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)
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51.Ivankov, Ana-Maria; Bobinec, Adriana; Boban, Ljubica; Sansović, Ivona; Barišić, IngeborgMikrodelecija 8q23.3-q24.11 povezana sa sindromima Langer- Giedion i Cornelia de Lange-4 // Paediatria Croatica, 60 (2016), 3; 106-110 (domaća recenzija, članak, stručni)
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52.Bobinec, Adriana; Ivankov, Ana-Maria; Čule, Marina; Sansović, Ivona; Barišić, IngeborgSekvenca kaudalne regresije i delecija 7q34-q36.3 // Paediatria Croatica, 60 (2016), 3; 112-115 doi:10.13112/PC.2016.17 (domaća recenzija, članak, stručni)
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53.Given, Joanne E.; Loane, Maria; Luteijn, Johannes M.; Morris, Joan K.; Jong van den Berg, Lolkje T.W.; Garne, Ester; Addor, Marie‐Claude; Barisic, Ingeborg; Walle, Hermien; Gatt, Miriam et al.EUROmediCAT signal detection: an evaluation of selected congenital anomaly‐medication associations // British Journal of Clinical Pharmacology, 82 (2016), 4; 1094-1109 doi:10.1111/bcp.12947 (međunarodna recenzija, članak, znanstveni)
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54.Dolk, Helen; Wang, Hao; Loane, Maria; Morris, Joan; Garne, Ester; Addor, Marie-Claude; Arriola, Larraitz; Bakker, Marian; Barisic, Ingeborg; Doray, Berenice et al.Lamotrigine use in pregnancy and risk of orofacial cleft and other congenital anomalies // Neurology, 86 (2016), 18; 1716-1725 doi:10.1212/wnl.0000000000002540 (međunarodna recenzija, članak, znanstveni)
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55.Luteijn, Johannes M.; Morris, Joan K.; Garne, Ester; Given, Joanne; de Jong-van den Berg, Lolkje; Addor, Marie-Claude; Bakker, Marian; Barisic, Ingeborg; Gatt, Miriam; Klungsoyr, Kari et al.EUROmediCAT signal detection: a systematic method for identifying potential teratogenic medication // British Journal of Clinical Pharmacology, 82 (2016), 4; 1110-1122 doi:10.1111/bcp.13056 (međunarodna recenzija, članak, znanstveni)
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56.Morris, Joan K; Rankin, Judith; Garne, Ester; Loane, Maria; Greenlees, Ruth; Addor, Marie-Claude; Arriola, Larraitz; Barisic, Ingeborg; Bergman, Jorieke E H; Csaky-Szunyogh, Melinda et al.Prevalence of microcephaly in Europe: population based study // BMJ, 13 (2016), 354; i4721, 6 doi:10.1136/bmj.i4721 (međunarodna recenzija, članak, znanstveni)
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57.Vulin, Katarina; Marković, Silvana; Fumić, Ksenija; Marjanović, Josip; Đaković, Ivana; Barišić, Ingeborg; Đuranović, VlastaKrabbeova bolest - prikaz bolesnice // Paediatria Croatica, Vol. 60, Suppl 3, 12. kongres Hrvatskog pedijatrijskog društva, Opatija, 13.-16.10.2016.
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58.Ivona Vrkić Boban, Ingeborg Barišić, Ivona Sansović, Vjekoslav Krželj, Bernarda LozićTeško globalno zaostajanje, epilepsija, hipospadija s kriptorhizmom i bulozna epidermoliza povezane s de novo delecijom 2q22.2-q22.3: prikaz slučaja // Paediatria Croatica. Supplement / Barišić, Ingeborg (ur.).
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59.Katušić Hećimović, Silva; Čermak, Stjepko; Malnar, Martina; Barišić, IngeborgMiotonična distrofija tipa 1 // Genetičko informiranje u praksi / Čulić, Vida ; Pavelić, Jasminka ; Radman, Maja (ur.).
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60.Katušić Hećimović, Silva; Malnar, Martina; Čermak, Stjepko; Barišić, IngeborgSindrom fragilnog X // Genetičko informiranje u praksi / Čulić, Vida ; Pavelić, Jasminka ; Radman, Maja (ur.).
