Andre Franke
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
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Packard C, Pers T, Person T, Peters A, Petersen E, Peyser P, Pirie A, Polasek O, Polderman T, Puolijoki H, Raitakari O, Perry J, Perry J, Perola M, Padmanabhan S, Palmer C, Palmer N, Pasterkamp G, Patel A, Pattie A, Pedersen O, Peissig P, Peloso G, Pennell C, Rasheed A, Rauramaa R, Reilly D, Samani N, Sapkota Y, Sattar N, Schoen R, Schreiner P, Schulze M, Scott R, Segura-Lepe M, Shah S, Sheu W, Salomaa V, Saleheen D, Ruth K, Renström F, Rheinberger M, Ridker P, Rioux J, Rivas M, Roberts D, Robertson N, Robino A, Rolandsson O, Rudan I, Sim X, Lin K, Lubitz S, Lyytikäinen L, Männistö S, Marenne G, Mazul A, McCarthy M, McKean-Cowdin R, Medland S, Meidtner K, Milani L, Luan J, Loukola A, Lotery A, Lin L, Lin X, Lind L, Lindström J, Linneberg A, Liu C, Liu D, Liu Y, Lo K, Lophatananon A, Mistry V, Mitchell P, Mohlke K, Neville M, Nielsen S, Nikus K, Njølstad P, Nordestgaard B, Nyholt D, O'Connel J, O'Donoghue M, Olde Loohuis L, Ophoff R, Nelson C, Narisu N, Nalls M, Moilanen L, Moitry M, Montgomery G, Mook-Kanamori D, Moore C, Mori T, Morris A, Morris A, Müller-Nurasyid M, Munroe P, Owen K, Slater A, Walker M, Witte D, Wood A, Wu Y, Yaghootkar H, Yao J, Yao P, Yerges-Armstrong L, Young R, Zeggini E, Zhan X, Wilson J, Willer C, White H, Wallentin L, Wang F, Wang C, Wang S, Wang Y, Ware E, Wareham N, Warren H, Waterworth D, Wessel J, Zhang W, Zhao J, Zhao W, CHD Exome+ Consortium, EPIC-CVD Consortium, ExomeBP Consortium, Global Lipids Genetic Consortium, GoT2D Genes Consortium, EPIC InterAct Consortium, INTERVAL Study, ReproGen Consortium, T2D-Genes Consortium, MAGIC Investigators, Loos R, Hirschhorn J, Lindgren C, Zhou W, Zondervan K, Rotter J, Pospisilik J, Rivadeneira F, Borecki I, Deloukas P, Frayling T, Lettre G, North K, Understanding Society Scientific Group, Small K, Swift A, Tada H, Tansey K, Tardif J, Taylor K, Teumer A, Thompson D, Thorleifsson G, Thorsteinsdottir U, Thuesen B, Surendran P, Sun L, Stumvoll M, Smith A, Southam L, Spector T, Speliotes E, Starr J, Stefansson K, Steinthorsdottir V, Stirrups K, Strauch K, Stringham H, Tönjes A, Tromp G, Trompet S, Varga T, Varma R, Velez Edwards D, Vermeulen S, Veronesi G, Vestergaard H, Vitart V, Vogt T, Völker U, Vuckovic D, Varbo A, Vanhala M, van Setten J, Tsafantakis E, Tuomilehto J, Tybjaerg-Hansen A, Tyrer J, Uher R, Uitterlinden A, Uusitupa M, Laan S, Duijn C, Leeuwen N, Wagenknecht L, Lin H, Bots M, Caulfield M, Chambers J, Chasman D, Chen Y, Chowdhury R, Christensen C, Chu A, Cocca M, Collins F, Cook J, Catamo E, Carey D, Cappellani S, Bottinger E, Bowden D, Brandslund I, Breen G, Brilliant M, Broer L, Brumat M, Burt A, Butterworth A, Campbell P, Corley J, Corominas Galbany J, Cox A, Ruijter H, Dennis J, Denny J, Di Angelantonio E, Drenos F, Du M, Dubé M, Dunning A, Easton D, Edwards T, Hollander A, Heijer M, Demerath E, Crosslin D, Cuellar-Partida G, D'Eustacchio A, Danesh J, Davies G, Bakker P, Groot M, Mutsert R, Deary I, Dedoussis G, Ellinghaus D, Turcot V, Locke A, Mahajan A, Marouli E, Sivapalaratnam