ReviewHuman genetics2003
The Finnish Disease Heritage III: the individual diseases.
Review in Human genetics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
34 citing papers in PubMed.
- Monoallelic TYROBP deletion is a novel risk factor for Alzheimer's disease.Molecular neurodegeneration · 2025Article
- Blood donor biobank as a resource in personalised biomedical genetic research.European journal of human genetics : EJHG · 2024Article
- Population-Based Biobanking.Genes · 2024Review
- Psychiatric symptoms in Salla disease.European child & adolescent psychiatry · 2023Review
- GENLIB: new function to simulate haplotype transmission in large complex genealogies.Bioinformatics (Oxford, England) · 2023Article
- Article
- Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort.Prenatal diagnosis · 2022Article
- Wilms tumor with Mulibrey Nanism: A case report and review of literature.Cancer reports (Hoboken, N.J.) · 2022Review
- Young woman with hypophosphatasia: A case report.Clinical case reports · 2022Article
- Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant.Molecular genetics & genomic medicine · 2022Article
- Review
- Review
- Genetic background of ataxia in children younger than 5 years in Finland.Neurology. Genetics · 2020Article
- Modifier genes for sudden cardiac death.European heart journal · 2018Review
- Fine-Scale Genetic Structure in Finland.G3 (Bethesda, Md.) · 2017Article
- Genetics in an isolated population like Finland: a different basis for genomic medicine?Journal of community genetics · 2017Article
- Retinal Degeneration In A Mouse Model Of CLN5 Disease Is Associated With Compromised Autophagy.Scientific reports · 2017Article
- Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder.Translational psychiatry · 2017Article
- The impact of recent population history on the deleterious mutation load in humans and close evolutionary relatives.Current opinion in genetics & development · 2016Review
- Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland.European journal of human genetics : EJHG · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This article is the third and last in a series entitled The Finnish Disease Heritage I-III. All the 36 rare hereditary diseases belonging to this entity are described for clinical and molecular genetic purposes, based on the Finnish experience gathered over a period of half a century. In addition, five other diseases are mentioned. They may be included in the list of the "Finnish diseases" after adequate complementary studies.
Indexed as
Identifiers
12627297What 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.