Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: PPP2R2B[original query] |
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CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Jan 116B (1): 45-50. Laurent Claudine, Niehaus Dana, Bauché Stéphanie, Levinson Douglas F, Soubigou Stéphane, Pimstone Simon, Hayden Michael, Mbanga Irena, Emsley Robin, Deleuze Jean-François, Mallet Jacqu |
Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia. Schizophrenia research 2005 Oct 78 (2-3): 131-6. Chen Chiung-Mei, Lane Hsien-Yuan, Wu Yih-Ru, Ro Long-Sun, Chen Fen-Lin, Hung Wei-Ling, Hou Yi-Ting, Lin Cheng-Yueh, Huang Shu-Yi, Chen I-Cheng, Soong Bing-Wen, Li Ming-Liang, Hsieh-Li Hsiu-Mei, Su Ming-Tsan, Lee-Chen Guey-J |
PPP2R2B CAG repeat length in the Han Chinese in Taiwan: Association analyses in neurological and psychiatric disorders and potential functional implications. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Jan 150B (1): 124-9. Chen Chiung-Mei, Hou Yi-Ting, Liu Ju-Yun, Wu Yih-Ru, Lin Chih-Hsin, Fung Hon-Chung, Hsu Wen-Chuin, Hsu Yuying, Lee Shen-Hung, Hsieh-Li Hsiu-Mei, Su Ming-Tsan, Chen Shui-Tein, Lane Hsien-Yuan, Lee-Chen Guey-J |
Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia. Neurologia i neurochirurgia polska 0 42 (6): 497-504. Rajkiewicz Marta, Su?ek-Piatkowska Anna, Krysa Wioletta, Zdzienicka Elzbieta, Szirkowiec Walentyna, Zaremba Jac |
A genetic variant in a PP2A regulatory subunit encoded by the PPP2R2B gene associates with altered breast cancer risk and recurrence. International journal of cancer. Journal international du cancer 2011 May 128 (10): 2335-43. Vazquez Alexei, Kulkarni Diptee, Grochola Lukasz F, Bond Gareth L, Barnard Nicola, Toppmeyer Deborah, Levine Arnold J, Hirshfield Kim |
Association between CAG repeat length in the PPP2R2B gene and Alzheimer disease in the Japanese population. Neuroscience letters 2011 Jan 487 (3): 354-7. Kimura Ryo, Morihara Takashi, Kudo Takashi, Kamino Kouzin, Takeda Masatos |
Association analyses identify multiple new lung cancer susceptibility loci and their interactions with smoking in the Chinese population. Nature genetics 2012 Jul . Dong J, Hu Z, Wu C, Guo H, Zhou B, Lv J, Lu D, Chen K, Shi Y, Chu M, Wang C, Zhang R, Dai J, Jiang Y, Cao S, Qin Z, Yu D, Ma H, Jin G, Gong J, Sun C, Zhao X, Yin Z, Yang L, Li Z, Deng Q, Wang J, Wu W, Zheng H, Zhou G, Chen H, Guan P, Peng Z, Chen Y, Shu Y, Xu L, Liu X, Liu L, Xu P, Han B, Bai C, Zhao Y, Zhang H, Yan Y, Amos CI, Chen F, Tan W, Jin L, Wu T, Lin D, Shen H |
Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5. BMC genetics 2012 13 12. Nolan Daniel K, Sutton Beth, Haynes Carol, Johnson Jessica, Sebek Jacqueline, Dowdy Elaine, Crosslin David, Crossman David, Sketch Michael H, Granger Christopher B, Seo David, Goldschmidt-Clermont Pascal, Kraus William E, Gregory Simon G, Hauser Elizabeth R, Shah Svati |
Germline variation in TP53 regulatory network genes associates with breast cancer survival and treatment outcome. International journal of cancer. Journal international du cancer 2012 Oct . Jamshidi M, Schmidt MK, Dörk T, Garcia-Closas M, Heikkinen T, Cornelissen S, van den Broek AJ, Schürmann P, Meyer A, Park-Simon TW, Figueroa J, Sherman M, Lissowska J, Teoh Hor Keong G, Irwanto A, Laakso M, Hautaniemi S, Aittomäki K, Blomqvist C, Liu J, Nevalinna H |
Functional genetic polymorphisms in PP2A subunit genes confer increased risks of lung cancer in southern and eastern Chinese. PloS one 2013 8 (10): e77285. Yang Rongrong, Yang Lei, Qiu Fuman, Zhang Lisha, Wang Hui, Yang Xiaorong, Deng Jieqiong, Fang Wenxiang, Zhou Yifeng, Lu Jiach |
