نتائج البحث - Minna Männikkö

تنقيح النتائج
  1. 1
    Heterozygous Mutations in the <i>LDL Receptor-Related Protein 5</i> (<i>LRP5</i>) Gene Are Associated With Primary Osteoporosis in Children

    Heterozygous Mutations in the <i>LDL Receptor-Related Protein 5</i> (<i>LRP5</i>) Gene Are Associated With Primary Osteoporosis in Children حسب Heini Hartikka, Outi Mäkitie, Minna Männikkö, Andréa S. Doria, Alan Daneman, William G. Cole, Leena Ala‐Kokko, Etienne Sochett

    منشور في 2005
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  2. 2
    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) حسب Tanja Nordström, Jouko Miettunen, Juha Auvinen, Leena Ala‐Mursula, Sirkka Keinänen‐Kiukaanniemi, Juha Veijola, Marjo‐Riitta Järvelin, Sylvain Sebért, Minna Männikkö

    منشور في 2021
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  3. 3
    Genetic predisposition for femoral neck stress fractures in military conscripts

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

    منشور في 2010
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  4. 4
    Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients

    Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients حسب Jaakko Patrakka, Marjo Kestilä, Jorma Wartiovaara, Vesa Ruotsalainen, Päivi Tissari, Ulla Lenkkeri, Minna Männikkö, Ilona Visapää, Christer Holmberg, Juhani Rapola, Karl Tryggvason, Hannu Jalanko

    منشور في 2000
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  5. 5
    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 حسب Eeva Sliz, Sylvain Sebért, Peter Würtz, Antti J. Kangas, Pasi Soininen, Terho Lehtimäki, Mika Kähönen, Jorma Viikari, Minna Männikkö, Mika Ala‐Korpela, Olli T. Raitakari, Johannes Kettunen

    منشور في 2018
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  6. 6
    Genetic Association Studies in Lumbar Disc Degeneration: A Systematic Review

    Genetic Association Studies in Lumbar Disc Degeneration: A Systematic Review حسب Pasi J Eskola, Susanna Lemmelä, Per Kjær, Svetlana Solovieva, Minna Männikkö, Niels Tommerup, Allan Lind-Thomsen, Kirsti Husgafvel‐Pursiainen, Kmc Cheung, Danny Chan, Dino Samartzis, Jaro Karppinen

    منشور في 2012
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  7. 7
    Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations

    Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations حسب Ulla Lenkkeri, Minna Männikkö, Paula McCready, Jane E. Lamerdin, Olivier Gribouval, Patrick Niaudet, Corinne Antignac, Clifford E. Kashtan, Christer Holmberg, Anne S. Olsen, Marjo Kestilä, Karl Tryggvason

    منشور في 1999
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  8. 8
    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 حسب Johanna Korvala, Harald Jüppner, Outi Mäkitie, Etienne Sochett, Dirk Schnabel, Stefano Mora, Cynthia F. Bartels, Matthew L. Warman, D J Deraska, William G. Cole, Heini Hartikka, Leena Ala‐Kokko, Minna Männikkö

    منشور في 2012
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  9. 9
    Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome

    Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome حسب Marjo Kestilä, Ulla Lenkkeri, Minna Männikkö, Jane E. Lamerdin, Paula McCready, Heli Putaala, Vesa Ruotsalainen, Takako Morita, Marja Nissinen, Riitta Herva, Clifford E. Kashtan, Leena Peltonen, Christer Holmberg, Anne S. Olsen, Karl Tryggvason

    منشور في 1998
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  10. 10
    Genetic susceptibility of intervertebral disc degeneration among young Finnish adults

    Genetic susceptibility of intervertebral disc degeneration among young Finnish adults حسب Anthi Kelempisioti, Pasi J Eskola, Annaleena Okuloff, Ulla Karjalainen, Jani Takatalo, Iita Daavittila, Jaakko Niinimäki, Roberto Blanco Sequeiros, Osmo Tervonen, Svetlana Solovieva, Patrick Y.P. Kao, You‐Qiang Song, Kmc Cheung, Danny Chan, Leena Ala‐Kokko, Marjo‐Riitta Järvelin, Jaro Karppinen, Minna Männikkö

    منشور في 2011
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  11. 11
    Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns

    Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns حسب Eeva Sliz, Marita Kalaoja, Ari Ahola‐Olli, Olli T. Raitakari, Markus Perola, Veikko Salomaa, Terho Lehtimäki, Toni Karhu, Heimo Viinamäki, Marko Salmi, Kristiina Santalahti, Sirpa Jalkanen, Jari Jokelainen, Sirkka Keinänen‐Kiukaanniemi, Minna Männikkö, Karl‐Heinz Herzig, Marjo‐Riitta Järvelin, Sylvain Sebért, Johannes Kettunen

    منشور في 2019
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  12. 12
    A <scp>GWAS</scp> meta‐analysis from 5 population‐based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome

    A <scp>GWAS</scp> meta‐analysis from 5 population‐based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome حسب Ferdinando Bonfiglio, Maria Henström, Abhishek Nag, Fatemeh Hadizadeh, Tenghao Zheng, María Carmen Cénit, Ettje F. Tigchelaar, Frances M. K. Williams, Anna Reznichenko, W. E. Ek, Natalia V. Rivera, Georg Homuth, Ali A. Aghdassi, Tim Kacprowski, Minna Männikkö, Ville Karhunen, Luís Bujanda, Joseph Rafter, Cisca Wijmenga, Jukka Ronkainen, Pirro G. Hysi, Alexandra Zhernakova, Mauro D’Amato

    منشور في 2018
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  13. 13
    Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland

    Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland حسب Mitja Kurki, Elmo Saarentaus, Olli Pietiläinen, Padhraig Gormley, Dennis Lal, Sini Kerminen, Minna Torniainen‐Holm, Eija Hämäläinen, Elisa Rahikkala, Riikka Keski‐Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen‐Ebrahim, Heli Helander, Päivi Vieira, Minna Männikkö, Markku Peltonen, Aki S. Havulinna, Veikko Salomaa, Matti Pirinen, Jaana Suvisaari, Jukka S. Moilanen, Jarmo Körkkö, Outi Kuismin, Mark J. Daly, Aarno Palotie

    منشور في 2019
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  14. 14
    Multiple chronic pain states are associated with a common amino acid–changing allele in KCNS1

    Multiple chronic pain states are associated with a common amino acid–changing allele in KCNS1 حسب Michael Costigan, Inna Belfer, Robert S. Griffin, Feng Dai, Lee Barrett, Giovanni Coppola, Tianxia Wu, Carly Kiselycznyk, Minakshi Poddar, Yan Lu, Luda Diatchenko, Shad B. Smith, Enrique J. Cobos, Dmitri V. Zaykin, Andrew Allchorne, Pei‐Hong Shen, Lone Nikolajsen, Jaro Karppinen, Minna Männikkö, Anthi Kelempisioti, David Goldman, William Maixner, Daniel H. Geschwind, Mitchell B. Max, Ze’ev Seltzer, Clifford J. Woolf

    منشور في 2010
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  15. 15
    Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

    Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland حسب Alicia R. Martin, Konrad J. Karczewski, Sini Kerminen, Mitja Kurki, Antti‐Pekka Sarin, Mykyta Artomov, Johan G. Eriksson, Tõnu Esko, Giulio Genovese, Aki S. Havulinna, Jaakko Kaprio, А. О. Конради, László Korányi, Anna Kostareva, Minna Männikkö, Andres Metspalu, Markus Perola, Rashmi B. Prasad, Olli T. Raitakari, Oxana Rotar, Veikko Salomaa, Leif Groop, Aarno Palotie, Benjamin M. Neale, Samuli Ripatti, Matti Pirinen, Mark J. Daly

    منشور في 2018
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  16. 16
    Pain perception is altered by a nucleotide polymorphism in <i>SCN9A</i>

    Pain perception is altered by a nucleotide polymorphism in <i>SCN9A</i> حسب Frank Reimann, James J. Cox, Inna Belfer, Luda Diatchenko, Dmitri V. Zaykin, Duncan P. McHale, Joost P.H. Drenth, Feng Dai, Jerry Wheeler, Frances Sanders, Linda S. Wood, Tianxia Wu, Jaro Karppinen, Lone Nikolajsen, Minna Männikkö, Mitchell B. Max, Carly Kiselycznyk, Minakshi Poddar, René H. M. te Morsche, Shad B. Smith, Dustin G. Gibson, Anthi Kelempisioti, William Maixner, Fiona M. Gribble, C. Geoffrey Woods

