1996. -

Doktor biomedicinskih znanosti

Biomedicina

Medicinski fakultet, Sveučilište u Rijeci

1985. - 1991.

Magistar znanosti

Poslijediplomski studij iz genetike

Prirodno-matematički fakultet Univerziteta u Beogradu

1978. - 1985.

Diplomirani biolog

Opća biologija

Prirodno-matematički fakultet Univerziteta u Beogradu

2013. -

Redoviti profesor u trajnom zvanju

Zavod za biologiju i medicinsku genetiku, Medicinski fakultet, Sveučilište u Rijeci

2008. -

Redoviti profesor

Zavod za biologiju i medicinsku genetiku, Medicinski fakultet, Sveučilište u Rijeci

2004. -

Izvanredni profesor

Zavod za biologiju i medicinsku genetiku, Medicinski fakultet, Sveučilište u Rijeci

2000. -

Docent

Zavod za biologiju i medicinsku genetiku, Medicinski fakultet, Sveučilište u Rijeci

1992. - 2000.

Asistent

Zavod za biologiju i medicinsku genetiku, Medicinski fakultet, Sveučilište u Rijeci

1987. - 1991.

Biolog na radu

Zavod za biologiju i medicinsku genetiku, Medicinski fakultet, Sveučilište u Rijeci

European Society of Human Genetics

Slovensko društvo za humanu genetiku

Hrvatsko društvo za neuroznanost

Hrvatsko antropološko društvo

Hrvatsko društvo za humanu genetiku

2017. -

Medicinska genetika

poslijediplomski specijalistički studij Obiteljska medicina

Medicinski fakultet Rijeka

voditelj

2013. -

Osnove humane genetike.

stručni studij Primaljstvo

Medicinski fakultet Rijeka

suradnik

2011. -

Humana genetika

stručni izvanredni studij medicinsko -laboratorijska dijagnostika

Medicinski fakultet Rijeka

voditelj

2011. -

Osnove molekularne medicine

preddiplomski sveučilišni studij Biotehnoligija i istraživanje ljekova

Odjel za biotehnologiju Sveučilišta u Rijeci

suradnik

2010. -

Medicinska genetika

sveučilišni studij Medicina

Medicinski fakultet Rijeka

suradnik

2006. -

Odstupanja od Mendelovih zakona nasljeđivanja

sveučilišni studij Medicina

Medicinski fakultet Rijeka

voditelj

2005. -

Humane genske bolesti

doktorski studij Biomedicina

Medicinski fakultet Rijeka

voditelj

2004. -

Osnove molekularne biologije

doktorski studij Biomedicina

Medicinski fakultet Rijeka

suradnik

2003. - 2011.

Biologija

sveučilišni studij Sanitarno inženjerstvo

Medicinski fakultet Rijeka

suradnik

2003. -

Higijena tla

diplomski sveučilišni studij Sanitarno inženjerstvo

Medicinski fakultet Rijeka

voditelj

2002. -

Humana genetika

stručni studij medicinsko -laboratorijska dijagnostika

Medicinski fakultet Rijeka

voditelj

1993. -

Sve je zapisano genima.

sveučilišni studij Medicina

Medicinski fakultet Rijeka

suradnik

1988. - 2016.

Medicinska genetika

stručni specijalistički studij Obiteljska medicina

Medicinski fakultet Rijeka

suradnik

1987. -

Stanična biologija s genetikom

sveučilišni studij Stomatologija

Medicinski fakultet Rijeka

suradnik

1987. -

Medicinska biologija

sveučilišni studij Medicina

Medicinski fakultet Rijeka

suradnik

29.09.2017. -

Utjecaj polimorfizma +49 A/G CTLA-4 gena na učinak terapije interferonom-beta u bolesnika s multiplom sklerozom.

Azemina Eminović

diplomski studij medicinsko-laboratorijske dijagnostike

Fakultet zdrastvenih studija

2015. -

Utjecaj CCR5?32 mutacije na učinak terapije interferonom-beta u bolesnika s multiplom sklerozom

Mateja Mikulčić

preddiplomski stručni studij medicinsko-laboratorijske dijagnostike

Fakultet zdrastvenih studija Sveučilišta u Rijeci

2012. -

Gen za matriksmetaloproteinazu-9 kao rizični čimbenik u multiploj sklerozi na području Gorskog kotara

Tea Viceić

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

2010. -

Angiotenzin I-konvertirajući enzim kao rizični čimbenik u multiploj sklerozi na području Gorskog kotara

Gorana Mlinar

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

2008. -

Polimorfizmi HFE i TF gena kao rizični čimbenici u multiploj sklerozi na području Gorskog kotara

Tomislav Vidulić

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

2007. -

Analiza mutacija gena za hemokromatozu C282Y i H63D u neplodnih muškaraca

Ivana Kuna

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

2007. -

Tkivni plazminogen activator kao rizični čimbenik u multiploj sklerozi na području Gorskog kotara

Romina Paliska

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

2005. -

Učestalost mutacija gena za hemokromatozu u populaciji Rijeke

Jelena Plazibat

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

2004. -

Analiza mutacija gena koje dovode do hemokromatoze u bolesnika s alkoholnom cirozom jetre

Nada Starčević Čizmarević

poslijediplomski studij iz toksikologije

PMF, Zagreb

2004. -

Inhibitor aktivatora plazminogena-1 kao rizični čimbenik u multiploj sklerozi

Mirela Mičić

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

2003. -

Učestalost mutacija gena za hemokromatozu u populaciji Gorskog kotara

Tatjana Ljepojević

Medicinsko-laboratorijska dijagnostika

Medicinski fakultet Rijeka

1995. -

Downov sindrom: incidencija, dijagnostika, prevencija.

Anđelo Mojsović

Medicina

Medicinski fakultet Rijeka

1992. -

Distribucija statičko-morfoloških fenotipskih svojstava u stanovništvu Rijeke.

Jadranka Stručić

Medicina

Medicinski fakultet Rijeka

1992. -

Populacijska genetika biokemijsko-fizioloških fenotipskih svojstava u stanovništvu Rijeke

Karlić Slađana

Medicina

Medicinski fakultet Rijeka

2006. -

Biologija - sažeci vježbi i seminara za studente sanitarnog inženjerstva.

Financiranje: Medicinski fakultet Sveučilišta u Rijeci

2006. -

Stanična biologija s genetikom - sažeci vježbi i seminara za studente stomatologije.

Financiranje: Medicinski fakultet Sveučilišta u Rijeci

2006. -

Medicinska biologija - sažeci vježbi i seminara za studente medicine.

Financiranje: Medicinski fakultet Sveučilišta u Rijeci

2000. -

Sve je zapisano u genima.

Financiranje: Medicinski fakultet Sveučilišta u Rijeci

2023.

The Influence of Hemochromatosis Gene (HFE) Mutations on SARS-CoV-2 Susceptibility and COVID- 19 Severity

Ristić, Smiljana ; Milić, Sandra ; Tatalović, Tanja ; Bilobrk, Matea ; Rončević, Dobrica ; Ćurko-Cofek, Božena ; Barac-Latas, Vesna ; Starčević Čizmarević, Nada

Balkan Medical Journal - 40 229-231

https://balkanmedicaljournal.org/abstract.php?id=2487

Q2

2022.

Association between Insertion-Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Treatment Response to Antipsychotic Medications: A Study of Antipsychotic-Naïve First-Episode Psychosis Patients and Nonadherent Chronic Psychosis Patients

Nadalin, Sergej ; Dević Pavlić, Sanja ; Peitl, Vjekoslav ; Karlović, Dalibor ; Zatković, Lena ; Ristić, Smiljana ; Buretić-Tomljanović, Alena ; Jakovac, Hrvoje

International Journal of Molecular Sciences - 23 1-11

https://www.mdpi.com/1422-0067/23/20/12180

Q1

2022.

Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta‑analysis

Starčević Čizmarević, Nada; Ćurko-Cofek, Božena; Barac-Latas, Vesna; Peterlin, Borut; Ristić, Smiljana

Biomedical Reports - 16 1-6

https://www.spandidos-publications.com/10.3892/br.2021.1495

Q2

2021.

Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?

Nada Starčević Čizmarević, Miljenko Kapović, Dobrica Rončević, Smiljana Ristić

Physiological Research - 70 249-252

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884372/

Q2

2021.

Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy

Zečkanović Aida, Maver Aleš, Ristić Smiljana, Starčević Čizmarević Nada, Peterlin Borut, Lovrečić Luca

Biomedical Reports - 15 1-5

https://www.spandidos-publications.com/10.3892/br.2021.1476

Q2

2021.

ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe

Ristić Smiljana, Dević Pavlić Sanja, Nadalin Sergej, Starčević Čizmarević, Nada

Journal of Infection - 83 381-412

https://www.journalofinfection.com/article/S0163-4453(21)00282-6/fulltext

Q1

2021.

COVID-19 prevalence and mortality is associated with the allele frequency of CCR5-Delta 32 Reply

Starčević Čizmarević Nada, Tota Marin, Ristić Smiljana

Croatian Medical Journal - 62 305-6

http://www.cmj.hr/default.aspx?id=13327&issue=yes

31.12.2020.

Does the CCR5-Δ32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?

Starčević Čizmarević N, Tota Marin, Ristić Smiljana

Croatian Medical Journal - 61 525-6

Q3

13.10.2020.

Association between the ACE‑I/D polymorphism and nicotine dependence amongst patients with lung cancer.

Nadalin, Sergej; Flego, Veljko; Dević Pavlić, Sanja; Volarić, Darian; Radojčić Badovinac, Anđelka; Kapović, Miljenko; Ristić, Smiljana.

Biomedical Reports - 13 1-7

https://www.spandidos-publications.com/10.3892/br.2020.1365

Q2

19.09.2020.

Could angiotensin-converting enzyme 1 I/D polymorphism be a modificator of COVID-19 response in different populations, diseases, and/or conditions?

Dević Pavlić, Sanja; Nadalin, Sergej; Starčević Čizmarević, Nada; Buretić-Tomljanović, Alena; Radojčić Badovinac, Anđelka; Ristić, Smiljana.

Journal of the Renin-Angiotensin-Aldosterone System - 21 1470320320957157

https://journals.sagepub.com/doi/full/10.1177/1470320320957157

Q3

24.06.2019.

Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes.

Vidmar Lovro, Maver Aleš, Drulović Jelena, Sepčić Juraj, Novaković Ivana, Ristić Smiljana, Šega Saša, Peterlin Borut.

Scientific Reports - 9 9171

https://www.nature.com/articles/s41598-019-45598-x

Q1

26.02.2019.

Pharmacogenomics of Multiple Sclerosis: A Systematic Review.

Hočevar K, Ristić S, Peterlin B.

Frontiers in Neurology - 10

https://www.frontiersin.org/articles/10.3389/fneur.2019.00134/full

Q1

11.01.2018.

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.

Lavtar P, Rudolf G, Maver A, Hodžić A, Starčević Čizmarević N, Živković M, Šega Jazbec S, Klemenc Ketiš Z, Kapović M, Dinčić E, Raičević R, Sepčić J, Lovrečić L, Stanković A, Ristić S, Peterlin B.

PLoS One. - 13 e0190601

http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0190601

Q1

01.04.2017.

Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-[beta] treatment response in multiple sclerosis patients: a preliminary report.

Smiljana Ristić, Nada Starčević Čizmarević, Polona Lavtar, Luca Lovrečić, Olivio Perković, Juraj Sepčić, Saša Šega Jazbec, Miljenko Kapović, Borut. Peterlin

Pharmacogenetics and Genomics - 27 232-235

http://journals.lww.com/jpharmacogenetics/Abstract/publishahead/Angiotensin_converting_enzyme_insertion_deletion.99254.aspx

Q2

2017.

The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients.

Sergej Nadalin, Smiljana Ristić, Jelena Rebić, Vesna Šendula Jengić, Miljenko Kapović, Alena Buretić-Tomljanović

Journal of Neural Transmission - 124 511-518

http://link.springer.com/article/10.1007/s00702-016-1670-y

Q1

2017.

The lack of association between angiotensin-converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis

Nadalin, Sergej; Buretić-Tomljanović, Alena; Lavtar, Polona; Starčević Čizmarević, Nada; Hodžić, Alenka; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut; Ristić, Smiljana.

Brain and Behavior - 7 e00600

http://onlinelibrary.wiley.com/doi/10.1002/brb3.600/full

Q2

17.11.2016.

Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis.

Ristić, Smiljana; Starčević Čizmarević, Nada; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut.

Neurological Sciences - 37 1955-9

Q2

15.11.2016.

Chronic iron overload induces gender-dependent changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis.

Ćurko-Cofek, Božena; Grubić Kezele, Tanja; Marinić, Jelena; Tota, Marin; Starčević Čizmarević, Nada; Milin, Čedomila; Ristić, Smiljana; Radošević-Stašić, Biserka; Barac-Latas, Vesna.

Neurotoxicology - 57 1-12

Q1

15.09.2016.

The Role of Iron and Iron Overload in Chronic Liver Disease.

Milić, Sandra; Mikolašević, Ivana; Orlić, Lidija; Devčić, Edita; Starčević-Čizmarević, Nada; Štimac, Davor; Kapović, Miljenko; Ristić, Smiljana.

Medical science monitor. - 22 2144-51

Q2

05.09.2016.

HLA-DQA1 i HLADQB1 geni u pacijenata s celijakijom.

Mijandrušić Sinčić, Brankica; Starčević Čizmarević, Nada; Licul, Vanja; Crnić-Martinović, Marija; Ristić, Smiljana; Kapović, Miljenko.

Medicina fluminensis. - 52 87-94.

Q4

30.12.2015.

MMP-2 -1575 G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?

Gašparović Iva, Starčević Čizmarević Nada, Lovrečić Luca, Perković Olivio, Lavtar Polona, Sepčić Juraj, Šega Jazbec Saša, Kapović Miljenko, Peterlin Borut, Ristić Smiljana.

Journal of Neuroimmunology - 286 13-15

http://www.sciencedirect.com/science/article/pii/S0165572815300023

Q1

05.11.2015.

The impact of ACE gene I/D polymorphism on plasma glucose and lipid concentrations in schizophrenia patients.

Nadalin S, Buretić-Tomljanović A, Ristić S, Jonovska S, Tomljanović D.

Psychiatry Res. - 227 71-2

http://www.psy-journal.com/article/S0165-1781%2815%2900138-9/abstract

Q1

03.11.2015.

Geni i celijakija

Starčević Čizmarević N, Mijandrušić-Sinčić B, Licul V, Kapović M, Ristić S.

Paediatria Croatica - 59 88-94

http://www.paedcro.com/hr/1700-geni-i-celijakija

Q4

13.08.2014.

The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis.

Živković Maja, Starčević Čizmarević Nada, Lovrečić Luca, Klupka-Sarić I, Stanković Aleksandra, Gašparović Iva, Lavtar Polona, Dinčić Evica, Stojković Ljiljana, Rudolf Gorazd, Šega Jazbec Saša, Perković Olivio, Sinanović Osman, Sepčić Juraj, Kapović Miljenko, Peterlin Borut, Ristić Smiljana.

Disease markers. - Volume 2014, Article ID 362708,

http://www.hindawi.com/journals/dm/2014/362708/

Q2

11.12.2013.

CTLA-4+ 49 and TNF-alpha-308 gene polymorphisms in celiac patients with exocrine pancreatic insufficiency.

Licul Vanja, Starčević Čizmarević Nada, Ristić Smiljana, Mikolasević Ivana, Mijandrušić Sinčić Brankica.

Collegium antropologicum - 37 1191-4

http://www.collantropol.hr/antropo/article/view/423

Q2

2013.

