Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: UNC5C[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 |
Variants in the netrin-1 receptor UNC5C prevent apoptosis and increase risk of familial colorectal cancer. Gastroenterology 2011 Dec 141 (6): 2039-46. Coissieux Marie-May, Tomsic Jerneja, Castets Marie, Hampel Heather, Tuupanen Sari, Andrieu Nadine, Comeras Ilene, Drouet Youenn, Lasset Christine, Liyanarachchi Sandya, Mazelin Laetitia, Puisieux Alain, Saurin Jean-Christophe, Scoazec Jean-Yves, Wang Qing, Aaltonen Lauri, Tanner Stephan M, de la Chapelle Albert, Bernet Agnès, Mehlen Patri |
Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China. Neurobiology of aging 2014 Oct 35 (10): 2422.e9-2422.e11. Jiao Bin, Liu Xiaoyan, Tang Beisha, Hou Lihua, Zhou Lin, Zhang Fufeng, Zhou Yafang, Guo Jifeng, Yan Xinxiang, Shen |
A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death. Nature medicine 2014 Dec 20 (12): 1452-7. Wetzel-Smith Monica K, Hunkapiller Julie, Bhangale Tushar R, Srinivasan Karpagam, Maloney Janice A, Atwal Jasvinder K, Sa Susan M, Yaylaoglu Murat B, Foreman Oded, Ortmann Ward, Rathore Nisha, Hansen David V, Tessier-Lavigne Marc, , Mayeux Richard, Pericak-Vance Margaret, Haines Jonathan, Farrer Lindsay A, Schellenberg Gerard D, Goate Alison, Behrens Timothy W, Cruchaga Carlos, Watts Ryan J, Graham Robert |
Whole-exome sequencing of muscle-invasive bladder cancer identifies recurrent mutations of UNC5C and prognostic importance of DNA repair gene mutations on survival. Clinical cancer research : an official journal of the American Association for Cancer Research 2014 Dec 20 (24): 6605-17. Yap Kai Lee, Kiyotani Kazuma, Tamura Kenji, Antic Tatjana, Jang Miran, Montoya Magdeline, Campanile Alexa, Yew Poh Yin, Ganshert Cory, Fujioka Tomoaki, Steinberg Gary D, O'Donnell Peter H, Nakamura Yusu |
Evaluation of the colorectal cancer risk conferred by rare UNC5C alleles. World journal of gastroenterology : WJG 2014 Jan 20 (1): 204-13. Küry Sébastien, Garrec Céline, Airaud Fabrice, Breheret Flora, Guibert Virginie, Frenard Cécile, Jiao Shuo, Bonneau Dominique, Berthet Pascaline, Bossard Céline, Ingster Olivier, Cauchin Estelle, Bezieau Stépha |
Alzheimer's disease: rare variants with large effect sizes. Current opinion in genetics & development 2015 Aug 33 49-55. Del-Aguila Jorge L, Koboldt Daniel C, Black Kathleen, Chasse Rachel, Norton Joanne, Wilson Richard K, Cruchaga Carl |
R47H Variant of TREM2 Associated With Alzheimer Disease in a Large Late-Onset Family: Clinical, Genetic, and Neuropathological Study. JAMA neurology 2015 Aug 72 (8): 920-7. Korvatska Olena, Leverenz James B, Jayadev Suman, McMillan Pamela, Kurtz Irina, Guo Xindi, Rumbaugh Malia, Matsushita Mark, Girirajan Santhosh, Dorschner Michael O, Kiianitsa Kostantin, Yu Chang-En, Brkanac Zoran, Garden Gwenn A, Raskind Wendy H, Bird Thomas |
The Impact of UNC5C Genetic Variations on Neuroimaging in Alzheimer's Disease. Molecular neurobiology 2015 Dec . Sun Jia-Hao, Wang Hui-Fu, Zhu Xi-Chen, Yu Wan-Jiang, Tan Chen-Chen, Jiang Teng, Tan Meng-Shan, Tan Lan, Yu Jin-Tai, |
Re: Whole-Exome Sequencing of Muscle-Invasive Bladder Cancer Identifies Recurrent Mutations of UNC5C and Prognostic Importance of DNA Repair Gene Mutations on Survival. The Journal of urology 2016 Aug 196 (2): 351-2. Chang Sam |
Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis. Scientific reports 2016 6 20697. Mur Pilar, Elena Sánchez-Cuartielles, Aussó Susanna, Aiza Gemma, Rafael Valdés-Mas, Pineda Marta, Navarro Matilde, Brunet Joan, Urioste Miguel, Lázaro Conxi, Moreno Victor, Capellá Gabriel, Puente Xose S, Valle Lau |
UNC5C variants are associated with cerebral amyloid angiopathy. Neurology. Genetics 2017 Aug 3 (4): e176. Yang Hyun-Sik, White Charles C, Chibnik Lori B, Klein Hans-Ulrich, Schneider Julie A, Bennett David A, De Jager Philip |
Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional data.
