Human Genome Epidemiology Literature Finder
Primary Immune Deficiency Diseases
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Multi-omics analysis identifies rare variation in leptin/PPAR gene sets and hypermethylation of ABCG1 contribute to antipsychotics-induced metabolic syndromes.
Molecular psychiatry 2022 9 27 (12): 5195-5205. Zhou Wei, Sun Jing, Huai Cong, Liu Yunxi, Chen Luan, Yi Zhenghui, Lv Qinyu, Song Chuanfu, Zhu Wenli, Liu Chuanxin, Weng Saizheng, Wu Hao, Sun Yidan, Zhang Runshuai, Wu Lianfeng, Li Mo, Zhu Jinhang, Zhang Yingtian, Wei Muyun, Guo Yujian, Huang Sijia, Zhang Na, Shen Ruoxi, Zhang Ying, Du Huihui, Huang Hailiang, He Lin, Sun Xiaofang, Shen Lu, Qin Shengyi |
| Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes.
Genome medicine 2022 3 14 (1): 28. Caron Barthelemy, Patin Etienne, Rotival Maxime, Charbit Bruno, Albert Matthew L, Quintana-Murci Lluis, Duffy Darragh, Rausell Antonio, |
| Common Genetic Variation and Age of Onset of Anorexia Nervosa.
Biological psychiatry global open science 2022 11 2 (4): 368-378. Watson Hunna J, Thornton Laura M, Yilmaz Zeynep, Baker Jessica H, Coleman Jonathan R I, Adan Roger A H, Alfredsson Lars, Andreassen Ole A, Ask Helga, Berrettini Wade H, Boehnke Michael, Boehm Ilka, Boni Claudette, Buehren Katharina, Bulant Josef, Burghardt Roland, Chang Xiao, Cichon Sven, Cone Roger D, Courtet Philippe, Crow Scott, Crowley James J, Danner Unna N, de Zwaan Martina, Dedoussis George, DeSocio Janiece E, Dick Danielle M, Dikeos Dimitris, Dina Christian, Djurovic Srdjan, Dmitrzak-Weglarz Monika, Docampo-Martinez Elisa, Duriez Philibert, Egberts Karin, Ehrlich Stefan, Eriksson Johan G, Escaramís Geòrgia, Esko Tõnu, Estivill Xavier, Farmer Anne, Fernández-Aranda Fernando, Fichter Manfred M, Föcker Manuel, Foretova Lenka, Forstner Andreas J, Frei Oleksandr, Gallinger Steven, Giegling Ina, Giuranna Johanna, Gonidakis Fragiskos, Gorwood Philip, Gratacòs Mònica, Guillaume Sébastien, Guo Yiran, Hakonarson Hakon, Hauser Joanna, Havdahl Alexandra, Hebebrand Johannes, Helder Sietske G, Herms Stefan, Herpertz-Dahlmann Beate, Herzog Wolfgang, Hinney Anke, Hübel Christopher, Hudson James I, Imgart Hartmut, Jamain Stephanie, Janout Vladimir, Jiménez-Murcia Susana, Jones Ian R, Julià Antonio, Kalsi Gursharan, Kaminská Deborah, Kaprio Jaakko, Karhunen Leila, Kas Martien J H, Keel Pamela K, Kennedy James L, Keski-Rahkonen Anna, Kiezebrink Kirsty, Klareskog Lars, Klump Kelly L, Knudsen Gun Peggy S, La Via Maria C, Le Hellard Stephanie, Leboyer Marion, Li Dong, Lilenfeld Lisa, Lin Bochao, Lissowska Jolanta, Luykx Jurjen, Magistretti Pierre, Maj Mario, Marsal Sara, Marshall Christian R, Mattingsdal Morten, Meulenbelt Ingrid, Micali Nadia, Mitchell Karen S, Monteleone Alessio Maria, Monteleone Palmiero, Myers Richard, Navratilova Marie, Ntalla Ionna, O'Toole Julie K, Ophoff Roel A, Padyukov Leonid, Pantel Jacques, Papežová Hana, Pinto Dalila, Raevuori Anu, Ramoz Nicolas, Reichborn-Kjennerud Ted, Ricca Valdo, Ripatti Samuli, Ripke Stephan, Ritschel