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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

High blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal genes and pathways. To better understand the genetics of blood pressure, we genotyped 242,296 rare, low-frequency and common genetic variants in up to ~19...

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Autores principales: Surendran, Praveen, Drenos, Fotios, Young, Robin, Warren, Helen, Cook, James P, Manning, Alisa K, Grarup, Niels, Sim, Xueling, Barnes, Daniel R, Witkowska, Kate, Staley, James R, Tragante, Vinicius, Tukiainen, Taru, Yaghootkar, Hanieh, Masca, Nicholas, Freitag, Daniel F, Ferreira, Teresa, Giannakopoulou, Olga, Tinker, Andrew, Harakalova, Magdalena, Mihailov, Evelin, Liu, Chunyu, Kraja, Aldi T, Fallgaard Nielsen, Sune, Rasheed, Asif, Samuel, Maria, Zhao, Wei, Bonnycastle, Lori L, Jackson, Anne U, Narisu, Narisu, Swift, Amy J, Southam, Lorraine, Marten, Jonathan, Huyghe, Jeroen R, Stančáková, Alena, Fava, Cristiano, Ohlsson, Therese, Matchan, Angela, Stirrups, Kathleen E, Bork-Jensen, Jette, Gjesing, Anette P, Kontto, Jukka, Perola, Markus, Shaw-Hawkins, Susan, Havulinna, Aki S, Zhang, He, Donnelly, Louise A, Groves, Christopher J, Rayner, N William, Neville, Matt J, Robertson, Neil R, Yiorkas, Andrianos M, Herzig, Karl-Heinz, Kajantie, Eero, Zhang, Weihua, Willems, Sara M, Lannfelt, Lars, Malerba, Giovanni, Soranzo, Nicole, Trabetti, Elisabetta, Verweij, Niek, Evangelou, Evangelos, Moayyeri, Alireza, Vergnaud, Anne-Claire, Nelson, Christopher P, Poveda, Alaitz, Varga, Tibor V, Caslake, Muriel, de Craen, Anton JM, Trompet, Stella, Luan, Jian’an, Scott, Robert A, Harris, Sarah E, Liewald, David CM, Marioni, Riccardo, Menni, Cristina, Farmaki, Aliki-Eleni, Hallmans, Göran, Renström, Frida, Huffman, Jennifer E, Hassinen, Maija, Burgess, Stephen, Vasan, Ramachandran S, Felix, Janine F, Uria-Nickelsen, Maria, Malarstig, Anders, Reily, Dermot F, Hoek, Maarten, Vogt, Thomas, Lin, Honghuang, Lieb, Wolfgang, Traylor, Matthew, Markus, Hugh F, Highland, Heather M, Justice, Anne E, Marouli, Eirini, Lindström, Jaana, Uusitupa, Matti, Komulainen, Pirjo, Lakka, Timo A, Rauramaa, Rainer, Polasek, Ozren, Rudan, Igor, Rolandsson, Olov, Franks, Paul W, Dedoussis, George, Spector, Timothy D, Jousilahti, Pekka, Männistö, Satu, Deary, Ian J, Starr, John M, Langenberg, Claudia, Wareham, Nick J, Brown, Morris J, Dominiczak, Anna F, Connell, John M, Jukema, J Wouter, Sattar, Naveed, Ford, Ian, Packard, Chris J, Esko, Tõnu, Mägi, Reedik, Metspalu, Andres, de Boer, Rudolf A, van der Meer, Peter, van der Harst, Pim, Gambaro, Giovanni, Ingelsson, Erik, Lind, Lars, de Bakker, Paul IW, Numans, Mattijs E, Brandslund, Ivan, Christensen, Cramer, Petersen, Eva RB, Korpi-Hyövälti, Eeva, Oksa, Heikki, Chambers, John C, Kooner, Jaspal S, Blakemore, Alexandra IF, Franks, Steve, Jarvelin, Marjo-Riitta, Husemoen, Lise L, Linneberg, Allan, Skaaby, Tea, Thuesen, Betina, Karpe, Fredrik, Tuomilehto, Jaakko, Doney, Alex SF, Morris, Andrew D, Palmer, Colin NA, Holmen, Oddgeir Lingaas, Hveem, Kristian, Willer, Cristen