Pregled po CROSBI profilu: Ingeborg Barišić (CROSBI Profil: 13659, MBZ: 168183)
Pronađeno 523 radova
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1.Mamasoula, Chrysovalanto; Bigirumurame, Theophile; Chadwick, Thomas; Addor, Marie‐Claude; Cavero‐ Carbonell, Clara; Dias, Carlos M.; Echevarría‐ González‐de‐Garibay, Luis‐Javier; Gatt, Miriam; Khoshnood, Babak; Klungsoyr, Kari et al.Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register‐ based study // Birth Defects Research, 115 (2023), 6; 583-594 doi:10.1002/bdr2.2152 (međunarodna recenzija, članak, znanstveni)
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2.Latos-Bieleńska, Anna; Marcus, Elena; Jamry- Dziurla, Anna; Rankin, Judith; Barisic, Ingeborg; Cavero- Carbonell, Clara; Den Hond, Elly; Garne, Ester; Genard, Lucas; João Santos, Ana et al.COVID-19 and children with congenital anomalies: a European survey of parents’ experiences of healthcare services // BMJ Open, 12 (2022), 7; 1-13 doi:10.1136/bmjopen-2022-061428 (međunarodna recenzija, članak, znanstveni)
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3.Coi, Alessio; Barisic, Ingeborg; Garne, Ester; Pierini, Anna; Addor, Marie‐Claude; Aizpurua Atxega, Amaia; Ballardini, Elisa; Braz, Paula; Broughan, Jennifer M.; Cavero‐Carbonell, Clara et al.Epidemiology of aplasia cutis congenita: A population‐based study in Europe // Journal of the European Academy of Dermatology and Venereology, 37 (2022), 3; 581-589 doi:10.1111/jdv.18690 (međunarodna recenzija, članak, znanstveni)
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4.Bergman, Jorieke E. H.; Barišić, Ingeborg; Addor, Marie‐Claude; Braz, Paula; Cavero‐ Carbonell, Clara; Draper, Elizabeth S.; Echevarría‐González‐de‐Garibay, Luis J.; Gatt, Miriam; Haeusler, Martin; Khoshnood, Babak et al.Amniotic band syndrome and limb body wall complex in Europe 1980–2019 // American Journal of Medical Genetics Part A, 191 (2022), 4; 995-1006 doi:10.1002/ajmg.a.63107 (međunarodna recenzija, članak, znanstveni)
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5.Marcus, Elena; Latos-Bielenska, Anna; Jamry- Dziurla, Anna; Barišić, Ingeborg; Cavero- Carbonell, Clara; Den Hond, Elly; Garne, Ester; Genard, Lucas; Santos, Ana João; Lutke, LRenée et al.Information needs of parents of children with congenital anomalies across Europe: a EUROlinkCAT survey // BMC Pediatrics, 22 (2022), 1; 1-13 doi:10.1186/s12887-022-03734-z (međunarodna recenzija, članak, znanstveni)
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6.Morris, Joan K.; Wellesley, Diana; Limb, Elizabeth; Bergman, Jorieke E. H.; Kinsner‐ Ovaskainen, Agnieszka; Addor, Marie Claude; Broughan, Jennifer M.; Cavero‐Carbonell, Clara; Dias, Carlos M.; Echevarría‐González‐de‐Garibay, Luis‐Javier et al.Prevalence of vascular disruption anomalies and association with young maternal age: A
EUROCAT study to compare the United Kingdom with other European countries // Birth Defects Research, 114 (2022), 20; 1417-1426 doi:10.1002/bdr2.2122 (međunarodna recenzija, članak, znanstveni) -
7.Mamasoula, Chrysovalanto; Addor, Marie‐Claude; Carbonell, Clara Cavero; Dias, Carlos M.; Echevarría‐González‐de‐Garibay, Luis‐Javier; Gatt, Miriam; Khoshnood, Babak; Klungsoyr, Kari; Randall, Kay; Stoianova, Sylvia et al.Prevalence of congenital heart defects in Europe, 2008–2015: A registry‐based study // Birth Defects Research, 114 (2022), 20; 1404-1416 doi:10.1002/bdr2.2117 (međunarodna recenzija, članak, znanstveni)
