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Screening of biobank SNP-array genotyping data to detect Lynch syndrome predisposing MLH1 copy number variants

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 12:54
  • Read more about Screening of biobank SNP-array genotyping data to detect Lynch syndrome predisposing MLH1 copy number variants

A systematic Mendelian randomized study of the effects of the gut microbiome and immune cells on pancreatic neuroendocrine tumors

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 12:46
  • Read more about A systematic Mendelian randomized study of the effects of the gut microbiome and immune cells on pancreatic neuroendocrine tumors

Causal association between periodontitis and oral cancer: a two-sample Mendelian randomization study

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 12:38
  • Read more about Causal association between periodontitis and oral cancer: a two-sample Mendelian randomization study

Genome-wide Association Study Identifies SORCS3 as a Novel Susceptibility Locus for Panic Disorder in the FinnGen Study

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 12:10
  • Read more about Genome-wide Association Study Identifies SORCS3 as a Novel Susceptibility Locus for Panic Disorder in the FinnGen Study

Etiological basis for chronic pain genetic variation in brain and dorsal root ganglia cell types

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 10:55
  • Read more about Etiological basis for chronic pain genetic variation in brain and dorsal root ganglia cell types

PGS Browser: a public platform for personalized polygenic score interpretation

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 10:48
  • Read more about PGS Browser: a public platform for personalized polygenic score interpretation

Assessing the impact of maternal blood pressure during pregnancy on perinatal health: A wide-angled Mendelian randomization study

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 10:37
  • Read more about Assessing the impact of maternal blood pressure during pregnancy on perinatal health: A wide-angled Mendelian randomization study

Genomics reveals eleven obesity endotypes with distinct biological and phenotypic signatures

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 10:23
  • Read more about Genomics reveals eleven obesity endotypes with distinct biological and phenotypic signatures

Barrier genes are associated with preterm birth

Submitted by Frida Mäkelä on Wed, 07/09/2025 - 09:55
  • Read more about Barrier genes are associated with preterm birth

Single-cell multi-omic integration analysis prioritizes druggable genes and reveals cell-type-specific causal effects in glioblastomagenesis

Submitted by Frida Mäkelä on Tue, 07/08/2025 - 15:54
  • Read more about Single-cell multi-omic integration analysis prioritizes druggable genes and reveals cell-type-specific causal effects in glioblastomagenesis

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The University of Helsinki is the organization responsible for the FinnGen research project. The Finnish consortium partners include all Finnish public biobanks and their background organisations, so the project covers the whole of Finland. All partners are listed on this page.

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