Pronađeno 501 radova, za izraz:
"OSOBA: Ingeborg Barišić (CROSBI Profil: 13659, MBZ: 168183)"
DODAJ/IZMIJENI OPERATORE PRETRAŽIVANJA
FILTRIRANO:
- Vrsta povezanosti: Autorstvo
- Profil osobe: Ingeborg Barišić (13659)
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1.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: Institute for Anthropological Research, 2022. str. 308-308 doi:10.54062/jb (predavanje, međunarodna recenzija, sažetak, znanstveni) -
2.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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3.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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4.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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5.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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6.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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7.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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8.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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9.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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10.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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11.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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12.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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13.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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14.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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15.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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16.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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17.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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18.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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19.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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20.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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21.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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22.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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23.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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24.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) -
25.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)
