Concepedia

Author

Dragan Marjanović

University of Southern DenmarkORCID

Also Known As

D Marjanovic, D Marjanović, Dragan Marjanovic, Dragan Marjanović, Trine Hammer

31

Publications

861

Citations

10

H-Index

26

Concepts

All Affiliations

University of Southern DenmarkUniversity of CopenhagenInsermCentre National de la Recherche ScientifiqueHospices Civils de Lyon
DM

About

Dragan Marjanović is an author at University of Southern Denmark specializing in synaptic signaling, neurogenetics, and medicine.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

259

2

Social Sciences

2

2

224

3

Molecular Biology

1

1

35

4

Molecular Genetics

1

1

35

5

Molecular Medicine

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35

Dragan Marjanović

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11

Publications

847

Citations

10

H-Index

YearCitations

Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies

Silvia Masnada, Ulrike B. S. Hedrich, Elena Gardella,

Brain

2017

158

The gain of function <i>SCN1A</i> disorder spectrum: novel epilepsy phenotypes and therapeutic implications

Andreas Brunklaus, Tobias Brünger, Tony Feng,

Brain

2022

137

Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

Rikke S. Møller, Line H.G. Larsen, Katrine M. Johannesen,

Molecular Syndromology

2016

126

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy

Wenshu XiangWei, Varun Kannan, Yuchen Xu,

Brain

2019

87

4-Aminopyridine is a promising treatment option for patients with gain-of-function <i>KCNA2</i> -encephalopathy

Ulrike B. S. Hedrich, Stephan Lauxmann, Markus Wolff,

Science Translational Medicine

2021

79

Utility of genetic testing for therapeutic decision‐making in adults with epilepsy

Katrine M. Johannesen, Natalya Nikanorova, Dragan Marjanović,

Epilepsia

2020

78

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Cyril Mignot, Aoife McMahon, Claire Bar,

Genetics in Medicine

2018

57

Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood

Hannah Stamberger, David Crosiers, Ganna Balagura,

Neurology

2022

53

Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis

Renzo Guerrini, Davide Mei, Katalin Kerti‐Szigeti,

Brain

2022

35

The epilepsy phenotypic spectrum associated with a recurrent <i>CUX2</i> variant

Nicolas Chatron, Rikke S. Møller, Neena L. Champaigne,

Annals of Neurology

2018

27

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