Alfa map Site map Forside Udskriv E-mail Få teksten læst op
Søg
 
Gl. Landevej 7  -  2600 Glostrup  -  Tlf: 43260100  -  man-tor kl. 8.00-16.00, fre kl. 8.00-15.00
Om Kennedy Centret Organisation Medarbejdere Ledige stillinger Årsrapport m.m. Ventetider Her bor vi Kontakt Om kennedy.dk Links English - Limited version Laboratory analyses Laboratory pricelist Laboratory profile Exclusion of liability Research profile PKU, Fragile X and Rett syndrome Center for Fragilt X Center for PKU Center for Rett syndrom Forskning Synshandicap Øjenmalformationer og øjenudvikling Aniridi USHER syndrom Oculocutaneous albinism (OCA) AMD (aldersrelateret makuladegeneration) Autosomal dominant opticus atrofi Glaukom Mental retardering Gilles de Tourette Syndrom (GTS) Kromosomale ubalancer Fragilt X Down syndrom Kobberstofskiftet Menkes sygdom Funktionelle studier af ATP7A proteinet Udvikling af nye behandlingsmuligheder Epigenetik Maternel hypomethyleringssyndrom Aldersrelateret ændring i X-kromosom reaktivering PKU og beslægtede tilstande Phenylketonuri (PKU) Co-faktor BH4 og smerteforskning Familiær Dopa-responsiv dystoni Nyt fra forskningen Publikationer 2014 2013 2012 2011 2010 2009 2008 2007 2006 Tidligere publikationer Links Genetisk rådgivning Information Arvelig cancer rådgivning Sjældne kromosomafvigelser Lokationsnummer Priser Links - Genetisk rådgivning Laboratoriet English Nye analysetilbud Rekvisitioner Priser Vejledninger og downloads Kvalitetspolitik Synsregisteret Øjenklinikken Rekvisitioner Selvbetjening Links Privatlivspolitik

Sidst opdateret: 16/11 2017
Cathrine Jespersgaard - Curriculum vitae and Publications

Education

2007

-

2010

PhD, Health Sciences, Copenhagen University

“Methodologies in screening for genetic variants – analysis of SNPs
and CNVs in Inflammatory Bowel Disease”.

Supervisors: Professor Zeynep Tümer, Kennedy Center and PhD Paal Skytt Andersen, Statens Serum Institut

 

1993

-

1999

M.Sc. Chemistry – Biotechnology, Aarhus University

Master thesis:”Identification of a mammalian homologue of the E.coli
chaperone ClpX.”

Student in the lab of associate professor Peter Bross and Professor Niels Gregersen, Research Unit for Molecular Medicine, Aarhus University Hospital Skejby.

Supervisor from Aarhus University: Associate professor Torsten Kristensen

Employment

2012

-

 

Post. doc. at the Kennedy Centre
2001

-

2012

Molecular Biologist, Department of Clinical Biochemistry and Immunology, Statens Serum Institut.

1999

-

2001

Biologist, Fertility Clinic, Aarhus University Hospital Skejby

Publications

31.
Boyle MI, Jespersgaard C, Brøndum-Nielsen K, Bisgaard AM, Tümer Z.
Cornelia de Lange Syndrome.
Clin Genet. 2014 Sep 11. doi: 10.1111/cge.12499. [Epub ahead of print]


30. Hedley PL, Durrheim GA, Hendricks F, Goosen A, Jespersgaard C, Støvring B, Pham TT, Christiansen M, Brink PA, Corfield VA. 2013 Long QT syndrome in South Africa: the results of comprehensive genetic screening. Cardiovasc J Afr.;24(6):231-7.


29. la Cour Sibbesen E, Jespersgaard C, Alosi D, Bisgaard AM, Tümer Z.
Ring Chromosome 9 in a Girl With Developmental Delay and Dysmorphic Features: Case Report and Review of the Literature.
Am J Med Genet A. 2013 Jun;161(6):1447-52. doi: 10.1002/ajmg.a.35901. Epub 2013 Apr 30.


28. Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jespersgaard C, Jensen M, Kanters JK, Moolman-Smook JC, Møller DV, Bundgaard H, Christiansen M. MT-CYB mutations in hypertrophic cardiomyopathy. Mol Genet Genomic Med. 2013 May;1(1):54-65.

27.  Voigt HM, Simon RL, Jespersgaard C, Rosenberg J, and Gogenur I (2012) There Is No Association Between the Circadian Clock Gene HPER3 and Cognitive Dysfunction After Noncardiac Surgery. Anesth Analg

26.  Steinmetz J, Jespersgaard C, Dalhoff K, Hedley P, Abildstrom H, Christiansen M, and Rasmussen LS (2012) Cytochrome P450 polymorphism and postoperative cognitive dysfunction. Minerva Anestesiol 78 (3):303-309

25.  Persson S, Petersen HM, Jespersgaard C, and Olsen KE (2012) Real-time TaqMan polymerase chain reaction-based genus-identification and pyrosequencing-based species identification of Campylobacter jejuni, C. coli, C. lari, C. upsaliensis, and C. fetus directly on stool samples. Diagn Microbiol Infect Dis 74 (1):6-10

24.  Harris RA, Nagy-Szakal D, Pedersen N, Opekun A, Bronsky J, Munkholm P, Jespersgaard C, Andersen P, Melegh B, Ferry G, Jess T, and Kellermayer R (2012) Genome-wide peripheral blood leukocyte DNA methylation microarrays identified a single association with inflammatory bowel diseases. Inflamm Bowel Dis:10

23.  Fode P, Larsen AR, Feenstra B, Jespersgaard C, Skov RL, Stegger M, Fowler VG, Jr., and Andersen PS (2012) Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia. PLoS One 7 (2):e32315

22.  Duus K, Larsen N, Tran TA, Guven E, Skov LK, Jespersgaard C, Gajhede M, and Houen G (2012) Chemical and thermal unfolding of calreticulin. Protein Pept Lett

21.  Jespersgaard C*, Fode P*, Dybdahl M, Vind I, Nielsen OH, Csillag C, Munkholm P, Vainer B, Riis L, Elkjaer M, Pedersen N, Knudsen E, and Andersen PS (2011) Alpha-defensin DEFA1A3 gene copy number elevation in Danish Crohn's disease patients. Dig Dis Sci 56 (12):3517-3524

20.  Harboe TL, Willems P, Jespersgaard C, Molgaard Poulsen ML, Sorensen FB, and Bisgaard ML (2011) Mosaicism in segmental Darier disease: an in-depth molecular analysis quantifying proportions of mutated alleles in various tissues. Dermatology 222 (4):292-296

19.  Fode P*, Jespersgaard C*, Hardwick RJ, Bogle H, Theisen M, Dodoo D, Lenicek M, Vitek L, Vieira A, Freitas J, Andersen PS, and Hollox EJ (2011) Determination of beta-defensin genomic copy number in different populations: a comparison of three methods. PLoS One 6 (2):e16768

18.  Stensvold CR, Lebbad M, Verweij JJ, Jespersgaard C, von Samson-Himmelstjerna G, Nielsen SS, and Nielsen HV (2010) Identification and delineation of members of the Entamoeba complex by pyrosequencing. Mol Cell Probes 24 (6):403-406

17.  Moller DV, Pecini R, Gustafsson F, Hassager C, Hedley P, Jespersgaard C, Torp-Pedersen C, Christiansen M, and Kober LV (2010) Hereditary hemochromatosis (HFE) genotypes in heart failure: relation to etiology and prognosis. BMC Med Genet 11:117.:117

16.  Sorensen M, Allermann L, Vogel U, Andersen PS, Jespersgaard C, Loft S, and Raaschou-Nielsen O (2009) Polymorphisms in inflammation genes, tobacco smoke and furred pets and wheeze in children. Pediatr Allergy Immunol 20 (7):614-623

