Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 64 Records) |
Query Trace: MEF2C[original query] |
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ADGRV1 is implicated in myoclonic epilepsy. Epilepsia 2017 Dec . Myers Kenneth A, Nasioulas Steven, Boys Amber, McMahon Jacinta M, Slater Howard, Lockhart Paul, Sart Desirée du, Scheffer Ingrid |
Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion. Haematologica 2018 9 104 (1): 128-137. Ohki Kentaro, Kiyokawa Nobutaka, Saito Yuya, Hirabayashi Shinsuke, Nakabayashi Kazuhiko, Ichikawa Hitoshi, Momozawa Yukihide, Okamura Kohji, Yoshimi Ai, Ogata-Kawata Hiroko, Sakamoto Hiromi, Kato Motohiro, Fukushima Keitaro, Hasegawa Daisuke, Fukushima Hiroko, Imai Masako, Kajiwara Ryosuke, Koike Takashi, Komori Isao, Matsui Atsushi, Mori Makiko, Moriwaki Koichi, Noguchi Yasushi, Park Myoung-Ja, Ueda Takahiro, Yamamoto Shohei, Matsuda Koichi, Yoshida Teruhiko, Matsumoto Kenji, Hata Kenichiro, Kubo Michiaki, Matsubara Yoichi, Takahashi Hiroyuki, Fukushima Takashi, Hayashi Yasuhide, Koh Katsuyoshi, Manabe Atsushi, Ohara Akira, |
The major depressive disorder GWAS-supported variant rs10514299 in TMEM161B-MEF2C predicts putamen activation during reward processing in alcohol dependence. Translational psychiatry 2018 Jul 8 (1): 131. Muench Christine, Schwandt Melanie, Jung Jeesun, Cortes Carlos R, Momenan Reza, Lohoff Falk |
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes.
Bone 2018 Jun . Gregson Celia L, Newell Felicity, Leo Paul J, Clark Graeme R, Paternoster Lavinia, Marshall Mhairi, Forgetta Vincenzo, Morris John A, Ge Bing, Bao Xiao, Duncan Bassett J H, Williams Graham R, Youlten Scott E, Croucher Peter I, Davey Smith George, Evans David M, Kemp John P, Brown Matthew A, Tobias Jon H, Duncan Emma |
Genome-wide association study of lncRNA polymorphisms with bone mineral density. Annals of human genetics 2018 Sep 82 (5): 244-253. Zeng Qin, Wu Ke-Hao, Liu Kun, Hu Yuan, Chen Xiang-Ding, Zhang Lei, Shen Hui, Tian Qin, Zhao Lan-Juan, Deng Hong-Wen, Tan Li-J |
Novel Loci Associated With Attention-Deficit/Hyperactivity Disorder Are Revealed by Leveraging Polygenic Overlap With Educational Attainment. Journal of the American Academy of Child and Adolescent Psychiatry 2018 Feb 57 (2): 86-95. Shadrin Alexey A, Smeland Olav B, Zayats Tetyana, Schork Andrew J, Frei Oleksandr, Bettella Francesco, Witoelar Aree, Li Wen, Eriksen Jon A, Krull Florian, Djurovic Srdjan, Faraone Stephen V, Reichborn-Kjennerud Ted, Thompson Wesley K, Johansson Stefan, Haavik Jan, Dale Anders M, Wang Yunpeng, Andreassen Ole |
Novel MEF2C point mutations in Chinese patients with Rett (-like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation. BMC medical genetics 2018 11 19 (1): 191. Wang Jiaping, Zhang Qingping, Chen Yan, Yu Shujie, Wu Xiru, Bao Xinhua, Wen Yongx |
JAG1, MEF2C and BDNF polymorphisms associated with bone mineral density in women from Northern México. Biomedica : revista del Instituto Nacional de Salud 2018 09 38 (3): 320-328. González-Peña Sandra Marlen, Campos-Góngora Eduardo, Ávila-Rodríguez Hilda Guadalupe, Ramírez-López Erik, Velázquez-Cruz Rafael, Jiménez-Salas Zacarí |
