Helena Kilpinen

E-postadresshelena.kilpinenhelsinkifi

PL 63 (Haartmaninkatu 8)
00014
Finland

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Vetenskapsgrenar

1184 Genetik, utvecklingsbiologi, fysiologi

23 Artikel
2 Mötesabstrakt
2 Översiktsartikel

CRISPR activation enables high-fidelity reprogramming into human pluripotent stem cells
Sokka, J. J., Yoshihara, M., Kvist, J., Laiho, L., Warren, A., Stadelmann, C., Jouhilahti, E-M., Kilpinen, H., Balboa, D., Katayama, S., Kyttälä, A., Kere, J., Otonkoski, T., Weltner, J. & Trokovic, R., 8 feb. 2022, I: Stem cell reports. 17, 2, s. 413–426 14 s.
Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

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Highly accurate quantification of allelic gene expression for population and disease genetics
Saukkonen, A., Kilpinen, H. & Hodgkinson, A., aug. 2022, I: Genome Research. 32, 8, s. 1565-1572 8 s.
Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

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Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics
HIPSCI Consortium, iPSCORE Consortium, Undiagnosed Dis Network, PhLiPS Consortium, Bonder, M. J., Li, X. & Kilpinen, H., 4 mars 2021, I: Nature Genetics. 53, 3, s. 313–321 25 s.
Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review
Tautimekanismien jäljille iPS-solujen ja biopankkien avulla
Kilpinen, H., Trokovic, R., Loukola, A. & Otonkoski, T., 2021, I: Duodecim. 137, 9, s. 918-924 7 s.
Forskningsoutput: Tidskriftsbidrag › Översiktsartikel › Peer review

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Genomic basis for RNA alterations in cancer
PCAWG Transcriptome Core Grp, PCAWG Transcriptome Working Grp, PCAWG Consortium, Calabrese, C. & Kilpinen, H., 6 feb. 2020, I: Nature. 578, 7793, s. 129-+ 50 s.
Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

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2 Aktiv

Yleisen geneettisen variaation vaikutus hermosolujen ilmiasuun harvinaisissa kehityshäiriöissä
Kilpinen, H.
Suomen akatemia
01/09/2021 → 31/08/2027
Projekt: Finlands Akademi: Akademiforskare
The effect of common genetic variation on neuronal phenotypes in rare developmental disorders
Kilpinen, H. & Sundaresh, A.
Suomen akatemia
01/09/2021 → 31/12/2025
Projekt: Finlands Akademi: Akademiforskarens forskningskostnader

Helena Kilpinen, assistant professor

Personlig profil

Vetenskapsgrenar

CRISPR activation enables high-fidelity reprogramming into human pluripotent stem cells

Highly accurate quantification of allelic gene expression for population and disease genetics

Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics

Tautimekanismien jäljille iPS-solujen ja biopankkien avulla

Genomic basis for RNA alterations in cancer

Yleisen geneettisen variaation vaikutus hermosolujen ilmiasuun harvinaisissa kehityshäiriöissä

The effect of common genetic variation on neuronal phenotypes in rare developmental disorders

Helena Kilpinen, assistant professor

Personlig profil

Vetenskapsgrenar

Publikationer

CRISPR activation enables high-fidelity reprogramming into human pluripotent stem cells

Highly accurate quantification of allelic gene expression for population and disease genetics

Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics

Tautimekanismien jäljille iPS-solujen ja biopankkien avulla

Genomic basis for RNA alterations in cancer

Projekter

Yleisen geneettisen variaation vaikutus hermosolujen ilmiasuun harvinaisissa kehityshäiriöissä

The effect of common genetic variation on neuronal phenotypes in rare developmental disorders