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171 peer-reviewed articles • 25,227 peer-reviewed citations • Sorted by year • Download PDF (PDF by citations)
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1The common, VTE-protective, G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding
Blood Advances, 2025, 9, 132-142
3.72Citations (PDF)
2Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Nature Genetics, 2024, 56, 1090-1099
14.964Citations (PDF)
3The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants
Blood, 2023, 142, 2055-2068
5.821Citations (PDF)
4A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk
Blood, 2023, 142, 1895-1908
5.88Citations (PDF)
5A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Nature Communications, 2023, 14, 1-19
11.426Citations (PDF)
6Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing
IScience, 2023, 26, 108214
2.611Citations (PDF)
7G protein–coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1
Blood Advances, 2022, 6, 2319-2330
3.725Citations (PDF)
8Circular RNAs exhibit limited evidence for translation, or translation regulation of the mRNA counterpart in terminal hematopoiesis
Rna, 2022, 28, 194-209
2.613Citations (PDF)
9Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease
Cell Genomics, 2022, 2, 100086
4.321Citations (PDF)
10Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites
American Journal of Human Genetics, 2022, 109, 1038-1054
4.638Citations (PDF)
11Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency
Thrombosis and Haemostasis, 2022, 122, 1369-1378
2.425Citations (PDF)
12Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke
Nature Communications, 2022, 13, 1-14
11.4119Citations (PDF)
13Neutrophil specific granule and NETosis defects in gray platelet syndrome
Blood Advances, 2021, 5, 549-564
3.727Citations (PDF)
14A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis
Communications Biology, 2021, 4, 1-14
3.3138Citations (PDF)
15Transcriptional characterization of human megakaryocyte polyploidization and lineage commitment
Journal of Thrombosis and Haemostasis, 2021, 19, 1236-1249
2.923Citations (PDF)
16Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates
International Journal of Obesity, 2021, 45, 2221-2229
3.151Citations (PDF)
17Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases
Nature Medicine, 2021, 27, 1564-1575
27.260Citations (PDF)
18Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Nature Genetics, 2021, 53, 1300-1310
14.91,840Citations (PDF)
19Elevated levels of tissue factor pathway inhibitor in patients with mild to moderate bleeding tendency
Blood Advances, 2021, 5, 391-398
3.733Citations (PDF)
20Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
Molecular Psychiatry, 2021, 26, 5239-5250
6.015Citations (PDF)
21Polygenic basis and biomedical consequences of telomere length variation
Nature Genetics, 2021, 53, 1425-1433
14.9317Citations (PDF)
22Comparison of four methods to measure haemoglobin concentrations in whole blood donors (COMPARE): A diagnostic accuracy study
Transfusion Medicine, 2021, 31, 94-103
0.627Citations (PDF)
23Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases
Nature Metabolism, 2021, 3, 1476-1483
15.777Citations (PDF)
24The role of haematological traits in risk of ischaemic stroke and its subtypes
Brain, 2020, 143, 210-221
6.155Citations (PDF)
25The Polygenic and Monogenic Basis of Blood Traits and Diseases
Cell, 2020, 182, 1214-1231.e11
24.4534Citations (PDF)
26Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Communications Biology, 2020, 3, 1-9
3.360Citations (PDF)
