Torthaí cuardaigh - Teppo Varilo

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  1. 1
    Molecular genetics of the Finnishdisease heritage

    Molecular genetics of the Finnishdisease heritage de réir Leena Peltonen, Anu Jalanko, Teppo Varilo

    Foilsithe / Cruthaithe 1999
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  2. 2
    Assignment of the Locus for Congenital Lactase Deficiency to 2q21, in the Vicinity of but Separate from the Lactase-Phlorizin Hydrolase Gene

    Assignment of the Locus for Congenital Lactase Deficiency to 2q21, in the Vicinity of but Separate from the Lactase-Phlorizin Hydrolase Gene de réir Irma Järvelä, Nabil Enattah, Jorma Kokkonen, Teppo Varilo, Erkki Savilahti, Leena Peltonen

    Foilsithe / Cruthaithe 1998
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  3. 3
    Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency

    Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency de réir Mikko Kuokkanen, Jorma Kokkonen, Nabil Enattah, Tero Ylisaukko‐oja, Hanna Komu, Teppo Varilo, Leena Peltonen, Erkki Savilahti, Irma Järvelä

    Foilsithe / Cruthaithe 2006
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  4. 4
    Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in Schizophrenia

    Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in Schizophrenia de réir Juho Wedenoja, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Anu Loukola, Tiina Paunio, Timo Partonen, Teppo Varilo, Jouko Lönnqvist, Leena Peltonen

    Foilsithe / Cruthaithe 2009
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  5. 5
    Genome-wide scan for loci of Asperger syndrome

    Genome-wide scan for loci of Asperger syndrome de réir Tero Ylisaukko‐oja, Taina Nieminen‐von Wendt, Elli Kempas, Susan Sarenius, Teppo Varilo, L. von Wendt, Leena Peltonen, Irma Järvelä

    Foilsithe / Cruthaithe 2004
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  6. 6
    A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27

    A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27 de réir Mari Auranen, Raija Vanhala, Teppo Varilo, Kristin L. Ayers, Elli Kempas, Tero Ylisaukko‐oja, Janet S. Sinsheimer, Leena Peltonen, Irma Järvelä

    Foilsithe / Cruthaithe 2002
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  7. 7
    Mutant<i>CHUK</i>and Severe Fetal Encasement Malformation

    Mutant<i>CHUK</i>and Severe Fetal Encasement Malformation de réir Jenni Lahtela, Heidi O. Nousiainen, Vedran Stefanović, Jonna Tallila, Heli Viskari, Riitta Karikoski, Massimiliano Gentile, Carola Saloranta, Teppo Varilo, Riitta Salonen, Marjo Kestilä

    Foilsithe / Cruthaithe 2010
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  8. 8
    A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci

    A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci de réir Iiris Hovatta, Teppo Varilo, Jaana Suvisaari, Joseph D. Terwilliger, Vesa Ollikainen, Ritva Arajärvi, Hannu Juvonen, Marja-Liisa Kokko-Sahin, Leena Väisänen, Heikki Mannila, Jouko Lönnqvist, Leena Peltonen

    Foilsithe / Cruthaithe 1999
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  9. 9
    Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

    Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects de réir William Hennah, Teppo Varilo, Marjo Kestilä, Tiina Paunio, Ritva Arajärvi, Jari Haukka, Alex Parker, Rory Martin, Steve Levitzky, Timo Partonen, Joanne M. Meyer, Jouko Lönnqvist, Leena Peltonen, Jesper Ekelund

    Foilsithe / Cruthaithe 2003
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  10. 10
    Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis

    Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis de réir Ritva Haataja, Minna K. Karjalainen, Aino Luukkonen, Kari Teramo, Hilkka Puttonen, Marja Ojaniemi, Teppo Varilo, Bimal P. Chaudhari, Jevon Plunkett, Jeffrey C. Murray, Steven A. McCarroll, Leena Peltonen, Louis J. Muglia, Aarno Palotie, Mikko Hallman

    Foilsithe / Cruthaithe 2011
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  11. 11
    The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population

