Publications by authors named "Jesper Graakjaer"

27Publications

Perturbations in RhoA signalling cause altered migration and impaired neuritogenesis in human iPSC-derived neural cells with PARK2 mutation.

Neurobiol Dis 2019 12 21;132:104581. Epub 2019 Aug 21.

Department of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, J.B. Winsloews Vej 21, st, DK5000 Odense C, Denmark; BRIDGE, Brain Research - Inter-Disciplinary Guided Excellence, Department of Clinical Research, University of Southern Denmark, J.B. Winsloews Vej 19, DK5000 Odense C, Denmark. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2019.104581DOI Listing
December 2019

Prostaglandin E -EP receptor subtype gene deletion in mother and son impairs platelet aggregation.

Br J Haematol 2019 03 13;184(5):851-853. Epub 2018 Mar 13.

Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark.

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http://dx.doi.org/10.1111/bjh.15196DOI Listing
March 2019

A case of penta X syndrome caused by nondisjunction in maternal meiosis 1 and 2.

Clin Case Rep 2017 07 1;5(7):1136-1140. Epub 2017 Jun 1.

Department of Clinical Genetics Aarhus University Hospital Aarhus Denmark.

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http://dx.doi.org/10.1002/ccr3.1004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494398PMC
July 2017

Microarray-Based Analysis of Methylation Status of CpGs in Placental DNA and Maternal Blood DNA--Potential New Epigenetic Biomarkers for Cell Free Fetal DNA-Based Diagnosis.

PLoS One 2015 31;10(7):e0128918. Epub 2015 Jul 31.

Department of Clinical Genetics, Vejle Hospital, 7100, Vejle, Denmark; Institute of Regional Health research, University of Southern Denmark, 5000, Odense, Denmark.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0128918PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521692PMC
May 2016

Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.

Am J Hum Genet 2014 Nov 6;95(5):565-78. Epub 2014 Nov 6.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.10.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225592PMC
November 2014

Duplication in the microtubule-actin cross-linking factor 1 gene causes a novel neuromuscular condition.

Sci Rep 2014 Jun 5;4:5180. Epub 2014 Jun 5.

University of Southern Denmark and Odense University Hospital, Institute of Clinical Research, Pathology, SDU muscle research cluster, J.B. Winsløws Vej 15, 2., 5000 Odense C, Denmark.

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http://dx.doi.org/10.1038/srep05180DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046130PMC
June 2014

Age-dependence of relative telomere length profiles during spermatogenesis in man.

Maturitas 2013 Aug 10;75(4):380-5. Epub 2013 Jun 10.

Laboratory of Reproductive Biology, Scientific Unit, Horsens Hospital, Denmark.

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http://dx.doi.org/10.1016/j.maturitas.2013.05.001DOI Listing
August 2013

Heart defects and other features of the 22q11 distal deletion syndrome.

Eur J Med Genet 2013 Feb 10;56(2):98-107. Epub 2012 Oct 10.

Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.

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http://dx.doi.org/10.1016/j.ejmg.2012.09.009DOI Listing
February 2013

The distribution pattern of critically short telomeres in human osteoarthritic knees.

Arthritis Res Ther 2012 Jan 18;14(1):R12. Epub 2012 Jan 18.

Department of Clinical Cell Biology, Vejle/Lillebaelt Hospital, Institute of Regional Health Research, University of Southern Denmark, Kabbeltoft 25, 7100 Vejle, Denmark.

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http://dx.doi.org/10.1186/ar3687DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392801PMC
January 2012

Further delineation of 17p13.3 microdeletion involving CRK. The effect of growth hormone treatment.

Eur J Med Genet 2012 Jan 24;55(1):22-6. Epub 2011 Oct 24.

Centre for Rare Diseases, Department of Paediatrics A, Aarhus University Hospital, Skejby. Brendstrupsgaardvej 100, DK-8200 Aarhus N, Denmark.

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http://dx.doi.org/10.1016/j.ejmg.2011.09.004DOI Listing
January 2012

A case study of "disorganized development" and its possible relevance to genetic determinants of aging.

Mech Ageing Dev 2009 May 24;130(5):350-6. Epub 2009 Feb 24.

University of South Florida College of Medicine, Tampa, FL, United States.

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http://dx.doi.org/10.1016/j.mad.2009.02.003DOI Listing
May 2009

Telomere stability and telomerase in mesenchymal stem cells.

Biochimie 2008 Jan 25;90(1):33-40. Epub 2007 Sep 25.

Southern Denmark University, Institute for Regional Health Research (IRS), Telomere and Aging Group, Biopark Vejle, Tysklandsvej 7,7100 Vejle, Denmark.

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http://dx.doi.org/10.1016/j.biochi.2007.09.005DOI Listing
January 2008

Allele-specific relative telomere lengths are inherited.

Hum Genet 2006 Apr 27;119(3):344-50. Epub 2006 Jan 27.

Telomeres and Cancer Lab, UMR7147, CNRS-I, Curie-UPMC, Paris, France.

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http://dx.doi.org/10.1007/s00439-006-0137-xDOI Listing
April 2006

Telomere length among the elderly and oldest-old.

Twin Res Hum Genet 2005 Oct;8(5):425-32

Institute of Human Genetics, Aarhus University, Denmark.

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http://dx.doi.org/10.1375/183242705774310079DOI Listing
October 2005

The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2.

Mol Cell 2004 Jun;14(6):763-74

Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.

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http://dx.doi.org/10.1016/j.molcel.2004.05.023DOI Listing
June 2004