Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: SGCG[original query] |
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Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India.
Diabetes 2013 May 62 (5): 1746-55. Saxena Richa, Saleheen Danish, Been Latonya F, Garavito Martha L, Braun Timothy, Bjonnes Andrew, Young Robin, Ho Weang Kee, Rasheed Asif, Frossard Philippe, Sim Xueling, Hassanali Neelam, Radha Venkatesan, Chidambaram Manickam, Liju Samuel, Rees Simon D, Ng Daniel Peng-Keat, Wong Tien-Yin, Yamauchi Toshimasa, Hara Kazuo, Tanaka Yasushi, Hirose Hiroshi, McCarthy Mark I, Morris Andrew P, , , , Basit Abdul, Barnett Anthony H, Katulanda Prasad, Matthews David, Mohan Viswanathan, Wander Gurpreet S, Singh Jai Rup, Mehra Narinder K, Ralhan Sarju, Kamboh M Ilyas, Mulvihill John J, Maegawa Hiroshi, Tobe Kazuyuki, Maeda Shiro, Cho Yoon S, Tai E Shyong, Kelly M Ann, Chambers John C, Kooner Jaspal S, Kadowaki Takashi, Deloukas Panos, Rader Daniel J, Danesh John, Sanghera Dharambir |
| A slowly progressive form of limb-girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican Hispanics. Molecular genetics & genomic medicine 2015 Mar 3 (2): 92-8. Al-Zaidy Samiah A, Malik Vinod, Kneile Kelley, Rosales Xiomara Q, Gomez Ana Maria, Lewis Sarah, Hashimoto Sayaka, Gastier-Foster Julie, Kang Peter, Darras Basil, Kunkel Louis, Carlo Jose, Sahenk Zarife, Moore Steven A, Pyatt Robert, Mendell Jerry |
| ?-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort. Muscle & nerve 2016 Oct . Dalichaouche Imene, Sifi Yamina, Roudaut Carinne, Sifi Karima, Hamri Abdelmadjid, Rouabah Leila, Abadi Noureddine, Richard Isabel |
| Three single nucleotide polymorphisms associated with type 2 diabetes mellitus in a Chinese population. Experimental and therapeutic medicine 2017 Jan 13 (1): 121-126. Chen Meijun, Zhang Xuelong, Fang Qingxiao, Wang Tongtong, Li Tingting, Qiao Ho |
| Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Nature genetics 2018 Jul . Nielsen Jonas B, Thorolfsdottir Rosa B, Fritsche Lars G, Zhou Wei, Skov Morten W, Graham Sarah E, Herron Todd J, McCarthy Shane, Schmidt Ellen M, Sveinbjornsson Gardar, Surakka Ida, Mathis Michael R, Yamazaki Masatoshi, Crawford Ryan D, Gabrielsen Maiken E, Skogholt Anne Heidi, Holmen Oddgeir L, Lin Maoxuan, Wolford Brooke N, Dey Rounak, Dalen Håvard, Sulem Patrick, Chung Jonathan H, Backman Joshua D, Arnar David O, Thorsteinsdottir Unnur, Baras Aris, O'Dushlaine Colm, Holst Anders G, Wen Xiaoquan, Hornsby Whitney, Dewey Frederick E, Boehnke Michael, Kheterpal Sachin, Mukherjee Bhramar, Lee Seunggeun, Kang Hyun M, Holm Hilma, Kitzman Jacob, Shavit Jordan A, Jalife José, Brummett Chad M, Teslovich Tanya M, Carey David J, Gudbjartsson Daniel F, Stefansson Kari, Abecasis Gonçalo R, Hveem Kristian, Willer Cristen |
| Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology 2019 3 37 (3): 210-220. Yi? Uluç, Diniz Gülden, Hazan Filiz, Daimagüler Hülya Sevcan, Baysal Bahar Toklu, Baydan Figen, Akinci Gülçin, Ünalp Aycan, Aktan Gül, Bayram Erhan, Hiz Semra, Paketçi Cem, Okur Derya, Özer Erdener, Danyeli Ayça Ersen, Polat Muzaffer, Uyanik Gökhan, Çirak Sebahatt |
| Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients. Clinical genetics 2019 3 96 (2): 126-133. Ten Dam Leroy, Frankhuizen Wendy S, Linssen Wim H J P, Straathof Chiara S, Niks Erik H, Faber Karin, Fock Annemarie, Kuks Jan B, Brusse Esther, de Coo René, Voermans Nicol, Verrips Aad, Hoogendijk Jessica E, van der Pol Ludo, Westra Dineke, de Visser Marianne, van der Kooi Anneke J, Ginjaar Ie |
| Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients. Orphanet journal of rare diseases 2019 2 14 (1): 43. Xie Zhiying, Hou Yue, Yu Meng, Liu Yilin, Fan Yanbin, Zhang Wei, Wang Zhaoxia, Xiong Hui, Yuan Y |
