Markus M Nöthen
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Mingardo E, Beaman G, Grote P, Nordenskjöld A, Newman W, Woolf A, Eckstein M, Hilger A, Dworschak G, Rösch W, Ebert A, Stein R, Brusco A, Di Grazia M, Tamer A, Torres F, Hernandez J, Erben P, Maj C, Olmos J, Riancho J, Valero C, Hostettler I, Houlden H, Werring D, Schumacher J, Gehlen J, Giel A, Buerfent B, Arkani S, Åkesson E, Rotstein E, Ludwig M, Holmdahl G, Giorgio E, Berettini A, Keene D, Cervellione R, Younsi N, Ortlieb M, Oswald J, Haid B, Promm M, Neissner C, Hirsch K, Stehr M, Schäfer F, Schmiedeke E, Boemers T, van Rooij I, Feitz W, Marcelis C, Lacher M, Nelson J, Ure B, Fortmann C, Gale D, Chan M, Ludwig K, Nöthen M, Heilmann S, Zwink N, Jenetzky E, Odermatt B, Knapp M, Reutter H. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Commun Biol 2022; 5:1203.
09.11.2022A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
09.11.2022Commun Biol 2022; 5:1203
Mingardo Enrico, Beaman Glenda, Grote Philip, Nordenskjöld Agneta, Newman William, Woolf Adrian S, Eckstein Markus, Hilger Alina C, Dworschak Gabriel C, Rösch Wolfgang, Ebert Anne-Karolin, Stein Raimund, Brusco Alfredo, Di Grazia Massimo, Tamer Ali, Torres Federico M, Hernandez Jose L, Erben Philipp, Maj Carlo, Olmos Jose M, Riancho Jose A, Valero Carmen, Hostettler Isabel, Houlden Henry, Werring David J, Schumacher Johannes, Gehlen Jan, Giel Ann-Sophie, Buerfent Benedikt C, Arkani Samara, Åkesson Elisabeth, Rotstein Emilia, Ludwig Michael, Holmdahl Gundela, Giorgio Elisa, Berettini Alfredo, Keene David, Cervellione Raimondo M, Younsi Nina, Ortlieb Melissa, Oswald Josef, Haid Bernhard, Promm Martin, Neissner Claudia, Hirsch Karin, Stehr Maximilian, Schäfer Frank-Mattias, Schmiedeke Eberhard, Boemers Thomas M, van Rooij Iris A L M, Feitz Wouter F J, Marcelis Carlo L M, Lacher Martin, Nelson Jana, Ure Benno, Fortmann Caroline, Gale Daniel P, Chan Melanie M Y, Ludwig Kerstin U, Nöthen Markus M, Heilmann Stefanie, Zwink Nadine, Jenetzky Ekkehart, Odermatt Benjamin, Knapp Michael, Reutter Heiko
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
van Rheenen W, van der Spek R, Bakker M, Van Vugt J, Hop P, Zwamborn R, de Klein N, Westra H, Bakker O, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, Dolzhenko E, Dekker A, Gawor K, Westeneng H, Tazelaar G, van Eijk K, Kooyman M, Byrne R, Doherty M, Heverin M, Al Khleifat A, Iacoangeli A, Shatunov A, Ticozzi N, Cooper-Knock J, Smith B, Gromicho M, Chandran S, Pal S, Morrison K, Shaw P, Hardy J, Orrell R, Sendtner M, Meyer T, Başak N, van der Kooi A, Ratti A, Fogh I, Gellera C, Lauria G, Corti S, Cereda C, Sproviero D, D'Alfonso S, Sorarù G, Siciliano G, Filosto M, Padovani A, Chio A, Calvo A, Moglia C, Brunetti M, Canosa A, Grassano M, Beghi E, Pupillo E, Logroscino G, Nefussy B, Osmanovic A, Nordin A, Lerner Y, Zabari M, Gotkine M, Baloh R, Bell S, Vourc'h P, Corcia P, Couratier P, Millecamps S, Meininger V, Salachas F, Mora Pardina J, Assialioui A, Rojas-García R, Dion P, Ross J, Ludolph A, Weishaupt J, Brenner D, Freischmidt A, Bensimon G, Brice A, Dürr A, Payan C, Saker-Delye S, Wood N, Topp S, Rademakers R, Tittmann L, Lieb W, Franke A, Ripke S, Braun A, Kraft J, Whiteman D, Olsen C, Uitterlinden A, Hofman A, Rietschel M, Cichon S, Nöthen M, Amouyel P, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor B, Singleton A, Mitne Neto M, Cauchi R, Ophoff R, Wiedau-Pazos M, Lomen-Hoerth C, Van Deerlin V, Grosskreutz J, Roediger A, Gaur N, Jörk A, Barthel T, Theele E, Ilse B, Stubendorff B, Witte O, Steinbach R, Hübner C, Graff C, Brylev L, Fominykh V, Demeshonok V, Ataulina A, Rogelj B, Koritnik B, Zidar J, Ravnik-Glavač M, Glavač D, Stević Z, Drory V, Povedano M, Blair I, Kiernan M, Benyamin B, Henderson R, Furlong S, Mathers S, McCombe P, Needham M, Ngo S, Nicholson G, Pamphlett R, Rowe D, Steyn F, Williams K, Mather K, Sachdev P, Henders A, Wallace L, de Carvalho M, Pinto S, Petri S, Weber M, Rouleau G, Silani V, Curtis C, Breen G, Glass J, Brown R, Landers J, Shaw C, Andersen P, Groen E, van Es M, Pasterkamp R, Fan D, Garton F, McRae A, Davey Smith G, Gaunt T, Eberle M, Mill J, McLaughlin R, Hardiman O, Kenna K, Wray N, Tsai E, Runz H, Franke L, Al-Chalabi A, Van Damme P, van den Berg L, Veldink J. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nat Genet 2022; 54:361.
01.03.2022Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
01.03.2022Nat Genet 2022; 54:361
van Rheenen Wouter, van der Spek Rick A A, Bakker Mark K, Van Vugt Joke J F A, Hop Paul J, Zwamborn Ramona A J, de Klein Niek, Westra Harm-Jan, Bakker Olivier B, Deelen Patrick, Shireby Gemma, Hannon Eilis, Moisse Matthieu, Baird Denis, Restuadi Restuadi, Dolzhenko Egor, Dekker Annelot M, Gawor Klara, Westeneng Henk-Jan, Tazelaar Gijs H P, van Eijk Kristel R, Kooyman Maarten, Byrne Ross P, Doherty Mark, Heverin Mark, Al Khleifat Ahmad, Iacoangeli Alfredo, Shatunov Aleksey, Ticozzi Nicola, Cooper-Knock Johnathan, Smith Bradley N, Gromicho Marta, Chandran Siddharthan, Pal Suvankar, Morrison Karen E, Shaw Pamela J, Hardy John, Orrell Richard W, Sendtner Michael, Meyer Thomas, Başak Nazli, van der Kooi Anneke J, Ratti Antonia, Fogh Isabella, Gellera Cinzia, Lauria Giuseppe, Corti Stefania, Cereda Cristina, Sproviero Daisy, D'Alfonso Sandra, Sorarù Gianni, Siciliano Gabriele, Filosto Massimiliano, Padovani Alessandro, Chio Adriano, Calvo Andrea, Moglia Cristina, Brunetti Maura, Canosa Antonio, Grassano Maurizio, Beghi Ettore, Pupillo Elisabetta, Logroscino Giancarlo, Nefussy Beatrice, Osmanovic Alma, Nordin Angelica, Lerner Yossef, Zabari Michal, Gotkine Marc, Baloh Robert H, Bell Shaughn, Vourc'h Patrick, Corcia Philippe, Couratier Philippe, Millecamps Stéphanie, Meininger Vincent, Salachas François, Mora Pardina Jesus S, Assialioui Abdelilah, Rojas-García Ricardo, Dion Patrick A, Ross Jay P, Ludolph Albert C, Weishaupt Jochen H, Brenner David, Freischmidt Axel, Bensimon Gilbert, Brice Alexis, Dürr Alexandra, Payan Christine A M, Saker-Delye Safa, Wood Nicholas W, Topp Simon, Rademakers Rosa, Tittmann Lukas, Lieb Wolfgang, Franke Andre, Ripke Stephan, Braun Alice, Kraft Julia, Whiteman David C, Olsen Catherine M, Uitterlinden André G, Hofman Albert, Rietschel Marcella, Cichon Sven, Nöthen Markus M, Amouyel Philippe, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor Bryan J, Singleton Andrew B, Mitne Neto Miguel, Cauchi Ruben J, Ophoff Roel A, Wiedau-Pazos Martina, Lomen-Hoerth Catherine, Van Deerlin Vivianna M, Grosskreutz Julian, Roediger Annekathrin, Gaur Nayana, Jörk Alexander, Barthel Tabea, Theele Erik, Ilse Benjamin, Stubendorff Beatrice, Witte Otto W, Steinbach Robert, Hübner Christian A, Graff Caroline, Brylev Lev, Fominykh Vera, Demeshonok Vera, Ataulina Anastasia, Rogelj Boris, Koritnik Blaž, Zidar Janez, Ravnik-Glavač Metka, Glavač Damjan, Stević Zorica, Drory Vivian, Povedano Monica, Blair Ian P, Kiernan Matthew C, Benyamin Beben, Henderson Robert D, Furlong Sarah, Mathers Susan, McCombe Pamela A, Needham Merrilee, Ngo Shyuan T, Nicholson Garth A, Pamphlett Roger, Rowe Dominic B, Steyn Frederik J, Williams Kelly L, Mather Karen A, Sachdev Perminder S, Henders Anjali K, Wallace Leanne, de Carvalho Mamede, Pinto Susana, Petri Susanne, Weber Markus, Rouleau Guy A, Silani Vincenzo, Curtis Charles J, Breen Gerome, Glass Jonathan D, Brown Robert H, Landers John E, Shaw Christopher E, Andersen Peter M, Groen Ewout J N, van Es Michael A, Pasterkamp R Jeroen, Fan Dongsheng, Garton Fleur C, McRae Allan F, Davey Smith George, Gaunt Tom R, Eberle Michael A, Mill Jonathan, McLaughlin Russell L, Hardiman Orla, Kenna Kevin P, Wray Naomi R, Tsai Ellen, Runz Heiko, Franke Lude, Al-Chalabi Ammar, Van Damme Philip, van den Berg Leonard H, Veldink Jan H
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