J, Tuomi, Tiinamaija, Groop, Leif, Käräjämäki, AnneMari, Palotie, Aarno, Ripatti, Samuli, Salomaa, Veikko, Alam, Dewan S, Shafi Majumder, Abdulla al, Di Angelantonio, Emanuele, Chowdhury, Rajiv, McCarthy, Mark I, Poulter, Neil, Stanton, Alice V, Sever, Peter, Amouyel, Philippe, Arveiler, Dominique, Blankenberg, Stefan, Ferrières, Jean, Kee, Frank, Kuulasmaa, Kari, Müller-Nurasyid, Martina, Veronesi, Giovanni, Virtamo, Jarmo, Deloukas, Panos, Elliott, Paul, Zeggini, Eleftheria, Kathiresan, Sekar, Melander, Olle, Kuusisto, Johanna, Laakso, Markku, Padmanabhan, Sandosh, Porteous, David, Hayward, Caroline, Scotland, Generation, Collins, Francis S, Mohlke, Karen L, Hansen, Torben, Pedersen, Oluf, Boehnke, Michael, Stringham, Heather M, Frossard, Philippe, Newton-Cheh, Christopher, Tobin, Martin D, Nordestgaard, Børge Grønne, Caulfield, Mark J, Mahajan, Anubha, Morris, Andrew P, Tomaszewski, Maciej, Samani, Nilesh J, Saleheen, Danish, Asselbergs, Folkert W, Lindgren, Cecilia M, Danesh, John, Wain, Louise V, Butterworth, Adam S, Howson, Joanna MM, Munroe, Patricia B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056636/
https://www.ncbi.nlm.nih.gov/pubmed/27618447
http://dx.doi.org/10.1038/ng.3654
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author Surendran, Praveen
Drenos, Fotios
Young, Robin
Warren, Helen
Cook, James P
Manning, Alisa K
Grarup, Niels
Sim, Xueling
Barnes, Daniel R
Witkowska, Kate
Staley, James R
Tragante, Vinicius
Tukiainen, Taru
Yaghootkar, Hanieh
Masca, Nicholas
Freitag, Daniel F
Ferreira, Teresa
Giannakopoulou, Olga
Tinker, Andrew
Harakalova, Magdalena
Mihailov, Evelin
Liu, Chunyu
Kraja, Aldi T
Fallgaard Nielsen, Sune
Rasheed, Asif
Samuel, Maria
Zhao, Wei
Bonnycastle, Lori L
Jackson, Anne U
Narisu, Narisu
Swift, Amy J
Southam, Lorraine
Marten, Jonathan
Huyghe, Jeroen R
Stančáková, Alena
Fava, Cristiano
Ohlsson, Therese
Matchan, Angela
Stirrups, Kathleen E
Bork-Jensen, Jette
Gjesing, Anette P
Kontto, Jukka
Perola, Markus
Shaw-Hawkins, Susan
Havulinna, Aki S
Zhang, He
Donnelly, Louise A
Groves, Christopher J
Rayner, N William
Neville, Matt J
Robertson, Neil R
Yiorkas, Andrianos M
Herzig, Karl-Heinz
Kajantie, Eero
Zhang, Weihua
Willems, Sara M
Lannfelt, Lars
Malerba, Giovanni
Soranzo, Nicole
Trabetti, Elisabetta
Verweij, Niek
Evangelou, Evangelos
Moayyeri, Alireza
Vergnaud, Anne-Claire
Nelson, Christopher P
Poveda, Alaitz
Varga, Tibor V
Caslake, Muriel
de Craen, Anton JM
Trompet, Stella
Luan, Jian’an
Scott, Robert A
Harris, Sarah E
Liewald, David CM
Marioni, Riccardo
Menni, Cristina
Farmaki, Aliki-Eleni
Hallmans, Göran
Renström, Frida
Huffman, Jennifer E
Hassinen, Maija
Burgess, Stephen
Vasan, Ramachandran S
Felix, Janine F
Uria-Nickelsen, Maria
Malarstig, Anders
Reily, Dermot F
Hoek, Maarten
Vogt, Thomas
Lin, Honghuang
Lieb, Wolfgang
Traylor, Matthew
Markus, Hugh F
Highland, Heather M
Justice, Anne E
Marouli, Eirini
Lindström, Jaana
Uusitupa, Matti
Komulainen, Pirjo
Lakka, Timo A
Rauramaa, Rainer
Polasek, Ozren
Rudan, Igor
Rolandsson, Olov
Franks, Paul W
Dedoussis, George
Spector, Timothy D
Jousilahti, Pekka
Männistö, Satu
Deary, Ian J
Starr, John M
