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Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations
Li, Yun Rose, Glessner, Joseph T., Coe, Bradley P., Li, Jin, Mohebnasab, Maede, Chang, Xiao, Connolly, John, Kao, Charlly, Wei, Zhi, Bradfield, Jonathan, Kim, Cecilia, Hou, Cuiping, Khan, Munir, Mentch, Frank, Qiu, Haijun, Bakay, Marina, Cardinale, Christopher, Lemma, Maria, Abrams, Debra, Bridglall-Jhingoor, Andrew, Behr, Meckenzie, Harrison, Shanell, Otieno, George, Thomas, Alexandria, Wang, Fengxiang, Chiavacci, Rosetta, Wu, Lawrence, Hadley, Dexter, Goldmuntz, Elizabeth, Elia, Josephine, Maris, John, Grundmeier, Robert, Devoto, Marcella, Keating, Brendan, March, Michael, Pellagrino, Renata, Grant, Struan F. A., Sleiman, Patrick M. A., Li, Mingyao, Eichler, Evan E., Hakonarson, Hakon
Published in Nature communications (14.01.2020)
Published in Nature communications (14.01.2020)
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Identification of Four Novel Loci in Asthma in European American and African American Populations
Almoguera, Berta, Vazquez, Lyam, Mentch, Frank, Connolly, John, Pacheco, Jennifer A., Sundaresan, Agnes S., Peissig, Peggy L., Linneman, James G., McCarty, Catherine A., Crosslin, David, Carrell, David S., Lingren, Todd, Namjou-Khales, Bahram, Harley, John B., Larson, Eric, Jarvik, Gail P., Brilliant, Murray, Williams, Marc S., Kullo, Iftikhar J., Hysinger, Erik B., Sleiman, Patrick M. A., Hakonarson, Hakon
Published in American journal of respiratory and critical care medicine (15.02.2017)
Published in American journal of respiratory and critical care medicine (15.02.2017)
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Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease
Sabater-Lleal, Maria, Huang, Jie, Chasman, Daniel, Naitza, Silvia, Dehghan, Abbas, Teumer, Alexander, Folkersen, Lasse, Basu, Saonli, Rudnicka, Alicja R., Trompet, Stella, Mälarstig, Anders, Baumert, Jens, Guo, Xiuqing, Hottenga, Jouke J., Shin, So-Youn, Lopez, Lorna M., Lahti, Jari, Oudot-Mellakh, Tiphaine, Wilson, James F., Navarro, Pau, Huffman, Jennifer E., Zemunik, Tatijana, Mehra, Reena, Rudan, Igor, Wright, Alan F., Campbell, Harry, Wallace, Robert, Liu, Simin, Eaton, Charles B., Becker, Diane M., Becker, Lewis C., Räikkönen, Katri, Widen, Elisabeth, Palotie, Aarno, Fornage, Myriam, Green, David, Gross, Myron, Harris, Sarah E., Starr, John M., Williams, Frances M.K., Spector, Timothy D., Strawbridge, Rona J., Silveira, Angela, Sennblad, Bengt, Uitterlinden, Andre G., Franco, Oscar H., Hofman, Albert, van Dongen, Jenny, Yao, Jie, Swords Jenny, Nancy, Haritunians, Talin, Lumley, Thomas, Taylor, Kent D., Peters, Annette, Illig, Thomas, Kocher, Thomas, Franzosi, Maria Grazia, Seedorf, Udo, Clarke, Robert, Schlessinger, David, Stott, David J., Sattar, Naveed, Buckley, Brendan M., Lowe, Gordon D., Chen, Ming-Huei, Tofler, Geoffrey H., Song, Jaejoon, Boerwinkle, Eric, Rose, Lynda M., Franco-Cereceda, Anders, Teichert, Martina, Mosley, Thomas H., Bevan, Steve, Dichgans, Martin, Sudlow, Cathie L.M., Hopewell, Jemma C., Chambers, John C., Saleheen, Danish, Kooner, Jaspal S., Danesh, John, Nelson, Christopher P., Reilly, Muredach P., Kathiresan, Sekar, Schunkert, Heribert, Morange, Pierre-Emmanuel, Ferrucci, Luigi, Eriksson, Johan G., Jacobs, David, Deary, Ian J., Soranzo, Nicole, Tracy, Russell P., Hayward, Caroline, Koenig, Wolfgang, Cucca, Francesco, Samani, Nilesh J., Smith, Nicholas L., Ridker, Paul M, Tang, Weihong, Hamsten, Anders, O’Donnell, Christopher J.
