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)
