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31 results for Fransson,+Susanne

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ArticlesPeer ReviewedFull Text
Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux
Author / Creator:Bartik, Zsuzsa I ; Sillén, Ulla ; Djos, Anna ; Lindholm, Anna ; Fransson, Susanne
Publisher:United States: Public Library of Science
Journal title:PloS one, 2022-11, Vol.17 (11), p.e0277524-e0277524
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Altered methylation of imprinted genes in neuroblastoma: implications for prognostic refinement
Author / Creator:Suman, Medha ; Löfgren, Maja ; Fransson, Susanne ; Yousuf, Jewahri Idris ; Svensson, Johanna ; Djos, Anna ; Martinsson, Tommy ; Kogner, Per ; Kling, Teresia ; Carén, Helena
Publisher:England: BioMed Central Ltd
Journal title:Journal of translational medicine, 2024-08, Vol.22 (1), p.808-25, Article 808
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Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance
Author / Creator:Fransson, Susanne ; Martinez-Monleon, Angela ; Johansson, Mathias ; Sjöberg, Rose-Marie ; Björklund, Caroline ; Ljungman, Gustaf ; Ek, Torben ; Kogner, Per ; Martinsson, Tommy
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2020-12, Vol.10 (1), p.22432-22432, Article 22432
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Joint single-cell genetic and transcriptomic analysis reveal pre-malignant SCP-like subclones in human neuroblastoma
Author / Creator:Olsen, Thale K ; Otte, Jörg ; Mei, Shenglin ; Embaie, Bethel Tesfai ; Kameneva, Polina ; Cheng, Huaitao ; Gao, Teng ; Zachariadis, Vasilios ; Tsea, Ioanna ; Björklund, Åsa ; Kryukov, Emil ; Hou, Ziyi ; Johansson, Anna ; Sundström, Erik ; Martinsson, Tommy ; Fransson, Susanne ; Stenman, Jakob ; Fard, Shahrzad Shirazi ; Johnsen, John Inge ; Kogner, Per ; Adameyko, Igor ; Enge, Martin ; Kharchenko, Peter V ; Baryawno, Ninib
Publisher:England: BioMed Central Ltd
Journal title:Molecular cancer, 2024-08, Vol.23 (1), p.180-12, Article 180
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TC-hunter: identification of the insertion site of a transgenic gene within the host genome
Author / Creator:Börjesson, Vanja ; Martinez-Monleon, Angela ; Fransson, Susanne ; Kogner, Per ; Johnsen, John Inge ; Milosevic, Jelena ; López, Marcela Dávila
Publisher:England: BioMed Central Ltd
Journal title:BMC genomics, 2022-02, Vol.23 (1), p.149-11, Article 149
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Amplification of CDK4 and MDM2: a detailed study of a high-risk neuroblastoma subgroup
Author / Creator:Martinez-Monleon, Angela ; Kryh Öberg, Hanna ; Gaarder, Jennie ; Berbegall, Ana P. ; Javanmardi, Niloufar ; Djos, Anna ; Ussowicz, Marek ; Taschner-Mandl, Sabine ; Ambros, Inge M. ; Øra, Ingrid ; Sandstedt, Bengt ; Beiske, Klaus ; Ladenstein, Ruth ; Noguera, Rosa ; Ambros, Peter F. ; Gordon Murkes, Lena ; Ljungman, Gustaf ; Kogner, Per ; Fransson, Susanne ; Martinsson, Tommy
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2022, Vol.12 (1), p.12420-12420, Article 12420
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PPM1D Is a Therapeutic Target in Childhood Neural Tumors
Author / Creator:Milosevic, Jelena ; Treis, Diana ; Fransson, Susanne ; Gallo-Oller, Gabriel ; Sveinbjörnsson, Baldur ; Eissler, Nina ; Tanino, Keiji ; Sakaguchi, Kazuyasu ; Martinsson, Tommy ; Wickström, Malin ; Kogner, Per ; Johnsen, John Inge
Publisher:Basel: MDPI AG
Journal title:Cancers, 2021-11, Vol.13 (23), p.6042
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High Expression of PPM1D Induces Tumors Phenotypically Similar to TP53 Loss-of-Function Mutations in Mice
Author / Creator:Milosevic, Jelena ; Fransson, Susanne ; Gulyas, Miklos ; Olsen, Thale K. ; Gallo-Oller, Gabriel ; Treis, Diana ; Elfman, Lotta H. M. ; Wilhelm, Margareta ; Martinsson, Tommy ; Baryawno, Ninib ; Kogner, Per ; Johnsen, John Inge
Publisher:Basel: MDPI AG
Journal title:Cancers, 2021-10, Vol.13 (21), p.5493
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Personalized circulating tumor DNA analysis for sensitive disease monitoring and detection of relapse in neuroblastoma
Author / Creator:Rahmqvist, Ida ; Engström, Enya ; Mellström, Elisabeth ; Ibrahim, Raghda R ; Pujol-Calderón, Fani ; Dahlstrand Rudin, Agnes ; Ordqvist Redfors, Anna ; Rostamzadeh, Niki ; Di Rienzo, Rita ; Franssila, Wilma ; Khashan, Robert ; Xylander, Moe ; Karlsson, Christin ; Ek, Torben ; Andersson, Daniel ; Österlund, Tobias ; Gaarder, Jennie ; Fagman, Henrik ; Fransson, Susanne ; Martinsson, Tommy ; Ståhlberg, Anders ; Dalin, Martin
Publisher:England: BioMed Central Ltd
Journal title:Biomarker research, 2024-11, Vol.12 (1), p.148-6, Article 148
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ArticlesPeer ReviewedFull Text
