Eriksson, Mats
Karolinska Institutet
3 papers on CoChatORCID 0000-0003-4756-1924
Most cited papers
- Verified
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature
Béna, F., Bruno, D. L., Eriksson, M., van Ravenswaaij‐Arts, C., Stark, Z., Dijkhuizen, T., Gerkes, E., Gimelli, S., Ganesamoorthy, D., Thuresson, A. C., et al. (2013) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
Cited by 109
- Verified
Developmental profiles in preschool children with autism spectrum disorders referred for intervention
Fernell, E., Hedvall, Å., Norrelgen, F., Eriksson, M., Höglund-Carlsson, L., Barnevik-Olsson, M., Svensson, L., Holm, A., Westerlund, J., & Gillberg, C. (2010) · Research in Developmental Disabilities
Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues
Cited by 98
- Verified
First-degree relatives of young children with autism spectrum disorders: Some gender aspects
Eriksson, M. A., Westerlund, J., Anderlid, B. M., Gillberg, C., & Fernell, E. (2012) · Research in Developmental Disabilities
Autism Spectrum Disorder ResearchFamily and Disability Support Research
Cited by 43
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