Johanna Lehtonen

• Kaustio, Meri; Nayebzadeh, Naemeh; Hinttala, Reetta; Tapiainen, Terhi; Åström, Pirjo & Mamia, Katariina Aino Inkeri [Vis alle 37 forfattere av denne artikkelen] (2021). Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunction. Journal of Allergy and Clinical Immunology. ISSN 0091-6749. 148(2), s. 599–611. doi: 10.1016/j.jaci.2020.12.656. Fulltekst i vitenarkiv
• Laitila, Jenni; Lehtonen, Johanna; Lehtokari, Vilma-Lotta; Sagath, Lydia; Wallgren-Pettersson, Carina & Grönholm, Mikaela [Vis alle 7 forfattere av denne artikkelen] (2019). A nebulin super-repeat panel reveals stronger actin binding toward the ends of the super-repeat region. Muscle and Nerve. ISSN 0148-639X. doi: 10.1002/mus.26350..

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• Lehtonen, Johanna (2022). A summary of the 20th Biennial meeting of the European Society for Immunodeficiencies.
• Lehtonen, Johanna & Batlle-Masó, Laura (2022). Genetic studies in autoimmune lymphoproliferative syndrome pediatric patients.
• 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.
• 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.
• Lehtonen, Johanna; Khattab, Ayman; Laitila, Jenni; Grönholm, Mikaela; Wallgren-Pettersson, Carina & Lehtokari, Vilma-Lotta [Vis alle 7 forfattere av denne artikkelen] (2019). The microscale thermophoresis method for the analysis of nebulin-tropomyosin interaction.

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