Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: DEPDC5[original query] |
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Neither MICA Nor DEPDC5 Genetic Polymorphisms Correlate with Hepatocellular Carcinoma Recurrence following Hepatectomy. HPB surgery : a world journal of hepatic, pancreatic and biliary surgery 2012 2012 185496. Motomura Takashi, Ono Yuki, Shirabe Ken, Fukuhara Takasuke, Konishi Hideyuki, Mano Yohei, Toshima Takeo, Yoshiya Shohei, Muto Jun, Ikegami Toru, Yoshizumi Tomoharu, Maehara Yoshihi |
Role of IFN-ks, IFN-ks related genes and the DEPDC5 gene in Hepatitis B virus-related liver disease. Journal of viral hepatitis 2014 Jul 21 (7): e29-38. Ma N, Zhang X, Yu F, Gao P, Fan Q, Liu L, Liu |
[Hepatitis C virus induced hepatocellular carcinoma associated genes]. Nihon rinsho. Japanese journal of clinical medicine 2015 Feb 73 (2): 333-8. Kato Naoya, Muroyama Ryosuke, Goto Ka |
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy. Annals of neurology 2015 Dec . Bagnall Richard D, Crompton Douglas E, Petrovski Slavé, Lam Lien, Cutmore Carina, Garry Sarah I, Sadleir Lynette G, Dibbens Leanne M, Cairns Anita, Kivity Sara, Afawi Zaid, Regan Brigid M, Duflou Johan, Berkovic Samuel F, Scheffer Ingrid E, Semsarian Christoph |
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy. Annals of neurology 2015 Oct . Ricos Michael G, Hodgson Bree L, Pippucci Tommaso, Saidin Akzam, Sze Ong Yeh, Heron Sarah E, Licchetta Laura, Bisulli Francesca, Bayly Marta A, Hughes James, Baldassari Sara, Palombo Flavia, , Santucci Margherita, Meletti Stefano, Berkovic Samuel F, Rubboli Guido, Thomas Paul Q, Scheffer Ingrid E, Tinuper Paolo, Geoghegan Joel, Schreiber Andreas W, Dibbens Leanne |
Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia. Annals of neurology 2015 Apr 77 (4): 720-5. D'Gama Alissa M, Geng Ying, Couto Javier A, Martin Beth, Boyle Evan A, LaCoursiere Christopher M, Hossain Amer, Hatem Nicole E, Barry Brenda J, Kwiatkowski David J, Vinters Harry V, Barkovich A James, Shendure Jay, Mathern Gary W, Walsh Christopher A, Poduri Annapur |
Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia. BMC infectious diseases 2014 14 (1): 632. Al-Anazi Mashael R, Matou-Nasri Sabine, Abdo Ayman A, Sanai Faisal M, Khan Mohammed Q, Albenmousa Ali, Al-Ashgar Hamad I, Khalaf Nisreen Z, Al-Ahdal Mohammed N, Al-Qahtani Ahmed |
Epileptic spasms are a feature of DEPDC5 mTORopathy. Neurology. Genetics 2015 Aug 1 (2): e17. Carvill Gemma L, Crompton Douglas E, Regan Brigid M, McMahon Jacinta M, Saykally Julia, Zemel Matthew, Schneider Amy L, Dibbens Leanne, Howell Katherine B, Mandelstam Simone, Leventer Richard J, Harvey A Simon, Mullen Saul A, Berkovic Samuel F, Sullivan Joseph, Scheffer Ingrid E, Mefford Heather |
Polymorphisms in MICA, but not in DEPDC5, HCP5 or PNPLA3, are associated with chronic hepatitis C-related hepatocellular carcinoma. Scientific reports 2017 09 7 (1): 11912. Hai Hoang, Tamori Akihiro, Thuy Le Thi Thanh, Yoshida Kanako, Hagihara Atsushi, Kawamura Etsushi, Uchida-Kobayashi Sawako, Morikawa Hiroyasu, Enomoto Masaru, Murakami Yoshiki, Kawada Norifu |
Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel. Frontiers in neurology 2018 7 9 515. Tsai Meng-Han, Chan Chung-Kin, Chang Ying-Chao, Lin Chih-Hsiang, Liou Chia-Wei, Chang Wen-Neng, Ng Ching-Ching, Lim Kheng-Seang, Hwang Daw-Ya |