S, Young K, Alfred T, Feitosa M, Masca N, Manning A, Medina-Gomez C, Lempradl A, Karaderi T, Hendricks A, Lu Y, Highland H, Schurmann C, Justice A, Fine R, Bradfield J, Esko T, Giri A, Graff M, Guo X, Mudgal P, Ng M, Reiner A, Barroso I, Bastarache L, Benn M, Bergmann S, Bielak L, Blüher M, Boehnke M, Boeing H, Boerwinkle E, Böger C, Bang L, Balkau B, Auer P, Vedantam S, Willems S, Winkler T, Abecasis G, Aben K, Alam D, Alharthi S, Allison M, Amouyel P, Asselbergs F, Bork-Jensen J, Ellinor P, Howson J, Jukema J, Kahali B, Kahn R, Kähönen M, Kamstrup P, Kanoni S, Kaprio J, Karaleftheri M, Kardia S, Karpe F, Jørgensen T, Jørgensen M, Johansson S, Hu Y, Huang P, Huffman J, Ikram M, Ingelsson E, Jackson A, Jansson J, Jarvik G, Jensen G, Jia Y, Kathiresan S, Kee F, Kiemeney L, Lamparter D, Lange E, Lange L, Langenberg C, Larson E, Lee N, Lehtimäki T, Lewis C, Li H, Li J, Lakka T, Laakso M, Kuusisto J, Kim E, Kitajima H, Komulainen P, Kooner J, Kooperberg C, Korhonen T, Kovacs P, Kuivaniemi H, Kutalik Z, Kuulasmaa K, Li-Gao R, Elliott P, Franks P, Friedrich N, Frikke-Schmidt R, Galesloot T, Gan W, Gandin I, Gasparini P, Gibson J, Giedraitis V, Gjesing A, Franke A, Franco O, Fornage M, Evangelou E, Farmaki A, Farooqi I, Faul J, Fauser S, Feng S, Ferrannini E, Ferrieres J, Florez J, Ford I, Gordon-Larsen P, Gorski M, Grabe H, Have C, Hayward C, He L, Heard-Costa N, Heath A, Heid I, Helgeland Ø, Hernesniemi J, Hewitt A, Holmen O, Hattersley A, Harris T, Harris K, Grant S, Grarup N, Griffiths H, Grove M, Gudnason V, Gustafsson S, Haessler J, Hakonarson H, Hammerschlag A, Hansen T, Hovingh G. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet 2017; 50:26-41.
22.12.2017Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
22.12.2017Nat Genet 2017; 50:26-41
Packard Chris J, Pers Tune H, Person Thomas N, Peters Annette, Petersen Eva R B, Peyser Patricia A, Pirie Ailith, Polasek Ozren, Polderman Tinca J, Puolijoki Hannu, Raitakari Olli T, Perry John R B, Perry James A, Perola Markus, Padmanabhan Sandosh, Palmer Colin N A, Palmer Nicholette D, Pasterkamp Gerard, Patel Aniruddh P, Pattie Alison, Pedersen Oluf, Peissig Peggy L, Peloso Gina M, Pennell Craig E, Rasheed Asif, Rauramaa Rainer, Reilly Dermot F, Samani Nilesh J, Sapkota Yadav, Sattar Naveed, Schoen Robert E, Schreiner Pamela J, Schulze Matthias B, Scott Robert A, Segura-Lepe Marcelo P, Shah Svati H, Sheu Wayne H-H, Salomaa Veikko, Saleheen Danish, Ruth Katherine S, Renström Frida, Rheinberger Myriam, Ridker Paul M, Rioux John D, Rivas Manuel A, Roberts David J, Robertson Neil R, Robino Antonietta, Rolandsson Olov, Rudan Igor, Sim Xueling, Lin Keng-Hung, Lubitz Steven A, Lyytikäinen Leo-Pekka, Männistö Satu, Marenne Gaëlle, Mazul Angela L, McCarthy Mark I, McKean-Cowdin Roberta, Medland Sarah E, Meidtner Karina, Milani Lili, Luan Jian'an, Loukola Anu, Lotery Andrew J, Lin Li-An, Lin Xu, Lind Lars, Lindström Jaana, Linneberg Allan, Liu Ching-Ti, Liu Dajiang J, Liu Yongmei, Lo Ken S, Lophatananon Artitaya, Mistry Vanisha, Mitchell Paul, Mohlke Karen L, Neville Matt, Nielsen Sune F, Nikus Kjell, Njølstad Pål R, Nordestgaard Børge