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Authors whose works are in public domain in at least one jurisdiction

List of works by Minna Männikkö

1-12 of 12 results

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Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome

scientific article published on March 1, 1998
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

scientific article
A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies

scientific article published on August 30, 2012
Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings

scientific article published on May 1, 2011
Candidate Gene Association Study of Magnetic Resonance Imaging-based Hip Osteoarthritis (OA): Evidence for COL9A2 Gene as a Common Predisposing Factor for Hip OA and Lumbar Disc Degeneration

article
Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

scientific article published in October 2016
Higher Prevalence of Autoimmune Diseases and Longer Spells of Vertigo in Patients Affected With Familial Ménière's Disease: A Clinical Comparison of Familial and Sporadic Ménière's Disease

scientific article published on June 1, 2014
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron
Functional polymorphisms in asporin and CILP together with joint loading predispose to hand osteoarthritis.

scientific article published on 12 December 2017
Polygenic Risk Scores and Physical Activity

scientific article published on 10 February 2020
Exome sequencing reveals a phenotype modifying variant in ZNF528 in primary osteoporosis with a COL1A2 deletion

scientific article published on 28 July 2020
Association of Body Mass Index with Fecal Microbial Diversity and Metabolites in the Northern Finland Birth Cohort

scientific article published on 27 August 2020

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