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Autori: Maver Ales

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Naslov Clinical Exome Sequencing in Serbian Patients with Movement Disorders - Single Centre Experience (Article)
Autori Brankovic Marija  Dragasevic Natasa T  Dobricic Valerija S  Maver Ales  Bergant Gaber  Petrovic Igor N  Peric Stojan Z  Marjanovic Ana  Jankovic Milena Z  Jancic Jasna B  Novakovic Ivana V  Peterlin Borut  Svetel Marina V  Kostic Vladimir K 
Info GENETIKA-BELGRADE, (2022), vol. 54 br. 1, str. 395-409
Projekat Serbian Ministry of education, science, and technological development [175090, 175091]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov De novo mutations in idiopathic male infertility-A pilot study (Article)
Autori Hodzic Alenka  Maver Ales  Plaseska-Karanfilska Dijana  Ristanovic Momcilo  Noveski Predrag  Zorn Branko  Terzic Marija  Kunej Tanja  Peterlin Borut 
Info ANDROLOGY, (2021), vol. 9 br. 1, str. 212-220
Projekat Slovenian Research Agency - Slovenia [P3-0326]; Ministry of Education and Science of R. Macedonia [17-4523/1]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (Article)
Autori Ruml-Stojanovic Jelena  Miletic Aleksandra  Peterlin Borut  Maver Ales  Mijovic Marija  Borlja Nikola  Dimitrijevic Brankica  Soldatovic Ivan A  Cuturilo Goran 
Info JOURNAL OF CHILD NEUROLOGY, (2020), vol. 35 br. 2, str. 116-131
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Clinical Next Generation Sequencing Reveals An H3f3a Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth Retardation (Article)
Autori Maver Ales  Cuturilo Goran  Stojanovic Ruml J  Peterlin Borut 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 65-68
Projekat Slovenian Research Agency - Slovenia [J3-8205, J3-9280, P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Rare missense TUBGCP5 gene variant in a patient with primary microcephaly (Article)
Autori Maver Ales  Cuturilo Goran  Kovanda Anja  Miletic Aleksandra  Peterlin Borut 
Info EUROPEAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 62 br. 12, str. -
Projekat ARRS research programme [P3-0326, J3-8205, J3-5506]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice (Article)
Autori Tumiene B  Maver Ales  Writzl Karin  Hodzic A  Cuturilo Goran  Kuzmanic-Samija Radenka  Culic V  Peterlin Borut 
Info CLINICAL GENETICS, (2018), vol. 93 br. 5, str. 1057-1062
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases (Article)
Autori Bergant Gaber  Maver Ales  Lovrecic Luca  Cuturilo Goran  Hodzic Alenka  Peterlin Borut 
Info GENETICS IN MEDICINE, (2018), vol. 20 br. 3, str. 303-312
Projekat Slovenian Research Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis (Article)
Autori Maver Ales  ...  Drulovic Jelena S  Pekmezovic Tatjana D  Novakovic Ivana V  ...  (broj koautora 19) 
Info SCIENTIFIC REPORTS, (2017), vol. 7 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility (Article)
Autori Hodzic Alenka  Ristanovic Momcilo  Zorn Branko  Tulic Cane Dz  Maver Ales  Novakovic Ivana V  Plaseska-Karanfilska Dijana  Peterlin Borut 
Info ANDROLOGY, (2017), vol. 5 br. 1, str. 70-74
Projekat Slovenian Research Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility (Article)
Autori Hodzic Alenka  Ristanovic Momcilo  Zorn Branko  Tulic Cane Dz  Maver Ales  Novakovic Ivana V  Peterlin Borut 
Info PLOS ONE, (2013), vol. 8 br. 3, str. -
Projekat National Research Agency of the Republic of Slovenia [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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