Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and SYNE1[original query] |
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| Genome-wide association study of alcohol dependence implicates a region on chromosome 11. Alcoholism, clinical and experimental research 2010 May 34 (5): 840-52. Edenberg Howard J, Koller Daniel L, Xuei Xiaoling, Wetherill Leah, McClintick Jeanette N, Almasy Laura, Bierut Laura J, Bucholz Kathleen K, Goate Alison, Aliev Fazil, Dick Danielle, Hesselbrock Victor, Hinrichs Anthony, Kramer John, Kuperman Sam, Nurnberger John I, Rice John P, Schuckit Marc A, Taylor Robert, Todd Webb B, Tischfield Jay A, Porjesz Bernice, Foroud Tatia |
| Using whole-exome sequencing to identify inherited causes of autism. Neuron 2013 Jan 77 (2): 2. Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, Leclair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA |
| Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1. BMC medical genetics 2014 15 (1): 2. Xu Wei, Cohen-Woods Sarah, Chen Qian, Noor Abdul, Knight Jo, Hosang Georgina, Parikh Sagar V, De Luca Vincenzo, Tozzi Federica, Muglia Pierandrea, Forte Julia, McQuillin Andrew, Hu Pingzhao, Gurling Hugh M D, Kennedy James L, McGuffin Peter, Farmer Anne, Strauss John, Vincent John |
| Systematic search for rare variants in Finnish early-onset colorectal cancer patients. Cancer genetics 0 208 (1-2): 35-40. Tanskanen Tomas, Gylfe Alexandra E, Katainen Riku, Taipale Minna, Renkonen-Sinisalo Laura, Järvinen Heikki, Mecklin Jukka-Pekka, Böhm Jan, Kilpivaara Outi, Pitkänen Esa, Palin Kimmo, Vahteristo Pia, Tuupanen Sari, Aaltonen Lauri |
| Genomic mapping and cellular expression of human CPG2 transcripts in the SYNE1 gene. Molecular and cellular neurosciences 2015 Dec . Loebrich Sven, Rathje Mette, Hager Emily, Ataman Bulent, Harmin David A, Greenberg Michael E, Nedivi El |
| Heterogeneity in clinical features and disease severity in ataxia-associated SYNE1 mutations. Journal of neurology 2016 May . Wiethoff Sarah, Hersheson Joshua, Bettencourt Conceicao, Wood Nicholas W, Houlden Hen |
| Novel genetic loci associated with long-term deterioration in blood lipid concentrations and coronary artery disease in European adults. International journal of epidemiology 2016 Nov . Varga Tibor V, Kurbasic Azra, Aine Mattias, Eriksson Pontus, Ali Ashfaq, Hindy George, Gustafsson Stefan, Luan Jian'an, Shungin Dmitry, Chen Yan, Schulz Christina-Alexandra, Nilsson Peter M, Hallmans Göran, Barroso Inês, Deloukas Panos, Langenberg Claudia, Scott Robert A, Wareham Nicholas J, Lind Lars, Ingelsson Erik, Melander Olle, Orho-Melander Marju, Renström Frida, Franks Paul |
| Identification of rare nonsynonymous variants in SYNE1/CPG2 in bipolar affective disorder. Psychiatric genetics 2017 Feb . Sharp Sally I, Lange Jenny, Kandaswamy Radhika, Daher Mazen, Anjorin Adebayo, Bass Nicholas J, McQuillin Andr |
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
Nature communications 2018 Sep 9 (1): 3636. Rafnar Thorunn, Gunnarsson Bjarni, Stefansson Olafur A, Sulem Patrick, Ingason Andres, Frigge Michael L, Stefansdottir Lilja, Sigurdsson Jon K, Tragante Vinicius, Steinthorsdottir Valgerdur, Styrkarsdottir Unnur, Stacey Simon N, Gudmundsson Julius, Arnadottir Gudny A, Oddsson Asmundur, Zink Florian, Halldorsson Gisli, Sveinbjornsson Gardar, Kristjansson Ragnar P, Davidsson Olafur B, Salvarsdottir Anna, Thoroddsen Asgeir, Helgadottir Elisabet A, Kristjansdottir Katrin, Ingthorsson Orri, Gudmundsson Valur, Geirsson Reynir T, Arnadottir Ragnheidur, Gudbjartsson Daniel F, Masson Gisli, Asselbergs Folkert W, Jonasson Jon G, Olafsson Karl, Thorsteinsdottir Unnur, Halldorsson Bjarni V, Thorleifsson Gudmar, Stefansson Ka |
