Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: DPP6[original query] |
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Screening for replication of genome-wide SNP associations in sporadic ALS.
European journal of human genetics : EJHG 2009 Feb 17 (2): 213-8. Cronin Simon, Tomik Barbara, Bradley Daniel G, Slowik Agnieszka, Hardiman Or |
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population. Neurobiology of aging 2011 May 32 (5): 966-7. Fogh Isabella, D'Alfonso Sandra, Gellera Cinzia, Ratti Antonia, Cereda Cristina, Penco Silvana, Corrado Lucia, Sorarù Gianni, Castellotti Barbara, Tiloca Cinzia, Gagliardi Stella, Cozzi Lorena, Lupton Michelle K, Ticozzi Nicola, Mazzini Letizia, Shaw Chris E, Al-Chalabi Ammar, Powell John, Silani Vincen |
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Human molecular genetics 2009 Apr 18 (8): 1524-32. Chiò Adriano, Schymick Jennifer C, Restagno Gabriella, Scholz Sonja W, Lombardo Federica, Lai Shiao-Lin, Mora Gabriele, Fung Hon-Chung, Britton Angela, Arepalli Sampath, Gibbs J Raphael, Nalls Michael, Berger Stephen, Kwee Lydia Coulter, Oddone Eugene Z, Ding Jinhui, Crews Cynthia, Rafferty Ian, Washecka Nicole, Hernandez Dena, Ferrucci Luigi, Bandinelli Stefania, Guralnik Jack, Macciardi Fabio, Torri Federica, Lupoli Sara, Chanock Stephen J, Thomas Gilles, Hunter David J, Gieger Christian, Wichmann H Erich, Calvo Andrea, Mutani Roberto, Battistini Stefania, Giannini Fabio, Caponnetto Claudia, Mancardi Giovanni Luigi, La Bella Vincenzo, Valentino Francesca, Monsurrò Maria Rosaria, Tedeschi Gioacchino, Marinou Kalliopi, Sabatelli Mario, Conte Amelia, Mandrioli Jessica, Sola Patrizia, Salvi Fabrizio, Bartolomei Ilaria, Siciliano Gabriele, Carlesi Cecilia, Orrell Richard W, Talbot Kevin, Simmons Zachary, Connor James, Pioro Erik P, Dunkley Travis, Stephan Dietrich A, Kasperaviciute Dalia, Fisher Elizabeth M, Jabonka Sibylle, Sendtner Michael, Beck Marcus, Bruijn Lucie, Rothstein Jeffrey, Schmidt Silke, Singleton Andrew, Hardy John, Traynor Bryan |
Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2010 Aug 11 (4): 389-91. Daoud Hussein, Valdmanis Paul N, Dion Patrick A, Rouleau Guy |
A large genome scan for rare CNVs in amyotrophic lateral sclerosis. Human molecular genetics 2010 Oct 19 (20): 4091-9. Blauw Hylke M, Al-Chalabi Ammar, Andersen Peter M, van Vught Paul W J, Diekstra Frank P, van Es Michael A, Saris Christiaan G J, Groen Ewout J N, van Rheenen Wouter, Koppers Max, Van't Slot Ruben, Strengman Eric, Estrada Karol, Rivadeneira Fernando, Hofman Albert, Uitterlinden Andre G, Kiemeney Lambertus A, Vermeulen Sita H M, Birve Anna, Waibel Stefan, Meyer Thomas, Cronin Simon, McLaughlin Russell L, Hardiman Orla, Sapp Peter C, Tobin Martin D, Wain Louise V, Tomik Barbara, Slowik Agnieszka, Lemmens Robin, Rujescu Dan, Schulte Claudia, Gasser Thomas, Brown Robert H, Landers John E, Robberecht Wim, Ludolph Albert C, Ophoff Roel A, Veldink Jan H, van den Berg Leonard |
Association between DPP6 polymorphism and the risk of sporadic amyotrophic lateral sclerosis in Chinese patients. Chinese medical journal 2009 Dec 122 (24): 2989-92. Li Xiao-Guang, Zhang Jiang-Hu, Xie Man-Qing, Liu Ming-Sheng, Li Ben-Hong, Zhao Yan-Huan, Ren Hai-Tao, Cui Li-Yi |
DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia.
