Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 52 Records) |
Query Trace: SCN9A[original query] |
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Na channel variants in patients with painful and nonpainful peripheral neuropathy. Neurology. Genetics 2017 Dec 3 (6): e207. Wadhawan Samir, Pant Saumya, Golhar Ryan, Kirov Stefan, Thompson John, Jacobsen Leslie, Qureshi Irfan, Ajroud-Driss Senda, Freeman Roy, Simpson David M, Smith A Gordon, Hoke Ahmet, Bristow Linda |
Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia. Scandinavian journal of pain 2018 6 5 (4): 217-225. Zhang Zhiping, Schmelz Martin, Segerdahl Märta, Quiding Hans, Centerholt Carina, Juréus Anna, Carr Thomas Hedley, Whiteley Jessica, Salter Hugh, Kvernebo Mari Skylstad, Ørstavik Kristin, Helås Tormod, Kleggetveit Inge-Petter, Lunden Lars Kristian, Jørum Ell |
Clinical and molecular analysis of epilepsy-related genes in patients with Dravet syndrome. Medicine 2018 12 97 (50): e13565. Jiang TieJia, Shen Yaping, Chen Huai, Yuan Zhefeng, Mao Shanshan, Gao Fe |
Homozygosity for the SCN10A Polymorphism rs6795970 Is Associated With Hypoalgesic Inflammatory Bowel Disease Phenotype. Frontiers in medicine 2018 12 5 324. Gonzalez-Lopez Eugene, Imamura Kawasawa Yuka, Walter Vonn, Zhang Lijun, Koltun Walter A, Huang Xuemei, Vrana Kent E, Coates Matthew |
No Association of Polymorphisms in Nav1.7 or Nerve Growth Factor Receptor Genes with Trigeminal Neuralgia. Pain medicine (Malden, Mass.) 2018 Oct . Costa Grazielle Mara Ferreira, Rocha Luiz Paulo C, Siqueira Silvia Regina Dowgan Tesseroli de, Moreira Paula Rocha, Almeida-Leite Camila Mega |
Sporadic Erythromelalgia Associated with a Homozygous Carrier of Common Missense Polymorphism in SCN9A Gene Coding for NaV1.7 Voltage-gated Sodium Channel. Cureus 2019 7 11 (5): e4587. Janicki Piotr K, Ruiz-Velasco Victor, Adhikary Sanj |
Small-fibre pathology has no impact on somatosensory system function in patients with fibromyalgia. Pain 2020 9 161 (10): 2385-2393. Fasolino Alessandra, Di Stefano Giulia, Leone Caterina, Galosi Eleonora, Gioia Chiara, Lucchino Bruno, Terracciano Alessandra, Di Franco Manuela, Cruccu Giorgio, Truini Andr |
Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes. Stem cells international 2020 9 2020 8842398. Barajas-Martinez Hector, Smith Maya, Hu Dan, Goodrow Robert J, Puleo Colleen, Hasdemir Can, Antzelevitch Charles, Pfeiffer Ryan, Treat Jacqueline A, Cordeiro Jonathan |
Genomic analysis of 21 patients with corneal neuralgia after refractive surgery. Pain reports 0 5 (4): e826. Yuan Jun-Hui, Schulman Betsy R, Effraim Philip R, Sulayman Dib-Hajj, Jacobs Deborah S, Waxman Stephen |
Identification of Candidate Genes Associated with Postherpetic Neuralgia Susceptibility. Pain physician 2020 Jun 23 (3): E281-E288. Xing Xiufang, Bai Yongyu, Sun Kai, Chen Qunshan, Huang Hao, Qiu Weidong, Yan M |
Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia. Biomedicines 2020 5 8 (5): . Maksemous Neven, Sutherland Heidi G, Smith Robert A, Haupt Larisa M, Griffiths Lyn |
Analysis of SCN9A Gene Variants for Acute and Chronic Postoperative Pain and Morphine Consumption After Total Hysterectomy. Pain medicine (Malden, Mass.) 2020 May . Yeo Junjie, Sia Alex T, Sultana Rehana, Sng Ban Leong, Tan Ene-Ch |
Taxane-induced sensory peripheral neuropathy is associated with an SCN9A single nucleotide polymorphism in Japanese patients. BMC cancer 2020 Apr 20 (1): 325. Tanabe Yuko, Shiraishi Seiji, Hashimoto Kenji, Ikeda Kazutaka, Nishizawa Daisuke, Hasegawa Junko, Shimomura Akihiko, Ozaki Yukinori, Tamura Nobuko, Yunokawa Mayu, Yonemori Kan, Takano Toshimi, Kawabata Hidetaka, Tamura Kenji, Fujiwara Yasuhiro, Shimizu Chika |
Molecular genetic analysis in 21 Chinese families with congenital insensitivity to pain with or without anhidrosis. European journal of neurology 2020 3 27 (8): 1697-1705. Zhao F, Mao B, Geng X, Ren X, Wang Y, Guan Y, Li S, Li L, Zhang S, You Y, Cao Y, Yang T, Zhao |
Single nucleotide polymorphisms associated with postoperative inadequate analgesia after single-port VATS in Chinese population. BMC anesthesiology 2020 Feb 20 (1): 38. Xing Xiufang, Bai Yongyu, Sun Kai, Yan M |
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 |
Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese population. PloS one 2020 11 15 (11): e0242793. Saadeh Fadi S, Morsi Rami Z, El-Kurdi Abdallah, Nemer Georges, Mahfouz Rami, Charafeddine Maya, Khoury Jessica, Najjar Marwan W, Khoueiry Pierre, Assi Hazem |
Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients. BMC neurology 2021 Sep 21 (1): 367. Lin Chih-Hsiang, Ho Chen-Jui, Lu Yan-Ting, Tsai Meng-H |
Genetic basis of cannabis use: a systematic review. BMC medical genomics 2021 8 14 (1): 203. Hillmer Alannah, Chawar Caroul, Sanger Stephanie, D'Elia Alessia, Butt Mehreen, Kapoor Raveena, Kapczinski Flavio, Thabane Lehana, Samaan Zain |
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohort. Journal of the neurological sciences 2021 6 427 117498. Cintra Vivian Pedigone, Dohrn Maike F, Tomaselli Pedro José, Figueiredo Fernanda Barbosa, Marques Sandra Elisabete, Camargos Sarah Teixeira, Barbosa Luiz Sergio Mageste, P Rebelo Adriana, Abreu Lisa, Danzi Matt, Marques Wilson, Züchner Steph |
Fatigue in Women with Fibromyalgia: A Gene-Physical Activity Interaction Study. Journal of clinical medicine 2021 4 10 (9): . Estévez-López Fernando, Salazar-Tortosa Diego F, Camiletti-Moirón Daniel, Gavilán-Carrera Blanca, Aparicio Virginia A, Acosta-Manzano Pedro, Segura-Jiménez Víctor, Álvarez-Gallardo Inmaculada C, Carbonell-Baeza Ana, Munguía-Izquierdo Diego, Geenen Rinie, Lacerda Eliana, Delgado-Fernández Manuel, Martínez-González Luis J, Ruiz Jonatan R, Álvarez-Cubero María |
Interplay between genetics and lifestyle on pain susceptibility in women with fibromyalgia: the al-Ándalus project. Rheumatology (Oxford, England) 2021 12 61 (8): 3180-3191. Estévez-López Fernando, Guerrero-González Juan M, Salazar-Tortosa Diego, Camiletti-Moirón Daniel, Gavilán-Carrera Blanca, Aparicio Virginia A, Acosta-Manzano Pedro, Álvarez-Gallardo Inmaculada C, Segura-Jiménez Víctor, Soriano-Maldonado Alberto, Geenen Rinie, Delgado-Fernández Manuel, Martínez-González Luis J, Ruiz Jonatan R, Álvarez-Cubero María |
Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
Intrafamilial Phenotypic Variability Associated with the I1739V Mutation in the SCN9A Gene. Case reports in neurology 2022 8 13 (1): 135-139. Peddareddygari Leema Reddy, Grewal Raji |
ADGRV1 Variants in Febrile Seizures/Epilepsy With Antecedent Febrile Seizures and Their Associations With Audio-Visual Abnormalities. Frontiers in molecular neuroscience 2022 7 15 864074. Zhou Peng, Meng Heng, Liang Xiaoyu, Lei Xiaoyun, Zhang Jingwen, Bian Wenjun, He Na, Lin Zhijian, Song Xingwang, Zhu Weiwen, Hu Bin, Li Bingmei, Yan Limin, Tang Bin, Su Tao, Liu Hankui, Mao Yong, Zhai Qiongxiang, Yi Yongho |
Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells. Neurobiology of aging 2022 5 116 16-24. Ruf Wolfgang P, Hannon Eilis, Freischmidt Axel, Grozdanov Veselin, Brenner David, Müller Kathrin, Knehr Antje, Günther Kornelia, Dorst Johannes, Ammerpohl Ole, Danzer Karin M, Mill Jonathan, Ludolph Albert C, Weishaupt Jochen |
Association Between Single-nucleotide Polymorphisms in Candidate Genes and Success of Pulpal Anesthesia after Inferior Alveolar Nerve Block. Journal of endodontics 2023 5 49 (1): 18-25. Ertu?rul Karata?, Meltem Sümbüllü, Çi?dem Y Kahraman, Fatma A Çakm |
Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohort. Brain communications 2023 3 5 (2): fcad037. Themistocleous Andreas C, Baskozos Georgios, Blesneac Iulia, Comini Maddalena, Megy Karyn, Chong Sam, Deevi Sri V V, Ginsberg Lionel, Gosal David, Hadden Robert D M, Horvath Rita, Mahdi-Rogers Mohamed, Manzur Adnan, Mapeta Rutendo, Marshall Andrew, Matthews Emma, McCarthy Mark I, Reilly Mary M, Renton Tara, Rice Andrew S C, Vale Tom A, van Zuydam Natalie, Walker Suellen M, Woods Christopher Geoffrey, Bennett David L |
Neanderthal introgression in SCN9A impacts mechanical pain sensitivity. Communications biology 2023 10 6 (1): 958. Pierre Faux, Li Ding, Luis Miguel Ramirez-Aristeguieta, J Camilo Chacón-Duque, Maddalena Comini, Javier Mendoza-Revilla, Macarena Fuentes-Guajardo, Claudia Jaramillo, William Arias, Malena Hurtado, Valeria Villegas, Vanessa Granja, Rodrigo Barquera, Paola Everardo-Martínez, Mirsha Quinto-Sánchez, Jorge Gómez-Valdés, Hugo Villamil-Ramírez, Caio C Silva de Cerqueira, Tábita Hünemeier, Virginia Ramallo, Rolando Gonzalez-José, Lavinia Schüler-Faccini, Maria-Cátira Bortolini, Victor Acuña-Alonzo, Samuel Canizales-Quinteros, Giovanni Poletti, Carla Gallo, Francisco Rothhammer, Winston Rojas, Annina B Schmid, Kaustubh Adhikari, David L Bennett, Andrés Ruiz-Linar |
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- Page last updated:Apr 22, 2024
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