Langenberg, Claudia
Wareham, Nick J
Brown, Morris J
Dominiczak, Anna F
Connell, John M
Jukema, J Wouter
Sattar, Naveed
Ford, Ian
Packard, Chris J
Esko, Tõnu
Mägi, Reedik
Metspalu, Andres
de Boer, Rudolf A
van der Meer, Peter
van der Harst, Pim
Gambaro, Giovanni
Ingelsson, Erik
Lind, Lars
de Bakker, Paul IW
Numans, Mattijs E
Brandslund, Ivan
Christensen, Cramer
Petersen, Eva RB
Korpi-Hyövälti, Eeva
Oksa, Heikki
Chambers, John C
Kooner, Jaspal S
Blakemore, Alexandra IF
Franks, Steve
Jarvelin, Marjo-Riitta
Husemoen, Lise L
Linneberg, Allan
Skaaby, Tea
Thuesen, Betina
Karpe, Fredrik
Tuomilehto, Jaakko
Doney, Alex SF
Morris, Andrew D
Palmer, Colin NA
Holmen, Oddgeir Lingaas
Hveem, Kristian
Willer, Cristen J
Tuomi, Tiinamaija
Groop, Leif
Käräjämäki, AnneMari
Palotie, Aarno
Ripatti, Samuli
Salomaa, Veikko
Alam, Dewan S
Shafi Majumder, Abdulla al
Di Angelantonio, Emanuele
Chowdhury, Rajiv
McCarthy, Mark I
Poulter, Neil
Stanton, Alice V
Sever, Peter
Amouyel, Philippe
Arveiler, Dominique
Blankenberg, Stefan
Ferrières, Jean
Kee, Frank
Kuulasmaa, Kari
Müller-Nurasyid, Martina
Veronesi, Giovanni
Virtamo, Jarmo
Deloukas, Panos
Elliott, Paul
Zeggini, Eleftheria
Kathiresan, Sekar
Melander, Olle
Kuusisto, Johanna
Laakso, Markku
Padmanabhan, Sandosh
Porteous, David
Hayward, Caroline
Scotland, Generation
Collins, Francis S
Mohlke, Karen L
Hansen, Torben
Pedersen, Oluf
Boehnke, Michael
Stringham, Heather M
Frossard, Philippe
Newton-Cheh, Christopher
Tobin, Martin D
Nordestgaard, Børge Grønne
Caulfield, Mark J
Mahajan, Anubha
Morris, Andrew P
Tomaszewski, Maciej
Samani, Nilesh J
Saleheen, Danish
Asselbergs, Folkert W
Lindgren, Cecilia M
Danesh, John
Wain, Louise V
Butterworth, Adam S
Howson, Joanna MM
Munroe, Patricia B
author_facet Surendran, Praveen
Drenos, Fotios
Young, Robin
Warren, Helen
Cook, James P
Manning, Alisa K
Grarup, Niels
Sim, Xueling
Barnes, Daniel R
Witkowska, Kate
Staley, James R
Tragante, Vinicius
Tukiainen, Taru
Yaghootkar, Hanieh
Masca, Nicholas
Freitag, Daniel F
Ferreira, Teresa
Giannakopoulou, Olga
Tinker, Andrew
Harakalova, Magdalena
Mihailov, Evelin
Liu, Chunyu
Kraja, Aldi T
Fallgaard Nielsen, Sune
Rasheed, Asif
Samuel, Maria
Zhao, Wei
Bonnycastle, Lori L
Jackson, Anne U
Narisu, Narisu
Swift, Amy J
Southam, Lorraine
Marten, Jonathan
Huyghe, Jeroen R
Stančáková, Alena
Fava, Cristiano
Ohlsson, Therese
Matchan, Angela
Stirrups, Kathleen E
Bork-Jensen, Jette
Gjesing, Anette P
Kontto, Jukka
Perola, Markus
Shaw-Hawkins, Susan
Havulinna, Aki S
Zhang, He
Donnelly, Louise A
Groves, Christopher J
Rayner, N William
Neville, Matt J
Robertson, Neil R
Yiorkas, Andrianos M
Herzig, Karl-Heinz
Kajantie, Eero
Zhang, Weihua
Willems, Sara M
Lannfelt, Lars
Malerba, Giovanni
Soranzo, Nicole
Trabetti, Elisabetta
Verweij, Niek
Evangelou, Evangelos
Moayyeri, Alireza
Vergnaud, Anne-Claire
Nelson, Christopher P
Poveda, Alaitz
Varga, Tibor V
Caslake, Muriel
de Craen, Anton JM
Trompet, Stella
Luan, Jian’an
Scott, Robert A
Harris, Sarah E
Liewald, David CM
Marioni, Riccardo
Menni, Cristina
Farmaki, Aliki-Eleni
Hallmans, Göran
Renström, Frida
Huffman, Jennifer E
Hassinen, Maija
Burgess, Stephen
Vasan, Ramachandran S