The pharmacogenomics journal 2013 Feb 13 (1): 27-34. Tanaka S, Syu A, Ishiguro H, Inada T, Horiuchi Y, Ishikawa M, Koga M, Noguchi E, Ozaki N, Someya T, Kakita A, Takahashi H, Nawa H, Arinami |
No association of five candidate genetic variants with amyotrophic lateral sclerosis in a Chinese population. Neurobiology of aging 2012 Jul . Chen Y, Zeng Y, Huang R, Yang Y, Chen K, Song W, Zhao B, Li J, Yuan L, Shang HF |
A high-density genome-wide association screen of sporadic ALS in US veterans.
PloS one 2012 7 (3): e32768. Kwee Lydia Coulter, Liu Yutao, Haynes Carol, Gibson Jason R, Stone Annjanette, Schichman Steven A, Kamel Freya, Nelson Lorene M, Topol Barbara, Van den Eeden Stephen K, Tanner Caroline M, Cudkowicz Merit E, Grasso Daniela L, Lawson Robert, Muralidhar Sumitra, Oddone Eugene Z, Schmidt Silke, Hauser Michael |
Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans. Neuroscience letters 2012 Nov 530 (2): 155-60. Brambilla Paola, Esposito Federica, Lindstrom Eva, Sorosina Melissa, Giacalone Giacomo, Clarelli Ferdinando, Rodegher Mariaemma, Colombo Bruno, Moiola Lucia, Ghezzi Angelo, Capra Ruggero, Collimedaglia Laura, Coniglio Gabriella, Celius Elisabeth G, Galimberti Daniela, Sørensen Per Soelberg, Martinelli Vittorio, Oturai Annette B, Harbo Hanne F, Hillert Jan, Comi Giancarlo, Martinelli-Boneschi Filip |
Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation. European journal of medical genetics 2013 Sep 56 (9): 484-9. Liao Can, Fu Fang, Li Ru, Yang Wen-Qing, Liao Hua-Yi, Yan Jia-Rong, Li Jian, Li Shi-Yuan, Yang Xin, Li Dong-Z |
Endometriosis is associated with rare copy number variants. PloS one 2014 9 (8): e103968. Chettier Rakesh, Ward Kenneth, Albertsen Hans |
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Jun 165B (4): 303-13. Noor Abdul, Lionel Anath C, Cohen-Woods Sarah, Moghimi Narges, Rucker James, Fennell Alanna, Thiruvahindrapuram Bhooma, Kaufman Liana, Degagne Bryan, Wei John, Parikh Sagar V, Muglia Pierandrea, Forte Julia, Scherer Stephen W, Kennedy James L, Xu Wei, McGuffin Peter, Farmer Anne, Strauss John, Vincent John |
A genome-wide association study of clinical symptoms of dissociation in a trauma-exposed sample.
Depression and anxiety 2014 Apr 31 (4): 352-60. Wolf Erika J, Rasmusson Ann M, Mitchell Karen S, Logue Mark W, Baldwin Clinton T, Miller Mark |
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families. Neurogenetics 2014 May 15 (2): 117-27. Egger Gerald, Roetzer Katharina M, Noor Abdul, Lionel Anath C, Mahmood Huda, Schwarzbraun Thomas, Boright Oliver, Mikhailov Anna, Marshall Christian R, Windpassinger Christian, Petek Erwin, Scherer Stephen W, Kaschnitz Wolfgang, Vincent John |
Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative.
