| 1 | Genetic variants associated with syncope implicate neural and autonomic processes | 2.3 | 18 | Citations (PDF) |
| 2 | Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study | 2.3 | 96 | Citations (PDF) |
| 3 | Sequence variants affecting voice pitch in humans | 11.0 | 16 | Citations (PDF) |
| 4 | Genome-wide association study on 13 167 individuals identifies regulators of blood CD34+cell levelsBlood, 2022, 139, 1659-1669 | 4.2 | 7 | Citations (PDF) |
| 5 | Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies | 5.5 | 14 | Citations (PDF) |
| 6 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation | 26.1 | 616 | Citations (PDF) |
| 7 | Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci | 2.3 | 17 | Citations (PDF) |
| 8 | Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis | 2.1 | 28 | Citations (PDF) |
| 9 | Thirty novel sequence variants impacting human intracranial volume | 3.6 | 7 | Citations (PDF) |
| 10 | Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in
<i>LDLR</i> | 3.3 | 22 | Citations (PDF) |
| 11 | Loss-of-Function Variants in the Tumor-Suppressor Gene <i>PTPN14</i> Confer Increased Cancer Risk | 0.6 | 27 | Citations (PDF) |
| 12 | Genetic insight into sick sinus syndrome | 2.3 | 48 | Citations (PDF) |
| 13 | Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency | 3.2 | 8 | Citations (PDF) |
| 14 | Germline variants at SOHLH2 influence multiple myeloma risk | 7.9 | 11 | Citations (PDF) |
| 15 | Distinction between the effects of parental and fetal genomes on fetal growth | 26.1 | 86 | Citations (PDF) |
| 16 | Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus | 3.0 | 32 | Citations (PDF) |
| 17 | Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour | 10.5 | 140 | Citations (PDF) |
| 18 | Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database | 3.2 | 5 | Citations (PDF) |
| 19 | Genetic variants associated with platelet count are predictive of human disease and physiological markers | 4.4 | 17 | Citations (PDF) |
| 20 | The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland | 7.4 | 56 | Citations (PDF) |
| 21 | Deciphering osteoarthritis genetics across 826,690 individuals from 9 populationsCell, 2021, 184, 4784-4818.e17 | 34.1 | 349 | Citations (PDF) |
| 22 | Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland | 6.3 | 21 | Citations (PDF) |
| 23 | Differences between germline genomes of monozygotic twins | 26.1 | 133 | Citations (PDF) |
| 24 | Large-scale integration of the plasma proteome with genetics and disease | 26.1 | 1,320 | Citations (PDF) |
| 25 | Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases | 2.0 | 11 | Citations (PDF) |
| 26 | Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood | 1.2 | 15 | Citations (PDF) |
| 27 | Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure | 13.9 | 745 | Citations (PDF) |
| 28 | A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies | 4.2 | 54 | Citations (PDF) |
| 29 | Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults | 10.4 | 47 | Citations (PDF) |
| 30 | Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming | 3.6 | 38 | Citations (PDF) |
| 31 | Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals | 26.1 | 167 | Citations (PDF) |
| 32 | Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease | 2.3 | 76 | Citations (PDF) |
| 33 | Humoral Immune Response to SARS-CoV-2 in Iceland | 43.7 | 896 | Citations (PDF) |
| 34 | Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus | 3.3 | 10 | Citations (PDF) |
| 35 | Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction | 13.9 | 105 | Citations (PDF) |
| 36 | FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease | 38.7 | 132 | Citations (PDF) |
| 37 | Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis | 13.9 | 91 | Citations (PDF) |
| 38 | Spread of SARS-CoV-2 in the Icelandic Population | 43.7 | 1,153 | Citations (PDF) |
| 39 | Sequence variants with large effects on cardiac electrophysiology and disease | 13.9 | 36 | Citations (PDF) |
| 40 | Disentangling the genetics of lean mass | 4.9 | 47 | Citations (PDF) |
| 41 | Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes | 3.6 | 17 | Citations (PDF) |
| 42 | Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | 13.9 | 207 | Citations (PDF) |
| 43 | Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels | 26.1 | 363 | Citations (PDF) |
| 44 | Characterizing mutagenic effects of recombination through a sequence-level genetic map | 36.4 | 378 | Citations (PDF) |