Loss of Chromatin-Remodeling Proteins and/or CDKN2A Associates With Metastasis of Pancreatic Neuroendocrine Tumors and Reduced Patient Survival Times. Gastroenterology 2018 2 154 (8): 2060-2063.e8. Roy Somak, LaFramboise William A, Liu Ta-Chiang, Cao Dengfeng, Luvison Alyssa, Miller Caitlyn, Lyons Maureen A, O'Sullivan Roderick J, Zureikat Amer H, Hogg Melissa E, Tsung Allan, Lee Kenneth K, Bahary Nathan, Brand Randall E, Chennat Jennifer S, Fasanella Kenneth E, McGrath Kevin, Nikiforova Marina N, Papachristou Georgios I, Slivka Adam, Zeh Herbert J, Singhi Aatur |
PNPLA3 and TM6SF2 variants as risk factors of hepatocellular carcinoma across various etiologies and severity of underlying liver diseases. International journal of cancer 2018 Oct . Yang Jie, Trépo Eric, Nahon Pierre, Cao Qian, Moreno Christophe, Letouzé Eric, Imbeaud Sandrine, Gustot Thierry, Deviere Jacques, Debette Stéphanie, Amouyel Philippe, Bioulac-Sage Paulette, Calderaro Julien, Ganne-Carrié Nathalie, Laurent Alexis, Blanc Jean Frédéric, Guyot Erwan, Sutton Angela, Ziol Marianne, Zucman-Rossi Jessica, Nault Jean-Charl |
Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical Development. Pediatric neurology 2019 9 103 27-34. Lee Sangbo, Kim Se Hee, Kim Borahm, Lee Seung-Tae, Choi Jong Rak, Kim Heung Dong, Lee Joon Soo, Kang Hoon-Ch |
Precise detection of low-level somatic mutation in resected epilepsy brain tissue. Acta neuropathologica 2019 Aug . Sim Nam Suk, Ko Ara, Kim Woo Kyeong, Kim Se Hoon, Kim Ju Seong, Shim Kyu-Won, Aronica Eleonora, Mijnsbergen Caroline, Spliet Wim G M, Koh Hyun Yong, Kim Heung Dong, Lee Joon Soo, Kim Dong Seok, Kang Hoon-Chul, Lee Jeong |
Exome sequencing identifies molecular diagnosis in children with drug-resistant epilepsy. Epilepsia open 2019 3 4 (1): 63-72. Tsang Mandy Ho-Yin, Leung Gordon Ka-Chun, Ho Alvin Chi-Chung, Yeung Kit-San, Mak Christopher Chun-Yu, Pei Steven Lim-Cho, Yu Mullin Ho-Chung, Kan Anita Sik-Yau, Chan Kelvin Yuen-Kwong, Kwong Karen Ling, Lee So-Lun, Yung Ada Wing-Yan, Fung Cheuk-Wing, Chung Brian Hon-Y |
A variant in the MICA gene is associated with liver fibrosis progression in chronic hepatitis C through TGF-?1 dependent mechanisms. Scientific reports 2019 2 9 (1): 1439. Sharkawy Rasha El, Bayoumi Ali, Metwally Mayada, Mangia Alessandra, Berg Thomas, Romero-Gomez Manuel, Abate Maria Lorena, Irving William L, Sheridan David, Dore Gregory J, Spengler Ulrich, Lampertico Pietro, Bugianesi Elisabetta, Weltman Martin, Mollison Lindsay, Cheng Wendy, Riordan Stephen, Santoro Rosanna, Gallego-Durán Rocío, Fischer Janett, Nattermann Jacob, D'Ambrosio Roberta, McLeod Duncan, Powell Elizabeth, Latchoumanin Olivier, Thabet Khaled, Najim Mustafa A M, Douglas Mark W, Liddle Christopher, Qiao Liang, George Jacob, Eslam Mohammed, |
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients. Seizure 2019 12 74 60-64. Licchetta Laura, Pippucci Tommaso, Baldassari Sara, Minardi Raffaella, Provini Federica, Mostacci Barbara, Plazzi Giuseppe, Tinuper Paolo, Bisulli Francesca, |
Rufinamide efficacy and association with phenotype and genotype in children with intractable epilepsy: A retrospective single center study. Epilepsy research 2019 10 168 106211. Oesch Gabriela, Bozarth Xiuhua Lia |
Correlation between the DEPDC5 rs1012068 polymorphism and the risk of HBV-related hepatocellular carcinoma. Clinics and research in hepatology and gastroenterology 2019 Jan . Liu Wenxuan, Ma Ning, Zhao Dongqiang, Gao Xia, Zhang Xiaolin, Yang Lei, Liu Dian |
Determining the best candidates for next-generation sequencing-based gene panel for evaluation of early-onset epilepsy. Molecular genetics & genomic medicine 2020 7 8 (9): e1376. Lee Jiwon, Lee Chung, Ki Chang-Seok, Lee Jeeh |
