Janna Saija Saarela

Bilde av Janna Saija Saarela
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Telefon +47 22840553
Brukernavn
Besøksadresse Gaustadalléen 21 Forskningsparken 0349 Oslo
Postadresse Postboks 1137 Blindern 0318 Oslo

Publikasjoner

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  • Lehtonen, Johanna; Hakonen, Anna H; Hassinen, Antti; Sulonen, Anna-Maija; Almusa, Henrikki & Palomäki, Maarit [Vis alle 14 forfattere av denne artikkelen] (2022). CCDC88A variants underly malformations of cortical development, profound developmental delay, epilepsy, and immune dysfunction.
  • Lehtonen, Johanna; Hakonen, Anna H; Hassinen, Antti; Sulonen, Anna-Maija; Almusa, Henrikki & Palomäki, Maarit [Vis alle 14 forfattere av denne artikkelen] (2022). CCDC88A variants underly malformations of cortical development, profound developmental delay, epilepsy, and immune dysfunction.
  • Lehtonen, Johanna; Hakonen, Anna H; Hassinen, Antti; Sulonen, Anna-Maija; Almusa, Henrikki & Palomäki, Maarit [Vis alle 13 forfattere av denne artikkelen] (2022). Genome sequencing reveals CCDC88A variants underlying malformations of cortical development, profound developmental delay, epilepsy, and immune dysfunction.
  • Lehtonen, Johanna; Sulonen, Anna-Maija; Almusa, Henrikki & Saarela, Janna Saija (2022). Gaining long-read information synthetically using linked reads.
  • Mamia, Katariina Aino Inkeri; Saarela, Janna Saija; Li, Zhuokun; Reint, Ganna; Fatkhutdinov, Nail & Haugen, Frida Høsøien [Vis alle 13 forfattere av denne artikkelen] (2022). CRISPR-Cas9 T cell editing pipeline for Finnish founder diseases.
  • Hashem, Hasan; Bucciol, Giorgia; Ozen, Seza; Unal, Sule; Bozkaya, Ikbal Ok & Akarsu, Nurten [Vis alle 51 forfattere av denne artikkelen] (2022). Correction to: Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients (Journal of Clinical Immunology, (2021), 41, 7, (1633-1647), 10.1007/s10875-021-01098-0). Journal of Clinical Immunology. ISSN 0271-9142. doi: 10.1007/s10875-022-01280-y.
  • Lehtonen, Johanna; Almusa, Henrikki; Savarese, Marco & Saarela, Janna Saija (2020). Haplotype and variant phasing of large muscle genes using linked-read sequencing.
  • Lehtonen, Johanna; Lehtokari, Vilma-Lotta; Almusa, Henrikki; Sulonen, Anna-Maija; Saarela, Janna Saija & Wallgren-Pettersson, Carina [Vis alle 7 forfattere av denne artikkelen] (2019). Linked-read whole genome sequencing in patients with congenital myopathy.
  • Madireddy, Lohith; Patsopoulos, Nikolaos A.; Cotsapas, Chris; Bos, Steffan Daniel; Beecham, Ashley H. & McCauley, Jacob [Vis alle 64 forfattere av denne artikkelen] (2019). Author Correction: A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis (Nature Communications, (2019), 10, 1, (2236), 10.1038/s41467-019-09773-y). Nature Communications. ISSN 2041-1723. 10(1). doi: 10.1038/s41467-019-10951-1.
  • Booth, DR; Heard, RN; Stewart, GJ; Cox, M; Scott, RJ & Lechner-Scott, J [Vis alle 42 forfattere av denne artikkelen] (2010). Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nature Genetics. ISSN 1061-4036. 42(6), s. 469–470.
  • Mero, Inger-Lise; Lorentzen, AR; Ban, Maria; SMESTAD, CATHRINE; Celius, Elisabeth Gulowsen & Aarseth, JH [Vis alle 20 forfattere av denne artikkelen] (2009). The TYK2 gene is associated with susceptibility to multiple sclerosis. Multiple Sclerosis. ISSN 1352-4585. 15(9), s. S186–S186.
  • Lorentzen, AR; SMESTAD, CATHRINE; Ekstrøm, Per Olaf; Oturai, Annette Bang; Åkesson, Eva & Saarela, Janna [Vis alle 13 forfattere av denne artikkelen] (2006). The role of SH2D2A gene polymorphisms in multiple sclerosis. Multiple Sclerosis. ISSN 1352-4585. 12(Suppl 1), s. S72–S72.
  • Lorentzen, Åslaug Rudjord; Smestad, C.; Ekstrom, PO; Ekström, Peter; Oturai, AB & Oturai, AB [Vis alle 10 forfattere av denne artikkelen] (2006). The role of SH2D2A gene polymorphisms in development of multiple sclerosis. Tissue Antigens. ISSN 0001-2815. 67(6 - P-179), s. 528–529.

Se alle arbeider i Cristin

Publisert 8. jan. 2019 14:30 - Sist endret 26. juli 2022 14:59

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