Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Dyslexia[original query] |
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Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.
BMC medical genetics 2007 8 Suppl 1 S15. Seshadri Sudha, DeStefano Anita L, Au Rhoda, Massaro Joseph M, Beiser Alexa S, Kelly-Hayes Margaret, Kase Carlos S, D'Agostino Ralph B, Decarli Charles, Atwood Larry D, Wolf Philip |
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
Molecular psychiatry 2011 Jan 16 (1): 97-107. Roeske D, Ludwig K U, Neuhoff N, Becker J, Bartling J, Bruder J, Brockschmidt F F, Warnke A, Remschmidt H, Hoffmann P, Müller-Myhsok B, Nöthen M M, Schulte-Körne |
PCSK6 is associated with handedness in individuals with dyslexia.
Human molecular genetics 2011 Feb 20 (3): 608-14. Scerri Thomas S, Brandler William M, Paracchini Silvia, Morris Andrew P, Ring Susan M, Richardson Alex J, Talcott Joel B, Stein John, Monaco Anthony |
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
PLoS genetics 2013 9 (9): e1003751. Brandler William M, Morris Andrew P, Evans David M, Scerri Thomas S, Kemp John P, Timpson Nicholas J, St Pourcain Beate, Smith George Davey, Ring Susan M, Stein John, Monaco Anthony P, Talcott Joel B, Fisher Simon E, Webber Caleb, Paracchini Silv |
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
Translational psychiatry 2013 3 e229. Ludwig K U, Sämann P, Alexander M, Becker J, Bruder J, Moll K, Spieler D, Czisch M, Warnke A, Docherty S J, Davis O S P, Plomin R, Nöthen M M, Landerl K, Müller-Myhsok B, Hoffmann P, Schumacher J, Schulte-Körne G, Czamara |
Common variation near ROBO2 is associated with expressive vocabulary in infancy.
Nature communications 2014 5 4831. St Pourcain Beate, Cents Rolieke A M, Whitehouse Andrew J O, Haworth Claire M A, Davis Oliver S P, O'Reilly Paul F, Roulstone Susan, Wren Yvonne, Ang Qi W, Velders Fleur P, Evans David M, Kemp John P, Warrington Nicole M, Miller Laura, Timpson Nicholas J, Ring Susan M, Verhulst Frank C, Hofman Albert, Rivadeneira Fernando, Meaburn Emma L, Price Thomas S, Dale Philip S, Pillas Demetris, Yliherva Anneli, Rodriguez Alina, Golding Jean, Jaddoe Vincent W V, Jarvelin Marjo-Riitta, Plomin Robert, Pennell Craig E, Tiemeier Henning, Davey Smith Geor |
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 |
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 |
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- Page last updated:Apr 22, 2024
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