Published in Circulation (New York, N.Y.) (17.09.2013)
Published in Circulation (New York, N.Y.) (17.09.2013)
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GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway
Kiryluk, Krzysztof, Li, Yifu, Moldoveanu, Zina, Suzuki, Hitoshi, Reily, Colin, Hou, Ping, Xie, Jingyuan, Mladkova, Nikol, Prakash, Sindhuri, Fischman, Clara, Shapiro, Samantha, LeDesma, Robert A., Bradbury, Drew, Ionita-Laza, Iuliana, Eitner, Frank, Rauen, Thomas, Maillard, Nicolas, Berthoux, Francois, Floege, Jürgen, Chen, Nan, Zhang, Hong, Scolari, Francesco, Wyatt, Robert J., Julian, Bruce A., Gharavi, Ali G., Novak, Jan
Published in PLoS genetics (10.02.2017)
Published in PLoS genetics (10.02.2017)
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Carbamazepine and phenytoin induced Stevens‐Johnson syndrome is associated with HLA‐B1502 allele in Thai population
Locharernkul, Chaichon, Loplumlert, Jakrin, Limotai, Chusak, Korkij, Wiwat, Desudchit, Tayard, Tongkobpetch, Siraprapa, Kangwanshiratada, Oratai, Hirankarn, Nattiya, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk
Published in Epilepsia (Copenhagen) (01.12.2008)
Published in Epilepsia (Copenhagen) (01.12.2008)
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TREM2 is associated with the risk of Alzheimer's disease in Spanish population
Benitez, Bruno A., Cooper, Breanna, Pastor, Pau, Jin, Sheng-Chih, Lorenzo, Elena, Cervantes, Sebastian, Cruchaga, Carlos
Published in Neurobiology of aging (01.06.2013)
Published in Neurobiology of aging (01.06.2013)
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Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue
Shi, Jianxin, Marconett, Crystal N., Duan, Jubao, Hyland, Paula L., Li, Peng, Wang, Zhaoming, Wheeler, William, Zhou, Beiyun, Campan, Mihaela, Lee, Diane S., Huang, Jing, Zhou, Weiyin, Triche, Tim, Amundadottir, Laufey, Warner, Andrew, Hutchinson, Amy, Chen, Po-Han, Chung, Brian S. I., Pesatori, Angela C., Consonni, Dario, Bertazzi, Pier Alberto, Bergen, Andrew W., Freedman, Mathew, Siegmund, Kimberly D., Berman, Benjamin P., Borok, Zea, Chatterjee, Nilanjan, Tucker, Margaret A., Caporaso, Neil E., Chanock, Stephen J., Laird-Offringa, Ite A., Landi, Maria Teresa
Published in Nature communications (27.02.2014)
Published in Nature communications (27.02.2014)
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Association between habitual coffee consumption and multiple disease outcomes: A Mendelian randomisation phenome-wide association study in the UK Biobank
Nicolopoulos, Konstance, Mulugeta, Anwar, Zhou, Ang, Hyppönen, Elina
Published in Clinical nutrition (Edinburgh, Scotland) (01.11.2020)
Published in Clinical nutrition (Edinburgh, Scotland) (01.11.2020)
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Implication of Genetic Variants Near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in Type 2 Diabetes and Obesity in 6,719 Asians
Ng, Maggie C.Y., Park, Kyong Soo, Oh, Bermseok, Tam, Claudia H.T., Cho, Young Min, Shin, Hyoung Doo, Lam, Vincent K.L., Ma, Ronald C.W., So, Wing Yee, Cho, Yoon Shin, Kim, Hyung-Lae, Lee, Hong Kyu, Chan, Juliana C.N., Cho, Nam H.
Published in Diabetes (New York, N.Y.) (01.08.2008)
Published in Diabetes (New York, N.Y.) (01.08.2008)
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Genomewide Association Study Using a High-Density Single Nucleotide Polymorphism Array and Case-Control Design Identifies a Novel Essential Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Synthase
Salvi, Erika, Kutalik, Zoltán, Glorioso, Nicola, Benaglio, Paola, Frau, Francesca, Kuznetsova, Tatiana, Arima, Hisatomi, Hoggart, Clive, Tichet, Jean, Nikitin, Yury P., Conti, Costanza, Seidlerova, Jitka, Tikhonoff, Valérie, Stolarz-Skrzypek, Katarzyna, Johnson, Toby, Devos, Nabila, Zagato, Laura, Guarrera, Simonetta, Zaninello, Roberta, Calabria, Andrea, Stancanelli, Benedetta, Troffa, Chiara, Thijs, Lutgarde, Rizzi, Federica, Simonova, Galina, Lupoli, Sara, Argiolas, Giuseppe, Braga, Daniele, DʼAlessio, Maria C., Ortu, Maria F., Ricceri, Fulvio, Mercurio, Maurizio, Descombes, Patrick, Marconi, Maurizio, Chalmers, John, Harrap, Stephen, Filipovsky, Jan, Bochud, Murielle, Iacoviello, Licia, Ellis, Justine, Stanton, Alice V., Laan, Maris, Padmanabhan, Sandosh, Dominiczak, Anna F., Samani, Nilesh J., Melander, Olle, Jeunemaitre, Xavier, Manunta, Paolo, Shabo, Amnon, Vineis, Paolo, Cappuccio, Francesco P., Caulfield, Mark J., Matullo, Giuseppe, Rivolta, Carlo, Munroe, Patricia B., Barlassina, Cristina, Staessen, Jan A., Beckmann, Jacques S., Cusi, Daniele