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8.Santoro, Michele; Coi, Alessio; Pierini, Anna; Rankin, Judith; Glinianaia, Svetlana V.; Tan, Joachim; Reid, Abigail; Garne, Ester; Loane, Maria; Given, Joanne et al.Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi‐registry cohort study // Paediatric and Perinatal Epidemiology, 36 (2022), 6; 792-803 doi:10.1111/ppe.12884 (međunarodna recenzija, članak, znanstveni)
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9.Urhoj, Stine Kjaer; Tan, Joachim; Morris, Joan K.; Given, Joanne; Astolfi, Gianni; Baldacci, Silvia; Barisic, Ingeborg; Brigden, Joanna; Cavero-Carbonell, Clara; Evans, Hannah et al.Hospital length of stay among children with and without congenital anomalies across 11 European regions—A population-based data linkage study // PLOS ONE, 17 (2022), 7; 1-17 doi:10.1371/journal.pone.0269874 (međunarodna recenzija, članak, znanstveni)
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10.Cindrić, Ana; Vučković, Frano; Alić, Ivan; Gough, Gillian; Koschut, David; Borelli, Vincenzo; Petrović, Dražen; Bekavac, Ana; Spector, Tim; Mitrečić, Dinko et al.Down syndrome biological age is accelerated on average by 19 years, beginning in early childhood, independent of co-morbidities, and trisomy of Down-syndrome-critical-region is a sufficient trigger // T21RS 4th International conference Book of abstracts
Long Beach (CA), Sjedinjene Američke Države, 2022. str. 273-274 (predavanje, međunarodna recenzija, sažetak, znanstveni) -
11.Tylki-Szymańska, Anna; Almássy, Zsuzsanna; Christophidou- Anastasiadou, Violetta; Avdjieva- Tzavella, Daniela; Barisic, Ingeborg; Cerkauskiene, Rimante; Cuturilo, Goran; Djiordjevic, Maja; Gucev, Zoran; Hlavata, Anna et al.The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers // Orphanet journal of rare diseases, 17 (2022), 1; 136-152 doi:10.1186/s13023-022-02285-x (međunarodna recenzija, članak, znanstveni)
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12.Vulin, Katarina; Odak, Ljubica; Morožin Pohovski, Leona; Đaković, Ivana; Tripalo Batoš, Ana; Meašić, Ana-Maria; Kero, Mijana; Sansović, Ivona; Bobinec, Adrana; Barišić, IngeborgChromosomal microarray in clinical diagnosis of cerebral palsy // Journal of Bioanthropology ; vol.2, no.1, 2022. Program and abstracts: The Twelfth ISABS Conference on Forensic and Anthropological Genetics and Mayo Clinic Lectures in Individualized Medicine ; June 22-27, 2022, Dubrovnik, Croatia. / Marjanović, D (ur.).
Zagreb: Institut za antropologiju, 2022. str. 308-308 doi:10.54062/jb (predavanje, međunarodna recenzija, sažetak, znanstveni) -
13.Krnjak, Goran; Vulin, Katarina; Pazanin, Leo; Barisic, Ingeborg; Duranovic, VlastaA case of macrophagic myofasciitis in a girl with developmental delay // Pediatrics International, 64 (2022), 1; 35139249, 2 doi:10.1111/ped.14930 (međunarodna recenzija, članak, stručni)
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14.Odak, Ljubica; Meašić, Ana-Marija; Bobinec, Adriana; Kero, Mijana; Sansović, Ivona; Vulin, Katarina; Tomić, Mirko; Barišić, Ingeborg.Clinical exome sequencing in the diagnosis of autism spectrum disorder // WebArchives of Disease in Childhood
Zagreb, Hrvatska, 2021. str. A41-A41 (poster, međunarodna recenzija, sažetak, znanstveni) -
15.Loane, M.; Given, J. E.; Tan, J.; Reid, A.; Akhmedzhanova, D.; Astolfi, G.; Barišić, I.; Bertille, N.; Bonet, L. B.; Carbonell, C. C. et al.Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records: A EUROlinkCAT study // PLOS ONE, 16 (2021), 8; 1-16 doi:10.1371/journal.pone.0256535 (međunarodna recenzija, članak, znanstveni)
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16.Leke, Aminkeng Zawuo; Dolk, Helen; Loane, Maria; Casson, Karen; Nelen, Vera; Barišić, Ingeborg; Garne, Ester; Rissman, Anke; O’Mahony, Mary; Neville, Amanda J. et al.Macrolide and lincosamide antibiotic exposure in the first trimester of pregnancy and risk of congenital anomaly: A European case- control study // Reproductive Toxicology, 100 (2021), 101-108 doi:10.1016/j.reprotox.2021.01.006 (međunarodna recenzija, članak, znanstveni)
