Lars Allan Larsen

Lars Allan Larsen

Professor

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    1 - 25 out of 83Page size: 25
    1. 2024
    2. Published

      TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant

      Møller Nielsen, A. K., Dehn, A. M., Hjortdal, Vibeke Elisabeth & Larsen, Lars Allan, 2024, In: European Journal of Medical Genetics. 68, 6 p., 104920.

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

    3. Published

      Pericardial delta like non-canonical NOTCH ligand 1 (Dlk1) augments fibrosis in the heart through epithelial to mesenchymal transition

      Jensen, C. H., Johnsen, R. H., Eskildsen, T., Baun, C., Ellman, D. G., Fang, S., Bak, S. T., Hvidsten, S., Larsen, Lars Allan, Rosager, A. M., Riber, L. P., Schneider, M., De Mey, J., Thomassen, Mads, Burton, M., Uchida, S., Laborda, J. & Andersen, D. C., 2024, In: Clinical and Translational Medicine. 14, 2, 18 p., e1565.

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

    4. 2023
    5. Published

      The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvement

      Munch, Tina Nørgaard, Hedley, P. L., Hagen, C. M., Baekvad-Hansen, M., Geller, F., Bybjerg-Grauholm, J., Nordentoft, Merete, Borglum, A. D., Werge, Thomas, Melbye, M., Hougaard, D. M., Larsen, Lars Allan, Christensen, Søren Tvorup & Christiansen, M., 2023, In: Brain Communications. 5, 1, 14 p., fcad004.

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

    6. 2022
    7. Published

      Comparison of Outcome in Patients With Familial Versus Spontaneous Atrial Septal Defect

      Nielsen, A. K. M., Ellesøe, S. G., Larsen, Lars Allan, Hjortdal, Vibeke Elisabeth & Nyboe, C., 2022, In: The American Journal of Cardiology. 173, p. 128-131

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

    8. 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

    9. 2021
    10. 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

    11. 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

    12. 2020
    13. Published

      RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

      Farooq, M., Lindbæk, L., Krogh, N., Doganli, C., Keller, C., Mönnich, M., Gonçalves, A. B., Sakthivel, S., Mang, Y., Fatima, A., Andersen, V. S., Hussain, M. S., Eiberg, H., Hansen, L., Kjaer, K. W., Gopalakrishnan, J., Pedersen, L. B., Møllgård, K., Nielsen, H., Baig, S. M. & 3 others, Tommerup, Niels, Christensen, Søren Tvorup & Larsen, Lars Allan, 2020, In: Nature Communications. 11, 16 p., 5816.

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

    14. Published

      Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

      Izarzugaza, J. M. G., Ellesøe, S. G., Doganli, Canan, Ehlers, Natasja Spring, Dalgaard, M. D., Audain, E., Dombrowsky, G., Banasik, Karina, Sifrim, A., Wilsdon, A., Thienpont, B., Breckpot, J., Gewillig, M., Brook, J. D., Hitz, M., Larsen, Lars Allan, Brunak, Søren & Competence Network for Congenital Heart Defects, Germany, C. N. F. C. H. D. G., 2020, In: Genome Medicine. 12, 1, 13 p., 76.

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

    15. 2019
    16. Published

      Haploinsufficiency of ARHGAP42 is associated with hypertension

      Fjorder, A. S., Rasmussen, Malene Bøgehus, Mehrjouy, M. M., Nazaryan, Lusine, Hansen, C., Bak, M., Grarup, Niels, Nørremølle, Anne, Larsen, Lars Allan, drb459, drb459, Hansen, Torben, Tommerup, Niels & Bache, Iben, 2019, In: European Journal of Human Genetics. 27, 8, p. 1296-1303 8 p.

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

    17. 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

    18. Published

      Patterns of 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, Vibeke Elisabeth, Brunak, Søren & Larsen, Lars Allan, 2019, In: European Journal of Human Genetics. 26, p. 106 1 p.

      Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

    19. 2018
    20. Published

      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. 1015–1022

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

    21. Published

      CEP128 Localizes to the Subdistal Appendages of the Mother Centriole and Regulates TGF-β/BMP Signaling at the Primary Cilium

      Mönnich, M., Borgeskov, L., Breslin, L., Jakobsen, L., Rogowski, M., Doganli, Canan, Schrøder, J. M., Mogensen, J. B., Blinkenkjær, L., Harder, L. M., Lundberg, E., Geimer, S., Christensen, Søren Tvorup, Andersen, J. S., Larsen, Lars Allan & Pedersen, Lotte Bang, 2018, In: Cell Reports. 22, 10, p. 2584-2592 9 p.

