Zhou, Y., Al-Saaidi, R. A., Guerra, P. F., Freude, K. K.
, Olsen, R. K. J., Jensen, U. B., Gregersen, N., Hyttel, P.
, Bolund, L., Aagaard, L., Bross, P. & Luo, Y. (2017).
Mitochondrial Spare Respiratory Capacity Is Negatively Correlated With Nuclear Reprogramming Efficiency.
Stem Cells and Development,
26(3), 166-176.
https://doi.org/10.1089/scd.2016.0162
Zankl, A., Duncan, E. L., Leo, P. J., Clark, G. R., Glazov, E. A., Addor, M.-C.
, Herlin, T., Kim, C. A., Leheup, B. P., McGill, J., McTaggart, S., Mittas, S., Mitchell, A. L., Mortier, G. R., Robertson, S. P., Schroeder, M., Terhal, P. & Brown, M. A. (2012).
Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB.
American Journal of Human Genetics,
90(3), 494-501.
https://doi.org/10.1016/j.ajhg.2012.01.003
Zangenberg, M., Grubach, L.
, Aggerholm, A., Silkjaer, T., Juhl-Christensen, C., Nyvold, C. G.
, Kjeldsen, E., Ommen, H. B. & Hokland, P. (2009).
The combined expression of HOXA4 and MEIS1 is an independent prognostic factor in patients with AML.
European Journal of Haematology,
83(5), 439-48.
https://doi.org/10.1111/j.1600-0609.2009.01309.x
Woo, S.-H., Stumpfova, M.
, Jensen, U. B., Lumpkin, E. A. & Owens, D. M. (2010).
Identification of epidermal progenitors for the Merkel cell lineage.
Development,
137(23), 3965-71.
https://doi.org/10.1242/dev.055970
Whitworth, J., Skytte, A.-B.
, Sunde, L., Lim, D. H., Arends, M. J., Happerfield, L., Frayling, I. M., van Minkelen, R., Woodward, E. R., Tischkowitz, M. D. & Maher, E. R. (2016).
Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review.
JAMA oncology,
2(3), 373-379.
https://doi.org/10.1001/jamaoncol.2015.4771
Whitworth, J., Smith, P. S., Martin, J.-E., West, H., Luchetti, A., Rodger, F., Clark, G., Carss, K., Stephens, J., Stirrups, K., Penkett, C., Mapeta, R., Ashford, S., Megy, K., Shakeel, H., Ahmed, M., Adlard, J., Barwell, J., Brewer, C. ... NIHR BioResource Rare Diseases Consortium (2018).
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes.
American Journal of Human Genetics,
103(1), 3-18.
https://doi.org/10.1016/j.ajhg.2018.04.013
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
Westergaard, M., Henningsen, J.
, Svendsen, M. L., Johansen, C., Jensen, U. B., Schrøder, H. D., Kratchmarova - Blagoeva, I. H., Berge, R. K.
, Iversen, L., Bolund, L., Kragballe, K. & Kristiansen, K. (2001).
Modulation of keratinocyte gene expression and differentiation by PPAR-selective ligands and tetradecylthioacetic acid.
Journal of Investigative Dermatology,
116(5), 702-12.
https://doi.org/10.1046/j.0022-202x.2001.doc.x
Wei, C. S.
, Becher, N., Friis, J. B., Ott, P., Vogel, I. & Grønbæk, H. (2020).
New tight junction protein 2 variant causing progressive familial intrahepatic cholestasis type 4 in adults: A case report.
World Journal of Gastroenterology,
26(5), 550-561.
https://doi.org/10.3748/wjg.v26.i5.550
Wallentin, M., Skakkebæk, A., Bojesen, A., Fedder, J., Peter, L.
, Østergaard, J. R., Hertz, J. M., Pedersen, A. D.
& Gravholt, C. H. (2016).
Klinefelter syndrome has increased brain responses to auditory stimuli and motor output, but not to visual stimuli or Stroop adaptation.
NeuroImage: Clinical,
11, 239-251.
https://doi.org/10.1016/j.nicl.2016.02.002
Walbum, P.
, Andreasen, L., Geilswijk, M., Niemann, I. & Sunde, L. (2024).
Aneuploidy is frequent in heterozygous diploid and triploid hydatidiform moles.
Scientific Reports,
14, Article 6876.
https://doi.org/10.1038/s41598-024-57465-5
Wadt, K. A. W., Aoude, L. G., Krogh, L.