PloS one 2015 10 (11): e0141647. Giri Ayush, Wu Jennifer M, Ward Renee M, Hartmann Katherine E, Park Amy J, North Kari E, Graff Mariaelisa, Wallace Robert B, Bareh Gihan, Qi Lihong, O'Sullivan Mary J, Reiner Alexander P, Edwards Todd L, Velez Edwards Digna |
Genomic Study of Cardiovascular Continuum Comorbidity. Acta naturae 0 7 (3): 89-99. Makeeva O A, Sleptsov A A, Kulish E V, Barbarash O L, Mazur A M, Prokhorchuk E B, Chekanov N N, Stepanov V A, Puzyrev V |
Next-generation sequencing of a large gene panel in patients initially diagnosed with idiopathic ventricular fibrillation. Heart rhythm 2017 1 14 (7): 1035-1040. Visser Marloes, Dooijes Dennis, van der Smagt Jasper J, van der Heijden Jeroen F, Doevendans Pieter A, Loh Peter, Asselbergs Folkert W, Hassink Rutger |
Cardiac arrhythmia and neuroexcitability gene variants in resected brain tissue from patients with sudden unexpected death in epilepsy (SUDEP). NPJ genomic medicine 2018 4 3 9. Friedman Daniel, Kannan Kasthuri, Faustin Arline, Shroff Seema, Thomas Cheddhi, Heguy Adriana, Serrano Jonathan, Snuderl Matija, Devinsky Orr |
Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases. Circulation. Genomic and precision medicine 2018 10 11 (10): e001797. Nannenberg Eline A, van Rijsingen Ingrid A W, van der Zwaag Paul A, van den Berg Maarten P, van Tintelen J Peter, Tanck Michael W T, Ackerman Michael J, Wilde Arthur A M, Christiaans Im |
Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers. PloS one 2019 14 (9): e0221957. Cunningham Patrick N, Wang Zhiying, Grove Megan L, Cooper-DeHoff Rhonda M, Beitelshees Amber L, Gong Yan, Gums John G, Johnson Julie A, Turner Stephen T, Boerwinkle Eric, Chapman Arlene |
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. Acta neuropathologica 2019 Feb . Pottier Cyril, Ren Yingxue, Perkerson Ralph B, Baker Matt, Jenkins Gregory D, van Blitterswijk Marka, DeJesus-Hernandez Mariely, van Rooij Jeroen G J, Murray Melissa E, Christopher Elizabeth, McDonnell Shannon K, Fogarty Zachary, Batzler Anthony, Tian Shulan, Vicente Cristina T, Matchett Billie, Karydas Anna M, Hsiung Ging-Yuek Robin, Seelaar Harro, Mol Merel O, Finger Elizabeth C, Graff Caroline, Öijerstedt Linn, Neumann Manuela, Heutink Peter, Synofzik Matthis, Wilke Carlo, Prudlo Johannes, Rizzu Patrizia, Simon-Sanchez Javier, Edbauer Dieter, Roeber Sigrun, Diehl-Schmid Janine, Evers Bret M, King Andrew, Mesulam M Marsel, Weintraub Sandra, Geula Changiz, Bieniek Kevin F, Petrucelli Leonard, Ahern Geoffrey L, Reiman Eric M, Woodruff Bryan K, Caselli Richard J, Huey Edward D, Farlow Martin R, Grafman Jordan, Mead Simon, Grinberg Lea T, Spina Salvatore, Grossman Murray, Irwin David J, Lee Edward B, Suh EunRan, Snowden Julie, Mann David, Ertekin-Taner Nilufer, Uitti Ryan J, Wszolek Zbigniew K, Josephs Keith A, Parisi Joseph E, Knopman David S, Petersen Ronald C, Hodges John R, Piguet Olivier, Geier Ethan G, Yokoyama Jennifer S, Rissman Robert A, Rogaeva Ekaterina, Keith Julia, Zinman Lorne, Tartaglia Maria Carmela, Cairns Nigel J, Cruchaga Carlos, Ghetti Bernardino, Kofler Julia, Lopez Oscar L, Beach Thomas G, Arzberger Thomas, Herms Jochen, Honig Lawrence S, Vonsattel Jean Paul, Halliday Glenda M, Kwok John B, White Charles L, Gearing Marla, Glass Jonathan, Rollinson Sara, Pickering-Brown Stuart, Rohrer Jonathan D, Trojanowski John Q, Van Deerlin Vivianna, Bigio Eileen H, Troakes Claire, Al-Sarraj Safa, Asmann Yan, Miller Bruce L, Graff-Radford Neill R, Boeve Bradley F, Seeley William W, Mackenzie Ian R A, van Swieten John C, Dickson Dennis W, Biernacka Joanna M, Rademakers Ro |