van Rheenen W, van der Spek R, Bakker M, Farei-Campagna J, Hop P, Zwamborn R, de Klein N, Westra H, Bakker O, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, Dolzhenko E, Dekker A, Gawor K, Westeneng H, Tazelaar G, van Eijk K, Kooyman M, Byrne R, Doherty M, Heverin M, Al Khleifat A, Iacoangeli A, Shatunov A, Ticozzi N, Cooper-Knock J, Smith B, Gromicho M, Chandran S, Pal S, Morrison K, Openshaw P, Hardy J, Orrell R, Sendtner M, Meyer T, Başak N, van der Kooi A, Ratti A, Fogh I, Gellera C, Lauria G, Corti S, Cereda C, Sproviero D, D'Alfonso S, Sorarù G, Siciliano G, Filosto M, Padovani A, Chio A, Calvo A, Moglia C, Brunetti M, Canosa A, Grassano M, Beghi E, Pupillo E, Logroscino G, Nefussy B, Osmanovic A, Nordin A, Lerner Y, Zabari M, Gotkine M, Baloh R, Bell S, Vourc'h P, Corcia P, Couratier P, Millecamps S, Meininger V, Salachas F, Mora J, Assialioui A, Rojas-García R, Dion P, Ross J, Ludolph A, Weishaupt J, Brenner D, Freischmidt A, Bensimon G, Brice A, Dürr A, Payan C, Saker-Delye S, Wood N, Topp S, Rademakers R, Tittmann L, Lieb W, Klein-Franke A, Ripke S, Braun A, Kraft J, Whiteman D, Olsen C, Uitterlinden A, Hofman A, Rietschel M, Cichon S, Nöthen M, Amouyel P, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor B, Singleton A, Mitne Neto M, Cauchi R, Ophoff R, Wiedau-Pazos M, Lomen-Hoerth C, Van Deerlin V, Grosskreutz J, Roediger A, Gaur N, Jörk A, Barthel T, Theele E, Ilse B, Stubendorff B, Witte O, Steinbach R, Hübner C, Graff C, Brylev L, Fominykh V, Demeshonok V, Ataulina A, Rogelj B, Koritnik B, Zidar J, Ravnik-Glavač M, Glavač D, Stević Z, Drory V, Povedano M, Blair I, Kiernan M, Benyamin B, Henderson R, Furlong S, Mathers S, McCombe P, Needham M, Ngo S, Nicholson G, Pamphlett R, Rowe D, Steyn F, Williams K, Mather K, Sachdev P, Henders A, Wallace L, de Carvalho M, Pinto S, Petri S, Weber M, Rouleau G, Silani V, Curtis C, Breen G, Glass J, Brown R, Landers J, Shaw C, Andersen P, Groen E, van Es M, Pasterkamp R, Fan D, Garton F, McRae A, Davey Smith G, Gaunt T, Eberle M, Mill J, McLaughlin R, Hardiman O, Kenna K, Wray N, Tsai E, Runz H, Franke L, Al-Chalabi A, Van Damme P, van den Berg L, Veldink J. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nat Genet 2021; 53:1636-1648.
06.12.2021Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
06.12.2021Nat Genet 2021; 53:1636-1648
van Rheenen Wouter, van der Spek Rick A A, Bakker Mark K, Farei-Campagna Jan Marino, Hop Paul J, Zwamborn Ramona A J, de Klein Niek, Westra Harm-Jan, Bakker Olivier B, Deelen Patrick, Shireby Gemma, Hannon Eilis, Moisse Matthieu, Baird Denis, Restuadi Restuadi, Dolzhenko Egor, Dekker Annelot M, Gawor Klara, Westeneng Henk-Jan, Tazelaar Gijs H P, van Eijk Kristel R, Kooyman Maarten, Byrne Ross P, Doherty Mark, Heverin Mark, Al Khleifat Ahmad, Iacoangeli Alfredo, Shatunov Aleksey, Ticozzi Nicola, Cooper-Knock Johnathan, Smith Bradley N, Gromicho Marta, Chandran Siddharthan, Pal Suvankar, Morrison Karen E, Openshaw Peter J M, Hardy John, Orrell Richard W, Sendtner Michael, Meyer Thomas, Başak Nazli A, van der Kooi Anneke J, Ratti Antonia, Fogh Isabella, Gellera Cinzia, Lauria Giuseppe, Corti Stefania, Cereda Cristina, Sproviero Daisy, D'Alfonso Sandra, Sorarù Gianni, Siciliano Gabriele, Filosto Massimiliano, Padovani Alessandro, Chio Adriano, Calvo Andrea, Moglia Cristina, Brunetti Maura, Canosa Antonio, Grassano Maurizio, Beghi Ettore, Pupillo Elisabetta, Logroscino Giancarlo, Nefussy Beatrice, Osmanovic Alma, Nordin Angelica, Lerner Yossef, Zabari Michal, Gotkine Marc, Baloh Robert H, Bell Shaughn, Vourc'h Patrick, Corcia Philippe, Couratier Philippe, Millecamps Stéphanie, Meininger Vincent, Salachas François, Mora Jesus S, Assialioui Abdelilah, Rojas-García Ricardo, Dion Patrick A, Ross Jay P, Ludolph Albert C., Weishaupt Jochen H, Brenner David, Freischmidt Axel, Bensimon Gilbert, Brice Alexis, Dürr Alexandra, Payan Christine A M, Saker-Delye Safaa, Wood Nicholas W, Topp Simon, Rademakers Rosa, Tittmann Lukas, Lieb Wolfgang, Klein-Franke Andreas, Ripke Stephan, Braun Alice, Kraft Julia, Whiteman David C, Olsen Catherine M, Uitterlinden André G, Hofman Albert, Rietschel Marcella, Cichon Sven, Nöthen Markus M, Amouyel Philippe, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor Bryan J, Singleton Andrew B, Mitne Neto Miguel, Cauchi Ruben J, Ophoff Roel A, Wiedau-Pazos Martina, Lomen-Hoerth Catherine, Van Deerlin Vivianna M, Grosskreutz Julian, Roediger Annekathrin, Gaur Nayana, Jörk Alexander, Barthel Tabea, Theele Erik, Ilse Benjamin, Stubendorff Beatrice, Witte Otto W, Steinbach Robert, Hübner Christian A, Graff Caroline, Brylev Lev, Fominykh Vera, Demeshonok Vera, Ataulina Anastasia, Rogelj Boris, Koritnik Blaž, Zidar Janez, Ravnik-Glavač Metka, Glavač Damjan, Stević Zorica, Drory Vivian E, Povedano Monica, Blair Ian P, Kiernan Matthew C, Benyamin Beben, Henderson Robert D, Furlong Sarah, Mathers Susan, McCombe Pamela A, Needham Merrilee, Ngo Shyuan T, Nicholson Garth A, Pamphlett Roger, Rowe Dominic B, Steyn Frederik J, Williams Kelly L, Mather Karen A, Sachdev Perminder S, Henders Anjali K, Wallace Leanne, de Carvalho Mamede, Pinto Susana, Petri Susanne, Weber Markus, Rouleau Guy A, Silani Vincenzo, Curtis Charles J, Breen Gerome, Glass Jonathan D, Brown Robert H, Landers John E, Shaw Christopher E, Andersen Peter Munch, Groen Ewout J N, van Es Michael A, Pasterkamp R Jeroen, Fan Dongsheng, Garton Fleur C, McRae Allan F, Davey Smith George, Gaunt Tom R, Eberle Michael A, Mill Jonathan, McLaughlin Russell L, Hardiman Orla, Kenna Kevin P, Wray Naomi R, Tsai Ellen, Runz Heiko, Franke Lude, Al-Chalabi Ammar, Van Damme Philip, van den Berg Leonard H, Veldink Jan H
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Zhang K, Arcuti S, Brunetti M, Moglia C, Calvo A, Ratti A, Tiloca C, Gellera C, Pensato V, Mazzini L, Capozzo R, Zecca C, Blair I, Stuit R, Muller B, Filosto M, Padovani A, Riva N, Penco S, Lunetta C, Sorarù G, Bertolin C, Blauw H, Curtis C, Hofman A, Estrada K, Rivadeneira F, Uitterlinden A, Dartigues J, Tzourio C, Amouyel P, van der Kooi A, de Visser M, D'Alfonso S, Comi G, Del Bo R, Cereda C, Pansarasa O, Smith B, Shaw C, Weber M, Goris A, Nöthen M, McCann E, Veldink J, Corcia P, Andersen P, Hardiman O, Landers J, Glass J, Brown R, Pers T, Franke L, Van Damme P, Vourc'h P, Silani V, van den Berg L, Al-Chalabi A, Breen G, Lewis C, Pasterkamp R, van Es M, de Bakker P, Visscher P, Wray N, Robberecht W, Weishaupt J, Stubendorff B, Prell T, Ringer T, Witte O, Grosskreutz J, Kiernan M, Pamphlett R, Rowe D, Nicholson G, Kurth I, Hübner C, Ludolph A, Powell J, Logroscino G, Tortelli R, Pupillo E, Beghi E, Chio A, Casale F, Leigh P, Fifita J, Chandran S, Koritnik B, Ravnik-Glavač M, Vrabec K, Rogelj B, Lin K, Ticozzi N, Vajda A, Menelaou A, Medic J, Zidar J, Leonardis L, Polak M, Rojas-García R, Mora J, Pinto S, de Carvalho M, Meininger V, Salachas F, Millecamps S, Grošelj L, Brands W, Schellevis R, Robinson M, de Jong S, Võsa U, van der Spek R, Pulit S, Diekstra F, McLaughlin R, Dekker A, Shatunov A, Yang J, Fogh I, Harschnitz O, van Eijk K, Kenna K, Jones A, Sproviero W, Blokhuis A, Koppers M, Tazelaar G, van Doormaal P, van Rheenen W, Colville S, Cichon S, Maurel C, Andres C, Radivojkov-Blagojevic M, Lichtner P, Meitinger T, Parman Y, Hamzeiy H, Tunca C, Basak A, Bensimon G, Landwehrmeyer B, Rietschel M, Franke A, Lieb W, Tittmann L, Wood N, Dürr A, Saker-Delye S, Payan C, Brice A, McCluskey L, Elman L, Topp S, Malaspina A, Fratta P, Sidle K, Pittman A, Orrell R, Hardy J, Shaw P, Morrison K, Petri S, Abdulla S, Trojanowski J, Van Deerlin V, Lomen-Hoerth C, Wiedau-Pazos M, Staats K, Ophoff R, Meyer T, Sendtner M, Drepper C, Swingler R. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat Genet 2016; 48:1043-8.
