COBISS Kooperativni online bibliografski sistem in servisi COBISS

Gašper Klančar

Osebna bibliografija za obdobje 2008-2025

2008

1. ŠUSTER, Katja, KLADNIK, Urška, KLANČAR, Gašper, KONONENKO, Veno, ŠUSTER, Katja, LAMPIČ, Maruša, MARIČ, Ajda, MOHORIČ, Luka. Pomen gostiteljske rastline za mineralno prehrano parazitske rastline. Collectanea studentium physiologiae plantarum. [Tiskana izd.]. 2008, vol. 3, št. 1, str. 3-6, graf. prikazi. ISSN 1854-4185. [COBISS.SI-ID 256069632]

2011

2. KLANČAR, Gašper. Primerjava metod izolacije mezenhimskih matičnih celic iz humanega kostnega mozga z imunomagnetno selekcijo in adherenco na plastiko : diplomsko delo = Comparison of isolation methods of mesenchymal stem cells from human bone marrow using imunomagnetic selection or plastic adherence : graduation thesis. Ljubljana: [G. Klančar], 2011. XVII, 83 f., [2] f. pril., ilustr., preglednice. Biotehniška fakulteta, Študij biotehnologije, Diplomska dela, 56. http://www.digitalna-knjiznica.bf.uni-lj.si/dn_klancar_gasper.pdf, Repozitorij Univerze v Ljubljani – RUL. [COBISS.SI-ID 6777209]

2012

3. KLANČAR, Gašper, GROŠELJ, Urh, BRATINA, Nataša, BRATANIČ, Nevenka, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Genetic analysis of the LDLR gene in children with hypercholesterolemia. V: HUDLER, Petra (ur.), VIDETIČ PASKA, Alja (ur.), JUVAN, Peter (ur.). Molekularna medicina in biotehnologija = Molecular medicine and biotechnology : book of abstracts. Simpozij z mednarodno udele bo ob 40. obletnici In tituta za biokemijo in 20. obletnici Medicinskega centra za molekularno biologijo = International Symposium at 40th Anniversary of Institute of Biochemistry and_ 20th Anniversary of Medical Centre for Molecular Biology, Ljubljana, 27-29 June 2012. Ljubljana: Inštitut za biokemijo, Medicinska fakulteta: = Institute of Biochemistry, Faculty of Medicine, 2012. Str. 82. ISBN 978-961-267-050-4. [COBISS.SI-ID 354220]
4. KLANČAR, Gašper, GROŠELJ, Urh, BRATINA, Nataša, BRATANIČ, Nevenka, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina. The LDLR gene analysis in the slovene familial hypercholesterolemia (fh) population : a preliminary report. V: Programme. Gozd Martuljek: MESPE, 2012. Str. 350. Slovenska Pediatrija, let. 19. ISSN 1318-4423. [COBISS.SI-ID 664236]
5. GROŠELJ, Urh, KLANČAR, Gašper, BRATINA, Nataša, BRATANIČ, Nevenka, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Some characteristics of the Slovene familial hypercholesterolemia (FH) pediatric population : a preliminary report. V: Programme. Gozd Martuljek: MESPE, 2012. Str. 349. Slovenska Pediatrija, let. 19. ISSN 1318-4423. [COBISS.SI-ID 663980]

2013

6. KLANČAR, Gašper. Analiza gena za LDL receptor z uporabo presejalne metode denaturacijske tekočinske kromatografije visoke ločljivosti. V: Zbornik predavanj. 26. strokovni sestanek Terme Olimia, Hotel Sotelia, Podčetrtek, 12. in 13. april 2013. Ljubljana: Hematološko društvo laboratorijskih tehnikov, 2013. F. 8-9. [COBISS.SI-ID 867756]
7. GROŠELJ, Urh, KLANČAR, Gašper, BRATINA, Nataša, BRATANIČ, Nevenka, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Clinical and genetic characteristics of the paediatric heterozygous familial hypercholesterolaemia population in Slovenia: a preliminary report. V: Predictive medicine to improve the care of children : [abstracts]. 9th Joint Meeting of Paediatric Endocrinology, September 19-22, 2013, Milan, Italy. Milan: ESPE, 2013. Str. 107. [COBISS.SI-ID 1031340]
8. KLANČAR, Gašper, GROŠELJ, Urh, BRATINA, Nataša, BRATANIČ, Nevenka, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Genetic analysis in Slovene population of the children and adolescents with autosomal dominamt hypercholesterolemia. V: AČIMOVIČ, Jure (ur.), PROSENC ZMRZLJAK, Uršula (ur.), JUVAN, Peter (ur.). Book of abstracts. Casym Training Event Systems Medicine of Multifactorial Disorders Workshop & Tutorial and 8th CFGBC Symposium, Ljubljana, 12-15 June 2013. Ljubljana: Faculty of Medicine, 2013. Str. 37. ISBN 978-961-267-060-3. [COBISS.SI-ID 865452]
9. KLANČAR, Gašper, GROŠELJ, Urh, BRATINA, Nataša, BRATANIČ, Nevenka, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Genetic characteristics of hypercholesterolemia in children and adolescents in Slovenia. V: LOVREČIĆ, Luca (ur.), MAVER, Aleš (ur.). Book of abstracts. 10th Balkan Congress of Human Genetics [and] 2nd Alpe Adria Meeting of Human Genetics, Bled, Slovenia, 10.-12. October 2013. Ljubljana: Slovenian Association of Medical Genetics, 2013. Str. 49. ISBN 978-961-93050-2-7. [COBISS.SI-ID 1095852]
10. GROŠELJ, Urh, KLANČAR, Gašper, BRATINA, Nataša, BRATANIČ, Nevenka, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Genetski in klinični vidiki družinke hiperholesterolemije pri otrocih in mladostnikih v Slovenijii. V: KRŽIŠNIK, Ciril (ur.), BATTELINO, Tadej (ur.). Novosti v intenzivnem zdravljenju otrok. V Ljubljani: Medicinska fakulteta, Katedra za pediatrijo, 2013. Str. 45-54. Izbrana poglavja iz pediatrije, 25. ISBN 978-961-6454-27-8. ISSN 1408-354X. [COBISS.SI-ID 1247148]
11. GROŠELJ, Urh, KLANČAR, Gašper, BRATINA, Nataša, BRATANIČ, Nevenka. Genetski in klinični vidiki družinske hiperholesterolemije v Sloveniji : vabljeno predavanje na 31. Derčevih dnevih, Ljubljana, 14. in 15. junij 2013. 2013. [COBISS.SI-ID 1030828]
12. KLANČAR, Gašper, GROŠELJ, Urh, BRATINA, Nataša, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. LDLR and APOB gene analysis in the Slovene population of the children and adolescents with hypercholesteromia. V: Abstracts. Basel: Nature Pub. Group, 2013. Str. 15. European journal of human genetics, vol. 21, Suppl. 2. ISSN 1018-4813. [COBISS.SI-ID 1030572]

