Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 79 Records) |
Query Trace: GABRG2[original query] |
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Mutational screening of GABRG2 gene in Pakistani population of Punjab with generalized tonic clonic seizures and children with childhood absence epilepsy. Journal of the Chinese Medical Association : JCMA 2018 Jun . Iqbal Muhammad Javed, Wasim Muhammad, Rashid Umer, Zeeshan Nadia, Ali Rizwan, Nayyab Sawera, Habib Sahrish, Manzoor Bushra, Zahid Noum |
Association of GABAA Receptor Gene with Epilepsy Syndromes. Journal of molecular neuroscience : MN 2018 May . Bhat Musadiq Ahmad, Guru Sameer Ahmad, Mir Rashid, Waza Ajaz Ahmad, Zuberi Mariyam, Sumi Mamta Pervin, Bodeliwala Shaam, Puri Vinod, Saxena Alpa |
Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease. Journal of cellular and molecular medicine 2018 Apr . Wang Yang, Yan Weihui, Wang Jun, Zhou Ying, Chen Jie, Gu Beilin, Cai W |
Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated with Reaction Time, Motor Time, and Ethanol Effects in Vivo. Frontiers in cellular neuroscience 2018 12 10. García-Martín Elena, Ramos María I, Cornejo-García José A, Galván Segismundo, Perkins James R, Rodríguez-Santos Laura, Alonso-Navarro Hortensia, Jiménez-Jiménez Félix J, Agúndez José A |
Lack of association between valproic acid response and polymorphisms of its metabolism, transport, and receptor genes in children with focal seizures. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Mar 40 (3): 523-528. Feng Weixing, Mei Shenghui, Han Jiaqi, Zhu Leting, Yu Yazhen, Gao Baoqin, Wu Yun, Li Jiuwei, Zhao Zhigang, Fang Fa |
Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel. Journal of human genetics 2019 Aug . Hirabayashi Kyoko, Uehara Daniela Tiaki, Abe Hidetoshi, Ishii Atsushi, Moriyama Keiji, Hirose Shinichi, Inazawa Joh |
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals. American journal of human genetics 2019 Jul . , |
Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence. Psychiatric genetics 2019 Apr . Hsieh Ai-Ru, Chen Li-Shiun, Li Ying-Ju, Fann Cathy S |
MAPT haplotype-stratified GWAS reveals differential association for AD risk variants. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 May . Strickland Samantha L, Reddy Joseph S, Allen Mariet, N'songo Aurelie, Burgess Jeremy D, Corda Morgane M, Ballard Travis, Wang Xue, Carrasquillo Minerva M, Biernacka Joanna M, Jenkins Gregory D, Mukherjee Shubhabrata, Boehme Kevin, Crane Paul, Kauwe John S, Ertekin-Taner Nilüfer, |
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Aging 2020 3 12 (5): 4379-4393. Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W |
Interactions of the GABRG2 polymorphisms and childhood trauma on suicide attempt and related traits in depressed patients. Journal of affective disorders 2020 Jan 266 447-455. Yin Honglei, Galfalvy Hanga, Zhang Bin, Tang Weiwei, Xin Qianqian, Li Enze, Xue Xiang, Li Qiyang, Ye Junping, Yan Na, Mann J Jo |
Genetic Association of Epilepsy and Anti-Epileptic Drugs Treatment in Jordanian Patients. Pharmacogenomics and personalized medicine 2020 10 13 503-510. Al-Eitan Laith N, Al-Dalala Islam M, Elshammari Afrah K, Khreisat Wael H, Nimiri Aseel F, Alnaamneh Adan H, Aljamal Hanan A, Alghamdi Mansour |
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature communications 2020 10 11 (1): 4932. Wang Tianyun, Hoekzema Kendra, Vecchio Davide, Wu Huidan, Sulovari Arvis, Coe Bradley P, Gillentine Madelyn A, Wilfert Amy B, Perez-Jurado Luis A, Kvarnung Malin, Sleyp Yoeri, Earl Rachel K, Rosenfeld Jill A, Geisheker Madeleine R, Han Lin, Du Bing, Barnett Chris, Thompson Elizabeth, Shaw Marie, Carroll Renee, Friend Kathryn, Catford Rachael, Palmer Elizabeth E, Zou Xiaobing, Ou Jianjun, Li Honghui, Guo Hui, Gerdts Jennifer, Avola Emanuela, Calabrese Giuseppe, Elia Maurizio, Greco Donatella, Lindstrand Anna, Nordgren Ann, Anderlid Britt-Marie, Vandeweyer Geert, Van Dijck Anke, Van der Aa Nathalie, McKenna Brooke, Hancarova Miroslava, Bendova Sarka, Havlovicova Marketa, Malerba Giovanni, Bernardina Bernardo Dalla, Muglia Pierandrea, van Haeringen Arie, Hoffer Mariette J V, Franke Barbara, Cappuccio Gerarda, Delatycki Martin, Lockhart Paul J, Manning Melanie A, Liu Pengfei, Scheffer Ingrid E, Brunetti-Pierri Nicola, Rommelse Nanda, Amaral David G, Santen Gijs W E, Trabetti Elisabetta, Sedlá?ek Zden?k, Michaelson Jacob J, Pierce Karen, Courchesne Eric, Kooy R Frank, , Nordenskjöld Magnus, Romano Corrado, Peeters Hilde, Bernier Raphael A, Gecz Jozef, Xia Kun, Eichler Evan |
The Effects of Gene Variations of GABRA2, GABRB1, GABRG2, GAD1 and SLC1A3 on Patients with Propofol During Anesthesia Induction. Pharmacogenomics and personalized medicine 2021 14 1185-1192. Zhang Lingyi, Zheng Zhuoling, Ma Wudi, Zhang Shuyu, Xue Faling, Wang Haini, He Yongqi, Ye Fang, Zhou Shouning, Wen Yongzi, Li Xiaoyan, Huang Wenqi, Huang Min, Li Jiali, Wang Zhongxi |
