Stefanie Brock

Laarbeeklaan 101
1090 Brussels
Belgium
Laarbeeklaan 101
1090 Jette
Belgium
Pleinlaan 2
1050 Brussel
Belgium

Onderzoeksresultaten per jaar

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108 Citaties
6 h-index
12 Article
2 Poster
1 Unpublished abstract
1 PhD Thesis

12 resultaten

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2022
Assessing Tumor-Infiltrating Lymphocytes in Breast Cancer: A Proposal for Combining Immunohistochemistry and Gene Expression Analysis to Refine Scoring
Locy, H., Verhulst, S., Cools, W., Waelput, W., Brock, S., Cras, L., Schiettecatte, A., Jonckheere, J., van Grunsven, L. A., Vanhoeij, M., Thielemans, K. & Breckpot, K., 11 feb 2022, In: Frontiers in Immunology. 13, blz. 1-13 13 blz., 794175.
Onderzoeksoutput: Article › peer review

Open Access
Bestand
4 Citaten (Scopus)

56 Downloads (Pure)
Malformations of cerebral development and clues from the peripheral nervous system: A systematic literature review
Rijckmans, E., Stouffs, K., Jansen, A. C. & Brock, S., mrt 2022, In: European Journal of Paediatric Neurology. 37, blz. 155-164 10 blz.
Onderzoeksoutput: Article › peer review
2021
A rare cause of postmenopausal hyperandrogenism
De Vis, M., Brock, S., Cosyns, S. & Velkeniers, B., 7 jan 2021, In: BMJ Case Reports. 14, 1, e237505.
Onderzoeksoutput: Article › peer review
Defining the phenotypical spectrum associated with variants in TUBB2A
Brock, S., Vanderhasselt, T., Vermaning, S., Keymolen, K., Régal, L., Romaniello, R., Wieczorek, D., Storm, T. M., Schaeferhoff, K., Hehr, U., Kuechler, A., Krägeloh-Mann, I., Haack, T. B., Kasteleijn, E., Schot, R., Mancini, G. M. S., Webster, R., Mohammad, S., Leventer, R. J., Mirzaa, G. & 5 anderen, Dobyns, W. B., Bahi-Buisson, N., Meuwissen, M., Jansen, A. C. & Stouffs, K., 1 jan 2021, In: Journal of Medical Genetics. 2020, 1, blz. 1-8 8 blz.
Onderzoeksoutput: Article › peer review

Open Access
7 Citaten (Scopus)
Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing
Stutterd, C. A., Brock, S., Stouffs, K., Jansen, A., Fanjul-Fernandez, M., Lockhart, P. J., McGillivray, G., Mandelstam, S., Pope, K., Delatycki, M. B. & Leventer, R., 2021, In: Brain Communications. 3, 1, 12 blz., fcaa221.
Onderzoeksoutput: Article › peer review

Open Access
Bestand
16 Citaten (Scopus)

123 Downloads (Pure)
Neuropathology of genetically defined malformations of cortical development - a systematic literature review
Brock, S., Cools, F. & Jansen, A. C., aug 2021, In: Neuropathology and applied neurobiology. 47, 5, blz. 585-602 18 blz.
Onderzoeksoutput: Article › peer review

Open Access
6 Citaten (Scopus)
Novel Variant in COL4A1 Causes Extensive Prenatal Intracranial Hemorrhage and Porencephaly
Brock, S., Michotte, A., Doné, E., Leus, A., Cannie, M., De Pierre, K., Forsyth, R., Stouffs, K., Keymolen, K., Dimitrov, B., Fieuw, A., Jansen, A. C. & Van Berkel, K., aug 2021, In: Journal of neuropathology and experimental neurology. 80, 8, blz. 807-810 4 blz.
Onderzoeksoutput: Article › peer review

Open Access
Overcoming the Challenges of High Quality RNA Extraction from Core Needle Biopsy
Locy, H., Correa, R. J. M., Autaers, D., Schiettecatte, A., Jonckheere, J., Waelput, W., Cras, L., Brock, S., Verhulst, S., Kwan, K., Vanhoeij, M., Thielemans, K. & Breckpot, K., mei 2021, In: Biomolecules. 11, 5, 19 blz., 621.
Onderzoeksoutput: Article › peer review

Open Access
Bestand
5 Citaten (Scopus)