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17.Goldsmith, Shona; McIntyre, Sarah; Scott, Heather; Himmelmann, Kate; Smithers‐Sheedy, Hayley; Andersen, Guro L; Blair, Eve; Badawi, Nadia; Garne, Ester; Barisic, Ingeborg et al.Congenital anomalies in children with postneonatally acquired cerebral palsy: an international data linkage study // Developmental Medicine & Child Neurology, 63 (2021), 4; 421-428 doi:10.1111/dmcn.14805 (međunarodna recenzija, članak, znanstveni)
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18.Dolk, Helen; Leke, Aminkeng Zawuo; Whitfield, Phil; Moore, Rebecca; Karnell, Katy; Barišić, Ingeborg; Barlow‐Mosha, Linda; Botto, Lorenzo D.; Garne, Ester; Guatibonza, Pilar et al.Global birth defects app: An innovative tool for describing and coding congenital anomalies at birth in low resource settings // Birth Defects Research, 113 (2021), 14; 1057-1073 doi:10.1002/bdr2.1898 (međunarodna recenzija, članak, znanstveni)
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19.Cavadino, Alana; Sandberg, Lovisa; Öhman, Inger; Bergvall, Tomas; Star, Kristina; Dolk, Helen; Loane, Maria; Addor, Marie- Claude; Barisic, Ingeborg; Cavero-Carbonell, Clara et al.Signal Detection in EUROmediCAT: Identification and Evaluation of Medication–Congenital Anomaly Associations and Use of VigiBase as a Complementary Source of Reference // Drug Safety, 44 (2021), 7; 765-785 doi:10.1007/s40264-021-01073-z (međunarodna recenzija, članak, znanstveni)
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20.Santoro, Michele; Coi, Alessio; Barišić, Ingeborg; Pierini, Anna; Addor, Marie‐Claude; Baldacci, Silvia; Ballardini, Elisa; Boban, Ljubica; Braz, Paula; Cavero‐Carbonell, Clara et al.Epidemiology of Pierre‐Robin sequence in Europe: A population‐ based EUROCAT study // Paediatric and Perinatal Epidemiology, 35 (2021), 5; 530-539 doi:10.1111/ppe.12776 (međunarodna recenzija, članak, znanstveni)
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21.Morris, Joan K.; Addor, Marie-Claude; Ballardini, Elisa; Barisic, Ingeborg; Barrachina-Bonet, Laia; Braz, Paula; Cavero-Carbonell, Clara; Den Hond, Elly; Garne, Ester; Gatt, Miriam et al.Prevention of Neural Tube Defects in Europe: A Public Health Failure // Frontiers in Pediatrics, 9 (2021), 10.3389/fped.2021.647038., 9 doi:10.3389/fped.2021.647038 (međunarodna recenzija, članak, znanstveni)
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22.Morris, Joan K; Garne, Ester; Loane, Maria; Barisic, Ingeborg; Densem, James; Latos-Bieleńska, Anna; Neville, Amanda; Pierini, Anna; Rankin, Judith; Rissmann, Anke et al.EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies // BMJ Open, 11 (2021), 6; e047859, 14 doi:10.1136/bmjopen-2020-047859 (međunarodna recenzija, članak, znanstveni)
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23.Morozin Pohovski, Leona; Bobinec, Adriana; Measic, Ana-Maria; Sansovic, Ivona; Barisic, IngeborgA new case of intragenic deletion of the TCF4 gene without features of Pitt-Hopkins syndrome // Molecular and experimental biology in medicine, 3 (2020), 2; 56-58 doi:10.33602/mebm.3.2.8 (recenziran, članak, stručni)
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24.Putte, Romy; Rooij, Iris A.L.M.; Haanappel, Cynthia P.; Marcelis, Carlo L.M.; Brunner, Han G.; Addor, Marie‐Claude; Cavero‐ Carbonell, Clara; Dias, Carlos M.; Draper, Elizabeth S.; Etxebarriarteun, Larraitz et al.Maternal risk factors for the VACTERL association: A EUROCAT case– control study // Birth Defects Research, 112 (2020), 9; 688-698 doi:10.1002/bdr2.1686 (međunarodna recenzija, članak, znanstveni)
