Published in Heredity (Edinb) on December 09, 2009
'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture. Investig Genet (2015) 1.39
The GenoChip: a new tool for genetic anthropology. Genome Biol Evol (2013) 1.12
Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits. Am J Hum Genet (2013) 0.92
Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island. Gene (2011) 0.83
An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. PLoS One (2012) 0.81
Serum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate. BMC Genet (2015) 0.75
A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers. PLoS Genet (2015) 0.75
Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate. Mol Vis (2017) 0.75
Increased accuracy of artificial selection by using the realized relationship matrix. Genet Res (Camb) (2009) 8.38
Strategies to utilize marker-quantitative trait loci associations. J Dairy Sci (1998) 4.91
Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Mol Psychiatry (2011) 4.16
Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Bioinformatics (2012) 3.97
Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Mol Psychiatry (2008) 3.85
Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner. Nat Genet (2000) 3.05
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. Mol Psychiatry (2010) 2.95
Beta-actin--an unsuitable internal control for RT-PCR. Mol Cell Probes (2001) 2.84
The pathogenesis of oral lichen planus. Crit Rev Oral Biol Med (2002) 2.78
Parents' accounts of obtaining a diagnosis of childhood cancer. Lancet (2001) 2.62
XVI. International Union of Pharmacology recommendations for the nomenclature of neuropeptide Y, peptide YY, and pancreatic polypeptide receptors. Pharmacol Rev (1998) 2.58
Mapping quantitative trait loci in complex pedigrees: a two-step variance component approach. Genetics (2000) 2.51
Strategies for reducing treatment default in drug-resistant tuberculosis: systematic review and meta-analysis. Int J Tuberc Lung Dis (2012) 2.09
Garden bird mortalities. Vet Rec (1995) 2.06
Meta-analysis of genome-wide association studies for personality. Mol Psychiatry (2010) 1.96
Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Mol Psychiatry (2011) 1.86
Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Mol Psychiatry (2011) 1.84
Estimation of linkage disequilibrium in a sample of the United Kingdom dairy cattle population using unphased genotypes. J Anim Sci (2003) 1.77
An autosomal genetic linkage map of the sheep genome. Genetics (1995) 1.75
Combined analyses of data from quantitative trait loci mapping studies. Chromosome 4 effects on porcine growth and fatness. Genetics (2000) 1.73
Highly prolific Booroola sheep have a mutation in the intracellular kinase domain of bone morphogenetic protein IB receptor (ALK-6) that is expressed in both oocytes and granulosa cells. Biol Reprod (2001) 1.71
The effects of red bull energy drink on human performance and mood. Amino Acids (2001) 1.71
Regional sympathetic nervous activity and oxygen consumption in obese normotensive human subjects. Circulation (1997) 1.60
Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Transl Psychiatry (2012) 1.52
Association of A vitamin D receptor polymorphism with sporadic breast cancer development. Int J Cancer (1999) 1.46
Necrotising fasciitis. Appropriate skin flap may reduce deformity. BMJ (1994) 1.46
Sheep linkage mapping: nineteen linkage groups derived from the analysis of paternal half-sib families. Genetics (1994) 1.43
Thymus-derived lymphocytes produce an immunologically specific macrophage-arming factor. J Exp Med (1972) 1.43
Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning. Lancet (2001) 1.43
Twin study of genetic and environmental influences on glucose tolerance and indices of insulin sensitivity and secretion. Diabetologia (2003) 1.42
Are there common genetic and environmental factors behind the endophenotypes associated with the metabolic syndrome? Diabetologia (2007) 1.40
Influence of family history on frequency of glucagon receptor Gly40Ser mutation in hypertensive subjects. Hypertension (1997) 1.39
Twin study of genetic and environmental influences on adult body size, shape, and composition. Int J Obes Relat Metab Disord (2004) 1.39
A genome scan for quantitative trait loci in a wild population of red deer (Cervus elaphus). Genetics (2002) 1.34
Inhalation aromatherapy during radiotherapy: results of a placebo-controlled double-blind randomized trial. J Clin Oncol (2003) 1.31
Association of a polymorphism of the angiotensin I-converting enzyme gene with essential hypertension. Biochem Biophys Res Commun (1992) 1.30
The sheep gene map database (SheepBase) is now available on the World Wide Web. Mamm Genome (1996) 1.30
Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936. Genes Brain Behav (2008) 1.29
A localized negative genetic correlation constrains microevolution of coat color in wild sheep. Science (2008) 1.27
A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Mol Psychiatry (2012) 1.21
A nonparametric bootstrap method for testing close linkage vs. pleiotropy of coincident quantitative trait loci. Genetics (1998) 1.21