Multifocal Neuroblastoma and Central Hypoventilation in An Infant with Germline ALK F1174I Mutation
Author / Creator:Djos, Anna ; Treis, Diana ; Fransson, Susanne ; Gordon Murkes, Lena ; Wessman, Sandra ; Ásmundsson, Jurate ; Markström, Agneta ; Kogner, Per ; Martinsson, Tommy
Publisher:Basel: MDPI AG
Journal title:Diagnostics (Basel), 2022-09, Vol.12 (9), p.2260
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Identification of recurrent 3q13.31 chromosomal rearrangement indicates LSAMP as a tumor suppressor gene in neuroblastoma
Author / Creator:Martinez‑Monleon, Angela ; Gaarder, Jennie ; Djos, Anna ; Kogner, Per ; Fransson, Susanne
Publisher:Athens: Spandidos Publications
Journal title:International journal of oncology, 2023-02, Vol.62 (2), p.1, Article 27
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High level of p37[delta]-mRNA relative to p110[delta]-mRNA in neuroblastoma tumors correlates with poor patient survival
Author / Creator:Fransson, Susanne ; Ejeskär, Katarina
Publisher:Middlesex: Springer Nature B.V
Journal title:Medical oncology (Northwood, London, England), 2013-12, Vol.30 (4), p.1
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Estimation of copy number aberrations: Comparison of exome sequencing data with SNP microarrays identifies homozygous deletions of 19q13.2 and CIC in neuroblastoma
Author / Creator:FRANSSON, SUSANNE ; ÖSTENSSON, MALIN ; DJOS, ANNA ; JAVANMARDI, NILOUFAR ; KOGNER, PER ; MARTINSSON, TOMMY
Publisher:Athens: D.A. Spandidos
Journal title:International journal of oncology, 2016-03, Vol.48 (3), p.1103-1116
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Rho-associated kinase is a therapeutic target in neuroblastoma
Author / Creator:Dyberg, Cecilia ; Fransson, Susanne ; Andonova, Teodora ; Sveinbjörnsson, Baldur ; Lännerholm-Palm, Jessika ; Olsen, Thale K. ; Forsberg, David ; Herlenius, Eric ; Martinsson, Tommy ; Brodin, Bertha ; Kogner, Per ; Johnsen, John Inge ; Wickström, Malin
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2017-08, Vol.114 (32), p.E6603-E6612
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Telomere Maintenance Mechanisms in a Cohort of High-Risk Neuroblastoma Tumors and Its Relation to Genomic Variants in the ITERT/I and IATRX/I Genes
Author / Creator:Djos, Anna ; Thombare, Ketan ; Vaid, Roshan ; Gaarder, Jennie ; Umapathy, Ganesh ; Reinsbach, Susanne E ; Georgantzi, Kleopatra ; Stenman, Jakob ; Carén, Helena ; Ek, Torben ; Mondal, Tanmoy ; Kogner, Per ; Ma ; Fransson, Susanne
Publisher:MDPI AG
Journal title:Cancers, 2023-12, Vol.15 (24)
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High level of p37δ-mRNA relative to p110δ-mRNA in neuroblastoma tumors correlates with poor patient survival
Author / Creator:Fransson, Susanne ; Ejeskär, Katarina
Publisher:Boston: Springer US
Journal title:Medical oncology (Northwood, London, England), 2013-12, Vol.30 (4), p.724-724, Article 724
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ArticlesPeer ReviewedFull Text
Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux
Author / Creator:Zsuzsa I. Bartik ; Ulla Sillén ; Anna Djos ; Anna Lindholm ; Susanne Fransson
Publisher:Public Library of Science (PLoS)
Journal title:PloS one, 2022-01, Vol.17 (11)
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Low Frequency ALK Hotspots Mutations In Neuroblastoma Tumours Detected By Ultra-deep Sequencing: Implications For ALK Inhibitor Treatment
Author / Creator:Javanmardi, Niloufar ; Fransson, Susanne ; Djos, Anna ; Sjöberg, Rose-Marie ; Nilsson, Staffan ; Truvé, Katarina ; Kogner, Per ; Martinsson, Tommy
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2019-02, Vol.9 (1), p.2199-2199, Article 2199
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Telomere Maintenance Mechanisms in a Cohort of High-Risk Neuroblastoma Tumors and Its Relation to Genomic Variants in the TERT and ATRX Genes
Author / Creator:Djos, Anna ; Thombare, Ketan ; Vaid, Roshan ; Gaarder, Jennie ; Umapathy, Ganesh ; Reinsbach, Susanne E ; Georgantzi, Kleopatra ; Stenman, Jakob ; Carén, Helena ; Ek, Torben ; Mondal, Tanmoy ; Kogner, Per ; Martinsson, Tommy ; Fransson, Susanne
Publisher:Switzerland: MDPI AG
Journal title:Cancers, 2023-12, Vol.15 (24), p.5732
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ArticlesFull Text
Estimation of copy number aberrations: Comparison of exome sequencing data with SNP microarrays identifies homozygous deletions of 19q13.2 and iin neuroblastoma
Author / Creator:Fransson, Susanne ; Östensson, Malin ; Djos, Anna ; Javanmardi, Niloufar ; Kogner, P. ; Martinsson, Tommy
Journal title:International journal of oncology, 2016, Vol.48 (3), p.1103
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Showing 1 to 20 of 31 results