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61.Bergman, Jorieke E. H.; Loane, Maria; Vrijheid, Martine; Pierini, Anna; Nijman, Rien J. M.; Addor, Marie-Claude; Barisic, Ingeborg; Béres, Judit; Braz, Paula; Budd, Judith et al.Epidemiology of hypospadias in Europe: a registry-based study // World Journal of Urology, 33 (2015), 12; 2159-2167 doi:10.1007/s00345-015-1507-6 (međunarodna recenzija, članak, znanstveni)
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62.Taruscio, Domenica; Mantovani, Alberto; Carbone, Pietro; Barisic, Ingeborg; Bianchi, Fabrizio; Garne, Ester; Nelen, Vera; Neville, Amanda Julie; Wellesley, Diana; Dolk, HelenPrimary Prevention of Congenital Anomalies: Recommendable, Feasible and Achievable // Public Health Genomics, 18 (2015), 3; 184-191 doi:10.1159/000379739 (međunarodna recenzija, pregledni rad, znanstveni)
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63.Garne, Ester; Hansen, Anne Vinkel; Morris, Joan; Zaupper, Louise; Addor, Marie-Claude; Barisic, Ingeborg; Gatt, Miriam; Lelong, Nathalie; Klungsøyr, Kari; O'Mahony, Mary et al.Use of asthma medication during pregnancy and risk of specific congenital anomalies: A European case-malformed control study // Journal of Allergy and Clinical Immunology, 136 (2015), 6; 1496-1502e7 doi:10.1016/j.jaci.2015.05.043 (međunarodna recenzija, članak, znanstveni)
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64.Khoshnood, Babak; Loane, Maria; Walle, Hermien de; Arriola, Larraitz; Addor, Marie-Claude; Barisic, Ingeborg; Beres, Judit; Bianchi, Fabrizio; Dias, Carlos; Draper, Elizabeth et al.Long term trends in prevalence of neural tube defects in Europe: population based study // BMJ, 351 (2015), h5949, 6 doi:10.1136/bmj.h5949 (međunarodna recenzija, članak, znanstveni)
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65.Barišić, Ingeborg; Boban, Ljubica; Loane, M; Garne, E; Wellesley, D; Calzolari, E; Dolk, H; Addor, MC; Bergman, J E; Braz, P et al.Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe // European journal of human genetics, 23 (2015), 6; 746-752 (međunarodna recenzija, članak, znanstveni)
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66.McGivern, MR; Best, KE; Rankin, J; Wellesley, D; Greenlees, R; Addor, MC; Arriola, L; de Walle, H; Barisic, I; Beres, J et al.Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study // Archives of disease in childhood, 100 (2015), 2; 137-144 (podatak o recenziji nije dostupan, članak, znanstveni)
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67.Roganović, Jelena; Barišić, Ingeborg; Jonjić, Nives; Fumić, Ksenija; Đorđević, AnaAngiokeratoma in Fabry Disease : Diagnostic but not Treatment Effectiveness Marker : Case Report // Global journal of medical and clinical case reports, 2 (2014), 1; 035-036 doi:10.17352/2455-5282.000012 (međunarodna recenzija, članak, stručni)
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68.Dumić, Katja; Yuen, T.; Grubić, Zorana; Kušec, Vesna; Barišić, Ingeborg; New, Maria I.Two novel CYP11B1 gene mutations in patients from two Croatian families with 11 β -Hydroxylase deficiency // International journal of endocrinology, / (2014), 185974-1 doi:10.1155/2014/185974 (međunarodna recenzija, članak, znanstveni)
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69.Morožin Pohovski, Leona; Barišić, IngeborgMultiplex ligation-dependent probe amplification (MLPA) genetic testing in the diagnostics of children with developmental delay/intellectual disabilities. // Folia medica Facultatis medicinae Universitatis Saraeviensis, 49 (2014), 1; 15-21 (podatak o recenziji nije dostupan, pregledni rad, ostalo)
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70.Dumić Kubat, Katja; Fumić, Ksenija; Škarić, Ivančica; Barišić, IngeborgPoremeća ciklusa ureje - rijedak uzrok iznenadne smrti dojenčeta // Pediatria Croatica Supplement
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71.Sansović, Ivona; Dumić Kubat, Katja; Barišić, IngeborgMetoda višestrukog umnažanja vezanih sondi u dijagnostici kongenitalne adrenalne hiperplazije uzrokovane deficitom 21-hidroksilaze // Pediatria Croatica Supplement
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72.Kero, Mijana; Morožin-Pohovski, Leona; Čače, Neven; Barišić, IngeborgSindrom Kleefstra: prikaz bolesnika s asimetričnom hipetrofičnom kardiomiopatijom // Pediatria Croatica Supplement
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73.Barišić Ingeborg; Boban, Ljubica; Loane, Maria; Garne, Ester; Wellesley, Diana; Calzolari, Elisa; Dolk, Helen; EUROCAT radna skupinaHolt Oramov sindrom - europska populacijska studija // Pediatria Croatica Supplement
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74.Morožin Pohovski, Leona; Barišić, Ingeborg; Riegel, Mariluce; Schinzel, AlbertMolekularna karakterizacija prstenastog kromosoma 9 primjenom tehnike komparativne genomske hibridizacije na mikropostroju // Pediatria Croatica Supplement