G, Nyholt Dale R, O'Connel Jeffrey R, O'Donoghue Michelle L, Olde Loohuis Loes M, Ophoff Roel A, Nelson Christopher P, Narisu Narisu, Nalls Mike A, Moilanen Leena, Moitry Marie, Montgomery Grant W, Mook-Kanamori Dennis O, Moore Carmel, Mori Trevor A, Morris Andrew D, Morris Andrew P, Müller-Nurasyid Martina, Munroe Patricia B, Owen Katharine R, Slater Andrew J, Walker Mark, Witte Daniel R, Wood Andrew R, Wu Ying, Yaghootkar Hanieh, Yao Jie, Yao Pang, Yerges-Armstrong Laura M, Young Robin, Zeggini Eleftheria, Zhan Xiaowei, Wilson James G, Willer Cristen J, White Harvey D, Wallentin Lars, Wang Feijie, Wang Carol A, Wang Shuai, Wang Yiqin, Ware Erin B, Wareham Nicholas J, Warren Helen R, Waterworth Dawn M, Wessel Jennifer, Zhang Weihua, Zhao Jing Hua, Zhao Wei, CHD Exome+ Consortium, EPIC-CVD Consortium, ExomeBP Consortium, Global Lipids Genetic Consortium, GoT2D Genes Consortium, EPIC InterAct Consortium, INTERVAL Study, ReproGen Consortium, T2D-Genes Consortium, MAGIC Investigators, Loos Ruth J F, Hirschhorn Joel N, Lindgren Cecilia M, Zhou Wei, Zondervan Krina T, Rotter Jerome I, Pospisilik John A, Rivadeneira Fernando, Borecki Ingrid B, Deloukas Panos, Frayling Timothy M, Lettre Guillaume, North Kari E, Understanding Society Scientific Group, Small Kerrin S, Swift Amy J, Tada Hayato, Tansey Katherine E, Tardif Jean-Claude, Taylor Kent D, Teumer Alexander, Thompson Deborah J, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Thuesen Betina H, Surendran Praveen, Sun Liang, Stumvoll Michael, Smith Albert V, Southam Lorraine, Spector Timothy D, Speliotes Elizabeth K, Starr John M, Stefansson Kari, Steinthorsdottir Valgerdur, Stirrups Kathleen E, Strauch Konstantin, Stringham Heather M, Tönjes Anke, Tromp Gerard, Trompet Stella, Varga Tibor V, Varma Rohit, Velez Edwards Digna R, Vermeulen Sita H, Veronesi Giovanni, Vestergaard Henrik, Vitart Veronique, Vogt Thomas F, Völker Uwe, Vuckovic Dragana, Varbo Anette, Vanhala Mauno, van Setten Jessica, Tsafantakis Emmanouil, Tuomilehto Jaakko, Tybjaerg-Hansen Anne, Tyrer Jonathan P, Uher Rudolf, Uitterlinden André G, Uusitupa Matti, Laan Sander W, Duijn Cornelia M, Leeuwen Nienke, Wagenknecht Lynne E, Lin Honghuang, Bots Michiel L, Caulfield Mark J, Chambers John C, Chasman Daniel I, Chen Yii-Der I, Chowdhury Rajiv, Christensen Cramer, Chu Audrey Y, Cocca Massimiliano, Collins Francis S, Cook James P, Catamo Eulalia, Carey David J, Cappellani Stefania, Bottinger Erwin P, Bowden Donald W, Brandslund Ivan, Breen Gerome, Brilliant Murray H, Broer Linda, Brumat Marco, Burt Amber A, Butterworth Adam S, Campbell Peter T, Corley Janie, Corominas Galbany Jordi, Cox Amanda J, Ruijter Hester M, Dennis Joe G, Denny Josh C, Di Angelantonio Emanuele, Drenos Fotios, Du Mengmeng, Dubé Marie-Pierre, Dunning Alison M, Easton Douglas F, Edwards Todd L, Hollander Anneke I, Heijer Martin, Demerath Ellen W, Crosslin David S, Cuellar-Partida Gabriel, D'Eustacchio Angela, Danesh John, Davies Gail, Bakker Paul I W, Groot Mark C H, Mutsert Renée, Deary Ian J, Dedoussis George, Ellinghaus David, Turcot Valérie, Locke Adam E, Mahajan Anubha, Marouli Eirini, Sivapalaratnam