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Melissa Rieger
Institutions:
Friedrich-Alexander-Universität Erlangen-Nürnberg,
Universitätsklinikum Erlangen
Observed institutions:
Friedrich-Alexander-Universität Erlangen-Nürnberg,
Universitätsklinikum Erlangen,
Centro de Investigación Médica Aplicada,
Ludwig-Maximilians-Universität München,
Universidad de Navarra
OpenAlex ID:
A5113741225
Acquired mutations in BCL2 family proteins conferring resistance to the BH3 mimetic ABT-199 in lymphoma
2014
·
Vicente Fresquet
, Melissa Rieger
, et al.
·
Blood
·
188
A cyclin-D1 interaction with BAX underlies its oncogenic role and potential as a therapeutic target in mantle cell lymphoma
2011
·
Elena Beltran
, Vicente Fresquet
, et al.
·
Proceedings of the National Academy of Sciences
·
57
Borrelia burgdorferi sensu stricto and Borrelia afzelii : Population structure and differential pathogenicity
2015
·
Sabrina Jungnick
, Gabriele Margos
, et al.
·
International Journal of Medical Microbiology
·
51
Long-term in vitro cultivation of Borrelia miyamotoi
2014
·
Gabriele Margos
, Sylvia Stockmeier
, et al.
·
Ticks and Tick-borne Diseases
·
39
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling
2022
·
Alexander M. Holtz
, Rachel VanCoillie
, et al.
·
Genetics in Medicine
·
22
SRD5A3-CDG: Twins with an intragenic tandem duplication
2022
·
Melissa Rieger
, Matthias Türk
, et al.
·
European Journal of Medical Genetics
·
10
CAMTA1‐related disorder: Phenotypic and molecular characterization of 26 new individuals and literature review
2023
·
Hussam Al‐Kateb
, P. Y. Billie Au
, et al.
·
Clinical Genetics
·
8
PDF
7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder
2020
·
Melissa Rieger
, Mandy Krumbiegel
, et al.
·
American Journal of Medical Genetics Part A
·
6
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay
2022
·
Melissa Rieger
, Sébastien Moutton
, et al.
·
European Journal of Medical Genetics
·
5
PDF
Author response for " CAMTA1‐related disorder: Phenotypic and molecular characterization of 26 new individuals and literature review"
2023
·
Hussam Al‐Kateb
, P. Y. Billie Au
, et al.
Author response for " CAMTA1‐related disorder: Phenotypic and molecular characterization of 26 new individuals and literature review"
2023
·
Hussam Al‐Kateb
, P. Y. Billie Au
, et al.
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Works count:
11
Citation count:
386
H-index:
7
I10-index:
6
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