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Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China
Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China
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Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China

Wu, Shan ; Wu, Zhidan ; Chen, Manlian ; Zhong, Xiangbin ; Gu, Haoyan ; Du, Wenjing ; Liu, Weidong ; Lang, Li ; Wang, Junyi

BMC medical genomics, 2024-01, Vol.17 (1), p.18-18, Article 18 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
The Application of Genetic Risk Scores in Rheumatic Diseases: A Perspective
The Application of Genetic Risk Scores in Rheumatic Diseases: A Perspective
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The Application of Genetic Risk Scores in Rheumatic Diseases: A Perspective

Vaskimo, Lotta M ; Gomon, Georgy ; Naamane, Najib ; Cordell, Heather J ; Pratt, Arthur ; Knevel, Rachel

Genes, 2023-12, Vol.14 (12), p.2167 [Periódico revisado por pares]

Switzerland: MDPI AG

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3
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
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Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

Zhao, Wei ; Rasheed, Asif ; Tikkanen, Emmi ; Lee, Jung-Jin ; Butterworth, Adam S ; Howson, Joanna M M ; Assimes, Themistocles L ; Chowdhury, Rajiv ; Orho-Melander, Marju ; Damrauer, Scott ; Small, Aeron ; Asma, Senay ; Imamura, Minako ; Yamauch, Toshimasa ; Chambers, John C ; Chen, Peng ; Sapkota, Bishwa R ; Shah, Nabi ; Jabeen, Sehrish ; Surendran, Praveen ; Lu, Yingchang ; Zhang, Weihua ; Imran, Atif ; Abbas, Shahid ; Majeed, Faisal ; Trindade, Kevin ; Qamar, Nadeem ; Mallick, Nadeem Hayyat ; Yaqoob, Zia ; Saghir, Tahir ; Rizvi, Syed Nadeem Hasan ; Memon, Anis ; Rasheed, Syed Zahed ; Memon, Fazal-Ur-Rehman ; Mehmood, Khalid ; Ahmed, Naveeduddin ; Qureshi, Irshad Hussain ; Tanveer-Us-Salam ; Iqbal, Wasim ; Malik, Uzma ; Mehra, Narinder ; Kuo, Jane Z ; Sheu, Wayne H-H ; Guo, Xiuqing ; Hsiung, Chao A ; Juang, Jyh-Ming J ; Taylor, Kent D ; Hung, Yi-Jen ; Lee, Wen-Jane ; Quertermous, Thomas ; Lee, I-Te ; Hsu, Chih-Cheng ; Bottinger, Erwin P ; Ralhan, Sarju ; Teo, Yik Ying ; Wang, Tzung-Dau ; Alam, Dewan S ; Di Angelantonio, Emanuele ; Epstein, Steve ; Nielsen, Sune F ; Nordestgaard, Børge G ; Tybjaerg-Hansen, Anne ; Young, Robin ; Benn, Marianne ; Frikke-Schmidt, Ruth ; Kamstrup, Pia R ; Jukema, J Wouter ; Sattar, Naveed ; Smit, Roelof ; Chung, Ren-Hua ; Liang, Kae-Woei ; Anand, Sonia ; Sanghera, Dharambir K ; Ripatti, Samuli ; Loos, Ruth J F ; Kooner, Jaspal S ; Tai, E Shyong ; Rotter, Jerome I ; Chen, Yii-Der Ida ; Frossard, Philippe ; Maeda, Shiro ; Kadowaki, Takashi ; Reilly, Muredach ; Pare, Guillaume ; Melander, Olle ; Salomaa, Veikko ; Rader, Daniel J ; Danesh, John ; Voight, Benjamin F ; Saleheen, Danish

Nature genetics, 2017-10, Vol.49 (10), p.1450-1457 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
A Journey through Genetic Architecture and Predisposition of Coronary Artery Disease
A Journey through Genetic Architecture and Predisposition of Coronary Artery Disease
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A Journey through Genetic Architecture and Predisposition of Coronary Artery Disease