25.07.2016Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
25.07.2016Nat Genet 2016; 48:1043-8
Zhang Katharine, Arcuti Simona, Brunetti Maura, Moglia Cristina, Calvo Andrea, Ratti Antonia, Tiloca Cinzia, Gellera Cinzia, Pensato Viviana, Mazzini Letizia, Capozzo Rosa, Zecca Chiara, Blair Ian, Stuit Robbert Jan, Muller Bernard, Filosto Massimiliano, Padovani Alessandro, Riva Nilo, Penco Silvana, Lunetta Christian, Sorarù Gianni, Bertolin Cinzia, Blauw Hylke M, Curtis Charles, Hofman Albert, Estrada Karol, Rivadeneira Fernando, Uitterlinden André G, Dartigues Jean-François, Tzourio Christophe, Amouyel Philippe, van der Kooi Anneke J, de Visser Marianne, D'Alfonso Sandra, Comi Giacomo P, Del Bo Roberto, Cereda Cristina, Pansarasa Orietta, Smith Bradley N, Shaw Christopher E, Weber Markus, Goris An, Nöthen Markus M, McCann Emily P, Veldink Jan H, Corcia Philippe, Andersen Peter M, Hardiman Orla, Landers John E, Glass Jonathan D, Brown Robert H, Pers Tune H, Franke Lude, Van Damme Philip, Vourc'h Patrick, Silani Vincenzo, van den Berg Leonard H, Al-Chalabi Ammar, Breen Gerome, Lewis Cathryn M, Pasterkamp R Jeroen, van Es Michael A, de Bakker Paul I W, Visscher Peter M, Wray Naomi R, Robberecht Wim, Weishaupt Jochen H, Stubendorff Beatrice, Prell Tino, Ringer Thomas, Witte Otto W, Grosskreutz Julian, Kiernan Matthew C, Pamphlett Roger, Rowe Dominic B, Nicholson Garth A, Kurth Ingo, Hübner Christian A, Ludolph Albert C, Powell John, Logroscino Giancarlo, Tortelli Rosanna, Pupillo Elisabetta, Beghi Ettore, Chio Adriano, Casale Federico, Leigh P Nigel, Fifita Jennifer A, Chandran Siddharthan, Koritnik Blaž, Ravnik-Glavač Metka, Vrabec Katarina, Rogelj Boris, Lin Kuang, Ticozzi Nicola, Vajda Alice, Menelaou Androniki, Medic Jelena, Zidar Janez, Leonardis Lea, Polak Meraida, Rojas-García Ricardo, Mora Jesus S, Pinto Susana, de Carvalho Mamede, Meininger Vincent, Salachas François, Millecamps Stéphanie, Grošelj Leja Dolenc, Brands William J, Schellevis Raymond D, Robinson Matthew R, de Jong Simone, Võsa Urmo, van der Spek Rick A A, Pulit Sara L, Diekstra Frank P, McLaughlin Russell L, Dekker Annelot M, Shatunov Aleksey, Yang Jian, Fogh Isabella, Harschnitz Oliver, van Eijk Kristel R, Kenna Kevin P, Jones Ashley R, Sproviero William, Blokhuis Anna M, Koppers Max, Tazelaar Gijs H P, van Doormaal Perry Tc, van Rheenen Wouter, Colville Shuna, Cichon Sven, Maurel Cindy, Andres Christian R, Radivojkov-Blagojevic Milena, Lichtner Peter, Meitinger Thomas, Parman Yesim, Hamzeiy Hamid, Tunca Ceren, Basak A Nazli, Bensimon Gilbert, Landwehrmeyer Bernhard, Rietschel Marcella, Franke Andre, Lieb Wolfgang, Tittmann Lukas, Wood Nicholas W, Dürr Alexandra, Saker-Delye Safaa, Payan Christine A M, Brice Alexis, McCluskey Leo, Elman Lauren, Topp Simon, Malaspina Andrea, Fratta Pietro, Sidle Katie, Pittman Alan, Orrell Richard W, Hardy John, Shaw Pamela J, Morrison Karen E, Petri Susanne, Abdulla Susanne, Trojanowski John Q, Van Deerlin Vivianna M, Lomen-Hoerth Catherine, Wiedau-Pazos Martina, Staats Kim A, Ophoff Roel A, Meyer Thomas, Sendtner Michael, Drepper Carsten, Swingler Robert
Immunochip analysis identifies association of the RAD50/IL13 region with human longevity
Flachsbart F, Brand S, Peters A, Strauch K, Müller-Nurasyid M, Hoffmann P, Nöthen M, Lieb W, Franke A, Schreiber S, Büning C, Galan P, Derbois C, Ellinghaus D, Gentschew L, Heinsen F, Caliebe A, Christiansen L, Nygaard M, Christensen K, Blanché H, Deleuze J, Nebel A. Immunochip analysis identifies association of the RAD50/IL13 region with human longevity. Aging Cell 2016; 15:585-8.
22.03.2016Immunochip analysis identifies association of the RAD50/IL13 region with human longevity
22.03.2016Aging Cell 2016; 15:585-8
Flachsbart Friederike, Brand Stephan, Peters Anette, Strauch Konstantin, Müller-Nurasyid Martina, Hoffmann Per, Nöthen Markus M, Lieb Wolfgang, Franke Andre, Schreiber Stefan, Büning Carsten, Galan Pilar, Derbois Céline, Ellinghaus David, Gentschew Liljana, Heinsen Femke-Anouska, Caliebe Amke, Christiansen Lene, Nygaard Marianne, Christensen Kaare, Blanché Hélène, Deleuze Jean-François, Nebel Almut
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk
Fischer A, Nöthen M, Herms S, Gieger C, Strauch K, Winkelmann J, Boehm B, Brand S, Büning C, Schürmann M, Ellinghaus E, Baurecht H, Lieb W, Nebel A, Müller-Quernheim J, Franke A, Schreiber S, Homolka J, Sterclova M, Ellinghaus D, Nutsua M, Hofmann S, Montgomery C, Iannuzzi M, Rybicki B, Petrek M, Mrazek F, Pabst S, Grohé C, Grunewald J, Ronninger M, Eklund A, Padyukov L, Mihailovic-Vucinic V, Jovanovic D. Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk. Am J Respir Crit Care Med 2015; 192:727-36.
15.09.2015Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk
15.09.2015Am J Respir Crit Care Med 2015; 192:727-36
Fischer Annegret, Nöthen Markus M, Herms Stefan, Gieger Christian, Strauch Konstantin, Winkelmann Juliane, Boehm Bernhard O, Brand Stephan, Büning Carsten, Schürmann Manfred, Ellinghaus Eva, Baurecht Hansjörg, Lieb Wolfgang, Nebel Almut, Müller-Quernheim Joachim, Franke Andre, Schreiber Stefan, Homolka Jiri, Sterclova Martina, Ellinghaus David, Nutsua Marcel, Hofmann Sylvia, Montgomery Courtney G, Iannuzzi Michael C, Rybicki Benjamin A, Petrek Martin, Mrazek Frantisek, Pabst Stefan, Grohé Christian, Grunewald Johan, Ronninger Marcus, Eklund Anders, Padyukov Leonid, Mihailovic-Vucinic Violeta, Jovanovic Dragana
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells
Li J, Gieger C, Nöthen M, Büning C, Brand S, Sullivan K, Orange J, Fevang B, Schreiber S, Lieb W, Aukrust P, Chapel H, Cunningham-Rundles C, Franke A, Karlsen T, Grimbacher B, Hakonarson H, Hammarström L, Winkelmann J, Nair R, Elder J, Jørgensen S, Maggadottir S, Bakay M, Warnatz K, Glessner J, Pandey R, Salzer U, Schmidt R, Perez E, Resnick E, Goldacker S, Buchta M, Witte T, Padyukov L, Videm V, Folseraas T, Atschekzei F, Ellinghaus E. Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. Nat Commun 2015; 6:6804.
