المؤلفون: Rissmann, A, Tan, J, Glinianaia, S, Rankin, J, Pierini, A, Santoro, M, Coi, A, Garne, E, Loane, M, Given, J, Reid, A, Aizpurua, A, Akhmedzhanova, D, Ballardini, E, Barisic, I, Cavero-Carbonell, C, de Walle, HEK, Gatt, M, Gissler, M, Heino, A, Jordan, S, Urhoj, SK, Klungsoyr, K, Lutke, R, Mokoroa, O, Neville, AJ, Thayer, DS, Wellesley, DG, Yevtushok, L, Zurriaga, O, Morris, J

المصدر: BMJ paediatrics open. 7(1)

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:153148384Test

المؤلفون: Morris, JK, Bergman, JEH, Barisic, I, Wellesley, D, Tucker, D, Limb, E, Addor, M-C, Cavero-Carbonell, C, Matias Dias, C, Draper, ES, Echevarría-González-de-Garibay, LJ, Gatt, M, Klungsøyr, K, Lelong, N, Luyt, K, Materna-Kiryluk, A, Nelen, V, Neville, A, Perthus, I, Pierini, A, Randrianaivo-Ranjatoelina, H, Rankin, J, Rissmann, A, Rouget, F, Sayers, G, Wertelecki, W, Kinsner-Ovaskainen, A, Garne, E

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: https://openaccess.sgul.ac.uk/id/eprint/115921/1/s41431-023-01502-w.pdfTest; https://openaccess.sgul.ac.uk/id/eprint/115921/6/41431_2023_1502_MOESM1_ESM.docxTest; Morris, JK; Bergman, JEH; Barisic, I; Wellesley, D; Tucker, D; Limb, E; Addor, M-C; Cavero-Carbonell, C; Matias Dias, C; Draper, ES; et al. Morris, JK; Bergman, JEH; Barisic, I; Wellesley, D; Tucker, D; Limb, E; Addor, M-C; Cavero-Carbonell, C; Matias Dias, C; Draper, ES; Echevarría-González-de-Garibay, LJ; Gatt, M; Klungsøyr, K; Lelong, N; Luyt, K; Materna-Kiryluk, A; Nelen, V; Neville, A; Perthus, I; Pierini, A; Randrianaivo-Ranjatoelina, H; Rankin, J; Rissmann, A; Rouget, F; Sayers, G; Wertelecki, W; Kinsner-Ovaskainen, A; Garne, E (2024) Surveillance of multiple congenital anomalies; searching for new associations. Eur J Hum Genet, 32 (4). pp. 407-412. ISSN 1476-5438 https://doi.org/10.1038/s41431-023-01502-wTest SGUL Authors: Morris, Joan Katherine

الإتاحة: https://doi.org/10.1038/s41431-023-01502-wTest
https://openaccess.sgul.ac.uk/id/eprint/115921Test/
https://openaccess.sgul.ac.uk/id/eprint/115921/1/s41431-023-01502-w.pdfTest
https://openaccess.sgul.ac.uk/id/eprint/115921/6/41431_2023_1502_MOESM1_ESM.docxTest

المؤلفون: Heino, A, Morris, JK, Garne, E, Baldacci, S, Barisic, I, Cavero-Carbonell, C, García-Villodre, L, Given, J, Jordan, S, Loane, M, Lutke, LR, Neville, AJ, Santoro, M, Scanlon, I, Tan, J, de Walle, HEK, Kiuru-Kuhlefelt, S, Gissler, M