| 45 | Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution | 26.1 | 106 | Citations (PDF) |
| 46 | Genetic predisposition to mosaic Y chromosome loss in blood | 38.7 | 300 | Citations (PDF) |
| 47 | Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes | 2.4 | 182 | Citations (PDF) |
| 48 | A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis | 26.1 | 118 | Citations (PDF) |
| 49 | Genome-wide analysis yields new loci associating with aortic valve stenosis | 13.9 | 114 | Citations (PDF) |
| 50 | Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease | 2.3 | 67 | Citations (PDF) |
| 51 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes | 26.1 | 429 | Citations (PDF) |
| 52 | Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition | 26.1 | 162 | Citations (PDF) |
| 53 | The nature of nurture: Effects of parental genotypes | 36.4 | 915 | Citations (PDF) |
| 54 | Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis | 26.1 | 289 | Citations (PDF) |
| 55 | Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria | 3.3 | 472 | Citations (PDF) |
| 56 | Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps | 26.1 | 1,673 | Citations (PDF) |
| 57 | Insights into imprinting from parent-of-origin phased methylomes and transcriptomes | 26.1 | 118 | Citations (PDF) |
| 58 | Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma | 13.9 | 106 | Citations (PDF) |
| 59 | Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation | 4.4 | 50 | Citations (PDF) |
| 60 | A rare missense mutation in <i>MYH6</i> associates with non-syndromic coarctation of the aorta | 2.3 | 67 | Citations (PDF) |
| 61 | Relatedness disequilibrium regression estimates heritability without environmental bias | 26.1 | 186 | Citations (PDF) |
| 62 | Sequence variants associating with urinary biomarkers | 3.0 | 39 | Citations (PDF) |
| 63 | Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes | 26.1 | 1,550 | Citations (PDF) |
| 64 | Selection against variants in the genome associated with educational attainment | 7.6 | 161 | Citations (PDF) |
| 65 | Rare and low-frequency coding variants alter human adult height | 38.7 | 612 | Citations (PDF) |
| 66 | Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci | 12.5 | 209 | Citations (PDF) |
| 67 | Identification of sequence variants influencing immunoglobulin levels | 26.1 | 107 | Citations (PDF) |
| 68 | Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci | 26.1 | 150 | Citations (PDF) |
| 69 | An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans | 4.4 | 717 | Citations (PDF) |
| 70 | A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease | 3.0 | 21 | Citations (PDF) |
| 71 | Genetic variation at 16q24.2 is associated with small vessel stroke | 6.3 | 84 | Citations (PDF) |
| 72 | Whole genome characterization of sequence diversity of 15,220 Icelanders | 5.7 | 118 | Citations (PDF) |
| 73 | A Missense Variant in PLEC Increases Risk of Atrial Fibrillation | 2.4 | 81 | Citations (PDF) |
| 74 | Large meta-analysis of genome-wide association studies identifies five loci for lean body mass | 13.9 | 168 | Citations (PDF) |
| 75 | A frameshift deletion in the sarcomere gene<i>MYL4</i>causes early-onset familial atrial fibrillation | 2.3 | 117 | Citations (PDF) |
| 76 | Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus | 3.0 | 58 | Citations (PDF) |
| 77 | Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks | 26.1 | 520 | Citations (PDF) |
| 78 | Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity | 26.1 | 387 | Citations (PDF) |
| 79 | A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma | 3.3 | 140 | Citations (PDF) |
| 80 | Variant<i>ASGR1</i>Associated with a Reduced Risk of Coronary Artery Disease | 43.7 | 180 | Citations (PDF) |
| 81 | Physical and neurobehavioral determinants of reproductive onset and success | 26.1 | 179 | Citations (PDF) |
| 82 | Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses | 26.1 | 1,005 | Citations (PDF) |
| 83 | Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease | 26.1 | 246 | Citations (PDF) |
| 84 | Adiposity-Dependent Regulatory Effects on Multi-tissue Transcriptomes | 6.5 | 33 | Citations (PDF) |
| 85 | A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis | 13.9 | 56 | Citations (PDF) |
| 86 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape | 13.9 | 90 | Citations (PDF) |
| 87 | The rate of meiotic gene conversion varies by sex and age | 26.1 | 105 | Citations (PDF) |
| 88 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals | 26.1 | 410 | Citations (PDF) |
