Human Genome Epidemiology Literature Finder
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Records 1 - 28 (of 28 Records) |
| Query Trace: Migraine[original query] |
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Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement.
Neurology. Genetics 2022 2 8 (1): e653. Daghals Iyas, Sargurupremraj Muralidharan, Danning Rebecca, Gormley Padhraig, Malik Rainer, Amouyel Philippe, Metso Tiina, Pezzini Alessandro, Kurth Tobias, Debette Stéphanie, Chasman Dani |
| A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches.
Phenomics (Cham, Switzerland) 2023 3 3 (1): 64-76. Meng Weihua, Reel Parminder S, Nangia Charvi, Rajendrakumar Aravind Lathika, Hebert Harry L, Guo Qian, Adams Mark J, Zheng Hua, Lu Zen Haut, , Ray Debashree, Colvin Lesley A, Palmer Colin N A, McIntosh Andrew M, Smith Blair |
| Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
Nature genetics 2010 Oct 42 (10): 869-73. Anttila Verneri, Stefansson Hreinn, Kallela Mikko, Todt Unda, Terwindt Gisela M, Calafato M Stella, Nyholt Dale R, Dimas Antigone S, Freilinger Tobias, Müller-Myhsok Bertram, Artto Ville, Inouye Michael, Alakurtti Kirsi, Kaunisto Mari A, Hämäläinen Eija, de Vries Boukje, Stam Anine H, Weller Claudia M, Heinze Axel, Heinze-Kuhn Katja, Goebel Ingrid, Borck Guntram, Göbel Hartmut, Steinberg Stacy, Wolf Christiane, Björnsson Asgeir, Gudmundsson Gretar, Kirchmann Malene, Hauge Anne, Werge Thomas, Schoenen Jean, Eriksson Johan G, Hagen Knut, Stovner Lars, Wichmann H-Erich, Meitinger Thomas, Alexander Michael, Moebus Susanne, Schreiber Stefan, Aulchenko Yurii S, Breteler Monique M B, Uitterlinden Andre G, Hofman Albert, van Duijn Cornelia M, Tikka-Kleemola Päivi, Vepsäläinen Salli, Lucae Susanne, Tozzi Federica, Muglia Pierandrea, Barrett Jeffrey, Kaprio Jaakko, Färkkilä Markus, Peltonen Leena, Stefansson Kari, Zwart John-Anker, Ferrari Michel D, Olesen Jes, Daly Mark, Wessman Maija, van den Maagdenberg Arn M J M, Dichgans Martin, Kubisch Christian, Dermitzakis Emmanouil T, Frants Rune R, Palotie Aarno, |
| Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.
PloS one 2011 6 (7): e22106. Schürks Markus, Buring Julie E, Ridker Paul M, Chasman Daniel I, Kurth Tobi |
| Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
Nature genetics 2011 Jul 43 (7): 695-8. Chasman Daniel I, Schürks Markus, Anttila Verneri, de Vries Boukje, Schminke Ulf, Launer Lenore J, Terwindt Gisela M, van den Maagdenberg Arn M J M, Fendrich Konstanze, Völzke Henry, Ernst Florian, Griffiths Lyn R, Buring Julie E, Kallela Mikko, Freilinger Tobias, Kubisch Christian, Ridker Paul M, Palotie Aarno, Ferrari Michel D, Hoffmann Wolfgang, Zee Robert Y L, Kurth Tobi |
| Meta-analysis of genome-wide association for migraine in six population-based European cohorts.
European journal of human genetics : EJHG 2011 Aug 19 (8): 901-7. Ligthart Lannie, de Vries Boukje, Smith Albert V, Ikram M Arfan, Amin Najaf, Hottenga Jouke-Jan, Koelewijn Stephany C, Kattenberg V Mathijs, de Moor Marleen H M, Janssens A Cecile J W, Aulchenko Yurii S, Oostra Ben A, de Geus Eco J C, Smit Johannes H, Zitman Frans G, Uitterlinden André G, Hofman Albert, Willemsen Gonneke, Nyholt Dale R, Montgomery Grant W, Terwindt Gisela M, Gudnason Vilmundur, Penninx Brenda W J H, Breteler Monique, Ferrari Michel D, Launer Lenore J, van Duijn Cornelia M, van den Maagdenberg Arn M J M, Boomsma Dorret |
| Genome-wide association analysis identifies susceptibility loci for migraine without aura.