Franziska, Roberts Marion, Rotondo Alessandro, Rujescu Dan, Rybakowski Filip, Scherag André, Scherer Stephen W, Schmidt Ulrike, Scott Laura J, Seitz Jochen, Silén Yasmina, Šlachtová Lenka, Slagboom P Eline, Slof-Op 't Landt Margarita C T, Slopien Agnieszka, Sorbi Sandro, ?wi?tkowska Beata, Tortorella Alfonso, Tozzi Federica, Treasure Janet, Tsitsika Artemis, Tyszkiewicz-Nwafor Marta, Tziouvas Konstantinos, van Elburg Annemarie A, van Furth Eric F, Walton Esther, Widen Elisabeth, Zerwas Stephanie, Zipfel Stephan, Bergen Andrew W, Boden Joseph M, Brandt Harry, Crawford Steven, Halmi Katherine A, Horwood L John, Johnson Craig, Kaplan Allan S, Kaye Walter H, Mitchell James E, Olsen Catherine M, Pearson John F, Pedersen Nancy L, Strober Michael, Werge Thomas, Whiteman David C, Woodside D Blake, Gordon Scott, Maguire Sarah, Larsen Janne T, Parker Richard, Petersen Liselotte V, Jordan Jennifer, Kennedy Martin, Wade Tracey D, Birgegård Andreas, Lichtenstein Paul, Landén Mikael, Martin Nicholas G, Mortensen Preben Bo, Breen Gerome, Bulik Cynthia |
| Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number.
HGG advances 2022 10 4 (1): 100147. Pillalamarri Vamsee, Shi Wen, Say Conrad, Yang Stephanie, Lane John, Guallar Eliseo, Pankratz Nathan, Arking Dan |
| STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency.
Frontiers in genetics 2022 1 12 736235. Lim Che Kang, Bronson Paola G, Varade Jezabel, Behrens Timothy W, Hammarström Lenna |
| Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study.
PloS one 2021 16 (7): e0249615. Streicher Samantha A, Lim Unhee, Park S Lani, Li Yuqing, Sheng Xin, Hom Victor, Xia Lucy, Pooler Loreall, Shepherd John, Loo Lenora W M, Darst Burcu F, Highland Heather M, Polfus Linda M, Bogumil David, Ernst Thomas, Buchthal Steven, Franke Adrian A, Setiawan Veronica Wendy, Tiirikainen Maarit, Wilkens Lynne R, Haiman Christopher A, Stram Daniel O, Cheng Iona, Le Marchand Lo |
| Genetic determinants of risk in autoimmune pulmonary alveolar proteinosis.
Nature communications 2021 02 12 (1): 1032. Sakaue Saori, Yamaguchi Etsuro, Inoue Yoshikazu, Takahashi Meiko, Hirata Jun, Suzuki Ken, Ito Satoru, Arai Toru, Hirose Masaki, Tanino Yoshinori, Nikaido Takefumi, Ichiwata Toshio, Ohkouchi Shinya, Hirano Taizou, Takada Toshinori, Miyawaki Satoru, Dofuku Shogo, Maeda Yuichi, Nii Takuro, Kishikawa Toshihiro, Ogawa Kotaro, Masuda Tatsuo, Yamamoto Kenichi, Sonehara Kyuto, Tazawa Ryushi, Morimoto Konosuke, Takaki Masahiro, Konno Satoshi, Suzuki Masaru, Tomii Keisuke, Nakagawa Atsushi, Handa Tomohiro, Tanizawa Kiminobu, Ishii Haruyuki, Ishida Manabu, Kato Toshiyuki, Takeda Naoya, Yokomura Koshi, Matsui Takashi, Watanabe Masaki, Inoue Hiromasa, Imaizumi Kazuyoshi, Goto Yasuhiro, Kida Hiroshi, Fujisawa Tomoyuki, Suda Takafumi, Yamada Takashi, Satake Yasuomi, Ibata Hidenori, Hizawa Nobuyuki, Mochizuki Hideki, Kumanogoh Atsushi, Matsuda Fumihiko, Nakata Koh, Hirota Tomomitsu, Tamari Mayumi, Okada Yukino |
| Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.
