Olof Bjerin

Statistics

Publications

Citations

144

H-Index

Active since

2019

Affiliations

Karolinska Institutet(Current)

Olof Bjerin is an author at Karolinska Institutet specializing in structural variant analysis, chromosomal microarray analysis, and genome-wide copy number variation analysis.

ORCID

Publications per year

2019–2019

Publications

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson et al. · Genome Medicine · 2019 · 144 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

1–1 of 1