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: https://openaccess.sgul.ac.uk/id/eprint/116202/7/s10995-024-03911-9.pdfTest; https://openaccess.sgul.ac.uk/id/eprint/116202/12/10995_2024_3911_MOESM1_ESM.docxTest; https://openaccess.sgul.ac.uk/id/eprint/116202/4/Prenatal%20diagnoses%2006062023%20title%20page%20REVISION%20FINAL%20clean.docxTest; https://openaccess.sgul.ac.uk/id/eprint/116202/1/Prenatal%20diagnoses%2006062023%20article%20REVISION%20FINAL%20clean.docxTest; https://openaccess.sgul.ac.uk/id/eprint/116202/3/Prenatal%20diagnoses%20Appendix%20FINAL.docxTest; Heino, A; Morris, JK; Garne, E; Baldacci, S; Barisic, I; Cavero-Carbonell, C; García-Villodre, L; Given, J; Jordan, S; Loane, M; et al. Heino, A; Morris, JK; Garne, E; Baldacci, S; Barisic, I; Cavero-Carbonell, C; García-Villodre, L; Given, J; Jordan, S; Loane, M; Lutke, LR; Neville, AJ; Santoro, M; Scanlon, I; Tan, J; de Walle, HEK; Kiuru-Kuhlefelt, S; Gissler, M (2024) The Association of Prenatal Diagnoses with Mortality and Long-Term Morbidity in Children with Specific Isolated Congenital Anomalies: A European Register-Based Cohort Study. Matern Child Health J. ISSN 1573-6628 https://doi.org/10.1007/s10995-024-03911-9Test SGUL Authors: Morris, Joan Katherine Tan, Joachim Wei Li

الإتاحة: https://doi.org/10.1007/s10995-024-03911-9Test
https://openaccess.sgul.ac.uk/id/eprint/116202Test/
https://openaccess.sgul.ac.uk/id/eprint/116202/7/s10995-024-03911-9.pdfTest
https://openaccess.sgul.ac.uk/id/eprint/116202/12/10995_2024_3911_MOESM1_ESM.docxTest
https://openaccess.sgul.ac.uk/id/eprint/116202/4/Prenatal%20diagnoses%2006062023%20title%20page%20REVISION%20FINAL%20clean.docxTest
https://openaccess.sgul.ac.uk/id/eprint/116202/1/Prenatal%20diagnoses%2006062023%20article%20REVISION%20FINAL%20clean.docxTest
https://openaccess.sgul.ac.uk/id/eprint/116202/3/Prenatal%20diagnoses%20Appendix%20FINAL.docxTest

المؤلفون: Bergman, JEH, Perraud, A, Barišić, I, Kinsner-Ovaskainen, A, Morris, JK, Tucker, D, Wellesley, D, Garne, E

وصف الملف: application/pdf; application/vnd.ms-excel

العلاقة: https://openaccess.sgul.ac.uk/id/eprint/116254/1/Birth%20Defects%20Research%20-%202024%20-%20Bergman%20-%20Updated%20EUROCAT%20guidelines%20for%20classification%20of%20cases%20with%20congenital%20anomalies.pdfTest; https://openaccess.sgul.ac.uk/id/eprint/116254/6/bdr22314-sup-0001-tables1.xlsxTest; Bergman, JEH; Perraud, A; Barišić, I; Kinsner-Ovaskainen, A; Morris, JK; Tucker, D; Wellesley, D; Garne, E (2024) Updated EUROCAT guidelines for classification of cases with congenital anomalies. Birth Defects Res, 116 (2). e2314. ISSN 2472-1727 https://doi.org/10.1002/bdr2.2314Test SGUL Authors: Morris, Joan Katherine

الإتاحة: https://doi.org/10.1002/bdr2.2314Test
https://openaccess.sgul.ac.uk/id/eprint/116254Test/
https://openaccess.sgul.ac.uk/id/eprint/116254/1/Birth%20Defects%20Research%20-%202024%20-%20Bergman%20-%20Updated%20EUROCAT%20guidelines%20for%20classification%20of%20cases%20with%20congenital%20anomalies.pdfTest
https://openaccess.sgul.ac.uk/id/eprint/116254/6/bdr22314-sup-0001-tables1.xlsxTest

المؤلفون: Bergman, JEH, Barišić, I., Addor, M.C., Braz, P., Cavero-Carbonell, C., Draper, E.S., Echevarría-González-de-Garibay, L.J., Gatt, M., Haeusler, M., Khoshnood, B., Klungsøyr, K., Kurinczuk, J.J., Latos-Bielenska, A., Luyt, K., Martin, D., Mullaney, C., Nelen, V., Neville, A.J., O'Mahony, M.T., Perthus, I., Pierini, A., Randrianaivo, H., Rankin, J., Rissmann, A., Rouget, F., Sayers, G., Schaub, B., Stevens, S., Tucker, D., Verellen-Dumoulin, C., Wiesel, A., Gerkes, E.H., Perraud, A., Loane, M.A., Wellesley, D., de Walle, HEK

