Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 59 Records) |
Query Trace: KIAA0319[original query] |
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Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Dec 165B (8): 627-34. Sun Yimin, Gao Yong, Zhou Yuxi, Chen Huan, Wang Guoqing, Xu Junquan, Xia Jiguang, Huen Michael S Y, Siok Wai Ting, Jiang Yuyang, Tan Li H |
A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children. Behavioral and brain functions : BBF 2014 10 23. Lim Cadmon King-Poo, Wong Amabel May-Bo, Ho Connie Suk-Han, Waye Mary Mui-Y |
DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development. The Journal of neuroscience : the official journal of the Society for Neuroscience 2014 Oct 34 (43): 14455-62. Darki Fahimeh, Peyrard-Janvid Myriam, Matsson Hans, Kere Juha, Klingberg Tork |
KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. Journal of human genetics 2014 Apr 59 (4): 189-97. Mascheretti Sara, Riva Valentina, Giorda Roberto, Beri Silvana, Lanzoni Lara Francesca Emilia, Cellino Maria Rosaria, Marino Cecil |
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family. Human genetics 2015 Sep . Einarsdottir Elisabet, Svensson Idor, Darki Fahimeh, Peyrard-Janvid Myriam, Lindvall Jessica M, Ameur Adam, Jacobsson Christer, Klingberg Torkel, Kere Juha, Matsson Ha |
The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants. Molecular neurobiology 2015 Jul . Shao Shanshan, Kong Rui, Zou Li, Zhong Rong, Lou Jiao, Zhou Jie, Guo Shengnan, Wang Jia, Zhang Xiaohui, Zhang Jiajia, Song Ranr |
Deep Sequencing in Conjunction with Expression and Functional Analyses Reveals Activation of FGFR1 in Ewing Sarcoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2015 Jul . Agelopoulos Konstantin, Richter Günther H S, Schmidt Eva, Dirksen Uta, von Heyking Kristina, Moser Benjamin, Klein Hans-Ulrich, Kontny Udo, Dugas Martin, Poos Kathrin, Korsching Eberhard, Buch Thorsten, Weckesser Matthias, Schulze Isabell, Besoke Regina, Witten Anika, Stoll Monika, Köhler Gabriele, Hartmann Wolfgang, Wardelmann Eva, Rossig Claudia, Baumhoer Daniel, Jürgens Heribert, Burdach Stefan, Berdel Wolfgang E, Müller-Tidow Carst |
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. Brain imaging and behavior 2015 May . Eicher John D, Montgomery Angela M, Akshoomoff Natacha, Amaral David G, Bloss Cinnamon S, Libiger Ondrej, Schork Nicholas J, Darst Burcu F, Casey B J, Chang Linda, Ernst Thomas, Frazier Jean, Kaufmann Walter E, Keating Brian, Kenet Tal, Kennedy David, Mostofsky Stewart, Murray Sarah S, Sowell Elizabeth R, Bartsch Hauke, Kuperman Joshua M, Brown Timothy T, Hagler Donald J, Dale Anders M, Jernigan Terry L, Gruen Jeffrey R, |
An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia. Human genetics 2015 Jul 134 (7): 749-60. Mascheretti S, Bureau A, Trezzi V, Giorda R, Marino |
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Journal of human genetics 2015 Jul 60 (7): 399-401. Matsson Hans, Huss Mikael, Persson Helena, Einarsdottir Elisabet, Tiraboschi Ettore, Nopola-Hemmi Jaana, Schumacher Johannes, Neuhoff Nina, Warnke Andreas, Lyytinen Heikki, Schulte-Körne Gert, Nöthen Markus M, Leppänen Paavo Ht, Peyrard-Janvid Myriam, Kere Ju |
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles. Journal of medical genetics 2015 Dec . Powers Natalie R, Eicher John D, Miller Laura L, Kong Yong, Smith Shelley D, Pennington Bruce F, Willcutt Erik G, Olson Richard K, Ring Susan M, Gruen Jeffrey |
Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Oct . Kong Rui, Shao Shanshan, Wang Jia, Zhang Xiaohui, Guo Shengnan, Zou Li, Zhong Rong, Lou Jiao, Zhou Jie, Zhang Jiajia, Song Ranr |
Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population. Scientific reports 2016 07 6 30454. Shao Shanshan, Niu Yanfeng, Zhang Xiaohui, Kong Rui, Wang Jia, Liu Lingfei, Luo Xiu, Zhang Jiajia, Song Ranr |
KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children. Journal of human genetics 2016 Apr . Zhao Hua, Chen Yun, Zhang Bao-Ping, Zuo Peng-Xia |
Dyslexia susceptibility genes influence brain atrophy in frontotemporal dementia. Neurology. Genetics 2015 Oct 1 (3): e24. Paternicó Donata, Premi Enrico, Alberici Antonella, Archetti Silvana, Bonomi Elisa, Gualeni Vera, Gasparotti Roberto, Padovani Alessandro, Borroni Barba |
Associations Between the KIAA0319 Dyslexia Susceptibility Gene Variants, Antenatal Maternal Stress, and Reading Ability in a Longitudinal Birth Cohort. Dyslexia (Chichester, England) 2016 Jul . D'Souza Stephanie, Backhouse-Smith Amelia, Thompson John M D, Slykerman Rebecca, Marlow Gareth, Wall Clare, Murphy Rinki, Ferguson Lynnette R, Mitchell Edwin A, Waldie Karen |