Genetika neurodegenerativnih bolesti (Genetics of neurodegenerative diseases).

Gašparović, Iva; Starčević-Čizmarević, Nada; Perković, Olivio; Antončić, Igor; Kapović, Miljenko; Ristić, Smiljana.

Medicina Fluminensis - 49 144-156

http://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=152153

2013.

Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor.

Flego, Veljko; Ristić, Smiljana; Dević Pavlić, Sanja; Matanić Lender, Dubravka; Bulat-Kardum, Ljiljana; Kapović, Miljenko; Radojčić Badovinac, Anđelka

Medical science monitor - 19 846-851

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3808239/

2012.

Angiotensin converting enzyme gene I/D polymorphim is not associated with schizophrenia in a Croatian population.

Nadalin, Sergej; Buretić-Tomljanović, Alena; Rubeša, Gordana; Jonovska, Suzana; Tomljanović, Draško; Ristić, Smiljana

Psychiatric genetics (0955-8829) - 22 267-268

http://journals.lww.com/psychgenetics/Citation/2012/10000/Angiotensin_converting_enzyme_gene.10.aspx

2012.

HFE mutations and transferrin C1/C2 polymorphism among Croatian patients with schizophrenia and schizoaffective disorder

Buretić-Tomljanović, Alena; Vraneković, Jadranka; Rubeša, Gordana; Jonovska, Suzana; Tomljanović, Draško; Šendula-Jengić, Vesna; Kapović, Miljenko; Ristić, Smiljana;

Molecular biology reports - 39 2253-2258

2012.

Angiotensin-converting enzyme insertion/deletion gene polymorphism in lung cancer patients.

Dević Pavlić, Sanja; Ristić, Smiljana; Flego, Veljko; Kapović, Miljenko; Radojčić Badovinac, Anđelka

Genetic Testing and Molecular Biomarkers (1945-0265) - 16 722-725

http://online.liebertpub.com/doi/abs/10.1089/gtmb.2011.0306

2011.

CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients

Starčević Čizmarević, Nada; Gašparović, Iva; Peterlin, Borut; Sepčić, Juraj; Rudolf, Gorazd; Kapović, Miljenko; Lavtar, Polona; Ristić, Smiljana.

International journal of immunogenetics (1744-3121) - 38 419-426

http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2011.01027.x/abstract

2011.

Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis

Milić, Sandra; Ristić, Smiljana; Starčević-Čizmarević, Nada; Brajenović-Milić, Bojana; Crnić-Martinović, Marija; Kapović, Miljenko; Peterlin, Boris; Štimac, Davor

Medical science monitor (1234-1010) - 17 552-556

http://www.medscimonit.com/abstract/index/idArt/881980

2011.

Angiotensin-Converting Enzyme Gene Polymorphism in Patients with Multiple Sclerosis from Bosnia and Herzegovina

Klupka-Sarić, Inge; Peterlin, Borut; Lovrečić, Luca; Sinanović, Osman; Vidović, Marija; Šehanović, Aida; Starčević Čizmarević, Nada; Sepčić, Juraj; Kapović, Miljenko; Ristić, Smiljana

Genetic testing and molecular biomarkers (1945-0265) - 15 835-838

http://www.liebertonline.com/doi/abs/10.1089/gtmb.2010.0257

2010.

Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia

Vraneković, Jadranka; Babić Božović, Ivana; Starčević Čizmarević, Nada; Buretić-Tomljanović, Alena; Ristić, Smiljana; Petrović, Oleg; Kapović, Miljenko; Brajenović- Milić, Bojana

Disease markers (0278-0240) 28 (2010), 5; 293-298 - 28 293-298

http://iospress.metapress.com/content/c816573304228j6r/?p=2efa72d639db451b9eea4104e2feb35b&pi=4

2010.

Interleukin 7 receptor alpha polymorphism rs6897932 and susceptibility to multiple sclerosis in the Western Balkans

Stanković, Aleksandra; Dinčić, Evica; Ristić, Smiljana; Lovrečić, Luca; Starčević Čizmarević, Nada; Djurić, Tamara; Sepčić, Juraj; Kapović, Miljenko; Raičević, Ranko; Peterlin, Borut; Alavantić, Dragan; Živković, Maja

Multiple Sclerosis (1352-4585) 16 (2010), 5; 533-536 - 16 553-536

http://intl-msj.sagepub.com

2010.

A case of lichen planus in a patient with familial multiple sclerosis

Sepčić, Juraj; Ristić, Smiljana; Perković, Olivio; Brinar, Vesna; Lipozenčić, Jasna; Crnić-Martinović, Marija; Starčević Čizmarević, Nada; Janko Labinac, Dolores; Kapović, Miljenko; Peterlin, Borut.

Journal of international medical research (0300-0605) - 38 1856-1860

2010.

Drug-induced aseptic meningitis, sensorineural hearing loss and vestibulopaty

Sepčić, Juraj; Bučuk, Mira; Petrović, Olivio; Šepić-Grahovac, Dubravka; Trošelj-Vukić, Biserka; Poljak, Ivica; Crnić-Martinović, Marica; Turel, Iztok; Ristić, Smiljana; Sepčić, Kristina

Collegium antropologicum (0350-6134) - 34 1101-1104

http://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=97081

2010.

The Town of Čabar, Croatia, Familiar Pseudocluster for Multiple Sclerosis –Descriptive Epidemiological Study

Perković, Olivio; Jurjević, Ante; Antončić, Igor; Dunatov, Siniša; Bralić, Marina; Ristić, Smiljana.

Collegium antropologicum (0350-6134) 34 (2010), S2; 141-144 - 34 141-144

http://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=79052

2009.

Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemics.

Biloglav, Zrinka; Zgaga, Lina; Smoljanović, Mladen; Hayward, Caroline; Polašek, Ozren; Kolčić, Ivana; Vitart, Veronique; Zemunik, Tatijana; Boraska, Vesna; Torlak, Vesela; Mulić, Rosanda; Ropac, Darko; Grković, Ivica; Rudan, Diana; Ristić, Smiljana; Barbalić, Maja; Campbell, Harry; Wright, Alan F.; Rudan, Igor

Croatian Medical Journal (0353-9504) 50 (2009), 1; 34-42 - 50 34-42

2009.

Primary lung cancer and TNF-alfa gene polymorphisms:A case-control study in a Croatian population

Flego, Veljko; Radojčić Badovinac, Anđelka; Bulat-Kardum, Ljiljana; Matanić, Dubravka; Crnić-Martinović, Marija; Kapović, Miljenko; Ristić, Smiljana.

Medical Science Monitor (1234-1010) - 15 361-365

2009.

The impact of hemochromatosis mutations and transferrin genotype on gonadotropin serum levels in infertile men

Buretić-Tomljanović, Alena; Vlastelić, Ivan; Radojčić Badovinac, Anđelka; Starčević Čizmarević, Nada; Nadalin, Sergej; Ristić, Smiljana

Fertility and Sterility (0015-0282) - 91 1793-1800

http://www.ncbi.nlm.nih.gov/pubmed/18395717?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum

2008.

PAI and TPA gene polymorphisms in multiple sclerosis

Lovrečić, Luca; Ristić, Smiljana; Starčević-Čizmarević, Nada; Brajenović-Milić, Bojana; Šega Jazbec, Saša; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut

Multiple Sclerosis (1352-4585) - 14 243-247

2008.

The prevalence of live birth Down syndrome in the region of Primorsko-goranska County in Croatia, 1996-2005: The impact of screening and amniocentesis

Brajenović-Milić, Bojana; Prpić, Igor; Petrović, Oleg; Ristić, Smiljana; Brumini, Gordana; Kapović, Miljenko

Maternal and Child Health Journal (1092-7875) - 12 620-623

http://www.springerlink.com/content/00712234ur841367/fulltext.pdf

2008.

