Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 40 Records) |
Query Trace: SOX5[original query] |
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Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma. Human genetics 2012 Sep 131 (9): 1507-17. Liu Yanhong, Melin Beatrice S, Rajaraman Preetha, Wang Zhaoming, Linet Martha, Shete Sanjay, Amos Christopher I, Lau Ching C, Scheurer Michael E, Tsavachidis Spiridon, Armstrong Georgina N, Houlston Richard S, Hosking Fay J, Claus Elizabeth B, Barnholtz-Sloan Jill, Lai Rose, Il'yasova Dora, Schildkraut Joellen, Sadetzki Siegal, Johansen Christoffer, Bernstein Jonine L, Olson Sara H, Jenkins Robert B, LaChance Daniel, Vick Nicholas A, Wrensch Margaret, Davis Faith, McCarthy Bridget J, Andersson Ulrika, Thompson Patricia A, Chanock Stephen, , Bondy Melissa |
Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population. PloS one 2013 8 (11): e80374. Xu Miaofei, Qin Yufeng, Qu Jianhua, Lu Chuncheng, Wang Ying, Wu Wei, Song Ling, Wang Shoulin, Chen Feng, Shen Hongbing, Sha Jiahao, Hu Zhibin, Xia Yankai, Wang Xin |
Pathogenic variants screening in five non-obstructive azoospermia-associated genes. Molecular human reproduction 2014 Feb 20 (2): 178-83. Lu Chuncheng, Xu Miaofei, Wang Rong, Qin Yufeng, Wang Ying, Wu Wei, Song Ling, Wang Shoulin, Shen Hongbing, Sha Jiahao, Miao Dengshun, Hu Zhibin, Xia Yankai, Wang Xin |
Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia. PloS one 2013 8 (1): e53042. Agim Zeynep Sena, Esendal Melda, Briollais Laurent, Uyan Ozgun, Meschian Mehran, Martinez Luis Antonio Mendoza, Ding Yongmei, Basak A Nazli, Ozcelik Hil |
A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation. The American journal of cardiology 2014 Aug 114 (4): 593-600. Kolek Matthew J, Edwards Todd L, Muhammad Raafia, Balouch Adnan, Shoemaker M Benjamin, Blair Marcia A, Kor Kaylen C, Takahashi Atsushi, Kubo Michiaki, Roden Dan M, Tanaka Toshihiro, Darbar Dawo |
The clinical and genetic features of COPD-asthma overlap syndrome. The European respiratory journal 2014 Aug 44 (2): 341-50. Hardin Megan, Cho Michael, McDonald Merry-Lynn, Beaty Terri, Ramsdell Joe, Bhatt Surya, van Beek Edwin J R, Make Barry J, Crapo James D, Silverman Edwin K, Hersh Craig |
Whole-genome analysis in Korean patients with autoimmune myasthenia gravis. Yonsei medical journal 2014 May 55 (3): 660-8. Na Sang-Jun, Lee Ji Hyun, Kim So Won, Kim Dae-Seong, Shon Eun Hee, Park Hyung Jun, Shin Ha Young, Kim Seung Min, Choi Young-Ch |
Association study between polymorphisms of PRMT6, PEX10, SOX5, and nonobstructive azoospermia in the Han Chinese population. Biology of reproduction 2014 May 90 (5): 96. Zou Shasha, Li Zheng, Wang Yanan, Chen Tingting, Song Pingping, Chen Jianhua, He Xiaojin, Xu Peng, Liang Ming, Luo Kailing, Zhu Xiaobin, Tian Erpo, Du Qiang, Wen Zujia, Li Zhiqiang, Wang Meng, Sha Yanwei, Cao Yunxia, Shi Yongyong, Hu Honglia |
Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia. Biology of reproduction 2015 Feb 92 (2): 41. Tu Wenling, Liu Yunqiang, Shen Ying, Yan Yuanlong, Wang Xianding, Yang Dong, Li Lei, Ma Yongxin, Tao Dachang, Zhang Sizhong, Yang Yu |
Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study.