15.  Bahl JM, Heegaard NH, Falkenhorst G, Laursen H, Hogenhaven H, Molbak K, Jespersgaard C, Hougs L, Waldemar G, Johannsen P, and Christiansen M (2009) The diagnostic efficiency of biomarkers in sporadic Creutzfeldt-Jakob disease compared to Alzheimer's disease. Neurobiol Aging 30 (11):1834-1841

14.  Vind I, Riis L, Jespersgaard C, Jess T, Knudsen E, Pedersen N, Elkjaere M, Hansen TS, Andersen IB, Paerregaard A, Bondesen S, Locht H, Larsen SO, Moesgaard F, Bendtsen F, Andersen PS, and Munkholm P (2008) Genetic and environmental factors as predictors of disease severity and extent at time of diagnosis in an inception cohort of inflammatory bowel disease, Copenhagen County and City 2003-2005. J Crohns Colitis 2 (2):162-169

13.  Stensvold CR, Arendrup MC, Jespersgaard C, Molbak K, and Nielsen HV (2007) Detecting Blastocystis using parasitologic and DNA-based methods: a comparative study. Diagn Microbiol Infect Dis 59 (3):303-307

12.  Stensvold CR, Traub RJ, von Samson-Himmelstjerna G, Jespersgaard C, Nielsen HV, and Thompson RC (2007) Blastocystis: subtyping isolates using pyrosequencing technology. Exp Parasitol 116 (2):111-119

11.  Sorensen KM, Jespersgaard C, Vuust J, Hougaard D, Norgaard-Pedersen B, and Andersen PS (2007) Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems. Genet Test 11 (1):65-71

10.  Larsen LA, Jespersgaard C, and Andersen PS (2007) Single-strand conformation polymorphism analysis using capillary array electrophoresis for large-scale mutation detection. Nat Protoc 2 (6):1458-1466

9.  Jespersgaard C, Larsen LA, Baba S, Kukita Y, Tahira T, Christiansen M, Vuust J, Hayashi K, and Andersen PS (2006) Optimization of capillary array electrophoresis single-strand conformation polymorphism analysis for routine molecular diagnostics. Electrophoresis 27 (19):3816-3822

8.  Vind I, Jespersgaard C, Hougs L, Riis L, Dinesen L, Andersen PS, Locht H, Jess T, and Munkholm P (2005) Genetic and environmental factors in monozygotic twins with Crohn's disease and their first-degree relatives: a case report. Digestion 71 (4):262-265

7.  Jess T, Riis L, Jespersgaard C, Hougs L, Andersen PS, Orholm MK, Binder V, and Munkholm P (2005) Disease concordance, zygosity, and NOD2/CARD15 status: follow-up of a population-based cohort of Danish twins with inflammatory bowel disease. Am J Gastroenterol 100 (11):2486-2492

6.  Frank-Hansen R, Larsen LA, Andersen P, Jespersgaard C, and Christiansen M (2005) Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome. Clin Chim Acta 351 (1-2):95-100

5.  Andersen PS, Jespersgaard C, Vuust J, Christiansen M, and Larsen LA (2003) Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening. Hum Mutat 21 (5):455-465

4.  Andersen PS, Jespersgaard C, Vuust J, Christiansen M, and Larsen LA (2003) High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method. Hum Mutat 21 (2):116-122

3.  Ingerslev HJ, Hindkjaer J, Jespersgaard C, Lind MP, and Kolvraa S (2001) [Preimplantation genetic diagnosis. The first experiences in Denmark]. Ugeskr Laeger 163 (40):5525-5528

2.  Ingerslev HJ, Jespersgaard C, and Hindkjaer J (2001) [Preimplantation diagnosis. The Danish Society of Obstetrics and Gynecology]. Ugeskr Laeger 19;163 (12):1706

1.  Corydon TJ*, Wilsbech M*, Jespersgaard C*, Andresen BS, Borglum AD, Pedersen S, Bolund L, Gregersen N, and Bross P (2000) Human and mouse mitochondrial orthologs of bacterial ClpX. Mamm Genome 11 (10):899-905

* Shared first authorship