| 89 | Epigenetic and genetic components of height regulation | 13.9 | 60 | Citations (PDF) |
| 90 | Genome-wide association study identifies multiple susceptibility loci for multiple myeloma | 13.9 | 168 | Citations (PDF) |
| 91 | Genome-wide analysis identifies 12 loci influencing human reproductive behavior | 26.1 | 323 | Citations (PDF) |
| 92 | Genetic variants linked to education predict longevity | 7.6 | 125 | Citations (PDF) |
| 93 | Two Rare Mutations in the<i>COL1A2</i>Gene Associate With Low Bone Mineral Density and Fractures in Iceland | 5.0 | 41 | Citations (PDF) |
| 94 | Insertion of an SVA-E retrotransposon into the<i>CASP8</i>gene is associated with protection against prostate cancer | 3.0 | 28 | Citations (PDF) |
| 95 | Multi-nucleotide de novo Mutations in Humans | 3.3 | 127 | Citations (PDF) |
| 96 | Sequence variants from whole genome sequencing a large group of Icelanders | 5.7 | 69 | Citations (PDF) |
| 97 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study | 3.3 | 393 | Citations (PDF) |
| 98 | Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation | 3.3 | 84 | Citations (PDF) |
| 99 | A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease | 3.3 | 33 | Citations (PDF) |
| 100 | Rare coding variants and X-linked loci associated with age at menarche | 13.9 | 39 | Citations (PDF) |
| 101 | New genetic loci link adipose and insulin biology to body fat distribution | 38.7 | 1,561 | Citations (PDF) |
| 102 | Genetic studies of body mass index yield new insights for obesity biology | 38.7 | 4,431 | Citations (PDF) |
| 103 | Common Sequence Variants Associated With Coronary Artery Disease Correlate With the Extent of Coronary Atherosclerosis | 6.3 | 21 | Citations (PDF) |
| 104 | Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk | 1.6 | 28 | Citations (PDF) |
| 105 | Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at <i>CCND2</i> Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion | 4.4 | 29 | Citations (PDF) |
| 106 | Large-scale whole-genome sequencing of the Icelandic population | 26.1 | 762 | Citations (PDF) |
| 107 | The impact of low-frequency and rare variants on lipid levels | 26.1 | 347 | Citations (PDF) |
| 108 | Genetically Determined Height and Coronary Artery Disease | 43.7 | 244 | Citations (PDF) |
| 109 | Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair | 26.1 | 417 | Citations (PDF) |
| 110 | Common and rare variants associated with kidney stones and biochemical traits | 13.9 | 151 | Citations (PDF) |
| 111 | Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome | 13.9 | 361 | Citations (PDF) |
| 112 | Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma | 13.9 | 109 | Citations (PDF) |
| 113 | New basal cell carcinoma susceptibility loci | 13.9 | 66 | Citations (PDF) |
| 114 | Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci | 26.1 | 408 | Citations (PDF) |
| 115 | Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma | 3.0 | 53 | Citations (PDF) |
| 116 | A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus | 3.9 | 37 | Citations (PDF) |
| 117 | Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process | 13.9 | 96 | Citations (PDF) |
| 118 | Assessment of Osteoarthritis Candidate Genes in a Meta‐Analysis of Nine Genome‐Wide Association Studies | 7.4 | 116 | Citations (PDF) |
| 119 | A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip | 12.4 | 113 | Citations (PDF) |
| 120 | Rare mutations associating with serum creatinine and chronic kidney disease | 3.0 | 59 | Citations (PDF) |
| 121 | Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms | 34.1 | 122 | Citations (PDF) |
| 122 | Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease | 6.0 | 324 | Citations (PDF) |
| 123 | Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer | 3.0 | 53 | Citations (PDF) |
| 124 | Defining the role of common variation in the genomic and biological architecture of adult human height | 26.1 | 1,965 | Citations (PDF) |
| 125 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility | 26.1 | 1,030 | Citations (PDF) |
| 126 | Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | 26.1 | 320 | Citations (PDF) |
| 127 | Discovery and refinement of loci associated with lipid levels | 26.1 | 2,993 | Citations (PDF) |
| 128 | Ischemic stroke is associated with the <i>ABO</i> locus: The EuroCLOT study | 6.3 | 156 | Citations (PDF) |
| 129 | Variant of<i>TREM2</i>Associated with the Risk of Alzheimer's Disease | 43.7 | 2,415 | Citations (PDF) |
| 130 | A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm | 3.0 | 96 | Citations (PDF) |
