Published in Am J Med Genet B Neuropsychiatr Genet on July 01, 2013
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. Acta Neuropathol (2014) 1.07
Do sleep disturbances and psychotic-like experiences in adolescence share genetic and environmental influences? J Abnorm Psychol (2015) 0.99
Sleep duration and depressive symptoms: a gene-environment interaction. Sleep (2014) 0.92
Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder. Proc Natl Acad Sci U S A (2015) 0.90
Expression and replication studies to identify new candidate genes involved in normal hearing function. PLoS One (2014) 0.85
Reduced Sleep Spindles in Schizophrenia: A Treatable Endophenotype That Links Risk Genes to Impaired Cognition? Biol Psychiatry (2015) 0.83
Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology. J Neuropathol Exp Neurol (2015) 0.83
ABCC9/SUR2 in the brain: Implications for hippocampal sclerosis of aging and a potential therapeutic target. Ageing Res Rev (2015) 0.81
Innovative approaches to bipolar disorder and its treatment. Ann N Y Acad Sci (2016) 0.80
A twin and molecular genetics study of sleep paralysis and associated factors. J Sleep Res (2015) 0.80
Cacna1c (Cav1.2) Modulates Electroencephalographic Rhythm and Rapid Eye Movement Sleep Recovery. Sleep (2015) 0.78
Genetic Correlates of Individual Differences in Sleep Behavior of Free-Living Great Tits (Parus major). G3 (Bethesda) (2016) 0.77
MZ twin pairs or MZ singletons in population family-based GWAS? More power in pairs. Mol Psychiatry (2014) 0.77
Hypersomnia in Mood Disorders: a Rapidly Changing Landscape. Curr Sleep Med Rep (2015) 0.76
Novel human ABCC9/SUR2 brain-expressed transcripts and an eQTL relevant to hippocampal sclerosis of aging. J Neurochem (2015) 0.76
A systematic review of calcium channel antagonists in bipolar disorder and some considerations for their future development. Mol Psychiatry (2016) 0.76
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hum Mol Genet (2015) 0.75
Genetic Pathways to Insomnia. Brain Sci (2016) 0.75
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium. Sleep (2016) 0.75
Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants. PLoS One (2017) 0.75
SNPs, linkage disequilibrium, and chronic mountain sickness in Tibetan Chinese. Hypoxia (Auckl) (2017) 0.75
Human genetics and sleep behavior. Curr Opin Neurobiol (2017) 0.75
Overexpression of Fto leads to increased food intake and results in obesity. Nat Genet (2010) 4.37
SCFFbxl3 controls the oscillation of the circadian clock by directing the degradation of cryptochrome proteins. Science (2007) 3.59
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse. Curr Biol (2003) 3.31
Depression and generalized anxiety disorder: cumulative and sequential comorbidity in a birth cohort followed prospectively to age 32 years. Arch Gen Psychiatry (2007) 3.23
The after-hours mutant reveals a role for Fbxl3 in determining mammalian circadian period. Science (2007) 3.05
Adolescent irritability: phenotypic associations and genetic links with depressed mood. Am J Psychiatry (2011) 2.33
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr Biol (2008) 2.27
Prospective longitudinal associations between persistent sleep problems in childhood and anxiety and depression disorders in adulthood. J Abnorm Child Psychol (2005) 1.94
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study. Physiol Genomics (2008) 1.76
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice. Proc Natl Acad Sci U S A (2009) 1.66
The direction of longitudinal associations between sleep problems and depression symptoms: a study of twins aged 8 and 10 years. Sleep (2009) 1.55
Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouse. Nat Genet (2002) 1.48
Novel ENU-induced eye mutations in the mouse: models for human eye disease. Hum Mol Genet (2002) 1.41
When clocks go bad: neurobehavioural consequences of disrupted circadian timing. PLoS Genet (2008) 1.41
The structure of language abilities at 4 years: a twin study. Dev Psychol (2002) 1.32
Prenatal mood disturbance predicts sleep problems in infancy and toddlerhood. Early Hum Dev (2006) 1.30
