Lars Allan Larsen

Lars Allan Larsen

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    1. Published

      Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

      Audain, E., Wilsdon, A., Breckpot, J., Izarzugaza, J. M. G., Fitzgerald, T. W., Kahlert, A. K., Sifrim, A., Wünnemann, F., Perez-Riverol, Y., Abdul-Khaliq, H., Bak, M., Bassett, A. S., Benson, W. D., Berger, F., Daehnert, I., Devriendt, K., Dittrich, S., Daubeney, P. E. F., Garg, V., Hackmann, K. & 30 others, Hoff, K., Hofmann, P., Dombrowsky, G., Pickardt, T., Bauer, U., Keavney, B. D., Klaassen, S., Kramer, H. H., Marshall, C. R., Milewicz, D. M., Lemaire, S., Coselli, J. S., Mitchell, M. E., Tomita-Mitchell, A., Prakash, S. K., Stamm, K., Stewart, A. F. R., Silversides, C. K., Siebert, R., Stiller, B., Rosenfeld, J. A., Vater, I., Postma, A. V., Caliebe, A., Brook, J. D., Andelfinger, G., Hurles, M. E., Thienpont, B., Larsen, Lars Allan & Hitz, M. P., 2021, In: PLOS Genetics. 17, 7, e1009679.

      Research output: Contribution to journal › Journal article › Research › peer-review

    2. Published

      Kromosomforandringer ved medfødt hjertemisdannelse

      Larsen, Lars Allan, 17 Jan 2011, In: Ugeskrift for Laeger. 173, 3, p. 194-6 3 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. Published

      MCPH1: A Novel Case Report and a Review of the Literature

      Caraffi, S. G., Pollazzon, M., Farooq, M., Fatima, A., Larsen, Lars Allan, Zuntini, R., Napoli, M. & Garavelli, L., 2022, In: Genes. 13, 4, 634.

      Research output: Contribution to journal › Review › Research › peer-review

    4. Published

      Mapping of 5q35 chromosomal rearrangements within a genomically unstable region

      Buysse, K., Crepel, A., Menten, B., Pattyn, F., Antonacci, F., Veltman, J. A., Larsen, Lars Allan, Tümer, Asuman Zeynep, de Klein, A., van de Laar, I., Devriendt, K., Mortier, G. & Speleman, F., 2008, In: Journal of Medical Genetics. 45, 10, p. 672-678 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    5. Published

      Model system identification of novel congenital heart disease gene candidates: focus on RPL13

      Schroeder, A. M., Allahyari, M., Vogler, G., Missinato, M. A., Nielsen, T., Yu, M. S., Theis, J. L., Larsen, Lars Allan, Goyal, P., Rosenfeld, J. A., Nelson, T. J., Olson, T. M., Colas, A. R., Grossfeld, P. & Bodmer, R., 2019, In: Human Molecular Genetics. 28, 23, p. 3954-3969 16 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    6. Published

      Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24

      Hilhorst-Hofstee, Y., Tümer, Asuman Zeynep, Born, P., Knijnenburg, J., Hansson, K., Yatawara, V., Steensberg, J., Ullmann, R., Arkesteijn, G., Tommerup, Niels & Larsen, Lars Allan, 2009, In: American Journal of Medical Genetics. Part A. 149A, 8, p. 1830-3 3 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    7. Published

      Multiplex Ligation-Dependent Probe Amplification Technique for Copy Number Analysis on Small Amounts of DNA Material

      Sørensen, K., Andersen, P., Larsen, Lars Allan, Schwartz, M., Schouten, J. & Nygren, A., 2008, In: Analytical Chemistry. 80, p. 9363-9368 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    8. Published

      Mutation burden in patients with small unrepaired atrial septal defects☆

      Nielsen, A. K. M., Nyboe, C., Ovesen, A. S. L., Udholm, S., Larsen, M. M. M., Hjortdal, Vibeke Elisabeth & Larsen, Lars Allan, 2021, In: International Journal of Cardiology Congenital Heart Disease. 4, 6 p., 100164.

      Research output: Contribution to journal › Journal article › Research › peer-review

    9. Published

      Mutation of the planar cell polarity gene VANGL1 in adolescent idiopathic scoliosis

      Andersen, M. R., Farooq, M., Rasmussen, K. K., Kjaer, K. W., Simony, A., Christensen, Søren Tvorup & Larsen, Lars Allan, 2017, In: Spine. 42, 12, p. E702–E707 6 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    10. Published

      Mutations in the HERG ion channel: A novel link between long QT syndrome and sudden death syndrome

      Christiansen, M., Tønder, N., Larsen, Lars Allan, Andersen, P. S., Simonsen, H. B., Øyen, N., Kanters, J. K., Jacobsen, J. R., Fosdal, I., Wettrell, G. & Kjeldsen, K., 2005, In: American Journal of Cardiology. Vol. 95, p. 433-434

      Research output: Contribution to journal › Journal article › Research › peer-review

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