Published in Genet Epidemiol on January 01, 1999
Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype? Am J Hum Genet (2000) 4.74
A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. Am J Hum Genet (1999) 2.15
A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. Am J Hum Genet (2006) 2.14
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nat Genet (2010) 2.04
Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Res (2011) 1.58
Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. Am J Hum Genet (2009) 1.51
The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics. PLoS One (2012) 1.49
Risk Factors and Relationship of Cutaneous and Uveal Melanocytic Lesions in Monozygotic and Dizygotic Twin Pairs. PLoS One (2016) 1.40
Genetic regulation of acquired immune responses to antigens of Mycobacterium tuberculosis: a study of twins in West Africa. Infect Immun (2001) 1.29
Heritability and genetic covariation of sensitivity to PROP, SOA, quinine HCl, and caffeine. Chem Senses (2006) 1.24
Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma. J Natl Cancer Inst (2014) 1.19
Genetic contribution to individual variation in binocular rivalry rate. Proc Natl Acad Sci U S A (2010) 1.08
Whole genome association scan for genetic polymorphisms influencing information processing speed. Biol Psychol (2010) 1.07
Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. BMC Med Genet (2011) 1.06
High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertil Steril (2011) 0.89
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Hum Mol Genet (2014) 0.87
Dissection of genetic associations with language-related traits in population-based cohorts. J Neurodev Disord (2011) 0.87
The etiology and molecular genetics of human pigmentation disorders. Wiley Interdiscip Rev Dev Biol (2012) 0.87
Genomewide scans of red cell indices suggest linkage on chromosome 6q23. J Med Genet (2006) 0.82
Association between melanocytic nevi and risk of breast diseases: The French E3N prospective cohort. PLoS Med (2014) 0.82
Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein. PLoS One (2012) 0.81
Five endometrial cancer risk loci identified through genome-wide association analysis. Nat Genet (2016) 0.80
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer. Endocr Relat Cancer (2015) 0.78
Accurate Imputation-Based Screening of Gln368Ter Myocilin Variant in Primary Open-Angle Glaucoma. Invest Ophthalmol Vis Sci (2015) 0.77
Assessment of PALB2 as a candidate melanoma susceptibility gene. PLoS One (2014) 0.77
Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis. Fertil Steril (2014) 0.75
Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric item response theory. BMC Psychiatry (2017) 0.75
NMRPipe: a multidimensional spectral processing system based on UNIX pipes. J Biomol NMR (1995) 93.94
B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion. Nat Med (1999) 16.91
A growth chart for premature and other infants. Arch Dis Child (1971) 8.04
Longitudinal effects of aging on serum total and free testosterone levels in healthy men. Baltimore Longitudinal Study of Aging. J Clin Endocrinol Metab (2001) 7.53
A beta peptide immunization reduces behavioural impairment and plaques in a model of Alzheimer's disease. Nature (2001) 6.78
Solution structure of a calmodulin-target peptide complex by multidimensional NMR. Science (1992) 6.16
Genetic and environmental contributions to alcohol dependence risk in a national twin sample: consistency of findings in women and men. Psychol Med (1997) 5.69
Abnormal bacterial colonisation of the genital tract and subsequent preterm delivery and late miscarriage. BMJ (1994) 5.07
Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype? Am J Hum Genet (2000) 4.74
Early-onset amyloid deposition and cognitive deficits in transgenic mice expressing a double mutant form of amyloid precursor protein 695. J Biol Chem (2001) 4.51
ALVAC-SIV-gag-pol-env-based vaccination and macaque major histocompatibility complex class I (A*01) delay simian immunodeficiency virus SIVmac-induced immunodeficiency. J Virol (2002) 4.11
B7-H3: a costimulatory molecule for T cell activation and IFN-gamma production. Nat Immunol (2001) 4.10
Measurement of homo- and heteronuclear J couplings from quantitative J correlation. Methods Enzymol (1994) 3.97
Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Mol Psychiatry (2008) 3.85
Randomised trial of personalised computer based information for cancer patients. BMJ (1999) 3.82
Demonstration of a spaser-based nanolaser. Nature (2009) 3.81
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol Psychiatry (2007) 3.49
Biological activities and molecular targets of the human papillomavirus E7 oncoprotein. Oncogene (2001) 3.44
Mechanism of NO-induced oxidation of myoglobin and hemoglobin. Biochemistry (1996) 3.36
What more do we have to do? Br Dent J (1992) 3.12
Prevalent vertebral deformities predict hip fractures and new vertebral deformities but not wrist fractures. Study of Osteoporotic Fractures Research Group. J Bone Miner Res (1999) 3.08
Model-fitting approaches to the analysis of human behaviour. Heredity (Edinb) (1978) 3.02
Vive la difference. Br Dent J (2001) 3.01
Origin and molecular changes associated with emergence of a highly pathogenic H5N2 influenza virus in Mexico. Virology (1995) 2.99
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. Mol Psychiatry (2010) 2.95
Student debt. Br Dent J (1995) 2.65
One-year outcome of elderly and young patients admitted to intensive care units. Crit Care Med (1993) 2.58
The heritability of general cognitive ability increases linearly from childhood to young adulthood. Mol Psychiatry (2009) 2.52
The genetical analysis of covariance structure. Heredity (Edinb) (1977) 2.45
