Published in Trends Genet on February 01, 2003
Heritability of cardiovascular and personality traits in 6,148 Sardinians. PLoS Genet (2006) 8.19
Runs of homozygosity in European populations. Am J Hum Genet (2008) 5.34
The distribution of fitness effects of new deleterious amino acid mutations in humans. Genetics (2006) 3.63
Genetic influence on human lifespan and longevity. Hum Genet (2006) 3.27
Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait. Nat Rev Genet (2010) 3.20
Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. Proc Natl Acad Sci U S A (2007) 2.81
Estimating selection on nonsynonymous mutations. Genetics (2005) 2.19
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases. Am J Epidemiol (2009) 2.15
Methodological Considerations in Studying Centenarians: Lessons Learned From the Georgia Centenarian Studies. Annu Rev Gerontol Geriatr (2007) 1.85
Effects of inbreeding, endogamy, genetic admixture, and outbreeding on human health: a (1001 Dalmatians) study. Croat Med J (2006) 1.64
A population threshold for functional polymorphisms. Genome Res (2003) 1.52
Quantitative genetics of age at reproduction in wild swans: support for antagonistic pleiotropy models of senescence. Proc Natl Acad Sci U S A (2006) 1.44
"10001 Dalmatians:" Croatia launches its national biobank. Croat Med J (2009) 1.38
Human genetics of infectious diseases: a unified theory. EMBO J (2007) 1.32
The impact of population demography and selection on the genetic architecture of complex traits. PLoS Genet (2014) 1.19
Genes, cognition, and communication: insights from neurodevelopmental disorders. Ann N Y Acad Sci (2009) 1.16
Evidence of inbreeding depression on human height. PLoS Genet (2012) 1.16
Genome-wide association study of anthropometric traits in Korcula Island, Croatia. Croat Med J (2009) 1.10
Directional dominance on stature and cognition in diverse human populations. Nature (2015) 1.07
Human genomic disease variants: a neutral evolutionary explanation. Genome Res (2012) 1.02
Negative selection on BRCA1 susceptibility alleles sheds light on the population genetics of late-onset diseases and aging theory. PLoS One (2007) 1.01
Functional polymorphisms of the brain serotonin synthesizing enzyme tryptophan hydroxylase-2. Cell Mol Life Sci (2006) 0.98
Demonstrating reduced environmental and genetic diversity in human isolates by analysis of blood lipid levels. Croat Med J (2006) 0.96
Common variant in myocilin gene is associated with high myopia in isolated population of Korcula Island, Croatia. Croat Med J (2009) 0.93
Genomics and epigenomics of the human glycome. Glycoconj J (2012) 0.90
Strategy for mapping quantitative trait loci (QTL) by using human metapopulations. Croat Med J (2006) 0.89
Consanguinity, endogamy, and genetic disorders in Tunisia. J Community Genet (2012) 0.86
Towards predictive genetic testing of complex diseases. Eur J Epidemiol (2006) 0.86
Micro-scale socioeconomic inequalities and health indicators in a small isolated community of Vis Island, Croatia. Croat Med J (2007) 0.84
A functional alternative splicing mutation in human tryptophan hydroxylase-2. Mol Psychiatry (2010) 0.83
High incidence of glucose-6-phosphate dehydrogenase deficiency in Croatian island isolate: example from Vis island, Croatia. Croat Med J (2006) 0.82
Neurogenetics II: complex disorders. J Neurol Neurosurg Psychiatry (2005) 0.81
Conference Scene: The great debate: genome-wide association studies in pharmacogenetics research, good or bad? Pharmacogenomics (2010) 0.79
Genomic architecture of inflammatory bowel disease in five families with multiple affected individuals. Hum Genome Var (2016) 0.78
The Effects of Background and Interference Selection on Patterns of Genetic Variation in Subdivided Populations. Genetics (2015) 0.77
Derived SNP alleles are used more frequently than ancestral alleles as risk-associated variants in common human diseases. J Bioinform Comput Biol (2012) 0.77
Human population structure, genome autozygosity and human health. Genome Med (2009) 0.77
A non-parametric approach for detecting gene-gene interactions associated with age-at-onset outcomes. BMC Genet (2014) 0.77
Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis Deformation. PLoS Genet (2016) 0.76
Co-morditities of environmental diseases: A common cause. Interdiscip Toxicol (2014) 0.76
Properties of human disease genes and the role of genes linked to Mendelian disorders in complex disease aetiology. Hum Mol Genet (2017) 0.75
Informed decision making about predictive DNA tests: arguments for more public visibility of personal deliberations about the good life. Med Health Care Philos (2010) 0.75
Detecting linkage between a trait and a marker in a random mating population without pedigree record. PLoS One (2009) 0.75
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Global, regional, and national causes of child mortality in 2008: a systematic analysis. Lancet (2010) 26.48
Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet (2012) 25.96
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet (2010) 23.08
Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature (2010) 20.01
