jessen, Pia Elisabeth Nørrisgaard, Raimo Joro, Ilkka Seppälä, Olli Raitakari, Tom Dudding & 23 others, Olja Grgic, Edwin Ongkosuwito, Anu Vierola, Aino Maija Eloranta, Nicola X. West, Steven J. Thomas, Daniel W. McNeil, Steven M. Levy, Rebecca Slayton, Ellen A. Nohr, Terho Lehtimäki, Timo Lakka, Hans Bisgaard, Craig Pennell, Jan Kühnisch, Mary L. Marazita, Mads Melbye, Frank Geller, Fernando Rivadeneira, Eppo B. Wolvius, Paul W. Franks, Ingegerd Johansson & Nicholas J. Timpson, 2018, In : Human Molecular Genetics. 27, 17, p. 3113-3127

    Research output: Contribution to journalArticle

  11. Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration

    Mariann Kremlitzka, Maartje J. Geerlings, Sarah De Jong, Bjorn Bakker, Sara C. Nilsson, Sascha Fauser, Carel B. Hoyng, Eiko K. De Jong, Anneke I. Den Hollander & Anna M. Blom, 2018, In : Human Molecular Genetics. 27, 15, p. 2678-2688 11 p.

    Research output: Contribution to journalArticle

  12. 2017
  13. Proteomics insights into infantile neuronal ceroid lipofuscinosis (CLN1) point to the involvement of cilia pathology in the disease

    Michal Segal-Salto, Karin Hansson, Tamar Sapir, Anna Kaplan, Talia Levy, Michaela Schweizer, Michael Frotscher, Peter James & Orly Reiner, 2017 May 1, In : Human Molecular Genetics. 26, 9, p. 1678-1693 16 p., ddx074.

    Research output: Contribution to journalArticle

  14. Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation

    Emma L. Clayton, Renzo Mancuso, Troels Tolstrup Nielsen, Sarah Mizielinska, Holly Holmes, Nicholas Powell, Frances Norona, Jytte Overgaard Larsen, Carmelo Milioto, Katherine M. Wilson, Mark F. Lythgoe, Sebastian Ourselin, Jörgen E. Nielsen, Peter Johannsen, Ida Holm, John Collinge, Peter L. Oliver, Diego Gomez-Nicola, Adrian M. Isaacs, Elisabet Englund & 1 others, FReJA FReJA, 2017 Mar 1, In : Human Molecular Genetics. 26, 5, p. 873-887

    Research output: Contribution to journalArticle

  15. 2016
  16. Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers

    Yan Borné, Martin Söderholm, Lars Barregard, Björn Fagerberg, Margaretha Persson, Olle Melander, Frank Thévenod, Bo Hedblad & Gunnar Engström, 2016 Jun 22, In : Human Molecular Genetics. 25, 11, p. 2342-2348

    Research output: Contribution to journalArticle

  17. Analysis with the exome array identifies multiple new independent variants in lipid loci

    Stavroula Kanoni, Nicholas G D Masca, Kathleen E. Stirrups, Tibor V. Varga, Helen R Warren, Robert A. Scott, Lorraine Southam, Weihua Zhang, Hanieh Yaghootkar, Martina Müller-Nurasyid, Alexessander Couto Alves, Rona J. Strawbridge, Lazaros Lataniotis, Nikman An Hashim, Céline Besse, Anne Boland, Peter S. Braund, John M. Connell, Anna Dominiczak, Aliki-Eleni Farmaki & 41 others, Stephen Franks, Harald Grallert, Jan-Håkan Jansson, Maria Karaleftheri, Sirkka Keinänen-Kiukaanniemi, Angela Matchan, Dorota Pasko, Annette Peters, Neil Poulter, Nigel W. Rayner, Frida Renström, Olov Rolandsson, Maria Sabater-Lleal, Bengt Sennblad, Peter Sever, Denis C Shields, Angela Silveira, Alice V Stanton, Konstantin Strauch, Maciej Tomaszewski, Emmanouil Tsafantakis, Melanie Waldenberger, Alexandra I. F. Blakemore, George Dedoussis, Stefan A Escher, Jaspal S Kooner, Mark I. McCarthy, Colin N. A. Palmer, Anders Hamsten, Mark J. Caulfield, Timothy M. Frayling, Martin D Tobin, Marjo Riitta Jarvelin, Eleftheria Zeggini, Christian Gieger, John C Chambers, Nick J. Wareham, Patricia B. Munroe, Paul W. Franks, Nilesh J. Samani & Panos Deloukas, 2016, In : Human Molecular Genetics. 25, 18, p. 4094-4106 13 p.

    Research output: Contribution to journalArticle

  18. Mutations in the polyglutamylase gene TTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility

    Nicola Bedoni, Lonneke Haer-Wigman, Veronika Vaclavik, Viet H. Tran, Pietro Farinelli, Sara Balzano, Beryl Royer-Bertrand, Mohammed E. El-Asrag, Olivier Bonny, Christos Ikonomidis, Yan Litzistorf, Konstantinos Nikopoulos, Georgia G. Yioti, Maria I. Stefaniotou, Martin McKibbin, Adam P. Booth, Jamie M. Ellingford, Graeme C. M. Black, Carmel Toomes, Chris F. Inglehearn & 11 others, Carel B. Hoyng, Nathalie Bax, Caroline C. W. Klaver, Alberta A. Thiadens, Fabien Murisier, Daniel F. Schorderet, Manir Ali, Frans P M Cremers, Sten Andréasson, Francis L. Munier & Carlo Rivolta, 2016, In : Human Molecular Genetics. 25, 20, p. 4546-4555 10 p.

    Research output: Contribution to journalArticle

  19. 2015
  20. Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus

    Nathalie Acevedo, Lovisa E Reinius, Dario Greco, Anna Gref, Christina Orsmark-Pietras, Helena Persson, Göran Pershagen, Gunilla Hedlin, Erik Melén, Annika Scheynius, Juha Kere & Cilla Söderhäll, 2015 Feb 1, In : Human Molecular Genetics. 24, 3, p. 875-90 16 p.