20.04.2015Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells
20.04.2015Nat Commun 2015; 6:6804
Li Jin, Gieger Christian, Nöthen Markus M, Büning Carsten, Brand Stephan, Sullivan Kathleen E, Orange Jordan S, Fevang Børre, Schreiber Stefan, Lieb Wolfgang, Aukrust Pål, Chapel Helen, Cunningham-Rundles Charlotte, Franke Andre, Karlsen Tom H, Grimbacher Bodo, Hakonarson Hakon, Hammarström Lennart, Winkelmann Juliane, Nair Rajan P, Elder James T, Jørgensen Silje F, Maggadottir S Melkorka, Bakay Marina, Warnatz Klaus, Glessner Joseph, Pandey Rahul, Salzer Ulrich, Schmidt Reinhold E, Perez Elena, Resnick Elena, Goldacker Sigune, Buchta Mary, Witte Torsten, Padyukov Leonid, Videm Vibeke, Folseraas Trine, Atschekzei Faranaz, Ellinghaus Eva
Genetic studies of body mass index yield new insights for obesity biology
Croteau-Chonka D, Bakker S, Esko T, Beilby J, Fall T, Bergman R, Ferreira T, Blangero J, Gustafsson S, Bovet P, Kutalik Z, Campbell H, Luan J, Caulfield M, Mägi R, Cesana G, Randall J, Chakravarti A, Chasman D, Wood A, Chines P, Collins F, Crawford D, Cupples L, Cusi D, Danesh J, de Faire U, den Ruijter H, Dominiczak A, Erbel R, Erdmann J, Eriksson J, Farrall M, Felix S, Ferrannini E, Ferrieres J, Ford I, Forouhi N, Forrester T, Deng G, Franco O, Ehret G, Gansevoort R, Feenstra B, Gejman P, Feitosa M, Gieger C, Fischer K, Gottesman O, Goel A, Gudnason V, Gong J, Gyllensten U, Jackson A, Hall A, Kanoni S, Harris T, Kleber M, Hattersley A, Kristiansson K, Hicks A, Lim U, Hindorff L, Lotay V, Hingorani A, Mangino M, Hofman A, Leach I, Homuth G, Medina-Gomez C, Hovingh G, Medland S, Humphries S, Nalls M, Hunt S, Palmer C, Hyppönen E, Pasko D, Illig T, Pechlivanis S, Jacobs K, Peters M, Jarvelin M, Prokopenko I, Jöckel K, Shungin D, Johansen B, Stančáková A, Jousilahti P, Strawbridge R, Jukema J, Sung Y, Jula A, Tanaka T, Kaprio J, Teumer A, Kastelein J, Trompet S, Keinanen-Kiukaanniemi S, van der Laan S, Kiemeney L, van Setten J, Knekt P, van Vliet-Ostaptchouk J, Kooner J, Wang Z, Kooperberg C, Yengo L, Kovacs P, Zhang W, Kraja A, Isaacs A, Kumari M, Albrecht E, Kuusisto J, Arnlöv J, Lakka T, Arscott G, Langenberg C, Attwood A, Marchand L, Bandinelli S, Lehtimäki T, Barrett A, Lyssenko V, Bas I, Männistö S, Bellis C, Marette A, Bennett A, Matise T, Berne C, McKenzie C, Blagieva R, McKnight B, Blüher M, Moll F, Böhringer S, Morris A, Bonnycastle L, Morris A, Böttcher Y, Murray J, Boyd H, Nelis M, Bruinenberg M, Ohlsson C, Caspersen I, Oldehinkel A, Chen Y, Ong K, Clarke R, Madden P, Daw E, Pasterkamp G, de Craen A, Peden J, Delgado G, Peters A, Dimitriou M, Postma D, Doney A, Pramstaller P, Eklund N, Price J, Estrada K, Qi L, Eury E, Raitakari O, Folkersen L, Rankinen T, Fraser R, Rao D, Garcia M, Rice T, Geller F, Ridker P, Giedraitis V, Rioux J, Gigante B, Ritchie M, Go A, Rudan I, Golay A, Salomaa V, Goodall A, Samani N, Gordon S, Saramies J, Gorski M, Sarzynski M, Grabe H, Schunkert H, Grallert H, Schwarz P, Grammer T, Sever P, Gräßler J, Shuldiner A, Grönberg H, Sinisalo J, Groves C, Stolk R, Gusto G, Strauch K, Haessler J, Tönjes A, Hall P, Trégouët D, Haller T, Tremblay A, Hallmans G, Tremoli E, Hartman C, Virtamo J, Hassinen M, Vohl M, Hayward C, Völker U, Heard-Costa N, Waeber G, Helmer Q, Willemsen G, Hengstenberg C, Witteman J, Holmen O, Zillikens M, Hottenga J, Adair L, James A, Amouyel P, Jeff J, Asselbergs F, Johansson Å, Assimes T, Jolley J, Bochud M, Juliusdottir T, Boehm B, Kinnunen L, Boerwinkle E, Koenig W, Bornstein S, Koskenvuo M, Bottinger E, Kratzer W, Bouchard C, Laitinen J, Cauchi S, Lamina C, Chambers J, Leander K, Chanock S, Lee N, Cooper R, Lichtner P, de Bakker P, Lind L, Dedoussis G, Lindström J, Ferrucci L, Lo K, Franks P, Lobbens S, Froguel P, Lorbeer R, Groop L, Lu Y, Haiman C, Mach F, Hamsten A, Magnusson P, Hui J, Mahajan A, Hunter D, McArdle W, Hveem K, McLachlan S, Kaplan R, Menni C, Kivimäki M, Merger S, Kuh D, Mihailov E, Laakso M, Milani L, Liu Y, Moayyeri A, Martin N, Monda K, März W, Morken M, Melbye M, Mulas A, Metspalu A, Müller G, Moebus S, Müller-Nurasyid M, Munroe P, Musk A, Njølstad I, Nagaraja R, Oostra B, Nöthen M, Palmer C, Nolte I, Pedersen N, Pilz S, Perola M, Rayner N, Pérusse L, Renström F, Peters U, Rettig R, Power C, Ried J, Quertermous T, Ripke S, Rauramaa R, Robertson N, Rivadeneira F, Rose L, Saaristo T, Sanna S, Saleheen D, Scharnagl H, Sattar N, Scholtens S, Schadt E, Schumacher F, Schlessinger D, Scott W, Slagboom P, Seufferlein T, Snieder H, Shi J, Spector T, Smith A, Thorsteinsdottir U, Smolonska J, Stumvoll M, Stanton A, Tuomilehto J, Steinthorsdottir V, Uitterlinden A, Stirrups K, Uusitupa M, Stringham H, van der Harst P, Sundstrom J, Walker M, Swertz M, Wallaschofski H, Swift A, Wareham N, Syvänen A, Watkins H, Tan S, Weir D, Tayo B, Wichmann H, Thorand B, Wilson J, Thorleifsson G, Zanen P, Tyrer J, Borecki I, Uh H, Deloukas P, Vandenput L, Fox C, Verhulst F, Heid I, Vermeulen S, O'Connell J, Verweij N, Strachan D, Vonk J, Stefansson K, Waite L, van Duijn C, Warren H, Abecasis G, Waterworth D, Franke L, Weedon M, Frayling T, Wilkens L, McCarthy M, Willenborg C, Visscher P, Wilsgaard T, Scherag A, Wojczynski M, Willer C, Wong A, Boehnke M, Wright A, Mohlke K, Zhang Q, Lindgren C, Beckmann J, Brennan E, Barroso I, Choi M, North K, Dastani Z, Ingelsson E, Drong A, Hirschhorn J, Eriksson P, Loos R, Franco-Cereceda A, Speliotes E, Gådin J, Gharavi A, Goddard M, Handsaker R, Huang J, Karpe F, Kathiresan S, Keildson S, Kiryluk K, Kubo M, Lee J, Liang L, Lifton R, Ma B, McCarroll S, McKnight A, Min J, Moffatt M, Montgomery G, Murabito J, Nicholson G, Nyholt D, Okada Y, Perry J, Dorajoo R, Reinmaa E, Salem R, Sandholm N, Scott R, Locke A, Stolk L, Kahali B, Takahashi A, Berndt S, Tanaka T, Justice A, van 't Hooft F, Pers T, Vinkhuyzen A, Day F, Westra H, Powell C, Zheng W, Vedantam S, Zondervan K, Buchkovich M, Heath A, Yang J, Arveiler D, Winkler T, Absher D, Amin N, Anderson D, Beekman M, Bolton J, Bragg-Gresham J, Buyske S, Demirkan A, Schmidt E, Karjalainen J, Workalemahu T, Faul J, Smith J, Zhao J, Zhao W, Chen J, Fehrmann R, Hedman Å. Genetic studies of body mass index yield new insights for obesity biology. Nature 2015; 518:197-206.