Felix, Janine F
Uria-Nickelsen, Maria
Malarstig, Anders
Reily, Dermot F
Hoek, Maarten
Vogt, Thomas
Lin, Honghuang
Lieb, Wolfgang
Traylor, Matthew
Markus, Hugh F
Highland, Heather M
Justice, Anne E
Marouli, Eirini
Lindström, Jaana
Uusitupa, Matti
Komulainen, Pirjo
Lakka, Timo A
Rauramaa, Rainer
Polasek, Ozren
Rudan, Igor
Rolandsson, Olov
Franks, Paul W
Dedoussis, George
Spector, Timothy D
Jousilahti, Pekka
Männistö, Satu
Deary, Ian J
Starr, John M
Langenberg, Claudia
Wareham, Nick J
Brown, Morris J
Dominiczak, Anna F
Connell, John M
Jukema, J Wouter
Sattar, Naveed
Ford, Ian
Packard, Chris J
Esko, Tõnu
Mägi, Reedik
Metspalu, Andres
de Boer, Rudolf A
van der Meer, Peter
van der Harst, Pim
Gambaro, Giovanni
Ingelsson, Erik
Lind, Lars
de Bakker, Paul IW
Numans, Mattijs E
Brandslund, Ivan
Christensen, Cramer
Petersen, Eva RB
Korpi-Hyövälti, Eeva
Oksa, Heikki
Chambers, John C
Kooner, Jaspal S
Blakemore, Alexandra IF
Franks, Steve
Jarvelin, Marjo-Riitta
Husemoen, Lise L
Linneberg, Allan
Skaaby, Tea
Thuesen, Betina
Karpe, Fredrik
Tuomilehto, Jaakko
Doney, Alex SF
Morris, Andrew D
Palmer, Colin NA
Holmen, Oddgeir Lingaas
Hveem, Kristian
Willer, Cristen J
Tuomi, Tiinamaija
Groop, Leif
Käräjämäki, AnneMari
Palotie, Aarno
Ripatti, Samuli
Salomaa, Veikko
Alam, Dewan S
Shafi Majumder, Abdulla al
Di Angelantonio, Emanuele
Chowdhury, Rajiv
McCarthy, Mark I
Poulter, Neil
Stanton, Alice V
Sever, Peter
Amouyel, Philippe
Arveiler, Dominique
Blankenberg, Stefan
Ferrières, Jean
Kee, Frank
Kuulasmaa, Kari
Müller-Nurasyid, Martina
Veronesi, Giovanni
Virtamo, Jarmo
Deloukas, Panos
Elliott, Paul
Zeggini, Eleftheria
Kathiresan, Sekar
Melander, Olle
Kuusisto, Johanna
Laakso, Markku
Padmanabhan, Sandosh
Porteous, David
Hayward, Caroline
Scotland, Generation
Collins, Francis S
Mohlke, Karen L
Hansen, Torben
Pedersen, Oluf
Boehnke, Michael
Stringham, Heather M
Frossard, Philippe
Newton-Cheh, Christopher
Tobin, Martin D
Nordestgaard, Børge Grønne
Caulfield, Mark J
Mahajan, Anubha
Morris, Andrew P
Tomaszewski, Maciej
Samani, Nilesh J
Saleheen, Danish
Asselbergs, Folkert W
Lindgren, Cecilia M
Danesh, John
Wain, Louise V
Butterworth, Adam S
Howson, Joanna MM
Munroe, Patricia B
author_sort Surendran, Praveen
collection PubMed
description High blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal genes and pathways. To better understand the genetics of blood pressure, we genotyped 242,296 rare, low-frequency and common genetic variants in up to ~192,000 individuals, and used ~155,063 samples for independent replication. We identified 31 novel blood pressure or hypertension associated genetic regions in the general population, including three rare missense variants in RBM47, COL21A1 and RRAS with larger effects (>1.5mmHg/allele) than common variants. Multiple rare, nonsense and missense variant associations were found in A2ML1 and a low-frequency nonsense variant in ENPEP was identified. Our data extend the spectrum of allelic variation underlying blood pressure traits and hypertension, provide new insights into the pathophysiology of hypertension and indicate new targets for clinical intervention.
