Elvir Bećirović - Concepedia

Author

Elvir Bećirović

Ludwig-Maximilians-Universität München ORCID

Also Known As

Becirovic, Elvir, E. Becirovic, E. Bećirović, Elvir Becirovic, Elvir Becirović, Elvir Bećirović

100

Publications

Citations

H-Index

Concepts

All Affiliations

Ludwig-Maximilians-Universität München Center for Integrated Protein Science Munich STZ eyetrial University of Tübingen University of Cologne

About

Elvir Bećirović is an author at Ludwig-Maximilians-Universität München specializing in medicine, signal transduction, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	888
2	Cell Biology	6	6	177
3	Natural Sciences	5	5	268
4	Molecular Biology	4	4	87
5	Biochemistry	3	3	452

Elvir Bećirović

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels S P H Alexander, Alistair Mathie, John A. Peters, British Journal of Pharmacology System PharmacologyExperimental PharmacologyPre-clinical PharmacologyTranslational PharmacologySystems Pharmacology	2021	248
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss Inga Ebermann, Hendrik P. N. Scholl, Peter Charbel Issa, Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderRetinitis PigmentosaGenetics	2006	229
The Concise Guide to PHARMACOLOGY 2023/24: Ion channels S P H Alexander, Alistair Mathie, John A. Peters, British Journal of Pharmacology Drug TargetSystem PharmacologyExperimental PharmacologyPre-clinical PharmacologyTranslational Pharmacology	2023	181
A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa François Paquet‐Durand, Susanne Beck, Stylianos Michalakis, Human Molecular Genetics	2010	112
Gene therapy restores vision and delays degeneration in the CNGB1-/- mouse model of retinitis pigmentosa Susanne Koch, Vithiyanjali Sothilingam, Marina Garcia Garrido, Human Molecular Genetics	2012	102
Sick Sinus Syndrome in HCN1-Deficient Mice Stefanie Fenske, Stefanie Krause, Sami Hassan, Circulation	2013	93
cAMP-dependent regulation of HCN4 controls the tonic entrainment process in sinoatrial node pacemaker cells Stefanie Fenske, Konstantin Hennis, René D. Rötzer, Nature Communications	2020	82
A gene therapy for inherited blindness using dCas9-VPR–mediated transcriptional activation Sybille Böhm, Victoria Splith, Lisa Maria Riedmayr, Science Advances	2020	64
mRNA trans-splicing dual AAV vectors for (epi)genome editing and gene therapy Lisa Maria Riedmayr, Klara Sonnie Hinrichsmeyer, Stefan Bernhard Thalhammer, Nature Communications	2023	57
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach Simon M. Petersen‐Jones, Laurence M. Occelli, Paige A. Winkler, Journal of Clinical Investigation Ocular DiseaseRetinal TherapiesSynaptic SignalingCngb1 MutationsRetina	2017	56

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