Kristina Fruerlund Rasmussen

An analysis of <i>PAX1</i> in the development of vertebral malformations

P F Giampietro, CL Raggio, CE Reynolds et al. · Clinical Genetics · 2005 · 67 citations

Mutations in endoglin and in activin receptor‐like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia

Klaus Brusgaard, Louise Ladefoged Poulsen, Hayley Moss et al. · Clinical Genetics · 2004 · 49 citations

Genetics, Genetic Epidemiology, Human Polymorphism +18

Mutations in theALK-1 gene and the phenotype of hereditary hemorrhagic telangiectasia in two large Danish families

Anette Drøhse Kjeldsen, Klaus Brusgaard, Louise Ladefoged Poulsen et al. · American Journal of Medical Genetics · 2001 · 41 citations

Genetic Status Affects Disease-Specific Mortality But Not the Incidence of Local Recurrence in Patients with Uveal Melanoma

Mette Bagger, Charlotte A. Espensen, Kristina Fruerlund Rasmussen et al. · Ophthalmology · 2023 · 11 citations · Full text

Translation, validation, and usability of the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool (Self‐ISTH‐BAT)

Rasmus Søgaard Hansen, Mette Carlsen, Kristina Fruerlund Rasmussen et al. · European Journal Of Haematology · 2021 · 10 citations · Full text