, Sunde, L., Bojesen, A., Grønskov, K., Wartacz, N., Ek, J., Tolstrup-Andersen, M., Klarskov-Andersen, M., Borg, Å., Heegaard, S., Kiilgaard, J. F., Hansen, T. V. O., Klein, K., Jönsson, G., Drzewiecki, K. T., Dunø, M., Hayward, N. K. & Gerdes, A.-M. (2015).
Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.
PLOS ONE,
10(3), e0122662.
https://doi.org/10.1371/journal.pone.0122662
Wadt, K. A. W., Aoude, L. G., Johansson, P., Solinas, A., Pritchard, A., Crainic, O., Andersen, M. T., Kiilgaard, J. F., Heegaard, S.
, Sunde, L., Federspiel, B., Madore, J., Thompson, J. F., McCarthy, S. W., Goodwin, A., Tsao, H., Jönsson, G., Busam, K., Gupta, R. ... Hayward, N. K. (2015).
A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma.
Clinical Genetics,
88(3), 267-72.
https://doi.org/10.1111/cge.12501
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
Vorup-Jensen, T., Jensen, U. B., Liu, H., Kawasaki, T., Uemura, K.
, Thiel, S., Dagnaes-Hansen, F.
& Jensen, T. G. (2001).
Tail-vein injection of mannan-binding lectin DNA leads to high expression levels of multimeric protein in liver.
Molecular Therapy,
3(6), 867-74.
https://doi.org/10.1006/mthe.2001.0335
Vorup-Jensen, T., Sørensen, E. S., Jensen, U. B., Schwaeble, W., Kawasaki, T., Ma, Y., Uemura, K., Wakamiya, N., Suzuki, Y.
, Jensen, T. G., Takahashi, K., Ezekowitz, R. A.
, Thiel, S. & Jensenius, J. C. (2001).
Recombinant expression of human mannan-binding lectin.
International Immunopharmacology,
1(4), 677-87.
Vogel, I., Glavind-Kristensen, M.
, Salvig, J. D., Secher, N. J., Thorsen, P.
, Sandager, K. P. & Uldbjerg, N. (2001).
Preterm delivery predicted by S-relaxin. In
Ikke angivet (pp. 518-4). Kluver Academic Press.
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
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
Vogel, I., Lyngbye, T., Nielsen, A., Pedersen, S. & Hertz, J. M. (2009).
Pallister-Killian syndrome in a girl with mild developmental delay and mosaicism for hexasomy 12p.
American Journal of Medical Genetics. Part A,
149A(3), 510-4.
https://doi.org/10.1002/ajmg.a.32681
Vogel, I., Hollegaard, M. V., Hougaard, D. M., Thorsen, P.
& Grove, J. (2009).
Polymorphisms in the promoter region of relaxin-2 and preterm birth: involvement of relaxin in the etiology of preterm birth.
In Vivo,
23(6), 1005-9.
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
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
Vogel, I., Rasmussen, M.
, Petersen, O. B., Cormier-Daire, V. & Pedersen, S. (2011).
Prenatal diagnostics of a DYNC2H1 deletion and a point mutation as a cause of Asphyxiating Thoracic Dysplasia. Abstract from 7th International DECIPHER Symposium , Hinxton, United Kingdom.
Vogel, I., Petersen, O. B., Christensen, R., Hyett, J.
, Lou, S. & Vestergaard, E. M. (2018).
Chromosomal microarray as a primary diagnostic genomic tool for pregnancies defined as being at increased risk within a population based combined first-trimester screening program.
Ultrasound in Obstetrics & Gynecology,
51(4), 480-486.
https://doi.org/10.1002/uog.17548
Vogel, I., Ott, P., Lildballe, D., Hamilton-Dutoit, S., Vilstrup, H. & Grønbæk, H. (2017).
Isolated congenital hepatic fibrosis associated with TMEM67 mutations: report of a new genotype-phenotype relationship.
Clinical Case Reports,
5(7), 1098-1102.
https://doi.org/10.1002/ccr3.981
Vogel, I., Fagerberg, C. R., Bache, I., Ekelund, C., Hoseth, E., Nørgaard, L. N., Sperling, L., Skibsted, L., Tabor, A.
& Petersen, O. B. (2018).
Prænatal kromosom mikroarray analyse (CMA). DFMS Guideline
http://www.dfms.dk/images/Guidelines/kromosom_mikro_array-2018-Final-rundsendt_090118.pdf
Vogel, I., Tabor, A., Ekelund, C.
, Lou, S., Hyett, J.
, Petersen, O. B. & The Danish Fetal Medicine Study Group, and the Danish Cytogenetic Study Group (2019).
