Ahvenainen, T., Lehtonen, HJ., Lehtonen, R., Aittomäki, K., Baynam, G., Dommering C, C., Eng, C., Gruber, SB., Grönberg, H., Harvima, R., Herva, R., Hietala, M., Kujala, M., Kääriäinen, H.
, Sunde, L., Vierimaa, O., Pollard, PJ., Tomlinson, IP., Björck, E. ... Launonen, V. (2008).
Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification: detection of exonic deletion in a patient with leiomyomatosis and renal cell cancer. Cancer Genetics and Cytogenetics,
183, 83-8.
Tørring, N., Jølving, L. R., Petersen, O. B. B., Holmskov, A.
, Hertz, J. M. & Uldbjerg, N. (2008).
Praenatal diagnostik i Arhus og Viborg Amter efter implementering af første trimester-risikovurdering.
Ugeskrift for Laeger,
170(1), 50-4.
Tørring, N., Holmskov, A., Hertz, J. M., Uldbjerg, N., Petersen, O. B. & Jølving, L. R. (2008).
Prænataldiagnostik i Århus og Viborg Amter efter implementering af første trimester-risikovurdering.
Ugeskrift for Laeger,
170(1), 50-54.
Menon, R.
, Thorsen, P., Vogel, I., Jacobsson, B., Morgan, N.
, Jiang, L., Li, C., Williams, S. M. & Fortunato, S. J. (2008).
Racial disparity in amniotic fluid concentrations of tumor necrosis factor (TNF)-alpha and soluble TNF receptors in spontaneous preterm birth.
American Journal of Obstetrics and Gynecology,
198(5), 533.e1-10.
https://doi.org/10.1016/j.ajog.2007.11.025
Lautrup, C. K., Kjaergaard, S., Brøndum-Nielsen, K., Fagerberg, C.
, Hertz, J. M., Petersen, O. B., Jørgensen, M. W.
& Vogel, I. (2008).
Testing for 22q11 microdeletion in 146 fetuses with nuchal translucency above the 99th percentile and a normal karyotype.
Acta Obstetricia et Gynecologica Scandinavica,
87(11), 1252-5.
https://doi.org/10.1080/00016340802482994
Møller, R. S., Kübart, S., Hoeltzenbein, M., Heye, B.
, Vogel, I., Hansen, C. P., Menzel, C., Ullmann, R., Tommerup, N., Ropers, H.-H., Tümer, Z. & Kalscheuer, V. M. (2008).
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.
American Journal of Human Genetics,
82(5), 1165-70.
https://doi.org/10.1016/j.ajhg.2008.03.001
Lexner, M. O., Bardow, A.
, juncker, I., Jensen, L. G., Almer, L., Kreiborg, S.
& Hertz, J. M. (2008).
X-linked hypohidrotic ectodermal dysplasia. Genetic and dental findings in 67 Danish patients from 19 families.
Clinical Genetics,
74(3), 252-9.
https://doi.org/10.1111/j.1399-0004.2008.01037.x
Vorup-Jensen, T., Chi, L.
, Gjelstrup, L. C., Jensen, U. B., Jewett, C. A., Xie, C., Shimaoka, M., Linhardt, R. J. & Springer, T. A. (2007).
Binding between the integrin alphaXbeta2 (CD11c/CD18) and heparin.
Journal of Biological Chemistry,
282(42), 30869-77.
https://doi.org/10.1074/jbc.M706114200
Vogel, I., Goepfert, A. R.
, Thorsen, P., Skogstrand, K., Hougaard, D. M., Curry, A. H., Cliver, S. & Andrews, W. W. (2007).
Early second-trimester inflammatory markers and short cervical length and the risk of recurrent preterm birth.
Journal of Reproductive Immunology,
75(2), 133-40.
https://doi.org/10.1016/j.jri.2007.02.008
Curry, A. E.
, Vogel, I., Drews, C.
, Schendel, D., Skogstrand, K., Flanders, W. D., Hougaard, D.
, Olsen, J. & Thorsen, P. (2007).
Mid-pregnancy maternal plasma levels of interleukin 2, 6, and 12, tumor necrosis factor-alpha, interferon-gamma, and granulocyte-macrophage colony-stimulating factor and spontaneous preterm delivery.
Acta Obstetricia et Gynecologica Scandinavica,
86(9), 1103-10.
https://doi.org/10.1080/00016340701515423
Vogel, I., Thorsen, P., Jeune, B.
, Jacobsson, B., Ebbesen, N., Arpi, M., Bremmelgaard, A. & Møller, B. R. (2006).
Acquisition and elimination of bacterial vaginosis during pregnancy: a Danish population-based study.
Infectious Diseases in Obstetrics and Gynecology,
2006, Article 94646.
https://doi.org/10.1155/IDOG/2006/94646
Hjermind, L. E., Johannsen, L. G., Blau, N., Wevers, R. A., Lucking, C.-B.
, Hertz, J. M., Friberg, L., Regeur, L., Nielsen, J. E. & Sørensen, S. A. (2006).
