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Journal Articles

High Throughput Sequencing in 3449 Patients with Bleeding and Platelet Disorders: Novel Gene Discovery and Robust Diagnosis

Claire Lentaigne, BSc, MB, MRCP, Bridge Consortium, Thrombogenomics Consortium
Journal: Blood
Blood (2017) 130 (Supplement 1): 5.
https://doi.org/10.1182/blood.V130.Suppl_1.5.5
Published: 2017
Journal Articles

Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort

Suthesh Sivapalaratnam, MD PhD, Willem Ouwehand, MD PhD, Bridge Consortium, ThromboGenomics Consortium
Journal: Blood
Blood (2016) 128 (22): 1359.
https://doi.org/10.1182/blood.V128.22.1359.1359
Published: 2016
Journal Articles

Pathogenic Variants in Thrombocytopenia Genes in 119 Cases with Undiagnosed Heritable Thrombocytopenia

Sarah K Westbury, BA(Hons) BM BCh MRCP, Bridge Consortium, ThromboGenomics Consortium
Journal: Blood
Blood (2016) 128 (22): 362.
https://doi.org/10.1182/blood.V128.22.362.362
Published: 2016
Journal Articles

αIIbβ3 Variants Defined By Next Generation Sequencing: Implications for Predicting Variants Likely to Cause Glanzmann Thrombasthenia and Alloimmune Disorders

Claudia Lorena Buitrago, PhD#, Augusto Rendon, PhD#~, Ernest Turro, PhD, Yupu Liang, PhD, Ilenia Simeoni, PhD, Ana Negri, PhD, ThromboGenomics Consortium, Marta Filizola, PhD, Willem H. Ouwehand, MDPhDFRCPath FMedSci #, Barry S. Coller, MD#
Journal: Blood
Blood (2014) 124 (21): 4151.
https://doi.org/10.1182/blood.V124.21.4151.4151
Published: 2014