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75.Boban, Ljubica; Barišić, Ingeborg; Loane, Maria; Garne, Rster; Wellesley, Diana; Calzolari, Elisa; Dolk, Helen; EUROCAT radna skupinaEllis van Creveldov sindrom - epidemiološka studija u europskoj populaciji // Pediatria Croatica Supplement
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76.Dumić Kubat, Katja; Grubić, Zorana; Barišić, Ingeborg; Štingl, Katarina; Yuen, Tony; Wilson, Robert; Dumić, Miroslav; Škrabic, Veselin; Kušec, Vesna; I New, MariaMolekularno-genetička analiza gena CYP21A2 i korelacija genotipa i fenotipa u bolesnika s klasičnim oblikom kongenitalne adrenalne hiperplazije u Hrvatskoj // Pediatria Croatica Supplement
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77.Boban LjubicaKlinički i biološka obilježja rijetkih genetskih sindroma u europskoj populaciji, 2014., doktorska disertacija, Medicinski fakultet Sveučilišta u Zagrebu, Zagreb
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78.Morožin Pohovski, L; Barišić, IIdentification of microdeletion 8q23.3q24.11 by MLPA in patient with multiple hereditary exostoses // European journal of human genetics Supplement 1
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79.Sansović, I; Morožin Pohovski, L; Barišić, IMicroduplication of Xp22.31 region involving the STS gene in two males with intellectual disability // European journal of human genetics
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80.Luteijn, J.M.; Dolk, H.; Addor, M.C.; Arriola, L.; Barišić, Ingeborg; Bianchi, F.; Calzolari, E.; Draper, E.; Garne, E.; Gatt, M. et al.Seasonality of congenital anomalies in Europe // Birth defects research. Part A. Clinical and molecular teratology, 100 (2014), 4; 260-269 doi:10.1002/bdra.23231 (međunarodna recenzija, članak, znanstveni)
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81.Taruscio, D; Arriola, L; Baldi, F; Barišić, I; Bermejo-Sánchez, E; Bianchi, F; Calzolari, E; Carbone, P; Curran, R; Garne, E et al.European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans // Public Health Genomics, 17 (2014), 115-123 doi:10.1159/00036060 (podatak o recenziji nije dostupan, ostalo)
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82.Calzolari, E.; Barišić, Ingeborg; Loane, M.; Morris, J.; Wellesley, D.; Dolk, H.; Addor, M.C.; Arriola, L.; Bianchi, F.; Neville, A.J. et al.Epidemiology of multiple congenital anomalies in Europe : A EUROCAT population-based registry study // Birth defects research. Part A. Clinical and molecular teratology, 100 (2014), 4; 270-276 doi:10.1002/bdra.23240 (međunarodna recenzija, članak, znanstveni)
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83.Morožin-Pohovski, L; Barišić, I:Multiple ligation-dependent proble amplification (MLPA) genetic testing in the diagnostics of children with developmental delay/intellectual disabilities // Folia Medica Facultatis Medicinae Universitatis Saraeviensis
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84.Best, K.E.; Addor, M.C.; Arriola, L.; Balku, E.; Barišićc, Ingeborg; Bianchi, F.; Calzolari, E.; Curran, R.; Doray, B.; Draper, E. et al.Hirschsprung's disease prevalence in Europe : A register based study // Birth defects research. Part A. Clinical and molecular teratology, 100 (2014), 9; 695-702 doi:10.1002/bdra.23269 (međunarodna recenzija, članak, znanstveni)
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85.Primorac, Dragan; Antičević, Darko; Barišić, Ingeborg; Hudetz, Damir; Ivković, AlanOsteogenesis Imperfecta – Multi-Systemic and Life - Long Disease that Affects Whole Family // Collegium antropologicum, 38 (2014), 767-772 (međunarodna recenzija, članak, znanstveni)
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86.Morris, J.K.; Garne, E.; Wellesley, D.; Addor, M.C.; Arriola, L.; Barišić, Ingrborg; Beres, J.; Bianchi, F.; Budd, J.; Dias, C.M. et al.Major congenital anomalies in babies born with Down syndrome : A EUROCAT population-based registry study // American journal of medical genetics. Part A, 164 (2014), 12; 2979-2986 doi:10.1002/ajmg.a.36780 (međunarodna recenzija, članak, znanstveni)
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87.Barisic, I; Boban, L; Greenlees, R; Garne, E; Wellesley, D; Calzolari, E; Addor, MC; Arriola, L; Bergman, J; Braz, P et al.Holt Oram syndrome: a registry-based study in Europe // Orphanet Journal of Rare Disease, 9 (2014), 156-156 (podatak o recenziji nije dostupan, članak, ostalo)
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88.Zergollern-Čupak, Ljiljana; Barišić, Ingeborg; Morožin-Pohovski, LeonaDevelopment of genetics in the world and in Croatia – forty years of the Croatian Society of Human Genetics of the Croatian Medical Association // Collegium antropologicum, 38 (2014), 3; 809-818 (podatak o recenziji nije dostupan, ostalo)
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89.Sansović, Ivona; Morožin Pohovski, Leona; Barišić, IngeborgMicroduplication of Xp22.31 region involving the STS gene in two males with intellectual disability // European Journal of Human Genetics, Volume 22, Supplement 1, May 2014 / G-J B van Ommen (ur.).