2014

13. HOVNIK, Tinka, ŠVIGELJ, Anja, KLANČAR, Gašper, BRATINA, Nataša, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina. APOE genetic variants are associated with plasma lipid levels in patients with type 1 diabetes. V: KOŠIR, Rok (ur.), JUVAN, Peter (ur.), PROSENC ZMRZLJAK, Uršula (ur.). From arrays and sequencing to understanding diseases : book of abstracts. Ljubljana: Faculty of Medicine, 2014. Str. 38. ISBN 978-961-267-081-8. http://cfgbc.mf.uni-lj.si/2014anniv9/abstracts/abstractsLectures.html, http://cfgbc.mf.uni-lj.si/2014anniv9/AbstractBook_2014.pdf. [COBISS.SI-ID 31639257]
14. KLANČAR, Gašper, MALOVRH, Petra, GROŠELJ, Urh, BRATINA, Nataša, BRATANIČ, Borut, BOŽIČ MIJOVSKI, Mojca, CEVC, Matija, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina. Early recognition of familial defective apolipoprotein B-100 with identification of common p.Arg3527Glu mutation. European journal of human genetics. 2014, vol. 22, suppl. 1, str. 119. ISSN 1018-4813. [COBISS.SI-ID 1648812]
15. KLANČAR, Gašper, MALOVRH, Petra, GROŠELJ, Urh, BRATANIČ, Nevenka, BRATINA, Nataša, BOŽIČ MIJOVSKI, Mojca, CEVC, Matija, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina. Familial defective apolipoprotein B-100 : early recognition with genetic testing. V: KOŠIR, Rok (ur.), JUVAN, Peter (ur.), PROSENC ZMRZLJAK, Uršula (ur.). From arrays and sequencing to understanding diseases : book of abstracts. Ljubljana: Faculty of Medicine, 2014. Str. 39. ISBN 978-961-267-081-8. http://cfgbc.mf.uni-lj.si/2014anniv9/abstracts/abstractsLectures.html, http://cfgbc.mf.uni-lj.si/2014anniv9/AbstractBook_2014.pdf. [COBISS.SI-ID 31639513]
16. GROŠELJ, Urh, KLANČAR, Gašper, POHLEVEN, Špela, BRATINA, Nataša, BRATANIČ, Nevenka, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Familial hypercholesterolemia in children and adolescents. V: BAJUK-STUDEN, Katica (ur.), et al. Zbornik predavanj in izvlečkov prostih tem = Book of proceedings and abstracts. Ljubljana: Združenje endokrinologov Slovenije pri Slovenskem zdravniškem društvu: Slovensko osteološko društvo, 2014. Str. 149-152. ISBN 978-961-91692-7-8. [COBISS.SI-ID 1998252]
17. KOVAČ, Jernej, KLANČAR, Gašper, BATTELINO, Saba, TREBUŠAK PODKRAJŠEK, Katarina. The identification of possible causative genetic variants in two siblings with idiopathic hearing loss using exome sequencing. V: 3rd Course in next generation sequencing. Bertinoro di Romagna: European Genetics Foundation, 2014. Str. 29-30. [COBISS.SI-ID 1482924]
18. KLANČAR, Gašper, TREBUŠAK PODKRAJŠEK, Katarina. Opredelitev genetskih vzrokov hiperholesterolomij : vabljeno predavanje na strokovnem srečanju ZLMS, Laboratorijska diagnostika, 19. 5. 2014, Ljubljana. 2014. [COBISS.SI-ID 1649068]
19. KLANČAR, Gašper, TREBUŠAK PODKRAJŠEK, Katarina. Opredelitev genskih vzrokov hiperholesterolemij = Determination of genetic causes of hypercholesterolemia. V: AVBERŠEK-LUŽNIK, Ivica (ur.), BOŽIČ, Borut (ur.). Zbornik delovanja ZLMS 2014. Ljubljana: Zbornica laboratorijske medicine Slovenije, 2014. Str. 82-85. ISBN 978-961-93148-1-4. [COBISS.SI-ID 2100396]
20. KOVAČ, Jernej, MACEDONI-LUKŠIČ, Marta, TREBUŠAK PODKRAJŠEK, Katarina, KLANČAR, Gašper, BATTELINO, Tadej. Rare single nucleotide polymorphisms in the regulatory regions of the superoxide dismutase genes in autism spectrum disorder. Autism research. 2014, vol. 7, iss. 1, str. 138-144. ISSN 1939-3806. http://onlinelibrary.wiley.com/doi/10.1002/aur.1345/abstracte, DOI: 10.1002/aur.1345. [COBISS.SI-ID 1272236]