| 131 | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture | 26.1 | 645 | Citations (PDF) |
| 132 | Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders | 26.1 | 308 | Citations (PDF) |
| 133 | Genetic Predisposition to Higher Blood Pressure Increases Coronary Artery Disease Risk | 6.9 | 74 | Citations (PDF) |
| 134 | Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits | 3.3 | 416 | Citations (PDF) |
| 135 | Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets | 3.3 | 155 | Citations (PDF) |
| 136 | The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis | 8.5 | 192 | Citations (PDF) |
| 137 | A Variant in
<i>LDLR</i>
Is Associated With Abdominal Aortic Aneurysm | 3.9 | 88 | Citations (PDF) |
| 138 | A genome-wide association study of early menopause and the combined impact of identified variants | 3.0 | 119 | Citations (PDF) |
| 139 | Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus | 26.1 | 294 | Citations (PDF) |
| 140 | Common and low-frequency variants associated with genome-wide recombination rate | 26.1 | 145 | Citations (PDF) |
| 141 | Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity | 2.4 | 36 | Citations (PDF) |
| 142 | Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis | 3.3 | 334 | Citations (PDF) |
| 143 | Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases | 3.3 | 206 | Citations (PDF) |
| 144 | Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study | 52.8 | 2,112 | Citations (PDF) |
| 145 | Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism | 2.4 | 168 | Citations (PDF) |
| 146 | Seventy-five genetic loci influencing the human red blood cell | 38.7 | 339 | Citations (PDF) |
| 147 | Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture | 26.1 | 1,190 | Citations (PDF) |
| 148 | Variants in<i>DENND1A</i>Are Associated with Polycystic Ovary Syndrome in Women of European Ancestry | 4.2 | 150 | Citations (PDF) |
| 149 | Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes | 26.1 | 1,863 | Citations (PDF) |
| 150 | Rate of de novo mutations and the importance of father’s age to disease risk | 38.7 | 2,087 | Citations (PDF) |
| 151 | Assessment of gene-by-sex interaction effect on bone mineral density | 5.0 | 50 | Citations (PDF) |
| 152 | Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways | 26.1 | 343 | Citations (PDF) |
| 153 | Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies | 18.4 | 483 | Citations (PDF) |
| 154 | Large-scale association analysis identifies new risk loci for coronary artery disease | 26.1 | 1,557 | Citations (PDF) |
| 155 | Common variants at VRK2 and TCF4 conferring risk of schizophrenia | 3.0 | 198 | Citations (PDF) |
| 156 | Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile | 26.1 | 311 | Citations (PDF) |
| 157 | Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22 | 12.4 | 133 | Citations (PDF) |
| 158 | A rare variant in MYH6 is associated with high risk of sick sinus syndrome | 26.1 | 288 | Citations (PDF) |
| 159 | Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1 | 6.5 | 204 | Citations (PDF) |
| 160 | Sequence variants at CYP1A1–CYP1A2 and AHR associate with coffee consumption | 3.0 | 135 | Citations (PDF) |
| 161 | Common genetic variants associated with open-angle glaucoma | 3.0 | 168 | Citations (PDF) |
| 162 | Genome-Wide Significant Association Between a Sequence Variant at 15q15.2 and Lung Cancer Risk | 0.6 | 27 | Citations (PDF) |
| 163 | Novel aspects of the pathogenesis of aneurysms of the abdominal aorta in humans | 5.7 | 334 | Citations (PDF) |
| 164 | Genome-wide association and genetic functional studies identify
<i>autism susceptibility candidate 2</i>
gene (
<i>AUTS2</i>
) in the regulation of alcohol consumption | 7.6 | 260 | Citations (PDF) |
| 165 | Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration | 3.0 | 242 | Citations (PDF) |
| 166 | European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene | 3.0 | 144 | Citations (PDF) |
| 167 | A sequence variant on 17q21 is associated with age at onset and severity of asthma | 3.2 | 133 | Citations (PDF) |
| 168 | Biological, clinical and population relevance of 95 loci for blood lipids | 38.7 | 3,429 | Citations (PDF) |
| 169 | Several common variants modulate heart rate, PR interval and QRS duration | 26.1 | 358 | Citations (PDF) |
| 170 | Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis | 26.1 | 1,700 | Citations (PDF) |
| 171 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution | 26.1 | 899 | Citations (PDF) |
