perinnölliset taudit

http://www.yso.fi/onto/yso/p19997

Liittyvät julkaisut ja muut tuotokset

  

  

  

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• Circulating metabolome landscape in Lynch syndrome (2024) Jokela, Tiina A.; et al.; A1; OA
• Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort (2024) Sipilä, Lauri J.; et al.; A1; OA
• Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects (2024) Broberg, Martin; et al.; A1; OA
• Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes : an EHTG, PLSD position statement (2023) Møller, Pal; et al.; A2; OA
• Lynch syndrome genetics and clinical implications (2023) Peltomäki, Päivi; et al.; A1; OA
• Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database (2023) Dominguez-Valentin, Mev; et al.; A1; OA
• Rare variant analyses across multiethnic cohorts identify novel genes for refractive error (2023) Musolf, Anthony M.; et al.; A1; OA
• Systemic circulating microRNA landscape in Lynch syndrome (2023) Sievänen, Tero; et al.; A1; OA
• Schizophrenia polygenic risk score and long-term success in the labour market : A cohort study (2022) Viinikainen, Jutta; et al.; A1; OA
• Testing for Lynch Syndrome in Endometrial Carcinoma : From Universal to Age-Selective MLH1 Methylation Analysis (2022) Pasanen, Annukka; et al.; A1; OA