221 Downloads (Pure)
2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
Ebrahimi-Fakhari, D., Teinert, J., Behne, R., Wimmer, M., D'Amore, A., Eberhardt, K., Brechmann, B., Ziegler, M., Jensen, D. M., Nagabhyrava, P., Geisel, G., Carmody, E., Shamshad, U., Dies, K. A., Yuskaitis, C. J., Salussolia, C. L., Ebrahimi-Fakhari, D., Pearson, T. S., Saffari, A., Ziegler, A. & 68 anderen, Kölker, S., Volkmann, J., Wiesener, A., Bearden, D. R., Lakhani, S., Segal, D., Udwadia-Hegde, A., Martinuzzi, A., Hirst, J., Perlman, S., Takiyama, Y., Xiromerisiou, G., Vill, K., Walker, W. O., Shukla, A., Dubey Gupta, R., Dahl, N., Aksoy, A., Verhelst, H., Delgado, M. R., Kremlikova Pourova, R., Sadek, A. A., Elkhateeb, N. M., Blumkin, L., Brea-Fernández, A. J., Dacruz-Álvarez, D., Smol, T., Ghoumid, J., Miguel, D., Heine, C., Schlump, J-U., Langen, H., Baets, J., Bulk, S., Darvish, H., Bakhtiari, S., Kruer, M. C., Lim-Melia, E., Aydinli, N., Alanay, Y., El-Rashidy, O., Nampoothiri, S., Patel, C., Beetz, C., Bauer, P., Yoon, G., Guillot, M., Miller, S. P., Bourinaris, T., Houlden, H., Robelin, L., Anheim, M., Alamri, A. S., Mahmoud, A. A. H., Inaloo, S., Habibzadeh, P., Faghihi, M. A., Jansen, A. C., Brock, S., Roubertie, A., Darras, B. T., Agrawal, P. B., Santorelli, F. M., Gleeson, J., Zaki, M. S., Sheikh, S. I., Bennett, J. T. & Sahin, M., 1 okt 2020, In: Brain. 143, 10, blz. 2929-2944 16 blz.
Onderzoeksoutput: Article › peer review

Open Access
26 Citaten (Scopus)
Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly
Stouffs, K., Verloo, P., Brock, S., Regal, L., Beysen, D., Ceulemans, B., Jansen, A. & Meuwissen, M., 5 feb 2020, In: Frontiers in Genetics. 11, 5 blz., 26.
Onderzoeksoutput: Article › peer review

Open Access
Bestand
8 Citaten (Scopus)

86 Downloads (Pure)
2019
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities
Vandervore, L. V., Schot, R., Milanese, C., Smits, D. J., Kasteleijn, E., Fry, A. E., Pilz, D. T., Brock, S., Börklü-Yücel, E., Post, M., Bahi-Buisson, N., Sánchez-Soler, M. J., van Slegtenhorst, M., Keren, B., Afenjar, A., Coury, S. A., Tan, W-H., Oegema, R., de Vries, L. S., Fawcett, K. A. & 29 anderen, Nikkels, P. G. J., Bertoli-Avella, A., Al Hashem, A., Alwabel, A. A., Tlili-Graiess, K., Efthymiou, S., Zafar, F., Rana, N., Bibi, F., Houlden, H., Maroofian, R., Person, R. E., Crunk, A., Savatt, J. M., Turner, L., Doosti, M., Karimiani, E. G., Saadi, N. W., Akhondian, J., Lequin, M. H., Kayserili, H., van der Spek, P. J., Jansen, A. C., Kros, J. M., Verdijk, R. M., Milošević, N. J., Fornerod, M., Mastroberardino, P. G. & Mancini, G. M. S., 5 dec 2019, In: American Journal of Human Genetics. 105, 6, blz. 1126-1147 22 blz.
Onderzoeksoutput: Article › peer review

Open Access
17 Citaten (Scopus)
2018
Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1
Brock, S., Stouffs, K., Scalais, E., D'Hooghe, M., Keymolen, K., Guerrini, R., Dobyns, W. B., Di Donato, N. & Jansen, A. C., 1 aug 2018, In: European Journal of Human Genetics. 26, 8, blz. 1132-1142 11 blz.
Onderzoeksoutput: Article › peer review

Open Access
19 Citaten (Scopus)

Stefanie Brock

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