X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
dcdc2 (68) 68
index medicus (63) 63
humans (52) 52
developmental dyslexia (47) 47
dyslexia (44) 44
dyslexia - genetics (41) 41
female (36) 36
male (36) 36
kiaa0319 (35) 35
reading-disability (34) 34
neurosciences (33) 33
susceptibility gene (33) 33
microtubule-associated proteins - genetics (27) 27
child (23) 23
genes (23) 23
article (22) 22
genetics & heredity (22) 22
nerve tissue proteins - genetics (19) 19
language (18) 18
children (17) 17
neuronal migration (17) 17
reading (17) 17
association (16) 16
candidate genes (16) 16
genetic predisposition to disease (15) 15
genetic research (15) 15
genetics (15) 15
behavioral sciences (14) 14
dyx1c1 (14) 14
polymorphism, single nucleotide (14) 14
brain (13) 13
genetic aspects (13) 13
genetic association studies (12) 12
linkage (12) 12
adolescent (11) 11
polymorphism, single nucleotide - genetics (11) 11
animals (10) 10
case-control studies (10) 10
neurology (10) 10
psychiatry (10) 10
dyslexia - physiopathology (9) 9
families (9) 9
haplotypes (9) 9
quantitative-trait locus (9) 9
alleles (8) 8
analysis (8) 8
gene expression (8) 8
genomes (8) 8
genotype (8) 8
neurodevelopmental disorders (8) 8
neurons (8) 8
risk factors (8) 8
adult (7) 7
biochemistry & molecular biology (7) 7
biomedicine (7) 7
cell movement - genetics (7) 7
cognitive ability (7) 7
disability (7) 7
expression (7) 7
genomics (7) 7
knockdown (7) 7
language impairment (7) 7
mice (7) 7
microtubule-associated proteins - metabolism (7) 7
multidisciplinary sciences (7) 7
original (7) 7
polymorphisms (7) 7
population (7) 7
research (7) 7
single-nucleotide polymorphism (7) 7
young adult (7) 7
dyslexia - epidemiology (6) 6
genetic variation (6) 6
genome-wide association (6) 6
medical research (6) 6
polymorphism (6) 6
pregnancy (6) 6
psychology (6) 6
psychology, experimental (6) 6
association study (5) 5
cell biology (5) 5
cell migration (5) 5
cognition (5) 5
cohort studies (5) 5
contrast sensitivity (5) 5
disease susceptibility (5) 5
dyslexia - pathology (5) 5
dyslexia - psychology (5) 5
longitudinal studies (5) 5
nuclear proteins - genetics (5) 5
reading disabilities (5) 5
reading disability (5) 5
single nucleotide polymorphisms (5) 5
studies (5) 5
age (4) 4
aged (4) 4
anopheles (4) 4
cerebral cortex (4) 4
chromosome 6p (4) 4
chromosome 6p influences (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Cerebral Cortex, ISSN 1047-3211, 10/2016, Volume 26, Issue 11, pp. 4356 - 4369
Although impaired auditory-phonological processing is the most popular explanation of developmental dyslexia (DD), the literature shows that the combination of... 
reading disorders | visual pathways | motion perception | perceptual learning | action video games | CONTRAST SENSITIVITY | READING ACQUISITION | DCDC2 GENETIC-VARIANTS | NEUROSCIENCES | FAMILIAL RISK | CHILDREN | SYMBOL-STRING SENSITIVITY | PERCEPTION | MOTION | ATTENTIONAL ENGAGEMENT DEFICITS | VISUAL-SPATIAL ATTENTION | Original
Journal Article
by Davies, Gail and Lam, M and Harris, Sarah and Trampush, J.W and Luciano, Michelle and Hill, W.D and Hagenaars, Saskia and Ritchie, S.J and Marioni, Riccardo and Fawns-Ritchie, C and Liewald, D.C.M and Okely, J.A and Ahola-Olli, A.V and Barnes, C.L.K and Bertram, Lars and Bis, Joshua and Burdick, K.E and Christoforou, Anea and Derosse, P and Djurovic, Srdjan and Espeseth, Thomas and Giakoumaki, S and Giddaluru, Sudheer and Gustavson, D.E and Hayward, Caroline and Hofer, Edith and Ikram, Arfan and Karlsson, Robert and Knowles, E and Lahti, Jari and Leber, Isabelle and Li, S and Mather, R and Melle, Ingrid and Morris, D and Oldmeadow, Christopher and Palviainen, T and Payton, Antony and Pazoki, Raha and Petrovic, Katja and Reynolds, C and Sargurupremraj, M and Scholz, Markus and Smith, Jennifer A and Smith, Albert and Terzikhan, Natalie and Thalamuthu, Anbupalam and Trompet, Stella and Lee, Sven and Ware, Erin B and Windham, B Gwen and Wright, M.J and Yang, J and Yu, J and Ames, David and Amin, Najaf and Amouyel, Philippe and Aneassen, Ole and Armstrong, Nicola J and Assareh, A.A and Attia, John and Attix, D and Avramopoulos, D and Bennett, David and Böhmer, Marcel and Boyle, P.A and Brodaty, Henry and Campbell, Harry and Cannon, T.D and Cirulli, E.T and Congdon, E and Conley, E.D and Corley, J and Cox, Simon R and Dale, Anders and Dehghan, Abbas and Dick, D and Dickinson, D and Hagen, Knut and Evangelou, Evangelos and Faul, Jessica D and Ford, Ian and Freimer, N.A and Gao, H and Giegling, Ina and Gillespie, N.A and Gordon, Scott D and Gottesman, Rebecca and Griswold, Michael and Gudnason, V and Harris, Tamara and Hartmann, Annette M and Hatzimanolis, A and Heiss, Gerardo and Holliday, Elizabeth and Joshi, Peter and Kähönen, Mika and Kardia, S.L.R and Karlsson, I and Kleineidam, L and ...
