Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: CTNNA2[original query] |
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Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
Journal of neural transmission (Vienna, Austria : 1996) 2008 Nov 115 (11): 1573-85. Lesch Klaus-Peter, Timmesfeld Nina, Renner Tobias J, Halperin Rebecca, Röser Christoph, Nguyen T Trang, Craig David W, Romanos Jasmin, Heine Monika, Meyer Jobst, Freitag Christine, Warnke Andreas, Romanos Marcel, Schäfer Helmut, Walitza Susanne, Reif Andreas, Stephan Dietrich A, Jacob Christi |
Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.
Annals of human genetics 2012 Sep 76 (5): 342-51. Cummings Anna C, Jiang Lan, Velez Edwards Digna R, McCauley Jacob L, Laux Renee, McFarland Lynne L, Fuzzell Denise, Knebusch Clare, Caywood Laura, Reinhart-Mercer Lori, Nations Laura, Gilbert John R, Konidari Ioanna, Tramontana Michael, Cuccaro Michael L, Scott William K, Pericak-Vance Margaret A, Haines Jonathan |
Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Translational psychiatry 2012 7 1 (10): e49. Terracciano A, Esko T, Sutin A R, de Moor M H M, Meirelles O, Zhu G, Tanaka T, Giegling I, Nutile T, Realo A, Allik J, Hansell N K, Wright M J, Montgomery G W, Willemsen G, Hottenga J-J, Friedl M, Ruggiero D, Sorice R, Sanna S, Cannas A, Räikkönen K, Widen E, Palotie A, Eriksson J G, Cucca F, Krueger R F, Lahti J, Luciano M, Smoller J W, van Duijn C M, Abecasis G R, Boomsma D I, Ciullo M, Costa P T, Ferrucci L, Martin N G, Metspalu A, Rujescu D, Schlessinger D, Uda |
Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.
Human genomics 2013 7 16. Ding Lili, Abebe Tilahun, Beyene Joseph, Wilke Russell A, Goldberg Arnon, Woo Jessica G, Martin Lisa J, Rothenberg Marc E, Rao Marepalli, Hershey Gurjit K Khurana, Chakraborty Ranajit, Mersha Tesfaye |
Five linkage regions each harbor multiple type 2 diabetes genes in the African American subset of the GENNID Study. Journal of human genetics 2013 Jun 58 (6): 378-83. Hasstedt Sandra J, Highland Heather M, Elbein Steven C, Hanis Craig L, Das Swapan K, |
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm.
Journal of medical genetics 2013 Jul 50 (7): 473-8. Zheng Hou-Feng, Duncan Emma L, Yerges-Armstrong Laura M, Eriksson Joel, Bergström Ulrica, Leo Paul J, Leslie William D, Goltzman David, Blangero John, Hanley David A, Carless Melanie A, Streeten Elizabeth A, Lorentzon Mattias, Brown Matthew A, Spector Tim D, Pettersson-Kymmer Ulrika, Ohlsson Claes, Mitchell Braxton D, Richards J Bre |
Genetics of eye colours in different rural populations on the Silk Road. European journal of human genetics : EJHG 2013 Mar . Ulivi S, Mezzavilla M, Gasparini P |
Cell-cell adhesion genes CTNNA2 and CTNNA3 are tumour suppressors frequently mutated in laryngeal carcinomas. Nature communications 2013 4 2531. Fanjul-Fernández Miriam, Quesada Víctor, Cabanillas Rubén, Cadiñanos Juan, Fontanil Tania, Obaya Alvaro, Ramsay Andrew J, Llorente José L, Astudillo Aurora, Cal Santiago, López-Otín Carl |
Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations.
