Stefan A Escher
Analysis with the exome array identifies multiple new independent variants in lipid loci
Deloukas P, Escher S, Dedoussis G, Blakemore A, Waldenberger M, Tsafantakis E, Tomaszewski M, Strauch K, Stanton A, Silveira A, Shields D, Sever P, Sennblad B, Sabater-Lleal M, Kooner J, McCarthy M, Palmer C, Samani N, Franks P, Munroe P, Wareham N, Chambers J, Gieger C, Zeggini E, Jarvelin M, Tobin M, Frayling T, Caulfield M, Hamsten A, Rolandsson O, Renström F, An Hashim N, Lataniotis L, Strawbridge R, Couto Alves A, Müller-Nurasyid M, Yaghootkar H, Zhang W, Southam L, Scott R, Warren H, Varga T, Stirrups K, Masca N, Besse C, Boland A, Braund P, Rayner N, Poulter N, Peters A, Pasko D, Matchan A, Keinänen-Kiukaanniemi S, Karaleftheri M, Jansson J, Grallert H, Franks S, Farmaki A, Dominiczak A, Connell J, Kanoni S. Analysis with the exome array identifies multiple new independent variants in lipid loci. Hum Mol Genet 2016; 25:4094-4106.
27.07.2016Analysis with the exome array identifies multiple new independent variants in lipid loci
27.07.2016Hum Mol Genet 2016; 25:4094-4106
Deloukas Panos, Escher Stefan A, Dedoussis George, Blakemore Alexandra I F, Waldenberger Melanie, Tsafantakis Emmanouil, Tomaszewski Maciej, Strauch Konstantin, Stanton Alice V, Silveira Angela, Shields Denis, Sever Peter, Sennblad Bengt, Sabater-Lleal Maria, Kooner Jaspal S, McCarthy Mark I, Palmer Colin N A, Samani Nilesh J, Franks Paul W, Munroe Patricia B, Wareham Nick J, Chambers John C, Gieger Christian, Zeggini Eleftheria, Jarvelin Marjo-Riitta, Tobin Martin D, Frayling Timothy M, Caulfield Mark J, Hamsten Anders, Rolandsson Olov, Renström Frida, An Hashim Nikman, Lataniotis Lazaros, Strawbridge Rona J, Couto Alves Alexessander, Müller-Nurasyid Martina, Yaghootkar Hanieh, Zhang Weihua, Southam Lorraine, Scott Robert A, Warren Helen R, Varga Tibor V, Stirrups Kathleen E, Masca Nicholas G D, Besse Céline, Boland Anne, Braund Peter S, Rayner Nigel W, Poulter Neil, Peters Annette, Pasko Dorota, Matchan Angela, Keinänen-Kiukaanniemi Sirkka, Karaleftheri Maria, Jansson Jan-Håkan, Grallert Harald, Franks Stephen, Farmaki Aliki-Eleni, Dominiczak Anna, Connell John M, Kanoni Stavroula
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
Franco O, Lorenzo C, Karter A, Ingelsson E, Hansen T, Cupples L, Brown J, Bis J, Becker D, Zengini E, Yanek L, Mathias R, Norris J, Peloso G, Ferrannini E, Deloukas P, Dedoussis G, Bottinger E, Boeing H, Wagenknecht L, Varma R, Vaidya D, Toniolo D, Sheu W, Javad S, Tsafantakis E, Traglia M, Rayner N, Peter A, Pasko D, Palmer N, Ntalla I, Muzny D, Mohlke K, Metcalf G, McLeod O, McKean-Cowdin R, Renström F, Rice K, Sala C, Torres M, Thanopoulou A, Tentolouris N, Stirrups K, Stahl E, Speliotes E, Soranzo N, Smith J, Serafetinidis I, Sennblad B, Matchan A, Goodarzi M, van Duijn C, Tai E, Psaty B, Pedersen