| 172 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | 26.1 | 2,774 | Citations (PDF) |
| 173 | Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies | 26.1 | 476 | Citations (PDF) |
| 174 | Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes | 3.0 | 202 | Citations (PDF) |
| 175 | Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels | 12.7 | 147 | Citations (PDF) |
| 176 | Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases | 3.3 | 185 | Citations (PDF) |
| 177 | Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene | 3.3 | 88 | Citations (PDF) |
| 178 | Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies | 2.4 | 86 | Citations (PDF) |
| 179 | Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus | 3.3 | 85 | Citations (PDF) |
| 180 | European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations | 2.4 | 82 | Citations (PDF) |
| 181 | Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution | 3.3 | 466 | Citations (PDF) |
| 182 | Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design? | 3.3 | 63 | Citations (PDF) |
| 183 | Parental origin of sequence variants associated with complex diseases | 38.7 | 545 | Citations (PDF) |
| 184 | Variant in the sequence of the LINGO1 gene confers risk of essential tremor | 26.1 | 230 | Citations (PDF) |
| 185 | A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke | 26.1 | 463 | Citations (PDF) |
| 186 | Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies | 26.1 | 686 | Citations (PDF) |
| 187 | Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture | 10.4 | 259 | Citations (PDF) |
| 188 | Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke | 6.3 | 262 | Citations (PDF) |
| 189 | Genetics of gene expression and its effect on disease | 38.7 | 1,267 | Citations (PDF) |
| 190 | Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer | 26.1 | 419 | Citations (PDF) |
| 191 | Two newly identified genetic determinants of pigmentation in Europeans | 26.1 | 352 | Citations (PDF) |
| 192 | Detection of sharing by descent, long-range phasing and haplotype imputation | 26.1 | 440 | Citations (PDF) |
| 193 | Male-pattern baldness susceptibility locus at 20p11 | 26.1 | 130 | Citations (PDF) |
| 194 | Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer | 26.1 | 365 | Citations (PDF) |
| 195 | On the Replication of Genetic Associations: Timing Can Be Everything! | 6.5 | 130 | Citations (PDF) |
| 196 | A Drastic Reduction in the Life Span of Cystatin C L68Q Carriers Due to Life-Style Changes during the Last Two Centuries | 3.3 | 29 | Citations (PDF) |
| 197 | Multiple Genetic Loci for Bone Mineral Density and Fractures | 43.7 | 602 | Citations (PDF) |
| 198 | Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity | 26.1 | 1,300 | Citations (PDF) |
| 199 | New sequence variants associated with bone mineral density | 26.1 | 344 | Citations (PDF) |
| 200 | The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts | 3.3 | 135 | Citations (PDF) |
| 201 | A Genetic Risk Factor for Periodic Limb Movements in Sleep | 43.7 | 603 | Citations (PDF) |
| 202 | PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden | 2.4 | 40 | Citations (PDF) |
| 203 | Genetic determinants of hair, eye and skin pigmentation in Europeans | 26.1 | 702 | Citations (PDF) |
| 204 | The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland | 8.5 | 62 | Citations (PDF) |
| 205 | Familial Risk of Lung Carcinoma in the Icelandic Population | 17.1 | 110 | Citations (PDF) |
| 206 | Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family | 8.5 | 254 | Citations (PDF) |
| 207 | The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke | 26.1 | 873 | Citations (PDF) |
| 208 | Interstitial deletions including chromosome 3 common eliminated region 1 (C3CER1) prevail in human solid tumors from 10 different tissues | 3.0 | 24 | Citations (PDF) |
| 209 | Overexpression of the myeloid leukemia–associatedHoxa9 gene in bone marrow cells induces stem cell expansion | 4.2 | 324 | Citations (PDF) |
| 210 | Defining Roles for
HOX
and
MEIS1
Genes in Induction of Acute Myeloid Leukemia | 2.5 | 262 | Citations (PDF) |
| 211 | The Oncoprotein E2A-Pbx1a Collaborates with Hoxa9 To Acutely Transform Primary Bone Marrow Cells | 2.5 | 69 | Citations (PDF) |
| 212 | HOX HOMEOBOX GENES AS REGULATORS OF NORMAL AND LEUKEMIC HEMATOPOIESIS | 2.3 | 63 | Citations (PDF) |
| 213 | Overexpression of HOXB3 in Hematopoietic Cells Causes Defective Lymphoid Development and Progressive Myeloproliferation | 23.3 | 173 | Citations (PDF) |