2015

21. HOVNIK, Tinka, KLANČAR, Gašper, ŠVIGELJ, Anja, BRATINA, Nataša, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Apolipoprotein E gene polymorphisms and lipid levels in patients with T1D. European journal of human genetics. 2015, vol. 23, suppl. 1, str. 329. ISSN 1018-4813. [COBISS.SI-ID 2418092]
22. TREBUŠAK PODKRAJŠEK, Katarina, KLANČAR, Gašper, KOVAČ, Jernej, BATTELINO, Tadej, BATTELINO, Saba. Autosomal recessive nonsyndromic hearing loss due to TMPRSS3 mutations in Slovenia. European journal of human genetics. 2015, vol. 23, suppl. 1, str. 73. ISSN 1018-4813. [COBISS.SI-ID 2417836]
23. BATTELINO, Saba, TREBUŠAK PODKRAJŠEK, Katarina, KLANČAR, Gašper, KOVAČ, Janko, BERTOK, Sara, BATTELINO, Tadej. Genetic background of autosomal recessive nonsyndromic hearing loss in Slovenian population. V: JAKŠE, Jernej (ur.), et al. Genetika 2015 : book of abstracts. 7th Congress of the Genetic Society of Slovenia and 7th Meeting of the Slovenian Society of Human Genetics, 20-23 September 2015, Rogaška Slatina, Slovenia. Ljubljana: Genetic Society of Slovenia: The Slovenian Society of Human Genetics, 2015. Str. 25. ISBN 978-961-93545-2-0. [COBISS.SI-ID 2623148]
24. KOVAČ, Jernej, TREBUŠAK PODKRAJŠEK, Katarina, KLANČAR, Gašper, BERTOK, Sara, AVBELJ STEFANIJA, Magdalena, MLAKAR, Gorazd, BATTELINO, Tadej. Identification of rare genetic disorders in paediatric population using NGS. V: LOVREČIĆ, Luca (ur.), MAVER, Aleš (ur.). New generation sequencing in clinical medicine : abstract book. Ljubljana: Slovenian Association of Medical Genetics, Slovene Medical Society, 2015. Str. 12-13. ISBN 978-961-93050-3-4. [COBISS.SI-ID 2503852]
25. KLANČAR, Gašper, GROŠELJ, Urh, KOVAČ, Jernej, BRATANIČ, Nevenka, BRATINA, Nataša, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina. Implementation of next generation sequencing in national universal hypercholesterolemia screening. V: LOVREČIĆ, Luca (ur.), MAVER, Aleš (ur.). New generation sequencing in clinical medicine : abstract book. Ljubljana: Slovenian Association of Medical Genetics, Slovene Medical Society, 2015. Str. 10-11. ISBN 978-961-93050-3-4. [COBISS.SI-ID 2446508]
26. DEBELJAK, Maruša, KLANČAR, Gašper, MAZIĆ, Uroš, ŠINKOVEC, Matjaž, KOVAČ, Jernej. New generation sequencing in Long QT syndrome. V: LOVREČIĆ, Luca (ur.), MAVER, Aleš (ur.). New generation sequencing in clinical medicine : abstract book. Ljubljana: Slovenian Association of Medical Genetics, Slovene Medical Society, 2015. Str. 16. ISBN 978-961-93050-3-4. [COBISS.SI-ID 2447020]
27. KOREN, Simon, TOPLAK, Nataša, TREBUŠAK PODKRAJŠEK, Katarina, KLANČAR, Gašper, BATTELINO, Saba, KOVAČ, Minka. Next generation sequencing and genetic variant analysis In otoslerosis. V: PFAFFL, Michael W. (ur.). qPCR & NGS 2015 : Advanced molecular diagnostics for biomarker discovery : event proceedings. 7th International qPCR & NGS Symposium Industrial Exhibition & Application Workshops, 23rd-27th March 2015, Freising-Weihenstephan, Germany. Freising: Technical University Munich (TUM): Technische Universität München (TUM), 2015. Str. 37. ISBN 978-3-00-048805-4. [COBISS.SI-ID 3552335]
28. KOVAČ, Urša, KOŠIR, Rok, FUŽIR, Natalija, LEWINSKA, Monika, KOVAČ, Jernej, KLANČAR, Gašper, TREBUŠAK PODKRAJŠEK, Katarina, KOTNIK, Primož, BATTELINO, Tadej, ROZMAN, Damjana. PNPLA3 as a potential marker for non-alcoholic fatty liver disease in children with familial hypercholesterolemia?. V: AČIMOVIČ, Jure (ur.), et al. Book of abstracts. 10th CFGBC Symposium with ISBE and CASyM workshops From functional genomics to systems biology and systems medicine & Hands-on tutorial systems biology/medicine, Ljubljana, June 30 - July 3, 2015. Ljubljana: Faculty of Medicine, 2015. Str. 28. ISBN 978-961-267-092-4. [COBISS.SI-ID 32057817]
29. KLANČAR, Gašper, KOVAČ, Jernej, BATTELINO, Tadej, BATTELINO, Saba, TREBUŠAK PODKRAJŠEK, Katarina. A rareform of autosomal recessive nonsyndromic hearing loss due to mutation in TMPRSS3 or ILDR1 genes. V: LOVREČIĆ, Luca (ur.), MAVER, Aleš (ur.). New generation sequencing in clinical medicine : abstract book. Ljubljana: Slovenian Association of Medical Genetics, Slovene Medical Society, 2015. Str. 15. ISBN 978-961-93050-3-4. [COBISS.SI-ID 2446764]
30. KLANČAR, Gašper, GROŠELJ, Urh, KOVAČ, Jernej, BRATANIČ, Nevenka, BRATINA, Nataša, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej. Universal screening for familial hypercholesterolemia in children. Journal of the American college of cardiology. [Print ed.]. Sep. 2015, vol. 66, iss. 11, str. 1250-1257. ISSN 0735-1097. http://www.sciencedirect.com/science/article/pii/S0735109715044629, DOI: 10.1016/j.jacc.2015.07.017. [COBISS.SI-ID 32206809]

