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Author Details

Keith Gomez
1998
66
23
PMIDPaper TitleJournal TitlePublished Year
36793181Effect of direct thrombin inhibitors on laboratory measurement of fibrinogen: Potential for errors in clinical decision-making.2023
37647632The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140â¿¿214 UK Biobank participants.Blood2023
36819179How will UK hospitals use andexanet alfa? A review of local protocols.2023
36877609An expert consensus to define how higher standards of equitable care for von Willebrand disease can be achieved in the UK and Republic of Ireland.2023
36737374Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021 Oct;19(10):2612-2617].J Thromb Haemost2023
36073900Reproductive health and hemostatic issues in women and girls with congenital factor VII deficiency: A systematic review.Journal of Thrombosis and Haemostasis2022
35845226Platelet storage pool disorder in pregnancy: Utilising thromboelastography to guide a risk-based delivery plan.Obstetric Medicine2022
35521730Diagnosis of rare bleeding disorders.Haemophilia2022
35389508Addendum to guidelines on the investigation and management of venous thrombosis at unusual sites (Br. J. Haematol. 2012;159:28-38): Use of Direct Oral Anticoagulants.British Journal of Haematology2022
34435350Clinical and laboratory diagnosis of heritable platelet disorders in adults and children: a British Society for Haematology Guideline.British Journal of Haematology2021
33749973Challenges of antithrombotic therapy in the management of cardiovascular disease in patients with inherited bleeding disorders: A single-centre experience.Haemophilia2021
33636748Genomic Analysis for the Detection of Bleeding and Thrombotic Disorders.Seminars in Thrombosis and Hemostasis2021
33521972The presentation and outcomes of Hermansky-Pudlak syndrome in obstetrics and gynecological settings: A systematic review.International Journal of Gynecology and Obstetrics2021
34343384European principles of care for women and girls with inherited bleeding disorders.Haemophilia2021
34355501GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis.J Thromb Haemost2021
32578312Diagnosis of rare bleeding disorders.Haemophilia2021
33236402Debate: Should the dose or duration of anticoagulants for the prevention of venous thrombosis be increased in patients with COVID-19 while we are awaiting the results of clinical trials?British Journal of Haematology2021
33079472Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH.J Thromb Haemost2020
31943138Addendum to British Society for Haematology Guidelines on Investigation and Management of Antiphospholipid syndrome, 2012 (Br. J. Haematol. 2012; 157: 47-58): use of direct acting oral anticoagulants.British Journal of Haematology2020
32110765Impaired platelet-dependent thrombin generation associated with thrombocytopenia is improved by prothrombin complex concentrates in vitro.Research and Practice in Thrombosis and Haemostasis2020
32166871The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers.Haemophilia2020
31562665Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variants.Hum Mutat2020
32333443The EAHAD blood coagulation factor VII variant database.Human Mutation2020
32693407Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome.Blood2020
30664826Recommendations for the clinical interpretation of genetic variants and presentation of results to patients with inherited bleeding disorders. A UK Haemophilia Centre Doctors' Organisation Good Practice Paper.Haemophilia2019
30467204Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia.Haematologica2019
30656286Evaluation of von Willebrand factor concentrates by platelet adhesion to collagen using an in vitro flow assay.Research and Practice in Thrombosis and Haemostasis2019
31168789NICE NG89 recommendations for extended pharmacological thromboprophylaxis - is it justified and is it cost effective: a rebuttal from the British Society for Haematology.British Journal of Haematology2019
30859551New information on rare diseases - how important is that for us?British Journal of Haematology2019
31217188Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.Blood2019
31064749Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.Blood2019
30232087Phenotype description and response to thrombopoietin receptor agonist in <i>DIAPH1</i>-related disorder.Blood Adv2018
28653330Quality assurance and tests of platelet function.British Journal of Haematology2018
27984638Dawning of the age of genomics for platelet granule disorders: improving insight, diagnosis and management.Br J Haematol2017
28374619Super-resolution microscopy in the diagnosis of platelet granule disorders.Expert Review of Hematology2017
28612396Diagnosis of inherited bleeding disorders in the genomic era.British Journal of Haematology2017
26663472Safety and efficacy of factor XI (FXI) concentrate use in patients with FXI deficiency: a single-centre experience of 19 years.Haemophilia2016
26806224Super-resolution microscopy as a potential approach to diagnosis of platelet granule disorders.Journal of Thrombosis and Haemostasis2016
26912466A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.Blood2016
27084890A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.Blood2016
26823395The ophthalmic presentation of Hermansky-Pudlak syndrome 6.Br J Ophthalmol2016
27451401Changes in thromboelastography parameters in pregnancy, labor, and the immediate postpartum period.International Journal of Gynecology and Obstetrics2016
26936507A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.Sci Transl Med2016
26492096What's in a name? The pharmacy of vitamin K.British Journal of Haematology2016
25244644A large-scale computational study of inhibitor risk in non-severe haemophilia A.Br J Haematol2015
25689278Presentation and management of acute coronary syndromes among adult persons with haemophilia: results of an international, retrospective, 10-year survey.Haemophilia2015
25949529Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.Genome Med2015
26238113The effects of angiotensin II signaling blockade on platelet activity in subjects with hypertension.Current Hypertension Reviews2015
24333092Key issues in inhibitor management in patients with haemophilia.2014
25258084Transcriptional diversity during lineage commitment of human blood progenitors.Science2014
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