Varilo, T : rechercher sur Z-Library

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Don't use scam websites

Livres
Articles (50)
Les plus populaires
Liste
- Liste
- Tableau

1

Association of DISC1 with autism and Asperger syndrome

Kilpinen, H, Ylisaukko-oja, T, Hennah, W, Palo, O M, Varilo, T, Vanhala, R, Nieminen-von Wendt, T, von Wendt, L, Paunio, T, Peltonen, L

Journal:

Molecular Psychiatry

Année:

2007

Langue:

english

Fichier:

PDF, 181 KB

english, 2007

2

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia

Annamari Tuulio-Henriksson, Jari Haukka, Timo Partonen, Teppo Varilo, Tiina Paunio, Jesper Ekelund, Tyrone D. Cannon, Joanne M. Meyer, Jouko Lönnqvist

Journal:

American Journal of Medical Genetics Part A

Année:

2002

Langue:

english

Fichier:

PDF, 89 KB

english, 2002

3

Evidence for allelic association on chromosome 3q25–27 in families with autism spectrum disorders originating from a subisolate of Finland

Auranen, M, Varilo, T, Alen, R, Vanhala, R, Ayers, K, Kempas, E, Ylisaukko-oja, T, Peltonen, L, Järvelä, I

Journal:

Molecular Psychiatry

Année:

2003

Langue:

english

Fichier:

PDF, 94 KB

english, 2003

4

Genome-wide scan for loci of Asperger syndrome

Ylisaukko-oja, T, Nieminen-von Wendt, T, Kempas, E, Sarenius, S, Varilo, T, Wendt, L von, Peltonen, L, Järvelä, I

Journal:

Molecular Psychiatry

Année:

2004

Langue:

english

Fichier:

PDF, 245 KB

english, 2004

5

Affective flattening and alogia associate with the familial form of schizophrenia

Ritva Arajärvi, Teppo Varilo, Jari Haukka, Jaana Suvisaari, Jaana Suokas, Hannu Juvonen, Maria Muhonen, Kirsi Suominen, Jukka Hintikka, Marjut Schreck, Annamari Tuulio-Henriksson, Timo Partonen, Jouko

Journal:

Psychiatry Research

Année:

2006

Langue:

english

Fichier:

PDF, 199 KB

english, 2006

6

The Finnish Disease Heritage Database (FinDis) Update-A Database for the Genes Mutated in the Finnish Disease Heritage Brought to the Next-Generation Sequencing Era

Polvi, Anne, Linturi, Henna, Varilo, Teppo, Anttonen, Anna-Kaisa, Byrne, Myles, Fokkema, Ivo F.A.C., Almusa, Henrikki, Metzidis, Anthony, Avela, Kristiina, Aula, Pertti, Kestilä, Marjo, Muilu, Juha

Journal:

Année:

2013

Langue:

english

Fichier:

PDF, 238 KB

english, 2013

7

Linkage analysis of schizophrenia controlling for population substructure

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

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 421 KB

english, 2009

8

Impact of the dopamine receptor gene family on temperament traits in a population-based birth cohort

Emma S. Nyman, Anu Loukola, Teppo Varilo, Jesper Ekelund, Juha Veijola, Matti Joukamaa, Anja Taanila, Anneli Pouta, Jouko Miettunen, Nelson Freimer, Marjo-Riitta Järvelin, Leena Peltonen

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 180 KB

english, 2009

9

Identification of susceptibility loci at 7q31 and 9p13 for bipolar disorder in an isolated population

Outi M. Palo, Pia Soronen, Kaisa Silander, Teppo Varilo, Katja Tuononen, Tuula Kieseppä, Timo Partonen, Jouko Lönnqvist, Tiina Paunio, Leena Peltonen

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 500 KB

english, 2010

10

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

Sabatti, Chiara, Service, Susan K, Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G, Zaitlen, Noah A, Varilo, Teppo, Kaakinen, Marika

Journal:

Nature Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 13.03 MB

english, 2008

11

Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo

Varilo, Teppo, Laan, Maris, Hovatta, Iiris, Wiebe, Victor, Terwilliger, Joseph D, Peltonen, Leena

Journal:

European Journal of Human Genetics

Année:

2000

Langue:

english

Fichier:

