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Query Trace: Dyslexia Or Learning Disability [original query] |
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A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN. Asian journal of psychiatry 2018 Aug 37 121-129. Devasenapathy Subhashree, Midha Rashi, Naskar Teesta, Mehta Anuradha, Prajapati Bharat, Ummekulsum Mariam, Sagar Rajesh, Singh Nandini C, Sinha Subra |
Genetic variants in the CNTNAP2 gene are associated with gender differences among dyslexic children in China. EBioMedicine 2018 Jul . Gu Huaiting, Hou Fang, Liu Lingfei, Luo Xiu, Nkomola Pauline Denis, Xie Xinyan, Li Xin, Song Ranr |
The Influence of Dyslexia Candidate Genes on Reading Skill in Old Age. Behavior genetics 2018 Jun . Luciano Michelle, Gow Alan J, Pattie Alison, Bates Timothy C, Deary Ian |
Dyslexia associated functional variants in Europeans are not associated with dyslexia in Chinese. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019 Jul . Liu Lingfei, Gu Huaiting, Hou Fang, Xie Xinyan, Li Xin, Zhu Bing, Zhang Jiajia, Wei Wen-Hua, Song Ranr |
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 |
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Translational psychiatry 2019 02 9 (1): 77. Gialluisi Alessandro, Andlauer Till F M, Mirza-Schreiber Nazanin, Moll Kristina, Becker Jessica, Hoffmann Per, Ludwig Kerstin U, Czamara Darina, St Pourcain Beate, Brandler William, Honbolygó Ferenc, Tóth Dénes, Csépe Valéria, Huguet Guillaume, Morris Andrew P, Hulslander Jacqueline, Willcutt Erik G, DeFries John C, Olson Richard K, Smith Shelley D, Pennington Bruce F, Vaessen Anniek, Maurer Urs, Lyytinen Heikki, Peyrard-Janvid Myriam, Leppänen Paavo H T, Brandeis Daniel, Bonte Milene, Stein John F, Talcott Joel B, Fauchereau Fabien, Wilcke Arndt, Francks Clyde, Bourgeron Thomas, Monaco Anthony P, Ramus Franck, Landerl Karin, Kere Juha, Scerri Thomas S, Paracchini Silvia, Fisher Simon E, Schumacher Johannes, Nöthen Markus M, Müller-Myhsok Bertram, Schulte-Körne Ge |
Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment.
Cortex; a journal devoted to the study of the nervous system and behavior 2019 Nov 124 137-153. Carrion-Castillo Amaia, Pepe Antonietta, Kong Xiang-Zhen, Fisher Simon E, Mazoyer Bernard, Tzourio-Mazoyer Nathalie, Crivello Fabrice, Francks Cly |
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 |
Isoform-specific NF1 mRNA levels correlate with disease severity in Neurofibromatosis type 1. Orphanet journal of rare diseases 2019 11 14 (1): 261. Assunto Antonia, Ferrara Ursula, De Luca Alessandro, Pivonello Claudia, Lombardo Lisa, Piscitelli Annapina, Tortora Cristina, Pinna Valentina, Daniele Paola, Pivonello Rosario, Russo Maria Giovanna, Limongelli Giuseppe, Colao Annamaria, Tartaglia Marco, Strisciuglio Pietro, Melis Danie |
A molecular-genetic and imaging-genetic approach to specific comprehension difficulties in children. NPJ science of learning 2018 3 20. Li Miao, Malins Jeffrey G, DeMille Mellissa M C, Lovett Maureen W, Truong Dongnhu T, Epstein Katherine, Lacadie Cheryl, Mehta Chintan, Bosson-Heenan Joan, Gruen Jeffrey R, Frijters Jan C, |
The associations of zinc and GRIN2B genetic polymorphisms with the risk of dyslexia. Environmental research 2020 Sep 110207. Liu Qi, Zhu Bing, Xue Qi, Xie Xinyan, Zhou Yu, Zhu Kaiheng, Wan Zihao, Wu Hao, Zhang Jiajia, Song Ranr |
Do Genes Associated with Dyslexia of Chinese Characters Evolve Neutrally? Genes 2020 6 11 (6): . Nishiyama Kumiko V, Satta Yoko, Gojobori J |
The Association of Scoliosis and NSD1 Gene Deletion in Sotos Syndrome Patients. Spine 2020 12 46 (13): E726-E733. Machida Masafumi, Katoh Hiroyuki, Machida Masayoshi, Miyake Atsushi, Taira Katsuaki, Ohashi Hirofu |
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular psychiatry 2020 Oct . Gialluisi Alessandro, Andlauer Till F M, Mirza-Schreiber Nazanin, Moll Kristina, Becker Jessica, Hoffmann Per, Ludwig Kerstin U, Czamara Darina, Pourcain Beate St, Honbolygó Ferenc, Tóth Dénes, Csépe Valéria, Huguet Guillaume, Chaix Yves, Iannuzzi Stephanie, Demonet Jean-Francois, Morris Andrew P, Hulslander Jacqueline, Willcutt Erik G, DeFries John C, Olson Richard K, Smith Shelley D, Pennington Bruce F, Vaessen Anniek, Maurer Urs, Lyytinen Heikki, Peyrard-Janvid Myriam, Leppänen Paavo H T, Brandeis Daniel, Bonte Milene, Stein John F, Talcott Joel B, Fauchereau Fabien, Wilcke Arndt, Kirsten Holger, Müller Bent, Francks Clyde, Bourgeron Thomas, Monaco Anthony P, Ramus Franck, Landerl Karin, Kere Juha, Scerri Thomas S, Paracchini Silvia, Fisher Simon E, Schumacher Johannes, Nöthen Markus M, Müller-Myhsok Bertram, Schulte-Körne Ge |
