Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 59 Records) |
Query Trace: SCN10A[original query] |
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Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.
Circulation. Cardiovascular genetics 2017 Aug 10 (4): . Christophersen Ingrid E, Magnani Jared W, Yin Xiaoyan, Barnard John, Weng Lu-Chen, Arking Dan E, Niemeijer Maartje N, Lubitz Steven A, Avery Christy L, Duan Qing, Felix Stephan B, Bis Joshua C, Kerr Kathleen F, Isaacs Aaron, Müller-Nurasyid Martina, Müller Christian, North Kari E, Reiner Alex P, Tinker Lesley F, Kors Jan A, Teumer Alexander, Petersmann Astrid, Sinner Moritz F, Buzkova Petra, Smith Jonathan D, Van Wagoner David R, Völker Uwe, Waldenberger Melanie, Peters Annette, Meitinger Thomas, Limacher Marian C, Wilhelmsen Kirk C, Psaty Bruce M, Hofman Albert, Uitterlinden Andre, Krijthe Bouwe P, Zhang Zhu-Ming, Schnabel Renate B, Kääb Stefan, van Duijn Cornelia, Rotter Jerome I, Sotoodehnia Nona, Dörr Marcus, Li Yun, Chung Mina K, Soliman Elsayed Z, Alonso Alvaro, Whitsel Eric A, Stricker Bruno H, Benjamin Emelia J, Heckbert Susan R, Ellinor Patrick |
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 |
[Rs17042171 at chromosome 4q25 is associated with atrial fibrillation in the Chinese Han population from the central plains]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2018 Jun 43 (6): 594-603. Wang Xu, Nie Yali, Ning Shuwei, Shi Yong, Zhao Yujie, Niu Siquan, Guo Chengxian, Meng Xiangguang, Yuan Yiqia |
Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest. Frontiers in physiology 2018 9 894. Andreasen Laura, Ghouse Jonas, Skov Morten W, Have Christian T, Ahlberg Gustav, Rasmussen Peter V, Linneberg Allan, Pedersen Oluf, Platonov Pyotr G, Haunsø Stig, Svendsen Jesper H, Hansen Torben, Kanters Jørgen K, Olesen Morten |
[Polymorphisms of the SCN10A Gene in Patients With Sick Sinus Syndrome]. Kardiologiia 2018 Apr (4): 53-59. Niculina S Y, Marilovceva O V, Chernova A A, Tret'jakova S S, Nikulin D A, Maksimov V |
Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction. Circulation. Genomic and precision medicine 2018 May 11 (5): e001663. Macri Vincenzo, Brody Jennifer A, Arking Dan E, Hucker William J, Yin Xiaoyan, Lin Honghuang, Mills Robert W, Sinner Moritz F, Lubitz Steven A, Liu Ching-Ti, Morrison Alanna C, Alonso Alvaro, Li Ning, Fedorov Vadim V, Janssen Paul M, Bis Joshua C, Heckbert Susan R, Dolmatova Elena V, Lumley Thomas, Sitlani Colleen M, Cupples L Adrienne, Pulit Sara L, Newton-Cheh Christopher, Barnard John, Smith Jonathan D, Van Wagoner David R, Chung Mina K, Vlahakes Gus J, O'Donnell Christopher J, Rotter Jerome I, Margulies Kenneth B, Morley Michael P, Cappola Thomas P, Benjamin Emelia J, Muzny Donna, Gibbs Richard A, Jackson Rebecca D, Magnani Jared W, Herndon Caroline N, Rich Stephen S, Psaty Bruce M, Milan David J, Boerwinkle Eric, Mohler Peter J, Sotoodehnia Nona, Ellinor Patrick |
A variant in the SCN10A enhancer may affect human mechanical pain sensitivity. Molecular pain 2018 2 14 1744806918763275. Duan Guangyou, Sun Jiaoli, Li Ningbo, Zheng Hua, Guo Shanna, Zhang Yuhao, Wang Qingli, Ying Ying, Zhang Mi, Huang Penghao, Zhang Xianw |
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 |
Putative role of Brugada syndrome genes in familial atrial fibrillation. European review for medical and pharmacological sciences 2019 9 23 (17): 7582-7598. Maltese P E, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli |
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.