PDF, 195 KB

english, 2000

12

Bipolar disorder susceptibility region on Xq24–q27.1 in Finnish families

Ekholm, J M, Pekkarinen, P, Pajukanta, P, Kieseppä, T, Partonen, T, Paunio, T, Varilo, T, Perola, M, Lönnqvist, J, Peltonen, L

Journal:

Molecular Psychiatry

Année:

2002

Langue:

english

Fichier:

PDF, 186 KB

english, 2002

13

A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia

Hennah, W, Tuulio-Henriksson, A, Paunio, T, Ekelund, J, Varilo, T, Partonen, T, Cannon, T D, Lönnqvist, J, Peltonen, L

Journal:

Molecular Psychiatry

Année:

2005

Langue:

english

Fichier:

PDF, 132 KB

english, 2005

14

Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families

Wedenoja, J, Loukola, A, Tuulio-Henriksson, A, Paunio, T, Ekelund, J, Silander, K, Varilo, T, Suvisaari, J, Partonen, T, Heikkilä, K

Journal:

Molecular Psychiatry

Année:

2007

Langue:

english

Fichier:

PDF, 239 KB

english, 2007

15

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

Eveliina Jakkula, Karola Rehnström, Teppo Varilo, Olli P.H. Pietiläinen, Tiina Paunio, Nancy L. Pedersen, Ulf deFaire, Marjo-Riitta Järvelin, Juha Saharinen, Nelson Freimer, Samuli Ripatti, Shaun Purc

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 596 KB

english, 2008

16

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

Eveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, Teppo Varilo, Suvi Kallio, Anu Kemppinen, Shaun Purcell, Keijo Koivisto, Pentti Tienari, Marja-Liisa Sumelahti, Irina Elovaara, Tuula Pirttilä, Mauri

Journal:

The American Journal of Human Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 507 KB

english, 2010

17

Fine-Scale Mapping of a Novel Dementia Gene, PLOSL, by Linkage Disequilibrium

P. Pekkarinen, M. Kestilä, J. Paloneva, J. Terwilliger, T. Varilo, O. Järvi, P. Hakola, L. Peltonen

Journal:

Année:

1998

Langue:

english

Fichier:

PDF, 155 KB

english, 1998

18

Isolates and their potential use in complex gene mapping efforts

Teppo Varilo, Leena Peltonen

Journal:

Current Opinion in Genetics & Development

Année:

2004

Langue:

english

Fichier:

PDF, 261 KB

english, 2004

19

Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria

Vineta Fellman, Juhani Rapola, Helena Pihko, Teppo Varilo, Kari O Raivio

Journal:

Année:

1998

Langue:

english

Fichier:

PDF, 75 KB

english, 1998

20

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

Irma Järvelä, Nabil Sabri Enattah, Jorma Kokkonen, Teppo Varilo, Erkki Savilahti, Leena Peltonen

Journal:

The American Journal of Human Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 1.31 MB

english, 1998

21

Assignment of the Locus for a New Lethal Neonatal Metabolic Syndrome to 2q33-37

Ilona Visapää, Vineta Fellman, Teppo Varilo, Aarno Palotie, Kari O. Raivio, Leena Peltonen

Journal:

The American Journal of Human Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 746 KB

english, 1998

22

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

Ilona Visapää, Riitta Salonen, Teppo Varilo, Paulina Paavola, Leena Peltonen

Journal:

The American Journal of Human Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 515 KB

english, 1999

23

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

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 Pel

Journal:

The American Journal of Human Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 907 KB

english, 1999

24

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

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

Journal:

The American Journal of Human Genetics

Année:

2002

Langue:

english

Fichier:

PDF, 2.09 MB

english, 2002

25

Minimum Description Length Block Finder, a Method to Identify Haplotype Blocks and to Compare the Strength of Block Boundaries

H. Mannila, M. Koivisto, M. Perola, T. Varilo, W. Hennah, J. Ekelund, M. Lukk, L. Peltonen, E. Ukkonen

Journal:

The American Journal of Human Genetics

Année:

2003

Langue:

english

Fichier:

PDF, 1.31 MB

english, 2003

26

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

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

Journal:

The American Journal of Human Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 754 KB

english, 2006

27

Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients

Annamari Tuulio-Henriksson, Ritva Arajärvi, Timo Partonen, Jari Haukka, Teppo Varilo, Marjut Schreck, Tyrone Cannon, Jouko Lönnqvist

