Lars Allan Larsen
Professor
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Familial co-occurrence of congenital heart defects follows distinct patterns
Ellesøe, S. G., Workman, C. T., Bouvagnet, P., Loffredo, C. A., McBride, K. L., Hinton, R. B., van Engelen, K., Gertsen, E. C., Mulder, B. J. M., Postma, A. V., Anderson, R. H., Hjortdal, V. E., Brunak, Søren & Larsen, Lars Allan, Mar 2018, In: European Heart Journal. 39, 12, p. 1015–1022Research output: Contribution to journal › Journal article › Research › peer-review
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Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature
Ellesøe, S. G., Johansen, M. M., Bjerre, J. V., Hjortdal, V. E., Brunak, Søren & Larsen, Lars Allan, 1 May 2016, In: Congenital Heart Disease. 11, 3, p. 283–290 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Expression analyses of human cleft palate tissue suggest a role for osteopontin and immune related factors in palatal development
Jakobsen, L. P., Borup, R., Vestergaard, J., Larsen, Lars Allan, Lage, K., Maroun, L. L., Kjær, Inger, Niemann, C. U., Andersen, M., Knudsen, M. A., Møllgård, Kjeld & Tommerup, Niels, 2009, In: Experimental & Molecular Medicine. 41, 2, p. 77-85 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Evaluation of two methods for generating cRNA for microarray experiments from nanogram amounts of total RNA.
Bak, M., Conley, L., Hedegaard, J., Larsen, Lars Allan, Sørensen, P., Bendixen, C. & Tommerup, Niels, 2006, In: Analytical Biochemistry. 358, 1, p. 111-9 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Does KCNE5 play a role in long QT syndrome?
Hofman-Bang, J., Jespersen, Thomas, Grunnet, Morten, Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Kjeldsen, K. & Christiansen, M., 2004, In: Clinica Chimica Acta. 345, 1-2, p. 49-53 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Dissecting spatio-temporal protein networks driving human heart development and related disorders
Hansen, K. L., Møllgård, K., Greenway, S., Wakimoto, H., Gorham, J. M., Workman, C. T., Bendsen, E., Hansen, N. T., Rigina, O., Roque, F. S., Wiese, C., Christoffels, V. M., Roberts, A. E., Smoot, L. B., Pu, W. T., Donahoe, P. K., Tommerup, N., Brunak, S., Seidman, C. E., Seidman, J. G. & 1 others, , 2010, In: Molecular Systems Biology. 6, p. 381Research output: Contribution to journal › Journal article › Research › peer-review
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Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives
Andersen, P. S., Havndrup, O., Hougs, L., Sørensen, K. M., Jensen, M., Larsen, Lars Allan, Hedley, P., Bie Thomsen, A. R., Moolman-Smook, J., Christiansen, M. & Bundgård, Henning, 2008, In: Human Mutation. 30, 3, p. 363-370 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot samples
Sørensen, K. M., Agergaard, P., Olesen, C., Andersen, P. S., Larsen, Lars Allan, Ostergaard, J. R., Schouten, J. P. & Christiansen, M., 2010, In: Journal of Molecular Diagnostics. 12, 2, p. 147-51 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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, Lars Allan, Tommerup, Niels & Brøndum-Nielsen, K., 2005, In: American Journal of Medical Genetics. Part A. Vol. 132, p. 324-328Research output: Contribution to journal › Journal article › Research › peer-review
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Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome
Boonen, S. E., Stahl, D., Kreiborg, Sven, Rosenberg, T., Kalscheuer, V., Larsen, Lars Allan, Tommerup, Niels, Brøndum-Nielsen, K. & Tümer, Asuman Zeynep, 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 132A, p. 324-328Research output: Contribution to journal › Journal article › Research › peer-review
ID: 2949
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281
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CEP128 Localizes to the Subdistal Appendages of the Mother Centriole and Regulates TGF-β/BMP Signaling at the Primary Cilium
Research output: Contribution to journal › Journal article › Research › peer-review
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216
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TGF-β Signaling Is Associated with Endocytosis at the Pocket Region of the Primary Cilium
Research output: Contribution to journal › Journal article › Research › peer-review
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198
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Challenges for the sustainability of university-run biobanks
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Published