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Grobarczyk Benjamin

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Main Referenced Co-authors
Malgrange, Brigitte  (6)
Lefèbvre, Philippe  (5)
Nguyen, Laurent  (5)
Czajkowski, Amandine  (4)
Borgs, Laurence (3)
Main Referenced Keywords
genome editing (2); ALMS1 (1); Alström Syndrome (1); Animals (1); Cas (1);
Main Referenced Unit & Research Centers
Giga Neurosciences - ULiège [BE] (3)
Main Referenced Disciplines
Biochemistry, biophysics & molecular biology (8)
Otolaryngology (3)
Neurology (1)
Anatomy (cytology, histology, embryology...) & physiology (1)
Biotechnology (1)

Publications (total 8)

The most downloaded
4 downloads
Grobarczyk, B., Franco, B., Hanon, K., & Malgrange, B. (2015). Generation of Isogenic Human iPS Cell Line Precisely Corrected by Genome Editing Using the CRISPR/Cas9 System. Stem Cell Reviews. doi:10.1007/s12015-015-9600-1 https://hdl.handle.net/2268/182774

The most cited

62 citations (OpenCitations)

Grobarczyk, B., Franco, B., Hanon, K., & Malgrange, B. (2015). Generation of Isogenic Human iPS Cell Line Precisely Corrected by Genome Editing Using the CRISPR/Cas9 System. Stem Cell Reviews. doi:10.1007/s12015-015-9600-1 https://hdl.handle.net/2268/182774

Czajkowski, A., Grobarczyk, B., Borgs, L., Hanon, K., LEFEBVRE, P., & Nguyen, L. (24 November 2017). Derivation of cochlear cells from human iPSCs for modeling hereditary hearing loss [Paper presentation]. BeSSCR.

Czajkowski, A., Grobarczyk, B., Borgs, L., Hanon, K., LEFEBVRE, P., Nguyen, L., & Malgrange, B. (May 2017). Derivation of cochlear cells from human iPSCs for modeling hereditary hearing loss [Poster presentation]. 9th International Meeting of the Stem Cell Network Noth Rhine Westphalia, Münster, Germany.

Czajkowski, A., Grobarczyk, B., Borgs, L., LEFEBVRE, P., Nguyen, L., & Malgrange, B. (16 September 2016). Derivation of cochlear cells from human iPSCs for modeling hereditary hearing loss [Poster presentation]. BeSSCR.

Czajkowski, A., Grobarczyk, B., Hanon, K., LEFEBVRE, P., Delacroix, L., & Malgrange, B. (May 2016). Derivation of cochlear cells from pathological or isogenic human iPSCs for modeling hereditary hearing loss [Poster presentation]. 10th Molecular Biology of Hearing and Deafness conference, Hinxton, United Kingdom.

Borgs, L.* , Peyre, E.* , Alix, P., Hanon, K., Grobarczyk, B., Godin, J., Purnelle, A., Krusy, N., Maquet, P., Lefèbvre, P., Seutin, V., Malgrange, B.* , & Nguyen, L.*. (2016). Dopaminergic neurons differentiating from LRRK2 G2019S induced pluripotent stem cells show early neuritic branching defects. Scientific Reports, 6, 33377. doi:10.1038/srep33377
Peer Reviewed verified by ORBi
* These authors have contributed equally to this work.

Grobarczyk, B. (2015). Utilisation des cellules souches humaines à pluripotence induite normales et mutantes pour l’étude et le traitement des surdités génétiques [Doctoral thesis, Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/315056

Grobarczyk, B., Franco, B., Hanon, K., & Malgrange, B. (2015). Generation of Isogenic Human iPS Cell Line Precisely Corrected by Genome Editing Using the CRISPR/Cas9 System. Stem Cell Reviews. doi:10.1007/s12015-015-9600-1
Peer Reviewed verified by ORBi

Malgrange, B., Borgs, L., Grobarczyk, B., Purnelle, A., Ernst, P., Moonen, G., & Nguyen, L. (2011). Using human pluripotent stem cells to untangle neurodegenerative disease mechanisms. Cellular and Molecular Life Sciences, 68 (4), 635-49. doi:10.1007/s00018-010-0557-6
Peer Reviewed verified by ORBi

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