Giovanni Malerba
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Palotie A, Linneberg A, Husemoen L, Jarvelin M, Franks S, Blakemore A, Kooner J, Chambers J, Oksa H, Korpi-Hyövälti E, Petersen E, Christensen C, Skaaby T, Thuesen B, Käräjämäki A, Groop L, Tuomi T, Willer C, Hveem K, Holmen O, Palmer C, Morris A, Doney A, Tuomilehto J, Karpe F, Brandslund I, Numans M, Jukema J, Connell J, Dominiczak A, Brown M, Wareham N, Langenberg C, Starr J, Deary I, Männistö S, Jousilahti P, Spector T, Sattar N, Ford I, de Bakker P, Lind L, Ingelsson E, Gambaro G, van der Harst P, van der Meer P, de Boer R, Metspalu A, Mägi R, Esko T, Packard C, Dedoussis G, Ripatti S, Munroe P, Tobin M, Newton-Cheh C, Frossard P, Stringham H, Boehnke M, Pedersen O, Hansen T, Mohlke K, Collins F, Scotland G, Hayward C, Nordestgaard B, Caulfield M, Howson J, Butterworth A, Wain L, Danesh J, Lindgren C, Asselbergs F, Saleheen D, Samani N, Tomaszewski M, Morris A, Mahajan A, Porteous D, Padmanabhan S, Blankenberg S, Arveiler D, Amouyel P, Sever P, Stanton A, Poulter N, McCarthy M, Chowdhury R, Di Angelantonio E, Shafi Majumder A, Alam D, Ferrieres J, Kee F, Laakso M, Kuusisto J, Melander O, Kathiresan S, Zeggini E, Elliott P, Deloukas P, Virtamo J, Veronesi G, Müller-Nurasyid M, Kuulasmaa K, Salomaa V, Franks P, Yiorkas A, Matchan A, Ohlsson T, Fava C, Stančáková A, Huyghe J, Marten J, Southam L, Swift A, Narisu N, Jackson A, Bonnycastle L, Stirrups K, Bork-Jensen J, Robertson N, Neville M, Rayner N, Groves C, Donnelly L, Zhang H, Havulinna A, Shaw-Hawkins S, Perola M, Kontto J, Gjesing A, Zhao W, Samuel M, Tragante V, Staley J, Witkowska K, Barnes D, Sim X, Grarup N, Manning A, Cook J, Warren H, Young R, Drenos F, Tukiainen T, Yaghootkar H, Rasheed A, Fallgaard Nielsen S, Kraja A, Liu C, Mihailov E, Harakalova M, Tinker A, Giannakopoulou O, Ferreira T, Freitag D, Masca N, Surendran P, Herzig K, Rolandsson O, Lin H, Vogt T, Hoek M, Reily D, Malarstig A, Uria-Nickelsen M, Felix J, Vasan R, Burgess S, Hassinen M, Lieb W, Traylor M, Rudan I, Polasek O, Rauramaa R, Lakka T, Komulainen P, Uusitupa M, Lindström J, Marouli E, Justice A, Highland H, Markus H, Huffman J, Renström F, Nelson C, Vergnaud A, Moayyeri A, Evangelou E, Verweij N, Trabetti E, Soranzo N, Malerba G, Lannfelt L, Willems S, Zhang W, Poveda A, Varga T, Hallmans G, Farmaki A, Menni C, Marioni R, Liewald D, Harris S, Scott R, Luan J, Trompet S, de Craen A, Caslake M, Kajantie E. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat Genet 2016; 48:1151-1161.