27Development and validation of a universal blood donor genotyping platform: a multinational prospective study Free
Blood Advances, 2020, 4, 3495-3506
3.749Citations (PDF)
28Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Blood, 2020, 136, 1956-1967
5.858Citations (PDF)
29Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Cell, 2020, 182, 1198-1213.e14
24.4511Citations (PDF)
30Treatment of COVID-19 with remdesivir in the absence of humoral immunity: a case report
Nature Communications, 2020, 11, 1-11
11.4104Citations (PDF)
31Whole-genome sequencing of a sporadic primary immunodeficiency cohort
Nature, 2020, 583, 90-95
32.8203Citations (PDF)
32Whole-genome sequencing of patients with rare diseases in a national health system
Nature, 2020, 583, 96-102
32.8460Citations (PDF)
33The influence of rare variants in circulating metabolic biomarkers
PLoS Genetics, 2020, 16, e1008605
2.314Citations (PDF)
34Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasia Free
Blood, 2020, 136, 1907-1918
5.866Citations (PDF)
35A coagulation defect arising from heterozygous premature termination of tissue factor
Journal of Clinical Investigation, 2020, 130, 5302-5312
7.125Citations (PDF)
36Longer-term efficiency and safety of increasing the frequency of whole blood donation (INTERVAL): extension study of a randomised trial of 20 757 blood donors
Lancet Haematology,the, 2019, 6, e510-e520
8.021Citations (PDF)
37Germline mutations in the transcription factor IKZF5 cause thrombocytopenia
Blood, 2019, 134, 2070-2081
5.839Citations (PDF)
38A catalog of genetic loci associated with kidney function from analyses of a million individuals
Nature Genetics, 2019, 51, 957-972
14.9702Citations (PDF)
39Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders Free
Blood, 2019, 134, 2082-2091
5.8201Citations (PDF)
40How common are single gene mutations as a cause for lacunar stroke?A targeted gene panel study
Neurology, 2019, 93, e2007-e2020
0.736Citations (PDF)
41Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Nature Communications, 2018, 9, 1-16
11.4333Citations (PDF)
42Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans
Journal of Allergy and Clinical Immunology, 2018, 142, 1285-1296
5.1214Citations (PDF)
43Nbeal2 interacts with Dock7, Sec16a, and Vac14 Free
Blood, 2018, 131, 1000-1011
5.843Citations (PDF)
44Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing
Genome Medicine, 2018, 10, 1-10
6.3140Citations (PDF)
45GNE variants causing autosomal recessive macrothrombocytopenia without associated muscle wasting Free
Blood, 2018, 132, 1851-1854
5.851Citations (PDF)
46Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils
Cell Reports, 2018, 24, 2784-2794
4.6120Citations (PDF)
47Phenotype description and response to thrombopoietin receptor agonist in DIAPH1-related disorder Free
Blood Advances, 2018, 2, 2341-2346
3.738Citations (PDF)
48Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study
Lancet Haematology,the, 2018, 5, e241-e251
8.076Citations (PDF)
49Genomic atlas of the human plasma proteome
Nature, 2018, 558, 73-79
32.81,750Citations (PDF)
50Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice Free
Blood, 2018, 132, 1399-1412
5.853Citations (PDF)
51The Human Phenotype Ontology in 2017.
Nucleic Acids Research, 2017, 45, D865-D876
11.4614Citations (PDF)
52Megakaryocytes in Myeloproliferative Neoplasms Have Unique Somatic Mutations
American Journal of Pathology, 2017, 187, 1512-1522
2.919Citations (PDF)
53Common genetic variation drives molecular heterogeneity in human iPSCs
Nature, 2017, 546, 370-375
32.8483Citations (PDF)
54Detection of Atherosclerotic Inflammation by 68Ga-DOTATATE PET Compared to [18F]FDG PET Imaging.