    Research output: Contribution to journalArticle

  21. Association of exome sequences with plasma C-reactive protein levels in >9000 participants.

    Ursula M Schick, Paul L Auer, Joshua C Bis, Honghuang Lin, Peng Wei, Nathan Pankratz, Leslie A Lange, Jennifer Brody, Nathan O Stitziel, Daniel S Kim, Christopher S Carlson, Myriam Fornage, Jeffery Haessler, Li Hsu, Rebecca D Jackson, Charles Kooperberg, Suzanne M Leal, Bruce M Psaty, Eric Boerwinkle, Russell Tracy & 24 others, Diego Ardissino, Svati Shah, Cristen Willer, Ruth Loos, Olle Melander, Ruth Mcpherson, Kees Hovingh, Muredach Reilly, Hugh Watkins, Domenico Girelli, Pierre Fontanillas, Daniel I Chasman, Stacey B Gabriel, Richard Gibbs, Deborah A Nickerson, Sekar Kathiresan, Ulrike Peters, Josée Dupuis, James G Wilson, Stephen S Rich, Alanna C Morrison, Emelia J Benjamin, Myron D Gross & Alex P Reiner, 2015, In : Human Molecular Genetics. 24, 2, p. 559-571

    Research output: Contribution to journalArticle

  22. FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

    Paolo Peterlongo, Irene Catucci, Mara Colombo, Laura Caleca, Eliseos Mucaki, Massimo Bogliolo, Maria Marin, Francesca Damiola, Loris Bernard, Valeria Pensotti, Sara Volorio, Valentina Dall'Olio, Alfons Meindl, Claus Bartram, Christian Sutter, Harald Surowy, Valérie Sornin, Marie-Gabrielle Dondon, Séverine Eon-Marchais, Dominique Stoppa-Lyonnet & 76 others, Nadine Andrieu, Olga M Sinilnikova, Gillian Mitchell, Paul A James, Ella Thompson, Marina Marchetti, Cristina Verzeroli, Carmen Tartari, Gabriele Lorenzo Capone, Anna Laura Putignano, Maurizio Genuardi, Veronica Medici, Isabella Marchi, Massimo Federico, Silvia Tognazzo, Laura Matricardi, Simona Agata, Riccardo Dolcetti, Lara Della Puppa, Giulia Cini, Viviana Gismondi, Valeria Viassolo, Chiara Perfumo, Maria Antonietta Mencarelli, Margherita Baldassarri, Bernard Peissel, Gaia Roversi, Valentina Silvestri, Piera Rizzolo, Francesca Spina, Caterina Vivanet, Maria Grazia Tibiletti, Maria Adelaide Caligo, Gaetana Gambino, Stefania Tommasi, Brunella Pilato, Carlo Tondini, Chiara Corna, Bernardo Bonanni, Monica Barile, Ana Osorio, Javier Benitez, Luisa Balestrino, Laura Ottini, Siranoush Manoukian, Marco A Pierotti, Alessandra Renieri, Liliana Varesco, Fergus J Couch, Xianshu Wang, Peter Devilee, Florentine S Hilbers, Christi J van Asperen, Alessandra Viel, Marco Montagna, Laura Cortesi, Orland Diez, Judith Balmaña, Jan Hauke, Rita K Schmutzler, Laura Papi, Miguel Angel Pujana, Conxi Lázaro, Anna Falanga, Kenneth Offit, Joseph Vijai, Ian Campbell, Barbara Burwinkel, Anders Kvist, Hans Ehrencrona, Sylvie Mazoyer, Sara Pizzamiglio, Paolo Verderio, Jordi Surralles, Peter K Rogan & Paolo Radice, 2015, In : Human Molecular Genetics. 24, 18, p. 5345-5355

    Research output: Contribution to journalArticle

  23. Gene×dietary pattern interactions in obesity: analysis of up to 68,317 adults of European ancestry.

    Jennifer A Nettleton, Jack L Follis, Julius S Ngwa, Caren E Smith, Shafqat Ahmad, Toshiko Tanaka, Mary K Wojczynski, Trudy Voortman, Rozenn N Lemaitre, Kati Kristiansson, Marja-Liisa Nuotio, Denise K Houston, Mia-Maria Perälä, Qibin Qi, Emily Sonestedt, Ani Manichaikul, Stavroula Kanoni, Andrea Ganna, Vera Mikkilä, Kari E North & 51 others, David S Siscovick, Kennet Harald, Nicola M McKeown, Ingegerd Johansson, Harri Rissanen, Yongmei Liu, Jari Lahti, Frank B Hu, Stefania Bandinelli, Gull Rukh, Stephen Rich, Lisanne Booij, Maria Dmitriou, Erika Ax, Olli Raitakari, Kenneth Mukamal, Satu Männistö, Göran Hallmans, Antti Jula, Ulrika Ericson, David R Jacobs, Frank J A van Rooij, Panos Deloukas, Per Sjögren, Mika Kähönen, Luc Djousse, Markus Perola, Inês Barroso, Albert Hofman, Kathleen Stirrups, Jorma Viikari, André G Uitterlinden, Ioanna P Kalafati, Oscar H Franco, Dariush Mozaffarian, Veikko Salomaa, Ingrid B Borecki, Paul Knekt, Stephen B Kritchevsky, Johan G Eriksson, George V Dedoussis, Lu Qi, Luigi Ferrucci, Marju Orho-Melander, M Carola Zillikens, Erik Ingelsson, Terho Lehtimäki, Frida Renström, L Adrienne Cupples, Ruth Loos & Paul Franks, 2015, In : Human Molecular Genetics. 24, 16, p. 4728-4738

    Research output: Contribution to journalArticle

  24. Identification of novel genes for glucose metabolism based upon expression pattern in human islets and effect on insulin secretion and glycemia.

    Jalal Taneera, Joao Fadista, Emma Ahlqvist, David Grubich Atac, Emilia Ottosson Laakso, Claes Wollheim & Leif Groop, 2015, In : Human Molecular Genetics. 24, 7, p. 1945-1955

    Research output: Contribution to journalArticle

  25. Impact of age, BMI and HbA1c levels on the genome-wide DNA methylation and mRNA expression patterns in human adipose tissue and identification of epigenetic biomarkers in blood.