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Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux

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Altered methylation of imprinted genes in neuroblastoma: implications for prognostic refinement

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Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance

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Joint single-cell genetic and transcriptomic analysis reveal pre-malignant SCP-like subclones in human neuroblastoma

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TC-hunter: identification of the insertion site of a transgenic gene within the host genome

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Amplification of CDK4 and MDM2: a detailed study of a high-risk neuroblastoma subgroup

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PPM1D Is a Therapeutic Target in Childhood Neural Tumors

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High Expression of PPM1D Induces Tumors Phenotypically Similar to TP53 Loss-of-Function Mutations in Mice

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Personalized circulating tumor DNA analysis for sensitive disease monitoring and detection of relapse in neuroblastoma

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Multifocal Neuroblastoma and Central Hypoventilation in An Infant with Germline ALK F1174I Mutation

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Identification of recurrent 3q13.31 chromosomal rearrangement indicates LSAMP as a tumor suppressor gene in neuroblastoma

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High level of p37[delta]-mRNA relative to p110[delta]-mRNA in neuroblastoma tumors correlates with poor patient survival

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Estimation of copy number aberrations: Comparison of exome sequencing data with SNP microarrays identifies homozygous deletions of 19q13.2 and CIC in neuroblastoma

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Rho-associated kinase is a therapeutic target in neuroblastoma

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Telomere Maintenance Mechanisms in a Cohort of High-Risk Neuroblastoma Tumors and Its Relation to Genomic Variants in the ITERT/I and IATRX/I Genes

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High level of p37δ-mRNA relative to p110δ-mRNA in neuroblastoma tumors correlates with poor patient survival

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Whole exome sequencing identifies KIF26B, LIFR and LAMC1 mutations in familial vesicoureteral reflux

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Low Frequency ALK Hotspots Mutations In Neuroblastoma Tumours Detected By Ultra-deep Sequencing: Implications For ALK Inhibitor Treatment

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Telomere Maintenance Mechanisms in a Cohort of High-Risk Neuroblastoma Tumors and Its Relation to Genomic Variants in the TERT and ATRX Genes

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Estimation of copy number aberrations: Comparison of exome sequencing data with SNP microarrays identifies homozygous deletions of 19q13.2 and iin neuroblastoma

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