Projects per year
Fingerprint
Dive into the research topics where Dusica Babovic-Vuksanovic is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
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
-
Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes
Oftedal, B. E., Assing, K., Baris, S., Safgren, S. L., Johansen, I. S., Jakobsen, M. A., Babovic-Vuksanovic, D., Agre, K., Klee, E. W., Majcic, E., Ferré, E. M. N., Schmitt, M. M., DiMaggio, T., Rosen, L. B., Rahman, M. O., Chrysis, D., Giannakopoulos, A., Garcia, M. T., González-Granado, L. I., Stanley, K., & 5 others , Jun 16 2023, In: iScience. 26, 6, 106818.Research output: Contribution to journal › Article › peer-review
Open Access -
Erratum: Impact of integrated translational research on clinical exome sequencing (Genetics in Medicine (2021) 23(3) (498–507), (S1098360021049455), (10.1038/s41436-020-01005-9))
Klee, E. W., Cousin, M. A., Pinto e Vairo, F., Morales-Rosado, J. A., Macke, E. L., Jenkinson, W. G., Ferrer, A., Schultz-Rogers, L. E., Olson, R. J., Oliver, G. R., Sigafoos, A. N., Schwab, T. L., Zimmermann, M. T., Urrutia, R. A., Kaiwar, C., Gupta, A., Blackburn, P. R., Boczek, N. J., Prochnow, C. A., Lowy, R. J., & 40 others , Feb 2023, In: Genetics in Medicine. 25, 2, 100359.Research output: Contribution to journal › Comment/debate › peer-review
-
Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway
Delanne, J., Lecat, M., Blackburn, P. R., Klee, E. W., Stumpel, C. T. R. M., Stegmann, S., Stevens, S. J. C., Nava, C., Heron, D., Keren, B., Mahida, S., Naidu, S., Babovic-Vuksanovic, D., Herkert, J. C., Torring, P. M., Kibæk, M., De Bie, I., Pfundt, R., Hendriks, Y. M. C., Ousager, L. B., & 15 others , Jan 2023, In: European Journal of Medical Genetics. 66, 1, 104670.Research output: Contribution to journal › Article › peer-review
-
Autosomal Recessive Cerebellar Atrophy and Spastic Ataxia in Patients With Pathogenic Biallelic Variants in GEMIN5
Rajan, D. S., Kour, S., Fortuna, T. R., Cousin, M. A., Barnett, S. S., Niu, Z., Babovic-Vuksanovic, D., Klee, E. W., Kirmse, B., Innes, M., Rydning, S. L., Selmer, K. K., Vigeland, M. D., Erichsen, A. K., Nemeth, A. H., Millan, F., DeVile, C., Fawcett, K., Legendre, A., Sims, D., & 10 others , Feb 28 2022, In: Frontiers in Cell and Developmental Biology. 10, 783762.Research output: Contribution to journal › Article › peer-review
Open Access -
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome
Cousin, M. A., Veale, E. L., Dsouza, N. R., Tripathi, S., Holden, R. G., Arelin, M., Beek, G., Bekheirnia, M. R., Beygo, J., Bhambhani, V., Bialer, M., Bigoni, S., Boelman, C., Carmichael, J., Courtin, T., Cogne, B., Dabaj, I., Doummar, D., Fazilleau, L., Ferlini, A., & 51 others , Dec 2022, In: Genome medicine. 14, 1, 62.Research output: Contribution to journal › Article › peer-review
Open Access