Journal of the American College of Cardiology, 2017, 69, 1774-1791
6.5410Citations (PDF)
55Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
American Journal of Human Genetics, 2017, 100, 75-90
4.6422Citations (PDF)
56Dawning of the age of genomics for platelet granule disorders: improving insight, diagnosis and management
British Journal of Haematology, 2017, 176, 705-720
1.726Citations (PDF)
57Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Lancet Neurology, The, 2017, 16, 898-907
25.9228Citations (PDF)
58Efficiency and safety of varying the frequency of whole blood donation (INTERVAL): a randomised trial of 45 000 donors
Lancet, The, 2017, 390, 2360-2371
49.6223Citations (PDF)
59Platelet function is modified by common sequence variation in megakaryocyte super enhancers
Nature Communications, 2017, 8, 1-12
11.446Citations (PDF)
60Chromosome contacts in activated T cells identify autoimmune disease candidate genes
Genome Biology, 2017, 18, 1-19
5.162Citations (PDF)
61Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia
Journal of Clinical Investigation, 2017, 127, 814-829
7.167Citations (PDF)
62Increased DNA methylation variability in type 1 diabetes across three immune effector cell types
Nature Communications, 2016, 7, 1-11
11.4139Citations (PDF)
63A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies
Science Translational Medicine, 2016, 8, 328ra30
8.993Citations (PDF)
64A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
Blood, 2016, 127, 2791-2803
5.8163Citations (PDF)
65Inherited platelet disorders: toward DNA-based diagnosis Free
Blood, 2016, 127, 2814-2823
5.8129Citations (PDF)
66eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data
Cell Reports, 2016, 17, 2137-2150
4.6106Citations (PDF)
67A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss
Blood, 2016, 127, 2903-2914
5.8139Citations (PDF)
68Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters
Cell, 2016, 167, 1369-1384.e19
24.4781Citations (PDF)
69The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Cell, 2016, 167, 1415-1429.e19
24.4951Citations (PDF)
70Distinct Trends of DNA Methylation Patterning in the Innate and Adaptive Immune Systems
Cell Reports, 2016, 17, 2101-2111
4.655Citations (PDF)
71DNA Methylation Dynamics of Human Hematopoietic Stem Cell Differentiation
Cell Stem Cell, 2016, 19, 808-822
12.4236Citations (PDF)
72Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
Cell, 2016, 167, 1398-1414.e24
24.4503Citations (PDF)
73Large-scale production of megakaryocytes from human pluripotent stem cells by chemically defined forward programming
Nature Communications, 2016, 7, 1-16
11.4218Citations (PDF)
74Recruitment and representativeness of blood donors in the INTERVAL randomised trial assessing varying inter-donation intervals
Trials, 2016, 17, 1-12
1.219Citations (PDF)
75Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Nature Neuroscience, 2016, 19, 571-577
12.5378Citations (PDF)
76Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.
Genome Medicine, 2015, 7, 36
6.3108Citations (PDF)
77αIIbβ3 variants defined by next-generation sequencing: Predicting variants likely to cause Glanzmann thrombasthenia
Proceedings of the National Academy of Sciences of the United States of America, 2015, 112, E1898-E1907
5.438Citations (PDF)
78Single Nucleotide Variants in the Protein C Pathway and Mortality in Dialysis Patients
PLoS ONE, 2014, 9, e97251
1.64Citations (PDF)
79A Loss of Function Screen of Identified Genome-Wide Association Study Loci Reveals New Genes Controlling Hematopoiesis
PLoS Genetics, 2014, 10, e1004450
2.323Citations (PDF)
80DNA methylation and body-mass index: a genome-wide analysis
Lancet, The, 2014, 383, 1990-1998
49.6702Citations (PDF)
81The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
Nucleic Acids Research, 2014, 42, D966-74
11.4635Citations (PDF)
82Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis
Nature Communications, 2014, 5, 1-11
11.4224Citations (PDF)
83Transcriptional diversity during lineage commitment of human blood progenitors
Science, 2014, 345, 1251033
