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Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting [electronic resource] by
- Järviaho, Tekla
- Bang, Benedicte
- Zachariadis, Vasilios
- Taylan, Fulya
- Moilanen, Jukka
- Möttönen, Merja
- Smith, C I Edvard
- Harila-Saari, Arja
- Niinimäki, Riitta
- Nordgren, Ann
Producer: 20200814
In:
Blood advances vol. 3
Availability: No items available.
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6.
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High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing. [electronic resource] by
- Tran, Anh Nhi
- Taylan, Fulya
- Zachariadis, Vasilios
- Ivanov Öfverholm, Ingegerd
- Lindstrand, Anna
- Vezzi, Francesco
- Lötstedt, Britta
- Nordenskjöld, Magnus
- Nordgren, Ann
- Nilsson, Daniel
- Barbany, Gisela
Producer: 20180625
In:
PloS one vol. 13
Availability: No items available.
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7.
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Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia. [electronic resource] by
- Ivanov Öfverholm, Ingegerd
- Tran, Anh Nhi
- Olsson, Linda
- Zachariadis, Vasilios
- Heyman, Mats
- Rudd, Eva
- Syk Lundberg, Elisabeth
- Nordenskjöld, Magnus
- Johansson, Bertil
- Nordgren, Ann
- Barbany, Gisela
Producer: 20180112
In:
Leukemia & lymphoma vol. 57
Availability: No items available.
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8.
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Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth. [electronic resource] by
- Frisk, Sofia
- Taylan, Fulya
- Blaszczyk, Izabela
- Nennesmo, Inger
- Annerén, Göran
- Herm, Bettina
- Stattin, Eva-Lena
- Zachariadis, Vasilios
- Lindstrand, Anna
- Tesi, Bianca
- Laurell, Tobias
- Nordgren, Ann
Producer: 20200812
In:
Clinical genetics vol. 96
Availability: No items available.
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9.
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The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013. [electronic resource] by
- Olsson, Linda
- Ivanov Öfverholm, Ingegerd
- Norén-Nyström, Ulrika
- Zachariadis, Vasilios
- Nordlund, Jessica
- Sjögren, Helene
- Golovleva, Irina
- Nordgren, Ann
- Paulsson, Kajsa
- Heyman, Mats
- Barbany, Gisela
- Johansson, Bertil
Producer: 20151120
In:
British journal of haematology vol. 170
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10.
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Transcription-coupled genetic instability marks acute lymphoblastic leukemia structural variation hotspots. [electronic resource] by
- 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
Producer: 20171116
In:
eLife vol. 5
Availability: No items available.
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11.
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Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemia. [electronic resource] by
- Järviaho, Tekla
- Zachariadis, Vasilios
- Tesi, Bianca
- Chiang, Samuel
- Bryceson, Yenan T
- Möttönen, Merja
- Niinimäki, Riitta
- Bang, Benedicte
- Rahikkala, Elisa
- Taylan, Fulya
- Uusimaa, Johanna
- Harila-Saari, Arja
- Nordgren, Ann
Producer: 20200504
In:
British journal of haematology vol. 185
Availability: No items available.
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12.
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PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia. [electronic resource] by
- 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
Producer: 20161005
In:
Haematologica vol. 101
Availability: No items available.
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13.
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Metabolic reprogramming of acute lymphoblastic leukemia cells in response to glucocorticoid treatment. [electronic resource] by
- Dyczynski, Matheus
- Vesterlund, Mattias
- Björklund, Ann-Charlotte
- Zachariadis, Vasilios
- Janssen, Jerry
- Gallart-Ayala, Hector
- Daskalaki, Evangelia
- Wheelock, Craig E
- Lehtiö, Janne
- Grandér, Dan
- Tamm, Katja Pokrovskaja
- Nilsson, Roland
Producer: 20191115
In:
Cell death & disease vol. 9
Availability: No items available.
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14.
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Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells. [electronic resource] by
- 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
Producer: 20091208
In:
Haematologica vol. 94
Availability: No items available.
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15.
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Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation. [electronic resource] by
- 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
Producer: 20180112
In:
Human mutation vol. 38
Availability: No items available.
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16.
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DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia. [electronic resource] by
- 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
Producer: 20150302
In:
Clinical epigenetics vol. 7
Availability: No items available.
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17.
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De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations. [electronic resource] by
- 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
Producer: 20160622
In:
American journal of human genetics vol. 98
Availability: No items available.
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