    Tina Rönn, Petr Volkov, Linn Gillberg, Milana Kokosar, Alexander Perfilyev, Anna Louisa Jacobsen, Sine W Jørgensen, Charlotte Brøns, Per-Anders Jansson, Karl-Fredrik Eriksson, Oluf Pedersen, Torben Hansen, Leif Groop, Elisabet Stener-Victorin, Allan Vaag, Emma A Nilsson & Charlotte Ling, 2015, In : Human Molecular Genetics. 24, 13, p. 3792-3813

    Research output: Contribution to journalArticle

  26. Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration.

    Diana Wiesner, Jérome Sinniger, Alexandre Henriques, Stéphane Dieterlé, Hans-Peter Müller, Volker Rasche, Boris Ferger, Sylvie Dirrig-Grosch, Rana Soylu, Åsa Petersén, Paul Walther, Birgit Linkus, Jan Kassubek, Philip C Wong, Albert C Ludolph & Luc Dupuis, 2015, In : Human Molecular Genetics. 24, 8, p. 2228-2240

    Research output: Contribution to journalArticle

  27. WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.

    Izabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, Jia Cao, Daniel Nilsson, Michael Ludwig, Markus Draaken, Gundela Holmdahl, Gillian Barker, Heiko Reutter, Vladana Vukojević, Christina Clementson Kockum, Johanna Lundin, Anna Lindstrand & Agneta Nordenskjöld, 2015, In : Human Molecular Genetics. 24, 18, p. 5069-5078

    Research output: Contribution to journalArticle

  28. 2014
  29. FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals.

    Qibin Qi, Tuomas O Kilpeläinen, Mary K Downer, Toshiko Tanaka, Caren E Smith, Ivonne Sluijs, Emily Sonestedt, Audrey Y Chu, Frida Renström, Xiaochen Lin, Lars H Angquist, Jinyan Huang, Zhonghua Liu, Yanping Li, Muhammad Asif Ali, Min Xu, Tarunveer Singh Ahluwalia, Jolanda M A Boer, Peng Chen, Makoto Daimon & 89 others, Johan Eriksson, Markus Perola, Yechiel Friedlander, Yu-Tang Gao, Denise H M Heppe, John W Holloway, Denise K Houston, Stavroula Kanoni, Yu-Mi Kim, Maarit A Laaksonen, Tiina Jääskeläinen, Nanette R Lee, Terho Lehtimäki, Rozenn N Lemaitre, Wei Lu, Robert N Luben, Ani Manichaikul, Satu Männistö, Pedro Marques-Vidal, Keri L Monda, Julius S Ngwa, Louis Perusse, Frank J A van Rooij, Yong-Bing Xiang, Wanqing Wen, Mary K Wojczynski, Jingwen Zhu, Ingrid B Borecki, Claude Bouchard, Qiuyin Cai, Cyrus Cooper, George V Dedoussis, Panos Deloukas, Luigi Ferrucci, Nita G Forouhi, Torben Hansen, Lene Christiansen, Albert Hofman, Ingegerd Johansson, Torben Jørgensen, Shigeru Karasawa, Kay-Tee Khaw, Mi-Kyung Kim, Kati Kristiansson, Huaixing Li, Xu Lin, Yongmei Liu, Kurt K Lohman, Jirong Long, Vera Mikkilä, Dariush Mozaffarian, Kari North, Oluf Pedersen, Olli Raitakari, Harri Rissanen, Jaakko Tuomilehto, Yvonne T van der Schouw, André G Uitterlinden, M Carola Zillikens, Oscar H Franco, E Shyong Tai, Xiao Ou Shu, David S Siscovick, Ulla Toft, W M Monique Verschuren, Peter Vollenweider, Nicholas J Wareham, Jacqueline C M Witteman, Wei Zheng, Paul M Ridker, Jae H Kang, Liming Liang, Majken K Jensen, Gary C Curhan, Louis R Pasquale, David J Hunter, Karen L Mohlke, Matti Uusitupa, L Adrienne Cupples, Tuomo Rankinen, Marju Orho-Melander, Tao Wang, Daniel I Chasman, Paul Franks, Thorkild I A Sørensen, Frank B Hu, Ruth J F Loos, Jennifer A Nettleton & Lu Qi, 2014, In : Human Molecular Genetics. 23, 25, p. 6961-6972

    Research output: Contribution to journalArticle

  30. Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

    Sachiko Yoneyama, Yiran Guo, Matthew B. Lanktree, Michael R. Barnes, Clara C. Elbers, Konrad J. Karczewski, Sandosh Padmanabhan, Florianne Bauer, Jens Baumert, Amber Beitelshees, Gerald S. Berenson, Jolanda M. A. Boer, Gregory Burke, Brian Cade, Wei Chen, Rhonda M. Cooper-Dehoff, Tom R. Gaunt, Christian Gieger, Yan Gong, Mathias Gorski & 54 others, Nancy Heard-Costa, Toby Johnson, Michael J. Lamonte, Caitrin Mcdonough, Keri L. Monda, N. Charlotte Onland-Moret, Christopher P. Nelson, Jeffrey R. O'Connell, Jose Ordovas, Inga Peter, Annette Peters, Jonathan Shaffer, Haiqinq Shen, Erin Smith, Liz Speilotes, Fridtjof Thomas, Barbara Thorand, W. M. Monique Verschuren, Sonia S. Anand, Anna Dominiczak, Karina W. Davidson, Robert A. Hegele, Iris Heid, Marten H. Hofker, Gordon S. Huggins, Thomas Illig, Julie A. Johnson, Susan Kirkland, Wolfgang Koenig, Taimour Y. Langaee, Jeanne Mccaffery, Olle Melander, Braxton D. Mitchell, Patricia Munroe, Sarah S. Murray, George Papanicolaou, Susan Redline, Muredach Reilly, Nilesh J. Samani, Nicholas J. Schork, Yvonne T. Van der Schouw, Daichi Shimbo, Alan R. Shuldiner, Martin D. Tobin, Cisca Wijmenga, Salim Yusuf, Hakon Hakonarson, Leslie A. Lange, Ellen W. Demerath, Caroline S. Fox, Kari E. North, Alex P. Reiner, Brendan Keating & Kira C. Taylor, 2014, In : Human Molecular Genetics. 23, 9, p. 2498-2510

    Research output: Contribution to journalArticle

  31. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of Dementia with Lewy Bodies.