2016

31. KLANČAR, Gašper. Genetske značilnosti hiperholesterolemij pri otrocih in mladostnikih v Sloveniji : doktorsko delo = Genetic charateristics of hypercholesterolemia in children and adolescents in Slovenia : doctoral thesis. Ljubljana: [G. Klančar], 2016. XV, 84 f., 1. f. pril., tabele, graf. prikazi. Repozitorij Univerze v Ljubljani – RUL, Digitalna knjižnica Slovenije - dLib.si. [COBISS.SI-ID 283890432]
32. KOVAČ, Jernej, KLANČAR, Gašper, TESOVNIK, Tine, GROŠELJ, Urh, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina. Introduction of a routine NGS-based genetic screening into the universal screening programme for hypercholesterolemia in Slovenian 5-years old children. European journal of human genetics. 2016, suppl. 1, vol. 24, str. 86. ISSN 1018-4813. [COBISS.SI-ID 3477420]
33. TREBUŠAK PODKRAJŠEK, Katarina, KLANČAR, Gašper, GROŠELJ, Urh, KOVAČ, Jernej, BATTELINO, Tadej. Next generation sequencing in clinical diagnosis of familial hypercholesterolemia. V: URLEP, Žiga (ur.), JUVAN, Peter (ur.). Book of abstracts. Elixir-si Launch & 11th CFGBC Symposium Data for Life, Ljubljana, September 20 - September 21, 2016. Ljubljana: Faculty of Medicine, 2016. Str. 15. ISBN 978-961-267-113-6. http://cfgbc.mf.uni-lj.si/2016data4life/abstracts/Book_of_Abstracts.pdf. [COBISS.SI-ID 3478188]
34. BATTELINO, Saba, KLANČAR, Gašper, KOVAČ, Jernej, BATTELINO, Tadej, TREBUŠAK PODKRAJŠEK, Katarina. TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss. European archives of oto-rhino-laryngology. May 2016, vol. 273, iss. 5, str. 1151-1154. ISSN 0937-4477. http://dx.doi.org/10.1007/s00405-015-3671-0, DOI: 10.1007/s00405-015-3671-0. [COBISS.SI-ID 2417580]

2017

35. KLANČAR, Gašper, ŠETRAJČIČ DRAGOŠ, Vita, NOVAKOVIĆ, Srdjan. Detection of copy number variations with next generation sequencing : laboratory validation. V: The ESHG 2017 programme planner : 1967-2017 - 50th Anniversary Meeting. Vienna: European Society of Human Genetics. 2017, str. p14.021a. http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=4ec03764-b275-4784-bf0e-8b0b491f3582&cKey=dd8d66d7-8c7b-4335-8ee3-63e7099e2c1a&mKey=15a3630e-7769-4d64-a80a-47f190ac2f4f. [COBISS.SI-ID 3174779]
36. KOVAČ, Jernej, KLANČAR, Gašper, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Saba. Discovering the unexpected with the utilization of NGS in diagnostics of non-syndromic hearing loss disorders : the family case of ILDR1-dependent hearing loss disorder. Frontiers in genetics. Jun. 2017, vol. 8, str. 1-6. ISSN 1664-8021. http://journal.frontiersin.org/article/10.3389/fgene.2017.00095/full, DOI: 10.3389/fgene.2017.00095. [COBISS.SI-ID 3926188]

2018

37. BLATNIK, Ana, STROJNIK, Ksenija, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, KRAJC, Mateja. Breast cancer in Slovene CHEK2 mutation carriers. V: The ESHG 2018 programme. Milan: European Society of Human Genetics, 2018. http://www.abstractsonline.com/pp8/#!/4652/presentation/2822. [COBISS.SI-ID 3002747]
38. ŠKOF, Erik, GORNJEC, Andreja, NOVAKOVIĆ, Srdjan, STEGEL, Vida, KRAJC, Mateja, STROJNIK, Ksenija, BLATNIK, Ana, BEBAR, Sonja, DJURIŠIĆ, Astrid, MERLO, Sebastjan, POHAR-MARINŠEK, Živa, KLOBOVES-PREVODNIK, Veronika, GAZIĆ, Barbara, HOČEVAR, Marko, ŠKERL, Petra, KLANČAR, Gašper, ŠETRAJČIČ DRAGOŠ, Vita. Detection of BRCA 1/2 mutations from cytological samples in patients with high grade serous ovarian cancer. International journal of gynecological cancer. [Print ed.]. 2018, vol. 28, suppl. 2, str. 840. ISSN 1048-891X. [COBISS.SI-ID 40883203]
39. KRAJC, Mateja, BLATNIK, Ana, NORČIČ, Gregor, NOVAKOVIĆ, Srdjan, STEGEL, Vida, TAVČAR, Jana, STROJNIK, Ksenija, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper. Genetic and clinical characteristics of registry-validated pedigrees of Lynch syndrome families in Slovenia : first report. V: Abstracts. Third meeting of the European Hereditary Tumour Group, 23-25 September 2018, Nice, France. Str. 27-28. https://ehtg.org/2018/08/n44-genetic-and-clinical-characteristics-of-registry-validated-pedigrees-of-lynch-syndrome-families-in-slovenia-first-report/. [COBISS.SI-ID 3046011]
40. ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, STEGEL, Vida, BLATNIK, Ana, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. The importance of functional mRNA analysis in clinical variant interpretation. V: SKOČAJ, Matej (ur.). Genetika 2018 : book of abstracts. 8th Congress of the Genetics Society of Slovenia [and] 8th Meeting of the Slovenian Society of Human Genetics, September 19-21, 2018. Ljubljana: Slovensko genetsko društvo: = Genetics Society of Slovenia, 2018. Str. 35. ISBN 978-961-93545-5-1. http://genetika2018.alfa-faktor.si/. [COBISS.SI-ID 3014779]