Deficits in memory and hippocampal long-term potentiation in mice with reduced calbindin D28K expression. Proc Natl Acad Sci U S A (1996) 1.19
Empirical nonparametric bootstrap strategies in quantitative trait loci mapping: conditioning on the genetic model. Genetics (1998) 1.17
Monoamine oxidase and tobacco dependence. Neurotoxicology (2006) 1.15
Identifying participation rates at outpatient cardiac rehabilitation programs in Victoria, Australia. J Cardiopulm Rehabil (2000) 1.14
Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep. Proc Biol Sci (2007) 1.13
Parental assignment in fish using microsatellite genetic markers with finite numbers of parents and offspring. Anim Genet (2002) 1.12
Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. Genomics (2001) 1.11
Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G x E) interaction. Int J Obes (Lond) (2008) 1.11
Immunologically specific activation of macrophages armed with the specific macrophage arming factor (SMAF). Proc Soc Exp Biol Med (1973) 1.10
A randomised controlled trial of prehospital intravenous fluid replacement therapy in serious trauma. Health Technol Assess (2000) 1.10
Determination of genetic relationships among five indigenous Chinese goat breeds with six microsatellite markers. Anim Genet (1999) 1.09
A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42. Mol Psychiatry (2004) 1.08
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Mol Psychiatry (2011) 1.08
Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations. Hum Mol Genet (2003) 1.08
Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant? Eur J Med Genet (2010) 1.08
Power to detect QTL in a free-living polygynous population. Heredity (Edinb) (1999) 1.08
Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults. Mol Psychiatry (2009) 1.07
Linkage disequilibrium analysis in the genetically isolated Norfolk Island population. Heredity (Edinb) (2007) 1.06
Flow cytometric quantitation of DNA and c-myc oncoprotein in archival biopsies of uterine cervix neoplasia. Br J Cancer (1987) 1.05
Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives. Clin Genet (1995) 1.04
Familial typical migraine: significant linkage and localization of a gene to Xq24-28. Hum Genet (2000) 1.04
Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes Brain Behav (2008) 1.03
Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Mol Psychiatry (2011) 1.03
Mapping of quantitative trait loci on porcine chromosome 4. Anim Genet (1998) 1.02
Linkage mapping of wool keratin and keratin-associated protein genes in sheep. Mamm Genome (1997) 1.01
Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and breast cancer susceptibility. Cancer Lett (2000) 1.00
Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine. Neurogenetics (2000) 1.00
Effect of the BDNF V166M polymorphism on working memory in healthy adolescents. Genes Brain Behav (2006) 1.00
Association of estrogen receptor and glucocorticoid receptor gene polymorphisms with sporadic breast cancer. Int J Cancer (2001) 0.99
On the use of linear regression and maximum likelihood for QTL mapping in half-sib designs. Genet Res (1998) 0.99
Mapping of quantitative trait loci for growth and carcass traits in commercial sheep populations. J Anim Sci (2004) 0.99
The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data. Transl Psychiatry (2011) 0.99
Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation. Mol Psychiatry (2009) 0.98
Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin. Transl Psychiatry (2013) 0.98
Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity. Neurology (1998) 0.97
22q11 deletion: a multisystem disorder requiring multidisciplinary input. Arch Dis Child (2003) 0.97
Linkage mapping of CVD risk traits in the isolated Norfolk Island population. Hum Genet (2008) 0.97
Changes in pulsatile LH secretion after ovariectomy in Ile-de-France ewes in two seasons. J Reprod Fertil (1985) 0.95
A genome-wide association study for reading and language abilities in two population cohorts. Genes Brain Behav (2013) 0.95
Acetylcholine receptor antibody in the diagnosis of myasthenia gravis. Med J Aust (1983) 0.95
Elevated total body noradrenaline spillover in normotensive members of hypertensive families. Clin Sci (Lond) (1993) 0.95
Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. Int J Obes (Lond) (2008) 0.95
G-protein beta3 subunit gene (GNB3) variant in causation of essential hypertension. Hypertension (1998) 0.95
Evidence for an X-linked genetic component in familial typical migraine. Hum Mol Genet (1998) 0.94
Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci. Int J Obes (Lond) (2009) 0.94
Genomic imprinting of the insulin-like growth factor 2 gene in sheep. Mamm Genome (1999) 0.94
The genetics of cognitive processes: candidate genes in humans and animals. Behav Genet (2001) 0.93
Effects of aging on epinephrine secretion and regional release of epinephrine from the human heart. J Clin Endocrinol Metab (1995) 0.93
Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Transl Psychiatry (2011) 0.93