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. Lancet (2010) 13.86
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature (2011) 13.25
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet (2008) 12.32
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet (2012) 11.09
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet (2007) 9.88
Global burden of childhood pneumonia and diarrhoea. Lancet (2013) 9.28
Epidemiology and etiology of childhood pneumonia. Bull World Health Organ (2008) 9.17
Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet (2010) 8.55
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet (2010) 7.94
Comparison of global estimates of prevalence and risk factors for peripheral artery disease in 2000 and 2010: a systematic review and analysis. Lancet (2013) 7.03
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet (2008) 6.97
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet (2008) 6.75
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet (2008) 6.26
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout. Nat Genet (2008) 5.93
New loci associated with kidney function and chronic kidney disease. Nat Genet (2010) 5.58
Global burden of respiratory infections due to seasonal influenza in young children: a systematic review and meta-analysis. Lancet (2011) 5.43
Runs of homozygosity in European populations. Am J Hum Genet (2008) 5.34
Causes of deaths in children younger than 5 years in China in 2008. Lancet (2010) 5.02
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet (2009) 4.97
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. N Engl J Med (2006) 4.95
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nat Genet (2012) 4.73
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science (2013) 4.71
Gaps in policy-relevant information on burden of disease in children: a systematic review. Lancet (2005) 4.64
Childhood pneumonia and diarrhoea: setting our priorities right. Lancet Infect Dis (2007) 4.42
Biological and biomedical implications of the co-evolution of pathogens and their hosts. Nat Genet (2002) 4.42
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat Genet (2012) 4.37
Evolution on the X chromosome: unusual patterns and processes. Nat Rev Genet (2006) 4.29
Direct estimation of per nucleotide and genomic deleterious mutation rates in Drosophila. Nature (2007) 4.27
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Nat Genet (2010) 4.20
Global estimate of the incidence of clinical pneumonia among children under five years of age. Bull World Health Organ (2005) 4.17
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet (2014) 4.13
Genome-wide association study identifies five loci associated with lung function. Nat Genet (2009) 4.10
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways. Diabetes (2010) 4.07
Global and regional burden of hospital admissions for severe acute lower respiratory infections in young children in 2010: a systematic analysis. Lancet (2013) 3.98
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. Nat Genet (2007) 3.93
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation (2011) 3.68
Abundant pleiotropy in human complex diseases and traits. Am J Hum Genet (2011) 3.60
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat Genet (2010) 3.55
Setting priorities in global child health research investments: guidelines for implementation of CHNRI method. Croat Med J (2008) 3.42
Interventions to address deaths from childhood pneumonia and diarrhoea equitably: what works and at what cost? Lancet (2013) 3.41
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet (2011) 3.40
Multilocus patterns of nucleotide variability and the demographic and selection history of Drosophila melanogaster populations. Genome Res (2005) 3.38
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet (2010) 3.37
The Lothian Birth Cohort 1936: a study to examine influences on cognitive ageing from age 11 to age 70 and beyond. BMC Geriatr (2007) 3.33
Epidemiology and etiology of childhood pneumonia in 2010: estimates of incidence, severe morbidity, mortality, underlying risk factors and causative pathogens for 192 countries. J Glob Health (2013) 3.30
Setting priorities for global mental health research. Bull World Health Organ (2009) 3.26
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet (2013) 3.25
Setting priorities in global child health research investments: assessment of principles and practice. Croat Med J (2007) 3.24
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet (2012) 3.21
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. Nat Genet (2012) 3.19
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. PLoS Genet (2009) 3.18
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat Genet (2012) 3.04
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Nat Genet (2011) 3.03
Epidemiology of Alzheimer's disease and other forms of dementia in China, 1990-2010: a systematic review and analysis. Lancet (2013) 3.02
Global and regional risk of disabling sequelae from bacterial meningitis: a systematic review and meta-analysis. Lancet Infect Dis (2010) 3.00