Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: ATP2B2[original query] |
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Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches. Biological psychiatry 2010 Feb 67 (3): 263-9. Ikeda Masashi, Tomita Yasuyuki, Mouri Akihiro, Koga Minori, Okochi Tomo, Yoshimura Reiji, Yamanouchi Yoshio, Kinoshita Yoko, Hashimoto Ryota, Williams Hywel J, Takeda Masatoshi, Nakamura Jun, Nabeshima Toshitaka, Owen Michael J, O'Donovan Michael C, Honda Hiroyuki, Arinami Tadao, Ozaki Norio, Iwata Nak |
Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects. Biological psychiatry 2011 Nov 70 (9): 880-7. Carayol Jérôme, Sacco Roberto, Tores Frédéric, Rousseau Francis, Lewin Patricia, Hager Jorg, Persico Antonio |
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families. Psychiatric genetics 2012 Aug 22 (4): 177-81. Prandini Paola, Pasquali Alessandra, Malerba Giovanni, Marostica Andrea, Zusi Chiara, Xumerle Luciano, Muglia Pierandrea, Da Ros Lucio, Ratti Emiliangelo, Trabetti Elisabetta, Pignatti Pier Franco, |
The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population. PloS one 2013 8 (4): e61021. Yang Wen, Liu Jing, Zheng Fanfan, Jia Meixiang, Zhao Linnan, Lu Tianlan, Ruan Yanyan, Zhang Jishui, Yue Weihua, Zhang Dai, Wang Lifa |
PON2 and ATP2B2 gene polymorphisms with noise-induced hearing loss. Journal of thoracic disease 2016 Mar 8 (3): 430-8. Li Xiuting, Cao Jinglian, Wang Jun, Song Haiyan, Ji Guixiang, Dong Qiu, Wei Chunlong, Cao Ying, Wang Boshen, Zhu Baoli, Xiao Ha |
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Molecular autism 2017 8 21. Authors are not available |
Genome-wide association meta-analysis of age at first cannabis use.
Addiction (Abingdon, England) 2018 Jul . Minic? Camelia C, Verweij Karin J H, van der Most Peter J, Mbarek Hamdi, Bernard Manon, van Eijk Kristel R, Lind Penelope A, Liu Meng Zhen, Maciejewski Dominique F, Palviainen Teemu, Sánchez-Mora Cristina, Sherva Richard, Taylor Michelle, Walters Raymond K, Abdellaoui Abdel, Bigdeli Timothy B, Branje Susan J T, Brown Sandra A, Casas Miguel, Corley Robin P, Davey-Smith George, Davies Gareth E, Ehli Erik A, Farrer Lindsay, Fedko Iryna O, Garcia-Martínez Iris, Gordon Scott D, Hartman Catharina A, Heath Andrew C, Hickie Ian B, Hickman Matthew, Hopfer Christian J, Hottenga Jouke Jan, Kahn René S, Kaprio Jaakko, Korhonen Tellervo, Kranzler Henry R, Krauter Ken, van Lier Pol A C, Madden Pamela A F, Medland Sarah E, Neale Michael C, Meeus Wim H J, Montgomery Grant W, Nolte Ilja M, Oldehinkel Albertine J, Pausova Zdenka, Ramos-Quiroga Josep A, Richarte Vanesa, Rose Richard J, Shin Jean, Stallings Michael C, Wall Tamara L, Ware Jennifer J, Wright Margaret J, Zhao Hongyu, Koot Hans M, Paus Tomas, Hewitt John K, Ribasés Marta, Loukola Anu, Boks Marco P, Snieder Harold, Munafò Marcus R, Gelernter Joel, Boomsma Dorret I, Martin Nicholas G, Gillespie Nathan A, Vink Jacqueline M, Derks Eske |
Research and Discussion on the Relationships between Noise-Induced Hearing Loss and ATP2B2 Gene Polymorphism. International journal of genomics 2019 12 2019 5048943. Zhang Suhao, Ding Enmin, Yin Haoyang, Zhang Hengdong, Zhu Bao |
Genetic Risk of Autism Spectrum Disorder in a Pakistani Population. Genes 2020 Oct 11 (10): . Khalid Madiha, Raza Hashim, M Driessen Terri, J Lee Paul, Tejwani Leon, Sami Abdul, Nawaz Muhammad, Mehmood Baig Shahid, Lim Janghoo, Kaukab Raja Ghaza |
Latent trait modeling of tau neuropathology in progressive supranuclear palsy.
Acta neuropathologica 2021 2 141 (5): 667-680. Kouri Naomi, Murray Melissa E, Reddy Joseph S, Serie Daniel J, Soto-Beasley Alexandra, Allen Mariet, Carrasquillo Minerva M, Wang Xue, Castanedes Monica Casey, Baker Matthew C, Rademakers Rosa, Uitti Ryan J, Graff-Radford Neill R, Wszolek Zbigniew K, Schellenberg Gerard D, Crook Julia E, Ertekin-Taner Nilüfer, Ross Owen A, Dickson Dennis |
Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia. Biological psychiatry global open science 2023 10 3 (4): 797-802. Cathal Ormond, Niamh M Ryan, Elizabeth A Heron, Michael Gill, William Byerley, Aiden Corv |
Genetic variants in ATP2B2 as risk factors for mortality in patients unrelated but not associated with families with severe COVID-19. Heliyon 2024 4 10 (8): e29493. María Fernanda López-Bielma, Ramcés Falfán-Valencia, Aurelio Fierro-Piña, Edgar Abarca-Rojano, Elizabeth Córdoba-Lanus, Ingrid Fricke-Galindo, Priscila Romero-Villaseñor, Ivette Buendía-Roldán, Leslie Chávez-Galán, María Esther Jaime-Capetillo, Gloria Pérez-Rub |
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