Suthesh, Young Kristin L, Alfred Tamuno, Feitosa Mary F, Masca Nicholas G D, Manning Alisa K, Medina-Gomez Carolina, Lempradl Adelheid, Karaderi Tugce, Hendricks Audrey E, Lu Yingchang, Highland Heather M, Schurmann Claudia, Justice Anne E, Fine Rebecca S, Bradfield Jonathan P, Esko Tõnu, Giri Ayush, Graff Mariaelisa, Guo Xiuqing, Mudgal Poorva, Ng Maggie C Y, Reiner Alex P, Barroso Inês, Bastarache Lisa, Benn Marianne, Bergmann Sven, Bielak Lawrence F, Blüher Matthias, Boehnke Michael, Boeing Heiner, Boerwinkle Eric, Böger Carsten A, Bang Lia E, Balkau Beverley, Auer Paul L, Vedantam Sailaja, Willems Sara M, Winkler Thomas W, Abecasis Goncalo, Aben Katja K, Alam Dewan S, Alharthi Sameer E, Allison Matthew, Amouyel Philippe, Asselbergs Folkert W, Bork-Jensen Jette, Ellinor Patrick T, Howson Joanna M M, Jukema J Wouter, Kahali Bratati, Kahn René S, Kähönen Mika, Kamstrup Pia R, Kanoni Stavroula, Kaprio Jaakko, Karaleftheri Maria, Kardia Sharon L R, Karpe Fredrik, Jørgensen Torben, Jørgensen Marit E, Johansson Stefan, Hu Yao, Huang Paul L, Huffman Jennifer E, Ikram M Arfan, Ingelsson Erik, Jackson Anne U, Jansson Jan-Håkan, Jarvik Gail P, Jensen Gorm B, Jia Yucheng, Kathiresan Sekar, Kee Frank, Kiemeney Lambertus A, Lamparter David, Lange Ethan M, Lange Leslie A, Langenberg Claudia, Larson Eric B, Lee Nanette R, Lehtimäki Terho, Lewis Cora E, Li Huaixing, Li Jin, Lakka Timo A, Laakso Markku, Kuusisto Johanna, Kim Eric, Kitajima Hidetoshi, Komulainen Pirjo, Kooner Jaspal S, Kooperberg Charles, Korhonen Tellervo, Kovacs Peter, Kuivaniemi Helena, Kutalik Zoltán, Kuulasmaa Kari, Li-Gao Ruifang, Elliott Paul, Franks Paul W, Friedrich Nele, Frikke-Schmidt Ruth, Galesloot Tessel E, Gan Wei, Gandin Ilaria, Gasparini Paolo, Gibson Jane, Giedraitis Vilmantas, Gjesing Anette P, Franke Andre, Franco Oscar H, Fornage Myriam, Evangelou Evangelos, Farmaki Aliki-Eleni, Farooqi I Sadaf, Faul Jessica D, Fauser Sascha, Feng Shuang, Ferrannini Ele, Ferrieres Jean, Florez Jose C, Ford Ian, Gordon-Larsen Penny, Gorski Mathias, Grabe Hans-Jörgen, Have Christian T, Hayward Caroline, He Liang, Heard-Costa Nancy L, Heath Andrew C, Heid Iris M, Helgeland Øyvind, Hernesniemi Jussi, Hewitt Alex W, Holmen Oddgeir L, Hattersley Andrew T, Harris Tamara B, Harris Kathleen Mullan, Grant Struan F A, Grarup Niels, Griffiths Helen L, Grove Megan L, Gudnason Vilmundur, Gustafsson Stefan, Haessler Jeff, Hakonarson Hakon, Hammerschlag Anke R, Hansen Torben, Hovingh G Kees
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
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
Lees C, van der Meulen-de Jong A, Theatre E, Schreiber S, Satsangi J, Lee J, Lawrance I, Kupcinskas L, Kennedy N, Weersma R, Wilson D, Barrett J, McGovern D, Radford-Smith G, Silverberg M, Mansfield J, Rioux J, Vermeire S, Parkes M, Huang H, Hov J, Halfvarson J, Annese V, Andrews J, Andersen V, Ahmad T, Zeissig S, Schumm L, Jostins L, Boucher G, Brand S, Brant S, Cho J, Hakonarson H, Goyette P, Gearry R, Franke A, Ferguson L, Duerr R, Dubinsky M, Daly M, Cleynen I. Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study. Lancet 2015; 387:156-67.