    Jose Bras, Rita Guerreiro, Lee Darwent, Laura Parkkinen, Olaf Ansorge, Valentina Escott-Price, Dena G Hernandez, Michael A Nalls, Lorraine Clark, Lawrence Honig, Karen Marder, Wiesje van der Flier, Afina Lemstra, Philip Scheltens, Ekaterina Rogaeva, Peter St George-Hyslop, Elisabet Londos, Henrik Zetterberg, Sara Ortega-Cubero, Pau Pastor & 22 others, Tanis J Ferman, Neill R Graff-Radford, Owen A Ross, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Walter Maetzler, Daniela Berg, Claire Troakes, Safa Al-Sarraj, Tammaryn Lashley, Yarko Compta, Tamas Revesz, Andrew Lees, Nigel Cairns, Glenda M Halliday, David Mann, Stuart Pickering-Brown, Dennis Dickson, Andrew Singleton & John Hardy, 2014, In : Human Molecular Genetics. 23, 23, p. 6139-6146

    Research output: Contribution to journalArticle

  32. Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

    Alireza Moayyeri, Yi-Hsiang Hsu, David Karasik, Karol Estrada, Su-Mei Xiao, Carrie Nielson, Priya Srikanth, Sylvie Giroux, Scott G. Wilson, Hou-Feng Zheng, Albert V. Smith, Stephen R. Pye, Paul J. Leo, Alexander Teumer, Joo-Yeon Hwang, Claes Ohlsson, Fiona McGuigan, Ryan L. Minster, Caroline Hayward, Jose M. Olmos & 110 others, Leo-Pekka Lyytikaeinen, Joshua R. Lewis, Karin M. A. Swart, Laura Masi, Chris Oldmeadow, Elizabeth G. Holliday, Sulin Cheng, Natasja M. van Schoor, Nicholas C. Harvey, Marcin Kruk, M. Fabiola Del Greco, Wilmar Igl, Olivia Trummer, Efi Grigoriou, Robert Luben, Ching-Ti Liu, Yanhua Zhou, Ling Oei, Carolina Medina-Gomez, Joseph Zmuda, Greg Tranah, Suzanne J. Brown, Frances M. Williams, Nicole Soranzo, Johanna Jakobsdottir, Kristin Siggeirsdottir, Kate L. Holliday, Anke Hannemann, Min Jin Go, Melissa Garcia, Ozren Polasek, Marika Laaksonen, Kun Zhu, Anke W. Enneman, Mark McEvoy, Roseanne Peel, Pak Chung Sham, Maciej Jaworski, Asa Johansson, Andrew A. Hicks, Pawel Pludowski, Rodney Scott, Rosalie A. M. Dhonukshe-Rutten, Nathalie van der Velde, Mika Kaehoenen, Jorma S. Viikari, Harri Sievaenen, Olli T. Raitakari, Jesus Gonzalez-Macias, Jose L. Hernandez, Dan Mellstroem, Oesten Ljunggren, Yoon Shin Cho, Uwe Voelker, Matthias Nauck, Georg Homuth, Henry Voelzke, Robin Haring, Matthew A. Brown, Eugene McCloskey, Geoffrey C. Nicholson, Richard Eastell, John A. Eisman, Graeme Jones, Ian R. Reid, Elaine M. Dennison, John Wark, Steven Boonen, Dirk Vanderschueren, Frederick C. W. Wu, Thor Aspelund, J. Brent Richards, Doug Bauer, Albert Hofman, Kay-Tee Khaw, George Dedoussis, Barbara Obermayer-Pietsch, Ulf Gyllensten, Peter P. Pramstaller, Roman S. Lorenc, Cyrus Cooper, Annie Wai Chee Kung, Paul Lips, Markku Alen, John Attia, Maria Luisa Brandi, Lisette C. P. G. M. de Groot, Terho Lehtimaeki, Jose A. Riancho, Harry Campbell, Yongmei Liu, Tamara B. Harris, Kristina Åkesson, Magnus Karlsson, Jong-Young Lee, Henri Wallaschofski, Emma L. Duncan, Terence W. O'Neill, Vilmundur Gudnason, Timothy D. Spector, Francois Rousseau, Eric Orwoll, Steven R. Cummings, Nick J. Wareham, Fernando Rivadeneira, Andre G. Uitterlinden, Richard L. Prince, Douglas P. Kiel, Jonathan Reeve & Stephen K. Kaptoge, 2014, In : Human Molecular Genetics. 23, 11, p. 3054-3068

