Jeroen G. Van Rooij
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 9 publications
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing.
Journal: medRxiv : the preprint server for health sciences
Published: July 09, 2024
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.
Journal: Nature communications
Published: June 05, 2024
Lifestyle factors and metabolomic aging biomarkers: Meta-analysis of cross-sectional and longitudinal associations in three prospective cohorts.
Journal: Mechanisms of ageing and development
Published: February 07, 2024
Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: March 21, 2022
Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy.
Journal: European journal of human genetics : EJHG
Published: April 02, 2017
A rare missense variant in RCL1 segregates with depression in extended families.
Journal: Molecular psychiatry
Published: September 08, 2016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.
Journal: Molecular psychiatry
Published: August 10, 2016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.
Journal: Molecular psychiatry
Published: August 25, 2015
Suspected bacterial endophthalmitis following intravitreal anti-VEGF injection: case series and literature review.
Journal: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde
Published: January 26, 2012
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Last Updated: 09/26/2026