Pregnant women's attitudes towards amniocentesis before receiving Down syndrome screening results

Brajenović-Milić, Bojana; Babić, Ivana; Ristić, Smiljana; Vraneković, Jadranka; Brumini, Gordana; Kapović, Miljenko

Women's Health Issues (1049-3867) - 18 79-84

http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6TD8-4RH8SGF-1-1&_cdi=5192&_user=3875467&_orig=browse&_coverDate=04%2F30%2F2008&_sk=999819997&view=c&wchp=dGLbVzW-zSkzS&md5=c47fabf9ccb9430bb3c0e34014356974&ie=/sdarticle.pdf

2007.

Tumor Necrosis Factor-alpha-308 Gene Polymorphism in Croatian and Slovenian Multiple Sclerosis Patients

Ristić, Smiljana; Lovrečić, Luca; Starčević-Čizmarević, Nada; Brajenović-Milić, Bojana; Šega Jazbec, Saša; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut

European Neurology (0014-3022) 57 (2007), 4; 203-207 - 57 203-207

2007.

Epidemiology of multiple sclerosis in western Herzegovina

Klupka-Sarić, Inge; Ristić, Smiljana; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut; Materljan, Eris; Jurišić, Tonka; Martinović Mamić, Dražena; Burina, Adnan; Šulentić, Vlatko

Clinical Neurology and Neurosurgery (0303-8467) 109 (2007), 9; 779-783 - 109 779-783

2007.

HLA Class II Polymorphism in Autochthonous Population of Gorski kotar, Croatia

Crnić-Martinović, Marija; Grahovac, Blaženka; Vidan Jeras, Blanka; Ristić, Smiljana; Sepčić, Juraj; Brajenović-Milić, Bojana, Kapović, Miljenko; Peterlin, Borut

Collegium Antropologicum (0350-6134) - 31 853-858

2007.

The influence of fetal sex, smoking and parity on AFP and free-hCG concentrations in amniotic fluid of unaffected second-trimester pregnancies

Brajenović-Milić, Bojana; Tišlarić, Dubravka; Petrović, Oleg; Prodan, Mirko; Ristić, Smiljana; Marout, Jasminka; Herman, Radoslav; Kapović, Miljenko

Gynaecologia et Perinatologia (1330-0091) 16 (2007), 1; 14-18 - 16 14-18

2006.

Angiotensin-converting enzyme I/D gene polymorphism and risk of multiple sclerosis

Lovrečić, Luca; Ristić, Smiljana; Starčević-Čizmarević, Nada; Šega Jazbec, Saša; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut

Acta Neurologica Scandinavica (0001-6314) - 114 374-377

2006.

Hemochromatosis gene mutations in patients with alcoholic cirrhosis

Starčević Eizmerević, Nada; Stepec, Srećko; Ristić, Smiljana; Milić, Sandra; Brajenović -Milić, Bojana; Štimac, Davor; Kapović, Miljenko; Peterlin, Borut

Clinical genetics (0009-9163) 70 (2006), 3; 257-259 - 70 257-259

2006.

No association of CCR5D32 gene mutation with multiple sclerosis in Croatian and Slovenian patients

Ristić, Smiljana; Lovrečić, Luca; Brajenović-Milić, Bojana; Starčević-Čizmarević, Nada; Šega Jazbec, Saša; Barac-Latas, Vesna; Vejnović, Danilo; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut

Multiple sclerosis (1352-4585) - 12 360-362

2006.

Region with persistant high frequency of multiple sclerosis in Croatia and Slovenia

Peterlin, Borut; Ristić, Smiljana; Sepčić, Juraj; Končan Vračko, Beatrika; Rako, Andreja; Lovrečič, Luca; Brajenović-Milić, Bojana; Rudež, Josip; Materljan, Eris; Kapović, Miljenko

Journal of the neurological sciences (0022-510X) - 247 169-172

2005.

The frequency of CCR5 gene 32-basepair deletion in Croatian normal population

Ristić, Smiljana; Starčević-Čizmarević, Nada; Brajenović-Milić, Bojana; Crnić-Martinović, Marija; Kapović, Miljenko

Croatian medical journal (0353-9504) - 46 693-694

2005.

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis

Ristić, Smiljana; Lovrečić, Luca; Brajenović-Milić, Bojana; Starčević-Čizmarević, Nada; Šega Jazbec, Saša; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut.

Neuroscience letters (0304-3940) - 383 301-304

2005.

Human Y-specific STR haplotypes in the Western Croatian population sample

Lovrečić, Luca; Ristić, Smiljana; Brajenović, Bojana; Kapović, Miljenko; Peterlin, Borut

Forensic science international (0379-0738) - 149 257-261

2004.

Secular change of body height and cephalic index of Croatian medical students (University of Rijeka)

Buretić-Tomljanović, Alena; Ristić, Smiljana; Brajenović-Milić, Bojana; Ostojić, Saša; Gombač, Elena; Kapović, Miljenko

American Journal of Physical Anthropology (0002-9483) - 123 91-96

2004.

Elevated Second-trimester Free beta-hCG as an Isolated Finding and Pregnancy Outcomes

Brajenović-Milić, Bojana; Tišlarić, Dubravka; Žuvić-Butorac, Marta; Bačić, Josip; Petrović, Oleg; Ristić, Smiljana; Mimica, Marko; Kapović, Miljenko

Fetal diagnosis and therapy (1015-3837) - 19 483-487

2004.

Mutacije gena za hemokromatozu u bolesnika s povišenim vrijednostima serumskog željeza (Hemochromatosis gene mutations in patients with abnormal iron metabolism )

Starčević Čizmarević, Nad; , Milić, Sandra; Ristić, Smiljana; Štimac, Davor; Kapović, Miljenko

Medicina (0025-7729) 42 (2004), 4; 265-270 - 42 265-270

2004.

Polimorfizam 4G/5G u promotorskoj regiji gena za inhibitor aktivatora plazminogena-1 kao rizični čimbenik u multiploj sklerozi( 4G/5G polymorphism in promoter region of plasminogen activator inhibitor-1 gene as risk factor in multiple sclerosis )

Ristić, Smiljana; Starčević-Čizmarević, Nada; Sepčić, Juraj; Rudež, Josip; Crnić-Martinović, Marija; Barac-Latas, Vesna; Kapović, Miljenko

Medicina (0025-7729) - 40 271-274

2003.

Hemochromatosis gene mutations in the Croatian and Slovenian populations.

Ristić, Smiljana; Makuc, Jana; Starčević, Nada; Logar, Nataša; Brajenović-Milić, Bojana; Stepec, Srećko; Pleša, Ivana; Kapović, Miljenko; Milić, Sandra; Štimac, Davor; Crnić-Martinović, Marija; Peterlin, Borut

Clinical genetics (0009-9163) - 64 444-446

2003.

The influence of smoking and parity on serum markers for Down's syndrome screening.

Tišlarić, Dubravka; Brajenović-Milić, Bojana; Ristić, Smiljana; Latin, Višnja; Žuvić-Butorac, Marta; Bačić, Josip; Petek, Marjan; Kapović, Miljenko

Fetal Diagnosis and Therapy (1015-3837) - 17 17-21

2002.

The effect of a compulsory curriculum on ethical attitudes of medical students

Brajenović-Milić, Bojana; Ristić, Smiljana; Kern, Josipa; Vuletić Smiljana; Ostojić, Saša; Kapović, Miljenko

Collegium Antropologicum (0350-6134) - 24 47-52

2002.

Androgenic/anabolic steroid-induced toxic hepatitis

Štimac, Davor; Milić, Sandra; Dobrila-Dintinjana, Renata; Ristić, Smiljana

Journal of Clinical Gastroenterology (0192-0790) - 35 350-352

2002.

HLA class I and class II polymorphism in the population of Rijeka, Croatia

Crnić-Martinović, Marija; Vujaklija-Stipanović, Ksenija; Ristić, Smiljana; Fučak, Marina; Kapović, Miljenko; Weiner, Mima; Sepčić, Juraj

Collegium Antropologicum (0350-6134) 26 (2002), 1; 69-75 - 26 69-75

2001.