    Research output: Contribution to journalArticle

  33. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

    Kristen S Purrington, Seth Slettedahl, Manjeet K Bolla, Kyriaki Michailidou, Kamila Czene, Heli Nevanlinna, Stig E Bojesen, Irene L Andrulis, Angela Cox, Per Hall, Jane Carpenter, Drakoulis Yannoukakos, Christopher A Haiman, Peter A Fasching, Arto Mannermaa, Robert Winqvist, Hermann Brenner, Annika Lindblom, Georgia Chenevix-Trench, Javier Benitez & 143 others, Anthony Swerdlow, Vessela Kristensen, Pascal Guénel, Alfons Meindl, Hatef Darabi, Mikael Eriksson, Rainer Fagerholm, Kristiina Aittomäki, Carl Blomqvist, Børge G Nordestgaard, Sune F Nielsen, Henrik Flyger, Xianshu Wang, Curtis Olswold, Janet E Olson, Anna Marie Mulligan, Julia A Knight, Sandrine Tchatchou, Malcolm W R Reed, Simon S Cross, Jianjun Liu, Jingmei Li, Keith Humphreys, Christine Clarke, Rodney Scott, Florentia Fostira, George Fountzilas, Irene Konstantopoulou, Brian E Henderson, Fredrick Schumacher, Loic Le Marchand, Arif B Ekici, Arndt Hartmann, Matthias W Beckmann, Jaana M Hartikainen, Veli-Matti Kosma, Vesa Kataja, Arja Jukkola-Vuorinen, Katri Pylkäs, Saila Kauppila, Aida Karina Dieffenbach, Christa Stegmaier, Volker Arndt, Sara Margolin, Rosemary Balleine, Jose Ignacio Arias Perez, M Pilar Zamora, Primitiva Menéndez, Alan Ashworth, Michael Jones, Nick Orr, Patrick Arveux, Pierre Kerbrat, Thérèse Truong, Peter Bugert, Amanda E Toland, Christine B Ambrosone, France Labrèche, Mark S Goldberg, Martine Dumont, Argyrios Ziogas, Eunjung Lee, Gillian S Dite, Carmel Apicella, Melissa C Southey, Jirong Long, Martha Shrubsole, Sandra Deming-Halverson, Filomena Ficarazzi, Monica Barile, Paolo Peterlongo, Katarzyna Durda, Katarzyna Jaworska-Bieniek, Robert A E M Tollenaar, Caroline Seynaeve, Thomas Brüning, Yon-Dschun Ko, Carolien H M van Deurzen, John W M Martens, Mieke Kriege, Jonine D Figueroa, Stephen J Chanock, Jolanta Lissowska, Ian Tomlinson, Michael J Kerin, Nicola Miller, Andreas Schneeweiss, William J Tapper, Susan M Gerty, Lorraine Durcan, Catriona McLean, Roger L Milne, Laura Baglietto, Isabel Dos Santos Silva, Olivia Fletcher, Nichola Johnson, Laura J Van't Veer, Sten Cornelissen, Asta Försti, Diana Torres, Thomas Rüdiger, Anja Rudolph, Dieter Flesch-Janys, Stefan Nickels, Caroline Weltens, Giuseppe Floris, Matthieu Moisse, Joe Dennis, Qin Wang, Alison M Dunning, Mitul Shah, Judith Brown, Jacques Simard, Hoda Anton-Culver, Susan L Neuhausen, John L Hopper, Natalia Bogdanova, Thilo Dörk, Wei Zheng, Paolo Radice, Anna Jakubowska, Jan Lubinski, Peter Devillee, Hiltrud Brauch, Maartje Hooning, Montserrat García-Closas, Elinor Sawyer, Barbara Burwinkel, Frederick Marmee, Diana M Eccles, Graham G Giles, Julian Peto, Marjanka Schmidt, Annegien Broeks, Ute Hamann, Jenny Chang-Claude, Diether Lambrechts, Paul D P Pharoah, Douglas Easton, V Shane Pankratz, Susan Slager, Celine M Vachon & Fergus J Couch, 2014, In : Human Molecular Genetics. 23, 22, p. 6034-6046

    Research output: Contribution to journalArticle

  34. Genome-wide association study and mouse expression data identify a highly conserved 32kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

    Heiko Reutter, Markus Draaken, Tracie Pennimpede, Lars Wittler, Felix F Brockschmidt, Anne-Karolin Ebert, Enrika Bartels, Wolfgang Rösch, Thomas M Boemers, Karin Hirsch, Eberhard Schmiedeke, Christian Meesters, Tim Becker, Raimund Stein, Boris Utsch, Elisabeth Mangold, Agneta Nordenskjöld, Gillian Barker, Christina Clementson Kockum, Nadine Zwink & 13 others, Gundula Holmdahl, Göran Läckgren, Ekkehart Jenetzky, Wouter Fj Feitz, Carlo Marcelis, Charlotte H W Wijers, Iris A L M van Rooij, John P Gearhart, Bernhard G Herrmann, Michael Ludwig, Simeon A Boyadjiev, Markus M Nöthen & Manuel Mattheisen, 2014, In : Human Molecular Genetics. 23, 20, p. 5536-5544

    Research output: Contribution to journalArticle

  35. Integrative Genome and Transcriptome Analyses Reveal Two Distinct Types of Ring Chromosome in Soft Tissue Sarcomas.

    Karolin Hansén Nord, Gemma Macchia, Johnbosco Tayebwa, Jenny Nilsson, Fredrik Vult von Steyern, Otte Brosjö, Nils Mandahl & Fredrik Mertens, 2014, In : Human Molecular Genetics. 23, 4, p. 878-888

    Research output: Contribution to journalArticle

  36. Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes.

    Vladimir Sharoyko, Mia Abels, Jiangming Sun, Lisa Nicholas, Ines Mollet, Jelena Stamenkovic, Isabel Göhring, Siri Malmgren, Petter Storm, Joao Fadista, Peter Spégel, Metodi D Metodiev, Nils-Göran Larsson, Lena Eliasson, Nils Wierup & Hindrik Mulder, 2014, In : Human Molecular Genetics. 23, 21, p. 5733-5749

    Research output: Contribution to journalArticle

  37. Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin

    J.L. Marshall, J. Oh, E. Chou, J.A. Lee, Johan Holmberg, D.J. Burkin & R.H. Crosbie-Watson, 2014, In : Human Molecular Genetics. 24, 7, p. 2011-2022 ddu615.