Milano, Italija: Nature Publishing Group, 2014. str. 163-164 (poster, međunarodna recenzija, sažetak, znanstveni) -
90.Sansović, Ivona; Dumić Kubat, Katja; Barišić, IngeborgMetoda višestrukog umnažanja vezanih sondi u dijagnostici kongenitalne adrenalne hiperplazije uzrokovane deficitom 21-hidroksilaze // PAEDIATRIA CROATICA, Vol. 58, Suppl 2 / Prof.dr.sc. Ingeborg Barišić, dr.med. (ur.).
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91.Barišić, Ingeborg; Odak, Ljubica; Loane, M.; Garne, Ester; Wellesley, Diana; Calzolari, Elisa; Dolk, Helen; Addor, Marie-Claude; Arriola, Larraitz; Bergman, Jorieke et al.Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe // European journal of human genetics, 22 (2014), 8; 1026-1033 doi:10.1038/ejhg.2013.287 (međunarodna recenzija, članak, znanstveni)
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92.Cohn, G.M.; Morin, I.; Whiteman, D.A.; ...; Barišič, Ingeborg; ...Development of a mnemonic screening tool for identifying subjects with Hunter syndrome // European journal of pediatrics, 172 (2013), 7; 965-970 doi:10.1007/s00431-013-1967-x (međunarodna recenzija, članak, znanstveni)
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93.Barišić IngeborgDijagnostički algoritam za dijete s razvojnim zaostajanjem // Pedijatrija danas 2013: neki dijagnostički i terapijski prijepori
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94.Odak, Ljubica; Morožin-Pohovski, Leona; Barišić, IngeborgMikrodelecija 17q21.31- prikaz dvaju bolesnika // Paediatria Croatica, 57 (2013), 1; 45-48 (recenziran, članak, stručni)
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95.Barišić, Ingeborg; Morožin Pohovski, LeonaNovi mikrodelecijski sindromi // Paediatria Croatica, 57 (2013), 4; 400-407 (recenziran, članak, stručni)
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96.Morožin Pohovski; Leona; Barišić, IngeborgMicrodeletion syndromes: copy number aberrations in patients with developmental delay/intellectual disability detected by MLPA // Chromosome Research. Supplement 1
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97.Luteijn, J.M.; Dolk, H.; Addor, M.C.; Arriola, L.; Bakker, M.; Barišić, Ingeborg; Bianchi, F.; Calzolari, E.; Draper, E.; Garne, E. et al.Seasonality of births and congenital anomalies in Europe // Birth defects research. Part A. Clinical and molecular teratology, 100 (2013), 4; 260-269 doi:10.1002/bdra.23231 (međunarodna recenzija, članak, znanstveni)
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98.Odak, Ljubica; Barišić, Ingeborg; Loane, Maria; Garne, Ester; Wellesley, Diana; Calzolari, Elisa; Dolk, HelenMeckel Gruber syndrome in Europe- population based study // The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine, Book of Abstracts
Split, Hrvatska, 2013. str. 253-253 (poster, međunarodna recenzija, sažetak, ostalo) -
99.Morožin Pohovski, Leona; Barišić, IngeborgDetection of subtelomeric copy number aberrations in patients with developmental delay/intellectual disability by MLPA // The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine, Book of Abstracts
Split, Hrvatska, 2013. str. 290-290 (poster, međunarodna recenzija, sažetak, ostalo) -
100.Dumić Kubat, Katja; Morava, Eva; Barišić, IngeborgPatient with autosomal recessive cutis laxa type 2B due to PYCR1 gene mutation // The Eighth ISABS Conference in Forensic, Anthropologic and Medical Genetics and Mayo Clinic Lectures in Translational Medicine, Book of Abstracts
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