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25.van Schie, Janne J. M.; Faramarz, Atiq; Balk, Jesper A.; Stewart, Grant S.; Cantelli, Erika; Oostra, Anneke B.; Rooimans, Martin A.; Parish, Joanna L.; de Almeida Estéves, Cynthia; Dumic, Katja et al.Warsaw Breakage Syndrome associated DDX11 helicase resolves G- quadruplex structures to support sister chromatid cohesion // Nature Communications, 11 (2020), 1; 4287-4305 doi:10.1038/s41467-020-18066-8 (međunarodna recenzija, članak, znanstveni)
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26.Morris, Joan K; Wellesley, Diana G; Barisic, Ingeborg; Addor, Marie-Claude; Bergman, Jorieke E H; Braz, Paula; Cavero- Carbonell, Clara; Draper, Elizabeth S; Gatt, Miriam; Haeusler, Martin et al.Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study // Archives of Disease in Childhood, 104 (2019), 12; 1181-1187 doi:10.1136/archdischild-2018-316733 (međunarodna recenzija, članak, znanstveni)
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27.Santoro, Michele; Coi, Alessio; Barišić, Ingeborg; Garne, Ester; Addor, Marie-Claude; Bergman, Jorieke E.H.; Bianchi, Fabrizio; Boban, Ljubica; Braz, Paula; Cavero-Carbonell, Clara et al.Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study // Neuroepidemiology, 53 (2019), 3-4; 169-179 doi:10.1159/000501238 (međunarodna recenzija, članak, znanstveni)
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28.van de Putte, Romy; van Rooij, Iris A. L. M.; Marcelis, Carlo L. M.; Guo, Michel; Brunner, Han G.; Addor, Marie-Claude; Cavero- Carbonell, Clara; Dias, Carlos M.; Draper, Elizabeth S.; Etxebarriarteun, Larraitz et al.Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study // Pediatric Research, 87 (2019), 3; 541-549 doi:10.1038/s41390-019-0561-y (međunarodna recenzija, članak, znanstveni)
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29.Cleary, Brian; Loane, Maria; Addor, Marie-Claude; Barisic, Ingeborg; de Walle, Hermien E K; Matias Dias, Carlos; Gatt, Miriam; Klungsoyr, Kari; McDonnell, Bob; Neville, Amanda et al.Methadone, Pierre Robin sequence and other congenital anomalies: case–control study // Archives of Disease in Childhood - Fetal and Neonatal Edition, 105 (2019), 2; 151-157 doi:10.1136/archdischild-2019-316804 (međunarodna recenzija, članak, ostalo)
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30.Coi, Alessio; Santoro, Michele; Garne, Ester; Pierini, Anna; Addor, Marie‐Claude; Alessandri, Jean‐Luc; Bergman, Jorieke E. H.; Bianchi, Fabrizio; Boban, Ljubica; Braz, Paula et al.Epidemiology of achondroplasia: A population‐based study in Europe // American Journal of Medical Genetics Part A, 179 (2019), 9; 1791-1798 doi:10.1002/ajmg.a.61289 (međunarodna recenzija, članak, znanstveni)
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31.Wang, Hao; Barisic, Ingeborg; Loane, Maria; Addor, Marie-Claude; Bailey, Linda M.; Gatt, Miriam; Klungsoyr, Kari; Mokoroa, Olatz; Nelen, Vera; Neville, Amanda J. et al.Congenital clubfoot in Europe: A population-based study // American Journal of Medical Genetics Part A, 179 (2019), 4; 595-601 doi:10.1002/ajmg.a.61067 (međunarodna recenzija, članak, ostalo)
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32.Morris, Joan K.; Springett, Anna L.; Greenlees, Ruth; Loane, Maria; Addor, Marie-Claude; Arriola, Larraitz; Barisic, Ingeborg; Bergman, Jorieke E. H.; Csaky-Szunyogh, Melinda; Dias, Carlos et al.Trends in congenital anomalies in Europe from 1980 to 2012 // PLOS ONE, 13 (2018), 4; e0194986, 18 doi:10.1371/journal.pone.0194986 (međunarodna recenzija, članak, znanstveni)