18.10.2015Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
18.10.2015Lancet 2015; 387:156-67
Lees Charlie W, van der Meulen-de Jong Andrea E, Theatre Emilie, Schreiber Stephan, Satsangi Jack, Lee James C, Lawrance Ian C, Kupcinskas Limas, Kennedy Nicholas A, Weersma Rinse K, Wilson David C, Barrett Jeffrey C, McGovern Dermot P B, Radford-Smith Graham, Silverberg Mark S, Mansfield John, Rioux John D, Vermeire Severine, Parkes Miles, Huang Hailang, Hov Johannes R, Halfvarson Jonas, Annese Vito, Andrews Jane M, Andersen Vibeke, Ahmad Tariq, Zeissig Sebastian, Schumm L Philip, Jostins Luke, Boucher Gabrielle, Brand Stephan, Brant Steven R, Cho Judy H, Hakonarson Hakon, Goyette Philippe, Gearry Richard B, Franke Andre, Ferguson Lynnette R, Duerr Richard H, Dubinsky Marla, Daly Mark J, Cleynen Isabelle
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
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
Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2
Diegelmann J, Glas J, Franke A, Göke B, Bedynek A, Olszak T, Zimmermann E, Le Bras E, Czamara D, Brand S. Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2. PloS one 2013; 8:e77773.
05.11.2013Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2
05.11.2013PloS one 2013; 8:e77773
Diegelmann Julia, Glas Jürgen, Franke Andre, Göke Burkhard, Bedynek Andrea, Olszak Torsten, Zimmermann Eva, Le Bras Emmanuelle, Czamara Darina, Brand Stephan
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
PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites
Glas J, Duerr R, Franke A, Kamboh M, Achkar J, Balschun T, Müller-Myhsok B, Wolf C, Olszak T, Wetzke M, Diegelmann J, Pasciuto G, Czamara D, Seiderer J, Brand S. PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites. PloS one 2012; 7:e52873.
27.12.2012PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites
27.12.2012PloS one 2012; 7:e52873
Glas Jürgen, Duerr Richard H, Franke Andre, Kamboh M Ilyas, Achkar Jean-Paul, Balschun Tobias, Müller-Myhsok Bertram, Wolf Christiane, Olszak Torsten, Wetzke Martin, Diegelmann Julia, Pasciuto Giulia, Czamara Darina, Seiderer Julia, Brand Stephan
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Kupcinskas L, Potocnik U, Prescott N, Regueiro M, Rotter J, Russell R, Sanderson J, Sans M, Satsangi J, Schreiber S, Simms L, Sventoraityte J, Ponsioen C, Palmieri O, Kugathasan S, Latiano A, Laukens D, Lawrance I, Lees C, Louis E, Mahy G, Mansfield J, Morgan A, Mowat C, Newman W, Targan S, Taylor K, Tremelling M, Hakonarson H, Brant S, Radford-Smith G, Mathew C, Rioux J, Schadt E, Daly M, Franke A, Parkes M, Vermeire S, Barrett J, Annese V, Silverberg M, Verspaget H, De Vos M, Wijmenga C, Wilson D, Winkelmann J, Xavier R, Zeissig S, Zhang B, Zhang C, Zhao H, Cho J, Karlsen T, Jostins L, Theatre E, Spain S, Raychaudhuri S, Goyette P, Wei Z, Abraham C, Achkar J, Ahmad T, Amininejad L, Ananthakrishnan A, Andersen V, Cleynen I, Ning K, Ripke S, Weersma R, Duerr R, McGovern D, Hui K, Lee J, Schumm L, Sharma Y, Anderson C, Essers J, Mitrovic M, Andrews J, Baidoo L, Balschun T, Ferguson L, Franchimont D, Fransen K, Gearry R, Georges M, Gieger C, Glas J, Haritunians T, Hart A, Hawkey C, Hedl M, Ellinghaus D, Edwards C, Bampton P, Bitton A, Boucher G, Brand S, Büning C, Cohain A, Cichon S, D'Amato M, De Jong D, Devaney K, Dubinsky M, Hu X. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 2012; 491:119-24.