26.9250Citations (PDF)
84Defining the role of common variation in the genomic and biological architecture of adult human height
Nature Genetics, 2014, 46, 1173-1186
14.91,487Citations (PDF)
85Expression of a single-chain human leukocyte antigen-DRA/DRB3*01:01 molecule and differential binding of a monoclonal antibody in the presence of specifically bound human platelet antigen-1a peptide
Transfusion, 2014, 54, 1478-1485
0.62Citations (PDF)
86Gray platelet syndrome: proinflammatory megakaryocytes and α-granule loss cause myelofibrosis and confer metastasis resistance in mice Free
Blood, 2014, 124, 3624-3635
5.883Citations (PDF)
87αIIbβ3 Variants Defined By Next Generation Sequencing: Implications for Predicting Variants Likely to Cause Glanzmann Thrombasthenia and Alloimmune Disorders
Blood, 2014, 124, 4151-4151
5.81Citations (PDF)
88Single Nucleotide Polymorphisms with Cis-Regulatory Effects on Long Non-Coding Transcripts in Human Primary Monocytes
PLoS ONE, 2014, 9, e102612
1.64Citations (PDF)
89A Novel β3 Intracytoplasmic Domain Mutation Associated with Macrothrombocytopenia: Structural Analysis in Comparison with Previously Reported Cases
Blood, 2014, 124, 1454-1454
5.81Citations (PDF)
90New insights into the genetic basis of TAR (thrombocytopenia-absent radii) syndrome
Current Opinion in Genetics and Development, 2013, 23, 316-323
2.4107Citations (PDF)
91Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci
Genome Research, 2013, 23, 1130-1141
3.533Citations (PDF)
92Common genetic variants do not associate with CAD in familial hypercholesterolemia
European Journal of Human Genetics, 2013, 22, 809-813
2.44Citations (PDF)
93In Vitro Production Of Megakaryocytes and Platelets From Human Induced Pluripotent Cells By GMP Compatible Methods Free
Blood, 2013, 122, 2401-2401
5.81Citations (PDF)
94Bayesian refinement of association signals for 14 loci in 3 common diseases
Nature Genetics, 2012, 44, 1294-1301
14.9397Citations (PDF)
95Seventy-five genetic loci influencing the human red blood cell
Nature, 2012, 492, 369-375
32.8269Citations (PDF)
96Transcription factor co-localization patterns affect human cell type-specific gene expression
BMC Genomics, 2012, 13, 1-12
2.29Citations (PDF)
97Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci
American Journal of Human Genetics, 2012, 91, 823-838
4.6212Citations (PDF)
98Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome
Nature Genetics, 2012, 44, 435-439
14.9351Citations (PDF)
99Comparison of Methods for Competitive Tests of Pathway Analysis
PLoS ONE, 2012, 7, e41018
1.644Citations (PDF)
100Image-based characterization of thrombus formation in time-lapse DIC microscopy
Medical Image Analysis, 2012, 16, 915-931
9.56Citations (PDF)
101Large-scale association analysis identifies new risk loci for coronary artery disease
Nature Genetics, 2012, 45, 25-33
14.91,429Citations (PDF)
102Effect of Single Nucleotide Polymorphism in the Gene RBM8A Together with the Microdeletion 1q21 in Thrombocytopenia-Absent Radii Syndrome.
Blood, 2012, 120, 2372-2372
5.80Citations (PDF)
103Dindel: Accurate indel calls from short-read data
Genome Research, 2011, 21, 961-973
3.5411Citations (PDF)
104Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
Nature Genetics, 2011, 43, 735-737
14.9273Citations (PDF)
105New gene functions in megakaryopoiesis and platelet formation
Nature, 2011, 480, 201-208
32.8374Citations (PDF)
106Genome-wide Analysis of Simultaneous GATA1/2, RUNX1, FLI1, and SCL Binding in Megakaryocytes Identifies Hematopoietic Regulators
Developmental Cell, 2011, 20, 597-609
5.5271Citations (PDF)
107Silencing of RhoA nucleotide exchange factor, ARHGEF3, reveals its unexpected role in iron uptake
Blood, 2011, 118, 4967-4976
5.827Citations (PDF)
108Detection of human platelet antigen-1a alloantibodies in cases of fetomaternal alloimmune thrombocytopenia using recombinant β3 integrin fragments coupled to fluorescently labeled beads
Transfusion, 2011, 51, 1261-1270
0.616Citations (PDF)
109Identification of candidate genes linking systemic inflammation to atherosclerosis; results of a human in vivoLPS infusion study
