Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: KCNJ10[original query] |
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No association between common variations in the human alpha 2 subunit gene (ATP1A2) of the sodium-potassium-transporting ATPase and idiopathic generalized epilepsy. Neuroscience letters 0 382 (1-2): 33-8. Lohoff Falk W, Ferraro Thomas N, Sander Thomas, Zhao Hongyu, Dahl John P, Berrettini Wade H, Buono Russell |
Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy. Epilepsy research 2005 Feb 63 (2-3): 113-8. Lenzen K P, Heils A, Lorenz S, Hempelmann A, Höfels S, Lohoff F W, Schmitz B, Sander |
Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss. Annals of human genetics 2009 Jul 73 (Pt 4): 411-21. Pawelczyk Malgorzata, Van Laer Lut, Fransen Erik, Rajkowska Elzbieta, Konings Annelies, Carlsson Per-Inge, Borg Erik, Van Camp Guy, Sliwinska-Kowalska Mario |
Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy. Epilepsy research 2010 Jan 88 (1): 55-64. Heuser Kjell, Nagelhus Erlend A, Taubøll Erik, Indahl Ulf, Berg Paul R, Lien Sigbjørn, Nakken Sigve, Gjerstad Leif, Ottersen Ole Pett |
Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct. International journal of pediatric otorhinolaryngology 2010 Sep 74 (9): 1049-53. Jonard Laurence, Niasme-Grare Magali, Bonnet Crystel, Feldmann Delphine, Rouillon Isabelle, Loundon Natalie, Calais Catherine, Catros Hélène, David Albert, Dollfus Hélène, Drouin-Garraud Valérie, Duriez Françoise, Eliot Marie Madeleine, Fellmann Florence, Francannet Christine, Gilbert-Dussardier Brigitte, Gohler Catherine, Goizet Cyril, Journel Hubert, Mom Thierry, Thuillier-Obstoy Marie-Françoise, Couderc Remy, Garabédian Eréa Noël, Denoyelle Françoise, Marlin Sandri |
No association between the KCNH1, KCNJ10 and KCNN3 genes and schizophrenia in the Han Chinese population. Neuroscience letters 2011 Jan 487 (1): 61-5. Shen Qi, Zhang Jing, Wang Yang, Liu Baocheng, Li Xingwang, Zhao Qingzhu, Chen Shiqing, Ji Jue, Yang Fengping, Wan Chunling, Gao Linghan, Xu Yifeng, Feng Guoyin, He Lin, He Gua |
Identification of SLC26A4 mutations in patients with hearing loss and enlarged vestibular aqueduct using high-resolution melting curve analysis. Genetic testing and molecular biomarkers 2011 May 15 (5): 365-8. Mercer Stephen, Mutton Patricia, Dahl Hans-Henrik |
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. The Journal of physiology 2011 Apr 589 (Pt 7): 1681-9. Thompson Dorothy A, Feather Sally, Stanescu Horia C, Freudenthal Bernard, Zdebik Anselm A, Warth Richard, Ognjanovic Milos, Hulton Sally A, Wassmer Evangeline, van't Hoff William, Russell-Eggitt Isabelle, Dobbie Angus, Sheridan Eamonn, Kleta Robert, Bockenhauer Detl |
Targeted next generation sequencing as a diagnostic tool in epileptic disorders. Epilepsia 2012 Aug 53 (8): 1387-98. Lemke Johannes R, Riesch Erik, Scheurenbrand Tim, Schubach Max, Wilhelm Christian, Steiner Isabelle, Hansen Jörg, Courage Carolina, Gallati Sabina, Bürki Sarah, Strozzi Susi, Simonetti Barbara Goeggel, Grunt Sebastian, Steinlin Maja, Alber Michael, Wolff Markus, Klopstock Thomas, Prott Eva C, Lorenz Rüdiger, Spaich Christiane, Rona Sabine, Lakshminarasimhan Maya, Kröll Judith, Dorn Thomas, Krämer Günter, Synofzik Matthis, Becker Felicitas, Weber Yvonne G, Lerche Holger, Böhm Detlef, Biskup Sask |
Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2012 Jun 146 (6): 972-8. Chen Kaitian, Wang Xianren, Sun Liang, Jiang Hongy |
Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China. American journal of medical genetics. Part A 2013 Sep 161A (9): 2226-33. Chai Yongchuan, Huang Zhiwu, Tao Zheng, Li Xiaohua, Li Lei, Li Yun, Wu Hao, Yang T |
Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts. BMC medical genetics 2013 14 85. Landa Priya, Differ Ann-Marie, Rajput Kaukab, Jenkins Lucy, Bitner-Glindzicz Mar |
KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects. PloS one 2014 9 (11): e108134. Zhao Jiandong, Yuan Yongyi, Huang Shasha, Huang Bangqing, Cheng Jing, Kang Dongyang, Wang Guojian, Han Dongyi, Dai |
Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene. Gene 2014 Feb 536 (2): 247-53. Phani Nagaraja M, Acharya Shreeshakala, Xavy Seethu, Bhaskaranand Nalini, Bhat Manoj K, Jain Aditya, Rai Padmalatha S, Satyamoorthy Kapaettu, Kapaettu Satyamoort |
Common variants of KCNJ10 are associated with susceptibility and anti-epileptic drug resistance in Chinese genetic generalized epilepsies. PloS one 2015 10 (4): e0124896. Guo Yong, Yan Kui Po, Qu Qiang, Qu Jian, Chen Zi Gui, Song Tao, Luo Xiang-Ying, Sun Zhong-Yi, Bi Chang-Long, Liu Jin-Fa |
The gene encoding the inwardly rectifying potassium channel Kir4.1 may be involved in sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2017 Sep 106 (9): 1474-1480. Opdal Siri H, Vege Åshild, Stray-Pedersen Arne, Rognum Torleiv |
Association study between inwardly rectifying potassium channels 2.1 and 4.1 and autism spectrum disorders. Life sciences 2018 Oct . Sun Caihong, Zou Mingyang, Li Ling, Li Dexin, Ma Yongjuan, Xia Wei, Wu Lijie, Ren Hu |
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct. The Journal of molecular diagnostics : JMD 2018 10 21 (1): 138-148. Lin Yin-Hung, Wu Chen-Chi, Lin Yi-Hsin, Lu Ying-Chang, Chen Chih-Shan, Liu Tien-Chen, Chen Pei-Lung, Hsu Chuan-J |
Analysis of mutations in the FOXI1 and KCNJ10 genes in infants with a single-allele SLC26A4 mutation. Bioscience trends 2019 6 13 (3): 261-266. Zhao Xuelei, Cheng Xiaohua, Huang Lihui, Wang Xianlei, Wen Cheng, Wang Xueyao, Zhao Lipi |
Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2020 5 277 (12): 3331-3339. Liu Yalan, Wen Jie, Sang Shushan, Mei Lingyun, He Chufeng, Jiang Lu, Huang Sida, Feng Yo |
Increased potassium excretion in children with monosymptomatic nocturnal enuresis: could it be related to Kir 4.1- KCNJ10 gene polymorphism? The Turkish journal of pediatrics 2020 62 (2): 208-214. Balat Ayse, Parlak Mesut, Balci Sibel Oguzkan, Gögebakan Bülent, Büyükçelik Mithat, Çöl Nilgün, Kul Seval, Tinaztepe Kerim |
Association Analysis of Candidate Gene Polymorphisms and Audiometric Measures of Noise-Induced Hearing Loss in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2020 3 41 (5): e538-e547. Bhatt Ishan Sunilkumar, Dias Raquel, Washnik Nilesh, Wang Jin, Guthrie O'neil, Skelton Michael, Lane Jeffery, Wilder Jas |
Effects of AQP4 and KCNJ10 Gene Polymorphisms on Drug Resistance and Seizure Susceptibility in Chinese Han Patients with Focal Epilepsy. Neuropsychiatric disease and treatment 2020 16 119-129. Zhu Haoyue, Zhang Mengqi, Fu Yujiao, Long Hongyu, Xiao Wenbiao, Feng Li, Xiao Bo, Zhou L |
Association of KCNJ10 variants and the susceptibility to clinical epilepsy. Clinical neurology and neurosurgery 2020 Oct 106340. Jiang Chuan, Li Lianping, Wu Mingxin, Hao Maolin, Feng Jian |
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul . Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A |
Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China. Frontiers in genetics 2021 12 637096. Cai Luhang, Liu Ya, Xu Yaping, Yang Hang, Lv Lihui, Li Yang, Chen Qiongqiong, Lin Xiaojiang, Yang Yihui, Hu Guangwei, Zheng Guofeng, Zhou Jing, Qian Qiyong, Xu Mei-Ai, Fang Jin, Ding Jianjun, Chen Wei, Gao Jio |
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA. Journal of the American Society of Nephrology : JASN 2021 10 33 (2): 305-325. Viering Daan, Schlingmann Karl P, Hureaux Marguerite, Nijenhuis Tom, Mallett Andrew, Chan Melanie M Y, van Beek André, van Eerde Albertien M, Coulibaly Jean-Marie, Vallet Marion, Decramer Stéphane, Pelletier Solenne, Klaus Günter, Kömhoff Martin, Beetz Rolf, Patel Chirag, Shenoy Mohan, Steenbergen Eric J, Anderson Glenn, Bongers Ernie M H F, Bergmann Carsten, Panneman Daan, Rodenburg Richard J, Kleta Robert, Houillier Pascal, Konrad Martin, Vargas-Poussou Rosa, Knoers Nine V A M, Bockenhauer Detlef, de Baaij Jeroen H F, |
Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability. Archives of Iranian medicine 2023 8 25 (12): 788-797. Naeim Ehtesham, Meysam Mosallaei, Maryam Beheshtian, Shahrouz Khoshbakht, Mahsa Fadaee, Raheleh Vazehan, Mehrshid Faraji Zonooz, Parvaneh Karimzadeh, Kimia Kahrizi, Hossein Najmaba |
Coexistence of temporal lobe epilepsy and idiopathic generalized epilepsy. Epilepsy & behavior : E&B 2023 12 151 109602. Ali A Asadi-Pooya, Mahdi Malekpour, Ehsan Taherifard, Arashk Mallahzadeh, Mohsen Farjoud Kouhanja |
Genetic predisposition to differentiated thyroid cancer among Polish population. Polish archives of internal medicine 2024 1 . Martyna Borowczyk, Mateusz Sypniewski, Joanna Szyda, Ma?gorzata Braszka, Katarzyna Ziemnicka, Marek Rucha?a, Michalina Oszywa, Zbigniew J Król, Paula Dobo |
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- Page last updated:Apr 16, 2024
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