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Sidst opdateret: 16/11 2017
Publikationer 2007
Kontakt: Webmaster

Videnskabelige publikationer

  • Abdallah BM, Ding M, Jensen CH, Ditzel N, Flyvbjerg A, Jensen TG, Dagnæs-Hansen F, Gasser JA, Kassem M.
    Dlk1/FA1 Is a Novel Endocrine Regulator of Bone and Fat Mass and Its Serum Level Is Modulated By Growth Hormone.
    Endocrinology, 2007, 148: 3111-21

  • Bache I, Brondum-Nielsen K, Tommerup N.
    Genetic counseling in adult carriers of a balanced chromosomal rearrangement ascertained in childhood: experiences from a nationwide reexamination of translocation carriers.
    Genet Med. 2007 Mar;9(3):185-7

  • Banin E, Mizrahi-Meissonnier L, Neis R, Silverstein S, Magyar I, Abeliovich D, Roepman R, Berger W, Rosenberg T, Sharon D.
    A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa.
    Am J Med Genet A. 2007 Jun 1;143(11):1150-8

  • Birk Møller L, Nygren AO, Scott P, Hougaard P, Bieber Nielsen J, Hartmann C, Güttler F, Tyfield L, Zschocke J.
    Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany.
    Hum Mutat. 2007 Feb;28(2):207

  • Bugge M, Collins A, Hertz JM, Eiberg H, Lundsteen C, Brandt CA, Bak M, Hansen C, Delozier CD, Lespinasse J, Tranebjaerg L, Hahnemann JM, Rasmussen K, Bruun-Petersen G, Duprez L, Tommerup N, Petersen MB.
    Non-disjunction of chromosome 13.
    Hum Mol Genet. 2007 Aug 15;16(16):2004-10. Epub 2007 Jun 21

  • Christoffersen N, Gade E, Knudsen L, Juel K, Larsen M.
    Mortality in patients with branch retinal vein occlusion.
    Ophthalmology. 2007 Jun;114(6):1186-9

  • Corydon TJ, Haagerup A, Jensen TG, Binderup HG, Petersen MS, Kaltoft K, Vestbo J, Kruse TA, Børglum AD.
    A functional CD86 polymorphism associated with asthma and related allergic disorders.
    J Med Genet. 2007 Aug;44(8):509-15. Epub 2007 May 18

  • Cremers FP, Kimberling WJ, Külm M, de Brouwer AP, van Wijk E, te Brinke H, Cremers CW, Hoefsloot LH, Banfi S, Simonelli F, Fleischhauer JC, Berger W, Kelley PM, Haralambous E, Bitner-Glindzicz M, Webster AR, Saihan Z, De Baere E, Leroy BP, Silvestri G, McKay GJ, Koenekoop RK, Millan JM, Rosenberg T, Joensuu T, Sankila EM, Weil D, Weston MD, Wissinger B, Kremer H.
    Development of a genotyping microarray for Usher syndrome.
    J Med Genet. 2007 Feb;44(2):153-60. Epub 2006 Sep 8

  • Dahl C, Grønskov K, Larsen LA, Guldberg P, Brøndum-Nielsen K.
    A homogeneous assay for analysis of FMR1 promoter methylation in patients with fragile X syndrome.
    Clin Chem. 2007 Apr;53(4):790-3. Epub 2007 Jan 26

  • Gjetting T, Hagedorn PH, Schweizer P, Thordal-Christensen H, Carver TL, Lyngkjaer MF.
    Single-cell transcript profiling of barley attacked by the powdery mildew fungus.
    Mol Plant Microbe Interact. 2007 Mar;20(3):235-46

  • Grarup N, Albrechtsen A, Ek J, Borch-Johnsen K, Jørgensen T, Schmitz O, Hansen T, Pedersen O.
    Variation in the peroxisome proliferator-activated receptor delta gene in relation to common metabolic traits in 7,495 middle-aged white people.
    Diabetologia. 2007 Jun;50(6):1201-8. Epub 2007 Apr 13

  • Gronskov K, Ek J, Brondum-Nielsen K.
    Oculocutaneous albinism.
    Orphanet J Rare Dis. 2007 Nov 2;2(1):43

