Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: VPS13C[original query] |
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Variants from GIPR, TCF7L2, DGKB, MADD, CRY2, GLIS3, PROX1, SLC30A8 and IGF1 are associated with glucose metabolism in the Chinese. PloS one 2010 5 (11): e15542. Hu Cheng, Zhang Rong, Wang Congrong, Wang Jie, Ma Xiaojing, Hou Xuhong, Lu Jingyi, Yu Weihui, Jiang Feng, Bao Yuqian, Xiang Kunsan, Jia Weipi |
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.
Nature genetics 2010 Feb 42 (2): 142-8. Saxena Richa, Hivert Marie-France, Langenberg Claudia, Tanaka Toshiko, Pankow James S, Vollenweider Peter, Lyssenko Valeriya, Bouatia-Naji Nabila, Dupuis Josée, Jackson Anne U, Kao W H Linda, Li Man, Glazer Nicole L, Manning Alisa K, Luan Jian'an, Stringham Heather M, Prokopenko Inga, Johnson Toby, Grarup Niels, Boesgaard Trine W, Lecoeur Cécile, Shrader Peter, O'Connell Jeffrey, Ingelsson Erik, Couper David J, Rice Kenneth, Song Kijoung, Andreasen Camilla H, Dina Christian, Köttgen Anna, Le Bacquer Olivier, Pattou François, Taneera Jalal, Steinthorsdottir Valgerdur, Rybin Denis, Ardlie Kristin, Sampson Michael, Qi Lu, van Hoek Mandy, Weedon Michael N, Aulchenko Yurii S, Voight Benjamin F, Grallert Harald, Balkau Beverley, Bergman Richard N, Bielinski Suzette J, Bonnefond Amelie, Bonnycastle Lori L, Borch-Johnsen Knut, Böttcher Yvonne, Brunner Eric, Buchanan Thomas A, Bumpstead Suzannah J, Cavalcanti-Proença Christine, Charpentier Guillaume, Chen Yii-Der Ida, Chines Peter S, Collins Francis S, Cornelis Marilyn, J Crawford Gabriel, Delplanque Jerome, Doney Alex, Egan Josephine M, Erdos Michael R, Firmann Mathieu, Forouhi Nita G, Fox Caroline S, Goodarzi Mark O, Graessler Jürgen, Hingorani Aroon, Isomaa Bo, Jørgensen Torben, Kivimaki Mika, Kovacs Peter, Krohn Knut, Kumari Meena, Lauritzen Torsten, Lévy-Marchal Claire, Mayor Vladimir, McAteer Jarred B, Meyre David, Mitchell Braxton D, Mohlke Karen L, Morken Mario A, Narisu Narisu, Palmer Colin N A, Pakyz Ruth, Pascoe Laura, Payne Felicity, Pearson Daniel, Rathmann Wolfgang, Sandbaek Annelli, Sayer Avan Aihie, Scott Laura J, Sharp Stephen J, Sijbrands Eric, Singleton Andrew, Siscovick David S, Smith Nicholas L, Sparsø Thomas, Swift Amy J, Syddall Holly, Thorleifsson Gudmar, Tönjes Anke, Tuomi Tiinamaija, Tuomilehto Jaakko, Valle Timo T, Waeber Gérard, Walley Andrew, Waterworth Dawn M, Zeggini Eleftheria, Zhao Jing Hua, , , Illig Thomas, Wichmann H Erich, Wilson James F, van Duijn Cornelia, Hu Frank B, Morris Andrew D, Frayling Timothy M, Hattersley Andrew T, Thorsteinsdottir Unnur, Stefansson Kari, Nilsson Peter, Syvänen Ann-Christine, Shuldiner Alan R, Walker Mark, Bornstein Stefan R, Schwarz Peter, Williams Gordon H, Nathan David M, Kuusisto Johanna, Laakso Markku, Cooper Cyrus, Marmot Michael, Ferrucci Luigi, Mooser Vincent, Stumvoll Michael, Loos Ruth J F, Altshuler David, Psaty Bruce M, Rotter Jerome I, Boerwinkle Eric, Hansen Torben, Pedersen Oluf, Florez Jose C, McCarthy Mark I, Boehnke Michael, Barroso Inês, Sladek Robert, Froguel Philippe, Meigs James B, Groop Leif, Wareham Nicholas J, Watanabe Richard |
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 |
Frameshift mutations of vacuolar protein sorting genes in gastric and colorectal cancers with microsatellite instability. Human pathology 2012 Jan 43 (1): 40-7. An Chang Hyeok, Kim Yoo Ri, Kim Ho Shik, Kim Sung Soo, Yoo Nam Jin, Lee Sug Hyu |
Effects of genetic variants in ADCY5, GIPR, GCKR and VPS13C on early impairment of glucose and insulin metabolism in children. PloS one 2011 6 (7): e22101. Windholz Jan, Kovacs Peter, Tönjes Anke, Dittrich Kathrin, Blüher Susann, Kiess Wieland, Stumvoll Michael, Körner Ant |
The diabetogenic VPS13C/C2CD4A/C2CD4B rs7172432 variant impairs glucose-stimulated insulin response in 5,722 non-diabetic Danish individuals. Diabetologia 2011 Apr 54 (4): 789-94. Grarup N, Overvad M, Sparsø T, Witte D R, Pisinger C, Jørgensen T, Yamauchi T, Hara K, Maeda S, Kadowaki T, Hansen T, Pedersen |
Genetic variants in GCKR, GIPR, ADCY5 and VPS13C and the risk of severe sulfonylurea-induced hypoglycaemia in patients with type 2 diabetes. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2013 Jan 121 (1): 54-7. Holstein J D, Patzer O, Körner A, Stumvoll M, Kovacs P, Holstein |
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- |
Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease. Clinical genetics 2017 9 93 (3): 603-612. Schormair B, Kemlink D, Mollenhauer B, Fiala O, Machetanz G, Roth J, Berutti R, Strom T M, Haslinger B, Trenkwalder C, Zahorakova D, Martasek P, Ruzicka E, Winkelmann |
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.
