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Lars Kjærsgaard Hansen

MD Consultant

20012019
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Fingerprint Dive into the research topics where Lars Kjærsgaard Hansen is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 14 Similar Profiles
Mosaicism Medicine & Life Sciences
Congenital Hyperinsulinism Medicine & Life Sciences
Mutation Medicine & Life Sciences
Cerebral Palsy Medicine & Life Sciences
Loose Anagen Hair Syndrome Medicine & Life Sciences
Comorbidity Medicine & Life Sciences
Methyl-CpG-Binding Protein 2 Medicine & Life Sciences
Uniparental Disomy Medicine & Life Sciences

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Research Output 2001 2019

Cerebral Palsy
Randomized Controlled Trials
Orthopedics
Quality of Life
Control Groups
6 Downloads (Pure)

Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movements

Schönewolf-Greulich, B., Bisgaard, A-M., Dunø, M., Jespersgaard, C., Rokkjaer, M., Hansen, L. K., Tsoutsou, E., Sofokleous, C., Topcu, M., Kaur, S., Van Bergen, N. J., Brøndum-Nielsen, K., Larsen, M. J., Sørensen, K. P., Christodoulou, J., Fagerberg, C. R. & Tümer, Z., Mar 2019, In : Clinical Genetics. 95, 3, p. 403-408

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
Methyl-CpG-Binding Protein 2
Rett Syndrome
Mosaicism
Fibroblasts
Exome
13 Downloads (Pure)

Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism

Christesen, H. T., Christensen, L. G., Löfgren, Å. M., Brøndum-Nielsen, K., Svensson, J., Brusgaard, K., Samuelsson, S., Elfving, M., Jonson, T., Grønskov, K., Rasmussen, L., Backman, T., Hansen, L. K., Larsen, A. R., Petersen, H. & Detlefsen, S., 1. Jan 2019, In : European Journal of Medical Genetics.

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
Congenital Hyperinsulinism
Uniparental Disomy
Focal Nodular Hyperplasia
Glandular and Epithelial Neoplasms
Liver
188 Downloads (Pure)

Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease

Zagaglia, S., Selch, C., Nisevic, J. R., Mei, D., Michalak, Z., Hernandez-Hernandez, L., Krithika, S., Vezyroglou, K., Varadkar, S. M., Pepler, A., Biskup, S., Leão, M., Gärtner, J., Merkenschlager, A., Jaksch, M., Møller, R. S., Gardella, E., Kristiansen, B. S., Hansen, L. K., Vari, M. S. & 29 others, Helbig, K. L., Desai, S., Smith-Hicks, C. L., Hino-Fukuyo, N., Talvik, T., Laugesaar, R., Ilves, P., Õunap, K., Körber, I., Hartlieb, T., Kudernatsch, M., Winkler, P., Schimmel, M., Hasse, A., Knuf, M., Heinemeyer, J., Makowski, C., Ghedia, S., Subramanian, G. M., Striano, P., Thomas, R. H., Micallef, C., Thom, M., Werring, D. J., Kluger, G. J., Cross, J. H., Guerrini, R., Balestrini, S. & Sisodiya, S. M., 27. Nov 2018, In : Neurology. 91, 22, p. e2078-e2088

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
Nervous System
Mutation
Electroencephalography
Genetic Association Studies
Pedigree
33 Downloads (Pure)
Open Access
File