Nature genetics 2012 Jul 44 (7): 777-82. Freilinger Tobias, Anttila Verneri, de Vries Boukje, Malik Rainer, Kallela Mikko, Terwindt Gisela M, Pozo-Rosich Patricia, Winsvold Bendik, Nyholt Dale R, van Oosterhout Willebrordus P J, Artto Ville, Todt Unda, Hämäläinen Eija, Fernández-Morales Jèssica, Louter Mark A, Kaunisto Mari A, Schoenen Jean, Raitakari Olli, Lehtimäki Terho, Vila-Pueyo Marta, Göbel Hartmut, Wichmann Erich, Sintas Cèlia, Uitterlinden Andre G, Hofman Albert, Rivadeneira Fernando, Heinze Axel, Tronvik Erling, van Duijn Cornelia M, Kaprio Jaakko, Cormand Bru, Wessman Maija, Frants Rune R, Meitinger Thomas, Müller-Myhsok Bertram, Zwart John-Anker, Färkkilä Markus, Macaya Alfons, Ferrari Michel D, Kubisch Christian, Palotie Aarno, Dichgans Martin, van den Maagdenberg Arn M J M, |
| Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Nature genetics 2013 Aug 45 (8): 912-7. Anttila Verneri, Winsvold Bendik S, Gormley Padhraig, Kurth Tobias, Bettella Francesco, McMahon George, Kallela Mikko, Malik Rainer, de Vries Boukje, Terwindt Gisela, Medland Sarah E, Todt Unda, McArdle Wendy L, Quaye Lydia, Koiranen Markku, Ikram M Arfan, Lehtimäki Terho, Stam Anine H, Ligthart Lannie, Wedenoja Juho, Dunham Ian, Neale Benjamin M, Palta Priit, Hamalainen Eija, Schürks Markus, Rose Lynda M, Buring Julie E, Ridker Paul M, Steinberg Stacy, Stefansson Hreinn, Jakobsson Finnbogi, Lawlor Debbie A, Evans David M, Ring Susan M, Färkkilä Markus, Artto Ville, Kaunisto Mari A, Freilinger Tobias, Schoenen Jean, Frants Rune R, Pelzer Nadine, Weller Claudia M, Zielman Ronald, Heath Andrew C, Madden Pamela A F, Montgomery Grant W, Martin Nicholas G, Borck Guntram, Göbel Hartmut, Heinze Axel, Heinze-Kuhn Katja, Williams Frances M K, Hartikainen Anna-Liisa, Pouta Anneli, van den Ende Joyce, Uitterlinden Andre G, Hofman Albert, Amin Najaf, Hottenga Jouke-Jan, Vink Jacqueline M, Heikkilä Kauko, Alexander Michael, Muller-Myhsok Bertram, Schreiber Stefan, Meitinger Thomas, Wichmann Heinz Erich, Aromaa Arpo, Eriksson Johan G, Traynor Bryan J, Trabzuni Daniah, Rossin Elizabeth, Lage Kasper, Jacobs Suzanne B R, Gibbs J Raphael, Birney Ewan, Kaprio Jaakko, Penninx Brenda W, Boomsma Dorret I, van Duijn Cornelia, Raitakari Olli, Jarvelin Marjo-Riitta, Zwart John-Anker, Cherkas Lynn, Strachan David P, Kubisch Christian, Ferrari Michel D, van den Maagdenberg Arn M J M, Dichgans Martin, Wessman Maija, Smith George Davey, Stefansson Kari, Daly Mark J, Nyholt Dale R, Chasman Daniel I, Palotie Aarno, , , |
| Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.
