Published in Mol Psychiatry on November 22, 2011
Sleep: a health imperative. Sleep (2012) 2.01
Update on energy homeostasis and insufficient sleep. J Clin Endocrinol Metab (2012) 1.37
Targeting MDR in breast and lung cancer: discriminating its potential importance from the failure of drug resistance reversal studies. Drug Resist Updat (2012) 1.23
Glutathione peroxidase activity is neuroprotective in models of Huntington's disease. Nat Genet (2013) 1.20
Dissociation of circadian and circatidal timekeeping in the marine crustacean Eurydice pulchra. Curr Biol (2013) 1.17
Common genetic variants in ARNTL and NPAS2 and at chromosome 12p13 are associated with objectively measured sleep traits in the elderly. Sleep (2013) 1.03
Chronopharmacology: new insights and therapeutic implications. Annu Rev Pharmacol Toxicol (2013) 1.02
A genome-wide association study of sleep habits and insomnia. Am J Med Genet B Neuropsychiatr Genet (2013) 0.98
Neuroimaging, cognition, light and circadian rhythms. Front Syst Neurosci (2014) 0.97
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Mol Psychiatry (2014) 0.94
Identification of Redeye, a new sleep-regulating protein whose expression is modulated by sleep amount. Elife (2014) 0.93
Sleep duration and depressive symptoms: a gene-environment interaction. Sleep (2014) 0.92
Cross-translational studies in human and Drosophila identify markers of sleep loss. PLoS One (2013) 0.91
Genetic basis of human circadian rhythm disorders. Exp Neurol (2012) 0.90
Genetic analysis of circadian responses to low frequency electromagnetic fields in Drosophila melanogaster. PLoS Genet (2014) 0.89
Genetic association study of circadian genes with seasonal pattern in bipolar disorders. Sci Rep (2015) 0.85
African Genetic Ancestry is Associated with Sleep Depth in Older African Americans. Sleep (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
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
ABCC9/SUR2 in the brain: Implications for hippocampal sclerosis of aging and a potential therapeutic target. Ageing Res Rev (2015) 0.81
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. PLoS Genet (2016) 0.80
A twin and molecular genetics study of sleep paralysis and associated factors. J Sleep Res (2015) 0.80
A human sleep homeostasis phenotype in mice expressing a primate-specific PER3 variable-number tandem-repeat coding-region polymorphism. FASEB J (2014) 0.80
Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits. Nat Genet (2016) 0.79
Genetics and epigenetics of circadian rhythms and their potential roles in neuropsychiatric disorders. Neurosci Bull (2015) 0.79
Modeling the genetic basis for human sleep disorders in Drosophila. Commun Integr Biol (2013) 0.79
Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration. Am J Med Genet B Neuropsychiatr Genet (2015) 0.79
The Role of Genes in the Insomnia Phenotype. Sleep Med Clin (2013) 0.79
Common variants in DRD2 are associated with sleep duration: the CARe consortium. Hum Mol Genet (2015) 0.79
Genetic variants associated with sleep disorders. Sleep Med (2014) 0.78
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
Circadian Rhythms and Sleep in Drosophila melanogaster. Genetics (2017) 0.75
Surprising view of insomnia and sleeping pills. Sleep (2013) 0.75
Genetic Pathways to Insomnia. Brain Sci (2016) 0.75
Control of sleep by a network of cell cycle genes. Fly (Austin) (2015) 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
Human genetics and sleep behavior. Curr Opin Neurobiol (2017) 0.75
SNPs, linkage disequilibrium, and chronic mountain sickness in Tibetan Chinese. Hypoxia (Auckl) (2017) 0.75
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. Nature (1998) 15.24
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet (2013) 9.46
Puerperal thromboembolism and suppression of lactation. Lancet (1967) 8.22
Nonsteroidal antiinflammatory drugs and the risk of Alzheimer's disease. N Engl J Med (2001) 7.85
A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection. N Engl J Med (1996) 7.66
Absence of expression of the FMR-1 gene in fragile X syndrome. Cell (1991) 7.04
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med (1995) 6.73
Radon in homes and risk of lung cancer: collaborative analysis of individual data from 13 European case-control studies. BMJ (2004) 6.48
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. Am J Hum Genet (1998) 5.24