| Whole Exome Sequencing Uncovers Germline Variants of Cancer-Related Genes in Sporadic Pheochromocytoma. International journal of genomics 2018 9 2018 6582014. Urbini Milena, Nannini Margherita, Astolfi Annalisa, Indio Valentina, Vicennati Valentina, De Luca Matilde, Tarantino Giuseppe, Corso Federica, Saponara Maristella, Gatto Lidia, Santini Donatella, Di Dalmazi Guido, Pagotto Uberto, Pasquali Renato, Pession Andrea, Biasco Guido, Pantaleo Maria |
| Acquired Cystic Kidney Disease-associated Renal Cell Carcinoma (ACKD-RCC) Harbor Recurrent Mutations in KMT2C and TSC2 Genes. The American journal of surgical pathology 2020 7 44 (11): 1479-1486. Shah Abhishek, Lal Priti, Toorens Erik, Palmer Matthew B, Schwartz Lauren, Vergara Norge, Guzzo Thomas, Nayak Anup |
| Circulating Tumor DNA Is Capable of Monitoring the Therapeutic Response and Resistance in Advanced Colorectal Cancer Patients Undergoing Combined Target and Chemotherapy. Frontiers in oncology 2020 4 10 466. Cao Hua, Liu Xinyi, Chen Yixin, Yang Pan, Huang Tanxiao, Song Lele, Xu Ruili |
| A novel genomic classification system of gastric cancer via integrating multidimensional genomic characteristics. Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2021 6 24 (6): 1227-1241. Wang Haiyong, Ding Yongfeng, Chen Yanyan, Jiang Junjie, Chen Yiran, Lu Jun, Kong Mei, Mo Fan, Huang Yingying, Zhao Wenyi, Fang Ping, Chen Xiangliu, Teng Xiaodong, Xu Nong, Lu Yimin, Yu Xiongfei, Li Zhongqi, Zhang Jing, Wang Haohao, Bao Xuanwen, Zhou Donghui, Chi Ying, Zhou Tianhua, Zhou Zhan, Chen Shuqing, Teng Liso |
| Effects of cyclophosphamide related genetic variants on clinical outcomes of adult hematopoietic cell transplant patients. Cancer chemotherapy and pharmacology 2022 Jan . Takahashi Takuto, Pearson Rachael, Cao Qing, Scheibner Aileen, Sanghavi Kinjal, Weisdorf Daniel, Brunstein Claudio, Rogosheske John, Bachanova Veronika, Warlick Erica D, Wiseman Anthony, Jacobson Pamala |
| SYNE1 Mutation Is Associated with Increased Tumor Mutation Burden and Immune Cell Infiltration in Ovarian Cancer. International journal of molecular sciences 2023 9 24 (18): . Laura M Harbin, Nan Lin, Frederick R Ueland, Jill M Koles |
| Clinical Exome Gene Panel Analysis of a Cohort of Urothelial Bladder Cancer Patients from Sri Lanka. Asian Pacific journal of cancer prevention : APJCP 2023 5 24 (5): 1533-1542. Ajith Malalasekera, Nilaksha Neththikumara, Praveenan Somasundaram, Sajeewani Pathirana, Chathumadavi Ediriweera, Dileepa Ediriweera, Serozsha As Goonewardena, Neville D Perera, Anuruddha Abeygunasekara, Rohan W Jayasekara, Kalum Wettasinghe, M Dilani S Lokuhetty, Vajira H W Dissanaye |
| DcR3-associated risk score: correlating better prognosis and enhanced predictive power in colorectal cancer. Discover oncology 2024 6 15 (1): 233. Ying Duan, Hangrong Fang, Juanhong Wang, Banlai Ruan, Juan Yang, Jie Liu, Siqi Gou, Yijie Li, Zhengyi Che |
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