Nature genetics 2015 Jan 47 (1): 78-83. Debette Stéphanie, Kamatani Yoichiro, Metso Tiina M, Kloss Manja, Chauhan Ganesh, Engelter Stefan T, Pezzini Alessandro, Thijs Vincent, Markus Hugh S, Dichgans Martin, Wolf Christiane, Dittrich Ralf, Touzé Emmanuel, Southerland Andrew M, Samson Yves, Abboud Shérine, Béjot Yannick, Caso Valeria, Bersano Anna, Gschwendtner Andreas, Sessa Maria, Cole John, Lamy Chantal, Medeiros Elisabeth, Beretta Simone, Bonati Leo H, Grau Armin J, Michel Patrik, Majersik Jennifer J, Sharma Pankaj, Kalashnikova Ludmila, Nazarova Maria, Dobrynina Larisa, Bartels Eva, Guillon Benoit, van den Herik Evita G, Fernandez-Cadenas Israel, Jood Katarina, Nalls Michael A, De Leeuw Frank-Erik, Jern Christina, Cheng Yu-Ching, Werner Inge, Metso Antti J, Lichy Christoph, Lyrer Philippe A, Brandt Tobias, Boncoraglio Giorgio B, Wichmann Heinz-Erich, Gieger Christian, Johnson Andrew D, Böttcher Thomas, Castellano Maurizio, Arveiler Dominique, Ikram M Arfan, Breteler Monique M B, Padovani Alessandro, Meschia James F, Kuhlenbäumer Gregor, Rolfs Arndt, Worrall Bradford B, , Ringelstein Erich-Bernd, Zelenika Diana, Tatlisumak Turgut, Lathrop Mark, Leys Didier, , Amouyel Philippe, Dallongeville Jean, |
| Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Nature genetics 2016 Aug 48 (8): 856-66. Gormley Padhraig, Anttila Verneri, Winsvold Bendik S, Palta Priit, Esko Tonu, Pers Tune H, Farh Kai-How, Cuenca-Leon Ester, Muona Mikko, Furlotte Nicholas A, Kurth Tobias, Ingason Andres, McMahon George, Ligthart Lannie, Terwindt Gisela M, Kallela Mikko, Freilinger Tobias M, Ran Caroline, Gordon Scott G, Stam Anine H, Steinberg Stacy, Borck Guntram, Koiranen Markku, Quaye Lydia, Adams Hieab H H, Lehtimäki Terho, Sarin Antti-Pekka, Wedenoja Juho, Hinds David A, Buring Julie E, Schürks Markus, Ridker Paul M, Hrafnsdottir Maria Gudlaug, Stefansson Hreinn, Ring Susan M, Hottenga Jouke-Jan, Penninx Brenda W J H, Färkkilä Markus, Artto Ville, Kaunisto Mari, Vepsäläinen Salli, Malik Rainer, Heath Andrew C, Madden Pamela A F, Martin Nicholas G, Montgomery Grant W, Kurki Mitja I, Kals Mart, Mägi Reedik, Pärn Kalle, Hämäläinen Eija, Huang Hailiang, Byrnes Andrea E, Franke Lude, Huang Jie, Stergiakouli Evie, Lee Phil H, Sandor Cynthia, Webber Caleb, Cader Zameel, Muller-Myhsok Bertram, Schreiber Stefan, Meitinger Thomas, Eriksson Johan G, Salomaa Veikko, Heikkilä Kauko, Loehrer Elizabeth, Uitterlinden Andre G, Hofman Albert, van Duijn Cornelia M, Cherkas Lynn, Pedersen Linda M, Stubhaug Audun, Nielsen Christopher S, Männikkö Minna, Mihailov Evelin, Milani Lili, Göbel Hartmut, Esserlind Ann-Louise, Christensen Anne Francke, Hansen Thomas Folkmann, Werge Thomas, , Kaprio Jaakko, Aromaa Arpo J, Raitakari Olli, Ikram M Arfan, Spector Tim, Järvelin Marjo-Riitta, Metspalu Andres, Kubisch Christian, Strachan David P, Ferrari Michel D, Belin Andrea C, Dichgans Martin, Wessman Maija, van den Maagdenberg Arn M J M, Zwart John-Anker, Boomsma Dorret I, Smith George Davey, Stefansson Kari, Eriksson Nicholas, Daly Mark J, Neale Benjamin M, Olesen Jes, Chasman Daniel I, Nyholt Dale R, Palotie Aar |
| Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.