Roberts, Robert ; Chang, Chih Chao

Current genomics, 2020-08, Vol.21 (5), p.382-398 [Periódico revisado por pares]

United Arab Emirates: Bentham Science Publishers Ltd

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5
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Mahajan, Anubha ; Petty, Lauren E ; Chiou, Joshua ; Miguel-Escalada, Irene ; Nakatochi, Masahiro ; Huerta-Chagoya, Alicia ; Bielak, Lawrence F ; Hai, Yang ; Kals, Mart ; Grarup, Niels ; Wuttke, Matthias ; Nousome, Darryl ; Long, Jirong ; Ahmad, Meraj ; Jensen, Richard A ; An, Ping ; Cade, Brian E ; Abaitua, Fernando ; Akiyama, Masato ; Bertoni, Alain ; Bian, Zheng ; Brummett, Chad M ; Chee, Miao-Li ; Das, Swapan K ; Du, Shufa ; Duan, Qing ; Eckardt, Kai-Uwe ; Fischer, Krista ; Floyd, James S ; Genter, Pauline ; González-Villalpando, Maria Elena ; Gordon-Larsen, Penny ; Gorkin, David ; Herder, Christian ; Hung, Yi-Jen ; Hwu, Chii-Min ; Ikram, Mohammad Arfan ; Ingelsson, Martin ; Islam, Md Tariqul ; Isono, Masato ; Kamatani, Yoichiro ; Katsuya, Tomohiro ; Khor, Chiea-Chuen ; Kohara, Katsuhiko ; Kriebel, Jennifer ; Kuusisto, Johanna ; Läll, Kristi ; Leong, Aaron ; Luan, Jian'an ; Lv, Jun ; Lyssenko, Valeriya ; Meitinger, Thomas ; Morris, Andrew D ; Nadkarni, Girish N ; Nayak, Uma ; Ntalla, Ioanna ; Peters, Annette ; Preissl, Sebastian ; Rasmussen-Torvik, Laura J ; Roden, Michael ; Sabanayagam, Charumathi ; Schönherr, Sebastian ; Shahriar, Mohammad ; Shi, Jinxiu ; Stančáková, Alena ; Strauch, Konstantin ; Thorleifsson, Gudmar ; Thorsteinsdottir, Unnur ; Tsai, Fuu-Jen ; Tusie-Luna, Teresa ; Udler, Miriam S ; Valladares-Salgado, Adan ; Yajnik, Chittaranjan S ; Yoon, Kyungheon ; Igase, Michiya ; Hanis, Craig L ; Ingelsson, Erik ; Zeggini, Eleftheria ; Rich, Stephen S ; Kooperberg, Charles ; Engert, James C ; Wilson, James G ; Kardia, Sharon L R ; Groop, Leif ; Bharadwaj, Dwaipayan ; Sale, Michèle M ; Cruz, Miguel ; Tai, E-Shyong ; Kato, Norihiro ; Laakso, Markku ; Köttgen, Anna ; Loos, Ruth J F ; Saleheen, Danish ; Hansen, Torben ; Kadowaki, Takashi ; Walters, Robin G ; Stefansson, Kari ; Meigs, James B ; Gloyn, Anna L ; Chambers, John C

Nature genetics, 2022-05, Vol.54 (5), p.560-572 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example
Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example
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Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example

Goldstein, Benjamin A ; Knowles, Joshua W ; Salfati, Elias ; Ioannidis, John P A ; Assimes, Themistocles L