Human lymphocyte antigens (HLA) class I and class II in the autochthonous population of Gorski kotar, Croatia

Crnić-Martinović, Marija; Sepčić, Juraj; Vujaklija-Stipanović, Ksenija; Materljan, Eris; Strenja-Linić, Ines; Ristić, Smiljana

Acta Facultatis medicae Fluminensis (0065-1206) - 26 1-5

2000.

Biokemijski biljezi za Downov sindrom i oštećenja neuralne cijevi: Utjecaj pušenja, pariteta i dobi trudnica na razinu alfa-fetoproteina i beta podjedinice HCG u serumu( Biochemical markers for Down syndrome and neural tube defects: The influence of smoking, gravidity and maternal age on alpha-fetoprotein and free beta HCG serum levels )

Tišlarić, Dubravka; Košec, Vesna; Brajenović-Milić, Bojana; Smoljo, Luka; Rušinović, Frane; Berigoj, Ujević; Rajhvajn, Branko; Relja, Zoran; Ristić, Smiljana; Petek, Marijan

Gynaecologia et Perinatologia (1331-0151) - 9 28-31

2000.

Analysis of some phenothypic traits in a sample of multiple sclerosis patients

Ristić, Smiljana; Sepčić, Juraj; Kapović, Miljenko; Brajenović-Milić, Bojana; Materljan, Eris; Rudež, Josip

Balkan Journal of Medical Genetics (1311-160) - 3 11-18

1998.

Screening for Down's syndrome and neural tube defect in Croatia : A regional prospective study

Brajenović-Milić, Bojana; Tišlarić, Dubravka; Bačić, Josip; Paravić, Jadranka; Slivar, Anđelo; Kapović, Miljenko; Košec, Vesna; Ristić, Smiljana; Rajhvajn, Branko

Fetal diagnosis and therapy (1015-3837) - 13 367-371

1998.

Chromosomal anomalies in abnormal human pregnancies

Brajenović-Milić, Bojana; Petrović, Oleg; Krasević, Maja; Ristić, Smiljana; Kapović, Miljenko

Fetal Diagnosis and Therapy (1015-3837) - 13 187-191

1996.

Population-Genetic Analysis of Certain Morphophysiological Traits in the Population of Rijeka, Croatia (III)

Ristić, Smiljana; Brajenović-Milić, Bojana; Buretić-Tomljanović, Alena; Kapović, Miljenko

Collegium Antropologicum (0350-6134) - 20 21-25

1993.

Down's syndrome: an ever-recurring problem

B Brajenović-Milić, S Ristić, I Medica, Z Modrušan-Mozetič .

Medicina - 29 9-12

1993.

Miotonička distrofija (Mb Steinert): fertilnost, anticipacija, transmisija

Ristić, S, Hadžiselimović, R, Marković, D, Janko D.

Neurologia Croatica (ISSN0353-8842) - 42 39-47

1989.

Kliničko-genetička ekspresija miotonične distrofije u Istri.

Smiljana Ristić, Dubravko Marković, Dolores Janko, Milena Kružić .

Liječnički vjesnik - 111 301-304

1989.

Fenomen anticipacije u bolesnika s miotoničnom distrofijom.

Smiljana Ristić, Dubravko Marković, Dolores Janko, Milena Kružić .

Medicina - 25 117-119

2005.

Historic, epidemiologic, clinical, genetic and socio-economic aspects of multiple sclerosis in Croatia.

Autor poglavlja u knjizi

Sepčić J, Materljan E, Ristić S, Crnić-Martinović M, Rudež J, Kapović M.

Progress in multiple sclerosis research.

Columbus Frank

Nova Science Publishers New York

https://bib.irb.hr/prikazi-rad?&rad=160346

2000.

Hemofilija: molekularna biologija u središtu bolesti čovjeka.

Prevoditelj poglavlja u knjizi

Ristić S, Kapović M.

Molekularna biologija u medicini.

Jonjić S. Lučin P, Crnek-Kunstelj V, Traven L.

Medicinska naklada Zagreb

28.09.2018.

Gender-related differences in hepcidin and matallothionein I/II expression in spinal cord of iron-overloaded EAE rats.

Grubić Kezele, Tanja; Radošević-Stašić, Biserka; Barac-Latas, Vesna; Starčević Čizmarević, Nada; Ristić, Smiljana; Ćurko-Cofek, Božena.

predavanje

The 12th Annual Symposium of the Croatian Physiological Society with internationl participation "Homeostasis - From Cell to Organ" Rijeka, Hrvatska

19.06.2018.

Hemochromatosis gene polymorphisms in multiple sclerosis: a meta-analysis.

Starčević Čizmarević, Nada; Ćurko-Cofek, Božena; Barac-Latas, Vesna; Peterlin, Borut; Ristić, Smiljana.

poster

European Human Genetics Conference Milano, Italija

20.06.2017.

Angiotensin-converting enzyme (ACE) I/D gene polymorphism and IFN-ß treatment response in multiple sclerosis patients.

Ristić, Smiljana; Starčević Čizmarević, Nada; Lavtar, Polona; Lovrečić, Luca; Perković, Olivio; Sepčić, Juraj; Šega Jazbec, Saša; Kapović, Miljenko; Peterlin, Borut.

poster

Peti dani humane genetike - prof.dr.sc.Ljiljana Zergollern-Čupak Dubrovnik

01.06.2017.

The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS).

Peterlin, Ana; Maver, Aleš; Hodžić, Alenka; Šega, Saša; Drulović, Jelena; Novaković, Ivana; Pekmezović, Tatjana; Ristić, Smiljana; Kapović, Miljenko, Peterlin, Borut.

poster

European Human Genetics Conference Kopenhagen

2016.

Sequencing in patients with familial and sporadic multiple sclerosis reveals the possible etiological role of rare and highly penetrant genetic variation.

Maver, Aleš; Hodžić, Alenka; Šega, Saša; Drulović, Jelena; Novaković, Ivana; Ristić, Smiljana; Kapović, Miljenko; Pekmezović, Tatjana; Peterlin, Borut.

poster

European Human Genetics Conference Barcelona, Španjolska.

2016.

Are rare coding mutations in the genes related to genetic peripheral neuropathies risk factors in multiple sclerosis (MS).

Peterlin, Ana; Maver Aleš;, Hodžić, Alenka; Šega, Saša; Drulović, Jelena; Novaković, Ivana; Pekmezović, Tatjana; Ristić, Smiljana; Kapović, Miljenko; Peterlin, Borut.

poster

European Human Genetics Conference Barcelona, Španjolska.

2016.

Effect of genes in iron metabolism on multiple sclerosis development.

Starčević Čizmarević, Nada; Lovrečić, Luca; Ćurko-Cofek, Božena; Barac-Latas,V esna; Kapović, Miljenko; Peterlin, Borut; Ristić, Smiljana.

poster

European Human Genetics Conference. Barcelona, Španjolska.

2016.

Chronic iron overload induces gender-specific changes in iron homeostasis, lipid peroxidation and clinical course of experimental autoimmune encephalomyelitis.

Ćurko-Cofek, Božena; Grubić-Kezele, Tanja; Marinić, Jelena; Tota, Marin; Starčević Čizmarević, Nada; Milin, Čedomila; Ristić, Smiljana; Radošević-Stašić, Biserka; Barac-Latas, Vesna.

poster

The 10th International Congress on Autoimmunity. Leipzig. Germany.

2015.

Global DNA hypomethylation in white blood cells represents a feature of multiple sclerosis.

Bundalo M, Živković M, Ristić S, Starčević-Čizmarević N, Babić-Božović I, Brajenović-Milić B, Stanković A.

poster

FEBS3+ Meeting „Molecules of Life“. Portorož, Slovenia.

2015.

Influence of CCR5?32 gene mutation on interferon-beta treatment response in multiple sclerosis

Ristić, Smiljana; Mikulčić, Mateja; Starčević Čizmarević, Nada; Lovrečić, Luca; Lavtar, Polona; Sepčić, Juraj; Šega Jazbec, Saša; Kapović, Miljenko; Peterlin, Borut

poster

11th Balkan Congress of Human Genetics Beograd

2015.

Polimorfizmi gena matriksmetaloproteinaze-2 i matriksmetaloproteinaze-9 u multiploj sklerozi ( Polymorphisms of matrixmetalloproteinase-2 and matrixmetalloproteinase-9 in multiple sclerosis).

Gašparović, Iva; Starčević-Čizmarević, Nada; Perković, Olivio; Lovrečić, Luca; Miljenko, Kapović; Peterlin, Borut; Ristić, Smiljana

poster

VI hrvatski kongres humane genetike s međunarodnim sudjelovanjem Split

2014.

Polimorfizmi CTLA-4 i TNF-a gena u bolesnika s celijakijom.

Starčević Čizmarević, Nada; Licul, Vanja; Pleša, Ivana; Sinčić Mijandrušić, Brankica; Kapović, Miljenko; Ristić, Smiljana

usmena prezentacija

2. dani humane genetike prof.dr.sc.Ljiljane Zergollern-Čupak Zagreb

2014.

CTLA-4 and TNF-a gene polymorphisms in celiac disease.

Licul, Vanja; Mijandrušić Sinčić, Brankica; Starčević Čizmarević, Nada; Ristić, Smiljana; Kapović, Miljenko; Štimac, Davor

poster

Celiac Disease and other Small Bowell Disease Amsterdam

2013.

Tumor necrosis factor-alpha gene promoter-308 and-238 polymorphisms in patients with lung cancer as a second primary tumor

Dević Pavlić, Sanja; Flego, Veljko; Ristić, Smiljana; Radojčić Badovinac, Andjelka;

2013.

Signal transducers and activators of transcription genes (STAT genes) and Multiple sclerosis (MS).

Lavtar, Polona; Maver, Aleš; Rudolf, Goražd; Starčević Čizmarević, Nada; Živković, Maja; Šega Jazbec, Saša; Klemenc Ketiš, Zalika; Kapović, Miljenko; Dinčić, Evica; Raičević, Ranko; Sepčić, Juraj; Stanković, Aleksandra; Ristić, Smiljana; Peterlin, Borut.

poster

European Human Genetics Conference Paris, France

2012.

Circadian rhythm genes and multiple sclerosis (MS)

Lavtar, P; Rudolf, G; Maver, A; Lovrecic, L; Ristic, S; Cizmarevic, N Starcevic; Kapovic, M; Sepcic, J; Stankovic, A; Zivkovic, M;

poster

European Human Genetics Conference Nurnberg, Njemačka

2011.

Polimorfizmi PAI i TPA gena u multiploj sklerozi

Ristić, Smiljana; Starčević Čizmarević, Nada; Sepčić, Juraj; Živković, Maja; Stanković, Aleksandra; Klupka-Šarić, Inge; Lovrečić, Luca; Peterlin, Borut;

predavanje

The Seventh ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Bol, Brač

2011.

Angiotensin-converting enzyme (ACE) I/D gene polymorphism in multiple sclerosis

Stanković, Aleksandra; Gašparović, Iva; Peterlin, Borut; Klupka-Sarić, Inge; Živković, Maja; Starčević Čizmarević, Nada; Lovrečić, Luca; Sinanović, Osman; Dinčić, Evica; Perković, Olivio;

poster

5th Joint triennial Congress of the European and Americas Committees For Treatment and Research in Multiple Sclerosis Amsterdam

2011.

HFE MUTACIJE I C1/C2 POLIMORFIZAM GENA ZA TRANSFERIN U HRVATSKIH BOLESNIKA SA SHIZOFRENIJOM I SHIZOAFEKTIVNIM POREMEĆAJEM

Buretić-Tomljanović, Alena; Vraneković, Jadranka; Rubeša, Gordana; Jonovska, Suzana; Tomljanović, Draško; Šendula-Jengić, Vesna; Kapović, Miljenko; Ristić, Smiljana;

predavanje

The Seventh ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Bol, Brač

2011.

HFE MUTACIJE I C1/C2 POLIMORFIZAM GENA ZA TRANSFERIN U HRVATSKIH BOLESNIKA SA SHIZOFRENIJOM I SHIZOAFEKTIVNIM POREMEĆAJEM (HFE MUTATIONS AND TRANSFERRIN C1/C2 POLYMORPHISM AMONG CROATIAN PATIENTS WITH SCHIZOPHRENIA AND SCHIZOAFFECTIVE DISORDER )

Buretić-Tomljanović, Alena; Vraneković, Jadranka; Rubeša, Gordana; Jonovska, Suzana; Tomljanović, Draško; Šendula-Jengić, Vesna; Kapović, Miljenko; Ristić, Smiljana

predavanje

The Seventh ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Cavtat

2011.

CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients

Starčević Čizmarević, Nada; Gašparović, Iva; Peterlin, Borut; Sepčić, Juraj; Rudolf, Gorazd; Kapović, Miljenko; Lavtar, Polona; Ristić, Smiljana

poster

The Seventh ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine Cavtat

2010.

HLA Class II gene polymorphism in multiple sclerosis patients from Gorski Kotar, Croatia

Crnic-Martinovic, Marija; Balen, Sanja; Katalinic, Natasa; Fucak, Marina; Grahovac, Blazenka; Sepcic, Juraj; Kapovic, Miljenko; Ristic, Smiljana;

2010.

The Impact of Transferrin Gene Polymorphism to Phenotypic Expression in Patients With Iron Overload

Milic, Sandra; Ristic, Smiljana; Cizmarevic, Nada Starcevic; Stimac, Davor;

2009.

The interaction of hemochromatosis gene mutations and transferrin gene polymorphism to phenotypic expression in patients with iron overload

Milić, Sandra; Ristić, S; Starčević Čizmarević, N; Štimac, Davor;

2009.

IL7RA polymorphism rs6897932 and susceptibility to multiple sclerosis in West Balkan region

Stanković, Aleksandra; Dinčić, Evica; Ristić, Smiljana; Lovrečić, Luca; Starčević Čizmarević, Nada; Djurić, Tamara; Sepčić, Juraj; Kapović, Miljenko; Raičević, Ranko; Peterlin, Borut;

predavanje

Balkan Meeting on Human Genetics Cavtat

2009.

TNF-?-238 Gene Polymorphism in Croatian and Slovenian Multiple Sclerosis Patients

Starčević Čizmarević, Nada; Ristić, Smiljana; Lovrečić, Luca; Sepčić, Juraj; Brajenović-Milić, Bojana; Kapović, Miljenko; Peterlin, Borut;

poster

Balkan Meeting on Human Genetics Cavtat

2009.

Polymorphisms of hemochromatosis and transferrin genes in multiple sclerosis

Starčević Čizmarević, Nada; Ristić, Smiljana; Lovrečić, Luca; Sepčić, Juraj; Brajenović-Milić, Bojana; Buretić-Tomljanović, Alena; Kapovic, Miljenko; Peterlin, Borut;

poster

European Human Genetics Conference Beč

2009.

Genetička analiza multiple skleroze

Ristić, Smiljana; Starčević Čizmarević, Nada; Sepčić, Juraj; Lovrečić, Luca; Janko-Labinac, Dolores; Šega Jazbec, S; Kapović, Miljenko; Peterlin, Borut;

poster

V.hrvatski neurološki kongres Zagreb

2008.

Plasminogen activator inhibitor-1 (PAI-1) genetic polymorphism and its role in the response to immunomodulatory treatment in multiple sclerosis

Lovrecic, L; Ristic, S; Starcevic-Cizmarevic, N; Jazbec, S Sega; Potisk, K Peterlin; Sepcic, J; Kapovic, M; Peterlin, B;

poster

European Human Genetics Conference Amsterdam

2007.

