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Publications for Cecilia Gunnarsson

Publications mentioned in social media 14 times*

Journal Articles

Antheia Kissopoulou, Cecilia Trinks, Anna Gréen, Jan-Erik Karlsson, Jon Jonasson and Cecilia Gunnarsson
  Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy
  ESC Heart Failure, 2018, 5(4), 716-723.
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Eva Fernlund, Anna Wålinder Österberg, Ekaterina Kuchinskaya, Mikael Gustafsson, Kjell Jansson and Cecilia Gunnarsson
  Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death
  Pediatric Cardiology, 2017, 38(6), 1262-1268.
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Anneli Svensson, Meriam Åström Aneq, Kjerstin Ferm Widlund, Christina Fluur, Anna Green, Malin Rehnberg and Cecilia Gunnarsson
  Arrhythmogenic Right Ventricular Cardiomyopathy - 4 Swedish families with an associated PKP2 c.2146-1G>C variant.
  American journal of cardiovascular disease, 2016, 6(2), 55-65.
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Viviana Cordeddu, Jiani C. Yin, Cecilia Gunnarsson, Carl Virtanen, Severine Drunat, Francesca Lepri, Alessandro De Luca, Cesare Rossi, Andrea Ciolfi, Trevor J. Pugh, Alessandro Bruselles, James R. Priest, Len A. Pennacchio, Zhibin Lu, Arnavaz Danesh, Rene Quevedo, Alaa Hamid, Simone Martinelli, Francesca Pantaleoni, Maria Gnazzo, Paola Daniele, Christina Lissewski, Gianfranco Bocchinfuso, Lorenzo Stella, Sylvie Odent, Nicole Philip, Laurence Faivre, Marketa Vlckova, Eva Seemanova, Cristina Digilio, Martin Zenker, Giuseppe Zampino, Alain Verloes, Bruno Dallapiccola, Amy E. Roberts, Helene Cave, Bruce D. Gelb, Benjamin G. Neel and Marco Tartaglia
  Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome
  Human Mutation, 2015, 36(11), 1080-1087.
 Web of Science® Times Cited: 19

Anna Gréen, Henrik Green, Malin Rehnberg, Anneli Svensson, Cecilia Gunnarsson and Jon Jonasson
  Assessment of HaloPlex Amplification for Sequence Capture and Massively Parallel Sequencing of Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes
  Journal of Molecular Diagnostics, 2015, 17(1), 31-42.
 Web of Science® Times Cited: 9

Ivan Shabo, Kristine Maria Midtbö, Henrik Andersson, Emma Åkerlund, Hans Olsson, Pia Wegman, Cecilia Gunnarsson and Annelie Lindström
  Macrophage traits in cancer cells are induced by macrophage-cancer cell fusion and cannot be explained by cellular interaction
  BMC Cancer, 2015, 15(1), 922.
   Fulltext  PDF  
 Web of Science® Times Cited: 10

Hans Olsson, Agneta Jansson, Birgitta Holmlund and Cecilia Gunnarsson
  Methods for evaluating HER2 status in breast cancer: comparison of IHC, FISH, and real-time PCR analysis of formalin-fixed paraffin-embedded tissue
  Pathology and Laboratory Medicine International, 2013, 5, 31-37.
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Tove Sivik, Cecilia Gunnarsson, Tommy Fornander, Bo Nordenskjöld, Lambert Skoog, Olle Stål and Agneta Jansson
  17β-hydroxysteroid dehydrogenase type 14 is a predictive marker for tamoxifen response in oestrogen receptor positive breast cancer
  PLoS ONE, 2012, 7(7), e40568.
   Fulltext  PDF  
 Web of Science® Times Cited: 6

Istvan Gati, Olof Danielsson, Cecilia Gunnarsson, Magnus Vrethem, Bo Häggqvist, Bengt-Arne Fredriksson and Anne-Marie Landtblom
  Letter: Bent Spine Syndrome: A Phenotype of Dysferlinopathy or a Symptomatic DYSF Gene Mutation Carrier
  European Neurology, 2012, 67(5), 300-302.
 Web of Science® Times Cited: 4

Meriam Aneq Åström, Christina Fluur, Malin Rehnberg, Peter Söderkvist, Jan Engvall, Eva Nylander and Cecilia Gunnarsson
  Novel plakophilin2 mutation. Three generation family with arrhythmogenic right ventricular cardiomyopathy
  Scandinavian Cardiovascular Journal, 2012, 46(2), 72-75.
 Web of Science® Times Cited: 1

Malin Rehnberg, Jon Jonasson and Cecilia Gunnarsson
  Letter: Novel L1CAM Splice Site Mutation in a Young Male With L1 Syndrome
  American Journal of Medical Genetics. Part A, 2011, 155A(2), 439-441.
 Web of Science® Times Cited: 1

Cecilia Gunnarsson and Cathrine Foyn Bruhn
  Molecular Characterization and Clinical Features of a Patient With an Interstitial Deletion of 3p25.3-p26.1
 Web of Science® Times Cited: 27