Population-Based Screening for Trisomies and Atypical Chromosomal Abnormalities: Improving Efficacy using the Combined First Trimester Screening Algorithm as well as Individual Risk Parameters.
Fetal Diagnosis and Therapy,
45(6), 424-429.
https://doi.org/10.1159/000492152
Vogel, I., Vestergaard, E. M., Lildballe, D. L., Christensen, R., Hoseth, G. E., Petersen, A. C., Bogaard, P. & Sørensen, A. N. (2020).
Placental mosaicism in the era of chromosomal microarrays.
European Journal of Medical Genetics,
63(4), Article 103778.
https://doi.org/10.1016/j.ejmg.2019.103778
Viuff, M., Skakkebæk, A., Nielsen, M. M., Chang, S.
& Gravholt, C. H. (2019).
Epigenetics and genomics in Turner syndrome.
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics,
181(1), 125-132.
https://doi.org/10.1002/ajmg.c.31683
Viuff, M. H., Berglund, A., Juul, S., Andersen, N. H.
, Stochholm, K. & Gravholt, C. H. (2020).
Sex hormone replacement therapy in Turner Syndrome - impact on morbidity and mortality.
The Journal of clinical endocrinology and metabolism,
105(2), Article dgz039.
https://doi.org/10.1210/clinem/dgz039
Viuff, M. H., Stochholm, K., Lin, A.
, Berglund, A., Juul, S. & Gravholt, C. H. (2021).
Cancer occurrence in Turner syndrome and the effect of sex hormone substitution therapy.
European Journal of Endocrinology,
184(1), 79-88.
https://doi.org/10.1530/EJE-20-0702
Viuff, M. H., Stochholm, K., Grønbaek, H., Berglund, A., Juul, S. & Gravholt, C. H. (2021).
Increased occurrence of liver and gastrointestinal diseases and anaemia in women with Turner syndrome - a nationwide cohort study.
Alimentary Pharmacology and Therapeutics,
53(7), 821-829.
https://doi.org/10.1111/apt.16277
Viuff, M., Skakkebæk, A., Johannsen, E. B., Chang, S.
, Pedersen, S. B., Lauritsen, K. M.
, Pedersen, M. G. B., Trolle, C., Just, J. & Gravholt, C. H. (2023).
X chromosome dosage and the genetic impact across human tissues.
Genome Medicine,
15(1), Article 21.
https://doi.org/10.1186/s13073-023-01169-4
Vigorito, E., Kuchenbaecker, K. B., Beesley, J., Adlard, J., Agnarsson, B. A., Andrulis, I. L., Arun, B. K., Barjhoux, L., Belotti, M., Benitez, J., Berger, A.
, Bojesen, A., Bonanni, B., Brewer, C., Caldes, T., Caligo, M. A., Campbell, I., Chan, S. B., Claes, K. B. M. ... Antoniou, A. C. (2016).
Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
PLOS ONE,
11(7), e0158801. Article e0158801.
https://doi.org/10.1371/journal.pone.0158801
Vestergaard, E. M., Singh, R., Schelde, P., Hatt, L., Ravn, K.
, Christensen, R., Lildballe, D. L., Petersen, O. B., Uldbjerg, N. & Vogel, I. (2017).
On the road to replacing invasive testing with cell-based NIPT: five clinical cases with aneuploidies, microduplication, unbalanced structural rearrangement or mosaicism.
Prenatal Diagnosis,
37(11), 1120-1124.
https://doi.org/10.1002/pd.5150
van der Sluijs, P. J., Joosten, M., Alby, C., Attié-Bitach, T., Gilmore, K., Dubourg, C., Fradin, M., Wang, T., Kurtz-Nelson, E. C., Ahlers, K. P., Arts, P., Barnett, C. P., Ashfaq, M., Baban, A., van den Born, M., Borrie, S., Busa, T., Byrne, A., Carriero, M. ... Santen, G. W. E. (2022).
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.
Genetics in Medicine,
24(8), 1753-1760.
https://doi.org/10.1016/j.gim.2022.04.010
Van De Looij, A., Singh, R., Hatt, L., Ravn, K.
, Jeppesen, L. D., Nicolaisen, B. H., Kølvraa, M.
, Vogel, I., Schelde, P.
& Uldbjerg, N. (2020).
Do fetal extravillous trophoblasts circulate in maternal blood postpartum? Acta Obstetricia et Gynecologica Scandinavica,
99(6), 751-756.
https://doi.org/10.1111/aogs.13880