Genetic Polymorphism of GABRG2 rs211037 is Associated with Drug Response and Adverse Drug Reactions to Valproic Acid in Chinese Southern Children with Epilepsy. Pharmacogenomics and personalized medicine 2021 14 1141-1150. Lu Jieluan, Xia Hanbing, Li Wenzhou, Shen Xianhuan, Guo Huijuan, Zhang Jianping, Fan Xiaom |
Association of rs211037 GABRG2 gene polymorphism with susceptibility to idiopathic generalized epilepsy. Medicinski glasnik : official publication of the Medical Association of Zenica-Doboj Canton, Bosnia and Herzegovina 2021 Aug 18 (2): . Milanovska Marija, Cvetkovska Emilija, Panov Sas |
Analysis of GABRG2 C588T polymorphism in genetic epilepsy and evaluation of GABRG2 in drug treatment. Clinical and translational science 2021 3 14 (5): 1725-1733. Wang Shitao, Zhang Xianjun, Zhou Liang, Wu Qian, Han Yanbi |
Influence of the GABA Receptor Subunit Gene Polymorphism and Childhood Sexual Abuse on Processing Speed in Major Depression and Suicide Attempt. Frontiers in psychiatry 2021 12 712231. Yin Honglei, Guo Jia, Xin Qianqian, Zheng Shuqiong, Xue Xiang, Li Enze, Liu Ting, Yan Na, Keilp John, Mann J Jo |
GABRA1 and GABRB2 Polymorphisms are Associated with Propofol Susceptibility. Pharmacogenomics and personalized medicine 2022 15 105-117. Zeng Youjie, Cao Si, Chen Minghua, Fang Chao, Ouyang W |
Impact of GABA receptor gene variants (rs2279020 and rs211037) on the risk of predisposition to epilepsy: a case-control study. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Feb . Amjad Maryam, Tabassum Atiya, Sher Khalid, Kumar Suneel, Zehra Sitwat, Fatima Sehri |
Clinical and genetic study of developmental and epileptic encephalopathy in Argentinean pediatric patients. Medicina 2022 12 82 (6): 856-865. Juanes Matías, Loos Mariana, Reyes Gabriela, Veneruzzo Gabriel, García Francisco Martín, Aschettino Giovanna, Calligaris Silvana, Martín María Eugenia, Foncuberta María Eugenia, Alonso Cristina N, Caraballo Roberto |
GABRG2 C588T Polymorphism Is Associated with Idiopathic Generalized Epilepsy but Not with Antiepileptic Drug Resistance in Pakistani Cohort. BioMed research international 2022 11 2022 3460792. Saleem Tayyaba, Maqbool Hafsa, Sheikh Nadeem, Tayyeb Asima, Mukhtar Maryam, Ashfaq Aq |
The likelihood approach for potential role of "GABRG2 (C588T, C315T) gene polymorphisms" on the poor response to carbamazepine therapy in Pakhtun population of Pakistan. Medicine 2022 Oct 101 (40): e30948. Ullah Shakir, Ali Niaz, Ahmad Sajjad, Sha Syed Wadood Ali, Ali Saad, Almarshad Fer |
A single nucleotide polymorphism-based formula to predict the risk of propofol TCI concentration being over 4?µg?mL at the time of loss of consciousness. The pharmacogenomics journal 2022 1 22 (2): 109-116. Zheng Zhuoling, Xue Faling, Wang Haini, He Yongqi, Zhang Lingyi, Ma Wudi, Zhang Caibin, Guan Yanping, Ye Fang, Wen Yongzi, Li Xiaoyan, Huang Min, Huang Wenqi, Wang Zhongxing, Li Jia |
Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia 2022 1 63 (3): 723-735. Koko Mahmoud, Motelow Joshua E, Stanley Kate E, Bobbili Dheeraj R, Dhindsa Ryan S, May Patrick, , , , , |
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 |
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes.
Brain : a journal of neurology 2022 1 145 (2): 555-568. Skotte Line, Fadista João, Bybjerg-Grauholm Jonas, Appadurai Vivek, Hildebrand Michael S, Hansen Thomas F, Banasik Karina, Grove Jakob, Albiñana Clara, Geller Frank, Bjurström Carmen F, Vilhjálmsson Bjarni J, Coleman Matthew, Damiano John A, Burgess Rosemary, Scheffer Ingrid E, Pedersen Ole Birger Vesterager, Erikstrup Christian, Westergaard David, Nielsen Kaspar René, Sørensen Erik, Bruun Mie Topholm, Liu Xueping, Hjalgrim Henrik, Pers Tune H, Mortensen Preben Bo, Mors Ole, Nordentoft Merete, Dreier Julie W, Børglum Anders D, Christensen Jakob, Hougaard David M, Buil Alfonso, Hviid Anders, Melbye Mads, Ullum Henrik, Berkovic Samuel F, Werge Thomas, Feenstra Bjar |
Association between the SLC6A11 rs2304725 and GABRG2 rs211037 polymorphisms and drug-resistant epilepsy: a meta-analysis. Frontiers in physiology 2023 6 14 1191927. Xuemei Hu, Mingyang Zhao, Xue Yang, Dongsen Wang, Qingjian |
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 |
Association between GABRG2 Gene Single Nucleotide Polymorphisms and Susceptibility to Ischemic Stroke in a Chinese Population. Journal of integrative neuroscience 2024 1 22 (6): 151. Mingming Ma, Jing Zhao, Dandan Xie, Juan Ch |
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- Page last updated:Apr 22, 2024
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