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+). Neurology. Genetics 2018 Feb 4 (1): e211. Mäkelä Mira, Kaivola Karri, Valori Miko, Paetau Anders, Polvikoski Tuomo, Singleton Andrew B, Traynor Bryan J, Stone David J, Peuralinna Terhi, Tienari Pentti J, Tanskanen Maarit, Myllykangas Lii |
Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human mutation 2019 Feb . Zhou Wei-Zhen, Zhang Jie, Li Ziyi, Lin Xiaojing, Li Jiarui, Wang Sheng, Yang Changhong, Wu Qixi, Ye Adam Yongxin, Wang Meng, Wang Dandan, Pu Tad Zhengzhang, Wu Yu-Yu, Wei Lipi |
Mutations Defining Patient Cohorts With Elevated PD-L1 Expression in Gastric Cancer. Frontiers in pharmacology 2019 1 9 1522. Menyhárt Otília, Pongor L?rinc Sándor, Gy?rffy Balá |
[Discovery and functional analysis of a novel ISL1 variant associated with congenital heart defect]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 8 37 (9): 972-975. Dong Binbin, Liu Xingyuan, Wang Tianming, Yang Yiqi |
ISL1 loss-of-function variation causes familial atrial fibrillation. European journal of medical genetics 2020 8 63 (11): 104029. Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi |
Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in Drosophila. The American journal of psychiatry 2020 (6): 526-536. Klein Marieke, Singgih Euginia L, van Rens Anne, Demontis Ditte, Børglum Anders D, Mota Nina Roth, Castells-Nobau Anna, Kiemeney Lambertus A, Brunner Han G, Arias-Vasquez Alejandro, Schenck Annette, van der Voet Monique, Franke Barba |
MEF2C Common Genetic Variation Is Associated With Different Aspects of Cognition in Non-Hispanic White and Caribbean Hispanic Non-demented Older Adults. Frontiers in genetics 2021 12 642327. Sunderaraman Preeti, Cosentino Stephanie, Schupf Nicole, Manly Jennifer, Gu Yian, Barral Sand |
Characterization of Brain Iron Deposition Pattern and Its Association With Genetic Risk Factor in Alzheimer's Disease Using Susceptibility-Weighted Imaging. Frontiers in human neuroscience 2021 6 15 654381. You Peiting, Li Xiang, Wang Zhijiang, Wang Huali, Dong Bin, Li Quanzhe |
Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions. Frontiers in genetics 2021 12 651971. Strafella Claudia, Caputo Valerio, Termine Andrea, Assogna Francesca, Pellicano Clelia, Pontieri Francesco E, Macchiusi Lucia, Minozzi Giulietta, Gambardella Stefano, Centonze Diego, Bossù Paola, Spalletta Gianfranco, Caltagirone Carlo, Giardina Emiliano, Cascella Raffael |
Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms. American journal of human genetics 2021 5 108 (6): 1083-1094. Wright Caroline F, Quaife Nicholas M, Ramos-Hernández Laura, Danecek Petr, Ferla Matteo P, Samocha Kaitlin E, Kaplanis Joanna, Gardner Eugene J, Eberhardt Ruth Y, Chao Katherine R, Karczewski Konrad J, Morales Joannella, Gallone Giuseppe, Balasubramanian Meena, Banka Siddharth, Gompertz Lianne, Kerr Bronwyn, Kirby Amelia, Lynch Sally A, Morton Jenny E V, Pinz Hailey, Sansbury Francis H, Stewart Helen, Zuccarelli Britton D, , Cook Stuart A, Taylor Jenny C, Juusola Jane, Retterer Kyle, Firth Helen V, Hurles Matthew E, Lara-Pezzi Enrique, Barton Paul J R, Whiffin Nico |
Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence.
