<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Salminen A</submitter><funding>Business Finland</funding><funding>Pfizer Inc.</funding><funding>Boehringer Ingelheim International GmbH</funding><funding>Biogen MA Inc.</funding><funding>Bristol-Myers Squibb Canada</funding><funding>Paulo Foundation</funding><funding>Academy of Finland</funding><funding>Genentech Inc.</funding><funding>Bristol Myers Squibb (and Celgene Corporation &amp; Celgene International II Sàrl)</funding><funding>Novartis AG</funding><funding>GlaxoSmithKline Intellectual Property Development Ltd.</funding><funding>Suomen Hammaslääkäriseura Apollonia</funding><funding>Novo Nordisk Fonden</funding><funding>Maze Therapeutics Inc.</funding><funding>Merck Sharp &amp; Dohme LLC</funding><funding>Sigrid Juséliuksen Säätiö</funding><funding>Pfizer</funding><funding>AstraZeneca UK Ltd.</funding><funding>AbbVie</funding><funding>AbbVie Inc.</funding><funding>Novartis</funding><funding>Sydäntutkimussäätiö</funding><funding>Finnish Foundation for Cardiovascular Research</funding><funding>Paulon Säätiö</funding><funding>Sanofi US Services Inc.</funding><funding>Janssen Biotech Inc.</funding><pagination>1263-1275</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12377943</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>52(9)</volume><pubmed_abstract>&lt;h4>Aim&lt;/h4>To perform a genome-wide association study (GWAS) for periodontitis in the FinnGen cohort, as genetic factors contribute to periodontitis.&lt;h4>Materials and methods&lt;/h4>We included nearly 250,000 Finnish individuals who had visited a dentist in the public healthcare sector for a clinical oral examination. We designed three periodontitis phenotypes based on diagnosis and procedure codes and CPI indexes in national health registers.&lt;h4>Results&lt;/h4>We identified 11 independent genetic loci associated with periodontitis, among which 6 were common and novel. A locus near the FST gene was associated with two phenotypes, whereas other lead SNPs were located near ARL15, MFHAS1, DEFB130A and APOE. Additionally, all phenotypes in the discovery and replication cohorts were associated with </pubmed_abstract><journal>Journal of clinical periodontology</journal><pubmed_title>Genetic Loci Associated With Periodontitis: The FinnGen Study Based on National Health Registers.</pubmed_title><pmcid>PMC12377943</pmcid><funding_grant_id>4685/31/2016</funding_grant_id><funding_grant_id>UH 4386/31/2016</funding_grant_id><pubmed_authors>Lahteenmaki S</pubmed_authors><pubmed_authors>Helminen M</pubmed_authors><pubmed_authors>Kaprio J</pubmed_authors><pubmed_authors>Biswas S</pubmed_authors><pubmed_authors>Estrada K</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Harju T</pubmed_authors><pubmed_authors>Pendergrass R</pubmed_authors><pubmed_authors>Smaoui N</pubmed_authors><pubmed_authors>John S</pubmed_authors><pubmed_authors>Blomster T</pubmed_authors><pubmed_authors>Arvas M</pubmed_authors><pubmed_authors>FinnGen</pubmed_authors><pubmed_authors>Vahatalo 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S</pubmed_authors><pubmed_authors>Kumar J</pubmed_authors><pubmed_authors>Palta P</pubmed_authors><pubmed_authors>Kallionpaa R</pubmed_authors><pubmed_authors>Garcia-Tabuenca J</pubmed_authors><pubmed_authors>Mattsson H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic Loci Associated With Periodontitis: The FinnGen Study Based on National Health Registers.</name><description>&lt;h4>Aim&lt;/h4>To perform a genome-wide association study (GWAS) for periodontitis in the FinnGen cohort, as genetic factors contribute to periodontitis.&lt;h4>Materials and methods&lt;/h4>We included nearly 250,000 Finnish individuals who had visited a dentist in the public healthcare sector for a clinical oral examination. We designed three periodontitis phenotypes based on diagnosis and procedure codes and CPI indexes in national health registers.&lt;h4>Results&lt;/h4>We identified 11 independent genetic loci associated with periodontitis, among which 6 were common and novel. A locus near the FST gene was associated with two phenotypes, whereas other lead SNPs were located near ARL15, MFHAS1, DEFB130A and APOE. Additionally, all phenotypes in the discovery and replication cohorts were associated with </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-10T01:44:12.139Z</modification><creation>2026-04-08T01:24:44.177Z</creation></dates><accession>S-EPMC12377943</accession><cross_references><pubmed>40682483</pubmed><doi>10.1111/jcpe.14193</doi></cross_references></HashMap>