ArticleJournal of community genetics2017
Genetics in an isolated population like Finland: a different basis for genomic medicine?
Article in Journal of community genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
22 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Genetic sub-structuring of Croatian island populations in the Southeastern European context: a meta-analysis.Croatian medical journal · 2022Pooled it
- Article
- Y chromosome sequencing data suggest dual paths of haplogroup N1a1 into Finland.European journal of human genetics : EJHG · 2025Article
- A Comprehensive Review of Syndromic Forms of Obesity: Genetic Etiology, Clinical Features and Molecular Diagnosis.Current obesity reports · 2024Review
- Association between migraine and venous thromboembolism: a Mendelian randomization and genetic correlation study.Frontiers in genetics · 2024Article
- NovelCancers · 2023Article
- Men with Crohn's disease may have an increased risk for head and neck squamous cell carcinoma - a nationwide register study.Clinical oral investigations · 2023Article
- Article
- Fecal microbiome alterations in treatment-naive de novo Parkinson's disease.NPJ Parkinson's disease · 2022Article
- Calabria as a Genetic Isolate: A Model for the Study of Neurodegenerative Diseases.Biomedicines · 2022Review
- Article
- Influence of genetic substructuring of statistical forensic parameters on genetic short tandem repeat markers in the populations of Southeastern Europe.Croatian medical journal · 2022Article
- Article
- Review
- C-reactive protein and temperament: An instrumental variable analysis.Brain, behavior, & immunity - health · 2021Article
- HLA-G polymorphism impacts the outcome of oral HPV infections in women.BMC infectious diseases · 2021Article
- Cutting the fat: advances and challenges in sleep apnoea genetics.The European respiratory journal · 2021Article
- Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants.Human mutation · 2021Article
- The Effects of Genetic Background for Diurnal Preference on Sleep Development in Early Childhood.Nature and science of sleep · 2021Article
- Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype.BMC medical genetics · 2020Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
A unique genetic background in an isolated population like that of Finland offers special opportunities for genetic research as well as for applying the genetic developments to the health care. On the other hand, the different genetic background may require local attempts to develop diagnostics and treatment as the selection of diseases and mutations differs from that in the other populations. In this review, we describe the experiences of research and health care in this genetic isolate starting from the identification of specific monogenic diseases enriched in the Finnish population all the way to implementing the knowledge of the unique genetic background to genomic medicine at population level.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.