    Research output: Contribution to journalArticle

  38. TCF7L2 is a master regulator of insulin production and processing.

    Yuedan Zhou, Soo-Young Park, Jing Su, Kathleen Bailey, Emilia Ottosson Laakso, Liliya Shcherbina, Nikolay Oskolkov, Enming Zhang, Thomas Thevenin, Joao Fadista, Hedvig Bennet, Petter Vikman, Nils Wierup, Malin Fex, Johan Rung, Claes Wollheim, Marcelo Nobrega, Erik Renström, Leif Groop & Ola Hansson, 2014, In : Human Molecular Genetics. 23, 24, p. 6419-6431

    Research output: Contribution to journalArticle

  39. Ubiquitin-specific protease-14 reduces cellular aggregates and protects against mutant huntingtin-induced cell degeneration: involvement of the proteasome and ER stress-activated kinase IRE1α

    Alise Hyrskyluoto, Céline Bruelle, Sofia Hult Lundh, Hai Thi Do, Jenny Kivinen, Elisabeth Rappou, Sami Reijonen, Tuure Waltimo, Åsa Petersén, Dan Lindholm & Laura Korhonen, 2014, In : Human Molecular Genetics. 23, 22, p. 5928-5939

    Research output: Contribution to journalArticle

  40. 2013
  41. Abnormal cerebellar development and ataxia in CARP VIII morphant zebrafish

    Ashok Aspatwar, Martti E. E. Tolvanen, Eija Jokitalo, Mataleena Parikka, Csaba Ortutay, Sanna-Kaisa E. Harjula, Mika Ramet, Mauno Vihinen & Seppo Parkkila, 2013, In : Human Molecular Genetics. 22, 3, p. 417-432

    Research output: Contribution to journalArticle

  42. Deciphering the 8q24.21 association for glioma

    Victor Enciso-Mora, Fay J. Hosking, Ben Kinnersley, Yufei Wang, Sanjay Shete, Diana Zelenika, Peter Broderick, Ahmed Idbaih, Jean-Yves Delattre, Khe Hoang-Xuan, Yannick Marie, Anna Luisa Di Stefano, Marianne Labussiere, Sara Dobbins, Blandine Boisselier, Pietro Ciccarino, Marta Rossetto, Georgina Armstrong, Yanhong Liu, Konstantinos Gousias & 18 others, Johannes Schramm, Ching Lau, Sarah J. Hepworth, Konstantin Strauch, Martina Mueller-Nurasyid, Stefan Schreiber, Andre Franke, Susanne Moebus, Lewin Eisele, Asta Försti, Kari Hemminki, Ian P. Tomlinson, Anthony Swerdlow, Mark Lathrop, Matthias Simon, Melissa Bondy, Marc Sanson & Richard S. Houlston, 2013, In : Human Molecular Genetics. 22, 11, p. 2293-2302

    Research output: Contribution to journalArticle

  43. Loci influencing blood pressure identified using a cardiovascular gene-centric array

    Santhi K. Ganesh, Vinicius Tragante, Wei Guo, Yiran Guo, Matthew B. Lanktree, Erin N. Smith, Toby Johnson, Berta Almoguera Castillo, John Barnard, Jens Baumert, Yen-Pei Christy Chang, Clara C. Elbers, Martin Farrall, Mary E. Fischer, Nora Franceschini, Tom R. Gaunt, Johannes M. I. H. Gho, Christian Gieger, Yan Gong, Aaron Isaacs & 116 others, Marcus E. Kleber, Irene Mateo Leach, Caitrin W. McDonough, Matthijs F. L. Meijs, Olle Melander, Cliona M. Molony, Ilja M. Nolte, Sandosh Padmanabhan, Tom S. Price, Ramakrishnan Rajagopalan, Jonathan Shaffer, Sonia Shah, Haiqing Shen, Nicole Soranzo, Peter J. van der Most, Erik P. A. Van Iperen, Jessic A. Van Setten, Judith M. Vonk, Li Zhang, Amber L. Beitelshees, Gerald S. Berenson, Deepak L. Bhatt, Jolanda M. A. Boer, Eric Boerwinkle, Ben Burkley, Amber Burt, Aravinda Chakravarti, Wei Chen, Rhonda M. Cooper-DeHoff, Sean P. Curtis, Albert Dreisbach, David Duggan, Georg B. Ehret, Richard R. Fabsitz, Myriam Fornage, Ervin Fox, Clement E. Furlong, Ron T. Gansevoort, Marten H. Hofker, G. Kees Hovingh, Susan A. Kirkland, Kandice Kottke-Marchant, Abdullah Kutlar, Andrea Z. LaCroix, Taimour Y. Langaee, Yun R. Li, Honghuang Lin, Kiang Liu, Steffi Maiwald, Rainer Malik, Gurunathan Murugesan, Christopher Newton-Cheh, Jeffery R. OConnell, N. Charlotte Onland-Moret, Willem H. Ouwehand, Walter Palmas, Brenda W. Penninx, Carl J. Pepine, Mary Pettinger, Joseph F. Polak, Vasan S. Ramachandran, Jane Ranchalis, Susan Redline, Paul M. Ridker, Lynda M. Rose, Hubert Scharnag, Nicholas J. Schork, Daichi Shimbo, Alan R. Shuldiner, Sathanur R. Srinivasan, Ronald P. Stolk, Herman A. Taylor, Barbara Thorand, Mieke D. Trip, Cornelia M. van Duijn, W. Monique Verschuren, Cisca Wijmenga, Bernhard R. Winkelmann, Sharon Wyatt, J. Hunter Young, Bernhard O. Boehm, Mark J. Caulfield, Daniel I. Chasman, Karina W. Davidson, Pieter A. Doevendans, Garret A. FitzGerald, John G. Gums, Hakon Hakonarson, Hans L. Hillege, Thomas Illig, Gail P. Jarvik, Julie A. Johnson, John J. P. Kastelein, Wolfgang Koenig, Winfried Maerz, Braxton D. Mitchell, Sarah S. Murray, Albertine J. Oldehinkel, Daniel J. Rader, Muredach P. Reilly, Alex P. Reiner, Eric E. Schadt, Roy L. Silverstein, Harold Snieder, Alice V. Stanton, Andre G. Uitterlinden, Pim van der Harst, Yvonne T. van der Schouw, Nilesh J. Samani, Andrew D. Johnson, Patricia B. Munroe, Paul I. W. de Bakker, Xiaofeng Zhu, Daniel Levy, Brendan J. Keating & Folkert W. Asselbergs, 2013, In : Human Molecular Genetics. 22, 8, p. 1663-1678

