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1.
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Mol Psychiatry
; 26(7): 3004-3017, 2021 07.
Article
in English
| MEDLINE | ID: mdl-33057169
2.
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.
Bioinformatics
; 33(2): 272-279, 2017 01 15.
Article
in English
| MEDLINE | ID: mdl-27663502
3.
Opportunities and Challenges in Establishing a Cohort Study: An Example From Cleft Lip/Palate Research in the United Kingdom.
Cleft Palate Craniofac J
; 53(3): 317-25, 2016 05.
Article
in English
| MEDLINE | ID: mdl-26068383
4.
Resolving the effects of maternal and offspring genotype on dyadic outcomes in genome wide complex trait analysis ("M-GCTA").
Behav Genet
; 44(5): 445-55, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-25060210
5.
Prenatal methylmercury exposure and genetic predisposition to cognitive deficit at age 8 years.
Epidemiology
; 24(5): 643-50, 2013 Sep.
Article
in English
| MEDLINE | ID: mdl-23903878
6.
Discovery of 42 genome-wide significant loci associated with dyslexia.
Nat Genet
; 54(11): 1621-1629, 2022 11.
Article
in English
| MEDLINE | ID: mdl-36266505
7.
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.
Hum Genet
; 135(8): 965, 2016 08.
Article
in English
| MEDLINE | ID: mdl-27299648
8.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
; 12(1): 24, 2021 01 05.
Article
in English
| MEDLINE | ID: mdl-33402679
9.
Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate.
Epigenomics
; 11(2): 133-145, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30638414
10.
Identification of common genetic risk variants for autism spectrum disorder.
Nat Genet
; 51(3): 431-444, 2019 03.
Article
in English
| MEDLINE | ID: mdl-30804558
11.
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.
Nat Genet
; 55(3): 520, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-36823321
12.
Genetic Overlap Between Schizophrenia and Developmental Psychopathology: Longitudinal and Multivariate Polygenic Risk Prediction of Common Psychiatric Traits During Development.
Schizophr Bull
; 43(6): 1197-1207, 2017 10 21.
Article
in English
| MEDLINE | ID: mdl-28338919
13.
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium.
Sci Rep
; 6: 25853, 2016 05 13.
Article
in English
| MEDLINE | ID: mdl-27174397
14.
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts.
J Am Acad Child Adolesc Psychiatry
; 55(10): 896-905.e6, 2016 10.
Article
in English
| MEDLINE | ID: mdl-27663945
15.
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Nat Commun
; 12(1): 995, 2021 Feb 08.
Article
in English
| MEDLINE | ID: mdl-33558525
16.
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Nat Genet
; 45(3): 314-8, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23396134
17.
Time outdoors and physical activity as predictors of incident myopia in childhood: a prospective cohort study.
Invest Ophthalmol Vis Sci
; 53(6): 2856-65, 2012 May 14.
Article
in English
| MEDLINE | ID: mdl-22491403
18.
Common variants at 12q15 and 12q24 are associated with infant head circumference.
Nat Genet
; 44(5): 532-538, 2012 Apr 15.
Article
in English
| MEDLINE | ID: mdl-22504419
19.
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.
Nat Genet
; 44(9): 991-1005, 2012 Sep.
Article
in English
| MEDLINE | ID: mdl-22885924
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