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Natasa Kovacevic‐Grujicic

Datos Biográficos

ID5209519
NOMBRENatasa Kovacevic‐Grujicic
NOMBRESNatasa
APELLIDOKovacevic‐Grujicic
FIRMAGRUJICIC N K
AFILIACIONESUniversity of Belgrade
ORCID0000-0002-3837-1283
VERIFICADOSí
TOTAL DE OBRAS3
TOTAL DE CITAS1
TOTAL COMO AUTOR3
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2015
AÑO MÁS RECIENTE DE PUBLICACIÓN2024
ÍNDICE H1
  • Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion

    Open Access•Marijana Rakonjac, Goran Čuturilo et al.•ARTICLE•Children•2024

    22q11.2 deletion syndrome (22q11.2DS), the most frequent microdeletion syndrome in humans, is related to a high risk of developing neurodevelopmental disorders. About 95% of patients with 22q11.2DS have speech and language impairments. Global articulation, story generation, and verbal memory tests were applied to compare articulatory characteristics of speech sounds, spontaneous language abilities, and immediate verbal memory between four groups …

  • Mitochondrial super-haplogroup U diversity in Serbians

    Open Access•Slobodan Davidovic, B А Malyarchuk et al.•ARTICLE•Annals of Human Biology•2017

    The exceptional diversity of maternal lineages found in Serbians may be associated with the genetic impact of both autochthonous pre-Slavic Balkan populations whose mtDNA gene pool was affected by migrations of various populations over time (e.g. Bronze Age pastoralists) and Slavic and Germanic newcomers in the early Middle Ages

  • Mitochondrial DNA perspective of Serbian genetic diversity

    Open Access•Slobodan Davidovic, B А Malyarchuk et al.•ARTICLE•American Journal of Physical…•2015•Citada por: 1•Referencias: 65

    Although south‐Slavic populations have been studied to date from various aspects, the population of Serbia, occupying the central part of the Balkan Peninsula, is still genetically understudied at least at the level of mitochondrial DNA (mtDNA) variation. We analyzed polymorphisms of the first and the second mtDNA hypervariable segments (HVS‐I and HVS‐II) and informative coding‐region markers in 139 Serbians to shed more light on their mtDNA vari…

  • Mitochondrial DNA perspective of Serbian genetic diversity

    Open Access•Slobodan Davidovic, B А Malyarchuk et al.•ARTICLE•American Journal of Physical…•2015•Citada por: 1•Referencias: 65

    Although south‐Slavic populations have been studied to date from various aspects, the population of Serbia, occupying the central part of the Balkan Peninsula, is still genetically understudied at least at the level of mitochondrial DNA (mtDNA) variation. We analyzed polymorphisms of the first and the second mtDNA hypervariable segments (HVS‐I and HVS‐II) and informative coding‐region markers in 139 Serbians to shed more light on their mtDNA vari…

  • Mitochondrial DNA perspective of Serbian genetic diversity

    Open Access•Slobodan Davidovic, B А Malyarchuk et al.•ARTICLE•American Journal of Physical…•2015•Citada por: 1•Referencias: 65

    Although south‐Slavic populations have been studied to date from various aspects, the population of Serbia, occupying the central part of the Balkan Peninsula, is still genetically understudied at least at the level of mitochondrial DNA (mtDNA) variation. We analyzed polymorphisms of the first and the second mtDNA hypervariable segments (HVS‐I and HVS‐II) and informative coding‐region markers in 139 Serbians to shed more light on their mtDNA vari…

  • Mitochondrial super-haplogroup U diversity in Serbians

    Open Access•Slobodan Davidovic, B А Malyarchuk et al.•ARTICLE•Annals of Human Biology•2017

    The exceptional diversity of maternal lineages found in Serbians may be associated with the genetic impact of both autochthonous pre-Slavic Balkan populations whose mtDNA gene pool was affected by migrations of various populations over time (e.g. Bronze Age pastoralists) and Slavic and Germanic newcomers in the early Middle Ages

  • Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion

    Open Access•Marijana Rakonjac, Goran Čuturilo et al.•ARTICLE•Children•2024

    22q11.2 deletion syndrome (22q11.2DS), the most frequent microdeletion syndrome in humans, is related to a high risk of developing neurodevelopmental disorders. About 95% of patients with 22q11.2DS have speech and language impairments. Global articulation, story generation, and verbal memory tests were applied to compare articulatory characteristics of speech sounds, spontaneous language abilities, and immediate verbal memory between four groups …

Biology (2 obras) · Demography (2 obras) · Evolutionary biology (2 obras) · Forensic and Genetic Research (2 obras) · Gene (2 obras) · Gene pool (2 obras) · Genetic diversity (2 obras) · Genetics (2 obras) · Geography (2 obras) · History (2 obras)

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