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

    22. Published

      Challenges for the sustainability of university-run biobanks

      Kongsholm, Nana Cecilie Halmsted, Christensen, Søren Tvorup, Herrmann, Janne Rothmar, Larsen, Lars Allan, Minssen, Timo, Pedersen, Lotte Bang, Rajam, N., Tommerup, Niels, Tupasela, A. M. & Schovsbo, Jens Hemmingsen, 2018, In: Biopreservation and Biobanking. 16, 4, p. 312-321 10 p.

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

    23. Published

      IFT20 modulates ciliary PDGFRα signaling by regulating the stability of Cbl E3 ubiquitin ligases

      Schmid, F. M., Schou, K. B., Vilhelm, M. J., Holm, M. S., Breslin, L., Farinelli, P., Larsen, Lars Allan, Andersen, J. S., Pedersen, Lotte Bang & Christensen, Søren Tvorup, 2018, In: Journal of Cell Biology. 217, 1, p. 151-161 11 p.

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

    24. Published

      The E3 ubiquitin ligase SMURF1 regulates cell-fate specification and outflow tract septation during mammalian heart development

      Rasmussen, K. K., Skat-Rørdam, Josephine, Andersen, P., Warzecha, C. B., Pye, M., Andersen, T. A., Ajbro, K. D., Bendsen, E., Narimatsu, M., Vilhardt, Frederik, Pedersen, Lotte Bang, Wrana, J. L., Anderson, R. H., Møllgård, Kjeld, Christensen, Søren Tvorup & Larsen, Lars Allan, 2018, In: Scientific Reports. 8, 1, 14 p., 9542.

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

    25. 2017
    26. Published

      A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family

      Abdullah, U., Farooq, M., Mang, Y., Marriam Bakhtiar, S., Fatima, A., Hansen, Lars, Kjaer, K. W., Larsen, Lars Allan, Faryal, S., Tommerup, Niels & Mahmood Baig, S., Dec 2017, In: European Journal of Medical Genetics. 60, 12, p. 627-630 4 p.

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

    27. Published

      Patient-specific three-dimensional explant spheroids derived from human nasal airway epithelium: a simple methodological approach for ex vivo studies of primary ciliary dyskinesia

      Marthin, J. K., Stevens, E. M., Larsen, Lars Allan, Christensen, Søren Tvorup & Nielsen, Kim G., 23 Mar 2017, In: Cilia. 6, 9 p., 3.

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

    28. 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

    29. 2016
    30. Published

      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

    31. Published

      A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family

      Farooq, M., Fatima, A., Mang, Y., Hansen, Lars, Kjaer, K. W., Baig, S. M., Larsen, Lars Allan & Tommerup, Niels, Mar 2016, In: Journal of Human Genetics. 61, 3, p. 271-273 3 p.

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

    32. Published

      How Suitable Are Registry Data for Recurrence Risk Calculations? Validation of Diagnoses on 1,593 Families With Congenital Heart Disease

      Ellesøe, S. G., Jensen, A. B., Ängquist, Lars, Hjortdal, V. E., Larsen, Lars Allan & Brunak, Søren, Mar 2016, In: World journal for pediatric & congenital heart surgery. 7, 2, p. 169-77 9 p.

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

    33. 2015
    34. Published

      Coordination of TGFβ/BMP signaling is associated with the primary cilium

      Lindbæk, L., Warzecha, C. B., Koefoed, K., Mogensen, J. B., Schmid, F., Pedersen, Lotte Bang, Larsen, Lars Allan & Christensen, Søren Tvorup, 2015, In: Cilia. 4, Suppl. 1, 1 p., P17.

      Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

    35. 2014
    36. Published

      Brain Barriers and a Subpopulation of Astroglial Progenitors of Developing Human Forebrain Are Immunostained for the Glycoprotein YKL-40

      Holst, Camilla Bjørnbak, Brøchner, Christian Beltoft, Larsen, Lars Allan, Johansen, Julia Sidenius & Møllgård, Kjeld, May 2014, In: Journal of Histochemistry and Cytochemistry. 62, 5, p. 369-88 20 p.

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

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