12.09.2016Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
12.09.2016Nat Genet 2016; 48:1151-1161
Palotie Aarno, Linneberg Allan, Husemoen Lise L, Jarvelin Marjo-Riitta, Franks Steve, Blakemore Alexandra If, Kooner Jaspal S, Chambers John C, Oksa Heikki, Korpi-Hyövälti Eeva, Petersen Eva Rb, Christensen Cramer, Skaaby Tea, Thuesen Betina, Käräjämäki AnneMari, Groop Leif, Tuomi Tiinamaija, Willer Cristen J, Hveem Kristian, Holmen Oddgeir Lingaas, Palmer Colin Na, Morris Andrew D, Doney Alex Sf, Tuomilehto Jaakko, Karpe Fredrik, Brandslund Ivan, Numans Mattijs E, Jukema J Wouter, Connell John M, Dominiczak Anna F, Brown Morris J, Wareham Nick J, Langenberg Claudia, Starr John M, Deary Ian J, Männistö Satu, Jousilahti Pekka, Spector Timothy D, Sattar Naveed, Ford Ian, de Bakker Paul Iw, Lind Lars, Ingelsson Erik, Gambaro Giovanni, van der Harst Pim, van der Meer Peter, de Boer Rudolf A, Metspalu Andres, Mägi Reedik, Esko Tõnu, Packard Chris J, Dedoussis George, Ripatti Samuli, Munroe Patricia B, Tobin Martin D, Newton-Cheh Christopher, Frossard Philippe, Stringham Heather M, Boehnke Michael, Pedersen Oluf, Hansen Torben, Mohlke Karen L, Collins Francis S, Scotland Generation, Hayward Caroline, Nordestgaard Børge Grønne, Caulfield Mark J, Howson Joanna Mm, Butterworth Adam S, Wain Louise V, Danesh John, Lindgren Cecilia M, Asselbergs Folkert W, Saleheen Danish, Samani Nilesh J, Tomaszewski Maciej, Morris Andrew P, Mahajan Anubha, Porteous David, Padmanabhan Sandosh, Blankenberg Stefan, Arveiler Dominique, Amouyel Philippe, Sever Peter, Stanton Alice V, Poulter Neil, McCarthy Mark I, Chowdhury Rajiv, Di Angelantonio Emanuele, Shafi Majumder Abdulla Al, Alam Dewan S, Ferrieres Jean, Kee Frank, Laakso Markku, Kuusisto Johanna, Melander Olle, Kathiresan Sekar, Zeggini Eleftheria, Elliott Paul, Deloukas Panos, Virtamo Jarmo, Veronesi Giovanni, Müller-Nurasyid Martina, Kuulasmaa Kari, Salomaa Veikko, Franks Paul W, Yiorkas Andrianos M, Matchan Angela, Ohlsson Therese, Fava Cristiano, Stančáková Alena, Huyghe Jeroen R, Marten Jonathan, Southam Lorraine, Swift Amy J, Narisu Narisu, Jackson Anne U, Bonnycastle Lori L, Stirrups Kathleen E, Bork-Jensen Jette, Robertson Neil R, Neville Matt J, Rayner N William, Groves Christopher J, Donnelly Louise A, Zhang He, Havulinna Aki S, Shaw-Hawkins Susan, Perola Markus, Kontto Jukka, Gjesing Anette P, Zhao Wei, Samuel Maria, Tragante Vinicius, Staley James R, Witkowska Kate, Barnes Daniel R, Sim Xueling, Grarup Niels, Manning Alisa K, Cook James P, Warren Helen, Young Robin, Drenos Fotios, Tukiainen Taru, Yaghootkar Hanieh, Rasheed Asif, Fallgaard Nielsen Sune, Kraja Aldi T, Liu Chunyu, Mihailov Evelin, Harakalova Magdalena, Tinker Andrew, Giannakopoulou Olga, Ferreira Teresa, Freitag Daniel F, Masca Nicholas, Surendran Praveen, Herzig Karl-Heinz, Rolandsson Olov, Lin Honghuang, Vogt Thomas, Hoek Maarten, Reily Dermot F, Malarstig Anders, Uria-Nickelsen Maria, Felix Janine F, Vasan Ramachandran S, Burgess Stephen, Hassinen Maija, Lieb Wolfgang, Traylor Matthew, Rudan Igor, Polasek Ozren, Rauramaa Rainer, Lakka Timo A, Komulainen Pirjo, Uusitupa Matti, Lindström Jaana, Marouli Eirini, Justice Anne E, Highland Heather M, Markus Hugh F, Huffman Jennifer E, Renström Frida, Nelson Christopher P, Vergnaud Anne-Claire, Moayyeri Alireza, Evangelou Evangelos, Verweij Niek, Trabetti Elisabetta, Soranzo Nicole, Malerba Giovanni, Lannfelt Lars, Willems Sara M, Zhang Weihua, Poveda Alaitz, Varga Tibor V, Hallmans Göran, Farmaki Aliki-Eleni, Menni Cristina, Marioni Riccardo, Liewald David Cm, Harris Sarah E, Scott Robert A, Luan Jian'an, Trompet Stella, de Craen Anton Jm, Caslake Muriel, Kajantie Eero
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