    The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population de réir Eveliina Jakkula, Karola Rehnström, Teppo Varilo, Olli Pietiläinen, Tiina Paunio, Nancy L. Pedersen, Ulf DeFaire, Marjo‐Riitta Järvelin, Juha Saharinen, Nelson B. Freimer, Samuli Ripatti, Shaun Purcell, Andrew Collins, Mark J. Daly, Aarno Palotie, Leena Peltonen

    Foilsithe / Cruthaithe 2008
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  12. 12
    Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin

    Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin de réir Anna H. Hakonen, Silja Heiskanen, Vesa Juvonen, Ilse Lappalainen, Petri Luoma, Maria Rantamäki, Gert Van Goethem, A. Löfgren, Peter Hackman, Anders Paetau, Seppo Kaakkola, Kari Majamaa, Teppo Varilo, Bjarne Udd, Helena Kääriäinen, Laurence A. Bindoff, Anu Suomalainen

    Foilsithe / Cruthaithe 2005
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  13. 13
    The Finnish genetic heritage in 2022 – from diagnosis to translational research

    The Finnish genetic heritage in 2022 – from diagnosis to translational research de réir Johanna Uusimaa, Johannes Kettunen, Teppo Varilo, Irma Järvelä, Jukka Kallijärvi, Helena Kääriäinen, Minna Laine, Risto Lapatto, Päivi Myllynen, Harri Niinikoski, Elisa Rahikkala, Anu Suomalainen, Ritva Tikkanen, Henna Tyynismaa, Päivi Vieira, Tomáš Zárybnický, Petra Sipilä, Satu Kuure, Reetta Hinttala

    Foilsithe / Cruthaithe 2022
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  14. 14
    Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

    Genome-wide association analysis of metabolic traits in a birth cohort from a founder population de réir Chiara Sabatti, Susan K. Service, Anna‐Liisa Hartikainen, Anneli Pouta, Samuli Ripatti, J.F. Brodsky, Chris G Jones, Noah Zaitlen, Teppo Varilo, Marika Kaakinen, Ulla Sovio, Aimo Ruokonen, Jaana Laitinen, Eveliina Jakkula, Lachlan Coin, Clive Hoggart, Andrew Collins, Hannu Turunen, Stacey B. Gabriel, Paul Elliot, Mark I. McCarthy, Mark J. Daly, Marjo‐Riitta Järvelin, Nelson B. Freimer, Leena Peltonen

    Foilsithe / Cruthaithe 2008
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  15. 15
    Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

    Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene de réir Eveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, Teppo Varilo, S. Kallio, Anu Kemppinen, Shaun Purcell, Keijo Koivisto, Pentti J. Tienari, Marja‐Liisa Sumelahti, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, Arpo Aromaa, Annette Oturai, Helle Bach Søndergaard, Hanne F. Harbo, Inger‐Lise Mero, Stacey B. Gabriel, Daniel B. Mirel, Stephen L. Hauser, Ludwig Kappos, Chris H. Polman, Philip L. De Jager, David A. Hafler, Mark J. Daly, Aarno Palotie, Janna Saarela, Leena Peltonen

    Foilsithe / Cruthaithe 2010
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  16. 16
    The Clinical Picture of the ERCC6L2 Disease - from Bone Marrow Failure to Acute Leukemia

    The Clinical Picture of the ERCC6L2 Disease - from Bone Marrow Failure to Acute Leukemia de réir Marja Hakkarainen, Ilse Kaaja, Suvi P. M. Douglas, Thomas J. Vulliamy, Inderjeet Dokal, Jean Soulier, Lise Larcher, Régis Peffault de Latour, Thierry Leblanc, Flore Sicre de Fontbrune, Timo Siitonen, Olli Lohi, Eva Hellström‐Lindberg, Gisela Barbany, Bianca Tesi, Akiko Shimamura, Fabian Beier, Sharon Jackson, Amir A. Kuperman, Tzipora C. Falik‐Zaccai, Hannah Tamary, Cristina Mecucci, Ilaria Capolsini, Kirsi Jahnukainen, Urpu Salmenniemi, Riitta Niinimäki, Teppo Varilo, Outi Kilpivaara, Ulla Wartiovaara‐Kautto

