Malene Bøgehus Rasmussen
Guest Researcher
Medical Genetics Program
Blegdamsvej 3
2200 København N.
- 2019
- Published
Big Data and the ethics of detail: the role of ethics work in the making of a cross-national research infrastructure for genetic research
Hoeyer, Klaus, Tupasela, A. & Rasmussen, Malene Bøgehus, 2019, Global Genes, Local Concerns- Legal, Ethical and Scientific Challenges in International Biobanking. Minssen, T., Rothmar Herrmann, J. & Schovsbo, J. (eds.). 1 ed. Cheltenham: Edward Elgar Publishing, p. 2-21 20 p.Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review
- Published
Codes d’éthique et travail éthique dans la recherché et le partage des données génétiques transnationales. Flux, non-flux et débordements
Hoeyer, Klaus, Tupasela, A. M. & Rasmussen, Malene Bøgehus, 2019, In: Revue d'Anthropologie des Connaissances. 13, 2, p. 455-478 24 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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
- 2017
- Published
Re-examination of carriers of balanced chromosomal inversions
Rasmussen, Malene Bøgehus, 27 Nov 2017Research output: Book/Report › Ph.D. thesis › Research
- Published
Ethics policies and ethics work in cross-national genetic research and data sharing: Flows, nonflows, and overflows
Hoeyer, Klaus, Tupasela, A. & Rasmussen, Malene Bøgehus, 1 May 2017, In: Science, Technology & Human Values. 42, 3, p. 381-404 24 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
NGS mapped breakpoints in balanced chromosomal rearrangements including the first large cohort of healthy carriers
Tommerup, N., Fonseca, A. C., Mehrjouy, M., Rasmussen, M. B., Bache, I., Halgren, C., Kroisel, P., Midyan, S., Vermeesch, J., Vianna-Morgante, A. M., Abe, K. T., Moretti-Ferreira, D., Paskulin, G., Angelova, L., Rajcan-Separovic, E., Sismani, C., Sedlacek, Z., Fagerberg, C., Brondum-Nielsen, K., Vogel, I. & 36 others, , 2017, In: Molecular Cytogenetics. 10, S1, p. 70 1 p., 7.P1.Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
- 2016
- Published
Re-Examination of Danish Carriers of Balanced Chromosomal Inversions
Rasmussen, Malene Bøgehus, Bache, Iben, Mehrjouy, M. M., Silahtaroglu, Asli, Kjaergaard, S., Brondum-Nielsen, K., Jensen, P. K. A., Vogel, I., Hertz, J. M., Fagerberg, C., Bojesen, Anders Miki, Petersen, M. B., Hansen, J., Halgren, C., Bak, M. & Tommerup, Niels, May 2016, In: Cancer genetics. 209, 5, p. 231-231Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
- Published
Phenotypic subregions within the split-hand/foot malformation 1 locus
Rasmussen, Malene Bøgehus, Kreiborg, Sven, Jensen, P., Bak, M., Mang, Y., Lodahl, M., Budtz-Joergensen, Esben, Tommerup, Niels, Tranebjærg, Lisbeth & Rendtorff, N. D., Mar 2016, In: Human Genetics. 135, 3, p. 345-457 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2014
- Published
Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes
Rasmussen, Malene Bøgehus, Nielsen, J. V., Lourenço, C. M., Melo, J. B., Harding, Christina Halgren, Geraldi, C. V. L., Marques, W., Rodrigues, G. R., Thomassen, M., Bak, M., Hansen, C., Ferreira, S. I., Venâncio, M., Henriksen, K. F., Lind-Thomsen, A., Carreira, I. M., Jensen, N. A. & Tommerup, Niels, Sep 2014, In: Journal of Medical Genetics. 51, 9, p. 605-613 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5
Baker, P. R., Friederich, M. W., Swanson, M. A., Shaikh, T., Bhattacharya, K., Scharer, G. H., Aicher, J., Creadon-Swindell, G., Geiger, E., MacLean, K. N., Lee, W-T., Deshpande, C., Freckmann, M-L., Shih, L-Y., Wasserstein, M., Rasmussen, M. B., Lund, A. M., Procopis, P., Cameron, J. M., Robinson, B. H. & 9 others, , Feb 2014, In: Brain. 137, 2, p. 366-79 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 337730903
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NGS mapped breakpoints in balanced chromosomal rearrangements including the first large cohort of healthy carriers
Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
Published -
50
downloads
Codes d’éthique et travail éthique dans la recherché et le partage des données génétiques transnationales. Flux, non-flux et débordements
Research output: Contribution to journal › Journal article › Research › peer-review
Published