Family studies have estimated that genetic risk factors contribute to nearly 60% of VTE risk*
*Kolin et al – Nature Scientific Reports
Genomics research in Thrombosis has recently resulted in:
There is a role for genomics in diagnostics of Thrombosis.
NIHR Rare Diseases BioResource recall study is open for recruitment - for further details please email: firstname.lastname@example.org
Please note, patients being referred must be identified by a clinician to make sure that they meet the criteria of the project, and the clinician must have the patient’s permission to refer.
RNA phenotyping in heritable platelet disorders
RNA phenotyping in unexplained inherited thrombosis