Identification of NCAN as a candidate gene for developmental dyslexia. Scientific reports 2017 8 7 (1): 9294. Einarsdottir Elisabet, Peyrard-Janvid Myriam, Darki Fahimeh, Tuulari Jetro J, Merisaari Harri, Karlsson Linnea, Scheinin Noora M, Saunavaara Jani, Parkkola Riitta, Kantojärvi Katri, Ämmälä Antti-Jussi, Yiu-Lin Yu Nancy, Matsson Hans, Nopola-Hemmi Jaana, Karlsson Hasse, Paunio Tiina, Klingberg Torkel, Leinonen Eira, Kere Ju |
The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects. Journal of human genetics 2017 10 62 (11): 949-955. Trezzi Vittoria, Forni Diego, Giorda Roberto, Villa Marco, Molteni Massimo, Marino Cecilia, Mascheretti Sa |
Association analysis of dyslexia candidate genes in a Dutch longitudinal sample. European journal of human genetics : EJHG 2017 1 25 (4): 452-460. Carrion-Castillo Amaia, Maassen Ben, Franke Barbara, Heister Angelien, Naber Marlies, van der Leij Aryan, Francks Clyde, Fisher Simon |
Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexia. Developmental cognitive neuroscience 2018 6 34 7-17. Centanni T M, Pantazis D, Truong D T, Gruen J R, Gabrieli J D E, Hogan T |
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia. International journal of molecular medicine 2019 Jan 43 (1): 57-82. Yamada Yoshiji, Kato Kimihiko, Oguri Mitsutoshi, Horibe Hideki, Fujimaki Tetsuo, Yasukochi Yoshiki, Takeuchi Ichiro, Sakuma J |
KIAA0319 Genotype Predicts the Number of Past Concussions in a Division I Football Team: A Pilot Study. Journal of neurotrauma 2019 Apr 36 (7): 1115-1124. Walter Alexa, Herrold Amy A, Gallagher Virginia T, Lee Rosa, Scaramuzzo Madeleine, Bream Tim, Seidenberg Peter H, Vandenbergh David, O'Connor Kailyn, Talavage Thomas M, Nauman Eric A, Slobounov Semyon M, Breiter Hans |
Association between KIAA0319 SNPs and risk of dyslexia: a meta-analysis. Journal of genetics 2019 6 98 (1): . Deng Ke-Gao, Zhao Hua, Zuo Peng-Xia |
Genetic Study on Small Insertions and Deletions in Psoriasis Reveals a Role in Complex Human Diseases. The Journal of investigative dermatology 2019 5 139 (11): 2302-2312.e14. Zhen Qi, Yang Zhenjun, Wang Wenjun, Li Bao, Bai Mingzhou, Wu Jing, Ge Huiyao, Dong Zirui, Shen Juan, Tang Huayang, Sun Silong, Qiu Ying, Xu Jinjin, Qu Xiaoxiao, Wang Ying, Yi Meihui, Hu Huaqing, Xu Yuanhong, Cheng Hui, Liang Bo, Gao Jinping, Shao Haojing, Jiang Zhengwen, Gao Qiang, Sun Liangd |
Assessment for familial pattern and association of polymorphisms in KIAA0319 gene with specific reading disorder in children from North India visiting a tertiary care centre: A case-control study. Dyslexia (Chichester, England) 2019 12 26 (1): 104-114. Sharma Pawan, Sagar Rajesh, Deep Raman, Mehta Manju, Subbiah Vivekanandh |
Toward Robust Functional Neuroimaging Genetics of Cognition. The Journal of neuroscience : the official journal of the Society for Neuroscience 2019 Sep . Uddén Julia, Hultén Annika, Bendtz Katarina, Mineroff Zachary, Kucera Katerina S, Vino Arianna, Fedorenko Evelina, Hagoort Peter, Fisher Simon |
Aotearoa New Zealand M?ori and Pacific Population-amplified Gout Risk Variants: CLNK Is a Separate Risk Gene at the SLC2A9 Locus. The Journal of rheumatology 2021 Jul . Ji Aichang, Shaukat Amara, Takei Riku, Bixley Matthew, Cadzow Murray, Topless Ruth K, Major Tanya J, Phipps-Green Amanda, Merriman Marilyn E, Hindmarsh Jennie Harré, Stamp Lisa K, Dalbeth Nicola, Li Changgui, Merriman Tony |
Multivariate genome-wide association study of depression, cognition, and memory phenotypes and validation analysis identify 12 cross-ethnic variants.
Translational psychiatry 2022 07 12 (1): 304. Sun Jing, Wang Weijing, Zhang Ronghui, Duan Haiping, Tian Xiaocao, Xu Chunsheng, Li Xue, Zhang Dongfe |
Genetic determinants of individual variation in the superior temporal sulcus of chimpanzees (Pan troglodytes). Cerebral cortex (New York, N.Y. : 1991) 2022 6 . Hopkins William D, Coulon Oliver, Meguerditchian Adrien, Staes Nicky, Sherwood Chet C, Schapiro Steven J, Mangin Jean-Francois, Bradley Bren |
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families. Medicina (Kaunas, Lithuania) 2023 8 59 (8): . Francesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, Mirella Vinci, Antonino Musumeci, Angelo Gloria, Donatella Greco, Daniela Rita Raciti, Alessandro Zagami, Biagio Rizzo, Santina Città, Concetta Federico, Luigi Vetri, Salvatore Saccone, Serafino Buo |
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- Page last updated:Mar 25, 2024
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