Genomics & informatics 2013 Sep 11 (3): 129-34. Hong Kyung-Won, Kim Sung Soo, Kim Yeonju |
TARV: tree-based analysis of rare variants identifying risk modifying variants in CTNNA2 and CNTNAP2 for alcohol addiction. Genetic epidemiology 2014 Sep 38 (6): 552-9. Song Chi, Zhang Hepi |
Whole-genome sequencing and comprehensive molecular profiling identify new driver mutations in gastric cancer. Nature genetics 2014 Jun 46 (6): 573-82. Wang Kai, Yuen Siu Tsan, Xu Jiangchun, Lee Siu Po, Yan Helen H N, Shi Stephanie T, Siu Hoi Cheong, Deng Shibing, Chu Kent Man, Law Simon, Chan Kok Hoe, Chan Annie S Y, Tsui Wai Yin, Ho Siu Lun, Chan Anthony K W, Man Jonathan L K, Foglizzo Valentina, Ng Man Kin, Chan April S, Ching Yick Pang, Cheng Grace H W, Xie Tao, Fernandez Julio, Li Vivian S W, Clevers Hans, Rejto Paul A, Mao Mao, Leung Suet |
Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption. PloS one 2014 9 (12): e116346. Denis Marie, Enquobahrie Daniel A, Tadesse Mahlet G, Gelaye Bizu, Sanchez Sixto E, Salazar Manuel, Ananth Cande V, Williams Michelle |
A pilot genome-wide association study of breast cancer susceptibility loci in Indonesia.
Asian Pacific journal of cancer prevention : APJCP 2015 16 (6): 2231-5. Haryono Samuel J, Datasena I Gusti Bagus, Santosa Wahyu Budi, Mulyarahardja Raymond, Sari Karti |
Cadherin-13 gene is associated with hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Mar . Salatino-Oliveira Angélica, Genro Julia Pasqualini, Polanczyk Guilherme, Zeni Cristian, Schmitz Marcelo, Kieling Christian, Anselmi Luciana, Menezes Ana Maria Baptista, Barros Fernando Cde, Polina Evelise Regina, Motta Nina R, Grevet Eugênio Horácio, Bau Claiton Henrique Dotto, Rohde Luis Augusto, Hutz Mara Hele |
New polymorphisms associated with response to anti-TNF drugs in patients with moderate-to-severe plaque psoriasis. The pharmacogenomics journal 2018 01 18 (1): 70-75. Prieto-Pérez R, Solano-López G, Cabaleiro T, Román M, Ochoa D, Talegón M, Baniandrés O, López-Estebaranz J L, de la Cueva P, Daudén E, Abad-Santos |
Association of genetic polymorphisms with survival of pancreatic ductal adenocarcinoma patients. Carcinogenesis 2016 10 37 (10): 957-64. Rizzato Cosmeri, Campa Daniele, Talar-Wojnarowska Renata, Halloran Christopher, Kupcinskas Juozas, Butturini Giovanni, Mohelníková-Duchonová Beatrice, Sperti Cosimo, Tjaden Christine, Ghaneh Paula, Hackert Thilo, Funel Niccola, Giese Nathalia, Tavano Francesca, Pezzilli Raffaele, Pedata Mariangela, Pasquali Claudio, Gazouli Maria, Mambrini Andrea, Soucek Pavel, di Sebastiano Pierluigi, Capurso Gabriele, Cantore Maurizio, Oliverius Martin, Offringa Rienk, Malecka-Panas Ewa, Strobel Oliver, Scarpa Aldo, Canzian Federi |
Plasma levels of vitamin K and the risk of ischemic heart disease: a Mendelian randomization study. Journal of thrombosis and haemostasis : JTH 2016 Apr . Schooling C Ma |
Identifying the genetic risk factors for treatment response to lurasidone by genome-wide association study: A meta-analysis of samples from three independent clinical trials.
Schizophrenia research 2018 May . Li Jiang, Loebel Antony, Meltzer Herbert |
A Genome-Wide Search for Bipolar Disorder Risk Loci Modified by Mitochondrial Genome Variation. Molecular neuropsychiatry 2018 Feb 3 (3): 125-134. Ryu Euijung, Nassan Malik, Jenkins Gregory D, Armasu Sebastian M, Andreazza Ana, McElroy Susan L, Vawter Marquis P, Frye Mark A, Biernacka Joanna |
A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
Genomic analyses in African populations identify novel risk loci for cleft palate.
