Transcription-coupled genetic instability marks acute lymphoblastic leukemia structural variation hotspots

Por Heinäniemi, Merja, Vuorenmaa, Tapio, Teppo, Susanna, Kaikkonen, Minna U, Bouvy-Liivrand, Maria, Mehtonen, Juha, Niskanen, Henri, Zachariadis, Vasilios, Laukkanen, Saara, Liuksiala, Thomas, Teittinen, Kaisa, Lohi, Olli
Publicado no eLife (2016)

PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia

Por Marincevic-Zuniga, Yanara, Zachariadis, Vasilios, Cavelier, Lucia, Castor, Anders, Barbany, Gisela, Forestier, Erik, Fogelstrand, Linda, Heyman, Mats, Abrahamsson, Jonas, Lönnerholm, Gudmar, Nordgren, Ann, Syvänen, Ann-Christine, Nordlund, Jessica
Publicado no Haematologica (2016)

Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells

Por Akagi, Tadayuki, Shih, Lee-Yung, Ogawa, Seishi, Gerss, Joachim, Moore, Stephen R., Schreck, Rhona, Kawamata, Norihiko, Liang, Der-Cherng, Sanada, Masashi, Nannya, Yasuhito, Deneberg, Stefan, Zachariadis, Vasilios, Nordgren, Ann, Song, Jee Hoon, Dugas, Martin, Lehmann, Sören, Koeffler, H. Phillip
Publicado em 2009

Whole genome sequencing of cytogenetically balanced chromosome translocations identifies potentially pathological gene disruptions and highlights the importance of microhomology in...

Por Nilsson, Daniel, Pettersson, Maria, Gustavsson, Peter, Förster, Alisa, Hofmeister, Wolfgang, Wincent, Josephine, Zachariadis, Vasilios, Anderlid, Britt-Marie, Nordgren, Ann, Mäkitie, Outi, Wirta, Valtteri, Käller, Max, Vezzi, Francesco, Lupski, James R, Nordenskjöld, Magnus, Lundberg, Elisabeth Syk, Carvalho, Claudia M. B., Lindstrand, Anna
Publicado no Hum Mutat (2016)

DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia

Por Nordlund, Jessica, Bäcklin, Christofer L, Zachariadis, Vasilios, Cavelier, Lucia, Dahlberg, Johan, Öfverholm, Ingegerd, Barbany, Gisela, Nordgren, Ann, Övernäs, Elin, Abrahamsson, Jonas, Flaegstad, Trond, Heyman, Mats M, Jónsson, Ólafur G, Kanerva, Jukka, Larsson, Rolf, Palle, Josefine, Schmiegelow, Kjeld, Gustafsson, Mats G, Lönnerholm, Gudmar, Forestier, Erik, Syvänen, Ann-Christine
Publicado no Clin Epigenetics (2015)

De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations

Por Reijnders, Margot R.F., Zachariadis, Vasilios, Latour, Brooke, Jolly, Lachlan, Mancini, Grazia M., Pfundt, Rolph, Wu, Ka Man, van Ravenswaaij-Arts, Conny M.A., Veenstra-Knol, Hermine E., Anderlid, Britt-Marie M., Wood, Stephen A., Cheung, Sau Wai, Barnicoat, Angela, Probst, Frank, Magoulas, Pilar, Brooks, Alice S., Malmgren, Helena, Harila-Saari, Arja, Marcelis, Carlo M., Vreeburg, Maaike, Hobson, Emma, Sutton, V. Reid, Stark, Zornitza, Vogt, Julie, Cooper, Nicola, Lim, Jiin Ying, Price, Sue, Lai, Angeline Hwei Meeng, Domingo, Deepti, Reversade, Bruno, Gecz, Jozef, Gilissen, Christian, Brunner, Han G., Kini, Usha, Roepman, Ronald, Nordgren, Ann, Kleefstra, Tjitske
Publicado no Am J Hum Genet (2016)