2019

41. STROJNIK, Ksenija, KRAJC, Mateja, BANJAC, Marta, STEGEL, Vida, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, BLATNIK, Ana. CDH1 pathogenic variants in patients who do not fulfill testing criteria are not necessarily incidental findings. V: ESHG 2019. Gothenburg: European Society of Human Genetics, 2019. Str. p12.031d. https://www.abstractsonline.com/pp8/#!/7874/presentation/2967. [COBISS.SI-ID 3273339]
42. ŠETRAJČIČ DRAGOŠ, Vita, ŠKERL, Petra, KLANČAR, Gašper, STEGEL, Vida, BOMBAČ, Alenka, NOVAKOVIĆ, Srdjan. Classification of novel variants in clinilally important genes beyond hotspot codons. V: ESHG 2019. Gothenburg: European Society of Human Genetics, 2019. Str. e-p12.21. https://www.abstractsonline.com/pp8/#!/7874/presentation/2759. [COBISS.SI-ID 3321467]
43. KRAJC, Mateja, BLATNIK, Ana, NORČIČ, Gregor, NOVAKOVIĆ, Srdjan, STEGEL, Vida, TAVČAR, Petra, STROJNIK, Ksenija, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper. Genetic and clinical characteristics of registry-validated pedigrees of Lynch syndrome families in Slovenia : first report. Hereditary Cancer in Clinical Practice. 2019, vol. 17, suppl. 2, str. 10. ISSN 1731-2302. [COBISS.SI-ID 3483515]
44. BANJAC, Marta, BLATNIK, Ana, STROJNIK, Ksenija, STEGEL, Vida, NOVAKOVIĆ, Srdjan, ŠETRAJČIČ DRAGOŠ, Vita, ŠKERL, Petra, KLANČAR, Gašper, KRAJC, Mateja. High prevalence of BRCA mutations among Slovenian triple-negative breast cancer patients. V: ESHG 2019. Gothenburg: European Society of Human Genetics, 2019. Str. p12.148a. https://www.abstractsonline.com/pp8/#!/7874/presentation/3095. [COBISS.SI-ID 3351163]
45. BLATNIK, Ana, STEGEL, Vida, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, STROJNIK, Ksenija, NOVAKOVIĆ, Srdjan, NORČIČ, Gregor, KRAJC, Mateja. Pathogenic variants in Slovenian patients with APC-associated polyposis. Familial cancer. [Print ed.]. 2020, vol. 19, iss. 4, str. 116. ISSN 1389-9600. [COBISS.SI-ID 29436163]
46. ŠETRAJČIČ DRAGOŠ, Vita, BLATNIK, Ana, KLANČAR, Gašper, STEGEL, Vida, KRAJC, Mateja, BLATNIK, Olga, NOVAKOVIĆ, Srdjan. Two novel NF1 pathogenic variants causing the creation of a new splice site in patients with neurofibromatosis type I. Frontiers in genetics. Aug. 2019, vol. 10, str. 1-8. ISSN 1664-8021. https://doi.org/10.3389/fgene.2019.00762, DOI: 10.3389/fgene.2019.00762. [COBISS.SI-ID 3321211]

2020

47. KLANČAR, Gašper, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, STEGEL, Vida, BLATNIK, Ana, STROJNIK, Ksenija, BANJAC, Marta, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Clinically important variants in slovene bilateral breast cancer patients tested between 2014 and 2019. V: ESHG 2020.2 : live in your living room : European Human Genetics Virtual Conference : June 6-9, 2020. Vienna: European Society of Human Genetics. 2020, [1] str. https://www.abstractsonline.com/pp8/#!/9102/presentation/1331. [COBISS.SI-ID 29452803]
48. STROJNIK, Ksenija, KRAJC, Mateja, BANJAC, Marta, STEGEL, Vida, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, BLATNIK, Ana. First results of germline genetic testing in Slovenian patients with prostate cancer. V: ESHG 2020.2 : live in your living room : European Human Genetics Virtual Conference : June 6-9, 2020. Vienna: European Society of Human Genetics. 2020, [1] str. https://www.abstractsonline.com/pp8/#!/9102/presentation/1505. [COBISS.SI-ID 29451267]
49. BOMBAČ, Alenka, ZAKOTNIK, Branko, BUČIĆ, Marina, ŠETRAJČIČ DRAGOŠ, Vita, GAZIĆ, Barbara, STEGEL, Vida, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan. Mutational spectrum and classification of novel mutations in patients with metastatic gastrointestinal stromal tumours. International journal of oncology. [Print ed.]. 2020, vol. 56, iss. 6, str. 1468-1478. ISSN 1019-6439. DOI: 10.3892/ijo.2020.5028. [COBISS.SI-ID 3514491]
50. KLANČAR, Gašper, BLATNIK, Ana, ŠETRAJČIČ DRAGOŠ, Vita, VOGRIČ, Vesna, STEGEL, Vida, BLATNIK, Olga, DREV, Primož, GAZIĆ, Barbara, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. A novel germline MLH1 in-frame deletion in a Slovenian Lynch syndrome family associated with uncommon isolated PMS2 loss in tumor tissue. Genes. 2020, vol. 11, no. 3, str. 325-1-325-14. ISSN 2073-4425. https://www.mdpi.com/2073-4425/11/3/325, DOI: 10.3390/genes11030325. [COBISS.SI-ID 3513723]
51. BLATNIK, Ana, BANJAC, Marta, STROJNIK, Ksenija, HOTUJEC, Simona, STEGEL, Vida, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, BORŠTNAR, Simona, BEŠIĆ, Nikola, ŽGAJNAR, Janez, PERHAVEC, Andraž, KRAJC, Mateja. Prevalence of BRCA1/2 pathogenic variants in triple negative breast cancer patients stratified according to age at diagnosis. V: ASCO Virtual Scientific Program : ASCO Meeting Library, 2020. https://meetinglibrary.asco.org/record/189576/abstract. [COBISS.SI-ID 15645443]