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse. J Neurosci (2003) 1.29
Objective sleep in pediatric anxiety disorders and major depressive disorder. J Am Acad Child Adolesc Psychiatry (2008) 1.28
Etiologies of associations between childhood sleep and behavioral problems in a large twin sample. J Am Acad Child Adolesc Psychiatry (2004) 1.25
Novel phenotypes identified by plasma biochemical screening in the mouse. Mamm Genome (2002) 1.22
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Dis Model Mech (2009) 1.22
Juvenile mental health histories of adults with anxiety disorders. Am J Psychiatry (2007) 1.21
Diurnal preference and sleep quality: same genes? A study of young adult twins. Chronobiol Int (2010) 1.19
First genome-wide association study on anxiety-related behaviours in childhood. PLoS One (2013) 1.19
Feeling anxious: a twin study of panic/somatic ratings, anxiety sensitivity and heartbeat perception in children. J Child Psychol Psychiatry (2007) 1.16
Disentangling gene-environment correlations and interactions on adolescent depressive symptoms. J Child Psychol Psychiatry (2008) 1.15
Gene-environment interactions differentially affect mouse strain behavioral parameters. Mamm Genome (2006) 1.14
Associations between sleep problems, anxiety, and depression in twins at 8 years of age. Pediatrics (2006) 1.13
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Proc Natl Acad Sci U S A (2005) 1.07
A twin-study of sleep difficulties in school-aged children. Child Dev (2006) 1.07
Sleep quality and diurnal preference in a sample of young adults: associations with 5HTTLPR, PER3, and CLOCK 3111. Am J Med Genet B Neuropsychiatr Genet (2011) 1.06
Quantitative genetic research on sleep: a review of normal sleep, sleep disturbances and associated emotional, behavioural, and health-related difficulties. Sleep Med Rev (2012) 1.05
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features. J Clin Invest (2014) 1.04
Short-term serotonergic but not noradrenergic antidepressant administration reduces attentional vigilance to threat in healthy volunteers. Int J Neuropsychopharmacol (2008) 1.04
Links between antisocial behavior and depressed mood: the role of life events and attributional style. J Abnorm Child Psychol (2006) 1.04
Predicting outcomes following cognitive behaviour therapy in child anxiety disorders: the influence of genetic, demographic and clinical information. J Child Psychol Psychiatry (2013) 1.03
Associations between sleep quality and anxiety and depression symptoms in a sample of young adult twins and siblings. J Psychosom Res (2011) 1.02
Associations between behaviour problems and verbal and nonverbal cognitive abilities and disabilities in early childhood. J Child Psychol Psychiatry (2002) 1.02
Changes in genetic and environmental influences on depressive symptoms across adolescence and young adulthood. Br J Psychiatry (2006) 1.02
Therapygenetics: Using genetic markers to predict response to psychological treatment for mood and anxiety disorders. Biol Mood Anxiety Disord (2013) 1.01
Attributional style as a risk marker of genetic effects for adolescent depressive symptoms. J Abnorm Psychol (2008) 1.01
The genetics of mood disorders. Annu Rev Clin Psychol (2010) 1.00
Genetic influences on anxiety in children: what we've learned and where we're heading. Clin Child Fam Psychol Rev (2007) 1.00
Tuning the period of the mammalian circadian clock: additive and independent effects of CK1εTau and Fbxl3Afh mutations on mouse circadian behavior and molecular pacemaking. J Neurosci (2011) 0.99
I think, therefore I am: a twin study of attributional style in adolescents. J Child Psychol Psychiatry (2006) 0.97
Preliminary evidence for an association between social anxiety symptoms and avoidance of negative faces in school-age children. J Clin Child Adolesc Psychol (2006) 0.97
Obsessive-compulsive disorder, tics and anxiety in 6-year-old twins. Psychol Med (2006) 0.96
Assessing gene-environment interactions on anxiety symptom subtypes across childhood and adolescence. Dev Psychopathol (2007) 0.96