Scientific reports 2021 Feb 11 (1): 3851. Donati Georgina, Dumontheil Iroise, Pain Oliver, Asbury Kathryn, Meaburn Emma |
Polymorphisms in Genes Involved in Osteoblast Differentiation and Function Are Associated with Anthropometric Phenotypes in Spanish Women. Genes 2021 12 12 (12): . Pertusa Clara, Ruzo Sofía P, Panach Layla, Mifsut Damián, Tarín Juan J, Cano Antonio, García-Pérez Miguel Áng |
[Clinical phenotype and genetic analysis of a case of 5q14.3 microdeletion syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 11 38 (11): 1127-1131. Xu Xin, Li Hongying, Zhang Li, Lu Fen, Tang Ji |
Molecular Mechanisms of ARID5B-Mediated Genetic Susceptibility to Acute Lymphoblastic Leukemia. Journal of the National Cancer Institute 2022 May . Zhao Xujie, Qian Maoxiang, Goodings Charnise, Zhang Yang, Yang Wenjian, Wang Ping, Xu Beisi, Tian Cheng, Pui Ching-Hon, Hunger Stephen P, Raetz Elizabeth A, Devidas Meenakshi, Relling Mary V, Loh Mignon L, Savic Daniel, Li Chunliang, Yang Jun |
MEF2C gene variations are associated with ADHD in the Chinese Han population: a case-control study. Journal of neural transmission (Vienna, Austria : 1996) 2022 3 129 (4): 431-439. Fu Xihang, Yao Ting, Chen Xinzhen, Li Huiru, Wu Ji |
Single-Nucleotide Polymorphisms in Exonic and Promoter Regions of Transcription Factors of Second Heart Field Associated with Sporadic Congenital Cardiac Anomalies. Balkan journal of medical genetics : BJMG 2021 Nov 24 (2): 39-47. Wang E, Fan X, Nie Y, Zheng Z, Hu |
[Clinical and genetic analysis of two children with Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language due to de novo variants of MEF2C gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 9 40 (10): 1252-1256. Lulu Yan, Danyan Zhuang, Youqu Tu, Yuxin Zhang, Yingwen Liu, Yan He, Haibo |
Association between MEF2 family gene polymorphisms and susceptibility to multiple sclerosis in Chinese population. Acta neurologica Belgica 2023 8 . Lei Wu, Bo Liu, Yanbing Wei, Peng |
Refining patterns of MEF2C effects in white matter microstructure and psychiatric features. Journal of neural transmission (Vienna, Austria : 1996) 2023 3 . de Araujo Tavares Maria Eduarda, Cupertino Renata Basso, Bandeira Cibele Edom, da Silva Bruna Santos, Vitola Eduardo Schneider, Salgado Carlos Alberto Iglesias, Dos Santos Soares Robson, Picon Felipe Almeida, Rohde Luis Augusto, Rovaris Diego Luiz, Grevet Eugenio Horacio, Bau Claiton Henrique Dot |
Genomic patterns linked to gray matter alterations underlying working memory deficits in adults and adolescents with attention-deficit/hyperactivity disorder. Translational psychiatry 2023 2 13 (1): 50. Duan Kuaikuai, Chen Jiayu, Calhoun Vince D, Jiang Wenhao, Rootes-Murdy Kelly, Schoenmacker Gido, Silva Rogers F, Franke Barbara, Buitelaar Jan K, Hoogman Martine, Oosterlaan Jaap, Hoekstra Pieter J, Heslenfeld Dirk, Hartman Catharina A, Sprooten Emma, Arias-Vasquez Alejandro, Turner Jessica A, Liu Jing |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
Genome-Wide Association Study and Identification of Candidate Genes for Intramuscular Fat Fatty Acid Composition in Ningxiang Pigs. Animals : an open access journal from MDPI 2023 10 13 (20): . Qinghua Zeng, Hu Gao, Shishu Yin, Yinglin Peng, Fang Yang, Yawei Fu, Xiaoxiao Deng, Yue Chen, Xiaohong Hou, Qian Wang, Zhao Jin, Gang Song, Jun He, Yulong Yin, Kang |
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