Human Genome Epidemiology Literature Finder
|
Records 1 - 10 (of 10 Records) |
| Query Trace: Learning and DCDC2[original query] |
|---|
| Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatric genetics 2008 Dec 18 (6): 310-2. Ludwig Kerstin U, Schumacher Johannes, Schulte-Körne Gerd, König Inke R, Warnke Andreas, Plume Ellen, Anthoni Heidi, Peyrard-Janvid Myriam, Meng Haiying, Ziegler Andreas, Remschmidt Helmut, Kere Juha, Gruen Jeffrey R, Müller-Myhsok Bertram, Nöthen Markus M, Hoffmann P |
| SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations. Behavior genetics 2011 Jan 41 (1): 134-40. Matsson Hans, Tammimies Kristiina, Zucchelli Marco, Anthoni Heidi, Onkamo Päivi, Nopola-Hemmi Jaana, Lyytinen Heikki, Leppanen Paavo H T, Neuhoff Nina, Warnke Andreas, Schulte-Körne Gert, Schumacher Johannes, Nöthen Markus M, Kere Juha, Peyrard-Janvid Myri |
| An examination of candidate gene SNPs for dyslexia in an Indian sample. Behavior genetics 2011 Jan 41 (1): 105-9. Venkatesh Shyamala K, Siddaiah Anand, Padakannaya Prakash, Ramachandra Nallur |
| Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment. American journal of human genetics 2013 Jul 93 (1): 19-28. Powers Natalie R, Eicher John D, Butter Falk, Kong Yong, Miller Laura L, Ring Susan M, Mann Matthias, Gruen Jeffrey |
| Study of candidate genes for dyslexia in Brazilian individuals. Genetics and molecular research : GMR 2013 12 (4): 5356-64. Svidnicki M C C M, Salgado C A, Lima R F, Ciasca S M, Secolin R, Pomilio M C A, Junqueira P A, Pinto M S, Pereira M M, Sartorato E |
| The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems. European child & adolescent psychiatry 2015 Mar 24 (3): 309-18. Riva Valentina, Marino Cecilia, Giorda Roberto, Molteni Massimo, Nobile Mar |
| 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 |
| Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children. Clinical practice and epidemiology in mental health : CP & EMH 2017 10 13 104-114. Waye Mary M Y, Poo Lim K, Ho Connie S |
| 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 |
| 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 |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 18, 2023
- Content source: