Laura Huilaja
Researcher Next ID · RN-027997
Researcher · Medicine
Oulu, Philippines
- Works count
- 200
- Citation count
- 11,519
- H-index
- 33
- i10-index
- 79
Research interests
Publications
FinnGen provides genetic insights from a well-phenotyped isolated population
Nature · 2023 · https://doi.org/10.1038/s41586-022-05473-8
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
Nature · 2023 · https://doi.org/10.1038/s41586-023-05837-8
FinnGen: Unique genetic insights from combining isolated population and national health register data
medRxiv · 2022 · 10.1101/2022.03.03.22271360
Skin cancers and their risk factors in older persons: a population-based study
BMC Geriatrics · 2022 · 10.1186/s12877-022-02964-1
Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis
Journal of Allergy and Clinical Immunology · 2021 · 10.1016/j.jaci.2021.07.043
The High Prevalence of Skin Diseases in Adults Aged 70 and Older
Journal of the American Geriatrics Society · 2020 · 10.1111/jgs.16706
Somatic and psychiatric comorbidities of hidradenitis suppurativa in children and adolescents
Journal of the American Academy of Dermatology · 2018 · 10.1016/j.jaad.2018.02.067
Vildagliptin Significantly Increases the Risk of Bullous Pemphigoid: A Finnish Nationwide Registry Study
Journal of Investigative Dermatology · 2018 · 10.1016/j.jid.2018.01.027
Patients with Hidradenitis Suppurativa Have a High Psychiatric Disease Burden: A Finnish Nationwide Registry Study
Journal of Investigative Dermatology · 2017 · 10.1016/j.jid.2017.06.020
Neurological and psychiatric associations in bullous pemphigoid—more than skin deep?
Experimental Dermatology · 2017 · 10.1111/exd.13401
Increased Levels of the Bullous Pemphigoid BP180 Autoantibody Are Associated with More Severe Dementia in Alzheimer’s Disease
Journal of Investigative Dermatology · 2016 · 10.1016/j.jid.2016.09.010
Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy
The American Journal of Human Genetics · 2016 · 10.1016/j.ajhg.2016.03.015
Gestational pemphigoid
Orphanet Journal of Rare Diseases · 2014 · 10.1186/s13023-014-0136-2
Pemphigoid gestationis autoantigen, transmembrane collagen XVII, promotes the migration of cytotrophoblastic cells of placenta and is a structural component of fetal membranes
Matrix Biology · 2007 · 10.1016/j.matbio.2007.10.007
Current projects
No projects listed.