2021

52. KLANČAR, Gašper, BLATNIK, Ana, ŠETRAJČIČ DRAGOŠ, Vita, VOGRIČ, Vesna, STEGEL, Vida, BLATNIK, Olga, DREV, Primož, GAZIĆ, Barbara, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Association of novel germline MLH1 in-frame deletion with uncommon isolated PMS2 loss in tumor tissue : Elektronski vir. V: Abstract library. [S. l.]: European Society of Human Genetics, 2021. Str. [1]. https://www.abstractsonline.com/pp8/#!/10372/presentation/1305. [COBISS.SI-ID 81416451]
53. ŠKERL, Petra, KLANČAR, Gašper, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, VOGRIČ, Vesna, BOMBAČ, Alenka, ZAGOŽEN KLASINC, Anja, KOKOVIĆ, Ira, BLATNIK, Ana, STROJNIK, Ksenija, BANJAC, Marta, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Determination of Lynch syndrome related colorectal cancer based on tumor testing for microsatellite instability, BRAF V600E and MLH1 promoter hypermethylation among Slovene patients : Elektronski vir. V: Abstract library. [S. l.]: European Society of Human Genetics, 2021. Str. [1]. https://www.abstractsonline.com/pp8/#!/10372/presentation/1277. [COBISS.SI-ID 77388547]
54. STEGEL, Vida, KLANČAR, Gašper, ANŽIČ, Nina, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, BOMBAČ, Alenka, ZAGOŽEN KLASINC, Anja, VOGRIČ, Vesna, KRAJC, Mateja, BLATNIK, Ana, STROJNIK, Ksenija, BANJAC, Marta, NOVAKOVIĆ, Srdjan. Frequency of pathogenic variants in Fanconi anemia genes in hereditary breast and ovarian cancer families : Elektronski vir. V: Abstract library. [S. l.]: European Society of Human Genetics, 2021. Str. [1]. https://www.abstractsonline.com/pp8/#!/10372/presentation/1236. [COBISS.SI-ID 77380867]
55. STROJNIK, Ksenija, OPALIČ, Iva, KRAJC, Mateja, BANJAC, Marta, STEGEL, Vida, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, BLATNIK, Ana. MUTYH-associated polyposis in a cohort of Slovenian patients with adenomatous polyposis : Elektronski vir. V: Abstract library. [S. l.]: European Society of Human Genetics, 2021. Str. 1297. https://www.abstractsonline.com/pp8/#!/10372/presentation/1297. [COBISS.SI-ID 77371907]
56. ŠETRAJČIČ DRAGOŠ, Vita, STEGEL, Vida, BLATNIK, Ana, KLANČAR, Gašper, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. New approach for detection of normal alternative splicing events and aberrant spliceogenic transcripts with long-range PCR and deep RNA sequencing. Biology. 2021, vol. 10, no. 8, str. 706-1-706-12. ISSN 2079-7737. https://www.mdpi.com/2079-7737/10/8/706, DiRROS - Digitalni repozitorij raziskovalnih organizacij Slovenije, DOI: 10.3390/biology10080706. [COBISS.SI-ID 74741763]
57. OPALIČ, Iva, STROJNIK, Ksenija, KRAJC, Mateja, BANJAC, Marta, STEGEL, Vida, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, BLATNIK, Ana. NTHL1-tumor syndrome in Slovenian patients with adenomatous polyposis : Elektronski vir. V: Abstract library. [S. l.]: European Society of Human Genetics, 2021. Str. 1306. https://www.abstractsonline.com/pp8/#!/10372/presentation/1306. [COBISS.SI-ID 77394947]
58. ŠETRAJČIČ DRAGOŠ, Vita, ZAGOŽEN KLASINC, Anja, KLANČAR, Gašper, ŠKERL, Petra, STEGEL, Vida, BLATNIK, Ana, STROJNIK, Ksenija, BANJAC, Marta, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Reevaluation of variants c.93C>G and c.993G>C in BRCA1 gene. Molecular genetics and metabolism. 2021, vol. 132, suppl. 1, str. s230-s231. ISSN 1096-7192. [COBISS.SI-ID 67007491]

2022

59. BLATNIK, Ana, RIBNIKAR, Domen, ŠETRAJČIČ DRAGOŠ, Vita, NOVAKOVIĆ, Srdjan, STEGEL, Vida, GRČAR-KUZMANOV, Biljana, BOC, Nina, PERIĆ, Barbara, ŠKERL, Petra, KLANČAR, Gašper, KRAJC, Mateja. BAP1-defficient breast cancer in a patient with BAP1 cancer syndrome. Breast cancer. 2022, vol. 29, str. 921–927. ISSN 1340-6868. DiRROS - Digitalni repozitorij raziskovalnih organizacij Slovenije, DOI: 10.1007/s12282-022-01354-0. [COBISS.SI-ID 104001539]
60. UNK, Mojca, BOMBAČ, Alenka, JEZERŠEK NOVAKOVIĆ, Barbara, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, BLATNIK, Olga, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan. Correlation of treatment outcome in sanger/RT-qPCR KIT/PDGFRA wild-type metastatic gastrointestinal stromal tumors with next-generation sequencing results : a single-center report. Oncology reports. 2022, vol. 48, no. 3, str. 167-1-167-10. ISSN 1021-335X. DOI: 10.3892/or.2022.8382. [COBISS.SI-ID 118337283]
61. ŠETRAJČIČ DRAGOŠ, Vita, STROJNIK, Ksenija, KLANČAR, Gašper, ŠKERL, Petra, STEGEL, Vida, BLATNIK, Ana, BANJAC, Marta, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Identification of spliceogenic variants beyond canonical GT-AG splice sites in hereditary cancer genes. International journal of molecular sciences. 2022, vol. 23, no. 13, str. 7446-1-7446-14. ISSN 1422-0067. https://www.mdpi.com/1422-0067/23/13/7446, DiRROS - Digitalni repozitorij raziskovalnih organizacij Slovenije, DOI: 10.3390/ijms23137446. [COBISS.SI-ID 114023427]
62. KLANČAR, Gašper, ŠETRAJČIČ DRAGOŠ, Vita. Novel germline MLH1 in-frame deletion associated with uncommon isolated PMS2 loss in tumor tissue. V: ZORC, Minja (ur.), DOVČ, Peter (ur.). Proceedings of Genetika 2022 : 9th Congress of the Genetic Society of Slovenia and [9th] meeting of the Slovenian Society for Human Genetics with international participation : Ljubljana, September 28-30, 2022. Ljubljana: Genetic Society of Slovenia, 2022. Str. 69. ISBN 978-961-93545-7-5. [COBISS.SI-ID 213430787]
63. STEGEL, Vida, BLATNIK, Ana, ŠKOF, Erik, ŠETRAJČIČ DRAGOŠ, Vita, KRAJC, Mateja, GREGORČIČ, Brigita, ŠKERL, Petra, STROJNIK, Ksenija, KLANČAR, Gašper, BANJAC, Marta, ŽGAJNAR, Janez, RAVNIK-OBLAK, Maja, NOVAKOVIĆ, Srdjan. Real-world data on detection of germline and somatic pathogenic/likely pathogenic variants in BRCA1/2 and other susceptibility genes in ovarian cancer patients using next generation sequencing. Cancers. Mar. 2022, vol. 14, no. 6, str. 1434-1-1434-17. ISSN 2072-6694. https://www.mdpi.com/2072-6694/14/6/1434, DiRROS - Digitalni repozitorij raziskovalnih organizacij Slovenije, DOI: 10.3390/cancers14061434. [COBISS.SI-ID 100563715]
64. BLATNIK, Ana, STROJNIK, Ksenija, BANJAC, Marta, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, ŠKERL, Petra, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, KRAJC, Mateja. Triple-negative breast cancer in association with RAD51C pathogenic variants. European journal of human genetics. Jun. 2022, vol. 31, suppl. 1, str. [1]. ISSN 1476-5438. https://www.nature.com/articles/s41431-023-01338-4. [COBISS.SI-ID 189779715]

