A
Anna Collin
Researcher at Lund University
Publications - 30
Citations - 1098
Anna Collin is an academic researcher from Lund University. The author has contributed to research in topics: Induced pluripotent stem cell & Fluorescence in situ hybridization. The author has an hindex of 14, co-authored 27 publications receiving 858 citations.
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Journal ArticleDOI
Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders.
Fiona M Ross,Hervé Avet-Loiseau,Geneviève Ameye,Norma C. Gutiérrez,Peter Liebisch,Sheila J.M. O’Connor,Klara Dalva,Sonia Fabris,Adele M. Testi,Marie Jarošová,Clare Hodkinson,Anna Collin,Gitte Kerndrup,Petr Kuglík,D. Ladon,Paolo Bernasconi,Brigitte Maes,Zuzana Zemanova,Kyra Michalova,Lucienne Michau,Kai Neben,N. Emil U. Hermansen,Katrina Rack,Alberto Rocci,Rebecca K.M. Protheroe,Laura Chiecchio,Hélène Poirel,Pieter Sonneveld,Mette Nyegaard,Hans Erik Johnsen +29 more
TL;DR: The primary clinical applications for FISH analysis were for newly diagnosed cases of MM or frank relapse cases and prospective analysis should be centralized for upcoming trials based on the recommendations made.
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Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor
Arezoo Mohajeri,Johnbosco Tayebwa,Anna Collin,Jenny Nilsson,Linda Magnusson,Fredrik Vult von Steyern,Otte Brosjö,Henryk A. Domanski,Olle Larsson,Raf Sciot,Maria Debiec-Rychter,Jason L. Hornick,Nils Mandahl,Karolin Hansén Nord,Fredrik Mertens +14 more
TL;DR: The hypothesis that the NAB2/STAT6 fusions will result in altered properties of the transcriptional co‐repressor NAB 2 ‐ a key regulator of the early growth response 1 (EGR1) transcription factor – was corroborated by global gene expression analysis; SFTs showed deregulated expression of EGR1 target genes, as well as of other, developmentally important genes.
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Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype
Hammurabi Bartuma,Karolin H. Hallor,Ioannis Panagopoulos,Anna Collin,Anders Rydholm,Pelle Gustafson,Henrik C. F. Bauer,Otte Brosjö,Henryk A. Domanski,Nils Mandahl,Fredrik Mertens +10 more
TL;DR: Correlation with clinical features revealed that lipomas with rings/giant markers were larger, occurred in older patients, were more often deep‐seated, and seemed to have an increased tendency to recur locally, compared with tumors with other chromosome aberrations.
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Creation of a library of induced pluripotent stem cells from Parkinsonian patients
Staffan Holmqvist,Šárka Lehtonen,Margarita Chumarina,Katja A. Puttonen,Carla Azevedo,O. V. Lebedeva,Marika Ruponen,Minna Oksanen,Mehdi Djelloul,Anna Collin,Stefano Goldwurm,Morten Meyer,Maria A. Lagarkova,Sergei L. Kiselev,Jari Koistinaho,Laurent Roybon +15 more
TL;DR: The generation of a comprehensive library of iPSC lines of familial PD and an associated synucleinopathy, multiple system atrophy is reported, which will be a valuable resource for identifying common and divergent mechanisms leading to neurodegeneration in PD and MSA.
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The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1
TL;DR: It is shown that a putative POU5F1P1 protein is localized in the nucleus, acts as a transcriptional activator and regulates the expression in a similar way to the POU4F1 isoform 1, but was a weaker activator than isoforms 1 and 2.