Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: KCNA1[original query] |
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First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.
PloS one 2015 10 (3): e0119333. Anderson Denise, Cordell Heather J, Fakiola Michaela, Francis Richard W, Syn Genevieve, Scaman Elizabeth S H, Davis Elizabeth, Miles Simon J, McLeay Toby, Jamieson Sarra E, Blackwell Jenefer |
Variations in potassium channel genes are associated with distinct trajectories of persistent breast pain after breast cancer surgery. Pain 2015 Mar 156 (3): 371-80. Langford Dale J, Paul Steven M, West Claudia M, Dunn Laura B, Levine Jon D, Kober Kord M, Dodd Marylin J, Miaskowski Christine, Aouizerat Bradley |
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies. Brain : a journal of neurology 2017 Jun 140 (6): 1579-1594. Coutelier Marie, Coarelli Giulia, Monin Marie-Lorraine, Konop Juliette, Davoine Claire-Sophie, Tesson Christelle, Valter Rémi, Anheim Mathieu, Behin Anthony, Castelnovo Giovanni, Charles Perrine, David Albert, Ewenczyk Claire, Fradin Mélanie, Goizet Cyril, Hannequin Didier, Labauge Pierre, Riant Florence, Sarda Pierre, Sznajer Yves, Tison François, Ullmann Urielle, Van Maldergem Lionel, Mochel Fanny, Brice Alexis, Stevanin Giovanni, Durr Alexandra, |
Potassium Channel Candidate Genes Predict the Development of Secondary Lymphedema Following Breast Cancer Surgery. Nursing research 0 66 (2): 85-94. Smoot Betty, Kober Kord M, Paul Steven M, Levine Jon D, Abrams Gary, Mastick Judy, Topp Kimberly, Conley Yvette P, Miaskowski Christine |
Genetic Variants Associated with Episodic Ataxia in Korea. Scientific reports 2017 10 7 (1): 13855. Choi Kwang-Dong, Kim Ji-Soo, Kim Hyo-Jung, Jung Ileok, Jeong Seong-Hae, Lee Seung-Han, Kim Dong Uk, Kim Sang-Ho, Choi Seo Young, Shin Jin-Hong, Kim Dae-Seong, Park Kyung-Pil, Kim Hyang-Sook, Choi Jae-Hw |
The Impact of Potassium Channel Gene Polymorphisms on Antiepileptic Drug Responsiveness in Arab Patients with Epilepsy. Journal of personalized medicine 2018 Nov 8 (4): . Al-Eitan Laith N, Al-Dalalah Islam M, Elshammari Afrah K, Khreisat Wael H, Almasri Ayah |
Genome-Wide Association Study for Reproductive Traits in a Duroc Pig Population. Animals : an open access journal from MDPI 2019 9 9 (10): . Zhang Zhe, Chen Zitao, Ye Shaopan, He Yingting, Huang Shuwen, Yuan Xiaolong, Chen Zanmou, Zhang Hao, Li Jia |
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 |
High polygenic burden is associated with blood DNA methylation changes in individuals with suicidal behavior. Journal of psychiatric research 2020 Jan 123 62-71. Cabrera-Mendoza Brenda, Martínez-Magaña José Jaime, Genis-Mendoza Alma Delia, Sarmiento Emmanuel, Ruíz-Ramos David, Tovilla-Zárate Carlos Alfonso, González-Castro Thelma Beatriz, Juárez-Rojop Isela Esther, García-de la Cruz Dulce Dajheanne, López-Armenta Mauro, Real Fernanda, García-Dolores Fernando, Flores Gonzalo, Vázquez-Roque Rubén Antonio, Lanzagorta Nuria, Escamilla Michael, Saucedo-Uribe Erasmo, Rodríguez-Mayoral Oscar, Jiménez-Genchi Janet, Castañeda-González Carlos, Roche-Bergua Andrés, Nicolini Humber |
A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy. European journal of medical genetics 2020 1 63 (4): 103848. Vetri Luigi, Calì Francesco, Vinci Mirella, Amato Carmelo, Roccella Michele, Granata Tiziana, Freri Elena, Solazzi Roberta, Romano Valentino, Elia Mauriz |
Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients. Neuromuscular disorders : NMD 2021 2 31 (4): 336-347. Brugnoni Raffaella, Maggi Lorenzo, Canioni Eleonora, Verde Federico, Gallone Annamaria, Ariatti Alessandra, Filosto Massimiliano, Petrelli Cristina, Logullo Francesco Ottavio, Esposito Marcello, Ruggiero Lucia, Tonin Paola, Riguzzi Pietro, Pegoraro Elena, Torri Francesca, Ricci Giulia, Siciliano Gabriele, Silani Vincenzo, Merlini Luciano, De Pasqua Silvia, Liguori Rocco, Pini Antonella, Mariotti Caterina, Moroni Isabella, Imbrici Paola, Desaphy Jean-Francois, Mantegazza Renato, Bernasconi P |
Genome-Wide Association of Proprotein Convertase Subtilisin/Kexin Type 9 Plasma Levels in the ELSA-Brasil Study.
Frontiers in genetics 2021 10 12 728526. Bensenor Isabela, Padilha Kallyandra, Lima Isabella Ramos, Santos Raul Dias, Lambert Gilles, Ramin-Mangata Stéphane, Bittencourt Marcio S, Goulart Alessandra C, Santos Itamar S, Mill Jose G, Krieger Jose E, Lotufo Paulo A, Pereira Alexandre |
Identification of novel genes by targeted exome sequencing in Retinoblastoma. Ophthalmic genetics 2022 8 43 (6): 771-788. Bisht Shilpa, Chawla Bhavna, Kumar Amit, Vijayan Viswanathan, Kumar Manoj, Sharma Pradeep, Dada Ri |
Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain. Neurology. Genetics 2022 12 8 (6): e200038. Baviera-Muñoz Raquel, Carretero-Vilarroig Lidón, Vázquez-Costa Juan Francisco, Morata-Martínez Carlos, Campins-Romeu Marina, Muelas Nuria, Sastre-Bataller Isabel, Martínez-Torres Irene, Pérez-García Julia, Sivera Rafael, Sevilla Teresa, Vilchez Juan J, Jaijo Teresa, Espinós Carmen, Millán Jose M, Bataller Luis, Aller Ele |
Factors predisposing to humoral autoimmunity against brain-antigens in health and disease: Analysis of 49 autoantibodies in over 7000 subjects. Brain, behavior, and immunity 2022 11 108 135-147. Daguano Gastaldi Vinicius, Bh Wilke Justus, Weidinger Cosima A, Walter Carolin, Barnkothe Nadine, Teegen Bianca, Luessi Felix, Stöcker Winfried, Lühder Fred, Begemann Martin, Zipp Frauke, Nave Klaus-Armin, Ehrenreich Hannelo |
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- Page last updated:Apr 22, 2024
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