Genetic polymorphisms associated with upper gastrointestinal bleeding: a systematic review. The pharmacogenomics journal 2020 Sep . Forgerini Marcela, Lucchetta Rosa Camila, Urbano Gustavo, de Nadai Tales Rubens, de Carvalho Mastroianni Patríc |
The rs2619566, rs10260404, and rs79609816 Polymorphisms Are Associated With Sporadic Amyotrophic Lateral Sclerosis in Individuals of Han Ancestry From Mainland China. Frontiers in genetics 2021 12 679204. Zhang Jie, Qiu Weiwen, Hu Fan, Zhang Xiong, Deng Youqing, Nie Hongbing, Xu Rens |
The Mediation Effects of Aluminum in Plasma and Dipeptidyl Peptidase Like Protein 6 (DPP6) Polymorphism on Renal Function via Genome-Wide Typing Association.
International journal of environmental research and public health 2021 Oct 18 (19): . Chen Ting-Hao, Yang Chen-Cheng, Luo Kuei-Hau, Dai Chia-Yen, Chuang Yao-Chung, Chuang Hung- |
Genome-Wide Association Study Identifies Multiple Susceptibility Loci for Malignant Neoplasms of the Brain in Taiwan. Journal of personalized medicine 2022 Jul 12 (7): . Lin Jang-Chun, Wu Yi-Chieh, Yang Fu-Chi, Tsai Jo-Ting, Huang David Yc, Liu Wei-Hs |
Gene-environment analyses reveal novel genetic candidates with prenatal tobacco exposure in relation to risk for childhood acute lymphoblastic leukemia. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2023 9 . Charlie Zhong, Shaobo Li, Katti Arroyo, Libby M Morimoto, Adam J de Smith, Catherine Metayer, Xiaomei Ma, Scott C Kogan, W James Gauderman, Joseph L Wieme |
Systematic Review and Meta-Analyses of Aminopeptidases as Prognostic Biomarkers in Amyotrophic Lateral Sclerosis. International journal of molecular sciences 2023 4 24 (8): . Bárbara Teruel-Peña, José Luís Gómez-Urquiza, Nora Suleiman-Martos, Isabel Prieto, Francisco José García-Cózar, Manuel Ramírez-Sánchez, Carmen Fernández-Martos, Germán Domínguez-Ví |
The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2023 11 . Lisa M Verheul, Martijn H van der Ree, Sanne A Groeneveld, Bart A Mulder, Imke Christiaans, Gijs F L Kapel, Marco Alings, Marianne Bootsma, Daniela Q C M Barge-Schaapveld, Jippe C Balt, Sing-Chien Yap, Ingrid P C Krapels, Rachel M A Ter Bekke, Paul G A Volders, Saskia N van der Crabben, Pieter G Postema, Arthur A M Wilde, Dennis Dooijes, Annette F Baas, Rutger J Hassi |
Whole-exome sequencing reveals the genomic profile and IL6ST mutations as a prognostic biomarker of paraneoplastic pemphigus associated unicentric Castleman disease. The Journal of investigative dermatology 2023 10 . Sai Wang, Rui Wang, Panpan Shang, Xuejun Zhu, Xixue Chen, Guohong Zhang, Mingyue Wa |
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- Page last updated:Apr 22, 2024
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