Search Results - Männikkö, Minna

Refine Results
  1. 1
    Functional polymorphisms in asporin and CILP together with joint loading predispose to hand osteoarthritis

    Functional polymorphisms in asporin and CILP together with joint loading predispose to hand osteoarthritis by Taipale, Mari, Solovieva, Svetlana, Leino-Arjas, Päivi, Männikkö, Minna

    Published 2017
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  2. 2
    New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s Disease

    New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s Disease by Skarp, Sini, Korvala, Johanna, Kotimäki, Jouko, Sorri, Martti, Männikkö, Minna, Hietikko, Elina

    Published 2022
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  3. 3
    A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients

    A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients by Parviainen, Roope, Skarp, Sini, Korhonen, Linda, Serlo, Willy, Männikkö, Minna, Sinikumpu, Juha-Jaakko

    Published 2020
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  4. 4
    TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway

    TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway by Sliz, Eeva, Taipale, Mari, Welling, Maiju, Skarp, Sini, Alaraudanjoki, Viivi, Ignatius, Jaakko, Ruddock, Lloyd, Nissi, Ritva, Männikkö, Minna

    Published 2017
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  5. 5
    Common interleukin-6 promoter variants associate with the more severe forms of distal interphalangeal osteoarthritis

    Common interleukin-6 promoter variants associate with the more severe forms of distal interphalangeal osteoarthritis by Kämäräinen, Olli-Pekka, Solovieva, Svetlana, Vehmas, Tapio, Luoma, Katariina, Riihimäki, Hilkka, Ala-Kokko, Leena, Männikkö, Minna, Leino-Arjas, Päivi

    Published 2008
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  6. 6
    Gender difference in genetic association between IL1A variant and early lumbar disc degeneration: a three-year follow-up

    Gender difference in genetic association between IL1A variant and early lumbar disc degeneration: a three-year follow-up by Eskola, Pasi J, Kjaer, Per, Sorensen, Joan S, Okuloff, Annaleena, Wedderkopp, Niels, Daavittila, Iita, Ala-Kokko, Leena, Männikkö, Minna, Karppinen, Jaro

    Published 2012
    Get full text Get full text
    Text
    Save to List
    Saved in:
  7. 7
    Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility

    Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility by Costantini, Alice, Skarp, Sini, Kämpe, Anders, Mäkitie, Riikka E., Pettersson, Maria, Männikkö, Minna, Jiao, Hong, Taylan, Fulya, Lindstrand, Anna, Mäkitie, Outi

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  8. 8
    Exome Sequencing Reveals a Phenotype Modifying Variant in ZNF528 in Primary Osteoporosis With a COL1A2 Deletion

    Exome Sequencing Reveals a Phenotype Modifying Variant in ZNF528 in Primary Osteoporosis With a COL1A2 Deletion by Skarp, Sini, Xia, Ji‐Han, Zhang, Qin, Löija, Marika, Costantini, Alice, Ruddock, Lloyd W, Mäkitie, Outi, Wei, Gong‐Hong, Männikkö, Minna

    Published 2020
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  9. 9
    Cohort Profile: 46 years of follow-up of the Northern Finland Birth Cohort 1966 (NFBC1966)

    Cohort Profile: 46 years of follow-up of the Northern Finland Birth Cohort 1966 (NFBC1966) by Nordström, Tanja, Miettunen, Jouko, Auvinen, Juha, Ala-Mursula, Leena, Keinänen-Kiukaanniemi, Sirkka, Veijola, Juha, Järvelin, Marjo-Riitta, Sebert, Sylvain, Männikkö, Minna

    Published 2021
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  10. 10
    The Collagen V Homotrimer [α1(V)](3) Production Is Unexpectedly Favored over the Heterotrimer [α1(V)](2)α2(V) in Recombinant Expression Systems

    The Collagen V Homotrimer [α1(V)](3) Production Is Unexpectedly Favored over the Heterotrimer [α1(V)](2)α2(V) in Recombinant Expression Systems by Roulet, Muriel, Välkkilä, Merja, Chanut-Delalande, Hélène, Hämäläinen, Eija-Riitta, Kessler, Efrat, Ala-Kokko, Leena, Männikkö, Minna, Bonod-Bidaud, Christelle, Ruggiero, Florence

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  11. 11
    Genetic predisposition for femoral neck stress fractures in military conscripts

    Genetic predisposition for femoral neck stress fractures in military conscripts by Korvala, Johanna, Hartikka, Heini, Pihlajamäki, Harri, Solovieva, Svetlana, Ruohola, Juha-Petri, Sahi, Timo, Barral, Sandra, Ott, Jürg, Ala-Kokko, Leena, Männikkö, Minna

