Sven Bölte
Sven Bölte
Karolinska Institutet - Center of Neurodevelopmental Disorders (KIND)
Verified email at - Homepage
Cited by
Cited by
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
Premature mortality in autism spectrum disorder
T Hirvikoski, E Mittendorfer-Rutz, M Boman, H Larsson, P Lichtenstein, ...
The British Journal of Psychiatry 208 (3), 232-238, 2016
The world federation of ADHD international consensus statement: 208 evidence-based conclusions about the disorder
SV Faraone, T Banaschewski, D Coghill, Y Zheng, J Biederman, ...
Neuroscience & biobehavioral reviews 128, 789-818, 2021
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
The contribution of environmental exposure to the etiology of autism spectrum disorder
S Bölte, S Girdler, PB Marschik
Cellular and Molecular Life Sciences 76, 1275-1297, 2019
Assessing autistic traits: cross‐cultural validation of the social responsiveness scale (SRS)
S Bölte, F Poustka, JN Constantino
Autism Research 1 (6), 354-363, 2008
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
International Molecular Genetic Study of Autism Consortium
Human Molecular Genetics 7 (3), 571-578, 1998
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
Autism spectrum disorders: Sex differences in autistic behaviour domains and coexisting psychopathology
M Holtmann, S Bölte, F Poustka
Developmental Medicine & Child Neurology 49 (5), 361-366, 2007
Functional imbalance of visual pathways indicates alternative face processing strategies in autism
D Hubl, S Bolte, S Feineis–Matthews, H Lanfermann, A Federspiel, ...
Neurology 61 (9), 1232-1237, 2003
Emotion recognition in children and adolescents with autism spectrum disorders
S Kuusikko, H Haapsamo, E Jansson-Verkasalo, T Hurtig, ML Mattila, ...
Journal of autism and developmental disorders 39, 938-945, 2009
Eye tracking in early autism research
T Falck-Ytter, S Bölte, G Gredebäck
Journal of neurodevelopmental disorders 5, 1-13, 2013
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia
Molecular autism 8, 1-17, 2017
The relation between general cognitive level and adaptive behavior domains in individuals with autism with and without co-morbid mental retardation
S Bölte, F Poustka
Child psychiatry and human development 33, 165-172, 2002
The recognition of facial affect in autistic and schizophrenic subjects and their first-degree relatives
S Bölte, F Poustka
Psychological medicine 33 (5), 907-915, 2003
The child and adolescent twin study in Sweden (CATSS)
H Anckarsäter, S Lundström, L Kollberg, N Kerekes, C Palm, E Carlström, ...
Twin Research and Human Genetics 14 (6), 495-508, 2011
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