2023

65. BLATNIK, Ana, ŠETRAJČIČ DRAGOŠ, Vita, STEGEL, Vida, ŠKERL, Petra, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, KRAJC, Mateja. Genetic analysis of archival tissue when testing for hereditary cancer predispositions. V: OSREDKAR, Joško (ur.). Book of Abstracts : 46th ISOBM Congress 13th - 17th October, Bled, Slovenia. Basel: [S. Karger], 2023. Str. [1]. Tumor Biology (Online), Vol.46, iss. s1. ISSN 1010-4283. https://content.iospress.com/journals/tumor-biology/45/s1. [COBISS.SI-ID 189628675]
66. ŠKERL, Petra, BOMBAČ, Alenka, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, ZAGOŽEN KLASINC, Anja, NOVAKOVIĆ, Srdjan. Methylation status of mismatch repair genes in endometrial and colorectal cancer. V: OSREDKAR, Joško (ur.). Book of Abstracts : 46th ISOBM Congress 13th - 17th October, Bled, Slovenia. Basel: [S. Karger], 2023. Str. [1]. Tumor Biology (Online), Vol.46, iss. s1. ISSN 1010-4283. https://content.iospress.com/journals/tumor-biology/45/s1. [COBISS.SI-ID 189631491]
67. BLATNIK, Ana, ŠETRAJČIČ DRAGOŠ, Vita, BLATNIK, Olga, STEGEL, Vida, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, DREV, Primož, ŽAGAR, Tina, STROJNIK, Ksenija, MERLO, Sebastjan, ŠKOF, Erik, PAVLOVA BOJADŽISKI, Mirjana. Molecular and clinical characteristics of Slovenian patients with small cell carcinoma of the ovary, hypercalcemic type. V: KRANJC BREZAR, Simona (ur.), ČEMAŽAR, Maja (ur.), MARKELC, Boštjan (ur.). 9th Colloquium of Genetics : book of abstracts : September 29th 2023, National Institute of Biology, Marine Biology Station Piran. Ljubljana: Genetic Society of Slovenia in collaboration with the Slovenian Society of Human Genetics, 2023. Str. 31-32. ISBN 978-961-93545-8-2. https://sgd.si/docs/Colloquium-9th-2023.pdf. [COBISS.SI-ID 168420355]
68. ŠETRAJČIČ DRAGOŠ, Vita, STEGEL, Vida, KLANČAR, Gašper, ŠKERL, Petra, ZAGOŽEN KLASINC, Anja, NOVAKOVIĆ, Srdjan. Mutation profile of metastatic castration-resistant prostate cancer patients prior to olaparib treatment - EMA vs. FDA. European journal of human genetics. Jun. 2023, vol. 31, suppl. 1, str. 548-549. ISSN 1476-5438. https://www.nature.com/articles/s41431-023-01338-4. [COBISS.SI-ID 189777923]
69. STEGEL, Vida, ŠKERL, Petra, ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, ZAGOŽEN KLASINC, Anja, BOMBAČ, Alenka, HERTL, Gregor, VOGRIČ, Vesna, STROJNIK, Ksenija, NOVAKOVIĆ, Aleksander, BLATNIK, Ana, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Pathogenic variants in genes involved in homologous recombination and mismatch repair among prostate cancer patient. European journal of human genetics. Jun. 2023, vol. 32, suppl. 1, str. [1]. ISSN 1476-5438. https://www.nature.com/articles/s41431-023-01481-y. [COBISS.SI-ID 189793283]
70. KLANČAR, Gašper, ŠETRAJČIČ DRAGOŠ, Vita, STEGEL, Vida, ZAGOŽEN KLASINC, Anja, BOMBAČ, Alenka, ŠKERL, Petra, NOVAKOVIĆ, Srdjan. Reclassification of germline variants in cancer susceptibility genes implementing ACMG/AMP guidelines. European journal of human genetics. Jun. 2023, vol. 31, suppl. 1, str. 264. ISSN 1476-5438. https://www.nature.com/articles/s41431-023-01339-3. [COBISS.SI-ID 189783555]
71. ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, STEGEL, Vida, ŠKERL, Petra, BLATNIK, Ana, STROJNIK, Ksenija, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Reklasifikacija različic nejasnega kliničnega pomena z analizo mRNA iz krvi. V: BABIĆ BOŽOVIĆ, Ivana (ur.), LOVREČIĆ, Luca (ur.). Novosti na področju redkih bolezni v Sloveniji : 8. simpozij slovenske medicinske genetike : knjiga povzetkov : UKC Ljubljana, 10. november 2023. Ljubljana: Združenje za medicinsko genetiko, Slovensko zdravniško društvo, 2023. Str. 32. ISBN 978-961-93050-6-5. https://www.dlib.si/stream/URN:NBN:SI:doc-HFSD25A0/761c7f29-27ec-498f-9c5b-4dc338f47240/PDF. [COBISS.SI-ID 189668099]
72. KLANČAR, Gašper, NOVAKOVIĆ, Aleksander, BLATNIK, Ana, ŠETRAJČIČ DRAGOŠ, Vita, STEGEL, Vida, ŠKERL, Petra, ZAGOŽEN KLASINC, Anja, STROJNIK, Ksenija, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Somatic APC mosaicism as a cause of adenomatous polyposis. European journal of human genetics. Jun. 2023, vol. 32, suppl. 1, str. [1]. ISSN 1476-5438. https://www.nature.com/articles/s41431-023-01481-y. [COBISS.SI-ID 189789955]
73. BLATNIK, Ana, STROJNIK, Ksenija, BANJAC, Marta, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, ŠKERL, Petra, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, KRAJC, Mateja. Triple-negative breast cancer in association with RAD51C pathogenic variants. European journal of human genetics. Jun. 2023, vol. 31, suppl. 1, str. 551. ISSN 1476-5438. https://www.nature.com/collections/idgiceffji. [COBISS.SI-ID 236630531]
74. ŠETRAJČIČ DRAGOŠ, Vita, STROJNIK, Ksenija, KLANČAR, Gašper, ŠKERL, Petra, STEGEL, Vida, BANJAC, Marta, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. The use of RNAseq in discovery of splicing abnormalities. V: OSREDKAR, Joško (ur.). Book of Abstracts : 46th ISOBM Congress 13th - 17th October, Bled, Slovenia. Basel: [S. Karger], 2023. Str. [1]. Tumor Biology (Online), Vol.46, iss. s1. ISSN 1010-4283. https://content.iospress.com/journals/tumor-biology/45/s1. [COBISS.SI-ID 189635587]
75. ŠETRAJČIČ DRAGOŠ, Vita, KLANČAR, Gašper, STEGEL, Vida, ŠKERL, Petra, BLATNIK, Ana, STROJNIK, Ksenija, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Variants causing splicing defects – challenging cases. European journal of human genetics. Jun. 2023, vol. 32, suppl. 1, str. [1]. ISSN 1476-5438. https://www.nature.com/articles/s41431-023-01482-x. [COBISS.SI-ID 189788675]

