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Orphanet journal of rare diseases, 2013-01, Vol.8 (1), p.12-12
2013
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Orphanet journal of rare diseases, 2015-05, Vol.10 (1), p.65-65, Article 65
2015
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Nature genetics, 2019-10, Vol.51 (10), p.1494-1505
- Calderon, Diego
- Nguyen, Michelle L T
- Mezger, Anja
- Kathiria, Arwa
- Müller, Fabian
- Nguyen, Vinh
- Lescano, Ninnia
- Wu, Beijing
- Trombetta, John
- Ribado, Jessica V
- Knowles, David A
- Gao, Ziyue
- Blaeschke, Franziska
- Parent, Audrey V
- Burt, Trevor D
- Anderson, Mark S
- Criswell, Lindsey A
- Greenleaf, William J
- Marson, Alexander
- Pritchard, Jonathan K
2019
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Journal of medical genetics, 2021-08, Vol.58 (8), p.570
- Olivier, Guillaume
- Corton, Marta
- Intartaglia, Daniela
- Verbakel, Sanne K
- Sergouniotis, Panagiotis I
- Le Meur, Guylène
- Dhaenens, Claire-Marie
- Naacke, Hélène
- Avila-Fernández, Almudena
- Hoyng, Carel B
- Klevering, Jeroen
- Bocquet, Béatrice
- Roubertie, Agathe
- Sénéchal, Audrey
- Banfi, Sandro
- Muller, Agnès
- Hamel, Christian L
- Black, Graeme C
- Conte, Ivan
- Roosing, Susanne
- Zanlonghi, Xavier
- Ayuso, Carmen
- Meunier, Isabelle
- Manes, Gaël
2021
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Genes, 2019-08, Vol.10 (9), p.633
- Pacot, Laurence
- Burin des Roziers, Cyril
- Laurendeau, Ingrid
- Briand-Suleau, Audrey
- Coustier, Audrey
- Mayard, Théodora
- Tlemsani, Camille
- Faivre, Laurence
- Thomas, Quentin
- Rodriguez, Diana
- Blesson, Sophie
- Dollfus, Hélène
- Muller, Yvon-Gauthier
- Parfait, Béatrice
- Vidaud, Michel
- Gilbert-Dussardier, Brigitte
- Yardin, Catherine
- Dauriat, Benjamin
- Derancourt, Christian
- Vidaud, Dominique
- Pasmant, Eric
2019
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Genome biology and evolution, 2015-09, Vol.7 (9), p.2484-2505
2015
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PLoS genetics, 2010-02, Vol.6 (2), p.e1000859
- Arsène-Ploetze, Florence
- Koechler, Sandrine
- Marchal, Marie
- Coppée, Jean-Yves
- Chandler, Michael
- Bonnefoy, Violaine
- Brochier-Armanet, Céline
- Barakat, Mohamed
- Barbe, Valérie
- Battaglia-Brunet, Fabienne
- Bruneel, Odile
- Bryan, Christopher G
- Cleiss-Arnold, Jessica
- Cruveiller, Stéphane
- Erhardt, Mathieu
- Heinrich-Salmeron, Audrey
- Hommais, Florence
- Joulian, Catherine
- Krin, Evelyne
- Lieutaud, Aurélie
- Lièvremont, Didier
- Michel, Caroline
- Muller, Daniel
- Ortet, Philippe
- Proux, Caroline
- Siguier, Patricia
- Roche, David
- Rouy, Zoé
- Salvignol, Grégory
- Slyemi, Djamila
- Talla, Emmanuel
- Weiss, Stéphanie
- Weissenbach, Jean
- Médigue, Claudine
- Bertin, Philippe N
- Moran, Nancy A.