BMC Medical Genomics, 2011, 4, 1-8
1.424Citations (PDF)
110Cross-domain inhibition of TACE ectodomain
Proceedings of the National Academy of Sciences of the United States of America, 2011, 108, 5578-5583
5.4110Citations (PDF)
111Platelets release novel thiol isomerase enzymes which are recruited to the cell surface following activation
British Journal of Haematology, 2010, 148, 627-637
1.794Citations (PDF)
112Transcription profiling in human platelets reveals LRRFIP1 as a novel protein regulating platelet function
Blood, 2010, 116, 4646-4656
5.884Citations (PDF)
113PECAM-1 expression and activity negatively regulate multiple platelet signaling pathways
FEBS Letters, 2009, 583, 3618-3624
1.942Citations (PDF)
114Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
Nature Genetics, 2009, 41, 1011-1015
14.9239Citations (PDF)
115Single domain antibodies against the collagen signalling receptor glycoprotein VI are inhibitors of collagen induced thrombus formation
Platelets, 2009, 20, 268-76
2.021Citations (PDF)
116A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function Open Access
Blood, 2009, 113, 3831-3837
5.8109Citations (PDF)
117Functional genomics in zebrafish permits rapid characterization of novel platelet membrane proteins
Blood, 2009, 113, 4754-4762
5.872Citations (PDF)
118Apheresis donors and platelet function: inherent platelet responsiveness influences platelet quality
Transfusion, 2008, 48, 673-680
0.621Citations (PDF)
119A single-nucleotide polymorphism in the human ITGB3 gene is associated with the platelet-specific alloantigen Vaa (HPA-17bw) involved in fetal maternal alloimmune thrombocytopenia
Transfusion, 2008, 48, 1432-1438
0.621Citations (PDF)
120Molecular characteristics of anti-self antibody fragments against neutrophil cytoplasmic antigens from human V gene phage display libraries
Clinical and Experimental Immunology, 2008, 102, 566-574
2.44Citations (PDF)
121Identification of variation in the platelet transcriptome associated with Glycoprotein 6 haplotype
Platelets, 2008, 19, 258-67
2.07Citations (PDF)
122A nonsynonymous SNP in the ITGB3 gene disrupts the conserved membrane-proximal cytoplasmic salt bridge in the αIIbβ3 integrin and cosegregates dominantly with abnormal proplatelet formation and macrothrombocytopenia
Blood, 2008, 111, 3407-3414
5.896Citations (PDF)
123Developing recombinant HPA-1a–specific antibodies with abrogated Fcγ receptor binding for the treatment of fetomaternal alloimmune thrombocytopenia
Journal of Clinical Investigation, 2008, 118, 2929-2938
7.149Citations (PDF)
124Recombinant Human HPA-1A Antibodies for Treatment of Fetomaternal Alloimmune Thrombocytopenia (FMAIT): Proof of Principle in An in Vivo Murine Model and Human Volunteer Studies
Blood, 2008, 112, 85-85
5.84Citations (PDF)
125Genomewide Association Analysis of Coronary Artery Disease
New England Journal of Medicine, 2007, 357, 443-53
25.21,782Citations (PDF)
126Structural Basis for the Platelet-Collagen InteractionTHE SMALLEST MOTIF WITHIN COLLAGEN THAT RECOGNIZES AND ACTIVATES PLATELET GLYCOPROTEIN VI CONTAINS TWO GLYCINE-PROLINE-HYDROXYPROLINE TRIPLETS*
Journal of Biological Chemistry, 2007, 282, 1296-1304
1.4125Citations (PDF)
127Comparative gene expression profiling of in vitro differentiated megakaryocytes and erythroblasts identifies novel activatory and inhibitory platelet membrane proteins
Blood, 2007, 109, 3260-3269
5.8150Citations (PDF)
128Molecular characterization of the variable domains of an αIIbβ3-specific immunoglobulin M κ platelet cold agglutinin in a follicular lymphoma patient with treatment refractory autoimmune thrombocytopenia: idiotypic overlap between αIIbβ3 integrin antibodies
Transfusion, 2007, 47, 499-510
0.62Citations (PDF)
129Management and outcome of 200 cases of fetomaternal alloimmune thrombocytopenia
Transfusion, 2007, 47, 901-910
0.6149Citations (PDF)
130HPA-1a antibody potency and bioactivity do not predict severity of fetomaternal alloimmune thrombocytopenia
Transfusion, 2007, 47, 1296-1305
0.655Citations (PDF)