01.11.2012Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
01.11.2012Nature 2012; 491:119-24
Kupcinskas Limas, Potocnik Uros, Prescott Natalie J, Regueiro Miguel, Rotter Jerome I, Russell Richard K, Sanderson Jeremy D, Sans Miquel, Satsangi Jack, Schreiber Stefan, Simms Lisa A, Sventoraityte Jurgita, Ponsioen Cyriel Y, Palmieri Orazio, Kugathasan Subra, Latiano Anna, Laukens Debby, Lawrance Ian C, Lees Charlie W, Louis Edouard, Mahy Gillian, Mansfield John, Morgan Angharad R, Mowat Craig, Newman William, Targan Stephan R, Taylor Kent D, Tremelling Mark, Hakonarson Hakon, Brant Steven R, Radford-Smith Graham, Mathew Christopher G, Rioux John D, Schadt Eric E, Daly Mark J, Franke Andre, Parkes Miles, Vermeire Severine, Barrett Jeffrey C, Annese Vito, Silverberg Mark S, Verspaget Hein W, De Vos Martine, Wijmenga Cisca, Wilson David C, Winkelmann Juliane, Xavier Ramnik J, Zeissig Sebastian, Zhang Bin, Zhang Clarence K, Zhao Hongyu, Cho Judy H, Karlsen Tom H, Jostins Luke, Theatre Emilie, Spain Sarah L, Raychaudhuri Soumya, Goyette Philippe, Wei Zhi, Abraham Clara, Achkar Jean-Paul, Ahmad Tariq, Amininejad Leila, Ananthakrishnan Ashwin N, Andersen Vibeke, Cleynen Isabelle, Ning Kaida, Ripke Stephan, Weersma Rinse K, Duerr Richard H, McGovern Dermot P, Hui Ken Y, Lee James C, Schumm L Philip, Sharma Yashoda, Anderson Carl A, Essers Jonah, Mitrovic Mitja, Andrews Jane M, Baidoo Leonard, Balschun Tobias, Ferguson Lynnette R, Franchimont Denis, Fransen Karin, Gearry Richard, Georges Michel, Gieger Christian, Glas Jürgen, Haritunians Talin, Hart Ailsa, Hawkey Chris, Hedl Matija, Ellinghaus David, Edwards Cathryn, Bampton Peter A, Bitton Alain, Boucher Gabrielle, Brand Stephan, Büning Carsten, Cohain Ariella, Cichon Sven, D'Amato Mauro, De Jong Dirk, Devaney Kathy L, Dubinsky Marla, Hu Xinli
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Phillips A, van den Berg L, Vatn M, Verspaget H, Walters T, Wijmenga C, Wilson D, Westra H, Xavier R, Zhao Z, Ponsioen C, Andersen V, Torkvist L, Targan S, Steinhart A, Prescott N, Proctor D, Roberts R, Russell R, Rutgeerts P, Sanderson J, Sans M, Schumm P, Seibold F, Sharma Y, Simms L, Seielstad M, Gazouli M, Anagnou N, Satsangi J, Cho J, Schreiber S, Daly M, Barrett J, Parkes M, Annese V, Hakonarson H, Radford-Smith G, Duerr R, Vermeire S, Weersma R, Chamaillard M, Brant S, Karlsen T, Kupcinskas L, Sventoraityte J, Mansfield J, Kugathasan S, Silverberg M, Halfvarson J, Rotter J, Mathew C, Griffiths A, Gearry R, Ahmad T, Rioux J, Panés J, Anderson C, Baldassano R, Barclay M, Bayless T, Brand S, Büning C, Colombel J, Denson L, De Vos M, Dubinsky M, Edwards C, Ellinghaus D, Fehrmann R, Baidoo L, Bumpstead S, Boucher G, Lees C, Franke A, D'Amato M, Taylor K, Lee J, Goyette P, Imielinski M, Latiano A, Lagacé C, Scott R, Amininejad L, Floyd J, Florin T, Libioulle C, Louis E, McGovern D, Milla M, Montgomery G, Morley K, Mowat C, Ng A, Newman W, Ophoff R, Papi L, Palmieri O, Levine A, Lemann M, Franchimont D, Franke L, Georges M, Glas J, Glazer N, Guthery S, Haritunians T, Hayward N, Hugot J, Jobin G, Laukens D, Lawrance I, Peyrin-Biroulet L. Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nat Genet 2011; 43:246-52.