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spelling pubmed-50566362017-03-12 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension Surendran, Praveen Drenos, Fotios Young, Robin Warren, Helen Cook, James P Manning, Alisa K Grarup, Niels Sim, Xueling Barnes, Daniel R Witkowska, Kate Staley, James R Tragante, Vinicius Tukiainen, Taru Yaghootkar, Hanieh Masca, Nicholas Freitag, Daniel F Ferreira, Teresa Giannakopoulou, Olga Tinker, Andrew Harakalova, Magdalena Mihailov, Evelin Liu, Chunyu Kraja, Aldi T Fallgaard Nielsen, Sune Rasheed, Asif Samuel, Maria Zhao, Wei Bonnycastle, Lori L Jackson, Anne U Narisu, Narisu Swift, Amy J Southam, Lorraine Marten, Jonathan Huyghe, Jeroen R Stančáková, Alena Fava, Cristiano Ohlsson, Therese Matchan, Angela Stirrups, Kathleen E Bork-Jensen, Jette Gjesing, Anette P Kontto, Jukka Perola, Markus Shaw-Hawkins, Susan Havulinna, Aki S Zhang, He Donnelly, Louise A Groves, Christopher J Rayner, N William Neville, Matt J Robertson, Neil R Yiorkas, Andrianos M Herzig, Karl-Heinz Kajantie, Eero Zhang, Weihua Willems, Sara M Lannfelt, Lars Malerba, Giovanni Soranzo, Nicole Trabetti, Elisabetta Verweij, Niek Evangelou, Evangelos Moayyeri, Alireza Vergnaud, Anne-Claire Nelson, Christopher P Poveda, Alaitz Varga, Tibor V Caslake, Muriel de Craen, Anton JM Trompet, Stella Luan, Jian’an Scott, Robert A Harris, Sarah E Liewald, David CM Marioni, Riccardo Menni, Cristina Farmaki, Aliki-Eleni Hallmans, Göran Renström, Frida Huffman, Jennifer E Hassinen, Maija Burgess, Stephen Vasan, Ramachandran S Felix, Janine F Uria-Nickelsen, Maria Malarstig, Anders Reily, Dermot F Hoek, Maarten Vogt, Thomas Lin, Honghuang Lieb, Wolfgang Traylor, Matthew Markus, Hugh F Highland, Heather M Justice, Anne E Marouli, Eirini Lindström, Jaana Uusitupa, Matti Komulainen, Pirjo Lakka, Timo A Rauramaa, Rainer Polasek, Ozren Rudan, Igor Rolandsson, Olov Franks, Paul W Dedoussis, George Spector, Timothy D Jousilahti, Pekka Männistö, Satu Deary, Ian J Starr, John M Langenberg, Claudia Wareham, Nick J Brown, Morris J Dominiczak, Anna F Connell, John M Jukema, J Wouter Sattar, Naveed Ford, Ian Packard, Chris J Esko, Tõnu Mägi, Reedik Metspalu, Andres de Boer, Rudolf A van der Meer, Peter van der Harst, Pim Gambaro, Giovanni Ingelsson, Erik Lind, Lars de Bakker, Paul IW Numans, Mattijs E Brandslund, Ivan Christensen, Cramer Petersen, Eva RB Korpi-Hyövälti, Eeva Oksa, Heikki Chambers, John C Kooner, Jaspal S Blakemore, Alexandra IF Franks, Steve Jarvelin, Marjo-Riitta Husemoen, Lise L Linneberg, Allan Skaaby, Tea Thuesen, Betina Karpe, Fredrik Tuomilehto, Jaakko Doney, Alex SF Morris, Andrew D Palmer, Colin NA Holmen, Oddgeir Lingaas Hveem, Kristian Willer, Cristen J Tuomi, Tiinamaija Groop, Leif Käräjämäki, AnneMari Palotie, Aarno Ripatti, Samuli Salomaa, Veikko Alam, Dewan S Shafi Majumder, Abdulla al Di Angelantonio, Emanuele Chowdhury, Rajiv McCarthy, Mark I Poulter, Neil Stanton, Alice V Sever, Peter Amouyel, Philippe