Whole-exome sequencing identifies distinct genomic aberrations in eccrine porocarcinomas and poromas by Maya Puttonen, Henrikki Almusa, Tom Böhling, Virve Koljonen, Harri Sihto

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Author Correction: Clonal hematopoiesis in patients with rheumatoid arthritis by Paula Savola, Sofie Lundgren, Mikko A. I. Keränen, Henrikki Almusa, Pekka Ellonen, Marjatta Leirisalo-Repo, Tiina Kelkka, Satu Mustjoki

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Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years by Johanna Hietamäki, Juho Kärkinen, Anna-Pauliina Iivonen, Kirsi Vaaralahti, Annika Tarkkanen, Henrikki Almusa, Hanna Huopio, Matti Hero, Päivi J. Miettinen, Taneli Raivio

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Reconstruction and validation of RefRec: a global model for the yeast molecular interaction network. by Tommi Aho, Henrikki Almusa, Jukka Matilainen, Antti Larjo, Pekka Ruusuvuori, Kaisa-Leena Aho, Thomas Wilhelm, Harri Lähdesmäki, Andreas Beyer, Manu Harju, Sharif Chowdhury, Kalle Leinonen, Christophe Roos, Olli Yli-Harja

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Haplotype information of large neuromuscular disease genes provided by linked-read sequencing has a potential to increase diagnostic yield by Johanna Lehtonen, Anna-Maija Sulonen, Henrikki Almusa, Vilma-Lotta Lehtokari, Mridul Johari, Aino Palva, Anna H. Hakonen, Kirmo Wartiovaara, Anna-Elina Lehesjoki, Bjarne Udd, Carina Wallgren-Pettersson, Katarina Pelin, Marco Savarese, Janna Saarela

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Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts by Jaakko Laaksonen, Pashupati P. Mishra, Ilkka Seppälä, Leo-Pekka Lyytikäinen, Emma Raitoharju, Nina Mononen, Maija Lepistö, Henrikki Almusa, Pekka Ellonen, Nina Hutri-Kähönen, Markus Juonala, Olli Raitakari, Mika Kähönen, Jukka T. Salonen, Terho Lehtimäki

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