Published in Hypertension (Dallas, Tex. 1979) (01.02.2012)
Published in Hypertension (Dallas, Tex. 1979) (01.02.2012)
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MHC associations of ankylosing spondylitis in East Asians are complex and involve non-HLA-B27 HLA contributions
Wang, Geng, Kim, Tae-Hwan, Li, Zhixiu, Cortes, Adrian, Kim, Kwangwoo, Bang, So-Young, Leo, Paul, Brown, Matthew A., Xu, Huji
Published in Arthritis research & therapy (09.04.2020)
Published in Arthritis research & therapy (09.04.2020)
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The Impact of PNPLA3 rs738409 Genetic Polymorphism and Weight Gain ≥10 kg after Age 20 on Non-Alcoholic Fatty Liver Disease in Non-Obese Japanese Individuals
Nishioji, Kenichi, Mochizuki, Naomi, Kobayashi, Masao, Kamaguchi, Mai, Sumida, Yoshio, Nishimura, Takeshi, Yamaguchi, Kanji, Kadotani, Hiroshi, Itoh, Yoshito
Published in PloS one (20.10.2015)
Published in PloS one (20.10.2015)
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DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease
Xia, Hong, Huang, Xiangjun, Deng, Sheng, Xu, Hongbo, Yang, Yan, Liu, Xin, Yuan, Lamei, Deng, Hao
Published in PloS one (16.06.2021)
Published in PloS one (16.06.2021)
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Interferon-λ3/4 genetic variants and interferon-λ3 serum levels are biomarkers of lupus nephritis and disease activity in Taiwanese
Chen, Ji-Yih, Wang, Chin-Man, Chen, Tai-Di, Jan Wu, Yeong-Jian, Lin, Jing-Chi, Lu, Ling Ying, Wu, Jianming
Published in Arthritis research & therapy (29.08.2018)
Published in Arthritis research & therapy (29.08.2018)
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Prediction model for pancreatic cancer risk in the general Japanese population
Nakatochi, Masahiro, Lin, Yingsong, Ito, Hidemi, Hara, Kazuo, Kinoshita, Fumie, Kobayashi, Yumiko, Ishii, Hiroshi, Ozaka, Masato, Sasaki, Takashi, Sasahira, Naoki, Morimoto, Manabu, Kobayashi, Satoshi, Ueno, Makoto, Ohkawa, Shinichi, Egawa, Naoto, Kuruma, Sawako, Mori, Mitsuru, Nakao, Haruhisa, Wang, Chaochen, Nishiyama, Takeshi, Kawaguchi, Takahisa, Takahashi, Meiko, Matsuda, Fumihiko, Kikuchi, Shogo, Matsuo, Keitaro
Published in PloS one (07.09.2018)
Published in PloS one (07.09.2018)
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Mitochondrial DNA variants modulate genetic susceptibility to Parkinson's disease in Han Chinese
Wu, Hong-Mei, Li, Ting, Wang, Zhen-Feng, Huang, Shi-Shi, Shao, Zi-Qiang, Wang, Ke, Zhong, Hai-Qing, Chen, Song-Fang, Zhang, Xiong, Zhu, Jian-Hong
Published in Neurobiology of disease (01.06.2018)
Published in Neurobiology of disease (01.06.2018)
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Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide
García-Redondo, Alberto, Dols-Icardo, Oriol, Rojas-García, Ricard, Esteban-Pérez, Jesús, Cordero-Vázquez, Pilar, Muñoz-Blanco, José Luis, Catalina, Irene, González-Muñoz, Miguel, Varona, Luis, Sarasola, Esther, Povedano, Monica, Sevilla, Teresa, Guerrero, Antonio, Pardo, Julio, de Munain, Adolfo López, Márquez-Infante, Celedonio, de Rivera, Francisco Javier Rodríguez, Pastor, Pau, Jericó, Ivonne, de Arcaya, Amaya Álvarez, Mora, Jesús S., Clarimón, Jordi, Gonzalo-Martínez, Juan Francisco, Juárez-Rufián, Alexandra, Atencia, Gabriela, Jiménez-Bautista, Rosario, Morán, Yolanda, Mascías, Javier, Hernández-Barral, María, Kapetanovic, Solange, García-Barcina, María, Alcalá, Carmen, Vela, Álvaro, Ramírez-Ramos, Concepción, Galán, Lucía, Pérez-Tur, Jordi, Quintáns, Beatriz, Sobrido, M Jesús, Fernández-Torrón, Roberto, Poza, Juan José, Gorostidi, Ana, Paradas, Carmen, Villoslada, Pablo, Larrodé, Pilar, Capablo, José Luis, Pascual-Calvet, Jordi, Goñi, Miguel, Morgado, Yolanda, Guitart, Miriam, Moreno-Laguna, Sira, Rueda, Almudena, Martín-Estefanía, Carlos, Cemillán, Carlos, Blesa, Rafael, Lleó, Alberto
Published in Human mutation (01.01.2013)
Published in Human mutation (01.01.2013)
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