06.02.2011Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
06.02.2011Nat Genet 2011; 43:246-52
Phillips Anne, van den Berg Leonard H, Vatn Morten, Verspaget Hein, Walters Thomas, Wijmenga Cisca, Wilson David C, Westra Harm-Jan, Xavier Ramnik J, Zhao Zhen Z, Ponsioen Cyriel Y, Andersen Vibeke, Torkvist Leif, Targan Stephan R, Steinhart A Hillary, Prescott Natalie J, Proctor Deborah D, Roberts Rebecca, Russell Richard, Rutgeerts Paul, Sanderson Jeremy, Sans Miquel, Schumm Philip, Seibold Frank, Sharma Yashoda, Simms Lisa A, Seielstad Mark, Gazouli Maria, Anagnou Nicholas P, Satsangi Jack, Cho Judy H, Schreiber Stefan, Daly Mark J, Barrett Jeffrey C, Parkes Miles, Annese Vito, Hakonarson Hakon, Radford-Smith Graham, Duerr Richard H, Vermeire Severine, Weersma Rinse K, Chamaillard Mathias, Brant Steven R, Karlsen Tom H, Kupcinskas Limas, Sventoraityte Jurgita, Mansfield John C, Kugathasan Subra, Silverberg Mark S, Halfvarson Jonas, Rotter Jerome I, Mathew Christopher G, Griffiths Anne M, Gearry Richard, Ahmad Tariq, Rioux John D, Panés Julián, Anderson Carl A, Baldassano Robert N, Barclay Murray, Bayless Theodore M, Brand Stephan, Büning Carsten, Colombel Jean-Frédéric, Denson Lee A, De Vos Martine, Dubinsky Marla, Edwards Cathryn, Ellinghaus David, Fehrmann Rudolf S N, Baidoo Leonard, Bumpstead Suzannah, Boucher Gabrielle, Lees Charlie W, Franke Andre, D'Amato Mauro, Taylor Kent D, Lee James C, Goyette Philippe, Imielinski Marcin, Latiano Anna, Lagacé Caroline, Scott Regan, Amininejad Leila, Floyd James A B, Florin Timothy, Libioulle Cecile, Louis Edouard, McGovern Dermot P, Milla Monica, Montgomery Grant W, Morley Katherine I, Mowat Craig, Ng Aylwin, Newman William, Ophoff Roel A, Papi Laura, Palmieri Orazio, Levine Arie, Lemann Marc, Franchimont Denis, Franke Lude, Georges Michel, Glas Jürgen, Glazer Nicole L, Guthery Stephen L, Haritunians Talin, Hayward Nicholas K, Hugot Jean-Pierre, Jobin Gilles, Laukens Debby, Lawrance Ian, Peyrin-Biroulet Laurent
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Glas J, Mowat C, Newman W, Panés J, Phillips A, Proctor D, Regueiro M, Russell R, Rutgeerts P, Sanderson J, Sans M, Louis E, Libioulle C, Van Gossum A, Guthery S, Halfvarson J, Verspaget H, Hugot J, Karban A, Laukens D, Lawrance I, Lemann M, Levine A, Seibold F, Steinhart A, Mansfield J, Vermeire S, Duerr R, Silverberg M, Satsangi J, Schreiber S, Cho J, Annese V, Hakonarson H, Daly M, Griffiths A, Kugathasan S, Stokkers P, Torkvist L, Kullak-Ublick G, Wilson D, Walters T, Targan S, Brant S, Rioux J, D'Amato M, Weersma R, Parkes M, Franke A, Ellinghaus D, Festen E, Georges M, Green T, Haritunians T, Jostins L, Latiano A, Mathew C, Montgomery G, Prescott N, Bumpstead S, Bis J, McGovern D, Barrett J, Wang K, Radford-Smith G, Ahmad T, Lees C, Balschun T, Lee J, Roberts R, Anderson C, Raychaudhuri S, Rotter J, Colombel J, Cottone M, Stronati L, Denson T, De Vos M, D'Inca R, Dubinsky M, Edwards C, Florin T, Franchimont D, Cohen A, Büning C, Schumm P, Sharma Y, Simms L, Taylor K, Whiteman D, Wijmenga C, Baldassano R, Barclay M, Bayless T, Brand S, Gearry R. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nat Genet 2010; 42:1118-25.
