Extensive somatic L1 retrotransposition in colorectal tumors
Solyom, Szilvia, Ewing, Adam D, Rahrmann, Eric P, Doucet, Tara, Nelson, Heather H, Burns, Michael B, Harris, Reuben S, Sigmon, David F, Casella, Alex, Erlanger, Bracha, Wheelan, Sarah, Upton, Kyle R, Shukla, Ruchi, Faulkner, Geoffrey J, Largaespada, David A, Kazazian, Jr, Haig H
Published in Genome research (01.12.2012)
Published in Genome research (01.12.2012)
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Widespread somatic L1 retrotransposition occurs early during gastrointestinal cancer evolution
Ewing, Adam D, Gacita, Anthony, Wood, Laura D, Ma, Florence, Xing, Dongmei, Kim, Min-Sik, Manda, Srikanth S, Abril, Gabriela, Pereira, Gavin, Makohon-Moore, Alvin, Looijenga, Leendert H J, Gillis, Ad J M, Hruban, Ralph H, Anders, Robert A, Romans, Katharine E, Pandey, Akhilesh, Iacobuzio-Donahue, Christine A, Vogelstein, Bert, Kinzler, Kenneth W, Kazazian, Jr, Haig H, Solyom, Szilvia
Published in Genome research (01.10.2015)
Published in Genome research (01.10.2015)
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Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon
Solyom, Szilvia, Ewing, Adam D., Hancks, Dustin C., Takeshima, Yasuhiro, Awano, Hiroyuki, Matsuo, Masafumi, Kazazian Jr, Haig H.
Published in Human mutation (01.02.2012)
Published in Human mutation (01.02.2012)
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High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients
Papp, Janos, Kovacs, Marietta Eva, Solyom, Szilvia, Kasler, Miklos, Børresen-Dale, Anne-Lise, Olah, Edith
Published in BMC medical genetics (30.11.2010)
Published in BMC medical genetics (30.11.2010)
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Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families
Pylkäs, Katri, Erkko, Hannele, Nikkilä, Jenni, Sólyom, Szilvia, Winqvist, Robert
Published in BMC cancer (26.05.2008)
Published in BMC cancer (26.05.2008)
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Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions
Solyom, Szilvia, Aressy, Bernadette, Pylkäs, Katri, Patterson-Fortin, Jeffrey, Hartikainen, Jaana M, Kallioniemi, Anne, Kauppila, Saila, Nikkilä, Jenni, Kosma, Veli-Matti, Mannermaa, Arto, Greenberg, Roger A, Winqvist, Robert
Published in Science translational medicine (22.02.2012)
Published in Science translational medicine (22.02.2012)
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Abstract 5599: Screening for large genomic rearrangements in the FANCA and FANCJ genes reveals extensive genomic FANCA deletion in a Finnish breast cancer family
Solyom, Szilvia, Winqvist, Robert, Nikkilä, Jenni, Pylkäs, Katri
Published in Cancer research (Chicago, Ill.) (15.04.2011)
Published in Cancer research (Chicago, Ill.) (15.04.2011)
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Screening for large genomic rearrangements in the FANCA gene reveals extensive deletion in a Finnish breast cancer family
Solyom, Szilvia, Winqvist, Robert, Nikkilä, Jenni, Rapakko, Katrin, Hirvikoski, Pasi, Kokkonen, Hannaleena, Pylkäs, Katri
Published in Cancer letters (28.03.2011)
Published in Cancer letters (28.03.2011)
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Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families
Solyom, Szilvia, Patterson-Fortin, Jeffery, Pylkäs, Katri, Greenberg, Roger A, Winqvist, Robert
Published in Breast cancer research and treatment (01.02.2010)
Published in Breast cancer research and treatment (01.02.2010)
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Journal Article
Screening for large genomic rearrangements in theFANCAgene reveals extensive deletion in a Finnish breast cancer family
Solyom, Szilvia, Winqvist, Robert, Nikkilä, Jenni, Rapakko, Katrin, Hirvikoski, Pasi, Kokkonen, Hannaleena, Pylkäs, Katri
Published in Cancer letters (28.03.2011)
Published in Cancer letters (28.03.2011)
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Journal Article
Pathogenic orphan transduction created by a non-reference LINE-1 retrotransposon
Solyom, Szilvia, Ewing, Adam D., Hancks, Dustin C., Takeshima, Yasuhiro, Awano, Hiroyuki, Matsuo, Masafumi, Kazazian, Haig. H.
Published in Human mutation (08.12.2011)
Published in Human mutation (08.12.2011)
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Journal Article
High prevalence of germline STK11mutations in Hungarian Peutz-Jeghers Syndrome patients
Papp, Janos, Kovacs, Marietta Eva, Solyom, Szilvia, Kasler, Miklos, Børresen-Dale, Anne-Lise, Olah, Edith
Published in BMC medical genetics (30.11.2010)
Published in BMC medical genetics (30.11.2010)
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