Nature genetics 2019 Aug 51 (8): 1207-1214. Watson Hunna J, Yilmaz Zeynep, Thornton Laura M, Hübel Christopher, Coleman Jonathan R I, Gaspar Héléna A, Bryois Julien, Hinney Anke, Leppä Virpi M, Mattheisen Manuel, Medland Sarah E, Ripke Stephan, Yao Shuyang, Giusti-Rodríguez Paola, , Hanscombe Ken B, Purves Kirstin L, , Adan Roger A H, Alfredsson Lars, Ando Tetsuya, Andreassen Ole A, Baker Jessica H, Berrettini Wade H, Boehm Ilka, Boni Claudette, Perica Vesna Boraska, Buehren Katharina, Burghardt Roland, Cassina Matteo, Cichon Sven, Clementi Maurizio, Cone Roger D, Courtet Philippe, Crow Scott, Crowley James J, Danner Unna N, Davis Oliver S P, de Zwaan Martina, Dedoussis George, Degortes Daniela, DeSocio Janiece E, Dick Danielle M, Dikeos Dimitris, Dina Christian, Dmitrzak-Weglarz Monika, Docampo Elisa, Duncan Laramie E, Egberts Karin, Ehrlich Stefan, Escaramís Geòrgia, Esko Tõnu, Estivill Xavier, Farmer Anne, Favaro Angela, Fernández-Aranda Fernando, Fichter Manfred M, Fischer Krista, Föcker Manuel, Foretova Lenka, Forstner Andreas J, Forzan Monica, Franklin Christopher S, Gallinger Steven, Giegling Ina, Giuranna Johanna, Gonidakis Fragiskos, Gorwood Philip, Mayora Monica Gratacos, Guillaume Sébastien, Guo Yiran, Hakonarson Hakon, Hatzikotoulas Konstantinos, Hauser Joanna, Hebebrand Johannes, Helder Sietske G, Herms Stefan, Herpertz-Dahlmann Beate, Herzog Wolfgang, Huckins Laura M, Hudson James I, Imgart Hartmut, Inoko Hidetoshi, Janout Vladimir, Jiménez-Murcia Susana, Julià Antonio, Kalsi Gursharan, Kaminská Deborah, Kaprio Jaakko, Karhunen Leila, Karwautz Andreas, Kas Martien J H, Kennedy James L, Keski-Rahkonen Anna, Kiezebrink Kirsty, Kim Youl-Ri, Klareskog Lars, Klump Kelly L, Knudsen Gun Peggy S, La Via Maria C, Le Hellard Stephanie, Levitan Robert D, Li Dong, Lilenfeld Lisa, Lin Bochao Danae, Lissowska Jolanta, Luykx Jurjen, Magistretti Pierre J, Maj Mario, Mannik Katrin, Marsal Sara, Marshall Christian R, Mattingsdal Morten, McDevitt Sara, McGuffin Peter, Metspalu Andres, Meulenbelt Ingrid, Micali Nadia, Mitchell Karen, Monteleone Alessio Maria, Monteleone Palmiero, Munn-Chernoff Melissa A, Nacmias Benedetta, Navratilova Marie, Ntalla Ioanna, O'Toole Julie K, Ophoff Roel A, Padyukov Leonid, Palotie Aarno, Pantel Jacques, Papezova Hana, Pinto Dalila, Rabionet Raquel, Raevuori Anu, Ramoz Nicolas, Reichborn-Kjennerud Ted, Ricca Valdo, Ripatti Samuli, Ritschel Franziska, Roberts Marion, Rotondo Alessandro, Rujescu Dan, Rybakowski Filip, Santonastaso Paolo, Scherag André, Scherer Stephen W, Schmidt Ulrike, Schork Nicholas J, Schosser Alexandra, Seitz Jochen, Slachtova Lenka, Slagboom P Eline, Slof-Op 