| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | A D Johnson | |
| P2860 | cites work | Clinical and hematologic findings in Noonan syndrome patients with PTPN11 gene mutations | Q59173912 |
| Platelet function and ABO blood group | Q69173054 | ||
| Epinephrine-induced platelet aggregation. A twin study | Q70799370 | ||
| Prevalence of impaired responsiveness to epinephrine in platelets among Japanese | Q71366333 | ||
| Genetic and environmental effects on blood cells | Q72581784 | ||
| Genetic influences on F cells and other hematologic variables: a twin heritability study | Q73295247 | ||
| v-ATPase V0 subunit d2-deficient mice exhibit impaired osteoclast fusion and increased bone formation | Q79383955 | ||
| Identification of ADRA2A polymorphisms related to shear-mediated platelet function | Q79947121 | ||
| Expression of cellular prion protein on platelets from patients with gray platelet or Hermansky-Pudlak syndrome and the protein's association with alpha-granules | Q80050272 | ||
| Identification of a unique co-operative phosphoinositide 3-kinase signaling mechanism regulating integrin alpha IIb beta 3 adhesive function in platelets | Q80730894 | ||
| Gene variants associated with deep vein thrombosis | Q80893876 | ||
| Quantitative trait loci for steady-state platelet count in mice | Q80947331 | ||
| Mean platelet volume as marker of restenosis after percutaneous transluminal coronary angioplasty in patients with stable and unstable angina pectoris | Q81813429 | ||
| Quantitative trait loci for porcine white blood cells and platelet-related traits in a White Duroc x Erhualian F resource population | Q83360016 | ||
| An open access database of genome-wide association results | Q95780251 | ||
| Heritability and demographic analyses in the large isolated population of Val Borbera suggest advantages in mapping complex traits genes | Q21142722 | ||
| Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study | Q21261432 | ||
| Genome-wide QTL mapping for three traits related to teat number in a White Duroc x Erhualian pig resource population | Q21261513 | ||
| Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1 | Q22010014 | ||
| IRAG mediates NO/cGMP-dependent inhibition of platelet aggregation and thrombus formation | Q24304178 | ||
| RGS18 is a myeloerythroid lineage-specific regulator of G-protein-signalling molecule highly expressed in megakaryocytes | Q24533459 | ||
| The Ashwell receptor mitigates the lethal coagulopathy of sepsis | Q24596452 | ||
| VAMP8/endobrevin is overexpressed in hyperreactive human platelets: suggested role for platelet microRNA | Q24609475 | ||
| Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants | Q24645076 | ||
| A HaemAtlas: characterizing gene expression in differentiated human blood cells | Q24646314 | ||
| CD226 mediates platelet and megakaryocytic cell adhesion to vascular endothelial cells | Q28185503 | ||
| Differential proteome analysis of TRAP-activated platelets: involvement of DOK-2 and phosphorylation of RGS proteins | Q28188035 | ||
| XPLN, a guanine nucleotide exchange factor for RhoA and RhoB, but not RhoC | Q28200973 | ||
| Heritability of platelet responsiveness to aspirin in activation pathways directly and indirectly related to cyclooxygenase-1 | Q28222652 | ||
| Platelet expression profiling and clinical validation of myeloid-related protein-14 as a novel determinant of cardiovascular events | Q28238975 | ||
| Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction | Q28308221 | ||
| Mean Platelet Volume on Admission Predicts Impaired Reperfusion and Long-Term Mortality in Acute Myocardial Infarction Treated With Primary Percutaneous Coronary Intervention | Q58841243 | ||
| Mean platelet volume is an independent risk factor for myocardial infarction but not for coronary artery disease | Q58959199 | ||
| A role of jumonji gene in proliferation but not differentiation of megakaryocyte lineage cells | Q28587124 | ||
| Cloning and characterization of a novel regulator of G protein signalling in human platelets | Q28611509 | ||
| CUBN is a gene locus for albuminuria | Q30428102 | ||
| Heritability of cardiovascular and personality traits in 6,148 Sardinians | Q33255344 | ||
| Sialyltransferase ST3Gal-IV operates as a dominant modifier of hemostasis by concealing asialoglycoprotein receptor ligands | Q33343091 | ||
| Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin | Q33369073 | ||
| Decreased platelet expression of myosin regulatory light chain polypeptide (MYL9) and other genes with platelet dysfunction and CBFA2/RUNX1 mutation: insights from platelet expression profiling | Q33373057 | ||
| Congenital disorders associated with platelet dysfunctions | Q33378658 | ||
| Role of sialic acid for platelet life span: exposure of beta-galactose results in the rapid clearance of platelets from the circulation by asialoglycoprotein receptor-expressing liver macrophages and hepatocytes | Q33384971 | ||