Cecilia Gunnarsson, Barbara Graffmann and Jon Jonasson
  Chromosome r(10)(p15.3q26.12) in a newborn child: case report.
  Molecular Cytogenetics, 2009, 2, 25.
   Fulltext  PDF  
 Web of Science® Times Cited: 6

Kjerstin Ferm Widlund, Cecilia Gunnarsson, Karin Nordin and Mats G Hansson
  Pregnant women are satisfied with the information they receive about prenatal diagnosis, but are their decisions well informed?
  Acta obstetricia et gynecologica Scandinavica, 2009, 88(10), 1128-1132.
 Web of Science® Times Cited: 11

Agneta Jansson, Lovisa Delander, Cecilia Gunnarsson, Tommy Fornander, Lambert Skoog, Bo Nordenskjöld and Olle Stål
  Ratio of 17HSD1 to 17HSD2 protein expression predicts the outcome of tamoxifen treatment in postmenopausal breast cancer patients.
  Clinical Cancer Research, 2009, 15(10), 3610-3616.
 Web of Science® Times Cited: 22

Cecilia Gunnarsson, Piiha-Lotta Jerevall, Karl Hammar, Birgit Olsson, Bo Nordenskjöld, Agneta Jansson and Olle Stål
  Amplification of HSD17B1 has prognostic significance in postmenopausal breast cancer
  Breast Cancer Research and Treatment, 2008, 108(1), 35-41.
 Web of Science® Times Cited: 25

Agneta Jansson, Jonas Carlsson, Anette Olsson, Petter Storm, Sara Margolin, Cecilia Gunnarsson, Marie Stenmark Askmalm, Annika Lindblom, Bengt Persson and Olle Stål
  A new polymorphism in the coding region of exon four in HSD17B2 in relation to risk of sporadic and hereditary breast cancer
  Breast Cancer Research and Treatment, 2007, 106(1), 57-64.
 Web of Science® Times Cited: 7

Agneta Jansson, Cecilia Gunnarsson, Maja Cohen, Tove Sivik and Olle Stål
  17β-hydroxysteroid dehydrogenase 14 affects estradiol levels in breast cancer cells and is a prognostic marker in estrogen receptor-positive breast cancer
  Cancer Research, 2006, 66(23), 11471-11477.
 Web of Science® Times Cited: 50

Cecilia Gunnarsson, Agneta Jansson, Birgitta Holmlund, Lilianne Ferraud, Bo Nordenskjöld, Lars Erik Rutqvist, Lambert Skoog and Olle Stål
  Expression of COX-2 and steroid converting enzymes in breast cancer
  Oncology Reports, 2006, 16(2), 219-224.
 Web of Science® Times Cited: 12

Agneta Jansson, Cecilia Gunnarsson and Olle Stål
  Proliferative responses to altered 17β-hydroxysteroid dehydrogenase (17HSD) type 2 expression in human breast cancer cells are dependent on endogenous expression of 17HSD type 1 and the oestradiol receptors
  Endocrine-Related Cancer, 2006, 13(3), 875-884.
 Web of Science® Times Cited: 14

Cecilia Gunnarsson, Eva Hellqvist and Olle Stål
  17β-hydroxysteroid dehydrogenases involved in local oestrogen synthesis have prognostic significance in breast cancer
  British Journal of Cancer, 2005, 92(3), 547-552.
 Web of Science® Times Cited: 74

Cecilia Gunnarsson, Marie Ahnström, Kristina Kirschner, Birgit Olsson, Bo Nordenskjöld, Lars Erik Rutqvist, Lambert Skoog and Olle Stål
  Amplification of HSD17B1 and ERBB2 in primary breast cancer
  Oncogene, 2003, 22(1), 34-40.
 Web of Science® Times Cited: 64

Cecilia Gunnarsson, Birgit Olsson, Olle Stål and Lars-Gunnar Arnesson
  Abnormal expression of 17β-hydroxysteroid dehydrogenases in breast cancer predicts late recurrence
  Cancer Research, 2001, 61(23), 8448-8451.
 Web of Science® Times Cited: 91

Miodrag Palfi and Cecilia Gunnarsson
  The frequency of anti-C + anti-G in the absence of anti-D in alloimmunized pregnancies
  Transfusion Medicine, 2001, 11(3), 207-210.
 Web of Science® Times Cited: 13

Richard Lindgren, Cecilia Gunnarsson, Anna Jakobsson and Mats Hammar
  Hypersecretion of ovarian androgens may be gonadotrophin dependent many years after menopause
  Maturitas, 2000, 34(1), 43-46.
 Web of Science® Times Cited: 7

Ph.D. Theses

Cecilia Gunnarsson
  Steroid converting enzymes in breast cancer

* Social media data based on publications from 2011 to present and with a DOI; data delivered by Altmetric.com.


Responsible for this page: Peter Berkesand
Last updated: 2010-08-30