Journal:

Biological Psychiatry

Année:

2003

Langue:

english

Fichier:

PDF, 57 KB

english, 2003

28

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

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

Journal:

Biological Psychiatry

Année:

2010

Langue:

english

Fichier:

PDF, 485 KB

english, 2010

29

The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland

Joni A. Turunen, Juho O. Peltonen, Olli P.H. Pietiläinen, William Hennah, Anu Loukola, Tiina Paunio, Kaisa Silander, Jesper Ekelund, Teppo Varilo, Timo Partonen, Jouko Lönnqvist, Leena Peltonen

Journal:

Schizophrenia Research

Année:

2007

Langue:

english

Fichier:

PDF, 529 KB

english, 2007

30

Clinical phenotype of schizophrenia in a Finnish isolate

Ritva Arajärvi, Jari Haukka, Teppo Varilo, Jaana Suokas, Hannu Juvonen, Jaana Suvisaari, Maria Muhonen, Kirsi Suominen, Annamari Tuulio-Henriksson, Marjut Schreck, Iiris Hovatta, Timo Partonen, Jouko

Journal:

Schizophrenia Research

Année:

2004

Langue:

english

Fichier:

PDF, 275 KB

english, 2004

31

ADHD Candidate Gene Study in a Population-Based Birth Cohort: Association with DBH and DRD2

NYMAN, EMMA S., OGDIE, MATTHEW N., LOUKOLA, ANU, VARILO, TEPPO, TAANILA, ANJA, HURTIG, TUULA, MOILANEN, IRMA K., LOO, SANDRA K., McGOUGH, JAMES J., JÄRVELIN, MARJO-RIITTA, SMALLEY, SUSAN L., NELSON, S

Journal:

Journal of the American Academy of Child & Adolescent Psychiatry

Année:

2007

Langue:

english

Fichier:

PDF, 167 KB

english, 2007

32

Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?

Torniainen, Minna, Wedenoja, Juho, Varilo, Teppo, Partonen, Timo, Suokas, Jaana, Häkkinen, Laura, Lönnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari

Journal:

Psychiatry Research

Année:

2013

Langue:

english

Fichier:

PDF, 232 KB

english, 2013

33

Prevalence and Psychiatric Comorbidity of Attention-Deficit/Hyperactivity Disorder in an Adolescent Finnish Population

SMALLEY, SUSAN L., McGOUGH, JAMES J., MOILANEN, IRMA K., LOO, SANDRA K., TAANILA, ANJA, EBELING, HANNA, HURTIG, TUULA, KAAKINEN, MARIKA, HUMPHREY, LORIE A., McCRACKEN, JAMES T., VARILO, TEPPO, YANG, M

Journal:

Journal of the American Academy of Child & Adolescent Psychiatry

Année:

2007

Langue:

english

Fichier:

PDF, 325 KB

english, 2007

34

Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland

Kilpinen, H., Ylisaukko-oja, T., Rehnstrom, K., Gaal, E., Turunen, J. A., Kempas, E., von Wendt, L., Varilo, T., Peltonen, L.

Journal:

Human Molecular Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 326 KB

english, 2009

35

Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.

Varilo, T, Nikali, K, Suomalainen, A, Lonnqvist, T, Peltonen, L

Journal:

Genome Research

Année:

1996

Langue:

english

Fichier:

PDF, 766 KB

english, 1996

36

Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort

Nyman, Emma S., Loukola, Anu, Varilo, Teppo, Taanila, Anja, Hurtig, Tuula, Moilanen, Irma, Loo, Sandra, McGough, James J., Järvelin, Marjo-Riitta, Smalley, Susan L., Nelson, Stanley F., Peltonen, Leen

Journal:

Psychiatric Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 278 KB

english, 2012

37

The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories

Journal:

Human Molecular Genetics

Année:

2003

Langue:

english

Fichier:

PDF, 1.24 MB

english, 2003

38

Om ungdomsaddiktionens etiologi

Journal:

Nordic Journal of Psychiatry

Année:

1970

Fichier:

PDF, 1004 KB

1970

39

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

Luukkonen, T. M., Poyhonen, M., Palotie, A., Ellonen, P., Lagstrom, S., Lee, J. H., Terwilliger, J. D., Salonen, R., Varilo, T.