PLoS medicine 2017 Apr 14 (4): e1002287. White Charles C, Yang Hyun-Sik, Yu Lei, Chibnik Lori B, Dawe Robert J, Yang Jingyun, Klein Hans-Ulrich, Felsky Daniel, Ramos-Miguel Alfredo, Arfanakis Konstantinos, Honer William G, Sperling Reisa A, Schneider Julie A, Bennett David A, De Jager Philip |
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function. Journal of Alzheimer's disease & Parkinsonism 2017 11 7 (4): . Cukier H N, Kunkle B K, Hamilton K L, Rolati S, Kohli M A, Whitehead P L, Jaworski J, Vance J M, Cuccaro M L, Carney R M, Gilbert J R, Farrer L A, Martin E R, Beecham G W, Haines J L, Pericak-Vance M |
Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population. Cancer biomarkers : section A of Disease markers 2017 Oct . Lu Nanhang, Wang Jinzeng, Zhu Bijun, Zhang Miaomiao, Qi Fazhi, Wang Xiangdong, Gu Jianyi |
Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study. Annals of human genetics 2017 Jan . Tabb Keri L, Hellwege Jacklyn N, Palmer Nicholette D, Dimitrov Latchezar, Sajuthi Satria, Taylor Kent D, Ng Maggie C Y, Hawkins Gregory A, Chen Yii-der Ida, Brown W Mark, McWilliams David, Williams Adrienne, Lorenzo Carlos, Norris Jill M, Long Jirong, Rotter Jerome I, Curran Joanne E, Blangero John, Wagenknecht Lynne E, Langefeld Carl D, Bowden Donald |
A logical relationship for schizophrenia, bipolar, and major depressive disorder. Part 4: Evidence from chromosome 4 high-density association screen. The Journal of comparative neurology 2019 Feb 527 (2): 392-405. Tang Jian, Chen Xing, Cai Bin, Chen Ga |
Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.
PloS one 2018 13 (1): e0189498. Gorlova Olga Y, Li Yafang, Gorlov Ivan, Ying Jun, Chen Wei V, Assassi Shervin, Reveille John D, Arnett Frank C, Zhou Xiaodong, Bossini-Castillo Lara, Lopez-Isac Elena, Acosta-Herrera Marialbert, Gregersen Peter K, Lee Annette T, Steen Virginia D, Fessler Barri J, Khanna Dinesh, Schiopu Elena, Silver Richard M, Molitor Jerry A, Furst Daniel E, Kafaja Suzanne, Simms Robert W, Lafyatis Robert A, Carreira Patricia, Simeon Carmen Pilar, Castellvi Ivan, Beltran Emma, Ortego Norberto, Amos Christopher I, Martin Javier, Mayes Maureen |
An UNC5C Allele Predicts Cognitive Decline and Hippocampal Atrophy in Clinically Normal Older Adults. Journal of Alzheimer's disease : JAD 2019 3 68 (3): 1161-1170. Yang Hyun-Sik, Chhatwal Jasmeer P, Xu Jishu, White Charles C, Hanseeuw Bernard, Rabin Jennifer S, Papp Kathryn V, Buckley Rachel F, Schultz Aaron P, Properzi Michael J, Gatchel Jennifer R, Amariglio Rebecca E, Donovan Nancy J, Mormino Elizabeth C, Hedden Trey, Marshall Gad A, Rentz Dorene M, Johnson Keith A, De Jager Philip L, Sperling Reisa |
Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis.
PLoS medicine 2020 06 17 (6): e1003132. Dapas Matthew, Lin Frederick T J, Nadkarni Girish N, Sisk Ryan, Legro Richard S, Urbanek Margrit, Hayes M Geoffrey, Dunaif Andr |
A potential prognostic model based on miRNA expression profile in The Cancer Genome Atlas for bladder cancer patients. Journal of biological research (Thessalonike, Greece) 2020 6 27 6. Liu Yan, Zhu Dong Yan, Xing Hong Jian, Hou Yi, Sun Y |
Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG Endophenotypes. Journal of Alzheimer's disease : JAD 2021 Jan . Macedo Ana, Gómez Carlos, Rebelo Miguel Ângelo, Poza Jesús, Gomes Iva, Martins Sandra, Maturana-Candelas Aarón, Pablo Víctor Gutiérrez-de, Durães Luis, Sousa Patrícia, Figueruelo Manuel, Rodríguez María, Pita Carmen, Arenas Miguel, Álvarez Luis, Hornero Roberto, Lopes Alexandra M, Pinto Nád |
Associations of risk genes with onset age and plasma biomarkers of Alzheimer's disease: a large case-control study in mainland China. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2022 1 47 (5): 1121-1127. Jiao Bin, Xiao Xuewen, Yuan Zhenhua, Guo Lina, Liao Xinxin, Zhou Yafang, Zhou Lu, Wang Xin, Liu Xixi, Liu Hui, Jiang Yaling, Lin Zhuojie, Zhu Yuan, Yang Qijie, Zhang Weiwei, Li Jinchen, Shen |
Interactions between genes involved in physiological dysregulation and axon guidance: role in Alzheimer's disease. Frontiers in genetics 2023 9 14 1236509. Konstantin G Arbeev, Svetlana Ukraintseva, Olivia Bagley, Hongzhe Duan, Deqing Wu, Igor Akushevich, Eric Stallard, Alexander Kulminski, Kaare Christensen, Mary F Feitosa, Jeffrey R O'Connell, Daniel Parker, Heather Whitson, Anatoliy I Yash |
The impact of blood MCP-1 levels on Alzheimer's disease with genetic variation of UNC5C and NAV3 loci. Research square 2023 10 . Jinghan Huang, Yixuan Wang, Thor D Stein, Ting Fang Alvin Ang, Yibo Zhu, Qiushan Tao, Kathryn L Lunetta, Jesse Mez, Rhoda Au, Lindsay A Farrer, Wei Qiao Qiu, Xiaoling Zha |
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