  • Hansen L, Eiberg H, Rosenberg T.
    Novel MAF mutation in a family with congenital cataract-microcornea syndrome.
    Mol Vis. 2007 Oct 18;13:2019-22

  • Hansen L, Yao W, Eiberg H, Kjaer KW, Baggesen K, Hejtmancik JF, Rosenberg T.
    Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.
    Invest Ophthalmol Vis Sci. 2007 Sep;48(9):3937-44

  • Hjortshøj TD, Grønskov K, Rosenberg T, Brøndum-Nielsen K, Olsen JH.
    Risk for cancer in patients with Bardet-Biedl syndrome and their relatives.
    Am j Med Genet A. 2007 Aug 1;143(15):1699-702

  • Jacobsen N, Jensen H, Goldschmidt E.
    Prevalence of myopia in Danish conscripts.
    Acta Ophthalmol Scand. 2007 Mar;85(2):165-70

  • Jacobsen N, Jensen H, Lund-Andersen H, Goldschmidt E.
    Is poor glycaemic control in diabetic patients a risk factor of myopia?
    Acta Ophthalmol Scand. 2007 Dec 12

  • Jensen MK, Rung JH, Gregersen PL, Gjetting T, Fuglsang AT, Hansen M, Joehnk N, Lyngkjaer MF, Collinge DB.
    The HvNAC6 transcription factor: a positive regulator of penetration resistance in barley and Arabidopsis.
    Plant Mol Biol. 2007 Sep;65(1-2):137-50. Epub 2007 Jul 6

  • Jensen TG.
    Cutaneous gene therapy.
    Ann Med. 2007;39(2):108-15. Review.

  • Jensen TG, Brøndum-Nielsen K; Dansk Selskab for Medicinsk Genetik. [Gene therapy. The Danish Society of Medical Genetics] Ugeskr Laeger.
    2007 Mar 19;169(12):1119. Danish. No abstract available.

  • Khamaisi M, Søndergaard M, Segev Y, Dagnaes-Hansen F, Jensen TG, Landau D, Raz I, and Flyvbjerg A (2007).
    Differential effects on kidney and liver growth of a non-viral hGH-producing vector in hypophysectomized mice.
    Growth Horm IGF Res. 17: 279-287

  • Lehmann K, Seemann P, Silan F, Goecke TO, Irgang S, Kjaer KW, Kjaergaard S, Mahoney MJ, Morlot S, Reissner C, Kerr B, Wilkie AO, Mundlos S.
    A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN.
    Am J Hum Genet. 2007 Aug;81(2):388-96. Epub Jun 8

  • Matalon R, Michals-Matalon K, Bhatia G, Burlina AB, Burlina AP, Braga C, Fiori L, Giovannini M, Grechanina E, Novikov P, Grady J, Tyring SK, Guttler F.
    Double blind placebo control trial of large neutral amino acids in treatment of PKU: effect on blood phenylalanine.
    J Inherit Metab Dis. 2007 Apr;30(2):153-8. Epub 2007 Feb 27

  • Michals-Matalon K, Bhatia G, Guttler F, Tyring SK, Matalon R.
    Response of phenylketonuria to tetrahydrobiopterin.
    J Nutr. 2007 Jun;137(6 Suppl 1):1564S-1567S; discussion 1573S-1575S

  • Munch IC, Sander B, Kessel L, Hougaard JL, Taarnhøj NC, Sørensen TI, Kyvik KO, Larsen M.
    Heredity of small hard drusen in twins aged 20-46 years.
    Invest Ophthalmol Vis Sci. 2007 Feb;48(2):833-8

  • Nielsen LS, Skov L, Jensen H.
    Vision screening in children with developmental delay can be improved: analysis of a screening programme outside the ophthalmic clinic.
    Dev Med Child Neurol. 2007 Jul;49(7):508-12

  • Nielsen LS, Skov L, Jensen H.
    Visual dysfunctions and ocular disorders in children with developmental delay. I. prevalence, diagnoses and aetiology of visual impairment.
    Acta Ophthalmol Scand. 2007 Mar;85(2):149-56