Cephalalgia : an international journal of headache 2017 Jan 333102417695105. Chen Shih-Pin, Fuh Jong-Ling, Chung Ming-Yi, Lin Ying-Chao, Liao Yi-Chu, Wang Yen-Feng, Hsu Chia-Lin, Yang Ueng-Cheng, Lin Ming-Wei, Chiou Jen-Jie, Wang Po-Jen, Chen Ping-Kun, Fan Pi-Chuan, Wu Jer-Yuan, Chen Yuan-Tsong, Kao Lung-Sen, Shen-Jang Fann Cathy, Wang Shuu-Ji |
| Heritability and genome-wide associations studies of cerebral blood flow in the general population.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2017 06 271678X17715861. Ikram M Arfan, Zonneveld Hazel I, Roshchupkin Gennady, Smith Albert V, Franco Oscar H, Sigurdsson Sigurdur, van Duijn Cornelia, Uitterlinden André G, Launer Lenore J, Vernooij Meike W, Gudnason Vilmundur, Adams Hieab |
| Common variants at 5q33.1 predispose to migraine in African-American children.
Journal of medical genetics 2018 Sep . Chang Xiao, Pellegrino Renata, Garifallou James, March Michael, Snyder James, Mentch Frank, Li Jin, Hou Cuiping, Liu Yichuan, Sleiman Patrick M A, Hakonarson Hak |
| A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773).
EBioMedicine 2018 Feb 28 180-186. Meng Weihua, Adams Mark J, Hebert Harry L, Deary Ian J, McIntosh Andrew M, Smith Blair |
| Association of genetic variants in migraineurs with and without restless legs syndrome.
Annals of clinical and translational neurology 2020 Sep . Lin Guan-Yu, Lin Yu-Kai, Liang Chih-Sung, Lee Jiunn-Tay, Tsai Chia-Lin, Hung Kuo-Sheng, Luo Wen-Jie, Tsai Chia-Kuang, Hsu Yu-Wei, Ho Tsung-Han, Yang Fu-C |
| A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.
Nature communications 2020 07 11 (1): 3368. Guo Yanjun, Rist Pamela M, Daghlas Iyas, Giulianini Franco, , , Kurth Tobias, Chasman Daniel |
| Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity.
Genes 2020 Feb 11 (3): . Adewuyi Emmanuel O, Sapkota Yadav, International Endogene Consortium Iec , andMe Research Team , International Headache Genetics Consortium Ihgc , Auta Asa, Yoshihara Kosuke, Nyegaard Mette, Griffiths Lyn R, Montgomery Grant W, Chasman Daniel I, Nyholt Dale |
| Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population.
Cephalalgia : an international journal of headache 2021 Aug 3331024211037269. Tsao Yu-Chien, Wang Shuu-Jiun, Hsu Chia-Lin, Wang Yen-Feng, Fuh Jong-Ling, Chen Shih-Pin, Fann Cathy Shen-Ja |
| Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan.
The journal of headache and pain 2021 Aug 22 (1): 89. Tsai Chia-Kuang, Liang Chih-Sung, Lin Guan-Yu, Tsai Chia-Lin, Lee Jiunn-Tay, Sung Yueh-Feng, Lin Yu-Kai, Hung Kuo-Sheng, Chen Wei-Liang, Yang Fu-C |
| Genome-Wide Association Study Identifies Risk Loci for Cluster Headache.
Annals of neurology 2021 Jun . O'Connor Emer, Fourier Carmen, Ran Caroline, Sivakumar Prasanth, Liesecke Franziska, Southgate Laura, Harder Aster V E, Vijfhuizen Lisanne S, Yip Janice, Giffin Nicola, Silver Nicholas, Ahmed Fayyaz, Hostettler Isabel C, Davies Brendan, Cader M Zameel, Simpson Benjamin S, Sullivan Roisin, Efthymiou Stephanie, Adebimpe Joycee, Quinn Olivia, Campbell Ciaran, Cavalleri Gianpiero L, Vikelis Michail, Kelderman Tim, Paemeleire Koen, Kilbride Emer, Grangeon Lou, Lagrata Susie, Danno Daisuke, Trembath Richard, Wood Nicholas W, Kockum Ingrid, Winsvold Bendik S, Steinberg Anna, Sjöstrand Christina, Waldenlind Elisabet, Vandrovcova Jana, Houlden Henry, Matharu Manjit, Belin Andrea Carmi |
| Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Nature communications 2021 10 12 (1): 6031. Georges Adrien, Yang Min-Lee, Berrandou Takiy-Eddine, Bakker Mark K, Dikilitas Ozan, Kiando Soto Romuald, Ma Lijiang, Satterfield Benjamin A, Sengupta Sebanti, Yu Mengyao, Deleuze Jean-François, Dupré Delia, Hunker Kristina L, Kyryachenko Sergiy, Liu Lu, Sayoud-Sadeg Ines, Amar Laurence, Brummett Chad M, Coleman Dawn M, d'Escamard Valentina, de Leeuw Peter, Fendrikova-Mahlay Natalia, Kadian-Dodov Daniella, Li Jun Z, Lorthioir Aurélien, Pappaccogli Marco, Prejbisz Aleksander, Smigielski Witold, Stanley James C, Zawistowski Matthew, Zhou Xiang, Zöllner Sebastian, , , , Amouyel Philippe, De Buyzere Marc L, Debette Stéphanie, Dobrowolski Piotr, Drygas Wojciech, Gornik Heather L, Olin Jeffrey W, Piwonski Jerzy, Rietzschel Ernst R, Ruigrok Ynte M, Vikkula Miikka, Warchol Celinska Ewa, Januszewicz Andrzej, Kullo Iftikhar J, Azizi Michel, , Jeunemaitre Xavier, Persu Alexandre, Kovacic Jason C, Ganesh Santhi K, Bouatia-Naji Nabi |
| Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities.