Serum IL-6 level and the development of disability in older persons. J Am Geriatr Soc (1999) 4.84
Bronchitis in two integrated steel works. I. Ventilatory capacity, age, and physique of non-bronchitic men. Br J Prev Soc Med (1968) 4.75
Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits. Proc Natl Acad Sci U S A (1997) 4.73
High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG. Eur J Hum Genet (2000) 4.63
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. Nature (2010) 4.52
Double-blind randomised controlled trial of folate treatment before conception to prevent recurrence of neural-tube defects. Br Med J (Clin Res Ed) (1981) 4.12
Natural family planning in the 1990s. Lancet (1995) 3.97
Genome-wide, large-scale production of mutant mice by ENU mutagenesis. Nat Genet (2000) 3.92
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis. Nat Genet (2000) 3.87
Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. Mol Psychiatry (2008) 3.68
A point mutation in the FMR-1 gene associated with fragile X mental retardation. Nat Genet (1993) 3.58
The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting. J Clin Endocrinol Metab (2001) 3.55
Obstetric practice and outcome of pregnancy in Cardiff residents 1965-73. Br Med J (1976) 3.54
Emphysema in coal workers' pneumoconiosis. Br Med J (1970) 3.48
Environmental epidemiology. IV. Chronic respiratory disease in an industrial town: a nine-year follow-up study. Preliminary report. Am J Public Health Nations Health (1968) 3.33
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). Nat Genet (1996) 3.31
Smoking and risk of dementia and Alzheimer's disease in a population-based cohort study: the Rotterdam Study. Lancet (1998) 3.26
The magnitude of mortality from acute respiratory infections in children under 5 years in developing countries. World Health Stat Q (1992) 3.14
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency. Am J Hum Genet (1998) 3.08
Noninvasive determination of age-related changes in the human arterial pulse. Circulation (1989) 3.08
Does television viewing increase obesity and reduce physical activity? Cross-sectional and longitudinal analyses among adolescent girls. Pediatrics (1993) 3.04
Naturalistic weight-reduction efforts prospectively predict growth in relative weight and onset of obesity among female adolescents. J Consult Clin Psychol (1999) 3.01
Characterization of porin and ompR mutants of a virulent strain of Salmonella typhimurium: ompR mutants are attenuated in vivo. Infect Immun (1989) 3.00
Weight-related attitudes and behaviors of black women. J Am Diet Assoc (1993) 2.93
Factors predicting the use of breast-conserving therapy in stage I and II breast carcinoma. J Clin Oncol (2001) 2.91
A new incompatibility locus in Neurospora crassa. Genetics (1966) 2.91
Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays. Genome Res (1997) 2.90
Rapid simulation of P values for product methods and multiple-testing adjustment in association studies. Am J Hum Genet (2005) 2.89
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome. Neuron (2005) 2.82
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. Nat Genet (2000) 2.82
Maternal use of antiepileptic drugs and the risk of major congenital malformations: a joint European prospective study of human teratogenesis associated with maternal epilepsy. Epilepsia (1997) 2.82
Genetic association of apolipoprotein E with age-related macular degeneration. Am J Hum Genet (1998) 2.82
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein. Hum Mol Genet (1998) 2.79
Weight concerns influence the development of eating disorders: a 4-year prospective study. J Consult Clin Psychol (1996) 2.76
Gastric emptying in health and in gastroduodenal disease. Gastroenterology (1968) 2.75
TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres. Gut (2011) 2.75
HETEROCARYOSIS AND PROTOPLASMIC INCOMPATIBILITY IN NEUROSPORA CRASSA. Proc Natl Acad Sci U S A (1956) 2.74
GATA3 haplo-insufficiency causes human HDR syndrome. Nature (2000) 2.73
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes. Neurology (2005) 2.69
Head trauma as a risk factor for Alzheimer's disease: a collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group. Int J Epidemiol (1991) 2.63
Assembling a clock for all seasons: are there M and E oscillators in the genes? J Biol Rhythms (2001) 2.62
Trend analysis of socioeconomic differentials in deaths from injury in childhood in Scotland, 1981-95. BMJ (1999) 2.59
