Thomas Folkmann Hansen

ORCID: 0000-0001-6703-7762 · 8 papers in corpus
observational 2026
·doi:10.64898/2026.06.18.26355987

Purpose Endometriosis is associated with pain, cardiometabolic, psychiatric, and immune comorbidities. We tested whether the genetic liability captured by an endometriosis polygenic risk score (PRS) extends to these comorbidities through s…

observational 2025
BMC medicine ·doi:10.1186/s12916-025-04398-z

BACKGROUND: Endometriosis is a complex condition with a wide range of comorbidities. It is widely underdiagnosed, with a diagnostic delay of 4 to 10 years, potentially leading to worsened disease progression and a higher burden of comorbidi…

meta-analysis 2024
Nature genetics ·doi:10.1038/s41588-024-01839-y

Bleeding in early pregnancy and postpartum hemorrhage (PPH) bear substantial risks, with the former closely associated with pregnancy loss and the latter being the foremost cause of maternal death, underscoring the severe impact on maternal…

other 2023
International journal of epidemiology ·doi:10.1093/ije/dyac194
2023
·doi:10.1101/2023.08.10.23293932

Bleeding in early pregnancy and postpartum hemorrhage (PPH) bear substantial risks, with the former closely associated with pregnancy loss and the latter being the foremost cause of maternal death, underscoring the severity of these complic…

observational 2019
BMJ open ·doi:10.1136/bmjopen-2018-028401

PURPOSE: To establish a cohort that enables identification of genomic factors that influence human health and empower increased blood donor health and safe blood transfusions. Human health is complex and involves several factors, a major on…

review 2018
The journal of headache and pain ·doi:10.1186/s10194-018-0856-0

BACKGROUND: The latest Genome-Wide Association Study identified 38 genetic variants associated with migraine. In this type of studies the significance level is very difficult to achieve (5 × 10- 8) due to multiple testing. Thus, the identif…

observational 2013
Nature genetics ·doi:10.1038/ng.2711

Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across disorders is unclear. To examine shared genetic etiology, we use genome-wide genotype da…