Human molecular genetics 2018 Nov . Butali Azeez, Mossey Peter A, Adeyemo Wasiu L, Eshete Mekonen A, Gowans Lord J J, Busch Tamara D, Jain Deepti, Yu Wenjie, Huan Liu, Laurie Cecelia A, Laurie Cathy C, Nelson Sarah, Li Mary, Sanchez-Lara Pedro A, Magee William P, Magee Kathleen S, Auslander Allyn, Brindopke Frederick, Kay Denise M, Caggana Michele, Romitti Paul A, Mills James L, Audu Rosemary, Onwuamah Chika, Oseni Ganiyu O, Owais Arwa, James Olutayo, Olaitan Peter B, Aregbesola Babatunde S, Braimah Ramat O, Oginni Fadekemi O, Oladele Ayodeji O, Bello Saidu A, Rhodes Jennifer, Shiang Rita, Donkor Peter, Obiri-Yeboah Solomon, Arthur Fareed Kow Nanse, Twumasi Peter, Agbenorku Pius, Plange-Rhule Gyikua, Oti Alexander Acheampong, Ogunlewe Olugbenga M, Oladega Afisu A, Adekunle Adegbayi A, Erinoso Akinwunmi O, Adamson Olatunbosun O, Elufowoju Abosede A, Ayelomi Oluwanifemi I, Hailu Taiye, Hailu Abiye, Demissie Yohannes, Derebew Miliard, Eliason Steve, Romero-Bustillous Miguel, Lo Cynthia, Park James, Desai Shaan, Mohammed Muiawa, Abate Firke, Abdur-Rahman Lukman O, Anand Deepti, Saadi Irfaan, Oladugba Abimibola V, Lachke Salil A, Amendt Brad A, Rotimi Charles N, Marazita Mary L, Cornell Robert A, Murray Jeffrey C, Adeyemo Adebowale |
Identification of novel risk loci with shared effects on alcoholism, heroin, and methamphetamine dependence.
Molecular psychiatry 2019 Aug . Sun Yan, Chang Suhua, Liu Zhen, Zhang Libo, Wang Fan, Yue Weihua, Sun Hongqiang, Ni Zhaojun, Chang Xiangwen, Zhang Yibing, Chen Yang, Liu Jiqiang, Lu Lin, Shi J |
A trans-ethnic two-stage polygenetic scoring analysis detects genetic correlation between osteoporosis and schizophrenia.
Clinical and translational medicine 2020 Feb 9 (1): 21. Liu Li, Wen Yan, Ning Yujie, Li Ping, Cheng Bolun, Cheng Shiqiang, Zhang Lu, Ma Mei, Qi Xin, Liang Chujun, Yang Tielin, Chen Xiangding, Tan Lijun, Shen Hui, Tian Qing, Deng Hong-Wen, Ma Xiancang, Zhang Feng, Zhu Fe |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. medRxiv : the preprint server for health sciences 2020 Nov . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
Catenin Alpha 2 May Be a Biomarker or Potential Drug Target in Psychiatric Disorders with Perseverative Negative Thinking. Pharmaceuticals (Basel, Switzerland) 2021 9 14 (9): . Eszlari Nora, Bagyura Zsolt, Millinghoffer Andras, Nagy Tamas, Juhasz Gabriella, Antal Peter, Merkely Bela, Bagdy Gyor |
Catenin Alpha-2 Mutation Changes the Immune Microenvironment in Lung Adenocarcinoma Patients Receiving Immune Checkpoint Inhibitors. Frontiers in pharmacology 2021 6 12 645862. Wen Yang, Lin Anqi, Zhu Weiliang, Wei Ting, Luo Peng, Guo Linlang, Zhang Ji |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 Apr . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, , Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
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