O, Chasman D, Borecki I, Laakso M, Zeggini E, Wong T, Wareham N, Waterworth D, Boerwinkle E, Scott R, Meigs J, Rotter J, Dupuis J, Siscovick D, Frayling T, Wilson J, Loos R, Florez J, Kao W, Watkins H, Walker M, Uitterlinden A, Launer L, Langenberg C, Jansson J, Hofman A, Hayward C, Hattersley A, Harris T, Hamsten A, Gudnason V, Gibbs R, Levy D, Oostra B, O'Donnell C, Smith B, Schulze M, Rudan I, Ridker P, Rich S, Province M, Polasek O, Pankow J, Padmanabhan S, O'Rahilly S, Franks P, Maruthur N, Amin N, Meidtner K, Hua Zhao J, Li M, Layton J, Lange L, Jakobsdottir J, Isaacs A, Hara K, Guo X, Garcia M, Morrison A, Nalls M, Peters M, Allin K, Varga T, Taylor K, Strawbridge R, Stoiber M, Southam L, Smith A, Silveira A, Schurmann C, Sabater-Lleal M, Freitag D, Fornage M, Bork-Jensen J, Hidalgo B, Lipovich L, Raghavan S, Hivert M, Dauriz M, Brody J, Yaghootkar H, Wang S, Willems S, Chu A, Fox K, Huffman J, An P, Boland A, Besse C, Abrol R, Stančáková A, Baldridge A, Li L, Ehm M, Grarup N, Rasmussen-Torvik L, Lu Y, Wessel J, Marouli E, Kirkpatrick A, Khor C, Karaleftheri M, Jørgensen T, Jørgensen M, Jensen R, Ikram M, Hoffmann P, Heo J, Hallmans G, Kraja A, Kuusisto J, Lange E, Mamakou V, Malerba G, Linneberg A, Lindgren C, Liu Y, Liu C, Liao J, Leong A, Lee W, Lee I, Hai Y, Gustafsson S, Grove M, Cheng C, Chen Y, Chen Y, Burns S, Bowden D, Bombieri C, Boehnke M, Bihlmeyer N, Barbieri C, Aung T, Correa A, Czajkowski J, Dehghan A, Gottesman O, Goel A, Goddard W, Giulianini F, Gambaro G, Frånberg M, Farmaki A, Escher S, Eiriksdottir G, Ehret G, Aponte J. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nat Commun 2015; 6:5897.
29.01.2015Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
29.01.2015Nat Commun 2015; 6:5897
Franco Oscar H, Lorenzo Carlos, Karter Andrew J, Ingelsson Erik, Hansen Torben, Cupples L Adrienne, Brown James B, Bis Joshua C, Becker Diane M, Zengini Eleni, Yanek Lisa R, Mathias Rasika A, Norris Jill M, Peloso Gina M, Ferrannini Ele, Deloukas Panos, Dedoussis George, Bottinger Erwin P, Boeing Heiner, Wagenknecht Lynne E, Varma Rohit, Vaidya Dhananjay, Toniolo Daniela, Sheu Wayne H-H, Javad Sundas, Tsafantakis Emmanouil, Traglia Michela, Rayner Nigel W, Peter Andreas, Pasko Dorota, Palmer Nicholette D, Ntalla Ioanna, Muzny Donna M, Mohlke Karen L, Metcalf Ginger A, McLeod Olga, McKean-Cowdin Roberta, Renström Frida, Rice Ken, Sala Cinzia F, Torres Mina, Thanopoulou Anastasia, Tentolouris Nikos, Stirrups Kathleen, Stahl Eli A, Speliotes Elizabeth K, Soranzo Nicole, Smith Jennifer A, Serafetinidis Ioannis, Sennblad Bengt, Matchan Angela, Goodarzi Mark O, van Duijn Cornelia M, Tai E Shyong, Psaty Bruce M, Pedersen Oluf, Chasman Daniel I, Borecki Ingrid B, Laakso Markku, Zeggini Eleftheria, Wong Tien Y, Wareham Nicholas J, Waterworth Dawn M, Boerwinkle Eric, Scott Robert A, Meigs James