| Analysis of 12,517 inhabitants of a Sardinian geographic isolate reveals that predispositions to thrombocytopenia and thrombocytosis are inherited traits. | Q33391781 | ||
| Class prediction models of thrombocytosis using genetic biomarkers | Q33579530 | ||
| A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease | Q33596843 | ||
| Detection of quantitative trait loci affecting haematological traits in swine via genome scanning | Q33618370 | ||
| A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1. | Q33772964 | ||
| Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels | Q33773714 | ||
| Rap1b is required for normal platelet function and hemostasis in mice | Q33778323 | ||
| Genetic regulation of platelet receptor expression and function: application in clinical practice and drug development | Q33988457 | ||
| Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy | Q34019082 | ||
| Genome-wide association study of hematological and biochemical traits in a Japanese population | Q34097468 | ||
| The genetics of normal platelet reactivity | Q34282183 | ||
| Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function | Q34374101 | ||
| Thrombopoietin, the Mp1 ligand, is essential for full megakaryocyte development | Q34425414 | ||
| Genetic variants in ABCB1 and CYP2C19 and cardiovascular outcomes after treatment with clopidogrel and prasugrel in the TRITON-TIMI 38 trial: a pharmacogenetic analysis | Q34564576 | ||
| Complex haplotypes derived from noncoding polymorphisms of the intronless alpha2A-adrenergic gene diversify receptor expression | Q34600291 | ||
| Effect of CYP2C19 and ABCB1 single nucleotide polymorphisms on outcomes of treatment with ticagrelor versus clopidogrel for acute coronary syndromes: a genetic substudy of the PLATO trial | Q34622955 | ||
| Reduced-function CYP2C19 genotype and risk of adverse clinical outcomes among patients treated with clopidogrel predominantly for PCI: a meta-analysis | Q34624862 | ||
| Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-gamma and PTEN. | Q34652580 | ||
| Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists | Q34674600 | ||
| Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals | Q34997022 | ||
| A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium | Q35025798 | ||
| PRIMe: a method for characterization and evaluation of pleiotropic regions from multiple genome-wide association studies | Q35029368 | ||
| Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children. | Q35193732 | ||
| Using proteomics to identify potential therapeutic targets in platelets. | Q36078636 | ||
| Pharmacogenomics of platelet responsiveness to aspirin | Q36989841 | ||
| Inherited traits affecting platelet function. | Q37052328 | ||
| Mean platelet volume as a predictor of cardiovascular risk: a systematic review and meta-analysis. | Q37127450 | ||
| Pharmacogenetics of aspirin resistance: a comprehensive systematic review | Q37145122 | ||
| Junctional adhesion molecule A interacts with Afadin and PDZ-GEF2 to activate Rap1A, regulate beta1 integrin levels, and enhance cell migration | Q37146658 | ||
| A genome-wide association study identifies three loci associated with mean platelet volume | Q37156159 | ||
| A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function | Q37270690 | ||
| Dynamin 3 participates in the growth and development of megakaryocytes | Q37309541 | ||
| The low-frequency isoform of platelet glycoprotein VIb attenuates ligand-mediated signal transduction but not receptor expression or ligand binding. | Q37334622 | ||
| A novel variant in the platelet endothelial aggregation receptor-1 gene is associated with increased platelet aggregability | Q37336145 | ||
| The genetics of antiplatelet drug resistance | Q37344920 | ||
| Sequence variants in three loci influence monocyte counts and erythrocyte volume | Q37417876 | ||
| ABO-identical versus nonidentical platelet transfusion: a systematic review | Q37630711 | ||
| ACCF/AHA clopidogrel clinical alert: approaches to the FDA "boxed warning": a report of the American College of Cardiology Foundation Task Force on clinical expert consensus documents and the American Heart Association endorsed by the Society for Ca | Q37773051 | ||
| Platelet endothelial aggregation receptor 1 (PEAR1), a novel epidermal growth factor repeat-containing transmembrane receptor, participates in platelet contact-induced activation | Q38327516 | ||
| Comparison of platelet function tests in predicting clinical outcome in patients undergoing coronary stent implantation | Q38375573 | ||
| Quantitative trait loci for peripheral blood cell counts: a study in baboons | Q40205381 | ||
| Quantitative trait loci for baseline white blood cell count, platelet count, and mean platelet volume. | Q40376064 | ||
| Genetic and environmental contributions to platelet aggregation: the Framingham heart study. | Q40700314 | ||
| Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies | Q41735608 | ||
| The Gi-coupled P2Y12 receptor regulates diacylglycerol-mediated signaling in human platelets. | Q41883110 | ||