المصدر: American journal of medical genetics. Part A, vol. 191, no. 4, pp. 995-1006

مصطلحات موضوعية: Pregnancy, Humans, Female, Infant, Newborn, Amniotic Band Syndrome/complications, Abnormalities, Multiple/epidemiology, Europe/epidemiology, Maternal Age, Stillbirth/epidemiology, Registries, Prevalence, ADAM sequence, Streeter anomaly, birth defects, body stalk anomaly, constriction bands

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36584346; info:eu-repo/semantics/altIdentifier/eissn/1552-4833; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_B90F6ED045DA9; https://serval.unil.ch/notice/serval:BIB_B90F6ED045DATest; urn:issn:1552-4825; https://serval.unil.ch/resource/serval:BIB_B90F6ED045DA.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B90F6ED045DA9Test

الإتاحة: https://doi.org/10.1002/ajmg.a.63107Test
https://serval.unil.ch/notice/serval:BIB_B90F6ED045DATest
https://serval.unil.ch/resource/serval:BIB_B90F6ED045DA.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B90F6ED045DA9Test

المؤلفون: Loane, M, Given, JE, Tan, J, Barišić, I, Barrachina-Bonet, L, Cavero-Carbonell, C, Coi, A, Densem, J, Garne, E, Gissler, M, Heino, A, Jordan, S, Lutke, R, Neville, AJ, Odak, L, Puccini, A, Santoro, M, Scanlon, I, Urhoj, SK, de Walle, HEK, Wellesley, D, Morris, JK

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: https://openaccess.sgul.ac.uk/id/eprint/115703/1/journal.pone.0290711.pdfTest; https://openaccess.sgul.ac.uk/id/eprint/115703/10/pone.0290711.s001.docxTest; https://openaccess.sgul.ac.uk/id/eprint/115703/11/pone.0290711.s002.docxTest; https://openaccess.sgul.ac.uk/id/eprint/115703/14/pone.0290711.s003.docxTest; Loane, M; Given, JE; Tan, J; Barišić, I; Barrachina-Bonet, L; Cavero-Carbonell, C; Coi, A; Densem, J; Garne, E; Gissler, M; et al. Loane, M; Given, JE; Tan, J; Barišić, I; Barrachina-Bonet, L; Cavero-Carbonell, C; Coi, A; Densem, J; Garne, E; Gissler, M; Heino, A; Jordan, S; Lutke, R; Neville, AJ; Odak, L; Puccini, A; Santoro, M; Scanlon, I; Urhoj, SK; de Walle, HEK; Wellesley, D; Morris, JK (2023) Creating a population-based cohort of children born with and without congenital anomalies using birth data matched to hospital discharge databases in 11 European regions: Assessment of linkage success and data quality. PLoS One, 18 (8). e0290711. ISSN 1932-6203 https://doi.org/10.1371/journal.pone.0290711Test SGUL Authors: Morris, Joan Katherine

الإتاحة: https://doi.org/10.1371/journal.pone.0290711Test
https://openaccess.sgul.ac.uk/id/eprint/115703Test/
https://openaccess.sgul.ac.uk/id/eprint/115703/1/journal.pone.0290711.pdfTest
https://openaccess.sgul.ac.uk/id/eprint/115703/10/pone.0290711.s001.docxTest
https://openaccess.sgul.ac.uk/id/eprint/115703/11/pone.0290711.s002.docxTest
https://openaccess.sgul.ac.uk/id/eprint/115703/14/pone.0290711.s003.docxTest

المؤلفون: Claridge, H, Tan, J, Loane, M, Garne, E, Barisic, I, Cavero-Carbonell, C, Dias, C, Gatt, M, Jordan, S, Khoshnood, B, Kiuru-Kuhlefelt, S, Klungsoyr, K, Mokoroa Carollo, O, Nelen, V, Neville, AJ, Pierini, A, Randrianaivo, H, Rissmann, A, Tucker, D, de Walle, H, Wertelecki, W, Morris, JK