2024

76. ŠKOF, Erik, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, BLATNIK, Ana, GREGORIČ, Brigita, ŠKERL, Petra, KLANČAR, Gašper, ZAGOŽEN KLASINC, Anja, BOMBAČ, Alenka, KRAJC, Mateja, NOVAKOVIĆ, Srdjan. Exploring the impact of BRCA1 and BRCA2 mutation type and location on olaparib maintenance therapy in platinum-sensitive relapsed ovarian cancer patients : a single center report. Gynecologic oncology. [Print ed.]. Nov. 2024, vol. 190, str. 104-112, ilustr. ISSN 0090-8258. DOI: 10.1016/j.ygyno.2024.08.012. [COBISS.SI-ID 205458179]
77. BLATNIK, Ana, ŠETRAJČIČ DRAGOŠ, Vita, BLATNIK, Olga, STEGEL, Vida, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, DREV, Primož, ŽAGAR, Tina, MERLO, Sebastjan, ŠKOF, Erik, PAVLOVA BOJADŽISKI, Mirjana, STROJNIK, Ksenija, KRAJC, Mateja. A population-based study of patients with small cell carcinoma of the ovary, hypercalcemic type, encompassing a 30-year period. Archives of pathology & Laboratory Medicine. Mar. 2024, vol. 148, iss. 3, str. 299-309. ISSN 0003-9985. DOI: 10.5858/arpa.2022-0297-OA. [COBISS.SI-ID 154465283]

2025

78. AVSEC, Eva, RAKOVEC, Tea, HERTL, Gregor, BLATNIK, Ana, STEGEL, Vida, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan, KRAJC, Mateja. Bilateral breast cancer in a patient with PTEN hamartoma tumour syndrome : case report. V: Clinical genomics and NGS, Bertinoro, Italy, May 3 - 9, 2025. Bertinoro: European Society of Human Genetics, 2025. Str. 45-46. [COBISS.SI-ID 260423171]
79. Cancers. KLANČAR, Gašper (recenzent 2022-). Basel: MDPI. ISSN 2072-6694. http://www.mdpi.com/journal/cancers. [COBISS.SI-ID 517914137]
80. Clinics and practice. KLANČAR, Gašper (recenzent 2022-). Pavia: PagePress PublicationsBasel: MDPI. ISSN 2039-7283. http://www.clinicsandpractice.org. [COBISS.SI-ID 519961881]
81. Frontiers in molecular biosciences. KLANČAR, Gašper (področni urednik 2024-). Lausanne: Frontiers Media S.A., 2014-. ISSN 2296-889X. http://www.frontiersin.org/Molecular_Biosciences. [COBISS.SI-ID 523095321]
82. Frontiers in neuroscience. KLANČAR, Gašper (recenzent 2023-). Lausanne: Frontiers Research Foundation, 2007-. ISSN 1662-453X. http://www.frontiersin.org/neuroscience/. [COBISS.SI-ID 522058521]
83. Human gene. KLANČAR, Gašper (gostujoči urednik 2024-). Amsterdam: Elsevier, 2022-. ISSN 2773-0441. https://www.sciencedirect.com/journal/human-gene/issues. [COBISS.SI-ID 121512451]
84. Human gene. KLANČAR, Gašper (recenzent 2024-). Amsterdam: Elsevier, 2022-. ISSN 2773-0441. https://www.sciencedirect.com/journal/human-gene/issues. [COBISS.SI-ID 121512451]
85. International journal of environmental research and public health. KLANČAR, Gašper (recenzent 2022-). [Print ed.]. Basel: MDPI, 2004-. ISSN 1661-7827. http://www.mdpi.com/journal/ijerph. [COBISS.SI-ID 1024430420]
86. Journal of personalized medicine. KLANČAR, Gašper (recenzent 2022-). Basel: MDPI, 2011-. ISSN 2075-4426. http://www.mdpi.com/journal/jpm. [COBISS.SI-ID 31207641]
87. KLANČAR, Gašper. Priprava in interpretacija izvidov. V: NOVAKOVIĆ, Srdjan (ur.). Molekularna diagnostika v onkologiji : 20. obletnica ustanovitve Oddelka za molekularno diagnostiko na OIL. Ljubljana: Onkološki inštitut, 2025. Str. 96-100. [COBISS.SI-ID 235090179]
88. ŠKERL, Petra, VOGRIČ, Vesna, STEGEL, Vida, ŠETRAJČIČ DRAGOŠ, Vita, BLATNIK, Olga, KLANČAR, Gašper, NOVAKOVIĆ, Srdjan. Real-world evaluation of microsatellite instability detection via targeted NGS panels in routine molecular diagnostics. International journal of molecular sciences. 2025, vol. 26, no. 15, str. 7138-1-7138-17. ISSN 1422-0067. https://www.mdpi.com/1422-0067/26/15/7138, DOI: 10.3390/ijms26157138. [COBISS.SI-ID 246495747]
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