Research output per year
Research output per year
Personal profile
Short presentation
In the group (Larsen Group) we are interested in understanding the fundamental aspects of human embryonic development and birth defects. We have special focus on the genetic and functional aspects of human cardiac development and congenital heart disease, but we are also interested in investigating genetic and molecular mechanisms involved in other areas of human embryonic development, including development of the brain.
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Research output
- 105 Citations
- 5 Journal article
-
Rare homozygous cilia gene variants identified in consanguineous congenital heart disease patients
Baird, D. A., Mubeen, H., Doganli, C., Miltenburg, J. B., Thomsen, O. K., Ali, Z., Naveed, T., Rehman, A. U., Baig, S. M., Christensen, S. T., Farooq, M. & Larsen, L. A., 2024, In: Human Genetics. 143, 11, p. 1323–1339 17 p.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile -
Extrarenal expression of α-klotho, the kidney related longevity gene, in Heterocephalus glaber, the long living Naked Mole Rat
Morevati, M., Mace, M. L., Egstrand, S., Nordholm, A., Doganli, C., Strand, J., Rukov, J. L., Torsetnes, S. B., Gorbunova, V., Olgaard, K. & Lewin, E., 2021, In: Scientific Reports. 11, 11 p., 15375.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile2 Citations (Scopus)15 Downloads (Pure) -
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, , 2020, In: Nature Communications. 11, 16 p., 5816.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile35 Citations (Scopus)68 Downloads (Pure) -
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease
Izarzugaza, J. M. G., Ellesøe, S. G., Doganli, C., Ehlers, N. S., Dalgaard, M. D., Audain, E., Dombrowsky, G., Banasik, K., Sifrim, A., Wilsdon, A., Thienpont, B., Breckpot, J., Gewillig, M., Brook, J. D., Hitz, M-P., Larsen, L. A., Brunak, S. & Competence Network for Congenital Heart Defects, Germany, 2020, In: Genome Medicine. 12, 1, 13 p., 76.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile16 Citations (Scopus)38 Downloads (Pure) -
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, C., Schrøder, J. M., Mogensen, J. B., Blinkenkjær, L., Harder, L. M., Lundberg, E., Geimer, S., Christensen, S. T., Andersen, J. S., Larsen, L. A. & Pedersen, L. B., 2018, In: Cell Reports. 22, 10, p. 2584-2592 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
Open AccessFile52 Citations (Scopus)317 Downloads (Pure)