White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant. Experimental brain research 2021 Jul . Perani Daniela, Scifo Paola, Cicchini Guido M, Rosa Pasquale Della, Banfi Chiara, Mascheretti Sara, Falini Andrea, Marino Cecilia, Morrone Maria Concet |
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family. Human genetics 2021 6 140 (8): 1183-1200. Carrion-Castillo Amaia, Estruch Sara B, Maassen Ben, Franke Barbara, Francks Clyde, Fisher Simon |
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. Human molecular genetics 2021 4 30 (12): 1160-1171. Martinelli Angela, Rice Mabel L, Talcott Joel B, Diaz Rebeca, Smith Shelley, Raza Muhammad Hashim, Snowling Margaret J, Hulme Charles, Stein John, Hayiou-Thomas Marianna E, Hawi Ziarih, Kent Lindsey, Pitt Samantha J, Newbury Dianne F, Paracchini Silv |
Neural entrainment to speech and nonspeech in dyslexia: Conceptual replication and extension of previous investigations. Cortex; a journal devoted to the study of the nervous system and behavior 2021 2 137 160-178. Lizarazu Mikel, Scotto di Covella Lou, van Wassenhove Virginie, Rivière Denis, Mizzi Raphael, Lehongre Katia, Hertz-Pannier Lucie, Ramus Fran |
Erratum to "Auditory brainstem measures and genotyping boost the prediction of literacy: A longitudinal study on early markers of dyslexia" [Dev. Cognit. Neurosci. 46 (2020) 100869]. Developmental cognitive neuroscience 2021 1 48 100889. Liebig Johanna, , Friederici Angela D, Neef Nicole |
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis. Neurology. Genetics 2022 9 8 (5): e200011. Grassano Maurizio, Brodini Giorgia, De Marco Giovanni, Casale Federico, Fuda Giuseppe, Salamone Paolina, Brunetti Maura, Sbaiz Luca, Gallone Salvatore, Cugnasco Paolo, Bombaci Alessandro, Vasta Rosario, Manera Umberto, Canosa Antonio, Moglia Cristina, Calvo Andrea, Traynor Bryan J, Chio Adria |
Interaction between manganese and SLC6A3 genetic polymorphisms in relation to dyslexia. Neurotoxicology 2022 09 92 102-109. Zhu Kaiheng, Liu Qi, Xie Xinyan, Jiang Qi, Feng Yanan, Xiao Pei, Wu Xiaoqian, Zhu Bing, Song Ranr |
The combined effect between BDNF genetic polymorphisms and exposure to metals on the risk of Chinese dyslexia. Environmental pollution (Barking, Essex : 1987) 2022 Jun 308 119640. Zhu Kaiheng, Liu Qi, Xie Xinyan, Jiang Qi, Feng Yanan, Xiao Pei, Wu Xiaoqian, Song Ranr |
BDNF Val66Met Polymorphism: Suggested Genetic Involvement in Some Children with Learning Disorder. Journal of molecular neuroscience : MN 2022 12 73 (1): 39-46. Elhadidy Mohamed E, Kilany Ayman, Gebril Ola Hosny, Nashaat Neveen Hassan, Zeidan Hala M, Elsaied Amal, Hashish Adel F, Abdelraouf Ehab Rag |
Discovery of 42 genome-wide significant loci associated with dyslexia.
Nature genetics 2022 10 54 (11): 1621-1629. Doust Catherine, Fontanillas Pierre, Eising Else, Gordon Scott D, Wang Zhengjun, Alagöz Gökberk, Molz Barbara, , , Pourcain Beate St, Francks Clyde, Marioni Riccardo E, Zhao Jingjing, Paracchini Silvia, Talcott Joel B, Monaco Anthony P, Stein John F, Gruen Jeffrey R, Olson Richard K, Willcutt Erik G, DeFries John C, Pennington Bruce F, Smith Shelley D, Wright Margaret J, Martin Nicholas G, Auton Adam, Bates Timothy C, Fisher Simon E, Luciano Michel |
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 |
Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants. American journal of medical genetics. Part A 2023 4 . Siracusano Martina, Riccioni Assia, Frattale Ilaria, Arturi Lucrezia, Dante Caterina, Galasso Cinzia, Gialloreti Leonardo Emberti, Conteduca Giuseppina, Testa Barbara, Malacarne Michela, Coviello Domenico, Mazzone Lui |
Evaluating the Association Between Genetically Proxied Neurodevelopmental Language Phenotypes and the Risk for Primary Progressive Aphasia. Neurology 2023 3 . Nassan Malik, Piras Ignazio S, Rogalski Emily, Geula Changiz, Mesulam M-Marsel, Huentelman Ma |
The Moderating Role of the DYX1C1 Gene in the Effect of Home Supervision on Chinese Children's Reading Achievements: Evidence from the Diathesis-Stress Model. Behavioral sciences (Basel, Switzerland) 2023 11 13 (11): . Yingnan Niu, He Cai, Li Zha |
Investigation of the forkhead box protein P2 gene by the next-generation sequence analysis method in children diagnosed with specific learning disorder. Psychiatric genetics 2023 1 33 (1): 8-19. Yaz?c? Merve, Yekta? Çi?dem, Eröz Recep, Kaplan Karakaya Elif Sümeyra, Sar?gedik En |
Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults. Cerebral cortex (New York, N.Y. : 1991) 2024 4 34 (4): . Nea Rinne, Patrik Wikman, Elisa Sahari, Juha Salmi, Elisabet Einarsdóttir, Juha Kere, Kimmo Al |
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- Page last updated:Apr 22, 2024
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