PloS one 2019 14 (6): e0217796. Swenson Brenton R, Louie Tin, Lin Henry J, Méndez-Giráldez Raúl, Below Jennifer E, Laurie Cathy C, Kerr Kathleen F, Highland Heather, Thornton Timothy A, Ryckman Kelli K, Kooperberg Charles, Soliman Elsayed Z, Seyerle Amanda A, Guo Xiuqing, Taylor Kent D, Yao Jie, Heckbert Susan R, Darbar Dawood, Petty Lauren E, McKnight Barbara, Cheng Susan, Bello Natalie A, Whitsel Eric A, Hanis Craig L, Nalls Mike A, Evans Daniel S, Rotter Jerome I, Sofer Tamar, Avery Christy L, Sotoodehnia No |
A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2019 5 21 (9): 1410-1421. El-Battrawy Ibrahim, Albers Sebastian, Cyganek Lukas, Zhao Zhihan, Lan Huan, Li Xin, Xu Qiang, Kleinsorge Mandy, Huang Mengying, Liao Zhenxing, Zhong Rujia, Rudic Boris, Müller Jonas, Dinkel Hendrik, Lang Siegfried, Diecke Sebastian, Zimmermann Wolfram-Hubertus, Utikal Jochen, Wieland Thomas, Borggrefe Martin, Zhou Xiaobo, Akin Ibrah |
Polymorphisms of the SCN10A Gene in Patients With Sick Sinus Syndrome. Kardiologiia 2018 Nov 58 (4): 53-59. Nikulina S Yu, Marilovceva Olga V, Chernova A A, Tret'Jakova S S, Nikulin D A, Maksimov V |
Impact of the Na1.8 variant, A1073V, on post-sigmoidectomy pain and electrophysiological function in rat sympathetic neurons. Journal of neurophysiology 2019 10 122 (6): 2591-2600. Coates Matthew D, Kim Joyce S, Carkaci-Salli Nurgul, Vrana Kent E, Koltun Walter A, Puhl Henry L, Adhikary Sanjib D, Janicki Piotr K, Ruiz-Velasco Vict |
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 |
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation. Circulation. Genomic and precision medicine 2020 8 13 (5): 387-395. Weng Lu-Chen, Hall Amelia Weber, Choi Seung Hoan, Jurgens Sean J, Haessler Jeffrey, Bihlmeyer Nathan A, Grarup Niels, Lin Honghuang, Teumer Alexander, Li-Gao Ruifang, Yao Jie, Guo Xiuqing, Brody Jennifer A, Müller-Nurasyid Martina, Schramm Katharina, Verweij Niek, van den Berg Marten E, van Setten Jessica, Isaacs Aaron, Ramírez Julia, Warren Helen R, Padmanabhan Sandosh, Kors Jan A, de Boer Rudolf A, van der Meer Peter, Sinner Moritz F, Waldenberger Melanie, Psaty Bruce M, Taylor Kent D, Völker Uwe, Kanters Jørgen K, Li Man, Alonso Alvaro, Perez Marco V, Vaartjes Ilonca, Bots Michiel L, Huang Paul L, Heckbert Susan R, Lin Henry J, Kornej Jelena, Munroe Patricia B, van Duijn Cornelia M, Asselbergs Folkert W, Stricker Bruno H, van der Harst Pim, Kääb Stefan, Peters Annette, Sotoodehnia Nona, Rotter Jerome I, Mook-Kanamori Dennis O, Dörr Marcus, Felix Stephan B, Linneberg Allan, Hansen Torben, Arking Dan E, Kooperberg Charles, Benjamin Emelia J, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven |
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand.
