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Publications by Minna Männikkö

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

Neuron
Neuroscience
2018English

Haplotype Sharing Provides Insights Into Fine-Scale Population History and Disease in Finland

American Journal of Human Genetics
Genetics
2018English

Genome-Wide Association Study Identifies Seven Novel Loci Associating With Circulating Cytokines and Cell Adhesion Molecules in Finns

Journal of Medical Genetics
Genetics
2019English

TUFT1, a Novel Candidate Gene for Metatarsophalangeal Osteoarthritis, Plays a Role in Chondrogenesis on a Calcium-Related Pathway

PLoS ONE
Multidisciplinary
2017English

Congenital Nephrotic Syndrome (NPHS1): Features Resulting From Different Mutations in Finnish Patients

Kidney International
Nephrology
2000English

Association of the Tag SNPs in the HumanSKTGene (KIAA1217) With Lumbar Disc Herniation

Journal of Bone and Mineral Research
EndocrinologyOrthopedicsSports MedicineMetabolismDiabetes
2009English

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