Assignment of the Locus for Hydrolethalus Syndrome to a Highly Restricted Region on 11q23-25

Por Visapää, Ilona, Salonen, Riitta, Varilo, Teppo, Paavola, Paulina, Peltonen, Leena
Publicado em 1999

A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate

Por Misiewicz, Zuzanna, Hiekkalinna, Tero, Paunio, Tiina, Varilo, Teppo, Terwilliger, Joseph D., Partonen, Timo, Hovatta, Iiris
Publicado no Sci Rep (2016)

A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27

Por Auranen, Mari, Vanhala, Raija, Varilo, Teppo, Ayers, Kristin, Kempas, Elli, Ylisaukko-oja, Tero, Sinsheimer, Janet S., Peltonen, Leena, Järvelä, Irma
Publicado em 2002

Linkage Analysis of Schizophrenia Controlling for Population Substructure

Por Paunio, Tiina, Arajärvi, Ritva, Terwilliger, Joseph D., Hiekkalinna, Tero, Haimi, Perttu, Partonen, Timo, Lönnqvist, Jouko, Peltonen, Leena, Varilo, Teppo
Publicado em 2009

Replication of Association Between Working Memory and Reelin, a Potential Modifier Gene in Schizophrenia

Por Wedenoja, Juho, Tuulio-Henriksson, Annamari, Suvisaari, Jaana, Loukola, Anu, Paunio, Tiina, Partonen, Timo, Varilo, Teppo, Lönnqvist, Jouko, Peltonen, Leena
Publicado em 2009

Mutations in the Translated Region of the Lactase Gene (LCT) Underlie Congenital Lactase Deficiency

Por Kuokkanen, Mikko, Kokkonen, Jorma, Enattah, Nabil Sabri, Ylisaukko-oja, Tero, Komu, Hanna, Varilo, Teppo, Peltonen, Leena, Savilahti, Erkki, Järvelä, Irma
Publicado em 2006

A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm

Por Luukkonen, Tiia, Pöyhönen, Minna, Palotie, Aarno, Ellonen, Pekka, Lagström, Sonja, Lee, Joseph H, Terwilliger, Joseph D, Salonen, Riitta, Varilo, Teppo
Publicado em 2012

Linkage and Linkage Disequilibrium Scan for Autism Loci in an Extended Pedigree from Finland

Por Kilpinen, Helena, Ylisaukko-oja, Tero, Rehnström, Karola, Gaál, Emilia, Turunen, Joni A., Kempas, Elli, von Wendt, Lennart, Varilo, Teppo, Peltonen, Leena
Publicado em 2009

A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci

Por Hovatta, Iiris, Varilo, Teppo, Suvisaari, Jaana, Terwilliger, Joseph D., Ollikainen, Vesa, Arajärvi, Ritva, Juvonen, Hannu, Kokko-Sahin, Marja-Liisa, Väisänen, Leena, Mannila, Heikki, Lönnqvist, Jouko, Peltonen, Leena
Publicado em 1999

Mapping a New Spontaneous Preterm Birth Susceptibility Gene, IGF1R, Using Linkage, Haplotype Sharing, and Association Analysis

Por Haataja, Ritva, Karjalainen, Minna K., Luukkonen, Aino, Teramo, Kari, Puttonen, Hilkka, Ojaniemi, Marja, Varilo, Teppo, Chaudhari, Bimal P., Plunkett, Jevon, Murray, Jeffrey C., McCarroll, Steven A., Peltonen, Leena, Muglia, Louis J., Palotie, Aarno, Hallman, Mikko
Publicado em 2011

Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin

Por Hakonen, Anna H., Heiskanen, Silja, Juvonen, Vesa, Lappalainen, Ilse, Luoma, Petri T., Rantamäki, Maria, Goethem, Gert Van, Löfgren, Ann, Hackman, Peter, Paetau, Anders, Kaakkola, Seppo, Majamaa, Kari, Varilo, Teppo, Udd, Bjarne, Kääriäinen, Helena, Bindoff, Laurence A., Suomalainen, Anu
Publicado em 2005

The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population

Por Jakkula, Eveliina, Rehnström, Karola, Varilo, Teppo, Pietiläinen, Olli P.H., Paunio, Tiina, Pedersen, Nancy L., deFaire, Ulf, Järvelin, Marjo-Riitta, Saharinen, Juha, Freimer, Nelson, Ripatti, Samuli, Purcell, Shaun, Collins, Andrew, Daly, Mark J., Palotie, Aarno, Peltonen, Leena
Publicado em 2008

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

Por Sabatti, Chiara, Service, Susan K, Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G, Zaitlen, Noah A, Varilo, Teppo, Kaakinen, Marika, Sovio, Ulla, Ruokonen, Aimo, Laitinen, Jaana, Jakkula, Eveliina, Coin, Lachlan, Hoggart, Clive, Collins, Andrew, Turunen, Hannu, Gabriel, Stacey, Elliot, Paul, McCarthy, Mark I, Daly, Mark J, Järvelin, Marjo-Riitta, Freimer, Nelson B, Peltonen, Leena
Publicado em 2008

Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

Por Jakkula, Eveliina, Leppä, Virpi, Sulonen, Anna-Maija, Varilo, Teppo, Kallio, Suvi, Kemppinen, Anu, Purcell, Shaun, Koivisto, Keijo, Tienari, Pentti, Sumelahti, Marja-Liisa, Elovaara, Irina, Pirttilä, Tuula, Reunanen, Mauri, Aromaa, Arpo, Oturai, Annette Bang, Søndergaard, Helle Bach, Harbo, Hanne F., Mero, Inger-Lise, Gabriel, Stacey B., Mirel, Daniel B., Hauser, Stephen L., Kappos, Ludwig, Polman, Chris, De Jager, Philip L., Hafler, David A., Daly, Mark J., Palotie, Aarno, Saarela, Janna, Peltonen, Leena
Publicado em 2010

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

Por Stoll, Georg, Pietiläinen, Olli P. H., Linder, Bastian, Suvisaari, Jaana, Brosi, Cornelia, Hennah, William, Leppä, Virpi, Torniainen, Minna, Ripatti, Samuli, Ala-Mello, Sirpa, Plöttner, Oliver, Rehnström, Karola, Tuulio-Henriksson, Annamari, Varilo, Teppo, Tallila, Jonna, Kristiansson, Kati, Isohanni, Matti, Kaprio, Jaakko, Eriksson, Johan G., Raitakari, Olli T., Lehtimäki, Terho, Jarvelin, Marjo-Riitta, Salomaa, Veikko, Hurles, Matthew, Stefansson, Hreinn, Peltonen, Leena, Sullivan, Patrick F., Paunio, Tiina, Lönnqvist, Jouko, Daly, Mark J., Fischer, Utz, Freimer, Nelson B., Palotie, Aarno
Publicado em 2013