131A naturally occurring Leu33Val mutation in β3-integrin impairs the HPA-1a epitope: the third allele of HPA-1
Transfusion, 2006, 46, 790-799
0.621Citations (PDF)
132Acquired thrombasthenia due to GPIIbIIIa platelet autoantibodies in a 4-yr-old child
European Journal of Haematology, 2006, 76, 89-90
1.613Citations (PDF)
133Selective Blockade of Glycoprotein VI Clustering on Collagen Helices*
Journal of Biological Chemistry, 2006, 281, 33505-33510
1.429Citations (PDF)
134Microarray-based genotyping for blood groups: comparison of gene array and 5′-nuclease assay techniques with human platelet antigen as a model†
Transfusion, 2005, 45, 654-659
0.658Citations (PDF)
135The dilemma of screening for antibodies against low-frequency human platelet antigens
Transfusion, 2005, 45, 288-289
0.66Citations (PDF)
136Teicoplanin-dependent antibodies: detection and characterization
British Journal of Haematology, 2005, 129, 279-281
1.717Citations (PDF)
137Platelet genomics and proteomics in human health and disease
Journal of Clinical Investigation, 2005, 115, 3370-3377
7.1140Citations (PDF)
138Platelet integrin α2 I-domain specific antibodies produced via domain specific DNA vaccination combined with variable gene phage display
Thrombosis and Haemostasis, 2005, 94, 1318-1326
2.43Citations (PDF)
139Integrin Activation State Determines Selectivity for Novel Recognition Sites in Fibrillar Collagens*
Journal of Biological Chemistry, 2004, 279, 47763-47772
1.4153Citations (PDF)
140Molecular studies of anti-HLA-A2 using light-chain shuffling: a structural model for HLA antibody binding
Tissue Antigens, 2004, 63, 345-354
0.610Citations (PDF)
141Platelet receptor interplay regulates collagen-induced thrombus formation in flowing human blood Free
Blood, 2004, 103, 1333-1341
5.8184Citations (PDF)
142The low-frequency allele of the platelet collagen signaling receptor glycoprotein VI is associated with reduced functional responses and expression
Blood, 2003, 101, 4372-4379
5.8128Citations (PDF)
143Single-chain antibody fragments derived from a human synthetic phage-display library bind thrombospondin and inhibit sickle cell adhesion
Blood, 2003, 102, 718-724
5.825Citations (PDF)
144HPA-1a phenotype–genotype discrepancy reveals a naturally occurring Arg93Gln substitution in the platelet β3 integrin that disrupts the HPA-1a epitope Free
Blood, 2002, 99, 1833-1839
5.834Citations (PDF)
145Platelet αIIbβ3 recombinant autoantibodies from the B-cell repertoire of a post-transfusion purpura patient
British Journal of Haematology, 2002, 116, 677-685
1.734Citations (PDF)
146Genotyping for platelet-specific antigens: techniques for the detection of single nucleotide polymorphisms
Vox Sanguinis, 2002, 83, 1-12
0.870Citations (PDF)
147Provision of platelet support for fetuses and neonates affected by severe fetomaternal alloimmune thrombocytopenia
British Journal of Haematology, 2001, 113, 40-42
1.750Citations (PDF)
148Detection of Gov system antibodies by MAIPA reveals an immunogenicity similar to the HPA-5 alloantigens
British Journal of Haematology, 2000, 110, 735-742
1.786Citations (PDF)
149Introduction to Antibody Engineering and Phage Display
Vox Sanguinis, 2000, 78, 72-79
0.838Citations (PDF)
150The isolation and characterisation of human monoclonal HLA-A2 antibodies from an immune V gene phage display library
Tissue Antigens, 2000, 55, 219-228
0.631Citations (PDF)
151Threonine-145/Methionine-145 variants of baculovirus produced recombinant ligand binding domain of GPIbα express HPA-2 epitopes and show equal binding of von Willebrand factor Free
Blood, 2000, 95, 205-211
5.830Citations (PDF)
152Human antibodies with specificity for the C2 domain of factor VIII are derived from VH1 germline genes Free
Blood, 2000, 95, 558-563
5.865Citations (PDF)
153The immunogenicity of Gov alloantigens is comparable to that of the HPA-5 system
Transfusion Medicine, 2000, 10, 329
0.61Citations (PDF)
154Increased binding of fibrinogen to glycoprotein IIIa-proline33 (HPA-1b, PlA2, Zwb) positive platelets in patients with cardiovascular disease.
