Anzahl der Einträge: 2.
2021
Grosche, Sarah,
Marenholz, Ingo,
Esparza-Gordillo, Jorge,
Arnau-Soler, Aleix,
Pairo-Castineira, Erola ,
Rüschendorf, Franz,
Ahluwalia, Tarunveer S. ,
Almqvist, Catarina,
Arnold, Andreas,
Baurecht, Hansjörg ,
Bisgaard, Hans ,
Bønnelykke, Klaus ,
Brown, Sara J.,
Bustamante, Mariona,
Curtin, John A.,
Custovic, Adnan,
Dharmage, Shyamali C.,
Esplugues, Ana,
Falchi, Mario ,
Fernandez-Orth, Dietmar,
Ferreira, Manuel A. R.,
Franke, Andre ,
Gerdes, Sascha ,
Gieger, Christian,
Hakonarson, Hakon,
Holt, Patrick G. ,
Homuth, Georg,
Hubner, Norbert,
Hysi, Pirro G.,
Jarvelin, Marjo-Riitta,
Karlsson, Robert,
Koppelman, Gerard H. ,
Lau, Susanne,
Lutz, Manuel,
Magnusson, Patrik K. E.,
Marks, Guy B.,
Müller-Nurasyid, Martina,
Nöthen, Markus M.,
Paternoster, Lavinia,
Pennell, Craig E.,
Peters, Annette ,
Rawlik, Konrad,
Robertson, Colin F.,
Rodriguez, Elke,
Sebert, Sylvain,
Simpson, Angela ,
Sleiman, Patrick M. A.,
Standl, Marie,
Stölzl, Dora,
Strauch, Konstantin,
Szwajda, Agnieszka,
Tenesa, Albert,
Thompson, Philip J.,
Ullemar, Vilhelmina,
Visconti, Alessia,
Vonk, Judith M.,
Wang, Carol A.,
Weidinger, Stephan,
Wielscher, Matthias ,
Worth, Catherine L.,
Xu, Chen-Jian und
Lee, Young-Ae
(2021)
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
Nature Communications 12 (1).
Volltext nicht vorhanden.
2009
Kaput, Jim,
Cotton, Richard G. H.,
Hardman, Lauren,
Watson, Michael,
Al Aqeel, Aida I.,
Al-Aama, Jumana Y.,
Al-Mulla, Fahd,
Alonso, Santos,
Aretz, Stefan,
Auerbach, Arleen D.,
Bapat, Bharati,
Bernstein, Inge T.,
Bhak, Jong,
Bleoo, Stacey L.,
Blöcker, Helmut,
Brenner, Steven E.,
Burn, John,
Bustamante, Mariona,
Calzone, Rita,
Cambon-Thomsen, Anne,
Cargill, Michele,
Carrera, Paola,
Cavedon, Lawrence,
Cho, Yoon Shin,
Chung, Yeun-Jun,
Claustres, Mireille,
Cutting, Garry,
Dalgleish, Raymond,
den Dunnen, Johan T.,
Díaz, Carlos,
Dobrowolski, Steven,
dos Santos, M. Rosário N.,
Ekong, Rosemary,
Flanagan, Simon B.,
Flicek, Paul,
Furukawa, Yoichi,
Genuardi, Maurizio,
Ghang, Ho,
Golubenko, Maria V.,
Greenblatt, Marc S.,
Hamosh, Ada,
Hancock, John M.,
Hardison, Ross,
Harrison, Terence M.,
Hoffmann, Robert,
Horaitis, Rania,
Howard, Heather J.,
Barash, Carol Isaacson,
Izagirre, Neskuts,
Jung, Jongsun,
Kojima, Toshio,
Laradi, Sandrine,
Lee, Yeon-Su,
Lee, Jong-Young,
Gil-da-Silva-Lopes, Vera L.,
Macrae, Finlay A.,
Maglott, Donna,
Marafie, Makia J.,
Marsh, Steven G. E.,
Matsubara, Yoichi,
Messiaen, Ludwine M.,
Möslein, Gabriela,
Netea, Mihai G.,
Norton, Melissa L.,
Oefner, Peter J.,
Oetting, William S.,
O'Leary, James C.,
de Ramirez, Ana Maria Oller,
Paalman, Mark H.,
Parboosingh, Jillian,
Patrinos, George P.,
Perozzi, Giuditta,
Phillips, Ian R.,
Povey, Sue,
Prasad, Suyash,
Qi, Ming,
Quin, David J.,
Ramesar, Rajkumar S.,
Richards, C. Sue,
Savige, Judith,
Scheible, Dagmar G.,
Scott, Rodney J.,
Seminara, Daniela,
Shephard, Elizabeth A.,
Sijmons, Rolf H.,
Smith, Timothy D.,
Sobrido, María-Jesús,
Tanaka, Toshihiro,
Tavtigian, Sean V.,
Taylor, Graham R.,
Teague, Jon,
Töpel, Thoralf,
Ullman-Cullere, Mollie,
Utsunomiya, Joji,
van Kranen, Henk J.,
Vihinen, Mauno,
Webb, Elizabeth,
Weber, Thomas K.,
Yeager, Meredith,
Yeom, Young I.,
Yim, Seon-Hee und
Yoo, Hyang-Sook
(2009)
Planning the human variome project: the Spain report.
Human mutation 30 (4), S. 496-510.
Volltext nicht vorhanden.
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