12.02.2015Genetic studies of body mass index yield new insights for obesity biology
12.02.2015Nature 2015; 518:197-206
Croteau-Chonka Damien C, Bakker Stephan J L, Esko Tõnu, Beilby John, Fall Tove, Bergman Richard N, Ferreira Teresa, Blangero John, Gustafsson Stefan, Bovet Pascal, Kutalik Zoltán, Campbell Harry, Luan Jian'an, Caulfield Mark J, Mägi Reedik, Cesana Giancarlo, Randall Joshua C, Chakravarti Aravinda, Chasman Daniel I, Wood Andrew R, Chines Peter S, Collins Francis S, Crawford Dana C, Cupples L Adrienne, Cusi Daniele, Danesh John, de Faire Ulf, den Ruijter Hester M, Dominiczak Anna F, Erbel Raimund, Erdmann Jeanette, Eriksson Johan G, Farrall Martin, Felix Stephan B, Ferrannini Ele, Ferrieres Jean, Ford Ian, Forouhi Nita G, Forrester Terrence, Deng Guohong, Franco Oscar H, Ehret Georg B, Gansevoort Ron T, Feenstra Bjarke, Gejman Pablo V, Feitosa Mary F, Gieger Christian, Fischer Krista, Gottesman Omri, Goel Anuj, Gudnason Vilmundur, Gong Jian, Gyllensten Ulf, Jackson Anne U, Hall Alistair S, Kanoni Stavroula, Harris Tamara B, Kleber Marcus E, Hattersley Andrew T, Kristiansson Kati, Hicks Andrew A, Lim Unhee, Hindorff Lucia A, Lotay Vaneet, Hingorani Aroon D, Mangino Massimo, Hofman Albert, Leach Irene Mateo, Homuth Georg, Medina-Gomez Carolina, Hovingh G Kees, Medland Sarah E, Humphries Steve E, Nalls Michael A, Hunt Steven C, Palmer Cameron D, Hyppönen Elina, Pasko Dorota, Illig Thomas, Pechlivanis Sonali, Jacobs Kevin B, Peters Marjolein J, Jarvelin Marjo-Riitta, Prokopenko Inga, Jöckel Karl-Heinz, Shungin Dmitry, Johansen Berit, Stančáková Alena, Jousilahti Pekka, Strawbridge Rona J, Jukema J Wouter, Sung Yun Ju, Jula Antti M, Tanaka Toshiko, Kaprio Jaakko, Teumer Alexander, Kastelein John J P, Trompet Stella, Keinanen-Kiukaanniemi Sirkka M, van der Laan Sander W, Kiemeney Lambertus A, van Setten Jessica, Knekt Paul, van Vliet-Ostaptchouk Jana V, Kooner Jaspal S, Wang Zhaoming, Kooperberg Charles, Yengo Loic, Kovacs Peter, Zhang Weihua, Kraja Aldi T, Isaacs Aaron, Kumari Meena, Albrecht Eva, Kuusisto Johanna, Arnlöv Johan, Lakka Timo A, Arscott Gillian M, Langenberg Claudia, Attwood Antony P, Marchand Loic Le, Bandinelli Stefania, Lehtimäki Terho, Barrett Amy, Lyssenko Valeriya, Bas Isabelita N, Männistö Satu, Bellis Claire, Marette André, Bennett Amanda J, Matise Tara C, Berne Christian, McKenzie Colin A, Blagieva Roza, McKnight Barbara, Blüher Matthias, Moll Frans L, Böhringer Stefan, Morris Andrew D, Bonnycastle Lori L, Morris Andrew P, Böttcher Yvonne, Murray Jeffrey C, Boyd Heather A, Nelis Mari, Bruinenberg Marcel, Ohlsson Claes, Caspersen Ida H, Oldehinkel Albertine J, Chen Yii-Der Ida, Ong Ken K, Clarke Robert, Madden Pamela A F, Daw E Warwick, Pasterkamp Gerard, de Craen Anton J M, Peden John F, Delgado Graciela, Peters Annette, Dimitriou Maria, Postma Dirkje S, Doney Alex S F, Pramstaller Peter P, Eklund Niina, Price Jackie F, Estrada Karol, Qi Lu, Eury Elodie, Raitakari Olli T, Folkersen Lasse, Rankinen Tuomo, Fraser Ross M, Rao D C, Garcia Melissa E, Rice Treva K, Geller Frank, Ridker Paul M, Giedraitis Vilmantas, Rioux John D, Gigante Bruna, Ritchie Marylyn D, Go Alan S, Rudan Igor, Golay Alain, Salomaa Veikko, Goodall Alison H, Samani Nilesh J, Gordon Scott D, Saramies Jouko, Gorski Mathias, Sarzynski Mark A, Grabe Hans-Jörgen, Schunkert Heribert, Grallert Harald, Schwarz Peter E H, Grammer Tanja B, Sever Peter, Gräßler Jürgen, Shuldiner Alan R, Grönberg Henrik, Sinisalo Juha, Groves Christopher J, Stolk Ronald P, Gusto Gaëlle, Strauch Konstantin, Haessler Jeffrey, Tönjes Anke, Hall Per, Trégouët David-Alexandre, Haller Toomas, Tremblay Angelo, Hallmans Göran, Tremoli Elena, Hartman Catharina A, Virtamo Jarmo, Hassinen Maija, Vohl Marie-Claude, Hayward Caroline, Völker Uwe, Heard-Costa Nancy L, Waeber Gerard, Helmer Quinta, Willemsen Gonneke, Hengstenberg Christian, Witteman Jacqueline C, Holmen Oddgeir, Zillikens M Carola, Hottenga Jouke-Jan, Adair Linda S, James Alan L, Amouyel Philippe, Jeff Janina M, Asselbergs Folkert W, Johansson Åsa, Assimes Themistocles L, Jolley Jennifer, Bochud Murielle, Juliusdottir Thorhildur, Boehm Bernhard O, Kinnunen Leena, Boerwinkle Eric, Koenig Wolfgang, Bornstein Stefan R, Koskenvuo Markku, Bottinger Erwin P, Kratzer Wolfgang, Bouchard Claude, Laitinen Jaana, Cauchi Stéphane, Lamina Claudia, Chambers John C, Leander Karin, Chanock Stephen J, Lee Nanette R, Cooper Richard S, Lichtner Peter, de Bakker Paul I W, Lind Lars, Dedoussis George, Lindström Jaana, Ferrucci Luigi, Lo Ken Sin, Franks Paul W, Lobbens Stephane, Froguel Philippe, Lorbeer Roberto, Groop Leif C, Lu Yingchang, Haiman Christopher A, Mach François, Hamsten Anders, Magnusson Patrik K E, Hui Jennie, Mahajan Anubha, Hunter David J, McArdle Wendy L, Hveem Kristian, McLachlan Stela, Kaplan Robert C, Menni Cristina, Kivimäki Mika, Merger Sigrun, Kuh Diana, Mihailov Evelin, Laakso Markku, Milani Lili, Liu Yongmei, Moayyeri Alireza, Martin Nicholas G, Monda Keri L, März Winfried, Morken Mario A, Melbye Mads, Mulas Antonella, Metspalu Andres, Müller Gabriele, Moebus Susanne, Müller-Nurasyid Martina, Munroe Patricia B, Musk Arthur W, Njølstad Inger, Nagaraja Ramaiah, Oostra Ben A, Nöthen Markus M, Palmer Colin N A, Nolte Ilja M, Pedersen Nancy L, Pilz Stefan, Perola Markus, Rayner Nigel W, Pérusse Louis, Renström Frida, Peters Ulrike, Rettig Rainer, Power Chris, Ried Janina S, Quertermous Thomas, Ripke Stephan, Rauramaa Rainer, Robertson Neil R, Rivadeneira Fernando, Rose Lynda M, Saaristo Timo E, Sanna Serena, Saleheen Danish, Scharnagl Hubert, Sattar Naveed, Scholtens Salome, Schadt Eric E, Schumacher Fredrick R, Schlessinger David, Scott William R, Slagboom P Eline, Seufferlein Thomas, Snieder Harold, Shi Jianxin, Spector Tim D, Smith Albert Vernon, Thorsteinsdottir Unnur, Smolonska Joanna, Stumvoll Michael, Stanton Alice V, Tuomilehto Jaakko, Steinthorsdottir Valgerdur, Uitterlinden André G, Stirrups Kathleen, Uusitupa Matti, Stringham Heather M, van der Harst Pim, Sundstrom Johan, Walker Mark, Swertz Morris A, Wallaschofski Henri, Swift Amy J, Wareham Nicholas J, Syvänen Ann-Christine, Watkins Hugh, Tan Sian-Tsung, Weir David R, Tayo Bamidele O, Wichmann H-Erich, Thorand Barbara, Wilson James F, Thorleifsson Gudmar, Zanen Pieter, Tyrer Jonathan P, Borecki Ingrid B, Uh Hae-Won, Deloukas Panos, Vandenput Liesbeth, Fox Caroline S, Verhulst Frank C, Heid Iris M, Vermeulen Sita H, O'Connell Jeffrey R, Verweij Niek, Strachan David P, Vonk Judith M, Stefansson Kari, Waite Lindsay L, van Duijn Cornelia M, Warren Helen R, Abecasis Gonçalo R, Waterworth Dawn, Franke Lude, Weedon Michael N, Frayling Timothy M, Wilkens Lynne R, McCarthy Mark I, Willenborg Christina, Visscher Peter M, Wilsgaard Tom, Scherag André, Wojczynski Mary K, Willer Cristen J, Wong Andrew, Boehnke Michael, Wright Alan F, Mohlke Karen L, Zhang Qunyuan, Lindgren Cecilia M, Beckmann Jacques S, Brennan Eoin P, Barroso Inês, Choi Murim, North Kari E, Dastani Zari, Ingelsson Erik, Drong Alexander W, Hirschhorn Joel N, Eriksson Per, Loos Ruth J F, Franco-Cereceda Anders, Speliotes Elizabeth K, Gådin Jesper R, Gharavi Ali G, Goddard Michael E, Handsaker Robert E, Huang Jinyan, Karpe Fredrik, Kathiresan Sekar, Keildson Sarah, Kiryluk Krzysztof, Kubo Michiaki, Lee Jong-Young, Liang Liming, Lifton Richard P, Ma Baoshan, McCarroll Steven A, McKnight Amy J, Min Josine L, Moffatt Miriam F, Montgomery Grant W, Murabito Joanne M, Nicholson George, Nyholt Dale R, Okada Yukinori, Perry John R B, Dorajoo Rajkumar, Reinmaa Eva, Salem Rany M, Sandholm Niina, Scott Robert A, Locke Adam E, Stolk Lisette, Kahali Bratati, Takahashi Atsushi, Berndt Sonja I, Tanaka Toshihiro, Justice Anne E, van 't Hooft Ferdinand M, Pers Tune H, Vinkhuyzen Anna A E, Day Felix R, Westra Harm-Jan, Powell Corey, Zheng Wei, Vedantam Sailaja, Zondervan Krina T, Buchkovich Martin L, Heath Andrew C, Yang Jian, Arveiler Dominique, Winkler Thomas W, Absher Devin, Amin Najaf, Anderson Denise, Beekman Marian, Bolton Jennifer L, Bragg-Gresham Jennifer L, Buyske Steven, Demirkan Ayse, Schmidt Ellen M, Karjalainen Juha, Workalemahu Tsegaselassie, Faul Jessica D, Smith Jennifer A, Zhao Jing Hua, Zhao Wei, Chen Jin, Fehrmann Rudolf, Hedman Åsa K
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms
Baurecht H, Mrowietz U, Nair R, Nöthen M, Novak N, O'Regan G, Schreiber S, Smith C, Strauch K, Stuart P, Trembath R, Tsoi L, Weichenthal M, Barker J, Elder J, Weidinger S, Cordell H, Morris D, McLean W, Marenholz I, Hotze M, Brand S, Büning C, Cormican P, Corvin A, Ellinghaus D, Ellinghaus E, Esparza-Gordillo J, Fölster-Holst R, Franke A, Gieger C, Hübner N, Illig T, Irvine A, Kabesch M, Lee Y, Lieb W, Brown S. Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. Am J Hum Genet 2015; 96:104-20.