  • Nielsen LS, Nielsen SK, Skov L, Jensen H.
    Contrast sensitivity--an unnoticed factor of visual perception in children with developmental delay: normal data of the Cambridge Low Contrast Gratings test in children.
    J Child Neurol. 2007 Feb;22(2):151-5

  • Olsen BS, Hahnemann JM, Schwartz M, Østergaard E.
    Thiamine-responsive megaloblastic anaemia: a cause of syndromic diabetes in childhood.
    Pediatr Diabetes. 2007 Aug;8(4):239-41

  • Ostergaard E, Christensen E, Kristensen E, Mogensen B, Duno M, Shoubridge EA, Wibrand F.
    Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion.
    Am J Hum Genet. 2007 Aug;81(2):383-7. Epub 2007 Jun 4

  • Ostergaard E, Hansen FJ, Sorensen N, Duno M, Vissing J, Larsen PL, Faeroe O, Thorgrimsson S, Wibrand F, Christensen E, Schwartz M.
    Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations.
    Brain. 2007 Mar;130(Pt 3):853-61. Epub 2007 Feb 7

  • Pedersen R, Soliman W, Lund-Andersen H, Larsen M.
    Treatment of choroidal neovascularization using intravitreal bevacizumab.
    Acta Ophthalmol Scand. 2007;85:526-33

  • Prokisch H, Hartig M, Hellinger R, Meitinger T, Rosenberg T.
    A population-based epidemiological and genetic study of X-linked retinitis pigmentosa.
    Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4012-8

  • Rosenberg T, Klie F, Garred P, Schwartz M.
    N965S is a common ABCA4 variant in Stargardt-related retinopathies in the Danish population.
    Mol Vis. 2007 Oct 17;13:1962-9

  • Szabo V, Kreienkamp HJ, Rosenberg T
    Gal A. p.Gln200Glu, a putative constitutively active mutant of rod alpha-transducin (GNAT1) in autosomal dominant congenital stationary night blindness.
    Hum Mutat. 2007 Jul;28(7):741-2

  • Tsang SH, Woodruff ML, Jun L, Mahajan V, Yamashita CK, Pedersen R, Lin CS, Goff SP, Rosenberg T, Larsen M, Farber DB, Nusinowitz S.
    Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness.
    Hum Mutat. 2007 Mar;28(3):243-54

  • Wang M, Munch IC, Hasler PW, Prünte C, Larsen M.
    Central serous chorioretinopathy.
    Acta Ophthalmol Scand. 2007 Jul 28. [Epub ahead of print]

  • Wang L, Surendran S, Michals-Matalon K, Bhatia G, Tanskley S, Koch R, Grady J, Tyring SK, Stevens RC, Guttler F, Matalon R.
    Mutations in the regulatory domain of phenylalanine hydroxylase and response to tetrahydrobiopterin.
    Genet Test. 2007 Summer;11(2):174-8


Andre publikationer

  • Dudjonsson T, Jensen TG & Skottman H. Stem cell research - from basic biology to therapeutic applications. In: Stem cell Research in the Nordic Countries. Science, Ethics, Public Debate and Law. Nordforsk Policy Briefs 2007-2. ISSN 1504-8640. pp 14-16.

  • von Troil H, Gudjonsson T, Jensen T & Uddenberg K. Stem cell research in the Nordic Countries. In: Stem cell Research in the Nordic Countries. Science, Ethics, Public Debate and Law. Nordforsk Policy Briefs 2007-2. ISSN 1504-8640. pp 17-20.

  • Arnason V, von Troil H, Sirnes T, Elster J, Jensen T, Welin S & Westerlund K. In: Stem cell Research in the Nordic Countries. Science, Ethics, Public Debate and Law. Nordforsk Policy Briefs 2007-2. ISSN 1504-8640. pp 40-45.


Kronikker/debatindlæg

  • Thomas G. Jensen & Peder Agger. Etisk Råds enighed ikke total. Kronik i Politiken 3. april 2007.

  • Thomas G. Jensen. Blandingsvæsener giver etiske problemer. Debatindlæg i Kristeligt Dagblad 30. oktober 2007.