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#TitleJournalYearCitations
1Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disordersNature Genetics20101,034
2Genome-wide association study identifies five loci associated with lung functionNature Genetics2010518
3Aberrations of EZH2 in CancerClinical Cancer Research2011503
4In vivo equilibrium of proinflammatory IL-17+ and regulatory IL-10+ Foxp3+ RORγt+ T cellsJournal of Experimental Medicine2008491
5JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasmsNature Genetics2009365
6Common variants near CAV1 and CAV2 are associated with primary open-angle glaucomaNature Genetics2010357
7C-reactive protein and its role in metabolic syndrome: mendelian randomisation studyLancet, The2005300
8Phenotypic and functional analyses show stem cell-derived hepatocyte-like cells better mimic fetal rather than adult hepatocytesJournal of Hepatology2015271
9Subcellular Localization of ALMS1 Supports Involvement of Centrosome and Basal Body Dysfunction in the Pathogenesis of Obesity, Insulin Resistance, and Type 2 DiabetesDiabetes2005212
10Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panelBMC Genomics2008203
11Lack of Conventional Dendritic Cells Is Compatible with Normal Development and T Cell Homeostasis, but Causes Myeloid Proliferative SyndromeImmunity2008198
12Dendritic Cells Ameliorate Autoimmunity in the CNS by Controlling the Homeostasis of PD-1 Receptor+ Regulatory T CellsImmunity2012184
13The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysisProceedings of the National Academy of Sciences of the United States of America2002170
14Influence of matrix metalloproteinase genotype on cardiovascular disease susceptibility and outcomeCardiovascular Research2006156
15A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitusHuman Genetics2006147
16Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myelomaLeukemia2006141
17Role of the JAK–STAT pathway in myocardial injuryTrends in Molecular Medicine2007137
18Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevanceLeukemia2011131
19The Early Human Germ Cell Lineage Does Not Express SOX2 During In Vivo Development or upon In Vitro Culture1Biology of Reproduction2008116
20Proteome‐wide analyses of human hepatocytes during differentiation and dedifferentiationHepatology2013113
21Loss of Caspase-8 Protects Mice Against Inflammation-Related Hepatocarcinogenesis but Induces Non-Apoptotic Liver InjuryGastroenterology2011105
2213q deletion anatomy and disease progression in patients with chronic lymphocytic leukemiaLeukemia2011104
23Haplotypic analysis of the MMP-9 gene in relation to coronary artery diseaseJournal of Molecular Medicine200397
24Centriolar Association of ALMS1 and Likely Centrosomal Functions of the ALMS Motif–containing Proteins C10orf90 and KIAA1731Molecular Biology of the Cell201097
25King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) geneNeuromuscular Disorders201197
26Different autonomous myogenic cell populations revealed by ablation of Myf5-expressing cells during mouse embryogenesisDevelopment (Cambridge)200893
27The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasmsBlood201093
28Characterization and Multipotentiality of Human Fetal Femur-Derived Cells: Implications for Skeletal Tissue RegenerationStem Cells200692
29Properties of linkage disequilibrium (LD) mapsProceedings of the National Academy of Sciences of the United States of America200289
30Identification of a novel gene, FGFR1OP2, fused to FGFR1 in 8p11 myeloproliferative syndromeGenes Chromosomes and Cancer200489
31The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1Leukemia200585
32Standardisation of molecular monitoring for chronic myeloid leukaemiaBest Practice and Research in Clinical Haematology200985
33IL-13 receptor α 2: A regulator of IL-13 and IL-4 signal transduction in primary human fibroblastsJournal of Allergy and Clinical Immunology200684
34Differences in Matrix Metalloproteinase-1 and Matrix Metalloproteinase-12 Transcript Levels Among Carotid Atherosclerotic Plaques With Different Histopathological CharacteristicsStroke200483
35Association of Tumor Necrosis Factor-α Polymorphisms and Ozone-induced Change in Lung FunctionAmerican Journal of Respiratory and Critical Care Medicine200580
36The histone deacetylase inhibitors vorinostat and romidepsin downmodulate IL‐10 expression in cutaneous T‐cell lymphoma cellsBritish Journal of Pharmacology201178
37Haplotype Effect of the Matrix Metalloproteinase-1 Gene on Risk of Myocardial InfarctionCirculation Research200577
38Variation in the toll-like receptor 4 gene and susceptibility to myocardial infarctionPharmacogenetics and Genomics200575
39A map of the human genome in linkage disequilibrium unitsProceedings of the National Academy of Sciences of the United States of America200575
40The role of Toll-like receptors and related receptors of the innate immune system in asthmaCurrent Opinion in Allergy and Clinical Immunology200675
41Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxaHuman Mutation200673
42Timing of acquisition of deletion 13 in plasma cell dyscrasias is dependent on genetic contextHaematologica200968
43Effects of Polyclonal IgG Derived from Patients with Different Clinical Types of the Antiphospholipid Syndrome on Monocyte Signaling PathwaysJournal of Immunology201067
44Free radical scavenging inhibits STAT phosphorylation following in vivo ischemia/reperfusion injuryFASEB Journal200666
45Frequent upregulation of MYC in plasma cell leukemiaGenes Chromosomes and Cancer200965
46Urocortin prevents mitochondrial permeability transition in response to reperfusion injury indirectly by reducing oxidative stressAmerican Journal of Physiology - Heart and Circulatory Physiology200760
47Host Cytokine Genotype is Related to Adverse Prognosis and Systemic Inflammation in Gastro-Oesophageal CancerAnnals of Surgical Oncology200760
48EGF +61 gene polymorphism and susceptibility to and prognostic markers in cutaneous malignant melanomaInternational Journal of Cancer200359
49Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traitsHuman Molecular Genetics200457
50Feeding a protein-restricted diet during pregnancy induces altered epigenetic regulation of peroxisomal proliferator-activated receptor-α in the heart of the offspringJournal of Developmental Origins of Health and Disease201157