08.01.2015Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms
08.01.2015Am J Hum Genet 2015; 96:104-20
Baurecht Hansjörg, Mrowietz Ulrich, Nair Rajan, Nöthen Markus M, Novak Natalija, O'Regan Grainne M, Schreiber Stefan, Smith Catherine, Strauch Konstantin, Stuart Philip E, Trembath Richard, Tsoi Lam C, Weichenthal Michael, Barker Jonathan, Elder James T, Weidinger Stephan, Cordell Heather J, Morris Derek W, McLean W H Irwin, Marenholz Ingo, Hotze Melanie, Brand Stephan, Büning Carsten, Cormican Paul, Corvin Aiden, Ellinghaus David, Ellinghaus Eva, Esparza-Gordillo Jorge, Fölster-Holst Regina, Franke Andre, Gieger Christian, Hübner Norbert, Illig Thomas, Irvine Alan D, Kabesch Michael, Lee Young A E, Lieb Wolfgang, Brown Sara J
Defining the role of common variation in the genomic and biological architecture of adult human height
Jousilahti P, Lakka T, Langenberg C, Le Marchand L, Lehtimäki T, Lupoli S, Madden P, Männistö S, Manunta P, Marette A, Matise T, McKnight B, Kuusisto J, Kumari M, Kraja A, Jula A, Kaprio J, Kastelein J, Kayser M, Kee F, Keinanen-Kiukaanniemi S, Kiemeney L, Kooner J, Kooperberg C, Koskinen S, Kovacs P, Meitinger T, Moll F, Montgomery G, Rankinen T, Rao D, Rice T, Ritchie M, Rudan I, Salomaa V, Samani N, Saramies J, Sarzynski M, Schwarz P, Sebert S, Raitakari O, Qi L, Price J, Morris A, Morris A, Murray J, Nelis M, Ohlsson C, Oldehinkel A, Ong K, Ouwehand W, Pasterkamp G, Peters A, Pramstaller P, Sever P, Jarvelin M, Wright A, Caulfield M, Chakravarti A, Collins R, Collins F, Crawford D, Cupples L, Danesh J, de Faire U, den Ruijter H, Erbel R, Erdmann J, Campbell H, Brown M, Brambilla P, Zhang Q, Arveiler D, Bakker S, Beilby J, Bergman R, Bergmann S, Biffar R, Blangero J, Boomsma D, Bornstein S, Bovet P, Eriksson J, Farrall M, Ferrannini E, Hattersley A, Heath A, Hengstenberg C, Hicks A, Hindorff L, Hingorani A, Hofman A, Hovingh G, Humphries S, Hunt S, Hyppönen E, Harris T, Hall A, Haas D, Ferrieres J, Ford I, Forouhi N, Forrester T, Gansevoort R, Gejman P, Gieger C, Golay A, Gottesman O, Gudnason V, Gyllensten U, Jacobs K, Shuldiner A, Reinmaa E, Völzke H, Walker M, Wareham N, Watkins H, Wichmann H, Wilson J, Zanen P, Deloukas P, Heid I, Lindgren C, Mohlke K, van der Harst P, Uusitupa M, Tuomilehto J, Ridker P, Rivadeneira F, Rotter J, Saaristo T, Saleheen D, Schlessinger D, Slagboom P, Snieder H, Spector T, Strauch K, Stumvoll M, Speliotes E, Thorsteinsdottir U, Barroso I, Price A, Lettre G, Loos R, Weedon M, Ingelsson E, O'Connell J, Abecasis G, Chasman D, Goddard M, Visscher P, Hirschhorn J, Willer C, Franke L, van Duijn C, Fox C, North K, Strachan D, Beckmann J, Berndt S, Boehnke M, Borecki I, McCarthy M, Metspalu A, Stefansson K, Uitterlinden A, Frayling T, Rauramaa R, Sinisalo J, Boerwinkle E, Bottinger E, Bouchard C, Cauchi S, Chambers J, Chanock S, Cooper R, de Bakker P, Dedoussis G, Ferrucci L, Franks P, Boehm B, Bochud M, Assimes T, Steinthorsdottir V, Stolk R, Tardif J, Tönjes A, Tremblay A, Tremoli E, Virtamo J, Vohl M, Amouyel P, Asselbergs F, Froguel P, Groop L, Haiman C, Moebus S, Munroe P, Njølstad I, Oostra B, Palmer C, Pedersen N, Perola M, Pérusse L, Peters U, Powell J, Power C, Melbye M, März W, Martin N, Hamsten A, Hayes M, Hui J, Hunter D, Hveem K, Jukema J, Kaplan R, Kivimäki M, Kuh D, Laakso M, Liu Y, Quertermous T, Nyholt D, van Setten J, van Vliet-Ostaptchouk J, Wang Z, Yengo L, Zhang W, Afzal U, Arnlöv J, Arscott G, Bandinelli S, Barrett A, Bellis C, van der Laan S, Trompet S, Teumer A, Palmer C, Pasko D, Pechlivanis S, Prokopenko I, Ried J, Ripke S, Shungin D, Stančáková A, Strawbridge R, Sung Y, Tanaka T, Bennett A, Berne C, Blüher M, Delgado G, Denny J, Dhonukshe-Rutten R, Dimitriou M, Doney A, Dörr M, Eklund N, Eury E, Folkersen L, Garcia M, Geller F, Deelen J, De Jong P, Daw E, Bolton J, Böttcher Y, Boyd H, Bruinenberg M, Buckley B, Buyske S, Caspersen I, Chines P, Clarke R, Claudi-Boehm S, Cooper M, Giedraitis V, Nalls M, Wood A, Fall T, Fehrmann R, Ferreira T, Jackson A, Karjalainen J, Lo K, Locke A, Mägi R, Mihailov E, Porcu E, Randall J, Duan Y, Day F, Croteau-Chonka D, Esko T, Yang J, Vedantam S, Pers T, Gustafsson S, Chu A, Estrada K, Luan J, Kutalik Z, Amin N, Buchkovich M, Scherag A, Vinkhuyzen A, Westra H, Goel A, Gong J, Justice A, Kanoni S, Kleber M, Kristiansson K, Lim U, Lotay V, Lui J, Mangino M, Mateo Leach I, Fraser R, Fischer K, Feitosa M, Winkler T, Workalemahu T, Zhao J, Absher D, Albrecht E, Anderson D, Baron J, Beekman M, Demirkan A, Ehret G, Feenstra B, Medina-Gomez C, Go A, Monda K, Roussel R, Sanna S, Scharnagl H, Scholtens S, Schumacher F, Schunkert H, Scott R, Sehmi J, Seufferlein T, Shi J, Silventoinen K, Rose L, Robertson N, Renström F, Morken M, Müller G, Müller-Nurasyid M, Musk A, Narisu N, Nauck M, Nolte I, Nöthen M, Oozageer L, Pilz S, Rayner N, Smit J, Smith A, Smolonska J, van Oort F, Vermeulen S, Verweij N, Vonk J, Waite L, Waldenberger M, Wennauer R, Wilkens L, Willenborg C, Wilsgaard T, Wojczynski M, van Heemst D, van der Velde N, van Schoor N, Stanton A, Stirrups K, Stott D, Stringham H, Sundstrom J, Swertz M, Syvänen A, Tayo B, Thorleifsson G, Tyrer J, van Dijk S, Wong A, Moayyeri A, Grallert H, Helmer Q, Hemani G, Henders A, Hillege H, Hlatky M, Hoffmann W, Hoffmann P, Holmen O, Houwing-Duistermaat J, Illig T, Isaacs A, Heard-Costa N, Hayward C, Hassinen M, Grammer T, Gräßler J, Grönberg H, de Groot L, Groves C, Haessler J, Hall P, Haller T, Hallmans G, Hannemann A, Hartman C, James A, Jeff J, Johansen B, Lu Y, Lyssenko V, Magnusson P, Mahajan A, Maillard M, McArdle W, McKenzie C, McLachlan S, McLaren P, Menni C, Merger S, Lorentzon M, Lobbens S, Lindström J, Johansson Å, Jolley J, Juliusdottir T, Junttila J, Kho A, Kinnunen L, Klopp N, Kocher T, Kratzer W, Lichtner P, Lind L, Milani L. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet 2014; 46:1173-86.
