Author

Steve Berggren

Region StockholmORCID 0000-0002-3040-911XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Kristiina TammimiesiD· 2 shared Sofia StamouliiD· 2 shared Sven BölteiD· 2 shared Ann NordgreniD· 1 shared Bhooma ThiruvahindrapuramiD· 1 shared Britt‐Marie AnderlidiD· 1 shared Charlotte WillforsiD· 1 shared Christina CocoiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Kristiina TammimiesORCID

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2 papers

Recent·Most cited

GeneticsScientific ReportsPeer-reviewedJul 8, 2019

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

Kristiina Tammimies, Danyang Li, Ielyzaveta Rabkina…·Sven Bölte

This study investigates whether rare copy number variations (CNVs) moderate response to social skills training in ASD, finding that large CNVs are associated with worse outcomes while small CNVs show mixed effects.

16 citations

humanstatistical model

𝕏 PostBluesky

GeneticsTwin Research and Human GeneticsPeer-reviewedJan 8, 2018

Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders

Sofia Stamouli, Britt‐Marie Anderlid, Charlotte Willfors…·Sven Bölte

The paper analyzes copy number variations in 100 twin pairs enriched for neurodevelopmental disorders, finding no postzygotic de novo CNVs but higher rates of CNVs overlapping nervous system genes in discordant pairs.

33 citations

humanwhole-genome sequencing

𝕏 PostBluesky