    Published 2010
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  12. 12
    Identification of disease-associated loci using machine learning for genotype and network data integration

    Identification of disease-associated loci using machine learning for genotype and network data integration by Leal, Luis G, David, Alessia, Jarvelin, Marjo-Riita, Sebert, Sylvain, Männikkö, Minna, Karhunen, Ville, Seaby, Eleanor, Hoggart, Clive, Sternberg, Michael J E

    Published 2019
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  13. 13
    Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis

    Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis by Skarp, Sini, Kämäräinen, Olli-Pekka, Wei, Gong-Hong, Jakkula, Eveliina, Kiviranta, Ilkka, Kröger, Heikki, Auvinen, Juha, Lehenkari, Petri, Ala-Kokko, Leena, Männikkö, Minna

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  14. 14
    Genetic risk factors of disc degeneration among 12-14-year-old Danish children: a population study

    Genetic risk factors of disc degeneration among 12-14-year-old Danish children: a population study by Eskola, Pasi J, Kjaer, Per, Daavittila, Iita M, Solovieva, Svetlana, Okuloff, Annaleena, Sorensen, Joan S, Wedderkopp, Niels, Ala-Kokko, Leena, Männikkö, Minna, Karppinen, Jaro I

    Published 2010
    Get full text Get full text
    Text
    Save to List
    Saved in:
  15. 15
    NAFLD risk alleles in PNPLA3, TM6SF2, GCKR and LYPLAL1 show divergent metabolic effects

    NAFLD risk alleles in PNPLA3, TM6SF2, GCKR and LYPLAL1 show divergent metabolic effects by Sliz, Eeva, Sebert, Sylvain, Würtz, Peter, Kangas, Antti J, Soininen, Pasi, Lehtimäki, Terho, Kähönen, Mika, Viikari, Jorma, Männikkö, Minna, Ala-Korpela, Mika, Raitakari, Olli T, Kettunen, Johannes

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  16. 16
    Polygenic Risk Scores and Physical Activity

    Polygenic Risk Scores and Physical Activity by KUJALA, URHO M., PALVIAINEN, TEEMU, PESONEN, PAULA, WALLER, KATJA, SILLANPÄÄ, ELINA, NIEMELÄ, MAISA, KANGAS, MAARIT, VÄHÄ-YPYÄ, HENRI, SIEVÄNEN, HARRI, KORPELAINEN, RAIJA, JÄMSÄ, TIMO, MÄNNIKKÖ, MINNA, KAPRIO, JAAKKO

    Published 2020
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  17. 17
    Genetic Association Studies in Lumbar Disc Degeneration: A Systematic Review

    Genetic Association Studies in Lumbar Disc Degeneration: A Systematic Review by Eskola, Pasi J., Lemmelä, Susanna, Kjaer, Per, Solovieva, Svetlana, Männikkö, Minna, Tommerup, Niels, Lind-Thomsen, Allan, Husgafvel-Pursiainen, Kirsti, Cheung, Kenneth M. C., Chan, Danny, Samartzis, Dino, Karppinen, Jaro

    Published 2012
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  18. 18
    Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity

    Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity by Korvala, Johanna, Jüppner, Harald, Mäkitie, Outi, Sochett, Etienne, Schnabel, Dirk, Mora, Stefano, Bartels, Cynthia F, Warman, Matthew L, Deraska, Donald, Cole, William G, Hartikka, Heini, Ala-Kokko, Leena, Männikkö, Minna

    Published 2012
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  19. 19
    Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population

    Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population by Salo, Perttu P., Havulinna, Aki S., Tukiainen, Taru, Raitakari, Olli, Lehtimäki, Terho, Kähönen, Mika, Kettunen, Johannes, Männikkö, Minna, Eriksson, Johan G., Jula, Antti, Blankenberg, Stefan, Zeller, Tanja, Salomaa, Veikko, Kristiansson, Kati, Perola, Markus

    Published 2017
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  20. 20
    Association of Body Mass Index with Fecal Microbial Diversity and Metabolites in the Northern Finland Birth Cohort

    Association of Body Mass Index with Fecal Microbial Diversity and Metabolites in the Northern Finland Birth Cohort by Loftfield, Erikka, Herzig, Karl-Heinz, Caporaso, J Gregory, Derkach, Andriy, Wan, Yunhu, Byrd, Doratha A., Vogtmann, Emily, Männikkö, Minna, Karhunen, Ville, Knight, Rob, Gunter, Marc J., Jӓrvelin, Marjo-Riitta, Sinha, Rashmi

    Published 2020
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: