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Lista de obras de Sini Skarp

A Whole Exome Study Identifies Novel Candidate Genes for Vertebral Bone Marrow Signal Changes (Modic Changes).

artículo científico publicado en 2016

Breast cancer carcinoma-associated fibroblasts differ from breast fibroblasts in immunological and extracellular matrix regulating pathways.

artículo científico publicado en 2016

Exome sequencing reveals a phenotype modifying variant in ZNF528 in primary osteoporosis with a COL1A2 deletion

artículo científico publicado en 2020

Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes

scientific article published on 26 February 2019

Intrauterine growth restriction and placental gene expression in severe preeclampsia, comparing early-onset and late-onset forms

artículo científico

Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions

NRF1 and NRF2 mRNA and Protein Expression Decrease Early during Melanoma Carcinogenesis: An Insight into Survival and MicroRNAs

scientific article published on 04 September 2019

New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s Disease

artículo científico publicado en 2022

Prognostic significance of Twist, ZEB1 and Slug in peripheral T-cell lymphomas

scientific article published on 01 December 2020

Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility.

artículo científico publicado en 2018

TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway

artículo científico publicado en 2017

Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis.

artículo científico publicado en 2015

The interplay of matrix metalloproteinase-8, transforming growth factor-β1 and vascular endothelial growth factor-C cooperatively contributes to the aggressiveness of oral tongue squamous cell carcinoma

artículo científico publicado en 2017

Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis

artículo científico publicado en 2018

Whole-exome sequencing suggests multiallelic inheritance for childhood-onset Ménière's disease

artículo científico publicado en 2019

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