Journal of nutrigenetics and nutrigenomics 2015 8 (1): 44-53. Rudkowska Iwona, Pérusse Louis, Bellis Claire, Blangero John, Després Jean-Pierre, Bouchard Claude, Vohl Marie-Clau |
Integrative analysis of genome-wide association studies and gene expression profiles identified candidate genes for osteoporosis in Kashin-Beck disease patients. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2015 Oct . Wen Y, Guo X, Hao J, Xiao X, Wang W, Wu C, Wang S, Yang T, Shen H, Chen X, Tan L, Tian Q, Deng H-W, Zhang |
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability. Nature neuroscience 2016 Aug . Lelieveld Stefan H, Reijnders Margot R F, Pfundt Rolph, Yntema Helger G, Kamsteeg Erik-Jan, de Vries Petra, de Vries Bert B A, Willemsen Marjolein H, Kleefstra Tjitske, Löhner Katharina, Vreeburg Maaike, Stevens Servi J C, van der Burgt Ineke, Bongers Ernie M H F, Stegmann Alexander P A, Rump Patrick, Rinne Tuula, Nelen Marcel R, Veltman Joris A, Vissers Lisenka E L M, Brunner Han G, Gilissen Christi |
Psoriasis risk SNPs and their association with HIV-1 control. Human immunology 2016 Oct . Nititham Joanne, Gupta Rashmi, Zeng Xue, Hartogensis Wendy, Nixon Douglas F, Deeks Steven G, Hecht Frederick M, Liao Wils |
Silencing of the Drosophila ortholog of SOX5 leads to abnormal neuronal development and behavioral impairment. Human molecular genetics 2017 04 26 (8): 1472-1482. Li Airong, Hooli Basavaraj, Mullin Kristina, Tate Rebecca E, Bubnys Adele, Kirchner Rory, Chapman Brad, Hofmann Oliver, Hide Winston, Tanzi Rudolph |
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain.
PLoS genetics 2018 Sep 14 (9): e1007601. Suri Pradeep, Palmer Melody R, Tsepilov Yakov A, Freidin Maxim B, Boer Cindy G, Yau Michelle S, Evans Daniel S, Gelemanovic Andrea, Bartz Traci M, Nethander Maria, Arbeeva Liubov, Karssen Lennart, Neogi Tuhina, Campbell Archie, Mellstrom Dan, Ohlsson Claes, Marshall Lynn M, Orwoll Eric, Uitterlinden Andre, Rotter Jerome I, Lauc Gordan, Psaty Bruce M, Karlsson Magnus K, Lane Nancy E, Jarvik Gail P, Polasek Ozren, Hochberg Marc, Jordan Joanne M, Van Meurs Joyce B J, Jackson Rebecca, Nielson Carrie M, Mitchell Braxton D, Smith Blair H, Hayward Caroline, Smith Nicholas L, Aulchenko Yurii S, Williams Frances M |
PR Interval Associated Genes, Atrial Remodeling and Rhythm Outcome of Catheter Ablation of Atrial Fibrillation-A Gene-Based Analysis of GWAS Data. Frontiers in genetics 2017 8 224. Husser Daniela, Büttner Petra, Stübner Dorian, Ueberham Laura, Platonov Pyotr G, Dinov Borislav, Arya Arash, Hindricks Gerhard, Bollmann Andre |
Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2019 Jun e12661. Seifert Mariam B, Olesen Morten S, Christophersen Ingrid E, Nielsen Jonas B, Carlson Jonas, Holmqvist Fredrik, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Platonov Pyotr |
PEX10, SIRPA-SIRPG, and SOX5 gene polymorphisms are strongly associated with nonobstructive azoospermia susceptibility. Journal of assisted reproduction and genetics 2019 Mar . Gu Xiuli, Li Honggang, Chen Xi, Zhang Xue, Mei Fen, Jia Mingzhu, Xiong Chenglia |
Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry.
Frontiers in genetics 2018 9 659. Rolfe Sara, Lee Su-In, Shapiro Lin |
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation. Circulation. Genomic and precision medicine 2020 8 13 (5): 387-395. Weng Lu-Chen, Hall Amelia Weber, Choi Seung Hoan, Jurgens Sean J, Haessler Jeffrey, Bihlmeyer Nathan A, Grarup Niels, Lin Honghuang, Teumer Alexander, Li-Gao Ruifang, Yao Jie, Guo Xiuqing, Brody Jennifer A, Müller-Nurasyid Martina, Schramm Katharina, Verweij Niek, van den Berg Marten E, van Setten Jessica, Isaacs Aaron, Ramírez Julia, Warren Helen R, Padmanabhan Sandosh, Kors Jan A, de Boer Rudolf A, van der Meer Peter, Sinner Moritz F, Waldenberger Melanie, Psaty Bruce M, Taylor Kent D, Völker Uwe, Kanters Jørgen K, Li Man, Alonso Alvaro, Perez Marco V, Vaartjes Ilonca, Bots Michiel L, Huang Paul L, Heckbert Susan R, Lin Henry J, Kornej Jelena, Munroe Patricia B, van Duijn Cornelia M, Asselbergs Folkert W, Stricker Bruno H, van der Harst Pim, Kääb Stefan, Peters Annette, Sotoodehnia Nona, Rotter Jerome I, Mook-Kanamori Dennis O, Dörr Marcus, Felix Stephan B, Linneberg Allan, Hansen Torben, Arking Dan E, Kooperberg Charles, Benjamin Emelia J, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven |
The Effects of Single Nucleotide Polymorphisms in Korean Patients with Early-onset Atrial Fibrillation after Catheter Ablation. Journal of Korean medical science 2020 Dec 35 (49): e411. Park Yae Min, Roh Seung Young, Lee Dae In, Shim Jaemin, Choi Jong Il, Park Sang Weon, Kim Young Ho |
[Variant analysis of SOX5 gene in a Lamb-Shaffer syndrome family]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 8 38 (8): 765-767. Cao Jinghe, Li Jianwei, Zhang Yuqin, Niu Huanfu, Zhou Yongan, Li Zhe, Sun Baogang, Li Ze |
Causal influences of neuroticism on mental health and cardiovascular disease. Human genetics 2021 May . Zhang Fuquan, Baranova Ancha, Zhou Chao, Cao Hongbao, Chen Jiu, Zhang Xiangrong, Xu Mingqi |
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort. Andrology 2021 Mar . Cerván-Martín Miriam, Bossini-Castillo Lara, Rivera-Egea Rocío, Garrido Nicolás, Luján Saturnino, Romeu Gema, Santos-Ribeiro Samuel, , Castilla José A, Gonzalvo María Del Carmen, Clavero Ana, Vicente Francisco Javier, Guzmán-Jiménez Andrea, Burgos Miguel, Barrionuevo Francisco Javier, Jiménez Rafael, Sánchez-Curbelo Josvany, López-Rodrigo Olga, Peraza María Fernanda, Pereira-Caetano Iris, Marques Patrícia Isabel, Carvalho Filipa, Barros Alberto, Bassas Lluís, Seixas Susana, Gonçalves João, Larriba Sara, Lopes Alexandra Manuel, Carmona Francisco David, Palomino-Morales Rogelio Jes |
A Higher Polygenic Risk Score Is Associated with a Higher Recurrence Rate of Atrial Fibrillation in Direct Current Cardioversion-Treated Patients. Medicina (Kaunas, Lithuania) 2021 11 57 (11): . Vogel Simon, Rudaka Irina, Rots Dmitrijs, Isakova Jekater?na, Kal?js Oskars, V?ksne Krist?ne, Gail?te Lin |
Low Back Pain With Persistent Radiculopathy; the Clinical Role of Genetic Variants in the Genes SOX5, CCDC26/GSDMC and DCC. Frontiers in genetics 2021 12 757632. Lie Marie Udnesseter, Pedersen Linda Margareth, Heuch Ingrid, Winsvold Bendik, Gjerstad Johannes, Hasvik Eivind, Nygaard Øystein Petter, Grotle Margreth, Matre Dagfinn, Zwart John-Anker, Nilsen Kristian Bernha |
Non-coding rare variants in PANX3 are associated with chronic back pain. Pain 2022 11 . Belonogova Nadezhda M, Kirichenko Anatoly V, Freidin Maxim B, Williams Frances M K, Suri Pradeep, Aulchenko Yurii S, Axenovich Tatiana I, Tsepilov Yakov |
Genome-wide association study meta-analysis of suicide death and suicidal behavior.
Molecular psychiatry 2022 Oct . Li Qingqin S, Shabalin Andrey A, DiBlasi Emily, Gopal Srihari, Canuso Carla M, , Palotie Aarno, Drevets Wayne C, Docherty Anna R, Coon Hila |
Shared genetic liability between major depressive disorder and osteoarthritis. Bone & joint research 2022 1 11 (1): 12-22. Zhang Fuquan, Rao Shuquan, Baranova Anc |