Brain : a journal of neurology 2021 10 144 (9): 2670-2682. Malik Rainer, Beaufort Nathalie, Frerich Simon, Gesierich Benno, Georgakis Marios K, Rannikmäe Kristiina, Ferguson Amy C, Haffner Christof, Traylor Matthew, Ehrmann Michael, Sudlow Cathie L M, Dichgans Mart |
| Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine.
Frontiers in aging neuroscience 2022 14 860604. Yeh Po-Kuan, Liang Chih-Sung, Tsai Chia-Lin, Lin Yu-Kai, Lin Guan-Yu, Tsai Chia-Kuang, Tsai Ming-Chen, Liu Yi, Tai Yueh-Ming, Hung Kuo-Sheng, Yang Fu-C |
| Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity.
Nature and science of sleep 2022 14 1075-1087. An Yu-Chin, Tsai Chia-Lin, Liang Chih-Sung, Lin Yu-Kai, Lin Guan-Yu, Tsai Chia-Kuang, Liu Yi, Chen Sy-Jou, Tsai Shih-Hung, Hung Kuo-Sheng, Yang Fu-C |
| Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.
Nature genetics 2022 02 54 (2): 152-160. Hautakangas Heidi, Winsvold Bendik S, Ruotsalainen Sanni E, Bjornsdottir Gyda, Harder Aster V E, Kogelman Lisette J A, Thomas Laurent F, Noordam Raymond, Benner Christian, Gormley Padhraig, Artto Ville, Banasik Karina, Bjornsdottir Anna, Boomsma Dorret I, Brumpton Ben M, Burgdorf Kristoffer Sølvsten, Buring Julie E, Chalmer Mona Ameri, de Boer Irene, Dichgans Martin, Erikstrup Christian, Färkkilä Markus, Garbrielsen Maiken Elvestad, Ghanbari Mohsen, Hagen Knut, Häppölä Paavo, Hottenga Jouke-Jan, Hrafnsdottir Maria G, Hveem Kristian, Johnsen Marianne Bakke, Kähönen Mika, Kristoffersen Espen S, Kurth Tobias, Lehtimäki Terho, Lighart Lannie, Magnusson Sigurdur H, Malik Rainer, Pedersen Ole Birger, Pelzer Nadine, Penninx Brenda W J H, Ran Caroline, Ridker Paul M, Rosendaal Frits R, Sigurdardottir Gudrun R, Skogholt Anne Heidi, Sveinsson Olafur A, Thorgeirsson Thorgeir E, Ullum Henrik, Vijfhuizen Lisanne S, Widén Elisabeth, van Dijk Ko Willems, , , , Aromaa Arpo, Belin Andrea Carmine, Freilinger Tobias, Ikram M Arfan, Järvelin Marjo-Riitta, Raitakari Olli T, Terwindt Gisela M, Kallela Mikko, Wessman Maija, Olesen Jes, Chasman Daniel I, Nyholt Dale R, Stefánsson Hreinn, Stefansson Kari, van den Maagdenberg Arn M J M, Hansen Thomas Folkmann, Ripatti Samuli, Zwart John-Anker, Palotie Aarno, Pirinen Mat |
| Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.