2010
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Orphanet journal of rare diseases, 2023-07, Vol.18 (1), p.180-180, Article 180
2023
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Human mutation, 2012-08, Vol.33 (8), p.1228-1238
- Houdayer, Claude
- Caux-Moncoutier, Virginie
- Krieger, Sophie
- Barrois, Michel
- Bonnet, Françoise
- Bourdon, Violaine
- Bronner, Myriam
- Buisson, Monique
- Coulet, Florence
- Gaildrat, Pascaline
- Lefol, Cédrick
- Léone, Mélanie
- Mazoyer, Sylvie
- Muller, Danielle
- Remenieras, Audrey
- Révillion, Françoise
- Rouleau, Etienne
- Sokolowska, Joanna
- Vert, Jean-Philippe
- Lidereau, Rosette
- Soubrier, Florent
- Sobol, Hagay
- Sevenet, Nicolas
- Bressac-de Paillerets, Brigitte
- Hardouin, Agnès
- Tosi, Mario
- Sinilnikova, Olga M.
- Stoppa-Lyonnet, Dominique
2012
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Human mutation, 2023-05, Vol.2023, p.1-17
- Lazarian, Grégory
- Leroy, Bernard
- Theves, Floriane
- Hormi, Myriam
- Letestu, Rémi
- Eclache, Virginie
- Tueur, Giulia
- Ameur, Adam
- Bidet, Audrey
- Cornillet-Lefebvre, Pascale
- Davi, Frédéric
- Delabesse, Eric
- Estienne, Marie-Hélène
- Etancelin, Pascaline
- Kosmider, Olivier
- Laibe, Sophy
- Muller, Marc
- Nadal, Nathalie
- Naguib, Dina
- Pastoret, Cédric
- Poulain, Stéphanie
- Sujobert, Pierre
- Veronese, Lauren
- Imache, Samia
- Lefebvre, Valérie
- Cymbalista, Florence
- Baran-Marszak, Fanny
- Soussi, Thierry
- Ganguly, Arupa
- Arupa Ganguly
2023
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American journal of human genetics, 2018-04, Vol.102 (4), p.557-573
- Vögtle, F.-Nora
- Brändl, Björn
- Larson, Austin
- Pendziwiat, Manuela
- Friederich, Marisa W.
- White, Susan M.
- Basinger, Alice
- Kücükköse, Cansu
- Muhle, Hiltrud
- Jähn, Johanna A.
- Keminer, Oliver
- Helbig, Katherine L.
- Delto, Carolyn F.
- Myketin, Lisa
- Mossmann, Dirk
- Burger, Nils
- Miyake, Noriko
- Burnett, Audrey
- van Baalen, Andreas
- Lovell, Mark A.
- Matsumoto, Naomichi
- Walsh, Maie
- Yu, Hung-Chun
- Shinde, Deepali N.
- Stephani, Ulrich
- Van Hove, Johan L.K.
- Müller, Franz-Josef
- Helbig, Ingo
2018
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Genome biology and evolution, 2017-12, Vol.9 (12), p.3413-3431
2017
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Journal of medical genetics, 2012-08, Vol.49 (8), p.525-532
- Spurdle, Amanda B
- Whiley, Phillip J
- Thompson, Bryony
- Feng, Bingjian
- Healey, Sue
- Brown, Melissa A
- Pettigrew, Christopher
- Van Asperen, Christi J
- Ausems, Margreet G E M
- Kattentidt-Mouravieva, Anna A
- van den Ouweland, Ans M W
- Belgium UV Consortium, Dutch
- Lindblom, Annika
- Pigg, Maritta H
- Schmutzler, Rita K
- Engel, Christoph
- Meindl, Alfons
- Caputo, Sandrine
- Sinilnikova, Olga M
- Lidereau, Rosette
- Couch, Fergus J
- Guidugli, Lucia
- Hansen, Thomas van Overeem
- Thomassen, Mads
- Eccles, Diana M
- Tucker, Kathy
- Benitez, Javier
- Domchek, Susan M
- Toland, Amanda E