05.10.2014Defining the role of common variation in the genomic and biological architecture of adult human height
05.10.2014Nat Genet 2014; 46:1173-86
Jousilahti Pekka, Lakka Timo A, Langenberg Claudia, Le Marchand Loic, Lehtimäki Terho, Lupoli Sara, Madden Pamela A F, Männistö Satu, Manunta Paolo, Marette André, Matise Tara C, McKnight Barbara, Kuusisto Johanna, Kumari Meena, Kraja Aldi T, Jula Antti M, Kaprio Jaakko, Kastelein John J P, Kayser Manfred, Kee Frank, Keinanen-Kiukaanniemi Sirkka M, Kiemeney Lambertus A, Kooner Jaspal S, Kooperberg Charles, Koskinen Seppo, Kovacs Peter, Meitinger Thomas, Moll Frans L, Montgomery Grant W, Rankinen Tuomo, Rao D C, Rice Treva K, Ritchie Marylyn, Rudan Igor, Salomaa Veikko, Samani Nilesh J, Saramies Jouko, Sarzynski Mark A, Schwarz Peter E H, Sebert Sylvain, Raitakari Olli T, Qi Lu, Price Jackie F, Morris Andrew D, Morris Andrew P, Murray Jeffrey C, Nelis Mari, Ohlsson Claes, Oldehinkel Albertine J, Ong Ken K, Ouwehand Willem H, Pasterkamp Gerard, Peters Annette, Pramstaller Peter P, Sever Peter, Jarvelin Marjo-Riitta, Wright Alan F, Caulfield Mark J, Chakravarti Aravinda, Collins Rory, Collins Francis S, Crawford Dana C, Cupples L Adrienne, Danesh John, de Faire Ulf, den Ruijter Hester M, Erbel Raimund, Erdmann Jeanette, Campbell Harry, Brown Morris J, Brambilla Paolo, Zhang Qunyuan, Arveiler Dominique, Bakker Stephan J L, Beilby John, Bergman Richard N, Bergmann Sven, Biffar Reiner, Blangero John, Boomsma Dorret I, Bornstein Stefan R, Bovet Pascal, Eriksson Johan G, Farrall Martin, Ferrannini Ele, Hattersley Andrew T, Heath Andrew C, Hengstenberg Christian, Hicks Andrew A, Hindorff Lucia A, Hingorani Aroon D, Hofman Albert, Hovingh G Kees, Humphries Steve E, Hunt Steven C, Hyppönen Elina, Harris Tamara B, Hall Alistair S, Haas David W, Ferrieres Jean, Ford Ian, Forouhi Nita G, Forrester Terrence, Gansevoort Ron T, Gejman Pablo V, Gieger Christian, Golay Alain, Gottesman Omri, Gudnason Vilmundur, Gyllensten Ulf, Jacobs Kevin B, Shuldiner Alan R, Reinmaa Eva, Völzke Henry, Walker Mark, Wareham Nicholas J, Watkins Hugh, Wichmann H-Erich, Wilson James F, Zanen Pieter, Deloukas Panos, Heid Iris M, Lindgren Cecilia M, Mohlke Karen L, van der Harst Pim, Uusitupa Matti, Tuomilehto Jaakko, Ridker Paul M, Rivadeneira Fernando, Rotter Jerome I, Saaristo Timo E, Saleheen Danish, Schlessinger David, Slagboom P Eline, Snieder Harold, Spector Tim D, Strauch Konstantin, Stumvoll Michael, Speliotes Elizabeth K, Thorsteinsdottir Unnur, Barroso Inês, Price Alkes L, Lettre Guillaume, Loos Ruth J F, Weedon Michael N, Ingelsson Erik, O'Connell Jeffrey R, Abecasis Gonçalo R, Chasman Daniel I, Goddard Michael E, Visscher Peter M, Hirschhorn Joel N, Willer Cristen J, Franke Lude, van Duijn Cornelia M, Fox Caroline S, North Kari E, Strachan David P, Beckmann Jacques S, Berndt Sonja I, Boehnke Michael, Borecki Ingrid B, McCarthy Mark I, Metspalu Andres, Stefansson Kari, Uitterlinden André G, Frayling Timothy M, Rauramaa Rainer, Sinisalo Juha, Boerwinkle Eric, Bottinger Erwin P, Bouchard Claude, Cauchi Stéphane, Chambers John C, Chanock Stephen J, Cooper Richard S, de Bakker Paul I W, Dedoussis George, Ferrucci Luigi, Franks Paul W, Boehm Bernhard O, Bochud Murielle, Assimes Themistocles L, Steinthorsdottir Valgerdur, Stolk Ronald P, Tardif Jean-Claude, Tönjes Anke, Tremblay Angelo, Tremoli Elena, Virtamo Jarmo, Vohl Marie-Claude, Amouyel Philippe, Asselbergs Folkert W, Froguel Philippe, Groop Leif C, Haiman Christopher A, Moebus Susanne, Munroe Patricia B, Njølstad Inger, Oostra Ben A, Palmer Colin N A, Pedersen Nancy L, Perola Markus, Pérusse Louis, Peters Ulrike, Powell Joseph E, Power Chris, Melbye Mads, März Winfried, Martin Nicholas G, Hamsten Anders, Hayes M Geoffrey, Hui Jennie, Hunter David J, Hveem Kristian, Jukema J Wouter, Kaplan Robert C, Kivimäki Mika, Kuh Diana, Laakso Markku, Liu Yongmei, Quertermous Thomas, Nyholt Dale R, van Setten Jessica, van Vliet-Ostaptchouk Jana V, Wang Zhaoming, Yengo Loic, Zhang Weihua, Afzal Uzma, Arnlöv Johan, Arscott Gillian M, Bandinelli Stefania, Barrett Amy, Bellis Claire, van der Laan Sander W, Trompet Stella, Teumer Alexander, Palmer Cameron D, Pasko Dorota, Pechlivanis Sonali, Prokopenko Inga, Ried Janina S, Ripke Stephan, Shungin Dmitry, Stančáková Alena, Strawbridge Rona J, Sung Yun Ju, Tanaka Toshiko, Bennett Amanda J, Berne Christian, Blüher Matthias, Delgado Graciela, Denny Josh C, Dhonukshe-Rutten Rosalie, Dimitriou Maria, Doney Alex S F, Dörr Marcus, Eklund Niina, Eury Elodie, Folkersen Lasse, Garcia Melissa E, Geller Frank, Deelen Joris, De Jong Pim A, Daw E Warwick, Bolton Jennifer L, Böttcher Yvonne, Boyd Heather A, Bruinenberg Marcel, Buckley Brendan M, Buyske Steven, Caspersen Ida H, Chines Peter S, Clarke Robert, Claudi-Boehm Simone, Cooper Matthew, Giedraitis Vilmantas, Nalls Michael A, Wood Andrew R, Fall Tove, Fehrmann Rudolf, Ferreira Teresa, Jackson Anne U, Karjalainen Juha, Lo Ken Sin, Locke Adam E, Mägi Reedik, Mihailov Evelin, Porcu Eleonora, Randall Joshua C, Duan Yanan, Day Felix R, Croteau-Chonka Damien C, Esko Tõnu, Yang Jian, Vedantam Sailaja, Pers Tune H, Gustafsson Stefan, Chu Audrey Y, Estrada Karol, Luan Jian'an, Kutalik Zoltán, Amin Najaf, Buchkovich Martin L, Scherag André, Vinkhuyzen Anna A E, Westra Harm-Jan, Goel Anuj, Gong Jian, Justice Anne E, Kanoni Stavroula, Kleber Marcus E, Kristiansson Kati, Lim Unhee, Lotay Vaneet, Lui Julian C, Mangino Massimo, Mateo Leach Irene, Fraser Ross M, Fischer Krista, Feitosa Mary F, Winkler Thomas W, Workalemahu Tsegaselassie, Zhao Jing Hua, Absher Devin, Albrecht Eva, Anderson Denise, Baron Jeffrey, Beekman Marian, Demirkan Ayse, Ehret Georg B, Feenstra Bjarke, Medina-Gomez Carolina, Go Alan S, Monda Keri L, Roussel Ronan, Sanna Serena, Scharnagl Hubert, Scholtens Salome, Schumacher Fredrick R, Schunkert Heribert, Scott Robert A, Sehmi Joban, Seufferlein Thomas, Shi Jianxin, Silventoinen Karri, Rose Lynda M, Robertson Neil R, Renström Frida, Morken Mario A, Müller Gabriele, Müller-Nurasyid Martina, Musk Arthur W, Narisu Narisu, Nauck Matthias, Nolte Ilja M, Nöthen Markus M, Oozageer Laticia, Pilz Stefan, Rayner Nigel W, Smit Johannes H, Smith Albert Vernon, Smolonska Joanna, van Oort Floor V A, Vermeulen Sita H, Verweij Niek, Vonk Judith M, Waite Lindsay L, Waldenberger Melanie, Wennauer Roman, Wilkens Lynne R, Willenborg Christina, Wilsgaard Tom, Wojczynski Mary K, van Heemst Diana, van der Velde Nathalie, van Schoor Natasja M, Stanton Alice V, Stirrups Kathleen, Stott David J, Stringham Heather M, Sundstrom Johan, Swertz Morris A, Syvänen Ann-Christine, Tayo Bamidele O, Thorleifsson Gudmar, Tyrer Jonathan P, van Dijk Suzanne, Wong Andrew, Moayyeri Alireza, Grallert Harald, Helmer Quinta, Hemani Gibran, Henders Anjali K, Hillege Hans L, Hlatky Mark A, Hoffmann Wolfgang, Hoffmann Per, Holmen Oddgeir, Houwing-Duistermaat Jeanine J, Illig Thomas, Isaacs Aaron, Heard-Costa Nancy L, Hayward Caroline, Hassinen Maija, Grammer Tanja B, Gräßler Jürgen, Grönberg Henrik, de Groot Lisette C P G M, Groves Christopher J, Haessler Jeffrey, Hall Per, Haller Toomas, Hallmans Göran, Hannemann Anke, Hartman Catharina A, James Alan L, Jeff Janina, Johansen Berit, Lu Yingchang, Lyssenko Valeriya, Magnusson Patrik K E, Mahajan Anubha, Maillard Marc, McArdle Wendy L, McKenzie Colin A, McLachlan Stela, McLaren Paul J, Menni Cristina, Merger Sigrun, Lorentzon Mattias, Lobbens Stephane, Lindström Jaana, Johansson Åsa, Jolley Jennifer, Juliusdottir Thorhildur, Junttila Juhani, Kho Abel N, Kinnunen Leena, Klopp Norman, Kocher Thomas, Kratzer Wolfgang, Lichtner Peter, Lind Lars, Milani Lili
High-density genotyping study identifies four new susceptibility loci for atopic dermatitis
Weidinger S, Duerr R, Boehm B, Illig T, Winkelmann J, Fölster-Holst R, Nöthen M, Hoffmann P, Zhang X, Yang S, Zuo X, Büning C, Brand S, Franke A, Lee Y, Schreiber S, Irvine A, McLean W, Brown S, Kabesch M, Fahy C, McAleer M, Glas J, Sun L, Elder J, Stuart P, Maintz L, Michel S, Novak N, Schaarschmidt H, Hübner N, Marenholz I, Matanovic A, Rodríguez E, Esparza-Gordillo J, Baurecht H, Werfel T, Meyer-Hoffert U, Tsoi L, Nakamura Y, Takahashi A, Kubo M, Tamari M, Hirota T, Herder C, Heim K, Prokisch H, Hotze M, Ellinghaus D. High-density genotyping study identifies four new susceptibility loci for atopic dermatitis. Nat Genet 2013; 45:808-12.