وصف الملف: application/pdf

العلاقة: https://openaccess.sgul.ac.uk/id/eprint/115586/1/e071687.full.pdfTest; Claridge, H; Tan, J; Loane, M; Garne, E; Barisic, I; Cavero-Carbonell, C; Dias, C; Gatt, M; Jordan, S; Khoshnood, B; et al. Claridge, H; Tan, J; Loane, M; Garne, E; Barisic, I; Cavero-Carbonell, C; Dias, C; Gatt, M; Jordan, S; Khoshnood, B; Kiuru-Kuhlefelt, S; Klungsoyr, K; Mokoroa Carollo, O; Nelen, V; Neville, AJ; Pierini, A; Randrianaivo, H; Rissmann, A; Tucker, D; de Walle, H; Wertelecki, W; Morris, JK (2023) Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies. BMJ Open, 13 (7). e071687. ISSN 2044-6055 https://doi.org/10.1136/bmjopen-2023-071687Test SGUL Authors: Morris, Joan Katherine

الإتاحة: https://doi.org/10.1136/bmjopen-2023-071687Test
https://openaccess.sgul.ac.uk/id/eprint/115586Test/
https://openaccess.sgul.ac.uk/id/eprint/115586/1/e071687.full.pdfTest

المؤلفون: Murray, A, Gough, G, Cindrić, A, Vučković, F, Koschut, D, Borelli, V, Petrović, DJ, Bekavac, A, Plećaš, A, Hribljan, V, Brunmeir, R, Jurić, J, Pučić-Baković, M, Slana, A, Deriš, H, Frkatović, A, Groet, J, O'Brien, NL, Chen, HY, Yeap, YJ, Delom, F, Havlicek, S, Gammon, L, Hamburg, S, Startin, C, D'Souza, H, Mitrečić, D, Kero, M, Odak, L, Krušlin, B, Krsnik, Ž, Kostović, I, Foo, JN, Loh, Y-H, Dunn, NR, de la Luna, S, Spector, T, Barišić, I, Thomas, MSC, Strydom, A, Franceschi, C, Lauc, G, Krištić, J, Alić, I, Nižetić, D

مصطلحات موضوعية: Ageing, Chromosome 21, DYRK1A, DYRK1A inhibitors, Down syndrome, Down syndrome critical region, IgG glycan, LaminB1, Adult, Humans, Aging, Cell Differentiation, Induced Pluripotent Stem Cells

وصف الملف: 104692 - ?

العلاقة: EBioMedicine; https://qmro.qmul.ac.uk/xmlui/handle/123456789/90700Test

الإتاحة: https://doi.org/10.1016/j.ebiom.2023.104692Test
https://qmro.qmul.ac.uk/xmlui/handle/123456789/90700Test

المؤلفون: Perković, D., Janković Danolić, M., Petrić, M., Barišić, I., Gugo, K., Božić, J.

المصدر: Scientific Abstracts

الإتاحة: https://doi.org/10.1136/annrheumdis-2024-eular.2726Test

المؤلفون: Mamasoula, C., Addor, M.C., Carbonell, C.C., Dias, C.M., Echevarría-González-de-Garibay, L.J., Gatt, M., Khoshnood, B., Klungsoyr, K., Randall, K., Stoianova, S., Haeusler, M., Nelen, V., Neville, A.J., Perthus, I., Pierini, A., Bertaut-Nativel, B., Rissmann, A., Rouget, F., Schaub, B., Tucker, D., Wellesley, D., Zymak-Zakutnia, N., Barisic, I., de Walle, HEK, Lanzoni, M., Mullaney, C., Pennington, L., Rankin, J.

المصدر: Birth defects research, vol. 114, no. 20, pp. 1404-1416

مصطلحات موضوعية: Pregnancy, Female, Humans, Prevalence, Stillbirth, Heart Defects, Congenital/epidemiology, Registries, Europe/epidemiology, European Surveillance of Congenital Anomalies, congenital heart disease, prevalence rate

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36345679; info:eu-repo/semantics/altIdentifier/eissn/2472-1727; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_99FAA6B7C8EB8; https://serval.unil.ch/notice/serval:BIB_99FAA6B7C8EBTest; https://serval.unil.ch/resource/serval:BIB_99FAA6B7C8EB.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_99FAA6B7C8EB8Test

الإتاحة: https://doi.org/10.1002/bdr2.2117Test
https://serval.unil.ch/notice/serval:BIB_99FAA6B7C8EBTest
https://serval.unil.ch/resource/serval:BIB_99FAA6B7C8EB.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_99FAA6B7C8EB8Test