Evidence of gene–gene interaction in hidradenitis suppurativa: a nationwide registry study of Danish twins
Kjærsgaard Andersen, R., Clemmensen, S.B., Larsen, L.A., Hjelmborg, J.v.B., Ødum, N., Jemec, G.B.E., Christensen, K.
Published in British journal of dermatology (1951) (01.01.2022)
Published in British journal of dermatology (1951) (01.01.2022)
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Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twins
Andersen, P. S., Larsen, L. A., Fowler, V. G., Stegger, M., Skov, R. L., Christensen, K.
Published in European journal of clinical microbiology & infectious diseases (01.10.2013)
Published in European journal of clinical microbiology & infectious diseases (01.10.2013)
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High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease
Erdogan, F, Larsen, L A, Zhang, L, Tümer, Z, Tommerup, N, Chen, W, Jacobsen, J R, Schubert, M, Jurkatis, J, Tzschach, A, Ropers, H-H, Ullmann, R
Published in Journal of medical genetics (01.11.2008)
Published in Journal of medical genetics (01.11.2008)
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Elastic Properties of Nonstoichiometric Reacted PDMS Networks
Larsen, A. L, Hansen, K, Sommer-Larsen, P, Hassager, O, Bach, A, Ndoni, S, Jørgensen, M
Published in Macromolecules (30.12.2003)
Published in Macromolecules (30.12.2003)
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Editor's Choice – High Heritability of Liability to Abdominal Aortic Aneurysms: A Population Based Twin Study
Joergensen, T.M.M., Christensen, K., Lindholt, J.S., Larsen, L.A., Green, A., Houlind, K.
Published in European journal of vascular and endovascular surgery (01.07.2016)
Published in European journal of vascular and endovascular surgery (01.07.2016)
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Mapping of 5q35 chromosomal rearrangements within a genomically unstable region
Buysse, K, Crepel, A, Menten, B, Pattyn, F, Antonacci, F, Veltman, J A, Larsen, L A, Tümer, Z, de Klein, A, van de Laar, I, Devriendt, K, Mortier, G, Speleman, F
Published in Journal of medical genetics (01.10.2008)
Published in Journal of medical genetics (01.10.2008)
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Higher resting-state activity in reward-related brain circuits in obese versus normal-weight females independent of food intake
Hogenkamp, P S, Zhou, W, Dahlberg, L S, Stark, J, Larsen, A L, Olivo, G, Wiemerslage, L, Larsson, E-M, Sundbom, M, Benedict, C, Schiöth, H B
Published in International Journal of Obesity (01.11.2016)
Published in International Journal of Obesity (01.11.2016)
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The E3 ubiquitin ligase SMURF1 regulates cell-fate specification and outflow tract septation during mammalian heart development
Koefoed, K, Skat-Rørdam, J, Andersen, P, Warzecha, C B, Pye, M, Andersen, T A, Ajbro, K D, Bendsen, E, Narimatsu, M, Vilhardt, F, Pedersen, L B, Wrana, J L, Anderson, R H, Møllgård, K, Christensen, S T, Larsen, L A
Published in Scientific reports (22.06.2018)
Published in Scientific reports (22.06.2018)
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Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome
Boonen, S.E., Stahl, D., Kreiborg, S., Rosenberg, T., Kalscheuer, V., Larsen, L.A., Tommerup, N., Brøndum‐Nielsen, K., Tümer, Z.
Published in American journal of medical genetics. Part A (30.01.2005)
Published in American journal of medical genetics. Part A (30.01.2005)
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Fine mapping of a de novo interstitial 10q22–q23 duplication in a patient with congenital heart disease and microcephaly
Erdogan, F, Belloso, J.M, Gabau, E, Ajbro, K.D, Guitart, M, Ropers, H.H, Tommerup, N, Ullmann, R, Tümer, Z, Larsen, L.A
Published in European journal of medical genetics (01.01.2008)
Published in European journal of medical genetics (01.01.2008)
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Genome-wide Gene Expression Profiling of SCID Mice with T-cell-mediated Colitis
Brudzewsky, D, Pedersen, A.E, Claesson, M.H, Gad, M, Kristensen, N.N, Lage, K, Jensen, T, Tommerup, N, Larsen, L.A, Knudsen, S, Tümer, Z
Published in Scandinavian journal of immunology (01.05.2009)
Published in Scandinavian journal of immunology (01.05.2009)
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A DNA methylation site within the KLF13 gene is associated with orexigenic processes based on neural responses and ghrelin levels
Wiemerslage, L, Islam, R, van der Kamp, C, Cao, H, Olivo, G, Ence-Eriksson, F, Castillo, S, Larsen, A L, Bandstein, M, Dahlberg, L S, Perland, E, Gustavsson, V, Nilsson, J, Vogel, H, Schürmann, A, Larsson, E-M, Rask-Andersen, M, Benedict, C, Schiöth, H B
Published in International Journal of Obesity (01.06.2017)
Published in International Journal of Obesity (01.06.2017)
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Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen
TYSON, Jessica, TRANEBJAERG, Lisbeth, PEMBREY, Marcus E, MALCOLM, Sue, BITNER-GLINDZICZ, Maria, MCENTAGART, Meriel, LARSEN, Lars A, CHRISTIANSEN, Michael, WHITEFORD, Margo L, BATHEN, Jørn, ASLAKSEN, Bjørn, SØRLAND, Svein Jan, LUND, Ole
Published in Human genetics (01.11.2000)
Published in Human genetics (01.11.2000)
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Eponymous Jacobsen syndrome: Mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome
Tümer, Z., Henriksen, A.M., Bache, I., Brixen, K., Kalschauer, V., Illum, N., Rasmussen, K., Larsen, L.A., Tommerup, N.
Published in American journal of medical genetics. Part A (15.06.2005)
Published in American journal of medical genetics. Part A (15.06.2005)
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A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome
Larsen, Lars Allan, Andersen, Paal Skytt, Kanters, Jørgen K, Jacobsen, Joes Ramsøe, Vuust, Jens, Christiansen, Michael
Published in Clinica chimica acta (01.02.1999)
Published in Clinica chimica acta (01.02.1999)
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Conference Proceeding
High throughput mutation screening by automated capillary electrophoresis
Larsen, L A, Christiansen, M, Vuust, J, Andersen, P S
Published in Combinatorial chemistry & high throughput screening (01.10.2000)
Published in Combinatorial chemistry & high throughput screening (01.10.2000)
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