Heart rhythm 2020 Jun . Makarawate Pattarapong, Glinge Charlotte, Khongphatthanayothin Apichai, Walsh Roddy, Mauleekoonphairoj John, Amnueypol Montawatt, Prechawat Somchai, Wongcharoen Wanwarang, Krittayaphong Rungroj, Anannab Alisara, Lichtner Peter, Meitinger Thomas, Tjong Fleur V Y, Lieve Krystien V V, Amin Ahmad S, Sahasatas Dujdao, Ngarmukos Tachapong, Wichadakul Duangdao, Payungporn Sunchai, Sutjaporn Boosamas, Wandee Pharawee, Poovorawan Yong, Tfelt-Hansen Jacob, Tanck Michael W T, Tadros Rafik, Wilde Arthur A M, Bezzina Connie R, Veerakul Gumpanart, Nademanee Koonlaw |
Family-based exome sequencing identifies rare coding variants in age-related macular degeneration. Human molecular genetics 2020 Apr . Ratnapriya Rinki, Acar ?lhan E, Geerlings Maartje J, Branham Kari, Kwong Alan, Saksens Nicole T M, Pauper Marc, Corominas Jordi, Kwicklis Madeline, Zipprer David, Starostik Margaret R, Othman Mohammad, Yashar Beverly, Abecasis Goncalo R, Chew Emily Y, Ferrington Deborah A, Hoyng Carel B, Swaroop Anand, den Hollander Anneke |
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2020 Apr . Foddha Hajer, Bouzidi Nadia, Foddha Abdelhak, Chouchene Saoussen, Touhami Rahma, Leban Nadia, Maatoug Mohamed Faouzi, Gamra Habib, Ferchichi Salima, Chibani Jemni Ben, Khelil Amel H |
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 |
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 |
Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases. Cardiovascular research 2020 1 116 (13): 2116-2130. Hayashi Kenshi, Teramoto Ryota, Nomura Akihiro, Asano Yoshihiro, Beerens Manu, Kurata Yasutaka, Kobayashi Isao, Fujino Noboru, Furusho Hiroshi, Sakata Kenji, Onoue Kenji, Chiang David Y, Kiviniemi Tuomas O, Buys Eva, Sips Patrick, Burch Micah L, Zhao Yanbin, Kelly Amy E, Namura Masanobu, Kita Yoshihito, Tsuchiya Taketsugu, Kaku Bunji, Oe Kotaro, Takeda Yuko, Konno Tetsuo, Inoue Masaru, Fujita Takashi, Kato Takeshi, Funada Akira, Tada Hayato, Hodatsu Akihiko, Nakanishi Chiaki, Sakamoto Yuichiro, Tsuda Toyonobu, Nagata Yoji, Tanaka Yoshihiro, Okada Hirofumi, Usuda Keisuke, Cui Shihe, Saito Yoshihiko, MacRae Calum A, Takashima Seiji, Yamagishi Masakazu, Kawashiri Masa-Aki, Takamura Masayu |
Common variants in SCN10A gene associated with Brugada syndrome. Human molecular genetics 2021 7 31 (2): 157-165. Huang Yan, Chen Xiao-Meng, Barajas-Martinez Hector, Jiang Hong, Antzelevitch Charles, Hu D |
Genetic predictors of sick sinus syndrome. Molecular biology reports 2021 7 48 (6): 5355-5362. Timasheva Yanina, Badykov Marat, Akhmadishina Leysan, Nasibullin Timur, Badykova Elena, Pushkareva Alfiya, Plechev Vladimir, Sagitov Ildus, Zagidullin Nauf |
Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals. JAMA cardiology 2021 5 6 (7): 811-819. Chalazan Brandon, Mol Denise, Darbar Faisal A, Ornelas-Loredo Aylin, Al-Azzam Bahaa, Chen Yining, Tofovic David, Sridhar Arvind, Alzahrani Zain, Ellinor Patrick, Darbar Dawo |
Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients. Anatolian journal of cardiology 2021 02 25 (2): 129-138. Ulus Taner, Dural Muhammet, Me?e Pelin, Yetmi? Furkan, Mert Kadir U?ur, Görenek Bülent, Çilingir O?uz, Erzurumluoglu Gökalp Ebru, Arslan Serap, Artan Sevilhan, Aykaç Özlem, Çolak Ertu?rul, Yorgun Hikmet, Canpolat U?ur, Aytemir Kudr |
Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.
Cancers 2021 Feb 13 (4): . Adjei Araba A, Lopez Camden L, Schaid Daniel J, Sloan Jeff A, Le-Rademacher Jennifer G, Loprinzi Charles L, Norman Aaron D, Olson Janet E, Couch Fergus J, Beutler Andreas S, Vachon Celine M, Ruddy Kathryn |
Genetic insight into sick sinus syndrome.
European heart journal 2021 Feb . Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
Genetic insight into sick sinus syndrome.
European heart journal 2021 May 42 (20): 1959-1971. Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
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 |
Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death. Heart rhythm 2023 2 . Isaacs Aaron, Barysenka Andrei, Ter Bekke Rachel M A, Helderman-van den Enden Apollonia T J M, van den Wijngaard Arthur, Volders Paul G A, Stoll Moni |
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