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33.Garne, Ester; Rissmann, Anke; Addor, Marie-Claude; Barisic, Ingeborg; Bergman, Jorieke; Braz, Paula; Cavero-Carbonell, Clara; Draper, Elizabeth S.; Gatt, Miriam; Haeusler, Martin et al.Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study // European Journal of Medical Genetics, 61 (2018), 9; 483-488 doi:10.1016/j.ejmg.2018.05.010 (međunarodna recenzija, članak, znanstveni)
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34.Barisic, Ingeborg; Boban, Ljubica; Akhmedzhanova, Diana; Bergman, Jorieke E.H.; Cavero-Carbonell, Clara; Grinfelde, Ieva; Materna-Kiryluk, Anna; Latos-Bieleńska, Anna; Randrianaivo, Hanitra; Zymak-Zakutnya, Natalya et al.Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe // European Journal of Medical Genetics, 61 (2018), 9; 499-507 doi:10.1016/j.ejmg.2018.05.014 (međunarodna recenzija, članak, znanstveni)
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35.O’Connor, Daniel J.; Sheean, Maria E.; Hofer, Matthias P.; Tsigkos, Stelios; Mariz, Segundo; Fregonese, Laura; Larsson, Kristina; Hivert, Virginie; Westermark, Kerstin; Naumann-Winter, Frauke et al.Defining orphan conditions in the context of the European orphan regulation: challenges and evolution // Nature Reviews Drug Discovery, 18 (2018), 7; 479-480 doi:10.1038/nrd.2018.128 (međunarodna recenzija, pregledni rad, stručni)
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36.Morris, Joan K.; Garne, Ester; Loane, Maria; Addor, Marie-Claude; Barisic, Ingeborg; Bianchi, Fabrizio; Gatt, Miriam; Lanzoni, Monica; Lynch, Catherine; Mokoroa, Olatz et al.Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study // European Journal of Medical Genetics, 61 (2018), 9; 479-482 doi:10.1016/j.ejmg.2018.05.008 (međunarodna recenzija, članak, znanstveni)
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37.Krnjak, Goran; Đuranović, Vlasta; Barišić, Ingeborg; Pažanin, Leo; Vulin, Katarina; Đaković, IvanaMakrofagni miofascitis u djevojčice s usporenim psihomotornim razvojem // 13. kongres Hrvatskog pedijatrijskog društva i 12. kongres Pedijatrijskog društva Hrvatske udruge medicinskih sestara / Paediatria Croatica, 62(Suppl.2) / Barišić, Ingeborg (ur.).
Zagreb: Klinika za dječje bolesti Zagreb, 2018. str. 234-234 (poster, međunarodna recenzija, sažetak, stručni) -
38.Bobinec, Adriana; Ivankov, Ana-Maria; Kero, Mijana; Sansović, Ivona; Barišić, IngeborgGenotipsko-fenotipska korelacija rijetke mikrodelecije 17q24.1-q24.3 // Paediatria Croatica, 61 (2017), 2; 84-89 doi:10.13112/PC.2017.13 (domaća recenzija, prikaz, ostalo)
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39.Ivankov, Ana-Maria; Bobinec, Adriana; Boban, Ljubica; Sansović, Ivona; Barišić, IngeborgDe novo složena kromosomska preraspodjela u regiji 2q32q35 // Paediatria Croatica, 61 (2017), 2; 78-83 doi:10.13112/PC.2017.12 (domaća recenzija, prikaz, ostalo)
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40.Dvorakova, L.; Vlaskova, H.; Sarajlija, A.; Ramadza, D. P.; Poupetova, H.; Hruba, E.; Hlavata, A.; Bzduch, V.; Peskova, K.; Storkanova, G. et al.Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II // Clinical Genetics, 91 (2017), 5; 787-796 doi:10.1111/cge.12927 (međunarodna recenzija, članak, znanstveni)
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41.Sansović, Ivona; Ivankov, Ana-Maria; Bobinec, Adriana; Kero, Mijana; Barišić, IngeborgChromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability // Croatian Medical Journal, 58 (2017), 3; 231-238 doi:10.3325/cmj.2017.58.231 (recenziran, članak, znanstveni)