't Landt Margarita C T, Slopien Agnieszka, Sorbi Sandro, Swiatkowska Beata, Szatkiewicz Jin P, Tachmazidou Ioanna, Tenconi Elena, Tortorella Alfonso, Tozzi Federica, Treasure Janet, Tsitsika Artemis, Tyszkiewicz-Nwafor Marta, Tziouvas Konstantinos, van Elburg Annemarie A, van Furth Eric F, Wagner Gudrun, Walton Esther, Widen Elisabeth, Zeggini Eleftheria, Zerwas Stephanie, Zipfel Stephan, Bergen Andrew W, Boden Joseph M, Brandt Harry, Crawford Steven, Halmi Katherine A, Horwood L John, Johnson Craig, Kaplan Allan S, Kaye Walter H, Mitchell James E, Olsen Catherine M, Pearson John F, Pedersen Nancy L, Strober Michael, Werge Thomas, Whiteman David C, Woodside D Blake, Stuber Garret D, Gordon Scott, Grove Jakob, Henders Anjali K, Juréus Anders, Kirk Katherine M, Larsen Janne T, Parker Richard, Petersen Liselotte, Jordan Jennifer, Kennedy Martin, Montgomery Grant W, Wade Tracey D, Birgegård Andreas, Lichtenstein Paul, Norring Claes, Landén Mikael, Martin Nicholas G, Mortensen Preben Bo, Sullivan Patrick F, Breen Gerome, Bulik Cynthia |
| Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis.
PLoS genetics 2019 Apr 15 (4): e1008038. Li Zhixiu, Akar Servet, Yarkan Handan, Lee Sau Kuen, Çetin P?nar, Can Gerçek, Kenar Gökce, Çapa Fernur, Pamuk Omer Nuri, Pehlivan Yavuz, Cremin Katie, De Guzman Erika, Harris Jessica, Wheeler Lawrie, Jamshidi Ahmadreza, Vojdanian Mahdi, Farhadi Elham, Ahmadzadeh Nooshin, Yüce Zeynep, Dalk?l?ç Ediz, Solmaz Dilek, Ak?n Berrin, Dönmez Salim, Sar? ?smail, Leo Paul J, Kenna Tony J, Önen Fatos, Mahmoudi Mahdi, Brown Matthew A, Akkoc Nurull |
| The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
Journal of human genetics 2017 Apr . Sugiura-Ogasawara Mayumi, Omae Yosuke, Kawashima Minae, Toyo-Oka Licht, Khor Seik-Soon, Sawai Hiromi, Horita Tetsuya, Atsumi Tatsuya, Murashima Atsuko, Fujita Daisuke, Fujita Tomio, Morimoto Shinji, Morishita Eriko, Katsuragi Shinji, Kitaori Tamao, Katano Kinue, Ozaki Yasuhiko, Tokunaga Katsus |
| Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
Nature genetics 2017 Jan . de Lange Katrina M, Moutsianas Loukas, Lee James C, Lamb Christopher A, Luo Yang, Kennedy Nicholas A, Jostins Luke, Rice Daniel L, Gutierrez-Achury Javier, Ji Sun-Gou, Heap Graham, Nimmo Elaine R, Edwards Cathryn, Henderson Paul, Mowat Craig, Sanderson Jeremy, Satsangi Jack, Simmons Alison, Wilson David C, Tremelling Mark, Hart Ailsa, Mathew Christopher G, Newman William G, Parkes Miles, Lees Charlie W, Uhlig Holm, Hawkey Chris, Prescott Natalie J, Ahmad Tariq, Mansfield John C, Anderson Carl A, Barrett Jeffrey |
| An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma.
