Clinical 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-Reference-Cited by-同舟云学术

Clinical 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

Published:2020-10 Issue:10 Volume:18 Page:2751-2758
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Downes Kate¹²,Borry Pascal³,Ericson Katrin⁴,Gomez Keith⁵^ORCID,Greinacher Andreas⁶^ORCID,Lambert Michele⁷⁸,Leinoe Eva⁹,Noris Patrizia¹⁰,Van Geet Chris¹¹,Freson Kathleen¹¹^ORCID,

Affiliation:

1. East Genomic Laboratory Hub Cambridge University Hospitals NHS Foundation Trust Cambridge UK

2. Department of Haematology University of CambridgeCambridge Biomedical Campus Cambridge UK

3. Department of Public Health and Primary Care KU Leuven Leuven Belgium

4. The RUNX1 Research Program Santa Barbara CA USA

5. Haemophilia Centre and Thrombosis Unit Royal Free London NHS Foundation Trust London UK

6. Institut für Immunologie und Transfusionsmedizin Universitätsmedizin Greifswald Greifswald Germany

7. Division of Hematology The Children’s Hospital of Philadelphia Philadelphia PA USA

8. Department of Pediatrics Perelman School of Medicine at the University of Pennsylvania Philadelphia PA USA

9. Department of Haematology RigshospitaletNational University Hospital Copenhagen Denmark

10. IRCCS Policlinico San Matteo Foundation and University of Pavia Pavia Italy

11. Department of Cardiovascular Sciences Center or Molecular and Vascular Biology KU Leuven Leuven Belgium

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jth.14993

Reference42 articles.

1. Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH

2. Inherited platelet disorders: toward DNA-based diagnosis

3. Recent advances in inherited platelet disorders

4. Inherited Platelet Disorders

5. High-throughput sequencing for diagnosing platelet disorders: lessons learned from exploring the causes of bleeding disorders

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Standardization of definition and management for bleeding disorder of unknown cause: communication from the SSC of the ISTH;Journal of Thrombosis and Haemostasis;2024-07

2. Thrombophilia Testing: from Genetic Predisposition to Discrimination;TH Open;2024-03-09

3. Bleeding Disorder of Unknown Cause: A Diagnosis of Exclusion;Hämostaseologie;2024-02-27

4. Application of Multigene Panel Testing for Bleeding, Thrombotic, and Platelet Disorders in Patients and the General Population in China;2024

5. Platelet expression of the transcription factor ETV6 associates with ETV6‐related thrombocytopenia and can be detected by immunofluorescence on the blood film;British Journal of Haematology;2023-11-20