Analiza gena za transferin i hemokromatozu u idiopatskoj neplodnosti muškaraca

Buretić-Tomljanović, Alena; Vlastelić, Ivan; Radojčić Badovinac, Anđelka; Starčević Čizmarević, Nada; Nadalin, Sergej; Kapović, Miljenko; Ristić, Smiljana;

poster

Četvrti hrvatski kongres iz humane genetike s međunarodnim sudjelovanjem Krk

2007.

Geni HLA razreda II u bolesnika s multiplom sklerozom u Gorskom kotaru, Hrvatska

Crnić-Martinović, Marija; Ristić, Smiljana; Sepčić, Juraj; Vidan-Jeras, Blanka; Grahovac, Blaženka; Peterlin, Borut; Kapović, Miljenko;

poster

IV kongres humane genetike s međunarodnim sudjelovanjem Krk

2006.

Multiple sclerosis in Gorski Kotar, Croatia: Ethnical and genetic aspects

Perkovic, O; Jurjevic, A; Rudez, J; Ristic, S; Antonelli, L; Skarpa-Prpic, I; Antocic, I; Dunatov, S; Skarpa-Prpic, I;

2006.

Plasminogen activator inhibitor-1 (PAI-1) genetic polymorphism and its role in the progression of multiple sclerosis

Lovrečić, Luca; Ristić, Smiljana; Starčević Čizmarević, Nada; Šega Jazbec, Saša; Sepčić, Juraj; Brajenović-Milić, Bojana; Kapović, Miljenko; Peterlin, Borut;

2005.

Genska mutacija CCR5D32 nije rizični niti preventivni čimbenik za multiplu sklerozu

Ristić, Smiljana; Lovrečić, Luca; Brajenović-Milić, Bojana; Starčević-Čizmarević, Nada; Šega Jazbec, Saša; Barac-Latas, Vesna; Vejnović, Danilo; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut;

poster

4.hrvatski neurološki kongres Osijek

2005.

C282Y, H63D and S65C mutations of the hemochromatosis gene (HFE) in patients with alcoholic cirrhosis

Starčević Čizmarević, Nada; Stepec, Srećko; Ristić, Smiljana; Milić, Sandra; Brajenović-Milić, Bojana; Štimac, Davor; Kapović, Miljenko; Peterlin, Borut

poster

European Human genetics Conference Prag

2005.

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis

Ristić, Smiljana; Lovrečić, Luca; Brajenović-Milić, Bojana; Starčević-Čizmarević, Nada; Šega Jazbec, Saša; Sepčić, Juraj; Kapović, Miljenko; Peterlin, Borut

poster

European Journal of Human genetics Prag

2005.

Correlation between fetal sex and maternal serum AFP and free beta-hCG during second trimester normal pregnancies

Brajenović-Milić, Bojana; Tišlarić, Dubravka; Ristić, Smiljana; Kapović, Miljenko

poster

European Journal of Human Genetics Prag

2003.

Secular change in body height and cephalic index of Croatian medical students (University of Rijeka)

Buretić-Tomljanović, Alena; Ristić, Smiljana; Brajenović-Milić, Bojana; Ostojić, Saša; Gombač, Elena; Kapović, Miljenko

poster

4. hrvatski kongres iz humane genetike s medjunarodnim sudjelovanjem. Zagreb

2001.

Multipla skleroza u regiji Gorski kotar-Kočevje

Ristić, Smiljana; Peterlin, Borut; Sepčić, Juraj; Končan-Vračko, Beatrika; Lovrečić, Luca; Crnić-Martinović, Marija; Reko, A; Brajenović-Milić, Bojana; Rudež, Josip; Materljan, Eris;

predavanje

3. hrvatski neurološki kongres Rijeka

2001.

Woodhouse-Sakati syndrome; report of a patient

Medica, Igor; Teran, N; Sepčić, Juraj; Ristić, Smiljana; Brajenović, Bojana; Peterlin, Borut

poster

10th International Congress of Human Genetics Beč

2000.

Analysis of multiple sclerosis in Gorski Kotar and Kočevje Regions

Kapović, Miljenko; Sepčić, Juraj; Končan-Vračko, Beatrika; Lovrečić, L.; Ristić, Smiljana; Crnić-Martinović, Marija; Brajenović-Milić, Bojana; Peterlin, Borut

predavanje

1st Alps-Adria Meeting on Human Genetics Zagreb

1998.

Prenatal screening test for Down syndrome and neural tube defects

Brajenoviae-Miliae, B; Paraviae, J; Ristiae, S; Kapoviae, M; Baeiae, J; Frkoviae, A; Slivar, A;

1998.

Populacijsko-genetička analiza određenih fenotipskih svojstava u autohtonoj populaciji otoka Krka (Population-genetic analysis of certain fenotypic traits in the autochtonous population of island of Krk )

Ristić, Smiljana; Brajenović-Milić, Bojana; Obersnel, Vojko; Buretić-Tomljanović, Alena; Ostojić, Saša; Verša, Damjana; Paić, Marin; Kapović, Miljenko

poster

Prirodoslovna istraživanja riječkog područja Rijeka

1997.

Familial reccurence and inheritance of multiple sclerosis in the western Croatia

Ristić, Smiljana; Sepčić, Juraj; Kapović, Miljenko; Brajenović-Milić, Bojana

poster

13th Congress of the European Committee for Treatment and Research in Multiple Sclerosis Istanbul

1996.

Visina tijela i indeks glave u riječkih studenata medicine

Buretić-Tomljanović, Alena; Ristić, Smiljana; Brajenović-Milić, Bojana; Ostojić, Saša; Kapović, Miljenko;

poster

Prirodoslovna istraživanja riječkog područja Rijeka

1996.

Populacijsko-genetička analiza određenih fenotipskih svojstava u populaciji Rijeke

Ristić, Smiljana; Brajenović-Milić, Bojana; Buretić-Tomljanović, Alena; Kapović, Miljenko;

poster

6. kongresa biologa Hrvatske s međunarodnim sudjelovanjem Opatija

1988.

Epidemiološko-genetska istraživanja miotoničke distrofije u Istri

Janko, Dolores; Marković, Dubravko; Ristić, Smiljana; Kružić, Milica; Sepčić, Juraj;

predavanje

VIII kongres neurologa Jugoslavije sa međunarodnim učešćem Novi Sad

1988.

Od neuroepidemiologije do neuroimunologije: plodnost i multipla skleroza

Antonelli, Licia; Matejčić, Nikola; Materljan, Eris; Morović, Miro; Ristić, Smiljana; Rukavina, Daniel; Sepčić, Juraj; Šepić-Grahovac, Dubravka;

predavanje

VIII Kongres neurologa Jugoslavije Novi Sad

2011. - 2015.

Polimorfizmi gena sustava matriks metaloproteinaza i fibrinolize u multiploj sklerozi

Iva Gašparović, dr.med. Doktorat

Biomedicina

Datum obrane: 27.11.2015.

2008. - 2011.

Polimorfizmi gena uključenih u proces fibrinolize kao rizični čimbenici u multiploj sklerozi

Inge Klupka-Sarić Doktorat

Biomedicina

Datum obrane: 22.07. 2011.

2004. - 2008.

Polimorfizmi gena za hemokromatozu, transferin i čimbenik nekroze tumora u multiploj sklerozi

Nada Starčević-Čizmarević Doktorat

Biomedicina

Datum obrane: 16.07.2008.

2000. - 2004.

Učestalost mutacija gena za hemokromatozu u bolesnika s povišenim vrijednostima serumskog željeza i aminotransferaza

Sandra Milić Doktorat

Biomedicina

Datum obrane: 24.07.2004.

2007. -

Četvrti hrvatski kongres iz humane genetike s međunarodnim sudjelovanjem

Krk član znanstvenog odbora

2013. -

"Medicina fluminensis" - Glasilo Hrvatskog liječničkog zbora - podružnice Rijeka (ISSN 0025-7729)

2011. -

BMC Neurology- Associate editor

http://www.biomedcentral.com/bmcneurol/about/edboard

2005. -

Journal of Aids and HIV Research

http://www.academicjournals.org/journal/JAHR/editors

2017.