    منشور في 2010
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  17. 17
    GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos

    GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos حسب Anne E. Sanders, Deepti Jain, Tamar Sofer, Kathleen F. Kerr, Cathy C. Laurie, John R. Shaffer, Mary L. Marazita, Linda M. Kaste, Gary D. Slade, Roger B. Fillingim, Richard Ohrbach, William Maixner, Thomas Kocher, Olaf Bernhardt, Alexander Teumer, Christian Schwahn, Kirsi Sipilä, Raija Lähdesmäki, Minna Männikkö, Paula Pesonen, Marjo‐Riitta Järvelin, Célia Marisa Rizzatti‐Barbosa, Carolina B. Meloto, Margarete Ribeiro-Dasilva, Luda Diatchenko, Priscila de Oliveira Serrano, Shad B. Smith

    منشور في 2017
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  18. 18
    Metabolomic Consequences of Genetic Inhibition of PCSK9 Compared With Statin Treatment

    Metabolomic Consequences of Genetic Inhibition of PCSK9 Compared With Statin Treatment حسب Eeva Sliz, Johannes Kettunen, Michael V. Holmes, Clare Oliver Williams, Charles Boachie, Qin Wang, Minna Männikkö, Sylvain Sebért, Robin Walters, Kuang Lin, Iona Y. Millwood, Robert B. Clarke, Liming Li, Naomi Rankin, Paul Welsh, Christian Delles, J. Wouter Jukema, Stella Trompet, Ian Ford, Markus Perola, Veikko Salomaa, Marjo‐Riitta Järvelin, Zhengming Chen, Debbie A. Lawlor, Mika Ala‐Korpela, John Danesh, George Davey Smith, Naveed Sattar, Adam S. Butterworth, Peter Würtz

    منشور في 2018
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  19. 19
    Circulating inflammatory cytokines and risk of five cancers: a Mendelian randomization analysis

    Circulating inflammatory cytokines and risk of five cancers: a Mendelian randomization analysis حسب Emmanouil Bouras, Ville Karhunen, Dipender Gill, Jian Huang, Philip Haycock, Marc J. Gunter, Mattias Johansson, Paul Brennan, Timothy J. Key, Sarah J. Lewis, Richard M. Martin, Neil Murphy, Elizabeth A. Platz, Ruth C. Travis, James Yarmolinsky, Verena Zuber, Paul Martin, Michail Katsoulis, Heinz Freisling, Therese Haugdahl Nøst, Matthias B. Schulze, Laure Dossus, Rayjean J. Hung, Christopher I. Amos, Ari Ahola‐Olli, Saranya Palaniswamy, Minna Männikkö, Juha Auvinen, Karl‐Heinz Herzig, Sirkka Keinänen‐Kiukaanniemi, Terho Lehtimäki, Veikko Salomaa, Olli T. Raitakari, Marko Salmi, Sirpa Jalkanen, CRUK, CAPS, PEGASUS, Marjo-Riitta Jarvelin, Abbas Dehghan, Konstantinos K. Tsilidis

    منشور في 2022
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  20. 20
    Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males

    Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males حسب Shad B. Smith, Marc Parisien, Eric Bair, Inna Belfer, Anne‐Julie Chabot‐Doré, Pavel Gris, Samar Khoury, Shannon Tansley, Yelizaveta Torosyan, Dmitri V. Zaykin, Olaf Bernhardt, Priscila de Oliveira Serrano, Richard H. Gracely, Deepti Jain, Marjo‐Riitta Järvelin, Linda M. Kaste, Kathleen F. Kerr, Thomas Kocher, Raija Lähdesmäki, Nadia Laniado, Cathy C. Laurie, Cecelia Laurie, Minna Männikkö, Carolina B. Meloto, Andrea G. Nackley, Sarah C. Nelson, Paula Pesonen, Margarete Ribeiro-Dasilva, Célia Marisa Rizzatti‐Barbosa, Anne E. Sanders, Christian Schwahn, Kirsi Sipilä, Tamar Sofer, Alexander Teumer, Jeffrey S. Mogil, Roger B. Fillingim, Joel D. Greenspan, Richard Ohrbach, Gary D. Slade, William Maixner, Luda Diatchenko

    منشور في 2018
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