| Rap1b is critical for glycoprotein VI-mediated but not ADP receptor-mediated alpha2beta1 activation | Q42079343 | ||
| Effects of CYP2C19 genotype on outcomes of clopidogrel treatment | Q42846150 | ||
| The PFA-100R cannot detect blood group-dependent inhibition of platelet function by eptifibatide or abciximab at therapeutic plasma concentrations | Q43178534 | ||
| Influence of platelet size on outcome after myocardial infarction | Q43705998 | ||
| The low-frequency allele of the platelet collagen signaling receptor glycoprotein VI is associated with reduced functional responses and expression | Q44298394 | ||
| Subtype-selective antagonists of lysophosphatidic Acid receptors inhibit platelet activation triggered by the lipid core of atherosclerotic plaques | Q44529184 | ||
| Association of mean platelet volume with risk of stroke among 3134 individuals with history of cerebrovascular disease | Q44771742 | ||
| PKC-theta selectively controls the adhesion-stimulating molecule Rap1. | Q45124437 | ||
| Genetic evidence for a predominant role of PI3Kbeta catalytic activity in ITAM- and integrin-mediated signaling in platelets. | Q45974289 | ||
| A functional genomics approach reveals novel quantitative trait loci associated with platelet signaling pathways. | Q46017492 | ||
| Mean platelet volume and the extent of coronary artery disease: results from a large prospective study. | Q46019640 | ||
| Downregulation of platelet responsiveness upon contact with LDL by the protein-tyrosine phosphatases SHP-1 and SHP-2. | Q46190554 | ||
| Heritability of platelet function in families with premature coronary artery disease | Q46213168 | ||
| Variables that affect platelet function analyzer-100 (PFA-100) closure times and establishment of reference intervals in Korean adults. | Q46420093 | ||
| Genetic and environmental influences on the size and number of cells in the blood | Q47229206 | ||
| Prognostic role of mean platelet volume and platelet count in ischemic and hemorrhagic stroke | Q48324404 | ||
| Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease | Q48850540 | ||
| Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. | Q51773327 | ||
| Estimates of genetic and environmental contribution to 43 quantitative traits support sharing of a homogeneous environment in an isolated population from South Tyrol, Italy. | Q53028824 | ||
| The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans. | Q53533032 | ||
| The expression patterns of RGS transcripts in platelets. | Q53585529 | ||
| Transfer of differentiation signal by membrane microvesicles harboring hedgehog morphogens. | Q53617685 | ||
| An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. | Q55067329 | ||
| Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q | Q56959481 | ||
| High platelet volume and increased risk of myocardial infarction: 39 531 participants from the general population | Q58007630 | ||
| P304 | page(s) | 246-257 | |
| P577 | publication date | 2011-07-01 | |
| P1433 | published in | Journal of Thrombosis and Haemostasis | Q6296004 |
| P1476 | title | The genetics of common variation affecting platelet development, function and pharmaceutical targeting | |
| P478 | volume | 9 Suppl 1 |
| Q37432574 | A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects |
| Q40618496 | Association of frequent genetic variants in platelet activation pathway genes with large-vessel ischemic stroke in Polish population. |
| Q35689156 | Cardiovascular correlates of platelet count and volume in the Framingham Heart Study |
| Q37066578 | Characterization of the platelet transcriptome by RNA sequencing in patients with acute myocardial infarction |
| Q38857206 | Common genetic variants in platelet surface receptors and its association with ischemic stroke |
| Q92132610 | Development of a Bioinformatics Framework for Identification and Validation of Genomic Biomarkers and Key Immunopathology Processes and Controllers in Infectious and Non-infectious Severe Inflammatory Response Syndrome |
| Q92718588 | GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort |
| Q34663589 | Genetic sequence analysis of inherited bleeding diseases |
| Q30840174 | Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia |
| Q40315017 | Platelet volume is associated with the Framingham risk score for cardiovascular disease in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil). |
| Q30276496 | Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals |
| Q38947978 | Replication and hematological characterization of human platelet reactivity genetic associations in men from the Caerphilly Prospective Study (CaPS). |
| Q39147666 | Standardization and reference intervals of platelet volume indices: Insight from the Brazilian longitudinal study of adult health (ELSA-BRASIL). |
| Q33442981 | The genetics of platelet count and volume in humans. |
| Q50673868 | Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation. |
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