Human molecular genetics 2016 Aug 25 (16): 3626-3634. Cui Qian, Feng Qi-Sheng, Mo Hao-Yuan, Sun Jian, Xia Yun-Fei, Zhang Hongxing, Foo Jia Nee, Guo Yun-Miao, Chen Li-Zhen, Li Ming, Liu Wen-Sheng, Xu Miao, Zhou Gangqiao, He Fuchu, Yu Xueqing, Jia Wei-Hua, Liu Jianjun, Zeng Yi-Xin, Bei Jin-X |
| Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expression.
Thrombosis and haemostasis 2016 Apr 116 (1): . Müller-Calleja Nadine, Rossmann Heidi, Müller Christian, Wild Philipp, Blankenberg Stefan, Pfeiffer Norbert, Binder Harald, Beutel Manfred E, Manukyan Davit, Zeller Tanja, Lackner Karl |
| Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs.
Translational psychiatry 2016 6 e731. den Braber A, Zilhão N R, Fedko I O, Hottenga J-J, Pool R, Smit D J A, Cath D C, Boomsma D |
| Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.
Nature genetics 2016 Nov 48 (11): 1425-1429. Bronson Paola G, Chang Diana, Bhangale Tushar, Seldin Michael F, Ortmann Ward, Ferreira Ricardo C, Urcelay Elena, Pereira Luis Fernández, Martin Javier, Plebani Alessandro, Lougaris Vassilios, Friman Vanda, Freiberger Tomáš, Litzman Jiri, Thon Vojtech, Pan-Hammarström Qiang, Hammarström Lennart, Graham Robert R, Behrens Timothy |
| Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy.
Nature genetics 2015 Mar 47 (3): 267-71. Liu Hong, Irwanto Astrid, Fu Xi'an, Yu Gongqi, Yu Yongxiang, Sun Yonghu, Wang Chuan, Wang Zhenzhen, Okada Yukinori, Low Huiqi, Li Yi, Liany Herty, Chen Mingfei, Bao Fangfang, Li Jinghui, You Jiabao, Zhang Qilin, Liu Jian, Chu Tongsheng, Andiappan Anand Kumar, Wang Na, Niu Guiye, Liu Dianchang, Yu Xiulu, Zhang Lin, Tian Hongqing, Zhou Guizhi, Rotzschke Olaf, Chen Shumin, Zhang Xuejun, Liu Jianjun, Zhang Fur |
| Genetics of rheumatoid arthritis contributes to biology and drug discovery.
Nature 2014 Feb 506 (7488): 376-81. Okada Yukinori, Wu Di, Trynka Gosia, Raj Towfique, Terao Chikashi, Ikari Katsunori, Kochi Yuta, Ohmura Koichiro, Suzuki Akari, Yoshida Shinji, Graham Robert R, Manoharan Arun, Ortmann Ward, Bhangale Tushar, Denny Joshua C, Carroll Robert J, Eyler Anne E, Greenberg Jeffrey D, Kremer Joel M, Pappas Dimitrios A, Jiang Lei, Yin Jian, Ye Lingying, Su Ding-Feng, Yang Jian, Xie Gang, Keystone Ed, Westra Harm-Jan, Esko Tõnu, Metspalu Andres, Zhou Xuezhong, Gupta Namrata, Mirel Daniel, Stahl Eli A, Diogo Dorothée, Cui Jing, Liao Katherine, Guo Michael H, Myouzen Keiko, Kawaguchi Takahisa, Coenen Marieke J H, van Riel Piet L C M, van de Laar Mart A F J, Guchelaar Henk-Jan, Huizinga Tom W J, Dieudé Philippe, Mariette Xavier, Bridges S Louis, Zhernakova Alexandra, Toes Rene E M, Tak Paul P, Miceli-Richard Corinne, Bang So-Young, Lee Hye-Soon, Martin Javier, Gonzalez-Gay Miguel A, Rodriguez-Rodriguez Luis, Rantapää-Dahlqvist Solbritt, Arlestig Lisbeth, Choi Hyon K, Kamatani