    Foilsithe / Cruthaithe 2023
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  17. 17
    Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

    Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders de réir Georg Stoll, Olli Pietiläinen, Bastian Linder, Jaana Suvisaari, Cornelia Brosi, William Hennah, Virpi Leppä, Minna Torniainen, Samuli Ripatti, Sirpa Ala‐Mello, Oliver Plöttner, Karola Rehnström, Annamari Tuulio‐Henriksson, Teppo Varilo, Jonna Tallila, Kati Kristiansson, Matti Isohanni, Jaakko Kaprio, Johan G. Eriksson, Olli T. Raitakari, Terho Lehtimäki, Marjo‐Riitta Järvelin, Veikko Salomaa, Matthew E. Hurles, Hreinn Stefánsson, Leena Peltonen, Patrick F. Sullivan, Tiina Paunio, Jouko Lönnqvist, Mark J. Daly, Utz Fischer, Nelson B. Freimer, Aarno Palotie

    Foilsithe / Cruthaithe 2013
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  18. 18
    Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

    Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders de réir Chelsea Lowther, Mana M. Mehrjouy, Ryan L. Collins, Mads Bak, Olga Dudchenko, Harrison Brand, Zirui Dong, Malene Bøgehus Rasmussen, Huiya Gu, David Weisz, Lusine Nazaryan‐Petersen, Amanda S. Fjorder, Yuan Mang, Allan Lind-Thomsen, Juan M. M. Mendez, Xabier Calle, Anuja Chopra, Claus Hansen, Merete Bugge, Roeland Broekema, Teppo Varilo, Tiia Maria Luukkonen, J.J.M. Engelen, Angela Maria Vianna‐Morgante, Ana Carolina Fonseca, Juliana F. Mazzeu, Halinna Dornelles-Wawruk, Kikue Terada Abe, Joris Vermeesch, Kris Van Den Bogaert, Carolina Sismani, Constantia Aristidou, Paola Evangelidou, Albert Schinzel, Damien Sanlaville, Caroline Schluth–Bolard, Vera M. Kalscheuer, Maren Wenzel, Hyung‐Goo Kim, Katrin Õunap, Laura Roht, Susanna Midyan, María Clara Bonaglia, Anna Lindstrand, Jesper Eisfeldt, Jesper Ottosson, Daniel Nilsson, Maria Pettersson, Elenice Ferreira Bastos, Evica Rajcan‐Separovic, Fatma Sılan, Frenny Sheth, Antonio Novelli, Eirik Frengen, Madeleine Fannemel, Petter Strømme, Nadja Kokalj Vokač, Cornelia Daumer‐Haas, Danilo Moretti‐Ferreira, Deise Helena de Souza, María A. Ramos‐Arroyo, Maria M. Igoa, Lyudmila Angelova, Peter M. Kroisel, Graciela del Rey, Társis Paiva Vieira, M. E. Suzanne Lewis, Hao Wang, Jana Drabova, Markéta Havlovičová, Miroslava Hančárová, Zdeněk Sedláček, Ida Vogel, Tina Duelund Hjortshøj, Rikke S. Møller, Zeynep Tümer, Christina Fagerberg, Lilian Bomme Ousager, Bitten Schönewolf‐Greulich, Mathilde Lauridsen, Juliette Piard, Céline Pebrel‐Richard, Sylvie Jaillard, Nadja Ehmke, Eunice G. Stefanou, Czakó Marta, Kosztolányi György, Ashwin Dalal, Usha R. Dutta, Rashmi Shukla, Fortunato Lonardo, Orsetta Zuffardi, Gunnar Houge, Doriana Misceo, Shahid Mahmood Baig, Alina T. Midro, Natalia Wawrusiewicz‐Kurylonek, Isabel M. Carreira, Joana Barbosa Melo, Laura Rodriguez Martinez

    Foilsithe / Cruthaithe 2022
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