Novaković, Ivana

Type

Date issued

391 2000 - 2027
3 1901 - 1999

Mp-cat.

187 М30/М60
47 M21
45 M22
39 M23
17 M21a
15 M10/M40
11 M20/M50
11 other
10 M21a+
4 M24
. next >

Date issued - custom

Year from:

Year to:

Results 61-80 of 394 Results/Page

Issue Date	Title	Author(s)	Type	Мp-cat.
2023	Novel GATOR1 variants in focal epilepsy	Kovačević, Maša ; Janković, Milena ; Branković, Marija ; Milićević, Ognjen ; Novaković, Ivana ; Sokić, Dragoslav ; Ristić, Aleksandar ; Shamsani, Jannah; Vojvodić, Nikola	Article	22M22
2023	Novel variants in established epilepsy genes in focal epilepsy	Kovačević, Maša ; Milićević, Ognjen ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Sokić, Dragoslav ; Ristić, Aleksandar ; Shamsani, Jannah; Vojvodić, Nikola	Article	22M22
2023	C9ORF72 intermediate repats in neurodegenerative disorders from Serbia	Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Perić, Stojan ; Dragašević-Mišković, Nataša ; Mandić, Gorana ; Ječmenica-Lukić, Milica ; Stanković, Iva ; Stefanova, Elka ; Stević, Zorica ; Novaković, Ivana ; Svetel, Marina ; Kostić, Vladimir ;	Conference Paper	Mp. category will be shown later
2023	Whole exome sequencing in Serbian patients with hereditary spastic paraplegia	Ivanović, Vukan ; Branković, Marija ; Božović, Ivo ; Stević, Zorica ; Basta, Ivana ; Marković, Vladana ; Svetel, Marina ; Tubić, Radoje ; Marjanović, Ana ; Veselinović, Nikola ; Mesaroš, Šarlota ; Janković, Milena ; Rakočević-Stojanović, Vidosava ; Savić-Pavićević, Dušanka ; Novaković, Ivana ; Perić, Stojan ;	Conference Paper	Mp. category will be shown later
2023	The importance of direct genetic testing to determine female carriers in dystrophinopathies	Maksić, Jasmina ; Maksimović, Nela ; Rasulić, Lukas ; Milankov, Olgica; Marjanović, Ana ; Cvetković, Dragana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana	Article	23M23
2023	Motor neuron involvement in facial muscles as characteristic of ANO10 mutation	Dragašević-Mišović, Nataša ; Milovanović, Andona ; Stanković, Iva ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija S. ; Petrović, Igor N. ; Svetel, Marina V. ; Novaković, Ivana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2023	Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience	Kresojević, Nikola ; Perović, Ivana; Stanković, Iva ; Tomić, Aleksandra ; Ječmenica-Lukić, Milica ; Marković, Vladana ; Stojković, Tanja ; Mandić, Gorana ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Novaković, Ivana ; Petrović, Igor ; Dragašević, Nataša ; Stefanova, Elka ; Svetel, Marina ; Kostić, Vladimir ;	Article	21M21
2023	Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”	Kresojević, Nikola ; Marković, Vladana ; Dobričić, Valerija ; Stanković, Iva ; Stojković, Tanja ; Tomić, Aleksandra ; Ječmenica-Lukić, MIlica ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Novaković, Ivana ; Petrović, Igor ; Dragašević, Nataša ; Svetel, Marina ; Kostić, Vladimir ;	Article	21a+M21a+
2023	TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients	Pešić, Milica ; Andrejić, Nikola; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka	Conference Paper	Mp. category will be shown later
2023	The association of R47H variant in the TREM2 gene and genetic susceptibility to Alzheimer's disease in Serbian population	Andrejić, Nikola; Pešić, Milica ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka	Article	53M53
2022	Analysis of “clinical exome” panel in Serbian patients with cognitive disorders	Branković, Marija ; Stefanova, Elka ; Mandić, Gorana ; Marjanović, Ana ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Stević, Zorica ; Janković, Milena ; Novaković, Ivana ; Peterlin, Borut; Kostić, Vladimir ;	Article	22M22
2022	Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia	Perić, Stojan ; Marković, Vladana ; Candayan, Ayse; De Vriendt, Els; Momčilović, Nikola; Savić, Andrija; Dragašević-Mišković, Nataša ; Svetel, Marina ; Stević, Zorica ; Božović, Ivo ; Mesaroš, Šarlota ; Drulović, Jelena ; Basta, Ivana ; Petrović, Igor ; Tamaš, Olivera; Mijajlović, Milija ; Novaković, Ivana ; Sokić, Dragoslav ; Jordanova, Albena;	Article	21M21
2022	Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages	Pereza, Nina; Terzic, Rifet; Plaseska-Karanfilska, Dijana; Miljanovic, Olivera; Novaković, Ivana V. ; Poslon, Zeljka; Ostojic, Sasa; Peterlin, Borut	Article	21M21
2022	Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation	Minić, Snežana B. ; Trpinac, Dušan P. ; Novaković, Ivana V. ; Cerovac, Nataša M. ; Dobrosavljević-Vukojević, Danijela ; Rosain, Jeremie	Article	21M21
2022	Impact of the Fetuin Gene Polymorphisms in Coronary Artery Calcification and Mortality of Patients with Chronic Kidney Disease and Renal Transplant	Jovičić-Pavlović, Svetlana; Simić-Ogrizović, Sanja P. ; Bukumirić, Zoran M. ; Erić, Milena; Pavlović, Natalija; Kotlica, Boba ; Novaković, Ivana V.	Article	22M22
2022	Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience	Kresojević, Nikola ; Dobričić, Valerija ; Ječmenica-Lukić, Milica ; Tomić, Aleksandra ; Petrović, Igor ; Dragašević, Nataša ; Perović, Ivana; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Svetel, Marina ; Kostić, Vladimir S. ;	Article	21aM21a
2022	Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience	Branković, Marija ; Dragašević, Nataša ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Petrović, Igor ; Perić, Stojan ; Marjanović, Ana ; Janković, Milena ; Jančić, Jasna ; Novaković, Ivana ; Peterlin, Borut; Svetel, Marina ; Kostić, Vladimir ;	Article	22M22
2022	The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options	Janković, Milena ; Petrović, Bojana ; Novaković, Ivana ; Branković, Slavko ; Radosavljević, Nataša ; Nikolić, Dejan	Article	21M21
2022	C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population	Marjanović, Ana ; Dobričić, Valerija ; Ječmenica-Lukić, Milica ; Stanković, Iva ; Milićević, Ognjen ; Dragašević-Mišković, Nataša ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Svetel, Marina ; Stefanova, Elka ; Kostić, Vladimir ;	Article	22M22
2022	Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients	Perović, Dijana ; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Dušanović-Pjević, Marija G. ; Grk, Milka B. ; Đuranovic, Ana S. ; Rašić, Milica ; Novaković, Ivana V. ; Maksimović, Nela S.	Article	22M22