Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and meta-analysis and VPS13C[original query] |
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Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
Diabetes 2011 Oct 60 (10): 2624-34. Strawbridge Rona J, Dupuis Josée, Prokopenko Inga, Barker Adam, Ahlqvist Emma, Rybin Denis, Petrie John R, Travers Mary E, Bouatia-Naji Nabila, Dimas Antigone S, Nica Alexandra, Wheeler Eleanor, Chen Han, Voight Benjamin F, Taneera Jalal, Kanoni Stavroula, Peden John F, Turrini Fabiola, Gustafsson Stefan, Zabena Carina, Almgren Peter, Barker David J P, Barnes Daniel, Dennison Elaine M, Eriksson Johan G, Eriksson Per, Eury Elodie, Folkersen Lasse, Fox Caroline S, Frayling Timothy M, Goel Anuj, Gu Harvest F, Horikoshi Momoko, Isomaa Bo, Jackson Anne U, Jameson Karen A, Kajantie Eero, Kerr-Conte Julie, Kuulasmaa Teemu, Kuusisto Johanna, Loos Ruth J F, Luan Jian'an, Makrilakis Konstantinos, Manning Alisa K, Martínez-Larrad María Teresa, Narisu Narisu, Nastase Mannila Maria, Ohrvik John, Osmond Clive, Pascoe Laura, Payne Felicity, Sayer Avan A, Sennblad Bengt, Silveira Angela, Stancáková Alena, Stirrups Kathy, Swift Amy J, Syvänen Ann-Christine, Tuomi Tiinamaija, van 't Hooft Ferdinand M, Walker Mark, Weedon Michael N, Xie Weijia, Zethelius Björn, , , , , , Ongen Halit, Mälarstig Anders, Hopewell Jemma C, Saleheen Danish, Chambers John, Parish Sarah, Danesh John, Kooner Jaspal, Ostenson Claes-Göran, Lind Lars, Cooper Cyrus C, Serrano-Ríos Manuel, Ferrannini Ele, Forsen Tom J, Clarke Robert, Franzosi Maria Grazia, Seedorf Udo, Watkins Hugh, Froguel Philippe, Johnson Paul, Deloukas Panos, Collins Francis S, Laakso Markku, Dermitzakis Emmanouil T, Boehnke Michael, McCarthy Mark I, Wareham Nicholas J, Groop Leif, Pattou François, Gloyn Anna L, Dedoussis George V, Lyssenko Valeriya, Meigs James B, Barroso Inês, Watanabe Richard M, Ingelsson Erik, Langenberg Claudia, Hamsten Anders, Florez Jose |
| Association of four new candidate genetic variants with Parkinson's disease in a Han Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Dec . Wang Ling, Cheng Lan, Li Nan-Nan, Yu Wen-Juan, Sun Xiao-Yi, Peng Ro |
| SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study. Journal of the neurological sciences 2016 Oct 369 1-4. Safaralizadeh Tannaz, Jamshidi Javad, Esmaili Shandiz Ehsan, Movafagh Abolfazl, Fazeli Atena, Emamalizadeh Babak, Manafi Navid, Taghavi Shaghayegh, Tafakhori Abbas, Darvish Hosse |
| Genome-wide association study of Parkinson's disease in East Asians.
Human molecular genetics 2016 Dec . Foo Jia Nee, Tan Louis C, Irwan Ishak D, Au Wing-Lok, Low Hui Qi, Prakash Kumar-M, Ahmad-Annuar Azlina, Bei Jinxin, Chan Anne Yy, Chen Chiung Mei, Chen Yi-Chun, Chung Sun Ju, Deng Hao, Lim Shen-Yang, Mok Vincent, Pang Hao, Pei Zhong, Peng Rong, Shang Hui-Fang, Song Kyuyoung, Tan Ai Huey, Wu Yih-Ru, Aung Tin, Cheng Ching-Yu, Chew Fook Tim, Chew Soo-Hong, Chong Siow-Ann, Ebstein Richard P, Lee Jimmy, Saw Seang-Mei, Seow Adeline, Subramaniam Mythily, Tai E-Shyong, Vithana Eranga N, Wong Tien-Yin, Heng Khai Koon, Meah Wee-Yang, Khor Chiea Chuen, Liu Hong, Zhang Furen, Liu Jianjun, Tan Eng-Ki |
| Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan. Neurobiology of aging 2016 Mar 39 221.e1-5. Chen Chiung-Mei, Chen Yi-Chun, Chiang Mu-Chun, Fung Hon-Chung, Chang Kuo-Hsuan, Lee-Chen Guey-Jen, Wu Yih- |
| Association analyses of variants of SIPA1L2, MIR4697, GCH1, VPS13C, and DDRGK1 with Parkinson's disease in East Asians. Neurobiology of aging 2018 Mar . Zou Ming, Li Rui, Wang Jian-Yong, Wang Ke, Wang Ya-Nan, Li Yang, Ji Fei-Xue, Sun Sheng-Nan, Huang Shi-Shi, Fan Hui-Hui, Huang Chen-Ping, Zhang Xiong, Zhu Jian-Ho |
| Analysis of common and rare VPS13C variants in late-onset Parkinson disease. Neurology. Genetics 2020 2 6 (1): 385. Rudakou Uladzislau, Ruskey Jennifer A, Krohn Lynne, Laurent Sandra B, Spiegelman Dan, Greenbaum Lior, Yahalom Gilad, Desautels Alex, Montplaisir Jacques Y, Fahn Stanley, Waters Cheryl H, Levy Oren, Kehoe Caitlin M, Narayan Sushma, Dauvilliers Yves, Dupré Nicolas, Hassin-Baer Sharon, Alcalay Roy N, Rouleau Guy A, Fon Edward A, Gan-Or Z |
| Association between VPS13C rs2414739 polymorphism and Parkinson's disease risk: A meta-analysis. Neuroscience letters 2021 4 754 135879. Bai Xinling, Liu Xian, Li Xiaoyuan, Li Wenjian, Xie An |
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