Annals of the rheumatic diseases 2022 11 82 (3): 384-392. Henkel Cecilie, Styrkársdóttir Unnur, Thorleifsson Gudmar, Stefánsdóttir Lilja, Björnsdóttir Gyda, Banasik Karina, Brunak Søren, Erikstrup Christian, Dinh Khoa Manh, Hansen Thomas Folkmann, Nielsen Kaspar René, Bruun Mie Topholm, Dowsett Joseph, Brodersen Thorsten, , Thorgeirsson Thorgeir E, Gromov Kirill, Boesen Mikael Ploug, Ullum Henrik, Ostrowski Sisse Rye, Pedersen Ole Birger, Stefánsson Kári, Troelsen Ande |
| Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes.
Genes 2022 10 13 (10): . Islam Md Rafiqul, The International Headache Genetics Consortium Ihgc , Nyholt Dale |
| The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Nature genetics 2023 3 55 (3): 423-436. Rahmioglu Nilufer, Mortlock Sally, Ghiasi Marzieh, Møller Peter L, Stefansdottir Lilja, Galarneau Geneviève, Turman Constance, Danning Rebecca, Law Matthew H, Sapkota Yadav, Christofidou Paraskevi, Skarp Sini, Giri Ayush, Banasik Karina, Krassowski Michal, Lepamets Maarja, Marciniak B?a?ej, Nõukas Margit, Perro Danielle, Sliz Eeva, Sobalska-Kwapis Marta, Thorleifsson Gudmar, Topbas-Selcuki Nura F, Vitonis Allison, Westergaard David, Arnadottir Ragnheidur, Burgdorf Kristoffer S, Campbell Archie, Cheuk Cecilia S K, Clementi Caterina, Cook James, De Vivo Immaculata, DiVasta Amy, Dorien O, Donoghue Jacqueline F, Edwards Todd, Fontanillas Pierre, Fung Jenny N, Geirsson Reynir T, Girling Jane E, Harkki Paivi, Harris Holly R, Healey Martin, Heikinheimo Oskari, Holdsworth-Carson Sarah, Hostettler Isabel C, Houlden Henry, Houshdaran Sahar, Irwin Juan C, Jarvelin Marjo-Riitta, Kamatani Yoichiro, Kennedy Stephen H, Kepka Ewa, Kettunen Johannes, Kubo Michiaki, Kulig Bartosz, Kurra Venla, Laivuori Hannele, Laufer Marc R, Lindgren Cecilia M, MacGregor Stuart, Mangino Massimo, Martin Nicholas G, Matalliotaki Charoula, Matalliotakis Michail, Murray Alison D, Ndungu Anne, Nezhat Camran, Olsen Catherine M, Opoku-Anane Jessica, Padmanabhan Sandosh, Paranjpe Manish, Peters Maire, Polak Grzegorz, Porteous David J, Rabban Joseph, Rexrode Kathyrn M, Romanowicz Hanna, Saare Merli, Saavalainen Liisu, Schork Andrew J, Sen Sushmita, Shafrir Amy L, Siewierska-Górska Anna, S?omka Marcin, Smith Blair H, Smolarz Beata, Szaflik Tomasz, Szy??o Krzysztof, Takahashi Atsushi, Terry Kathryn L, Tomassetti Carla, Treloar Susan A, Vanhie Arne, Vincent Katy, Vo Kim C, Werring David J, Zeggini Eleftheria, Zervou Maria I, , , , , , Adachi Sosuke, Buring Julie E, Ridker Paul M, D'Hooghe Thomas, Goulielmos George N, Hapangama Dharani K, Hayward Caroline, Horne Andrew W, Low Siew-Kee, Martikainen Hannu, Chasman Daniel I, Rogers Peter A W, Saunders Philippa T, Sirota Marina, Spector Tim, Strapagiel Dominik, Tung Joyce Y, Whiteman David C, Giudice Linda C, Velez-Edwards Digna R, Uimari Outi, Kraft Peter, Salumets Andres, Nyholt Dale R, Mägi Reedik, Stefansson Kari, Becker Christian M, Yurttas-Beim Piraye, Steinthorsdottir Valgerdur, Nyegaard Mette, Missmer Stacey A, Montgomery Grant W, Morris Andrew P, Zondervan Krina |
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