Journal:

Journal of Medical Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 552 KB

english, 2012

40

MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features

Auranen, M., Vanhala, R., Vosman, M., Levander, M., Varilo, T., Hietala, M., Riikonen, R., Peltonen, L., Jarvela, I.

Journal:

Année:

2001

Langue:

english

Fichier:

PDF, 221 KB

english, 2001

41

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

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.,

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 827 KB

english, 2011

42

Mutant CHUK and Severe Fetal Encasement Malformation

Lahtela, Jenni, Nousiainen, Heidi O., Stefanovic, Vedran, Tallila, Jonna, Viskari, Heli, Karikoski, Riitta, Gentile, Massimiliano, Saloranta, Carola, Varilo, Teppo, Salonen, Riitta, Kestilä, Marjo

Journal:

Boston Medical and Surgical Journal

Année:

2010

Langue:

english

Fichier:

PDF, 1.15 MB

english, 2010

43

Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia

Hennah, William, Varilo, Teppo, Paunio, Tiina, Peltonen, Leena

Journal:

Annals of Medicine

Année:

2004

Langue:

english

Fichier:

PDF, 366 KB

english, 2004

44

Regional variation in the incidence of schizophrenia in Finland: a study of birth cohorts born from 1950 to 1969

HAUKKA, J., SUVISAARI, J., VARILO, T., LÖNNQVIST, J.

Journal:

Psychological Medicine

Année:

2001

Langue:

english

Fichier:

PDF, 781 KB

english, 2001

45

Identification of C12orf4 as a gene for autosomal recessive intellectual disability

Philips, A.K., Pinelli, M., de Bie, C.I., Mustonen, A., Määttä, T., Arts, H.H., Wu, K., Roepman, R., Moilanen, J.S., Raza, S., Varilo, T., Scala, G., Cocozza, S., Gilissen, C., van Gassen, K.L.I., Jär

Journal:

Clinical Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 1.23 MB

english, 2016

46

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

Misiewicz, Zuzanna, Hiekkalinna, Tero, Paunio, Tiina, Varilo, Teppo, Terwilliger, Joseph D., Partonen, Timo, Hovatta, Iiris

Journal:

Scientific Reports

Année:

2016

Langue:

english

Fichier:

PDF, 677 KB

english, 2016

47

Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes

Luukkonen, Tiia Maria, Mehrjouy, Mana M., Pöyhönen, Minna, Anttonen, Anna-Kaisa, Lahermo, Päivi, Ellonen, Pekka, Paulin, Lars, Tommerup, Niels, Palotie, Aarno, Varilo, Teppo

Journal:

Molecular Genetics & Genomic Medicine

Année:

2017

Langue:

english

Fichier:

PDF, 2.07 MB

english, 2017

48

NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease

Uusimaa, Johanna, Kaarteenaho, Riitta, Paakkola, Teija, Tuominen, Hannu, Karjalainen, Minna K., Nadaf, Javad, Varilo, Teppo, Uusi-Mäkelä, Meri, Suo-Palosaari, Maria, Pietilä, Ilkka, Hiltunen, Anniina

Journal:

Acta Neuropathologica

Année:

2018

Langue:

english

Fichier:

PDF, 4.98 MB

english, 2018

49

Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Polla, Daniel L., Rahikkala, Elisa, Bode, Michaela K., Määttä, Tuomo, Varilo, Teppo, Loman, Thyrza, Philips, Anju K., Kurki, Mitja, Palotie, Aarno, Körkkö, Jarmo, Vieira, Päivi, Avela, Kristiina, Jacq

Journal:

European Journal of Human Genetics

Année:

2019

Langue:

english

Fichier:

PDF, 237 KB

english, 2019

50

Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Polla, Daniel L., Rahikkala, Elisa, Bode, Michaela K., Määttä, Tuomo, Varilo, Teppo, Loman, Thyrza, Philips, Anju K., Kurki, Mitja, Palotie, Aarno, Körkkö, Jarmo, Vieira, Päivi, Avela, Kristiina, Jacq

Journal:

European Journal of Human Genetics

Année:

2019

Fichier:

PDF, 237 KB

2019