| New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy. Brain : a journal of neurology 2020 9 143 (9): 2696-2708. Alonso-Pérez Jorge, González-Quereda Lidia, Bello Luca, Guglieri Michela, Straub Volker, Gallano Pia, Semplicini Claudio, Pegoraro Elena, Zangaro Vittoria, Nascimento Andrés, Ortez Carlos, Comi Giacomo Pietro, Dam Leroy Ten, De Visser Marianne, van der Kooi A J, Garrido Cristina, Santos Manuela, Schara Ulrike, Gangfuß Andrea, Løkken Nicoline, Storgaard Jesper Helbo, Vissing John, Schoser Benedikt, Dekomien Gabriele, Udd Bjarne, Palmio Johanna, D'Amico Adele, Politano Luisa, Nigro Vincenzo, Bruno Claudio, Panicucci Chiara, Sarkozy Anna, Abdel-Mannan Omar, Alonso-Jimenez Alicia, Claeys Kristl G, Gomez-Andrés David, Munell Francina, Costa-Comellas Laura, Haberlová Jana, Rohlenová Marie, Elke De Vos, De Bleecker Jan L, Dominguez-González Cristina, Tasca Giorgio, Weiss Claudia, Deconinck Nicolas, Fernández-Torrón Roberto, López de Munain Adolfo, Camacho-Salas Ana, Melegh Béla, Hadzsiev Kinga, Leonardis Lea, Koritnik Blaz, Garibaldi Matteo, de Leon-Hernández Juan Carlos, Malfatti Edoardo, Fraga-Bau Arturo, Richard Isabelle, Illa Isabel, Díaz-Manera Jor |
| SGCG rs679482 Associates With Weight Loss Success in Response to an Intensively Supervised Outpatient Program. Diabetes 2020 6 69 (9): 2017-2026. Nikpay Majid, Lau Paulina, Soubeyrand Sébastien, Whytock Katey L, Beehler Kaitlyn, Pileggi Chantal, Ghosh Sujoy, Harper Mary-Ellen, Dent Robert, McPherson Ru |
| First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European journal of human genetics : EJHG 2020 Mar . Hengel Holger, Buchert Rebecca, Sturm Marc, Haack Tobias B, Schelling Yvonne, Mahajnah Muhammad, Sharkia Rajech, Azem Abdussalam, Balousha Ghassan, Ghanem Zaid, Falana Mohammed, Balousha Osama, Ayesh Suhail, Keimer Reinhard, Deigendesch Werner, Zaidan Jimmy, Marzouqa Hiyam, Bauer Peter, Schöls Ludg |
| Ethnic similarities in genetic polymorphisms associated with atrial fibrillation: Far East Asian vs European populations.
European journal of clinical investigation 2021 5 51 (9): e13584. Hong Myunghee, Ebana Yusuke, Shim Jaemin, Choi Eue-Keun, Lim Hong Euy, Hwang Inseok, Yu Hee Tae, Kim Tae-Hoon, Uhm Jae-Sun, Joung Boyoung, Oh Seil, Lee Moon-Hyoung, Kim Young-Hoon, Jee Sun Ha, Pak Hui-N |
| Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year's Journey. Journal of neuromuscular diseases 2021 1 8 (2): 261-272. Ten Dam L, de Visser M, Ginjaar Ieke B, van Duyvenvoorde Hermine A, van Koningsbruggen Silvana, van der Kooi Anneke |
| Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A?>?C. Neurogenetics 2022 4 23 (3): 187-202. Bardhan Mainak, Anjanappa Ram Murthy, Polavarapu Kiran, Preethish-Kumar Veeramani, Vengalil Seena, Nashi Saraswati, Sanga Shamita, Padmanabh Hansashree, Valasani Ravi Kiran, Nishadham Vikas, Keerthipriya Muddasu, Geetha Thenral S, Ramprasad Vedam, Arunachal Gautham, Thomas Priya Treesa, Acharya Moulinath, Nalini Atchayar |
| Genetic findings in Czech patients with limb girdle muscular dystrophy. Clinical genetics 2023 8 . Jana Zídková, Tereza Kramá?ová, Johana Kop?ilová, Kamila Réblová, Jana Haberlová, Radim Mazanec, Stanislav Vohá?ka, Andrea G?ego?ová, Martina Langová, Tomáš Honzík, Jana Šoukalová, Hana Ošlejšková, Pavla Sola?ová, Emílie Vyhnálková, Lenka Fajkuso |
| Genetic spectrum of sarcoglycanopathies in a cohort of Russian patients. Gene 2024 6 927 148680. Maria Bulakh, Daria Polyakova, Elena Dadali, Galina Rudenskaya, Inna Sharkova, Tatiana Markova, Aysylu Murtazina, Nina Demina, Sergei Kurbatov, Natalia Nikitina, Vasilisa Udalova, Aleksander Polyakov, Oxana Ryzhko |
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