02.06.2013High-density genotyping study identifies four new susceptibility loci for atopic dermatitis
02.06.2013Nat Genet 2013; 45:808-12
Weidinger Stephan, Duerr Richard H, Boehm Bernhard O, Illig Thomas, Winkelmann Juliane, Fölster-Holst Regina, Nöthen Markus M, Hoffmann Per, Zhang Xuejun, Yang Sen, Zuo Xianbo, Büning Carsten, Brand Stephan, Franke Andre, Lee Young-Ae, Schreiber Stefan, Irvine Alan D, McLean W H Irwin, Brown Sara, Kabesch Michael, Fahy Caoimhe M, McAleer Maeve A, Glas Jürgen, Sun Liangdan, Elder James T, Stuart Philip, Maintz Laura, Michel Sven, Novak Natalija, Schaarschmidt Heidi, Hübner Norbert, Marenholz Ingo, Matanovic Anja, Rodríguez Elke, Esparza-Gordillo Jorge, Baurecht Hansjörg, Werfel Thomas, Meyer-Hoffert Ulf, Tsoi Lam C, Nakamura Yusuke, Takahashi Atsushi, Kubo Michiaki, Tamari Mayumi, Hirota Tomomitsu, Herder Christian, Heim Katharina, Prokisch Holger, Hotze Melanie, Ellinghaus David
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies
Franke A, Büning C, Duerr R, Nöthen M, Wang J, Vatn M, Mathew C, Sanderson J, Rutgeerts P, Vermeire S, McArdle W, Strachan D, Wijmenga C, Sans M, Brand S, Glas J, Parkes M, Schreiber S, Rosenstiel P, Subramani S, Karlsen T, Nothnagel M, Daly M, D'Amato M, Halfvarson J, Annese V, Latiano A, Illig T, Winkelmann J, Ponsioen C, Weersma R, Nikolaus S, Liu X, Doncheva N, Skieceviciene J, Rivas M, Keller A, Ellinghaus E, Bromberg Y, Stade B, Jiang T, Till A, Lipinski S, Zeissig S, Zhang H, Liu Q, Jiang F, Krawczak M, Kayser M, Kupcinskas L, Vogel U, Andersen V, Lee J, Berzuini C, Goodall J, Boehm B, Häsler R, Albrecht M, Mayr G, Forster M, Ellinghaus D. Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies. Gastroenterology 2013; 145:339-47.
25.04.2013Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies
25.04.2013Gastroenterology 2013; 145:339-47
Franke Andre, Büning Carsten, Duerr Richard H, Nöthen Markus M, Wang Jun, Vatn Morten H, Mathew Christopher G, Sanderson Jeremy D, Rutgeerts Paul, Vermeire Severine, McArdle Wendy L, Strachan David P, Wijmenga Cisca, Sans Miquel, Brand Stephan, Glas Jürgen, Parkes Miles, Schreiber Stefan, Rosenstiel Philip, Subramani Suresh, Karlsen Tom H, Nothnagel Michael, Daly Mark J, D'Amato Mauro, Halfvarson Jonas, Annese Vito, Latiano Anna, Illig Thomas, Winkelmann Juliane, Ponsioen Cyriel Y, Weersma Rinse K, Nikolaus Susanna, Liu Xiao, Doncheva Nadezhda T, Skieceviciene Jurgita, Rivas Manuel A, Keller Andreas, Ellinghaus Eva, Bromberg Yana, Stade Björn, Jiang Tao, Till Andreas, Lipinski Simone, Zeissig Sebastian, Zhang Hu, Liu Qing, Jiang Fuman, Krawczak Michael, Kayser Manfred, Kupcinskas Limas, Vogel Ulla, Andersen Vibeke, Lee James, Berzuini Carlo R, Goodall Jane, Boehm Bernhard O, Häsler Robert, Albrecht Mario, Mayr Gabriele, Forster Michael, Ellinghaus David
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
Thomsen I, Vatn M, Silverberg M, Duerr R, Padyukov L, Brand S, Sans M, Annese V, Achkar J, Melum E, Durie P, Sandford R, Mayr G, König I, Hveem K, Cleynen I, Gutierrez-Achury J, Ricaño-Ponce I, van Heel D, Björnsson E, Boberg K, Marschall H, Schreiber S, Manns M, Färkkilä M, Dale A, Chapman R, Lazaridis K, Franke A, Anderson C, Cho J, Bergquist A, Alexander G, Chazouillères O, Bowlus C, Wijmenga C, Schrumpf E, Vermeire S, Albrecht M, Rioux J, Karlsen T, Næss S, Liu J, Gotthardt D, Pares A, Ellinghaus D, Shah T, Juran B, Milkiewicz P, Rust C, Schramm C, Hirschfield G, Invernizzi P, Eksteen B, Hov J, Folseraas T, Ellinghaus E, Rushbrook S, Doncheva N, Andreassen O, Weersma R, Weismüller T, Müller T, Srivastava B, Saarela J, Leppa V, Dorfman R, Alvaro D, Floreani A, Onengut-Gumuscu S, Rich S, Thompson W, Mason A, Teufel A, Sterneck M, Dalekos G, Nöthen M, Herms S, Winkelmann J, Mitrovic M, Braun F, Ponsioen C, Croucher P, Schork A. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat Genet 2013; 45:670-5.
21.04.2013Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
21.04.2013Nat Genet 2013; 45:670-5
Thomsen Ingo, Vatn Morten H, Silverberg Mark S, Duerr Richard H, Padyukov Leonid, Brand Stephan, Sans Miquel, Annese Vito, Achkar Jean-Paul, Melum Espen, Durie Peter R, Sandford Richard N, Mayr Gabriele, König Inke R, Hveem Kristian, Cleynen Isabelle, Gutierrez-Achury Javier, Ricaño-Ponce Isis, van Heel David, Björnsson Einar, Boberg Kirsten Muri, Marschall Hanns-Ulrich, Schreiber Stefan, Manns Michael P, Färkkilä Martti, Dale Anders M, Chapman Roger W, Lazaridis Konstantinos N, Franke Andre, Anderson Carl A, Cho Judy, Bergquist Annika, Alexander Graeme, Chazouillères Olivier, Bowlus Christopher L, Wijmenga Cisca, Schrumpf Erik, Vermeire Severine, Albrecht Mario, Rioux John D, Karlsen Tom H, Næss Sigrid, Liu Jimmy Z, Gotthardt Daniel Nils, Pares Albert, Ellinghaus David, Shah Tejas, Juran Brian D, Milkiewicz Piotr, Rust Christian, Schramm Christoph, Hirschfield Gideon M, Invernizzi Pietro, Eksteen Bertus, Hov Johannes Roksund, Folseraas Trine, Ellinghaus Eva, Rushbrook Simon M, Doncheva Nadezhda T, Andreassen Ole A, Weersma Rinse K, Weismüller Tobias J, Müller Tobias, Srivastava Brijesh, Saarela Janna, Leppa Virpi, Dorfman Ruslan, Alvaro Domenico, Floreani Annarosa, Onengut-Gumuscu Suna, Rich Stephen S, Thompson Wesley K, Mason Andrew L, Teufel Andreas, Sterneck Martina, Dalekos Georgios, Nöthen Markus M, Herms Stefan, Winkelmann Juliane, Mitrovic Mitja, Braun Felix, Ponsioen Cyriel Y, Croucher Peter J P, Schork Andrew J