Heart-beat perception, panic/somatic symptoms and anxiety sensitivity in children. Behav Res Ther (2004) 0.96
Running endurance abnormality in mdx mice. Muscle Nerve (2002) 0.95
Distinct and separable roles for endogenous CRY1 and CRY2 within the circadian molecular clockwork of the suprachiasmatic nucleus, as revealed by the Fbxl3(Afh) mutation. J Neurosci (2013) 0.95
Genetic influences on the cognitive biases associated with anxiety and depression symptoms in adolescents. J Affect Disord (2009) 0.95
Heterogeneity in antisocial behaviours and comorbidity with depressed mood: a behavioural genetic approach. J Child Psychol Psychiatry (2008) 0.93
Examining the state-trait anxiety relationship: a behavioural genetic approach. J Abnorm Child Psychol (2006) 0.93
Individual differences in children's facial expression recognition ability: The role of nature and nurture. Dev Neuropsychol (2009) 0.92
Mutations in gasdermin 3 cause aberrant differentiation of the hair follicle and sebaceous gland. J Invest Dermatol (2005) 0.92
The development of antisocial behaviour from childhood to adolescence. A longitudinal twin study. Eur Child Adolesc Psychiatry (2005) 0.92
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2. J Bone Miner Res (2007) 0.91
A comparison of physiological and behavioural parameters in C57BL/6J mice undergoing food or water restriction regimes. Behav Brain Res (2006) 0.91
Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours. PLoS One (2012) 0.91
Is there room for 'development' in developmental models of information processing biases to threat in children and adolescents? Clin Child Fam Psychol Rev (2010) 0.91
Stringent requirement of a proper level of canonical WNT signalling activity for head formation in mouse embryo. Development (2011) 0.90
Behavioral genetic analyses of prosocial behavior in adolescents. Dev Sci (2009) 0.90
The Genesis 12-19 (G1219) Study: a twin and sibling study of gene-environment interplay and adolescent development in the UK. Twin Res Hum Genet (2013) 0.89
In the face of uncertainty: a twin study of ambiguous information, anxiety and depression in children. J Abnorm Child Psychol (2007) 0.89
Genes of experience: explaining the heritability of putative environmental variables through their association with behavioural and emotional traits. Behav Genet (2013) 0.89
A longitudinal, genetically informative, study of associations between anxiety sensitivity, anxiety and depression. Behav Genet (2012) 0.88
Longitudinal genetic analysis of anxiety sensitivity. Dev Psychol (2011) 0.88
Dependent negative life events and sleep quality: an examination of gene-environment interplay. Sleep Med (2011) 0.88
Phenotypic and genetic differentiation of anxiety-related behaviors in middle childhood. Depress Anxiety (2009) 0.88
Genetic and environmental influences on different components of the Pittsburgh Sleep Quality Index and their overlap. Sleep (2010) 0.87
Stable genetic influence on anxiety-related behaviours across middle childhood. J Abnorm Child Psychol (2012) 0.87
A systematic evaluation and validation of subtypes of adolescent alcohol use motives: genetic and environmental contributions. Alcohol Clin Exp Res (2010) 0.87
Pathways to childhood depressive symptoms: the role of social, cognitive, and genetic risk factors. Dev Psychol (2007) 0.87
Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model. Am J Hum Genet (2007) 0.86
A monozygotic twin differences study of nonshared environmental influence on adolescent depressive symptoms. Child Dev (2005) 0.84
Prevalence and genetic and environmental influences on anxiety disorders in 6-year-old twins. Psychol Med (2005) 0.83
Polymorphisms in the circadian expressed genes PER3 and ARNTL2 are associated with diurnal preference and GNβ3 with sleep measures. J Sleep Res (2014) 0.83
Anxiety sensitivity in adolescence and young adulthood: the role of stressful life events, 5HTTLPR and their interaction. Depress Anxiety (2012) 0.83
N-ethyl-N-nitrosourea mouse mutants in the dissection of behavioural and psychiatric disorders. Eur J Pharmacol (2003) 0.83