Distinct functional and pharmacological properties of tonic and quantal inhibitory postsynaptic currents mediated by gamma-aminobutyric acid(A) receptors in hippocampal neurons. Mol Pharmacol (2001) 2.43
Prevalence of faecal incontinence in adults aged 40 years or more living in the community. Gut (2002) 2.41
Genetic and environmental causes of variation in basal levels of blood cells. Twin Res (1999) 2.36
Relating body mass index to figural stimuli: population-based normative data for Caucasians. Int J Obes Relat Metab Disord (2001) 2.36
Quality of life measures before and one year after admission to an intensive care unit. Crit Care Med (1995) 2.35
Common genetic risk factors for conduct disorder and alcohol dependence. J Abnorm Psychol (1998) 2.30
A whole genome association study of neuroticism using DNA pooling. Mol Psychiatry (2007) 2.30
Anthropometric determination of leg fat and muscle plus bone volumes in young male and female adults. J Physiol (1969) 2.28
Combined effects of obesity, acid reflux and smoking on the risk of adenocarcinomas of the oesophagus. Gut (2007) 2.28
Histopathology of ischemic optic neuropathy. Am J Ophthalmol (1970) 2.24
The power of the classical twin study. Heredity (Edinb) (1978) 2.23
Childhood sun exposure as a risk factor for melanoma: a systematic review of epidemiologic studies. Cancer Causes Control (2001) 2.21
Inferring the direction of causation in cross-sectional twin data: theoretical and empirical considerations. Genet Epidemiol (1994) 2.20
Modulation of T-cell-mediated immunity in tumor and graft-versus-host disease models through the LIGHT co-stimulatory pathway. Nat Med (2000) 2.18
A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. Am J Hum Genet (1999) 2.15
Identifying variables associated with inaccurate self-monitoring of blood glucose: proposed guidelines to improve accuracy. Diabetes Educ (2002) 2.12
Genetics of asthma and hay fever in Australian twins. Am Rev Respir Dis (1990) 2.12
Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci. Am J Hum Genet (1992) 2.12
The genetics of smoking persistence in men and women: a multicultural study. Behav Genet (1999) 2.11
Gastric emptying in acute overdose: a prospective randomised controlled trial. Med J Aust (1995) 2.10
Altered glucose metabolism in microvessels from patients with Alzheimer's disease. Ann Neurol (1989) 2.08
Genetic models for the natural history of smoking: evidence for a genetic influence on smoking persistence. Addict Behav (1993) 2.07
Natural selection and quantitative genetics of life-history traits in Western women: a twin study. Evolution (2001) 2.06
Tissue donation: benefits, legal issues and the nurse's role. Nurs Stand (2006) 2.05
Genetic and environmental contributions to cannabis dependence in a national young adult twin sample. Psychol Med (2002) 2.04
Dentists in the chair. Br Dent J (1998) 2.04
Future of the CDS. Community Dental Service. Br Dent J (1997) 2.03
The first step. Br Dent J (1994) 2.03
How much does it cost? Br Dent J (2001) 2.03
Want or need? Br Dent J (1995) 2.03
The scientific method. Br Dent J (1994) 2.03
Paradigm busters. Br Dent J (1997) 2.02
Nothing but the evidence. Br Dent J (1998) 2.02
The dentist's responsibility? Br Dent J (1993) 2.01
Genetic differences in alcohol sensitivity and the inheritance of alcoholism risk. Psychol Med (1999) 2.01
Fraud in dentistry. Br Dent J (1998) 2.00
Meta-analysis of genome-wide association studies for personality. Mol Psychiatry (2010) 1.96
Protective role of appendicectomy on onset and severity of ulcerative colitis and Crohn's disease. Gut (2002) 1.96
Time course of vasospasm in man. J Neurosurg (1978) 1.93
NHS or private--a balanced choice. Br Dent J (1996) 1.93
Safety in radiation. Br Dent J (1992) 1.92
Clinically essential. Br Dent J (1995) 1.91
Epidemiology of endometrial cancer. Best Pract Res Clin Obstet Gynaecol (2001) 1.90
Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins. Am J Hum Genet (2000) 1.89
Acute myoglobinuria associated with heroin addiction. JAMA (1971) 1.88
Quantitative studies of dorsal root ganglia and neuropathologic observations on spinal cords in familial dysautonomia. J Neurol Sci (1978) 1.87
Poiseuille and his law. Anaesthesia (1976) 1.81
Monitoring osteoporosis therapy with bone densitometry: misleading changes and regression to the mean. Fracture Intervention Trial Research Group. JAMA (2000) 1.79
Costimulation of T cells by B7-H2, a B7-like molecule that binds ICOS. Blood (2000) 1.76
Symptoms of anxiety and symptoms of depression. Same genes, different environments? Arch Gen Psychiatry (1987) 1.75
Suicidal behaviour: an epidemiological and genetic study. Psychol Med (1998) 1.74
Gastric mucus: isolation and polymeric structure of the undegraded glycoprotein: its breakdown by pepsin. Gastroenterology (1980) 1.74
Genetic covariation between neuroticism and the symptoms of anxiety and depression. Genet Epidemiol (1984) 1.73
Use of statins in general practices, 1996-8: cross sectional study. BMJ (2000) 1.73
Cigarette smoking and diabetic retinopathy. Diabetes (1977) 1.71
Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair. Hum Mol Genet (1997) 1.70
Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma. J Invest Dermatol (2001) 1.69
B7-H1 costimulation preferentially enhances CD28-independent T-helper cell function. Blood (2001) 1.69
Aid to diagnosis of melanoma in primary medical care. BMJ (1995) 1.68
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. Am J Hum Genet (2001) 1.67
Stimulated emission of surface plasmon polaritons. Phys Rev Lett (2008) 1.67
Increased DNA methylation at the AXIN1 gene in a monozygotic twin from a pair discordant for a caudal duplication anomaly. Am J Hum Genet (2006) 1.66