Dopa-responsive dystonia and early-onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency? Movement Disorders,
21(5), 679-82.
https://doi.org/10.1002/mds.20773
Vogel, I., Goepfert, A. R.
, Møller, H. J., Cliver, S.
, Thorsen, P. & Andrews, W. W. (2006).
Early mid-trimester serum relaxin, soluble CD163, and cervical length in women at high risk for preterm delivery.
American Journal of Obstetrics and Gynecology,
195(1), 208-14.
https://doi.org/10.1016/j.ajog.2005.12.009
Menon, R., Velez, D. R.
, Thorsen, P., Vogel, I., Jacobsson, B., Williams, S. M. & Fortunato, S. J. (2006).
Ethnic differences in key candidate genes for spontaneous preterm birth: TNF-alpha and its receptors.
Human Heredity,
62(2), 107-18.
https://doi.org/10.1159/000096301
Severinsen, J. E., Bjarkam, C. R., Kiaer-Larsen, S.
, Olsen, I. M., Nielsen, M. M., Blechingberg, J., Nielsen, A. L., Holm, I. E., Foldager, L., Young, B. D., Muir, W. J., Blackwood, D. H. R.
, Corydon, T. J., Mors, O. & Børglum, A. D. (2006).
Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder.
Molecular Psychiatry,
11(12), 1126-38.
https://doi.org/10.1038/sj.mp.4001885
Hertz, J. M., Ostergaard, K., Juncker, I., Pedersen, S., Romstad, A., Güttler, F., Møller, L. B.
& Dupont, E. (2006).
Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease.
European Journal of Neurology,
13(4), 385-90.
https://doi.org/10.1111/j.1468-1331.2006.01249.x
Menon, R., Velez, D. R., Simhan, H., Ryckman, K.
, Jiang, L., Thorsen, P., Vogel, I., Jacobsson, B., Merialdi, M., Williams, S. M. & Fortunato, S. J. (2006).
Multilocus interactions at maternal tumor necrosis factor-alpha, tumor necrosis factor receptors, interleukin-6 and interleukin-6 receptor genes predict spontaneous preterm labor in European-American women.
American Journal of Obstetrics and Gynecology,
194(6), 1616-24.
https://doi.org/10.1016/j.ajog.2006.03.059
Johansen, C., Funding, A. T., Otkjaer, K., Kragballe, K., Jensen, U. B., Madsen, M., Binderup, L., Skak-Nielsen, T., Fjording, M. S.
& Iversen, L. (2006).
Protein expression of TNF-alpha in psoriatic skin is regulated at a posttranscriptional level by MAPK-activated protein kinase 2.
Journal of Immunology,
176(3), 1431-8.
Singh, R., Kølvraa, S., Bross, P., Jensen, U. B., Gregersen, N., Tan, Q.
, Knudsen, C. & Rattan, S. I. S. (2006).
Reduced heat shock response in human mononuclear cells during aging and its association with polymorphisms in HSP70 genes.
Cell Stress & Chaperones,
11(3), 208-215.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1576475/
Thorsen, P., Vogel, I., Molsted, K.
, Jacobsson, B., Arpi, R. M., Møller, B. L. & Jeune, B. (2006).
Risk factors for bacterial vaginosis in pregnancy: a population-based study on Danish women.
Acta Obstetricia et Gynecologica Scandinavica,
85(8), 906-11.
https://doi.org/10.1080/00016340500432655
Langhoff-Roos, J.
, Kesmodel, U., Jacobsson, B., Rasmussen, S.
& Vogel, I. (2006).
Spontaneous preterm delivery in primiparous women at low risk in Denmark: population based study.
B M J,
332(7547), 937-9.
https://doi.org/10.1136/bmj.38751.524132.2F
Vogel, I., Thorsen, P., Hogan, V. K., Schieve, L. A.
, Jacobsson, B. & Ferre, C. D. (2006).
The joint effect of vaginal Ureaplasma urealyticum and bacterial vaginosis on adverse pregnancy outcomes.
Acta Obstetricia et Gynecologica Scandinavica,
85(7), 778-85.
https://doi.org/10.1080/00016340500442423
Bojesen, A., Kristensen, K., Birkebaek, N. H., Fedder, J., Mosekilde, L., Bennett, E. P.
, Laurberg, P., Frystyk, J., Flyvbjerg, A., Christiansen, J. S. & Gravholt, C. H. (2006).
The metabolic syndrome is frequent in Klinefelter's syndrome and is associated with abdominal obesity and hypogonadism.
Diabetes Care,
29(7), 1591-8.
https://doi.org/10.2337/dc06-0145
Rockenbauer, E., Petersen, K., Vogel, U.
, Bolund, L., Kølvraa, S., Nielsen, K. V. & Nexø, B. A. (2005).
SNP genotyping using microsphere-linked PNA and flow cytometric detection. Cytometry. Part A,
64A(2), 80-86.
https://doi.org/10.1002/cyto.a.20123
Bugge, M., deLozier-Blanchet, C., Bak, M., Brandt, C. A.
, Hertz, J. M., Nielsen, J. B., Duprez, L. & Petersen, M. B. (2005).
Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases.
American Journal of Medical Genetics. Part A,
132A(3), 310-3.
https://doi.org/10.1002/ajmg.a.30474
Hertz, J. M., Sivertsen, B., Silahtaroglu, A., Bugge, M., Kalscheuer, V.
, Weber, A., Wirth, J., Ropers, H.-H., Tommerup, N. & Tümer, Z. (2004).
Early onset, non-progressive, mild cerebellar ataxia co-segregating with a familial balanced translocation t(8;20)(p22;q13).
Journal of Medical Genetics,
41(3), e25.
Sorensen, C. B., Andresen, B. S., Jensen, U. B., Jensen, T. G., Jensen, P. K. A., Gregersen, N. & Bolund, L. (2004).
Erratum: Functional testing of keratin 14 mutant proteins associated with the three major types of epidermolysis bullosa simplex (Experimental Dermatology (2003) vol. 12 (472-479)).
Experimental Dermatology,
13(7).
Persson, U.
, Hertz, J. M., Carlsson, M., Hellmark, T.
, juncker, I., Wieslander, J. & Segelmark, M. (2004).
Patients with Goodpasture's disease have two normal COL4A3 alleles encoding the NC1 domain of the type IV collagen alpha 3 chain.
Nephrology, Dialysis, Transplantation,
19(8), 2030-5.
https://doi.org/10.1093/ndt/gfh355
Petersen, K., Vogel, U., Rockenbauer, E.
, Nielsen, K. V., Kølvraa, S., Bolund, L. & Nexø, B. A. (2004).
Short PNA molecular beacons for real-time PCR allelic discrimination of single nucleotide polymorphisms.
Molecular and Cellular Probes,
18(2), 117-122.
https://doi.org/10.1016/j.mcp.2003.10.003
Triel, C., Vestergaard, M. E.
, Bolund, L., Jensen, T. G., Jensen, U. B. & Jensen, U. B. (2004).
Side population cells in human and mouse epidermis lack stem cell characteristics.
Experimental Cell Research,
295(1), 79-90.
https://doi.org/10.1016/j.yexcr.2003.11.032
Miraglia Del Giudice, E., Coppola, G., Bellini, G., Ledaal, P.
, Hertz, J. M. & Pascotto, A. (2003).
A novel mutation (R218Q) at the boundary between the N-terminal and the first transmembrane domain of the glycine receptor in a case of sporadic hyperekplexia.
Journal of Medical Genetics,
40(5), e71.
Westergaard, M., Henningsen, J.
, Johansen, C., Rasmussen, S.
, Svendsen, M. L., Jensen, U. B., Schrøder, H. D., Staels, B.
, Iversen, L., Bolund, L., Kragballe, K. & Kristiansen, K. (2003).
Expression and localization of peroxisome proliferator-activated receptors and nuclear factor kappaB in normal and lesional psoriatic skin.
Journal of Investigative Dermatology,
121(5), 1104-17.
https://doi.org/10.1046/j.1523-1747.2003.12536.x
Braun, K. M., Niemann, C.
, Jensen, U. B., Sundberg, J. P., Silva-Vargas, V. & Watt, F. M. (2003).
Manipulation of stem cell proliferation and lineage commitment: visualisation of label-retaining cells in wholemounts of mouse epidermis.
Development,
130(21), 5241-55.
https://doi.org/10.1242/dev.00703
Rollman, O.
, Jensen, U. B., Ostman, A.
, Bolund, L., Gústafsdóttir, S. M.
& Jensen, T. G. (2003).
Platelet derived growth factor (PDGF) responsive epidermis formed from human keratinocytes transduced with the PDGF beta receptor gene.
Journal of Investigative Dermatology,
120(5), 742-9.
https://doi.org/10.1046/j.1523-1747.2003.12129.x
Legg, J.
, Jensen, U. B., Broad, S., Leigh, I. & Watt, F. M. (2003).
Role of melanoma chondroitin sulphate proteoglycan in patterning stem cells in human interfollicular epidermis.
Development,
130(24), 6049-63.
https://doi.org/10.1242/dev.00837
Puig-Kröger, A., Sanchez-Elsner, T., Ruiz, N., Andreu, E. J., Prosper, F.
, Jensen, U. B., Gil, J., Erickson, P., Drabkin, H., Groner, Y. & Corbi, A. L. (2003).
RUNX/AML and C/EBP factors regulate CD11a integrin expression in myeloid cells through overlapping regulatory elements.
Blood,
102(9), 3252-61.
https://doi.org/10.1182/blood-2003-02-0618
Jais, J. P., Knebelmann, B., Giatras, I., De Marchi, M., Rizzoni, G., Renieri, A., Weber, M., Gross, O., Netzer, K.-O., Flinter, F., Pirson, Y., Dahan, K., Wieslander, J., Persson, U., Tryggvason, K., Martin, P.
, Hertz, J. M., Schröder, C., Sanak, M. ... Gubler, M. C. (2003).
X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study.
Journal of the American Society of Nephrology,
14(10), 2603-10.