Lichtenstein P

ORCID: 0000-0003-3037-5287 · 6 papers in corpus
observational 2025
BMJ open ·doi:10.1136/bmjopen-2025-105694

OBJECTIVES: To determine whether hormonal contraceptives are associated with subsequent risks of suicidal behaviour and depression among women of reproductive age. DESIGN: Nationwide register-based study. SETTING: Swedish national populat…

observational 2024
The journal of pain ·doi:10.1016/j.jpain.2024.02.016

Chronic overlapping pain conditions (COPCs) by definition, frequently co-occur, perhaps reflecting their shared etiologies. Their overlapping nature presents a methodological challenge, possibly masking associations between COPCs and health…

review 2024
Journal of translational medicine ·doi:10.1186/s12967-024-05333-1

Fibrosis is a pathological process involving the abnormal deposition of connective tissue, resulting from improper tissue repair in response to sustained injury caused by hypoxia, infection, or physical damage. It can impact any organ, lead…

observational 2023
BMC medicine ·doi:10.1186/s12916-022-02703-8

BACKGROUND: Understanding the relationship between chronic pain conditions and suicidal behavior-suicide attempt, other intentional self-harm, and death by suicide-is imperative for suicide prevention efforts. Although chronic pain conditio…

observational 2022
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians ·doi:10.1080/14767058.2021.1875436

INTRODUCTION: Research has consistently shown individuals with mental health conditions are more likely to be prescribed opioid analgesic medications and to engage in heavier utilization. However, it is unclear whether these findings apply …

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…