How temperature changes reset a circadian oscillator. Science (1998) 2.56
Respiratory health and individual estimated exposure to traffic-related air pollutants in a cohort of young children. Occup Environ Med (2006) 2.55
Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study. Arch Neurol (1998) 2.53
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease. Neurology (2007) 2.51
Evaluation of a computerized field data collection system for health surveys. Bull World Health Organ (1991) 2.51
Dextran 70 in prophylaxis of thromboembolic disease after surgery: a clinically oriented randomized double-blind trial. Br Med J (1975) 2.51
Screening for people with a family history of colorectal cancer. BMJ (1997) 2.50
Circadian rhythm mutations in Drosophila melanogaster affect short-term fluctuations in the male's courtship song. Proc Natl Acad Sci U S A (1980) 2.50
Development and technical basis of simplified guidelines for emergency triage assessment and treatment in developing countries. WHO Integrated Management of Childhood Illness (IMCI) Referral Care Project. Arch Dis Child (1999) 2.49
Pursuit of thinness and onset of eating disorder symptoms in a community sample of adolescent girls: a three-year prospective analysis. Int J Eat Disord (1994) 2.49
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet (1998) 2.48
Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex. EMBO J (1988) 2.44
MITOP, the mitochondrial proteome database: 2000 update. Nucleic Acids Res (2000) 2.43
Familial aggregation of Parkinson's disease in Iceland. N Engl J Med (2000) 2.41
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene. Nat Genet (1992) 2.40
National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology. J Med Genet (2002) 2.39
Alcohol and tobacco consumption as risk factors for Alzheimer's disease: a collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group. Int J Epidemiol (1991) 2.36
Characterization and localization of the FMR-1 gene product associated with fragile X syndrome. Nature (1993) 2.36
Genetic risk of age-related maculopathy. Population-based familial aggregation study. Arch Ophthalmol (1998) 2.31
Comparison of the effects of dexamphetamine and 1-benzylpiperazine in former addicts. Eur J Clin Pharmacol (1973) 2.31
Pulmonary disability in coal workers' pneumoconiosis. Br Med J (1972) 2.29
Genome-wide association scan for five major dimensions of personality. Mol Psychiatry (2008) 2.29
Increased factor IX levels in puerperium during administration of diethylstilboestrol. Br Med J (1968) 2.29
A pilot evaluation of radiography of the acute abdomen. Clin Radiol (1984) 2.28
Assignment of circadian function for the Neurospora clock gene frequency. Nature (1999) 2.27
Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group. Am J Hum Genet (1997) 2.27
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease. Hum Mol Genet (1998) 2.26
Natural variation in a Drosophila clock gene and temperature compensation. Science (1997) 2.24
P-element transformation with period locus DNA restores rhythmicity to mutant, arrhythmic Drosophila melanogaster. Cell (1984) 2.24
FMRP expression as a potential prognostic indicator in fragile X syndrome. Am J Med Genet (1999) 2.23
Behaviour modification by in vitro mutagenesis of a variable region within the period gene of Drosophila. Nature (1987) 2.22
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE. Nat Genet (1994) 2.19
CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease. Neurology (2006) 2.19
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology (2008) 2.16
Informatics and medicine--from molecules to populations. Methods Inf Med (2008) 2.13
Y chromosomes traveling south: the cohen modal haplotype and the origins of the Lemba--the "Black Jews of Southern Africa". Am J Hum Genet (2000) 2.11
Body-image and eating disturbances predict onset of depression among female adolescents: a longitudinal study. J Abnorm Psychol (2000) 2.11
Breast-conserving therapy vs mastectomy in early-stage breast cancer: a meta-analysis of 10-year survival. Cancer J Sci Am (1997) 2.09
A PEST-like element in FREQUENCY determines the length of the circadian period in Neurospora crassa. EMBO J (2001) 2.08
A 5S rRNA/L5 complex is a precursor to ribosome assembly in mammalian cells. J Cell Biol (1988) 2.08
Evidence for a differential role of HPA-axis function, inflammation and metabolic syndrome in melancholic versus atypical depression. Mol Psychiatry (2012) 2.06