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2098 - 16
textabstractGeneral cognitive function is a prominent and relatively stable human trait that is associated with many important life outcomes. We combine... 
COMMON VARIANTS | METAANALYSIS | REACTION-TIME | PROCESSING SPEED | MULTIDISCIPLINARY SCIENCES | INTELLIGENCE DIFFERENCES | SCHIZOPHRENIA | DCDC2 | DISCOVERY | GENOME-WIDE ASSOCIATION | REVEALS | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genetic Loci - genetics | Neurodegenerative Diseases - genetics | Neurodevelopmental Disorders - genetics | Reaction Time - genetics | Young Adult | Mental Disorders - genetics | Adolescent | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Hypertension | Brain | Cognitive ability | Genomes | Gene expression | Neurodevelopmental disorders | Loci | Consortia | Illnesses | Mathematical analysis | Reaction time | Heritability | Gene loci | Polygenic inheritance | brain cortex | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | osteoarthritis | Article | heart infarction | Klinisk medicin | lung cancer | identification method | longevity | grip strength | angina pectoris | genetic correlation | human | major depression | Neurologi | cognition | data set | aged | brain | gene locus | Clinical Medicine | Neurology | genome | vision | genetic analysis | controlled study | response time | adolescent | nervous system disorder | adult | hypertension | gene expression
Journal Article
Neuropsychologia, ISSN 0028-3932, 07/2019, Volume 130, pp. 52 - 58
Developmental dyslexia (DD) is a complex neurodevelopmental heritable disorder. Among DD candidate genes, DCDC2 is one of the most replicated, with rs793862,... 
Developmental dyslexia | Association study | DCDC2 | Pleiotropy | Haplotype | DYSLEXIA CANDIDATE GENES | LANGUAGE | DYX1C1 | NEUROSCIENCES | PSYCHOLOGY, EXPERIMENTAL | DISABILITY | SUSCEPTIBILITY GENE | BEHAVIORAL SCIENCES | LINKAGE | KNOCKDOWN | ASSOCIATION | KIAA0319 | Genetic research | Dyslexia | Research institutes | Psychology, Pathological
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 05/2018, Volume 115, Issue 19, pp. 4951 - 4956
DCDC2 is a gene strongly associated with components of the phonological processing system in animal models and in multiple independent studies of populations... 
READ1 | DCDC2 | Genetics | Language | Phoneme | POPULATION | MULTIDISCIPLINARY SCIENCES | phoneme | language | GENOME | GENETIC-VARIATION | MUTATIONS CAUSE | genetics | EVOLUTION | POLYMORPHISMS | DISCRIMINATION | MICROSATELLITES | DEVELOPMENTAL DYSLEXIA | NEONATAL SCLEROSING CHOLANGITIS | Genetic research | Genetic variation | Research | Biological Sciences | Social Sciences
Journal Article
Nature Communications, ISSN 2041-1723, 07/2014, Volume 5, Issue 1, p. 4204
Journal Article
Scientific Reports, ISSN 2045-2322, 06/2016, Volume 6, Issue 1, p. 27901
Dyslexia is a severe disorder in the acquisition of reading and writing. Several studies investigated the role of genetics for reading, writing and spelling... 
POLYMORPHISMS | TRANS-EQTLS | SINGLE-BASE EXTENSION | MULTIDISCIPLINARY SCIENCES | CANDIDATE GENES | REGIONS | SUSCEPTIBILITY GENE | DCDC2 | EXPRESSION | KIAA0319 | GENOME-WIDE ASSOCIATION
Journal Article
Clinical Practice and Epidemiology in Mental Health, ISSN 1745-0179, 08/2017, Volume 13, Issue 1, pp. 104 - 114
Doublecortin domain-containing 2 (DCDC2) is a doublecortin domain-containing gene family member and the doublecortin domain has been demonstrated to bind to... 
Journal Article