Yoichiro, Galan Pilar, Lathrop Mark, , , Eyre Steve, Bowes John, Barton Anne, de Vries Niek, Moreland Larry W, Criswell Lindsey A, Karlson Elizabeth W, Taniguchi Atsuo, Yamada Ryo, Kubo Michiaki, Liu Jun S, Bae Sang-Cheol, Worthington Jane, Padyukov Leonid, Klareskog Lars, Gregersen Peter K, Raychaudhuri Soumya, Stranger Barbara E, De Jager Philip L, Franke Lude, Visscher Peter M, Brown Matthew A, Yamanaka Hisashi, Mimori Tsuneyo, Takahashi Atsushi, Xu Huji, Behrens Timothy W, Siminovitch Katherine A, Momohara Shigeki, Matsuda Fumihiko, Yamamoto Kazuhiko, Plenge Robert |
| Genome-wide association study identifies TNFSF13 as a susceptibility gene for IgA in a South Chinese population in smokers.
Immunogenetics 2012 Aug . Yang C, Jie W, Yanlong Y, Xuefeng G, Aihua T, Yong G, Zheng L, Youjie Z, Haiying Z, Xue Q, Min Q, Linjian M, Xiaobo Y, Yanling H, Zengnan M |
| Multiple loci influencing hippocampal degeneration identified by genome scan.
Annals of neurology 2012 Jul 72 (1): 65-75. Melville Scott A, Buros Jacqueline, Parrado Antonio R, Vardarajan Badri, Logue Mark W, Shen Li, Risacher Shannon L, Kim Sungeun, Jun Gyungah, DeCarli Charles, Lunetta Kathryn L, Baldwin Clinton T, Saykin Andrew J, Farrer Lindsay A, |
| Genome-wide association and functional follow-up reveals new loci for kidney function.
PLoS genetics 2012 8 (3): e1002584. Pattaro Cristian, Köttgen Anna, Teumer Alexander, Garnaas Maija, Böger Carsten A, Fuchsberger Christian, Olden Matthias, Chen Ming-Huei, Tin Adrienne, Taliun Daniel, Li Man, Gao Xiaoyi, Gorski Mathias, Yang Qiong, Hundertmark Claudia, Foster Meredith C, O'Seaghdha Conall M, Glazer Nicole, Isaacs Aaron, Liu Ching-Ti, Smith Albert V, O'Connell Jeffrey R, Struchalin Maksim, Tanaka Toshiko, Li Guo, Johnson Andrew D, Gierman Hinco J, Feitosa Mary, Hwang Shih-Jen, Atkinson Elizabeth J, Lohman Kurt, Cornelis Marilyn C, Johansson Åsa, Tönjes Anke, Dehghan Abbas, Chouraki Vincent, Holliday Elizabeth G, Sorice Rossella, Kutalik Zoltan, Lehtimäki Terho, Esko Tõnu, Deshmukh Harshal, Ulivi Sheila, Chu Audrey Y, Murgia Federico, Trompet Stella, Imboden Medea, Kollerits Barbara, Pistis Giorgio, , , , , Harris Tamara B, Launer Lenore J, Aspelund Thor, Eiriksdottir Gudny, Mitchell Braxton D, Boerwinkle Eric, Schmidt Helena, Cavalieri Margherita, Rao Madhumathi, Hu Frank B, Demirkan Ayse, Oostra Ben A, de Andrade Mariza, Turner Stephen T, Ding Jingzhong, Andrews Jeanette S, Freedman Barry I, Koenig Wolfgang, Illig Thomas, Döring Angela, Wichmann H-Erich, Kolcic Ivana, Zemunik Tatijana, Boban Mladen, Minelli Cosetta, Wheeler Heather E, Igl Wilmar, Zaboli Ghazal, Wild Sarah H, Wright Alan F, Campbell Harry, Ellinghaus David, Nöthlings Ute, Jacobs Gunnar, Biffar Reiner, Endlich Karlhans, Ernst Florian, Homuth Georg, Kroemer Heyo K, Nauck Matthias, Stracke Sylvia, Völker Uwe, Völzke Henry, Kovacs Peter, Stumvoll Michael, Mägi Reedik, Hofman Albert, Uitterlinden Andre G, Rivadeneira Fernando, Aulchenko Yurii S, Polasek Ozren, Hastie Nick, Vitart Veronique, Helmer Catherine, Wang Jie Jin, Ruggiero Daniela, Bergmann Sven, Kähönen Mika, Viikari Jorma, Nikopensius Tiit, Province Michael, Ketkar Shamika, Colhoun Helen, Doney Alex, Robino Antonietta, Giulianini Franco, Krämer Bernhard K, Portas Laura, Ford Ian, Buckley Brendan M, Adam Martin, Thun Gian-Andri, Paulweber Bernhard, Haun Margot, Sala Cinzia, Metzger Marie, Mitchell Paul, Ciullo Marina, Kim Stuart K, Vollenweider Peter, Raitakari Olli, Metspalu Andres, Palmer Colin, Gasparini Paolo, Pirastu Mario, Jukema J Wouter, Probst-Hensch Nicole M, Kronenberg Florian, Toniolo Daniela, Gudnason Vilmundur, Shuldiner Alan R, Coresh Josef, Schmidt Reinhold, Ferrucci Luigi, Siscovick David S, van Duijn Cornelia M, Borecki Ingrid, Kardia Sharon L R, Liu Yongmei, Curhan Gary C, Rudan Igor, Gyllensten Ulf, Wilson James F, Franke Andre, Pramstaller Peter P, Rettig Rainer, Prokopenko Inga, Witteman Jacqueline C M, Hayward Caroline, Ridker Paul, Parsa Afshin, Bochud Murielle, Heid Iris M, Goessling Wolfram, Chasman Daniel I, Kao W H Linda, Fox Caroline |
| A comprehensive genetic association study of Alzheimer disease in African Americans.
Archives of neurology 2011 Dec 68 (12): 1569-79. Logue Mark W, Schu Matthew, Vardarajan Badri N, Buros Jacki, Green Robert C, Go Rodney C P, Griffith Patrick, Obisesan Thomas O, Shatz Rhonna, Borenstein Amy, Cupples L Adrienne, Lunetta Kathryn L, Fallin M Daniele, Baldwin Clinton T, Farrer Lindsay A, |
| Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.
Nature genetics 2010 Sep 42 (9): 777-80. Ferreira Ricardo C, Pan-Hammarström Qiang, Graham Robert R, Gateva Vesela, Fontán Gumersindo, Lee Annette T, Ortmann Ward, Urcelay Elena, Fernández-Arquero Miguel, Núñez Concepción, Jorgensen Gudmundur, Ludviksson Björn R, Koskinen Sinikka, Haimila Katri, Clark Hilary F, Klareskog Lars, Gregersen Peter K, Behrens Timothy W, Hammarström Lenna |
| Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.
Proceedings of the National Academy of Sciences of the United States of America 2010 May 107 (20): 9293-8. Levy Daniel, Neuhausen Susan L, Hunt Steven C, Kimura Masayuki, Hwang Shih-Jen, Chen Wei, Bis Joshua C, Fitzpatrick Annette L, Smith Erin, Johnson Andrew D, Gardner Jeffrey P, Srinivasan Sathanur R, Schork Nicholas, Rotter Jerome I, Herbig Utz, Psaty Bruce M, Sastrasinh Malinee, Murray Sarah S, Vasan Ramachandran S, Province Michael A, Glazer Nicole L, Lu Xiaobin, Cao Xiaojian, Kronmal Richard, Mangino Massimo, Soranzo Nicole, Spector Tim D, Berenson Gerald S, Aviv Abrah |
| Multiple common variants for celiac disease influencing immune gene expression.