    Research output: Contribution to journalArticle

  44. Role of Gα(olf) in Familial and Sporadic Adult-Onset Primary Dystonia.

    Satya R Vemula, Andreas Puschmann, Jianfeng Xiao, Monika Rudzinska, Karen P Frei, Daniel D Truong, Zbigniew K Wszolek & Mark S LeDoux, 2013, In : Human Molecular Genetics. 22, 12, p. 2510-2519

    Research output: Contribution to journalArticle

  45. Role of WT1-ZNF224 interaction in the expression of apoptosis-regulating genes

    Giorgia Montano, Elena Cesaro, Luigi Fattore, Karina Vidovic, Chiara Palladino, Rossella Crescitelli, Paola Izzo, Maria Caterina Turco & Paola Costanzo, 2013, In : Human Molecular Genetics. 22, 9, p. 1771-1782

    Research output: Contribution to journalArticle

  46. 2012
  47. Cdk1, but not Cdk2, is the sole Cdk that is essential and sufficient to drive resumption of meiosis in mouse oocytes

    Deepak Adhikari, Wenjing Zheng, Yan Shen, Nagaraju Gorre, Yao Ning, Guillaume Halet, Philipp Kaldis & Kui Liu, 2012 Jun 1, In : Human Molecular Genetics. 21, 11, p. 2476-2484 dds061.

    Research output: Contribution to journalArticle

  48. A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations

    Lara Bossini-Castillo, Jose-Ezequiel Martin, Jasper Broen, Olga Gorlova, Carmen P. Simeon, Lorenzo Beretta, Madelon C. Vonk, Jose Luis Callejas, Ivan Castellvi, Patricia Carreira, Francisco Jose Garcia-Hernandez, Monica Fernandez Castro, Marieke J. H. Coenen, Gabriela Riemekasten, Torsten Witte, Nicolas Hunzelmann, Alexander Kreuter, Joerg H. W. Distler, Bobby P. Koeleman, Alexandre E. Voskuyl & 20 others, Annemie J. Schuerwegh, Oyvind Palm, Roger Hesselstrand, Annika Nordin, Paolo Airo, Claudio Lunardi, Raffaella Scorza, Paul Shiels, Jacob M. van Laar, Ariane Herrick, Jane Worthington, Christopher Denton, Filemon K. Tan, Frank C. Arnett, Sandeep K. Agarwal, Shervin Assassi, Carmen Fonseca, Maureen D. Mayes, Timothy R. D. J. Radstake & Javier Martin, 2012, In : Human Molecular Genetics. 21, 4, p. 926-933

    Research output: Contribution to journalArticle

  49. alpha-Synuclein expression and Nrf2 deficiency cooperate to aggravate protein aggregation, neuronal death and inflammation in early-stage Parkinson's disease

    Isabel Lastres-Becker, Ayse Ulusoy, Nadia G. Innamorato, Gurdal Sahin, Alberto Rabano, Deniz Kirik & Antonio Cuadrado, 2012, In : Human Molecular Genetics. 21, 14, p. 3173-3192

    Research output: Contribution to journalArticle

  50. Bezafibrate administration improves behavioral deficits and tau pathology in P301S mice

    Magali Dumont, Cliona Stack, Ceyhan Elipenahli, Shari Jainuddin, Meri Gerges, Natalia Starkova, Noel Y. Calingasan, Lichuan Yang, Davide Tampellini, Anatoly A. Starkov, Robin B. Chan, Gilbert Di Paolo, Aurora Pujol & M. Flint Beal, 2012, In : Human Molecular Genetics. 21, 23, p. 5091-5105

    Research output: Contribution to journalArticle

  51. Pharmacological interference with the glucocorticoid system influences symptoms and lifespan in a mouse model of Rett syndrome.

    Sebastian Braun, Denise Kottwitz & Ulrike Nuber, 2012, In : Human Molecular Genetics. 21, 8, p. 1673-1680

    Research output: Contribution to journalArticle

  52. Selective neuroprotective effects of the S18Y polymorphic variant of UCH-L1 in the dopaminergic system

    Maria Xilouri, Elli Kyratzi, Pothitos M. Pitychoutis, Zoi Papadopoulou-Daifoti, Celine Perier, Miquel Vila, Matina Maniati, Ayse Ulusoy, Deniz Kirik, David S. Park, Keiji Wada & Leonidas Stefanis, 2012, In : Human Molecular Genetics. 21, 4, p. 874-889

    Research output: Contribution to journalArticle

  53. Survival of pancreatic beta cells is partly controlled by a TCF7L2-p53-p53INP1-dependent pathway.

    Yuedan Zhou, Enming Zhang, Christine Berggreen, Xingjun Jing, Peter Osmark, Stefan Lang, Corrado Cilio, Olga Göransson, Leif Groop, Erik Renström & Ola Hansson, 2012, In : Human Molecular Genetics. 21, p. 196-207

    Research output: Contribution to journalArticle

  54. 2011
  55. Genome-wide association study identifies novel loci predisposing to cutaneous melanoma

    Christopher I Amos, Li-E Wang, Jeffrey E Lee, Jeffrey E Gershenwald, Wei V Chen, Shenying Fang, Roman Kosoy, Mingfeng Zhang, Abrar A Qureshi, Selina Vattathil, Christopher W Schacherer, Julie M Gardner, Yuling Wang, D Tim Bishop, Jennifer H Barrett, Stuart MacGregor, Nicholas K Hayward, Nicholas G Martin, David L Duffy, Graham J Mann & 15 others, Anne Cust, John Hopper, Kevin M Brown, Elizabeth A Grimm, Yaji Xu, Younghun Han, Kaiyan Jing, Caitlin McHugh, Cathy C Laurie, Kim F Doheny, Elizabeth W Pugh, Michael F Seldin, Jiali Han, Qingyi Wei & GenoMEL Investigators GenoMEL Investigators, 2011 Dec 15, In : Human Molecular Genetics. 20, 24, p. 5012-23 12 p.