01.12.2010Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
01.12.2010Nat Genet 2010; 42:1118-25
Glas Jürgen, Mowat Craig, Newman William, Panés Julián, Phillips Anne, Proctor Deborah D, Regueiro Miguel, Russell Richard, Rutgeerts Paul, Sanderson Jeremy, Sans Miquel, Louis Edouard, Libioulle Cecile, Van Gossum Andre, Guthery Stephen L, Halfvarson Jonas, Verspaget Hein W, Hugot Jean-Pierre, Karban Amir, Laukens Debby, Lawrance Ian, Lemann Marc, Levine Arie, Seibold Frank, Steinhart A Hillary, Mansfield John C, Vermeire Severine, Duerr Richard H, Silverberg Mark S, Satsangi Jack, Schreiber Stefan, Cho Judy H, Annese Vito, Hakonarson Hakon, Daly Mark J, Griffiths Anne M, Kugathasan Subra, Stokkers Pieter C F, Torkvist Leif, Kullak-Ublick Gerd, Wilson David, Walters Thomas, Targan Stephan R, Brant Steven R, Rioux John D, D'Amato Mauro, Weersma Rinse K, Parkes Miles, Franke Andre, Ellinghaus David, Festen Eleonora M, Georges Michel, Green Todd, Haritunians Talin, Jostins Luke, Latiano Anna, Mathew Christopher G, Montgomery Grant W, Prescott Natalie J, Bumpstead Suzanne, Bis Joshua C, McGovern Dermot P B, Barrett Jeffrey C, Wang Kai, Radford-Smith Graham L, Ahmad Tariq, Lees Charlie W, Balschun Tobias, Lee James, Roberts Rebecca, Anderson Carl A, Raychaudhuri Soumya, Rotter Jerome I, Colombel Jean-Frederick, Cottone Mario, Stronati Laura, Denson Ted, De Vos Martine, D'Inca Renata, Dubinsky Marla, Edwards Cathryn, Florin Tim, Franchimont Denis, Cohen Albert, Büning Carsten, Schumm Philip, Sharma Yashoda, Simms Lisa A, Taylor Kent D, Whiteman David, Wijmenga Cisca, Baldassano Robert N, Barclay Murray, Bayless Theodore M, Brand Stephan, Gearry Richard
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Horn D, Illig T, Bezzina C, Franke A, Spranger S, Villavicencio-Lorini P, Seifert W, Rosenfeld J, Klopocki E, Rappold G, Wohlleber E, Riess O, Bonin M, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco A, Strom T. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum Mutat 2010; 31:E1851-60.
01.11.2010Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
01.11.2010Hum Mutat 2010; 31:E1851-60
Horn Denise, Illig Thomas, Bezzina Connie R, Franke Andre, Spranger Stephanie, Villavicencio-Lorini Pablo, Seifert Wenke, Rosenfeld Jochen, Klopocki Eva, Rappold Gudrun A, Wohlleber Eva, Riess Olaf, Bonin Michael, Kapeller Johannes, Rivera-Brugués Núria, Moog Ute, Lorenz-Depiereux Bettina, Eck Sebastian, Hempel Maja, Wagenstaller Janine, Gawthrope Alex, Monaco Anthony P, Strom Tim M