The Association Between Somatic Health, Autism Spectrum Disorder, and Autistic Traits

ανά Pan, Pei-Yin, Tammimies, Kristiina, Bölte, Sven
Τόπος έκδοσης Behav Genet (2019)

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

ανά Tapia-Páez, Isabel, Tammimies, Kristiina, Massinen, Satu, Roy, Ananda L., Kere, Juha
Έκδοση 2008

2D:4D Ratio in Neurodevelopmental Disorders: A Twin Study

ανά Myers, Lynnea, van’t Westeinde, Annelies, Kuja-Halkola, Ralf, Tammimies, Kristiina, Bölte, Sven
Τόπος έκδοσης J Autism Dev Disord (2018)

Recurrence quantification analysis to characterize cyclical components of environmental elemental exposures during fetal and postnatal development

ανά Curtin, Paul, Curtin, Austen, Austin, Christine, Gennings, Chris, Tammimies, Kristiina, Bölte, Sven, Arora, Manish
Τόπος έκδοσης PLoS One (2017)

The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder

ανά Li, Danyang, Choque-Olsson, Nora, Jiao, Hong, Norgren, Nina, Jonsson, Ulf, Bölte, Sven, Tammimies, Kristiina
Τόπος έκδοσης NPJ Genom Med (2020)

The rs3743205 SNP Is Important for the Regulation of the Dyslexia Candidate Gene DYX1C1 by Estrogen Receptor β and DNA Methylation

ανά Tammimies, Kristiina, Tapia-Páez, Isabel, Rüegg, Joëlle, Rosin, Gustaf, Kere, Juha, Gustafsson, Jan-Åke, Nalvarte, Ivan
Τόπος έκδοσης Mol Endocrinol (2012)

Minor physical anomalies in neurodevelopmental disorders: a twin study

ανά Myers, Lynnea, Anderlid, Britt-Marie, Nordgren, Ann, Willfors, Charlotte, Kuja-Halkola, Ralf, Tammimies, Kristiina, Bölte, Sven
Τόπος έκδοσης Child Adolesc Psychiatry Ment Health (2017)

Copy number variation and neuropsychiatric problems in females and males in the general population

ανά Martin, Joanna, Tammimies, Kristiina, Karlsson, Robert, Lu, Yi, Larsson, Henrik, Lichtenstein, Paul, Magnusson, Patrik K. E.
Τόπος έκδοσης Am J Med Genet B Neuropsychiatr Genet (2018)

Dynamical properties of elemental metabolism distinguish attention deficit hyperactivity disorder from autism spectrum disorder

ανά Austin, Christine, Curtin, Paul, Curtin, Austen, Gennings, Chris, Arora, Manish, Tammimies, Kristiina, Isaksson, Johan, Willfors, Charlotte, Bölte, Sven
Τόπος έκδοσης Transl Psychiatry (2019)

Actionable and incidental neuroradiological findings in twins with neurodevelopmental disorders

ανά Myers, Lynnea, Ho, Mai-Lan, Cauvet, Elodie, Lundin, Karl, Carlsson, Torkel, Kuja-Halkola, Ralf, Tammimies, Kristiina, Bölte, Sven
Τόπος έκδοσης Sci Rep (2020)

Fetal and postnatal metal dysregulation in autism

ανά Arora, Manish, Reichenberg, Abraham, Willfors, Charlotte, Austin, Christine, Gennings, Chris, Berggren, Steve, Lichtenstein, Paul, Anckarsäter, Henrik, Tammimies, Kristiina, Bölte, Sven
Τόπος έκδοσης Nat Commun (2017)

Long-term social skills group training for children and adolescents with autism spectrum disorder: a randomized controlled trial

ανά Jonsson, Ulf, Olsson, Nora Choque, Coco, Christina, Görling, Anders, Flygare, Oskar, Råde, Anna, Chen, Qi, Berggren, Steve, Tammimies, Kristiina, Bölte, Sven
Τόπος έκδοσης Eur Child Adolesc Psychiatry (2018)

EU-AIMS Longitudinal European Autism Project (LEAP): the autism twin cohort

ανά Isaksson, Johan, Tammimies, Kristiina, Neufeld, Janina, Cauvet, Élodie, Lundin, Karl, Buitelaar, Jan K., Loth, Eva, Murphy, Declan G. M., Spooren, Will, Bölte, Sven
Τόπος έκδοσης Mol Autism (2018)

Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes

ανά Tervaniemi, Mari H., Katayama, Shintaro, Skoog, Tiina, Siitonen, H. Annika, Vuola, Jyrki, Nuutila, Kristo, Tammimies, Kristiina, Suomela, Sari, Kankuri, Esko, Kere, Juha, Elomaa, Outi
Τόπος έκδοσης BMC Genomics (2018)

Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs

ανά Tammimies, Kristiina, Bieder, Andrea, Lauter, Gilbert, Sugiaman-Trapman, Debora, Torchet, Rachel, Hokkanen, Marie-Estelle, Burghoorn, Jan, Castrén, Eero, Kere, Juha, Tapia-Páez, Isabel, Swoboda, Peter
Τόπος έκδοσης FASEB J (2016)

Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder

ανά Tammimies, Kristiina, Li, Danyang, Rabkina, Ielyzaveta, Stamouli, Sofia, Becker, Martin, Nicolaou, Veronika, Berggren, Steve, Coco, Christina, Falkmer, Torbjörn, Jonsson, Ulf, Choque-Olsson, Nora, Bölte, Sven
Τόπος έκδοσης Sci Rep (2019)

Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications

ανά Myers, Lynnea, Blyth, Moira, Moradkhani, Kamran, Hranilović, Dubravka, Polesie, Sam, Isaksson, Johan, Nordgren, Ann, Bucan, Maja, Vincent, Marie, Bölte, Sven, Anderlid, Britt‐Marie, Tammimies, Kristiina
Τόπος έκδοσης Mol Genet Genomic Med (2019)

Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons

ανά Massinen, Satu, Hokkanen, Marie-Estelle, Matsson, Hans, Tammimies, Kristiina, Tapia-Páez, Isabel, Dahlström-Heuser, Vanina, Kuja-Panula, Juha, Burghoorn, Jan, Jeppsson, Kristian E., Swoboda, Peter, Peyrard-Janvid, Myriam, Toftgård, Rune, Castrén, Eero, Kere, Juha
Έκδοση 2011

Copy number variation in Han Chinese individuals with autism spectrum disorder

ανά Gazzellone, Matthew J, Zhou, Xue, Lionel, Anath C, Uddin, Mohammed, Thiruvahindrapuram, Bhooma, Liang, Shuang, Sun, Caihong, Wang, Jia, Zou, Mingyang, Tammimies, Kristiina, Walker, Susan, Selvanayagam, Thanuja, Wei, John, Wang, Zhuozhi, Wu, Lijie, Scherer, Stephen W
Έκδοση 2014

Presynaptic dysfunction in CASK-related neurodevelopmental disorders

ανά Becker, Martin, Mastropasqua, Francesca, Reising, Jan Philipp, Maier, Simon, Ho, Mai-Lan, Rabkina, Ielyzaveta, Li, Danyang, Neufeld, Janina, Ballenberger, Lea, Myers, Lynnea, Moritz, Viveka, Kele, Malin, Wincent, Josephine, Willfors, Charlotte, Sitnikov, Rouslan, Herlenius, Eric, Anderlid, Britt-Marie, Falk, Anna, Bölte, Sven, Tammimies, Kristiina
Τόπος έκδοσης Transl Psychiatry (2020)