High genetic burden in 163 Chinese children with status epilepticus. Seizure 2020 12 84 40-46. Wang Tianqi, Wang Ji, Ma Yu, Zhou Hao, Ding Ding, Li Chunpei, Du Xiaonan, Jiang Yong-Hui, Wang Yi, Long Shasha, Li Shuang, Lu Guoping, Chen Weiming, Zhou Yuanfeng, Zhou Shuizhen, Wang |
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy. Annals of clinical and translational neurology 2021 May . Wolking Stefan, Moreau Claudia, McCormack Mark, Krause Roland, Krenn Martin, , Berkovic Samuel, Cavalleri Gianpiero L, Delanty Norman, Depondt Chantal, Johnson Michael R, Koeleman Bobby P C, Kunz Wolfram S, Lerche Holger, Marson Anthony G, O'Brien Terence J, Petrovski Slave, Sander Josemir W, Sills Graeme J, Striano Pasquale, Zara Federico, Zimprich Fritz, Sisodiya Sanjay M, Girard Simon L, Cossette Patri |
Epilepsy with auditory features: Contribution of known genes in 112 patients. Seizure 2021 1 85 115-118. Bisulli F, Rinaldi C, Pippucci T, Minardi R, Baldassari S, Zenesini C, Mostacci B, Fanella M, Avoni P, Menghi V, Caporali L, Muccioli L, Tinuper P, Licchetta |
Disheveled EGL-10 and pleckstrin domain-containing 5 rs1012068 T/G gene polymorphism among Egyptian chronic HCV-infected patients: disease progression and related complications. The Egyptian journal of immunology 2022 Jul 29 (3): 36-43. Farhan Hanan M, Abougabal Khadiga, Gaber Heba F, Attia Di |
Genetic and molecular features of seizure-freedom following surgical resections for focal epilepsy: A pilot study. Frontiers in neurology 2022 10 13 942643. Louis Shreya, Busch Robyn M, Lal Dennis, Hockings Jennifer, Hogue Olivia, Morita-Sherman Marcia, Vegh Deborah, Najm Imad, Ghosh Chaitali, Bazeley Peter, Eng Charis, Jehi Lara, Rotroff Daniel |
Genetic Determinants of Sudden Unexpected Death in Pediatrics. Genetics in medicine : official journal of the American College of Medical Genetics 2022 1 24 (4): 839-850. Koh Hyun Yong, Haghighi Alireza, Keywan Christine, Alexandrescu Sanda, Plews-Ogan Erin, Haas Elisabeth A, Brownstein Catherine A, Vargas Sara O, Haynes Robin L, Berry Gerard T, Holm Ingrid A, Poduri Annapurna H, Goldstein Richard |
Detection of brain somatic mutations in focal cortical dysplasia during epilepsy presurgical workup. Brain communications 2023 6 5 (3): fcad174. Rayann Checri, Mathilde Chipaux, Sarah Ferrand-Sorbets, Emmanuel Raffo, Christine Bulteau, Sarah Dominique Rosenberg, Marion Doladilhe, Georg Dorfmüller, Homa Adle-Biassette, Sara Baldassari, Stéphanie Baul |
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition. Brain : a journal of neurology 2023 4 . Martins Custodio Helena, Clayton Lisa M, Bellampalli Ravishankara, Pagni Susanna, Silvennoinen Katri, Caswell Richard, , Brunklaus Andreas, Guerrini Renzo, Koeleman Bobby P C, Lemke Johannes R, Møller Rikke S, Scheffer Ingrid E, Weckhuysen Sarah, Zara Federico, Zuberi Sameer, Kuchenbaecker Karoline, Balestrini Simona, Mills James D, Sisodiya Sanjay |
The role of copy number variants in the genetic architecture of common familial epilepsies. Epilepsia 2023 12 . Authors are not available |
Clinical and genetic features of GATOR1 complex-associated epilepsy. Journal of medical genetics 2023 1 . Yin Kaili, Lei Xingxing, Yan Zhaofen, Yang Yujiao, Deng Qinqin, Lu Qiang, Zhang Xue, Wang Mengyang, Liu Qi |
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- Page last updated:Apr 22, 2024
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