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Autori: Dobricic Valerija S

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Naslov The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia (Meeting Abstract)
Autori Mandic-Stojmenovic Gorana B  Stefanova Elka D  Novakovic Ivana V  Dobricic Valerija S  Stojkovic Tanja  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2019), vol. 26 br. , Suppl. 1, str. 120-120
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease (Meeting Abstract)
Autori Jankovic Milena Z  Dobricic Valerija S  Kresojevic Nikola D  Markovic Vladana V  Petrovic Igor N  Svetel Marina V  Pekmezovic Tatjana D  Novakovic Ivana V  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 410-411
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders (Meeting Abstract)
Autori Marjanovic Ana  Dobricic Valerija S  Marjanovic Ivan V  Brankovic Marija  Jankovic Milena Z  Mandic Gorana B  Stevic Zorica D  Novakovic Ivana V  Stefanova Elka D  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 376-376
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Contribution to the knowledge on the distribution of freshwater sponges - the Danube and Sava rivers case study (Article)
Autori Andjus Stefan P  Nikolic Nadja S  Dobricic Valerija S  Marjanovic Ana  Gacic Zoran M  Brankovic Goran O  Akovic Maja R  Paunovic Momir M 
Info JOURNAL OF LIMNOLOGY, (2018), vol. 77 br. 2, str. 199-208
Projekat Ministry of Education, Science and Technological Development of the Republic of Serbia [176018]; European Union [603629-ENV-2013-6.2.1-GLOBAQUA]; European Commission
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease (Article)
Autori Jankovic Milena Z  Dobricic Valerija S  Kresojevic Nikola D  Markovic Vladana V  Petrovic Igor N  Svetel Marina V  Pekmezovic Tatjana D  Novakovic Ivana V  Kostic Vladimir K 
Info JOURNAL OF THE NEUROLOGICAL SCIENCES, (2018), vol. 393 br. , str. 27-30
Projekat Serbian Ministry of Science and Technological Development [ON175090, ON175091]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients (Meeting Abstract)
Autori Mitropoulos Konstantinos  ...  Dobricic Valerija S  Novakovic Ivana V  Kostic Vladimir S  ...  (broj koautora 30) 
Info PUBLIC HEALTH GENOMICS, (2018), vol. 21 br. , Suppl. 1, str. 17-17
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype (Editorial Material)
Autori Kulikovskaja Leonora  Sarajlija Adrijan  Savic-Pavicevic Dusanka Lj  Dobricic Valerija S  Klein Christine  Westenberger Ana 
Info NEUROLOGY-GENETICS, (2018), vol. 4 br. 2, str. -
Projekat Hermann and Lilly Schilling Foundation; Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia (Article)
Autori Dobricic Valerija S  Tomic Aleksandra D  Brankovic Vesna  Kresojevic Nikola D  Jankovic Milena Z  Westenberger Ana  Milic-Rasic Vedrana M  Klein Christine  Novakovic Ivana V  Svetel Marina V  Kostic Vladimir S 
Info PARKINSONISM & RELATED DISORDERS, (2017), vol. 45 br. , str. 81-84
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation; German Research Foundation (DFG) Research Unit [FOR2488]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients (Article)
Autori Mitropoulos Konstantinos  ...  Dobricic Valerija S  Novakovic Ivana V  Kostic Vladimir S  ...  (broj koautora 33) 
Info HUMAN GENOMICS, (2017), vol. 11 br. , str. -
Projekat European Commission [RD-Connect] [FP7-305444]; European Commission [U-PGx] [H2020-668353]; Greek General Secretariat of Research and Technology [eMoDiA] [PiDeltaE11_0415]; Golden Helix Foundation; Serbian Ministry of Education, Science and Technology deve
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans (Article)
Autori Lohmann Katja  ...  Dobricic Valerija S  ...  Savic-Pavicevic Dusanka Lj  ...  (broj koautora 18) 
Info HUMAN MOLECULAR GENETICS, (2017), vol. 26 br. 6, str. 1078-1086
Projekat NIH [NS081282, HL105550]; German Ministry of Education and Research (BMBF, DYSTRACT consortium) [01GM1514B]; Ministry of Education, Science and Technological Development, Republic of Serbia [173016, 175090]; Hermann and Lilly Schilling Foundation
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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