European Heart Journal, 1999, 20, 742-7
7.493Citations (PDF)
155Synthesis of Rh Fv phage-antibodies using VH and VL germline genes
British Journal of Haematology, 1999, 105, 811-816
1.772Citations (PDF)
156Rapid phenotyping of HPA-1a using either diabody-based hemagglutination or recombinant IgG1-based assays
Transfusion, 1999, 39, 781-789
0.621Citations (PDF)
157A fatal case of autoimmune thrombocytopenia with an IgM anti-GPIb/IX following one antigen mismatched unrelated donor bone marrow transplantation
Bone Marrow Transplantation, 1999, 23, 739-741
2.619Citations (PDF)
158The Natural History of Fetomaternal Alloimmunization to the Platelet-Specific Antigen HPA-1a (PlA1, Zwa) as Determined by Antenatal Screening
Blood, 1998, 92, 2280-2287
5.8418Citations (PDF)
159Human autoimmune anti-proteinase 3 scFv from a phage display library
Clinical and Experimental Immunology, 1997, 107, 269-281
2.446Citations (PDF)
160Activation during preparation of therapeutic platelets affects deterioration during storage: a comparative flow cytometric study of different production methods
British Journal of Haematology, 1997, 98, 86-95
1.7155Citations (PDF)
161Characterization of human variable domain antibody fragments against the U1 RNA-associated A protein, selected from a synthetic and a patient-derived combinatorial V gene library
European Journal of Immunology, 1996, 26, 629-639
2.472Citations (PDF)
162Human platelet antigen-2 and -3 genotyping by PCR-SSP
Transfusion Medicine, 1995, 5, 285-288
0.64Citations (PDF)
163A human monoclonal antibody specific for the leucine-33 (P1A1, HPA-1a) form of platelet glycoprotein IIIa from a V gene phage display library
Blood, 1995, 86, 4430-4436
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164Characterization of human blood group scFv antibodies derived from a V gene phage-display library
British Journal of Haematology, 1994, 88, 180-186
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165No Beneficial Effect of Low-Dose Fetal Intravenous Gammaglobulin Administration in Combination with Intravascular Transfusions in Severe Rh D Haemolytic Disease
Vox Sanguinis, 1994, 66, 253-257
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166Human Antibody Fragments Specific for Human Blood Group Antigens from a Phage Display Library
Bio/technology, 1993, 11, 1145-1149
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167Leucine-proline substitution in human platelet glycoprotein IIIa determines HLA-DRw52a (DW24) association of the immune response against HPA-1a (Zw/PI) and HPA-1b (Zw/PI)
Human Immunology, 1992, 34, 253-256
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168Detection of platelet activation with monoclonal antibodies and flow cytometry. Changes during platelet storage
Transfusion, 1990, 30, 20-25
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169Theoretic and Practical Aspects of Platelet Crossmatching
Transfusion Medicine Reviews, 1990, 4, 265-278
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17011 Immunology of platelet disorders
Best Practice and Research: Clinical Haematology, 1989, 2, 749-781
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171Array genotyping of transfusion-relevant blood cell antigens in 6946 ancestrally diverse study participants Open Access
Blood, 0, 146, 1511-1524
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