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Autori: Maver Ales

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Naslov Discovery of PHB1 as a Novel Candidate Gene in Dominant Optic Atrophy (Article; Early Access)
Autori Volk Marija  Maver Ales  Vidmar Martina Jarc  Trost Nusa  Visnjar Tanja  Fakin Ana  Kovac Lea  Habjan Maja Sustar  Malinar Lucija  Petrovic Pajic Sanja MI  Jerman Urska Dragin  Romih Rok  Hawlina Marko  Peterlin Borut 
Info CLINICAL GENETICS, (2026), vol. br. , str. -
Projekat Slovenian Research Agency [P3-0326, P3-0333]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis (Meeting Abstract)
Autori Turk Aleksander  Maver Ales  Juvan Peter  Drulovic Jelena S  Mesaros Sarlota T  Novakovic Ivana V  Cizmarevic Nada S  Ristic Smiljana  Matic Ivana S  Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 1046-1046
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population (Meeting Abstract)
Autori Kovanda Anja  Susmelj Lara  Lukezic Tadeja  Maver Ales  Racki Valentino  Vuletic Vladimira  Svetel Marina V  Novakovic Ivana V  Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 797-798
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesis (Meeting Abstract)
Autori Podgrajsek Rebeka  Hodzic Alenka  Maver Ales  Stimpfel Martin  Andjelic Aleksander  Miljanovic Olivera  Ristanovic Momcilo  Novakovic Ivana V  Plaseska-Karanfilska Dijana  Noveski Predrag  Ostojic Sasa  Buretic-Tomljanovic Alena  Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 570-570
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Discovery of PHB1 as a novel candidate gene in dominant optic atrophy (Meeting Abstract)
Autori Volk Marija  Trost Nusa  Visnjar Tanja  Maver Ales  Vidmar Martina Jarc  Fakin Ana  Petrovic-Pajic Sanja  Hawlina Marko  Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 93-93
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study (Review)
Autori Podgrajsek Rebeka  Hodzic Alenka  Maver Ales  Stimpfel Martin  Andjelic Aleksander  Miljanovic Olivera  Ristanovic Momcilo  Novakovic Ivana V  Plaseska-Karanfilska Dijana  Noveski Predrag  Ostojic Sasa  Buretic-Tomljanovic Alena  Peterlin Borut 
Info REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, (2025), vol. 23 br. 1, str. -
Projekat Slovenian Research and Innovation Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility (Article)
Autori Podgrajsek Rebeka  Hodzic Alenka  Maver Ales  Stimpfel Martin  Andjelic Aleksander  Miljanovic Olivera  Ristanovic Momcilo  Novakovic Ivana V  Plaseska-Karanfilska Dijana  Noveski Predrag  Ostojic Sasa  Grskovic Antun  Buretic-Tomljanovic Alena  Peterlin Borut 
Info WORLD JOURNAL OF MENS HEALTH, (2025), vol. 43 br. 4, str. 908-917
Projekat Slovenian Research and Innovation Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease (Editorial Material; Early Access)
Autori Kovanda Anja  Susmelj Lara  Jaklic Helena  Lukezic Tadeja  Maver Ales  Petrovic Igor N  Dragasevic-Miskovic Natasa T  Svetel Marina V  Racki Valentino  Vuletic Vladimira  Novakovic Ivana V  Peterlin Borut 
Info CLINICAL GENETICS, (2025), vol. br. , str. -
Projekat Slovenian Research and Innovation Agency (ARIS) [P3-0326, J3-4517]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis (Article)
Autori Turk Aleksander  Maver Ales  Juvan Peter  Drulovic Jelena S  Mesaros Sarlota T  Novakovic Ivana V  Starcevic-Cizmarevic Nada  Ristic Smiljana  Stankovic-Matic Ivana  Peterlin Borut 
Info SCIENTIFIC REPORTS, (2025), vol. 15 br. 1, str. -
Projekat Slovenian Research Agency [P3-0326, P4-0220]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility (Article; Early Access)
Autori Podgrajsek Rebeka  Hodzic Alenka  Maver Ales  Stimpfel Martin  Andjelic Aleksander  Miljanovic Olivera  Ristanovic Momcilo  Novakovic Ivana V  Plaseska-Karanfilska Dijana  Noveski Predrag  Ostojic Sasa  Grskovic Antun  Buretic-Tomljanovic Alena  Peterlin Borut 
Info WORLD JOURNAL OF MENS HEALTH, (2025), vol. br. , str. -
Projekat Slovenian Research and Inno-vation Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
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