Morphogenetic variability and genetic loads amnong patients with different expression of developmental hip dysplasia. Genetika

2016.

Telegenetics: an update on availability and use of telemedicine in clinical genetics service, Journal of Medical Systems.

2016.

Association of matrix metalloproteinase-9 with risk and clinical course in Multiple Sclerosis, Neuroscience Letters.

2016.

Renin-angiotensin system gene polymorphisms as risk factors for multiple sclerosis, Journal of the Neurological Sciences.

2015.

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis, European journal of neurology.

2015.

Expression of SIRT1 and MMP-1 in human degenerated intervertebral disc, Central European Journal of Medicine.

2013.

Integration of data from omic studies with literature-based discovery towards identification of novel treatments for neovascularization in diabetic retinopathy, BioMed Research International

2013.

The Glutathione S-Transferase T1 deletion is associated with susceptibility to multiple sclerosis, Journal of the Neurological Sciences

2012.

Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility, PLOS ONE

2011.

Rezenzije većeg broja znanstvenih radova kao Associate editor u BMC Neurology.

2011.

Polymorphism in the CC-chemokine receptor-5 (CCR5) gene and risk of AIDS among Kashmiri population. Journal of AIDS and HIV Research (JAHR)

2011.

The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: Preliminary study. Molecular Biology Reports

2010.

HFE gene polymorphism and severity in multiple sclerosis Portuguese patients. European Journal of Neurology

2010.

Hemochromatosis gene mutations in the general population of Slovakia. Central European Journal of Medicine

2009.

Multiple Sclerosis and Cancers in Croatia – A Possible Protective Role of the “Mediterranean Diet. Collegium Antropologicum

2009.

Morphogenetic variability during selection of elite water polo players. Journal of Sports Sciences

2009.

CCR5-delta32 allele is associated with the risk of developing multiple sclerosis in the Iranian population. Cellular and Molecular Neurobiology

2009.

Lung cancer and pulmonary tuberculosis- a comparative population genetic-study. Balkan Journal of Human Genetics (BJHG)

2008.

The “PREXCEL-Q Method’ for qPCR. International Journal of Biological Sciences

2007.

Association of angiotensin-converting enzyme/DD genotype with sarcoidosis susceptibility in Slovenian patients. Medical Science Monitor

2007.

Matrix metalloproteinase 9-1562 C/T gene polymorphism in Serbian patients with multiple sclerosis. Journal of Neuroimmunology

2007.

Chromosome Aberrations in Peripheral Blood Lymphocytes of Croatian Hospital Workers Occupationally Exposed to Low Levels of Ionizing Radiation. Croatian Medical Journal (CMJ)

2007.

Stable and unstable chromosome aberrations measured after occupational exposure to ionizing radiation and ultrasound, Croatian Medical Journal (CMJ)

2007. -

Opremanje laboratorija za praktičnu nastavu iz molekularne genetike

Zavod za biologiju i medicinsku genetiku MF Rijeka

Nabava i instalacija opreme za praktične vježbe iz molekularne genetike

2001. -

Vođenje laboratorija za molekularnu genetiku

Zavod za biologiju i medicinsku genetiku MF Rijeka

Uvođenje tehnika i metoda za dijagnostiku određenih genskih bolesti

2019. -

Farmakogenetika multiple skleroze: odgovor na imunomodulacijsku terapiju

suradnik

Sveučilište u Rijeci, uniri-biomed-18-137

2019. -

Genetska epidemiologija Parkinsonove bolesti u Hrvatskoj

suradnik

Sveučilište u Rijeci, uniri-biomed-18-198

2019. -

Epidemiologija Parkinsonove bolesti u Hrvatskoj i utjecaj genetskih čimbenika i mikrobiote na progresiju bolesti i ishod liječenja

suradnik

Hrvatska zaklada za znanost

2017. - 2018.

Genetički i biokemijski biljezi metabolizma membranskih fosfolipida i masnih kiselina kao predskazatelji odgovora na antipsihotičnu terapiju u bolesnika s psihotičnom epizodom

suradnik

Sveučilište u Rijeci, 4722

2017. - 2018.

Genetska predispozicija za nastanak nealkoholne masne bolesti jetre nakon transplantacije jetre

suradnik

Sveučilište u Rijeci, 4951

2016. - 2017.

Polimorfizmi gena za fosfolipaze A2, ciklooksigenazu-2 i peroksisomnim proliferatorom aktivirani receptor alfa i odgovor na antipsihotičnu terapiju u bolesnika s prvom psihotičnom epizodom

Suradnik

Sveučilište u Rijeci, potpora broj

https://portal.uniri.hr/Projekti/807?controler=projekti

2014. - 2019.

Korelacija genotipa i fenotipa u bolesnika s povišenim vrijednostima serumskog željeza

Suradnik

Sveučilište u Rijeci, potpora broj 13.06.1.4.51

https://portal.uniri.hr/project/hemokromatoza

2014. - 2019.

Genetska analiza multiple skleroze

Voditelj

Sveučilište u Rijeci, potpora broj 13.06.1.1.10

https://portal.uniri.hr/project/genetikaMS

2014. - 2019.

Uloga željeza u etiopatogenezi multiple skleroze

Suradnik

Sveučilište u Rijeci, potpora broj 13.06.2.2.61

https://portal.uniri.hr/project/zeljezo-etiopatogenezaMS

2012. - 2013.

Pharmacogenetics of immunomodulatory therapy in multiple sclerosis and the influence of genetic polymorphisms of certain metabolic pathways.

Suradnik

MZOŠ Republike Hrvatske i Ministarstvo znanosti Republike Slovenije

2010. - 2015.

Genetska osnova vaskularnih i inflamatornih bolesti

Savjetnik

Ministarstvo nauke Republike Srbije

2009. - 2010.

Genetic analysis of multiple sclerosis.

Voditelj

MZOŠ Republike Hrvatske i Ministarstvo znanosti Republike Srbije

2009. - 2010.

Genetic factors in multiple sclerosis.

Voditelj

MZOŠ Republike Hrvatske i Ministarstvo znanosti Republike Slovenije

2007. - 2014.

Genetska analiza multiple skleroze

Voditelj

MZOŠ Republike Hrvatske

https://bib.irb.hr/lista-radova?sif_proj=062-1962766-0470&period=2007

2007. - 2013.

Prenatalni probir za Downov sindrom

Suradnik

MZOŠ Republike Hrvatske

https://bib.irb.hr/lista-radova?sif_proj=062-0000000-1349&period=2007

2006. - 2008.

Genetic factors in multiple sclerosis.

Voditelj

MZOŠ Republike Hrvatske i Ministarstvo znanosti Republike Slovenije

2003. - 2005.

Genetic factors in multiple sclerosis.

Voditelj

MZOŠ Republike Hrvatske i Ministarstvo znanosti Republike Slovenije

2002. - 2007.

Genetski čimbenici u multiploj sklerozi

Voditelj

MZOŠ Republike Hrvatske

https://bib.irb.hr/lista-radova?sif_proj=0062016&period=2002

2002. - 2006.

Biokemijski test probira za Downov sindrom i oštećenje neuralne cijevi

Savjetnik

MZOŠ Republike Hrvatske

https://bib.irb.hr/lista-radova?sif_proj=0062017&period=2002

2002. - 2006.

Ekspresija kemokina u eksperimentalnom alergijskom encefalomijelitisu

Savjetnik

MZOŠ Republike Hrvatske

https://bib.irb.hr/lista-radova?sif_proj=0062052&period=2002

1987. - 1991.

Toksično djelovanje teških metala na embrionalni razvoj i odrasle eksperimentalne životinje

Suradnik

Ministarstvo znanosti Republike Hrvatske

1987. - 1991.

Kromosomske aberacije kao mogući uzrok smanjene reproduktivne sposobnosti i njihova prenatalna dijagnostika

Suradnik

Ministarstvo znanosti Republike Hrvatske