Nature genetics 2010 Apr 42 (4): 295-302. Dubois Patrick C A, Trynka Gosia, Franke Lude, Hunt Karen A, Romanos Jihane, Curtotti Alessandra, Zhernakova Alexandra, Heap Graham A R, Adány Róza, Aromaa Arpo, Bardella Maria Teresa, van den Berg Leonard H, Bockett Nicholas A, de la Concha Emilio G, Dema Bárbara, Fehrmann Rudolf S N, Fernández-Arquero Miguel, Fiatal Szilvia, Grandone Elvira, Green Peter M, Groen Harry J M, Gwilliam Rhian, Houwen Roderick H J, Hunt Sarah E, Kaukinen Katri, Kelleher Dermot, Korponay-Szabo Ilma, Kurppa Kalle, MacMathuna Padraic, Mäki Markku, Mazzilli Maria Cristina, McCann Owen T, Mearin M Luisa, Mein Charles A, Mirza Muddassar M, Mistry Vanisha, Mora Barbara, Morley Katherine I, Mulder Chris J, Murray Joseph A, Núñez Concepción, Oosterom Elvira, Ophoff Roel A, Polanco Isabel, Peltonen Leena, Platteel Mathieu, Rybak Anna, Salomaa Veikko, Schweizer Joachim J, Sperandeo Maria Pia, Tack Greetje J, Turner Graham, Veldink Jan H, Verbeek Wieke H M, Weersma Rinse K, Wolters Victorien M, Urcelay Elena, Cukrowska Bozena, Greco Luigi, Neuhausen Susan L, McManus Ross, Barisani Donatella, Deloukas Panos, Barrett Jeffrey C, Saavalainen Paivi, Wijmenga Cisca, van Heel David |
| Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.
PLoS genetics 2010 Nov 6 (11): e1001213. Marzi Carola, Albrecht Eva, Hysi Pirro G, Lagou Vasiliki, Waldenberger Melanie, Tönjes Anke, Prokopenko Inga, Heim Katharina, Blackburn Hannah, Ried Janina S, Kleber Marcus E, Mangino Massimo, Thorand Barbara, Peters Annette, Hammond Christopher J, Grallert Harald, Boehm Bernhard O, Kovacs Peter, Geistlinger Ludwig, Prokisch Holger, Winkelmann Bernhard R, Spector Tim D, Wichmann H-Erich, Stumvoll Michael, Soranzo Nicole, März Winfried, Koenig Wolfgang, Illig Thomas, Gieger Christi |
| Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.
Nature genetics 2011 Feb 43 (2): 117-20. , , Zhou Kaixin, Bellenguez Celine, Spencer Chris C A, Bennett Amanda J, Coleman Ruth L, Tavendale Roger, Hawley Simon A, Donnelly Louise A, Schofield Chris, Groves Christopher J, Burch Lindsay, Carr Fiona, Strange Amy, Freeman Colin, Blackwell Jenefer M, Bramon Elvira, Brown Matthew A, Casas Juan P, Corvin Aiden, Craddock Nicholas, Deloukas Panos, Dronov Serge, Duncanson Audrey, Edkins Sarah, Gray Emma, Hunt Sarah, Jankowski Janusz, Langford Cordelia, Markus Hugh S, Mathew Christopher G, Plomin Robert, Rautanen Anna, Sawcer Stephen J, Samani Nilesh J, Trembath Richard, Viswanathan Ananth C, Wood Nicholas W, , Harries Lorna W, Hattersley Andrew T, Doney Alex S F, Colhoun Helen, Morris Andrew D, Sutherland Calum, Hardie D Grahame, Peltonen Leena, McCarthy Mark I, Holman Rury R, Palmer Colin N A, Donnelly Peter, Pearson Ewan |
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