Germline genetics of the p53 pathway affect longevity in a gender specific manner. Current aging science 2014 7 (2): 91-100. Groß Sebastian, Immel Uta-Dorothee, Klintschar Michael, Bartel Fra |
De novo mutations in moderate or severe intellectual disability. PLoS genetics 2014 Oct 10 (10): e1004772. Hamdan Fadi F, Srour Myriam, Capo-Chichi Jose-Mario, Daoud Hussein, Nassif Christina, Patry Lysanne, Massicotte Christine, Ambalavanan Amirthagowri, Spiegelman Dan, Diallo Ousmane, Henrion Edouard, Dionne-Laporte Alexandre, Fougerat Anne, Pshezhetsky Alexey V, Venkateswaran Sunita, Rouleau Guy A, Michaud Jacques |
Association of functional genetic variation in PP2A with prefrontal working memory processing. Behavioural brain research 2016 Aug 316 125-130. Rampino Antonio, Di Carlo Pasquale, Fazio Leonardo, Ursini Gianluca, Pergola Giulio, De Virgilio Caterina, Gadaleta Gemma, Giordano Giulia Maria, Bertolino Alessandro, Blasi Giusep |
Exome chip analyses in adult attention deficit hyperactivity disorder. Translational psychiatry 2016 Oct 6 (10): e923. Zayats T, Jacobsen K K, Kleppe R, Jacob C P, Kittel-Schneider S, Ribasés M, Ramos-Quiroga J A, Richarte V, Casas M, Mota N R, Grevet E H, Klein M, Corominas J, Bralten J, Galesloot T, Vasquez A A, Herms S, Forstner A J, Larsson H, Breen G, Asherson P, Gross-Lesch S, Lesch K P, Cichon S, Gabrielsen M B, Holmen O L, Bau C H D, Buitelaar J, Kiemeney L, Faraone S V, Cormand B, Franke B, Reif A, Haavik J, Johansson |
Antipsychotic Drug Responsiveness and Dopamine Receptor Signaling; Old Players and New Prospects. Frontiers in psychiatry 2018 9 702. Rampino Antonio, Marakhovskaia Aleksandra, Soares-Silva Tiago, Torretta Silvia, Veneziani Federica, Beaulieu Jean Mart |
Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
Live births following preimplantation genetic testing for dynamic mutation diseases by karyomapping: a report of three cases. Journal of assisted reproduction and genetics 2020 3 37 (3): 539-548. Shi Dayuan, Xu Jiawei, Niu Wenbin, Liu Yidong, Shi Hao, Yao Guidong, Shi Senlin, Li Gang, Song Wenyan, Jin Haixia, Sun Ying |
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy. Clinical autonomic research : official journal of the Clinical Autonomic Research Society 2021 Jan . Wernick Anna I, Walton Ronald L, Soto-Beasley Alexandra I, Koga Shunsuke, Heckman Michael G, Valentino Rebecca R, Milanowski Lukasz M, Hoffman-Zacharska Dorota, Koziorowski Dariusz, Hassan Anhar, Uitti Ryan J, Cheshire William P, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Low Phillip A, Ross Owen |
Variants in PPP2R2B and IGF2BP3 are associated with higher tau deposition.
Brain communications 2021 (2): fcaa159. Ramanan Vijay K, Wang Xuewei, Przybelski Scott A, Raghavan Sheelakumari, Heckman Michael G, Batzler Anthony, Kosel Matthew L, Hohman Timothy J, Knopman David S, Graff-Radford Jonathan, Lowe Val J, Mielke Michelle M, Jack Clifford R, Petersen Ronald C, Ross Owen A, Vemuri Prashant |
Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar Ataxia. Neurology. Genetics 2023 12 9 (1): e200050. Fatemeh Ghorbani, Eddy N de Boer, Marloes Benjamins-Stok, Corien C Verschuuren-Bemelmans, Jurjen Knapper, Jelkje de Boer-Bergsma, Jeroen J de Vries, Birgit Sikkema-Raddatz, Dineke S Verbeek, Helga Westers, Cleo C van Diem |
Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population.
PloS one 2023 1 18 (1): e0276700. Shen Yiran, Khatri Bhuwan, Rananaware Santosh, Li Danmeng, Ostrov David A, Jain Piyush K, Lessard Christopher J, Nguyen Cuong |
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- Page last updated:Apr 29, 2024
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