Arveiler, Dominique Blankenberg, Stefan Ferrières, Jean Kee, Frank Kuulasmaa, Kari Müller-Nurasyid, Martina Veronesi, Giovanni Virtamo, Jarmo Deloukas, Panos Elliott, Paul Zeggini, Eleftheria Kathiresan, Sekar Melander, Olle Kuusisto, Johanna Laakso, Markku Padmanabhan, Sandosh Porteous, David Hayward, Caroline Scotland, Generation Collins, Francis S Mohlke, Karen L Hansen, Torben Pedersen, Oluf Boehnke, Michael Stringham, Heather M Frossard, Philippe Newton-Cheh, Christopher Tobin, Martin D Nordestgaard, Børge Grønne Caulfield, Mark J Mahajan, Anubha Morris, Andrew P Tomaszewski, Maciej Samani, Nilesh J Saleheen, Danish Asselbergs, Folkert W Lindgren, Cecilia M Danesh, John Wain, Louise V Butterworth, Adam S Howson, Joanna MM Munroe, Patricia B Nat Genet Article High blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal genes and pathways. To better understand the genetics of blood pressure, we genotyped 242,296 rare, low-frequency and common genetic variants in up to ~192,000 individuals, and used ~155,063 samples for independent replication. We identified 31 novel blood pressure or hypertension associated genetic regions in the general population, including three rare missense variants in RBM47, COL21A1 and RRAS with larger effects (>1.5mmHg/allele) than common variants. Multiple rare, nonsense and missense variant associations were found in A2ML1 and a low-frequency nonsense variant in ENPEP was identified. Our data extend the spectrum of allelic variation underlying blood pressure traits and hypertension, provide new insights into the pathophysiology of hypertension and indicate new targets for clinical intervention. 2016-09-12 2016-10 /pmc/articles/PMC5056636/ /pubmed/27618447 http://dx.doi.org/10.1038/ng.3654 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Surendran, Praveen
Drenos, Fotios
Young, Robin
Warren, Helen
Cook, James P
Manning, Alisa K
Grarup, Niels
Sim, Xueling
Barnes, Daniel R
Witkowska, Kate
Staley, James R
Tragante, Vinicius
Tukiainen, Taru
Yaghootkar, Hanieh
Masca, Nicholas
Freitag, Daniel F
Ferreira, Teresa
Giannakopoulou, Olga
Tinker, Andrew
Harakalova, Magdalena
Mihailov, Evelin
Liu, Chunyu
Kraja, Aldi T
Fallgaard Nielsen, Sune
Rasheed, Asif
Samuel, Maria
Zhao, Wei
Bonnycastle, Lori L
Jackson, Anne U
Narisu, Narisu
Swift, Amy J
Southam, Lorraine
Marten, Jonathan
Huyghe, Jeroen R
Stančáková, Alena
Fava, Cristiano
Ohlsson, Therese
Matchan, Angela
Stirrups, Kathleen E
Bork-Jensen, Jette
Gjesing, Anette P
Kontto, Jukka
Perola, Markus
Shaw-Hawkins, Susan
Havulinna, Aki S
Zhang, He
Donnelly, Louise A
Groves, Christopher J
Rayner, N William
Neville, Matt J
Robertson, Neil R
Yiorkas, Andrianos M
Herzig, Karl-Heinz
Kajantie, Eero
Zhang, Weihua
Willems, Sara M
Lannfelt, Lars
Malerba, Giovanni
Soranzo, Nicole
Trabetti, Elisabetta
Verweij, Niek
Evangelou, Evangelos
Moayyeri, Alireza
Vergnaud, Anne-Claire
Nelson, Christopher P
Poveda, Alaitz
Varga, Tibor V
Caslake, Muriel
de Craen, Anton JM
Trompet, Stella
Luan, Jian’an
