Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients
2021 · BMC Cardiovascular Disorders · 50 citations
https://doi.org/10.1186/s12872-021-01927-5
I
Inka Saarinen
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
41
Papers
189
Citations
8
h-index
8
i10-index
Inka Saarinen is an academic researcher from Blueprint Genetics (Finland). The author has contributed to research in topics: Genomics and Rare Diseases & Cardiomyopathy and Myosin Studies & Connective tissue disorders research. The author has an h-index of 8, co-authored 35 publications.
ORCID: 0000-0001-8079-379XPapers by this author
worksP577: Genetic findings in afor cohort of over 1,800 patients tested with a combined cardiomyopathy and arrhythmia panel*
2024 · Genetics in Medicine Open · 0 citations
https://doi.org/10.1016/j.gimo.2024.101483
Additional file 3 of Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia
2021 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.16779522
Additional file 1 of Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients
2021 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.14173959
Additional file 2 of Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients
2021 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.14173962
Additional file 2 of Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia
2021 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.16779519
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat