Outi Elomaa

University of Helsinki — Finland

Biochemistry, Genetics and Molecular Biology · Life Sciences

25h-index2.4kcitations50works0.02yr avg
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Research Topics

Skin and Cellular Biology Research(10), Estrogen and related hormone effects(7), Immune Response and Inflammation(6), Psoriasis: Treatment and Pathogenesis(6), Wnt/β-catenin signaling in development and cancer(6)

Publications50 total

<i>DSP</i> -palmoplantar epidermal differentiation disorder: a distinct phenotype and red flag for cardiomyopathy
Clinical and Experimental Dermatology·2025Open Access
The <scp>HRAS</scp> Variant c. <scp>175G</scp> &gt;A (p. <scp>Ala59Thr</scp> ) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features
American Journal of Medical Genetics Part A·2025Open Access
<i>SERPINB8</i>‐associated peeling skin with palmoplantar keratoderma—A new variant and phenotypic expansion
Journal of the European Academy of Dermatology and Venereology·2025
A novel <i>SERPINA12</i> variant and first European patients with diffuse palmoplantar keratoderma
Journal of the European Academy of Dermatology and Venereology·2023· 6 citedOpen Access
A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign
Journal of the European Academy of Dermatology and Venereology·2022· 8 citedOpen Access
Hereditary palmoplantar keratoderma – phenotypes and mutations in 64 patients
Journal of the European Academy of Dermatology and Venereology·2021· 13 citedOpen Access
Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma
Acta Dermato Venereologica·2020· 3 citedOpen Access
Discovery of increased epidermal DNAH10 expression after regeneration of dermis in a randomized with-in person trial — reflections on psoriatic inflammation
Scientific Reports·2019· 5 citedOpen Access
Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutation
Journal of the American Academy of Dermatology·2019· 18 citedOpen Access
Novel DSP Spectrin 6 Region Variant Causes Neonatal Erythroderma, Failure to Thrive, Severe Herpes Simplex Infections and Brain Lesions
Acta Dermato Venereologica·2019· 16 citedOpen Access
Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
BMC Genomics·2018· 24 citedOpen Access
Additional file 4: of Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
Figshare·2018Open Access
Additional file 5: of Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
Figshare·2018Open Access
Additional file 2: of Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
Figshare·2018Open Access
Additional file 7: of Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
Figshare·2018Open Access
Additional file 1: of Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
Figshare·2018Open Access
Additional file 3: of Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
Figshare·2018Open Access
Additional file 6: of Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
Figshare·2018Open Access
A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR
Scientific Reports·2017· 25 citedOpen Access
NOD-like receptor signaling and inflammasome-related pathways are highlighted in psoriatic epidermis
Scientific Reports·2016· 92 citedOpen Access
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Frequent Co-authors

Juha Kere(35), Sari Suomela(18), Tiina Skoog(13), Jyrki Vuola(12), Ulpu Saarialho‐Kere(11), Mari Tervaniemi(11), H. Annika Siitonen(11), Esko Kankuri(11), Karl Tryggvason(10), Shintaro Katayama(10), Kristo Nuutila(10), Katariina Hannula‐Jouppi(9), Kristiina Tammimies(8), Liisa Harjama(8), K Kettunen(8), Sirpa Kivirikko(6), Annamari Ranki(6), Georg Kraal(5), Inkeri Tiala(5), Janna Saarela(5)