Scott, Robert A
Harris, Sarah E
Liewald, David CM
Marioni, Riccardo
Menni, Cristina
Farmaki, Aliki-Eleni
Hallmans, Göran
Renström, Frida
Huffman, Jennifer E
Hassinen, Maija
Burgess, Stephen
Vasan, Ramachandran S
Felix, Janine F
Uria-Nickelsen, Maria
Malarstig, Anders
Reily, Dermot F
Hoek, Maarten
Vogt, Thomas
Lin, Honghuang
Lieb, Wolfgang
Traylor, Matthew
Markus, Hugh F
Highland, Heather M
Justice, Anne E
Marouli, Eirini
Lindström, Jaana
Uusitupa, Matti
Komulainen, Pirjo
Lakka, Timo A
Rauramaa, Rainer
Polasek, Ozren
Rudan, Igor
Rolandsson, Olov
Franks, Paul W
Dedoussis, George
Spector, Timothy D
Jousilahti, Pekka
Männistö, Satu
Deary, Ian J
Starr, John M
Langenberg, Claudia
Wareham, Nick J
Brown, Morris J
Dominiczak, Anna F
Connell, John M
Jukema, J Wouter
Sattar, Naveed
Ford, Ian
Packard, Chris J
Esko, Tõnu
Mägi, Reedik
Metspalu, Andres
de Boer, Rudolf A
van der Meer, Peter
van der Harst, Pim
Gambaro, Giovanni
Ingelsson, Erik
Lind, Lars
de Bakker, Paul IW
Numans, Mattijs E
Brandslund, Ivan
Christensen, Cramer
Petersen, Eva RB
Korpi-Hyövälti, Eeva
Oksa, Heikki
Chambers, John C
Kooner, Jaspal S
Blakemore, Alexandra IF
Franks, Steve
Jarvelin, Marjo-Riitta
Husemoen, Lise L
Linneberg, Allan
Skaaby, Tea
Thuesen, Betina
Karpe, Fredrik
Tuomilehto, Jaakko
Doney, Alex SF
Morris, Andrew D
Palmer, Colin NA
Holmen, Oddgeir Lingaas
Hveem, Kristian
Willer, Cristen J
Tuomi, Tiinamaija
Groop, Leif
Käräjämäki, AnneMari
Palotie, Aarno
Ripatti, Samuli
Salomaa, Veikko
Alam, Dewan S
Shafi Majumder, Abdulla al
Di Angelantonio, Emanuele
Chowdhury, Rajiv
McCarthy, Mark I
Poulter, Neil
Stanton, Alice V
Sever, Peter
Amouyel, Philippe
Arveiler, Dominique
Blankenberg, Stefan
Ferrières, Jean
Kee, Frank
Kuulasmaa, Kari
Müller-Nurasyid, Martina
Veronesi, Giovanni
Virtamo, Jarmo
Deloukas, Panos
Elliott, Paul
Zeggini, Eleftheria
Kathiresan, Sekar
Melander, Olle
Kuusisto, Johanna
Laakso, Markku
Padmanabhan, Sandosh
Porteous, David
Hayward, Caroline
Scotland, Generation
Collins, Francis S
Mohlke, Karen L
Hansen, Torben
Pedersen, Oluf
Boehnke, Michael
Stringham, Heather M
Frossard, Philippe
Newton-Cheh, Christopher
Tobin, Martin D
Nordestgaard, Børge Grønne
Caulfield, Mark J
Mahajan, Anubha
Morris, Andrew P
Tomaszewski, Maciej
Samani, Nilesh J
Saleheen, Danish
Asselbergs, Folkert W
Lindgren, Cecilia M
Danesh, John
Wain, Louise V
Butterworth, Adam S
Howson, Joanna MM
Munroe, Patricia B
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
title Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
title_full Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
title_fullStr Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
title_full_unstemmed Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
title_short Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
title_sort trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056636/
https://www.ncbi.nlm.nih.gov/pubmed/27618447
http://dx.doi.org/10.1038/ng.3654
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