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42.Boyle, Breidge; Addor, Marie-Claude; Arriola, Larraitz; Barisic, Ingeborg; Bianchi, Fabrizio; Csáky-Szunyogh, Melinda; de Walle, Hermien E K; Dias, Carlos Matias; Draper, Elizabeth; Gatt, Miriam et al.Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data // Archives of Disease in Childhood - Fetal and Neonatal Edition, 103 (2017), 1; F22-F28 doi:10.1136/archdischild-2016-311845 (međunarodna recenzija, članak, znanstveni)
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43.Given, Joanne E.; Loane, Maria; Garne, Ester; Nelen, Vera; Barisic, Ingeborg; Randrianaivo, Hanitra; Khoshnood, Babak; Wiesel, Awi; Rissmann, Anke; Lynch, Catherine et al.Gastroschisis in Europe - A Case-malformed-Control Study of Medication and Maternal Illness during Pregnancy as Risk Factors // Paediatric and Perinatal Epidemiology, 31 (2017), 6; 549-559 doi:10.1111/ppe.12401 (međunarodna recenzija, članak, znanstveni)
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44.Ecker, Andrea; Mariz, Segundo; Naumann-Winter, Frauke; Norga, Koenraad; Barisic, Ingeborg; Girard, Thomas; Tomasi, Paolo; Mentzer, Dirk; Sepodes, BrunoComparative analysis of the scope of European Union paediatric investigation plans with corresponding orphan designations // Archives of Disease in Childhood, 103 (2017), 5; 427-430 doi:10.1136/archdischild-2017-313352 (međunarodna recenzija, članak, znanstveni)
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45.Bergman, Jorieke E. H.; Lutke, L. Renée; Gans, Rijk O. B.; Addor, Marie-Claude; Barisic, Ingeborg; Cavero-Carbonell, Clara; Garne, Ester; Gatt, Miriam; Klungsoyr, Kari; Lelong, Nathalie et al.Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study // Drug Safety, 41 (2017), 4; 415-427 doi:10.1007/s40264-017-0627-x (međunarodna recenzija, članak, znanstveni)
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46.Gagro, Alenka; Roić, Goran; Sansović, Ivona; Ivankov, AM; Bobinec, A; Antičević, Darko; Barišić, IngeborgInflammatory polyarthritis in patient with 18q deletion syndrome. // Program and abstracts Book of 10th ISABS Conference on Forensic and Anthropologic Genetics and Mayo Clinic lectures in Individualized Medicine.
Dubrovnik, Hrvatska, 2017. str. 309-309 (predavanje, međunarodna recenzija, sažetak, stručni) -
47.Barišić, I; Turkalj, M; Primorac, D.Osteogenesis imperfecta: klinička procjena i liječenje // Paediatria Croatica, 61 (2017), 3; 97-105 (recenziran, članak, znanstveni)
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48.Dumić, Katja K.; Grubić, Zorana; Yuen, Tony; Wilson, Robert C.; Kušec, Vesna; Barišić, Ingeborg; Stingl, Katarina; Sansović, Ivona; Škrabić, Veselin; Dumić, Miroslav; New, Maria I.Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia // Journal of steroid biochemistry and molecular biology, 165 (2017), Part A; 51-56 doi:10.1016/j.jsbmb.2016.03.035 (podatak o recenziji nije dostupan, pregledni rad, znanstveni)
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49.Sansović, Ivona; Ivankov, Ana-Maria; Bobinec, Adriana; Barišić, IngeborgRazlike u broju kopija u genomu kao uzrok razvojnih poremećaja, kongenitalnih anomalija i autističkog spektra poremećaja // Paediatria Croatica. Supplement, 60 (Suppl 3) (2016), 35-44 (domaća recenzija, članak, znanstveni)
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50.Sansović, Ivona; Ivankov, Ana-Maria; Bobinec, Adriana; Barišić, IngeborgKROMOSOMSKI MICROARRAY U KLINIČKOJ DIJAGNOSTICI OSOBA S RAZVOJNIM POREMEĆAJIMA // Paediatria Croatica. Supplement, 60 (Suppl 1) (2016), 58-64 (domaća recenzija, pregledni rad, znanstveni)