    Research output: Contribution to journalArticle

  56. Phenotype mining in CNV carriers from a population cohort

    Olli P H Pietiläinen, Karola Rehnström, Eveliina Jakkula, Susan K. Service, Eliza Congdon, Carola Tilgmann, Anna Liisa Hartikainen, Anja Taanila, Ulla Heikura, Tiina Paunio, Samuli Ripatti, Marjo Riitta Jarvelin, Matti Isohanni, Chiara Sabatti, Aarno Palotie, Nelson B. Freimer & Leena Peltonen, 2011 Jul, In : Human Molecular Genetics. 20, 13, p. 2686-2695 10 p., ddr162.

    Research output: Contribution to journalArticle

  57. A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa

    Francois Paquet-Durand, Susanne Beck, Stylianos Michalakis, Tobias Goldmann, Gesine Huber, Regine Muehlfriedel, Dragana Trifunovic, M. Dominik Fischer, Edda Fahl, Gabriele Duetsch, Elvir Becirovic, Uwe Wolfrum, Theo van Veen, Martin Biel, Naoyuki Tanimoto & Mathias W. Seeliger, 2011, In : Human Molecular Genetics. 20, 5, p. 941-947

    Research output: Contribution to journalArticle

  58. Autophagy is increased in laminin {alpha}2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.

    Virginie Carmignac, Martina Svensson, Zandra Körner, Linda Elowsson, Cintia Matsumura, Kinga Gawlik, Valerie Allamand & Madeleine Durbeej-Hjalt, 2011, In : Human Molecular Genetics. 20, 24, p. 4891-4902

    Research output: Contribution to journalArticle

  59. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

    Antonis C. Antoniou, Christiana Kartsonaki, Olga M. Sinilnikova, Penny Soucy, Lesley McGuffog, Sue Healey, Andrew Lee, Paolo Peterlongo, Siranoush Manoukian, Bernard Peissel, Daniela Zaffaroni, Elisa Cattaneo, Monica Barile, Valeria Pensotti, Barbara Pasini, Riccardo Dolcetti, Giuseppe Giannini, Anna Laura Putignano, Liliana Varesco, Paolo Radice & 161 others, Phuong L. Mai, Mark H. Greene, Irene L. Andrulis, Gord Glendon, Hilmi Ozcelik, Mads Thomassen, Anne-Marie Gerdes, Torben A. Kruse, Uffe Birk Jensen, Dorthe G. Crueger, Maria A. Caligo, Yael Laitman, Roni Milgrom, Bella Kaufman, Shani Paluch-Shimon, Eitan Friedman, Niklas Loman, Katja Harbst, Annika Lindblom, Brita Arver, Hans Ehrencrona, Beatrice Melin, Katherine L. Nathanson, Susan M. Domchek, Timothy Rebbeck, Ania Jakubowska, Jan Lubinski, Jacek Gronwald, Tomasz Huzarski, Tomasz Byrski, Cezary Cybulski, Bohdan Gorski, Ana Osorio, Teresa Ramon y Cajal, Florentia Fostira, Raquel Andres, Javier Benitez, Ute Hamann, Frans B. Hogervorst, Matti A. Rookus, Maartje J. Hooning, Marcel R. Nelen, Rob B. van der Luijt, Theo A. M. van Os, Christi J. van Asperen, Peter Devilee, Hanne E. J. Meijers-Heijboer, Encarna B. Gomez Garcia, Susan Peock, Margaret Cook, Debra Frost, Radka Platte, Jean Leyland, D. Gareth Evans, Fiona Lalloo, Ros Eeles, Louise Izatt, Julian Adlard, Rosemarie Davidson, Diana Eccles, Kai-ren Ong, Jackie Cook, Fiona Douglas, Joan Paterson, M. John Kennedy, Zosia Miedzybrodzka, Andrew Godwin, Dominique Stoppa-Lyonnet, Bruno Buecher, Muriel Belotti, Carole Tirapo, Sylvie Mazoyer, Laure Barjhoux, Christine Lasset, Dominique Leroux, Laurence Faivre, Myriam Bronner, Fabienne Prieur, Catherine Nogues, Etienne Rouleau, Pascal Pujol, Isabelle Coupier, Marc Frenay, John L. Hopper, Mary B. Daly, Mary B. Terry, Esther M. John, Saundra S. Buys, Yosuf Yassin, Alexander Miron, David Goldgar, Christian F. Singer, Muy-Kheng Tea, Georg Pfeiler, Anne Catharina Dressler, Thomas v. O. Hansen, Lars Jonson, Bent Ejlertsen, Rosa Bjork Barkardottir, Tomas Kirchhoff, Kenneth Offit, Marion Piedmonte, Gustavo Rodriguez, Laurie Small, John Boggess, Stephanie Blank, Jack Basil, Masoud Azodi, Amanda Ewart Toland, Marco Montagna, Silvia Tognazzo, Simona Agata, Evgeny Imyanitov, Ramunas Janavicius, Conxi Lazaro, Ignacio Blanco, Paul D. P. Pharoah, Lara Sucheston, Beth Y. Karlan, Christine S. Walsh, Edith Olah, Aniko Bozsik, Soo-Hwang Teo, Joyce L. Seldon, Mary S. Beattie, Elizabeth J. van Rensburg, Michelle D. Sluiter, Orland Diez, Rita K. Schmutzler, Barbara Wappenschmidt, Christoph Engel, Alfons Meindl, Ina Ruehl, Raymonda Varon-Mateeva, Karin Kast, Helmut Deissler, Dieter Niederacher, Norbert Arnold, Dorothea Gadzicki, Ines Schoenbuchner, Trinidad Caldes, Miguel de la Hoya, Heli Nevanlinna, Kristiina Aittomaki, Martine Dumont, Jocelyne Chiquette, Marc Tischkowitz, Xiaoqing Chen, Jonathan Beesley, Amanda B. Spurdle, Susan L. Neuhausen, Yuan Chun Ding, Zachary Fredericksen, Xianshu Wang, Vernon S. Pankratz, Fergus Couch, Jacques Simard, Douglas F. Easton, Georgia Chenevix-Trench, Åke Borg & Håkan Olsson, 2011, In : Human Molecular Genetics. 20, 16, p. 3304-3321

    Research output: Contribution to journalArticle

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