Diabetes 2017 May . Wood Andrew R, Jonsson Anna, Jackson Anne U, Wang Nan, van Leewen Nienke, Palmer Nicholette D, Kobes Sayuko, Deelen Joris, Boquete-Vilarino Lorena, Paananen Jussi, Stan?áková Alena, Boomsma Dorret I, de Geus Eco Jc, Eekhoff Elisabeth Mw, Fritsche Andreas, Kramer Mark, Nijpels Giel, Simonis-Bik Annemarie, van Haeften Timon W, Mahajan Anubha, Boehnke Michael, Bergman Richard N, Tuomilehto Jaakko, Collins Francis S, Mohlke Karen L, Banasik Karina, Groves Christopher J, McCarthy Mark I, Pearson Ewan R, Natali Andrea, Mari Andrea, Buchanan Thomas A, Taylor Kent D, Xiang Anny H, Gjesing Anette P, Grarup Niels, Eiberg Hans, Pedersen Oluf, Chen Yii-Derr, Laakso Markku, Norris Jill M, Smith Ulf, Wagenknecht Lynne E, Baier Leslie, Bowden Donald W, Hansen Torben, Walker Mark, Watanabe Richard M, 't Hart Leen M, Hanson Robert L, Frayling Timothy |
Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population. Neuroscience letters 2017 05 650 8-11. Yang Xinglong, Zheng Jinhua, An Ran, Tian Sijia, Zhao Quanzhen, Chen Yalan, Huang Hongyan, Ning Ping Ping, Song Yi, Xu Yanmi |
Identification of novel mutations in endometrial cancer patients by whole-exome sequencing. International journal of oncology 2017 Mar . Chang Ya-Sian, Huang Hsien-Da, Yeh Kun-Tu, Chang Jan-Gow |
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 |
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor molecular case studies 2019 12 5 (6): . Cochran J Nicholas, McKinley Emily C, Cochran Meagan, Amaral Michelle D, Moyers Bryan A, Lasseigne Brittany N, Gray David E, Lawlor James M J, Prokop Jeremy W, Geier Ethan G, Holt James M, Thompson Michelle L, Newberry J Scott, Yokoyama Jennifer S, Worthey Elizabeth A, Geldmacher David S, Love Marissa Natelson, Cooper Gregory M, Myers Richard M, Roberson Erik |
Parkin is the most common causative gene in a cohort of mainland Chinese patients with sporadic early-onset Parkinson's disease. Brain and behavior 2020 Jul e01765. Jiang Yanyan, Yu Meng, Chen Jing, Zhou Hong, Sun Wei, Sun Yunchuang, Li Fan, Wei Luhua, Pinkhardt Elmar H, Zhang Lin, Yuan Yun, Wang Zhaox |
Mutation screening and burden analysis of VPS13C in Chinese patients with early-onset Parkinson's disease. Neurobiology of aging 2020 6 94 311.e1-311.e4. Gu Xiaojing, Li Chunyu, Chen Yongping, Ou Ruwei, Cao Bei, Wei Qianqian, Hou Yanbing, Zhang Lingyu, Song Wei, Zhao Bi, Wu Ying, Shang Huifa |
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society 2020 Apr . Hopfner Franziska, Mueller Stefanie H, Szymczak Silke, Junge Olaf, Tittmann Lukas, May Sandra, Lohmann Katja, Grallert Harald, Lieb Wolfgang, Strauch Konstantin, Müller-Nurasyid Martina, Berger Klaus, Schormair Barbara, Winkelmann Juliane, Mollenhauer Brit, Trenkwalder Claudia, Maetzler Walter, Berg Daniela, Kasten Meike, Klein Christine, Höglinger Günter U, Gasser Thomas, Deuschl Günther, Franke André, Krawczak Michael, Dempfle Astrid, Kuhlenbäumer Greg |
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 |
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder. Movement disorders : official journal of the Movement Disorder Society 2020 10 36 (1): 235-240. Mufti Kheireddin, Rudakou Uladzislau, Yu Eric, Krohn Lynne, Ruskey Jennifer A, Asayesh Farnaz, Laurent Sandra B, Spiegelman Dan, Arnulf Isabelle, Hu Michele T M, Montplaisir Jacques Y, Gagnon Jean-François, Desautels Alex, Dauvilliers Yves, Gigli Gian Luigi, Valente Mariarosaria, Janes Francesco, Högl Birgit, Stefani Ambra, Holzknecht Evi, Šonka Karel, Kemlink David, Oertel Wolfgang, Janzen Annette, Plazzi Giuseppe, Antelmi Elena, Figorilli Michela, Puligheddu Monica, Mollenhauer Brit, Trenkwalder Claudia, Sixel-Döring Friederike, Cochen De Cock Valérie, Monaca Christelle Charley, Heidbreder Anna, Ferini-Strambi Luigi, Dijkstra Femke, Viaene Mineke, Abril Beatriz, Boeve Bradley F, Postuma Ronald B, Rouleau Guy A, Gan-Or Z |
Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease. Frontiers in neurology 2021 8 12 656342. Torrealba-Acosta Gabriel, Yu Eric, Lobo-Prada Tanya, Ruíz-Martínez Javier, Gorostidi-Pagola Ana, Gan-Or Ziv, Carazo-Céspedes Kenneth, Trempe Jean-François, Mata Ignacio F, Fornaguera-Trías Jai |
Rare Variants Analysis of Lysosomal Related Genes in Early-Onset and Familial Parkinson's Disease in a Chinese Cohort. Journal of Parkinson's disease 2021 7 11 (4): 1845-1855. Chen Yong-Ping, Gu Xiao-Jing, Song Wei, Hou Yan-Bing, Ou Ru-Wei, Zhang Ling-Yu, Liu Kun-Cheng, Su Wei-Ming, Cao Bei, Wei Qian-Qian, Zhao Bi, Wu Ying, Shang Hui-Fa |
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 |
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease. Acta neuropathologica communications 2021 Feb 9 (1): 25. Smolders Stefanie, Philtjens Stéphanie, Crosiers David, Sieben Anne, Hens Elisabeth, Heeman Bavo, Van Mossevelde Sara, Pals Philippe, Asselbergh Bob, Dos Santos Dias Roberto, Vermeiren Yannick, Vandenberghe Rik, Engelborghs Sebastiaan, De Deyn Peter Paul, Martin Jean-Jacques, Cras Patrick, Annaert Wim, Van Broeckhoven Christine, |
Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India. Advanced biology 2022 Jul e2101326. Kukkle Prashanth Lingappa, Geetha Thenral S, Chaudhary Ruchi, Sathirapongsasuti Jarupon F, Goyal Vinay, Kandadai Rukmini Mridula, Kumar Hrishikesh, Borgohain Rupam, Mukherjee Adreesh, Oliver Merina, Sunil Meeta, Mootor Mohammed Faizal Eeman, Kapil Shruti, Mandloi Nitin, Wadia Pettarusp M, Yadav Ravi, Desai Soaham, Kumar Niraj, Biswas Atanu, Pal Pramod Kumar, Muthane Uday B, Das Shymal Kumar, Sakthivel Murugan Sakthivel M, Peterson Andrew S, Stawiski Eric W, Seshagiri Somasekar, Gupta Ravi, Ramprasad Vedam L, Prai Parkinson Research Alliance Of Ind |
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients. Journal of molecular neuroscience : MN 2023 5 . Imane Smaili, Houyam Tibar, Mounia Rahmani, Najlaa Machkour, Rachid Razine, Hajar Naciri Darai, Naima Bouslam, Ali Benomar, Wafa Regragui, Ahmed Bouhouc |
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population.
NPJ Parkinson's disease 2023 2 9 (1): 22. Pan Hongxu, Liu Zhenhua, Ma Jinghong, Li Yuanyuan, Zhao Yuwen, Zhou Xiaoxia, Xiang Yaqin, Wang Yige, Zhou Xun, He Runcheng, Xie Yali, Zhou Qiao, Yuan Kai, Xu Qian, Sun Qiying, Wang Junling, Yan Xinxiang, Zhang Hainan, Wang Chunyu, Lei Lifang, Liu Weiguo, Wang Xuejing, Ding Xuebing, Wang Tao, Xue Zheng, Zhang Zhentao, Chen Ling, Wang Qing, Liu Yonghong, Tang Jiayu, Zhang Xuewei, Peng Shifang, Wang Chaodong, Ding Jianqing, Liu Chunfeng, Wang Lijuan, Chen Haibo, Shen Lu, Jiang Hong, Wu Xinyin, Tan Hongzhuan, Luo Dan, Xiao Shuiyuan, Chen Xiang, Tan Jieqiong, Hu Zhengmao, Chen Chao, Xia Kun, Zhang Zhuohua, Foo Jia Nee, Blauwendraat Cornelis, Nalls Mike A, Singleton Andrew B, Liu Jun, Chan Piu, Zheng Houfeng, Li Jinchen, Guo Jifeng, Yang Jian, Tang Beisha, |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
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