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. The American journal of psychiatry 2023 10 180 (10): 723-738. Anna R Docherty, Niamh Mullins, Allison E Ashley-Koch, Xuejun Qin, Jonathan R I Coleman, Andrey Shabalin, JooEun Kang, Balasz Murnyak, Frank Wendt, Mark Adams, Adrian I Campos, Emily DiBlasi, Janice M Fullerton, Henry R Kranzler, Amanda V Bakian, Eric T Monson, Miguel E Rentería, Consuelo Walss-Bass, Ole A Andreassen, Chittaranjan Behera, Cynthia M Bulik, Howard J Edenberg, Ronald C Kessler, J John Mann, John I Nurnberger, Giorgio Pistis, Fabian Streit, Robert J Ursano, Renato Polimanti, Michelle Dennis, Melanie Garrett, Lauren Hair, Philip Harvey, Elizabeth R Hauser, Michael A Hauser, Jennifer Huffman, Daniel Jacobson, Ravi Madduri, Benjamin McMahon, David W Oslin, Jodie Trafton, Swapnil Awasthi, Wade H Berrettini, Martin Bohus, Xiao Chang, Hsi-Chung Chen, Wei J Chen, Erik D Christensen, Scott Crow, Philibert Duriez, Alexis C Edwards, Fernando Fernández-Aranda, Hanga Galfalvy, Michael Gandal, Philip Gorwood, Yiran Guo, Jonathan D Hafferty, Hakon Hakonarson, Katherine A Halmi, Akitoyo Hishimoto, Sonia Jain, Stéphane Jamain, Susana Jiménez-Murcia, Craig Johnson, Allan S Kaplan, Walter H Kaye, Pamela K Keel, James L Kennedy, Minsoo Kim, Kelly L Klump, Daniel F Levey, Dong Li, Shih-Cheng Liao, Klaus Lieb, Lisa Lilenfeld, Christian R Marshall, James E Mitchell, Satoshi Okazaki, Ikuo Otsuka, Dalila Pinto, Abigail Powers, Nicolas Ramoz, Stephan Ripke, Stefan Roepke, Vsevolod Rozanov, Stephen W Scherer, Christian Schmahl, Marcus Sokolowski, Anna Starnawska, Michael Strober, Mei-Hsin Su, Laura M Thornton, Janet Treasure, Erin B Ware, Hunna J Watson, Stephanie H Witt, D Blake Woodside, Zeynep Yilmaz, Lea Zillich, Rolf Adolfsson, Ingrid Agartz, Martin Alda, Lars Alfredsson, Vivek Appadurai, María Soler Artigas, Sandra Van der Auwera, M Helena Azevedo, Nicholas Bass, Claiton H D Bau, Bernhard T Baune, Frank Bellivier, Klaus Berger, Joanna M Biernacka, Tim B Bigdeli, Elisabeth B Binder, Michael Boehnke, Marco P Boks, David L Braff, Richard Bryant, Monika Budde, Enda M Byrne, Wiepke Cahn, Enrique Castelao, Jorge A Cervilla, Boris Chaumette, Aiden Corvin, Nicholas Craddock, Srdjan Djurovic, Jerome C Foo, Andreas J Forstner, Mark Frye, Justine M Gatt, Ina Giegling, Hans J Grabe, Melissa J Green, Eugenio H Grevet, Maria Grigoroiu-Serbanescu, Blanca Gutierrez, Jose Guzman-Parra, Marian L Hamshere, Annette M Hartmann, Joanna Hauser, Stefanie Heilmann-Heimbach, Per Hoffmann, Marcus Ising, Ian Jones, Lisa A Jones, Lina Jonsson, René S Kahn, John R Kelsoe, Kenneth S Kendler, Stefan Kloiber, Karestan C Koenen, Manolis Kogevinas, Marie-Odile Krebs, Mikael Landén, Marion Leboyer, Phil H Lee, Douglas F Levinson, Calwing Liao, Jolanta Lissowska, Fermin Mayoral, Susan L McElroy, Patrick McGrath, Peter McGuffin, Andrew McQuillin, Divya Mehta, Ingrid Melle, Philip B Mitchell, Esther Molina, Gunnar Morken, Caroline Nievergelt, Markus M Nöthen, Michael C O'Donovan, Roel A Ophoff, Michael J Owen, Carlos Pato, Michele T Pato, Brenda W J H Penninx, James B Potash, Robert A Power, Martin Preisig, Digby Quested, Josep Antoni Ramos-Quiroga, Andreas Reif, Marta Ribasés, Vanesa Richarte, Marcella Rietschel, Margarita Rivera, Andrea Roberts, Gloria Roberts, Guy A Rouleau, Diego L Rovaris, Alan R Sanders, Peter R Schofield, Thomas G Schulze, Laura J Scott, Alessandro Serretti, Jianxin Shi, Lea Sirignano, Pamela Sklar, Olav B Smeland, Jordan W Smoller, Edmund J S Sonuga-Barke, Maciej Trzaskowski, Ming T Tsuang, Gustavo Turecki, Laura Vilar-Ribó, John B Vincent, Henry Völzke, James T R Walters, Cynthia Shannon Weickert, Thomas W Weickert, Myrna M Weissman, Leanne M Williams, Naomi R Wray, Clement C Zai, Esben Agerbo, Anders D Børglum, Gerome Breen, Ditte Demontis, Annette Erlangsen, Joel Gelernter, Stephen J Glatt, David M Hougaard, Hai-Gwo Hwu, Po-Hsiu Kuo, Cathryn M Lewis, Qingqin S Li, Chih-Min Liu, Nicholas G Martin, Andrew M McIntosh, Sarah E Medland, Ole Mors, Merete Nordentoft, Catherine M Olsen, David Porteous, Daniel J Smith, Eli A Stahl, Murray B Stein, Danuta Wasserman, Thomas Werge, David C Whiteman, Virginia Willour, , , , , , , , , Hilary Coon, Jean C Beckham, Nathan A Kimbrel, Douglas M Ruderf |
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- Page last updated:Apr 22, 2024
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