Frontiers in genetics, 2014-08, Vol.5, p.254-254 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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7
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
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Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Chia, Ruth ; Sabir, Marya S ; Saez-Atienzar, Sara ; Gustavsson, Emil ; Walton, Ronald L ; Ahmed, Sarah ; Makarious, Mary B ; Diez-Fairen, Monica ; Portley, Makayla K ; Shah, Zalak ; Hernandez, Dena G ; Blauwendraat, Cornelis ; Stone, David J ; Eicher, John ; Parkkinen, Laura ; Ansorge, Olaf ; Honig, Lawrence S ; Marder, Karen ; Lemstra, Afina ; Londos, Elisabet ; Morgan, Kevin ; Warner, Thomas T ; Jaunmuktane, Zane ; Galasko, Douglas ; Tienari, Pentti J ; Oinas, Minna ; Morris, John C ; Halliday, Glenda M ; Van Deerlin, Vivianna M ; Trojanowski, John Q ; Calvo, Andrea ; Canosa, Antonio ; Floris, Gianluca ; Bohannan, Ryan C ; Gan-Or, Ziv ; Geiger, Joshua T ; Krüger, Rejko ; Lopez, Grisel ; Sidransky, Ellen ; Norcliffe-Kaufmann, Lucy ; Kaufmann, Horacio ; Shakkottai, Vikram G ; Perkins, Matthew ; Newell, Kathy L ; Gasser, Thomas ; Schulte, Claudia ; Landi, Francesco ; Cusi, Daniele ; Monuki, Edwin S ; Brunetti, Maura ; Dawson, Ted M ; Rosenthal, Liana S ; Pletnikova, Olga ; Flanagan, Margaret E ; Rodríguez-Rodríguez, Eloy ; Infante, Jon ; Lage, Carmen ; Black, Sandra E ; Masellis, Mario ; Rogaeva, Ekaterina ; Duyckaerts, Charles ; Brice, Alexis ; Tilley, Bension S ; Gentleman, Steve ; Logroscino, Giancarlo ; Serrano, Geidy E ; Beach, Thomas G ; McKeith, Ian G ; Morris, Christopher M ; Al-Sarraj, Safa ; Hodges, Angela K ; Aarsland, Dag ; Klein, Gregory ; Kaiser, Scott M ; Woltjer, Randy ; Bekris, Lynn M ; Leverenz, James B ; Besser, Lilah M ; Kuzma, Amanda ; Morris, Huw R ; Albani, Diego ; Pickering-Brown, Stuart ; Faber, Kelley ; Morenas-Rodriguez, Estrella ; Fortea, Juan ; Alcolea, Daniel ; Nalls, Mike A ; Ferrucci, Luigi ; Resnick, Susan M ; Foroud, Tatiana M ; Graff-Radford, Neill R ; Ferman, Tanis ; Hardy, John A ; Torkamani, Ali ; Ryten, Mina ; Chiò, Adriano ; Ross, Owen A ; Gibbs, J Raphael ; Dalgard, Clifton L ; Traynor, Bryan J

Nature genetics, 2021-03, Vol.53 (3), p.294-303 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Weiner, Daniel J ; Wigdor, Emilie M ; Ripke, Stephan ; Walters, Raymond K ; Kosmicki, Jack A ; Grove, Jakob ; Samocha, Kaitlin E ; Goldstein, Jacqueline I ; Okbay, Aysu ; Bybjerg-Grauholm, Jonas ; Werge, Thomas ; Hougaard, David M ; Taylor, Jacob ; Skuse, David ; Devlin, Bernie ; Anney, Richard ; Sanders, Stephan J ; Bishop, Somer ; Mortensen, Preben Bo ; Børglum, Anders D ; Smith, George Davey ; Daly, Mark J ; Robinson, Elise B

Nature genetics, 2017-07, Vol.49 (7), p.978-985 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Low copy number of the salivary amylase gene predisposes to obesity
Low copy number of the salivary amylase gene predisposes to obesity
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Low copy number of the salivary amylase gene predisposes to obesity