B, Rotter Jerome I, Dupuis Josée, Siscovick David S, Frayling Timothy M, Wilson James G, Loos Ruth J F, Florez Jose C, Kao W H Linda, Watkins Hugh, Walker Mark, Uitterlinden André G, Launer Lenore J, Langenberg Claudia, Jansson Jan-Håkan, Hofman Albert, Hayward Caroline, Hattersley Andrew T, Harris Tamara B, Hamsten Anders, Gudnason Vilmundur, Gibbs Richard A, Levy Daniel, Oostra Ben A, O'Donnell Christopher J, Smith Blair H, Schulze Matthias B, Rudan Igor, Ridker Paul M, Rich Stephen S, Province Michael A, Polasek Ozren, Pankow James S, Padmanabhan Sandosh, O'Rahilly Stephen, Franks Paul W, Maruthur Nisa M, Amin Najaf, Meidtner Karina, Hua Zhao Jing, Li Man, Layton Jill C, Lange Leslie A, Jakobsdottir Johanna, Isaacs Aaron, Hara Kazuo, Guo Xiuqing, Garcia Melissa E, Morrison Alanna C, Nalls Mike A, Peters Marjolein J, Allin Kristine H, Varga Tibor V, Taylor Kent D, Strawbridge Rona J, Stoiber Marcus H, Southam Lorraine, Smith Albert V, Silveira Angela, Schurmann Claudia, Sabater-Lleal Maria, Freitag Daniel F, Fornage Myriam, Bork-Jensen Jette, Hidalgo Bertha, Lipovich Leonard, Raghavan Sridharan, Hivert Marie-France, Dauriz Marco, Brody Jennifer A, Yaghootkar Hanieh, Wang Shuai, Willems Sara M, Chu Audrey Y, Fox Keolu, Huffman Jennifer E, An Ping, Boland Anne, Besse Céline, Abrol Ravinder, Stančáková Alena, Baldridge Abigail S, Li Li, Ehm Margaret G, Grarup Niels, Rasmussen-Torvik Laura J, Lu Yingchang, Wessel Jennifer, Marouli Eirini, Kirkpatrick Andrea, Khor Chiea C, Karaleftheri Maria, Jørgensen Torben, Jørgensen Marit E, Jensen Richard A, Ikram Mohammad K, Hoffmann Per, Heo Jiyoung, Hallmans Göran, Kraja Aldi T, Kuusisto Johanna, Lange Ethan M, Mamakou Vasiliki, Malerba Giovanni, Linneberg Allan, Lindgren Cecilia M, Liu Yongmei, Liu Chunyu, Liao Jiemin, Leong Aaron, Lee Wen-Jane, Lee I T, Hai Yang, Gustafsson Stefan, Grove Megan L, Cheng Ching-Yu, Chen Yii-DerI, Chen Yuning, Burns Sean M, Bowden Donald W, Bombieri Cristina, Boehnke Michael, Bihlmeyer Nathan A, Barbieri Caterina, Aung Tin, Correa Adolfo, Czajkowski Jacek, Dehghan Abbas, Gottesman Omri, Goel Anuj, Goddard William A, Giulianini Franco, Gambaro Giovanni, Frånberg Mattias, Farmaki Aliki-Eleni, Escher Stefan A, Eiriksdottir Gudny, Ehret Georg B, Aponte Jennifer L
Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study
Varga T, Renström F, Orho-Melander M, Melander O, Nilsson P, Barroso I, Escher S, Hallmans G, Koivula R, Shungin D, Sonestedt E, Franks P. Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study. PLoS Genet 2014; 10:e1004388.
12.06.2014Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study
12.06.2014PLoS Genet 2014; 10:e1004388
Varga Tibor V, Renström Frida, Orho-Melander Marju, Melander Olle, Nilsson Peter, Barroso Inês, Escher Stefan A, Hallmans Göran, Koivula Robert W, Shungin Dmitry, Sonestedt Emily, Franks Paul W