Dušanka Savić‐Pavićević

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia

Jonathan Baets, Le­onardo Almeida-Souza, Els De Vriendt et al. · Nature Genetics · 2012 · 129 citations

Life Sciences, Neurology, Neuroscience +12

Novel <i>GNB1</i> mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans

Katja Lohmann, Ikuo Masuho, Dipak N. Patil et al. · Human Molecular Genetics · 2017 · 61 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells

Jovan Pešović, Stojan Perić, Miloš Brkušanin et al. · Frontiers in Genetics · 2018 · 51 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Joint effect of<i>ADARB1</i>gene,<i>HTR2C</i>gene and stressful life events on suicide attempt risk in patients with major psychiatric disorders

J Karanović, Saša Šviković, Maja Pantović-Stefanović et al. · The World Journal of Biological Psychiatry · 2015 · 44 citations

Medicine, Molecular Genetics, Psychiatry +15

Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2

Stojan Perić, Vidosava Rakočević Stojanović, Gorana Mandić Stojmenović et al. · Neurological Sciences · 2016 · 44 citations

Medicine, Neurology, Neuroscience +14