Falchi, Mario ; El-Sayed Moustafa, Julia Sarah ; Takousis, Petros ; Pesce, Francesco ; Bonnefond, Amélie ; Andersson-Assarsson, Johanna C ; Sudmant, Peter H ; Dorajoo, Rajkumar ; Al-Shafai, Mashael Nedham ; Bottolo, Leonardo ; Ozdemir, Erdal ; So, Hon-Cheong ; Davies, Robert W ; Patrice, Alexandre ; Dent, Robert ; Mangino, Massimo ; Hysi, Pirro G ; Dechaume, Aurélie ; Huyvaert, Marlène ; Skinner, Jane ; Pigeyre, Marie ; Caiazzo, Robert ; Raverdy, Violeta ; Vaillant, Emmanuel ; Field, Sarah ; Balkau, Beverley ; Marre, Michel ; Visvikis-Siest, Sophie ; Weill, Jacques ; Poulain-Godefroy, Odile ; Jacobson, Peter ; Sjostrom, Lars ; Hammond, Christopher J ; Deloukas, Panos ; Sham, Pak Chung ; McPherson, Ruth ; Lee, Jeannette ; Tai, E Shyong ; Sladek, Robert ; Carlsson, Lena M S ; Walley, Andrew ; Eichler, Evan E ; Pattou, Francois ; Spector, Timothy D ; Froguel, Philippe

Nature genetics, 2014-05, Vol.46 (5), p.492-497 [Periódico revisado por pares]

United States: Nature Publishing Group

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10
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
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Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Moser, Gerhard ; Agartz, Ingrid ; Andreassen, Ole A. ; Anjorin, Adebayo ; Bass, Nicholas ; Bergen, Sarah E. ; Betancur, Catalina ; Black, Donald W. ; Bloss, Cinnamon S. ; Buxbaum, Joseph D. ; Cantor, Rita M. ; Cormand, Bru ; Coryell, William H. ; Craig, Ian W. ; Crosbie, Jennifer ; Djurovic, Srdjan ; Ebstein, Richard P. ; Etain, Bruno ; Faraone, Stephen V. ; Farmer, Anne E. ; Ferrier, I. Nicol ; Fombonne, Eric ; Frank, Josef ; Franke, Barbara ; Freitag, Christine M. ; Friedl, Marion ; Gershon, Elliot S. ; Gill, Michael ; Gordon, Scott D. ; Green, Elaine K. ; De Haan, Lieuwe ; Haines, Jonathan L. ; Hakonarson, Hakon ; Hallmayer, Joachim ; Hamilton, Steven P. ; Hamshere, Marian L. ; Hoogendijk, Witte J. ; Hottenga, Jouke-Jan ; Hus, Vanessa ; Jamain, Stéphane ; Jones, Lisa ; Kenny, Elaine ; Krabbendam, Lydia ; Kuntsi, Jonna ; Landén, Mikael ; Lesch, Klaus-Peter ; Lichtenstein, Paul ; Lieberman, Jeffrey A. ; Linszen, Don H. ; Loo, Sandra K. ; Lowe, Jennifer K. ; Lucae, Susanne ; Magnusson, Patrik K.E. ; Mahon, Pamela B. ; Martin, Christa L. ; McGhee, Kevin A. ; McGuffin, Peter ; McInnis, Melvin G. ; McIntosh, Andrew ; McLean, Alan W. ; McMahon, William M. ; Meier, Sandra ; Meng, Fan ; Meyer, Jobst ; Middeldorp, Christel M. ; Miranda, Ana ; Montgomery, Grant W. ; Mühleisen, Thomas W. ; Neale, Benjamin M. ; Nyholt, Dale R. ; O’Donovan, Michael C. ; Olsen, Line ; Penninx, Brenda W. ; Pergadia, Michele L. ; Pericak-Vance, Margaret A. ; Perlis, Roy H. ; Posthuma, Danielle ; Rasmussen, Henrik B. ; Reif, Andreas ; Ribasés, Marta ; Rice, John P. ; Rossin, Lizzy ; Sanders, Stephan J. ; Schachar, Russell ; Schellenberg, Gerard D. ; Schumacher, Johannes ; Scott, Laura J. ; Smalley, Susan L. ; Smit, Johannes H. ; Szelinger, Szabocls ; Thapar, Anita ; Thirumalai, Srinivasa ; Treutlein, Jens ; Visscher, Peter M. ; Willemsen, Gonneke ; Young, Allan H. ; Zammit, Stanley ; Zitman, Frans G. ; Potash, James B. ; Shi, Jianxin

American journal of human genetics, 2015-02, Vol.96 (2), p.283-294 [Periódico revisado por pares]

United States: Elsevier Inc

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