- Van Rensburg, Elizabeth J
- Wappenschmidt, Barbara
- Borg, Åke
- Vreeswijk, Maaike P G
- Goldgar, David E
2012
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Circulation. Cardiovascular genetics, 2012-04, Vol.5 (2), p.202
2012
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Human molecular genetics, 2011-08, Vol.20 (16), p.3304-3321
- Antoniou, Antonis C
- Soucy, Penny
- McGuffog, Lesley
- Healey, Sue
- Lee, Andrew
- Peterlongo, Paolo
- Manoukian, Siranoush
- Peissel, Bernard
- Zaffaroni, Daniela
- Barile, Monica
- Pasini, Barbara
- Dolcetti, Riccardo
- Giannini, Giuseppe
- Varesco, Liliana
- Radice, Paolo
- Mai, Phuong L
- Andrulis, Irene L
- Glendon, Gord
- Birk Jensen, Uffe
- Crüger, Dorthe G
- Laitman, Yael
- Milgrom, Roni
- Kaufman, Bella
- Friedman, Eitan
- Lindblom, Annika
- Ehrencrona, Hans
- Rebbeck, Timothy
- Jakubowska, Ania
- Gronwald, Jacek
- Byrski, Tomasz
- Cybulski, Cezary
- Osorio, Ana
- Ramón y Cajal, Teresa
- Fostira, Florentia
- Rookus, Matti A
- Hooning, Maartje J
- van der Luijt, Rob B
- van Os, Theo A.M
- Meijers-Heijboer, Hanne E.J
- Gómez Garcia, Encarna B
- Peock, Susan
- Platte, Radka
- Lalloo, Fiona
- Eeles, Ros
- Davidson, Rosemarie
- Eccles, Diana
- Ong, Kai-ren
- Cook, Jackie
- Douglas, Fiona
- Paterson, Joan
- Miedzybrodzka, Zosia
- Godwin, Andrew
- Stoppa-Lyonnet, Dominique
- Buecher, Bruno
- Tirapo, Carole
- Barjhoux, Laure
- Faivre, Laurence
- Nogues, Catherine
- Rouleau, Etienne
- Pujol, Pascal
- Coupier, Isabelle
- Frénay, Marc
- Hopper, John L
- Terry, Mary B
- Singer, Christian F
- Catharina Dressler, Anne
- Offit, Kenneth
- Rodriguez, Gustavo
- Small, Laurie
- Boggess, John
- Blank, Stephanie
- Basil, Jack
- Ewart Toland, Amanda
- Montagna, Marco
- Tognazzo, Silvia
- Blanco, Ignacio
- Walsh, Christine S
- Olah, Edith
- Bozsik, Aniko
- Teo, Soo-Hwang
- Beattie, Mary S
- Diez, Orland
- Schmutzler, Rita K
- Engel, Christoph
- Meindl, Alfons
- Ruehl, Ina
- Varon-Mateeva, Raymonda
- Niederacher, Dieter
- Arnold, Norbert
- Gadzicki, Dorothea
- Caldes, Trinidad
- de la Hoya, Miguel
- Chen, Xiaoqing
- Spurdle, Amanda B
- Neuhausen, Susan L
- Chun Ding, Yuan
- Fredericksen, Zachary
- Couch, Fergus
- Simard, Jacques
- Easton, Douglas F
2011
Link zum Volltext
American journal of human genetics, 2004-01, Vol.74 (1), p.11-19
- Zimprich, Alexander
- Müller-Myhsok, Bertram
- Farrer, Matthew
- Leitner, Petra
- Sharma, Manu
- Hulihan, Mary
- Lockhart, Paul
- Strongosky, Audrey
- Kachergus, Jennifer
- Calne, Donald B.
- Stoessl, Jon
- Uitti, Ryan J.
- Pfeiffer, Ronald F.
- Trenkwalder, Claudia
- Homann, Nikolaus
- Ott, Erwin
- Wenzel, Karoline
- Asmus, Friedrich
- Hardy, John
- Wszolek, Zbigniew
- Gasser, Thomas
2004
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Human mutation, 2011-09, Vol.32 (9), p.1004-1007
2011
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European journal of human genetics : EJHG, 2016-07, Vol.24 (7), p.1001-1008
2016
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