Renée Lutke

2024

Hospital care in the first 10 years of life of children with congenital anomalies in six European countries: Data from the EUROlinkCAT cohort linkage study

Morris, J. K., Loane, M., Wahlich, C., Tan, J., Baldacci, S., Ballardini, E., Cavero-Carbonell, C., Damkjær, M., García-Villodre, L., Gissler, M., Given, J., Gorini, F., Heino, A., Limb, E., Lutke, R., Neville, A., Rissmann, A., Scanlon, L., Tucker, D. F. & Urhoj, S. K. & 2 anderen, de Walle, H. E. K. & Garne, E., 18-apr.-2024, In: Archives of disease in childhood. 109, 5, blz. 402-408 7 blz.

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The Association of Prenatal Diagnoses with Mortality and Long-Term Morbidity in Children with Specific Isolated Congenital Anomalies: A European Register-Based Cohort Study

Heino, A., Morris, J. K., Garne, E., Baldacci, S., Barisic, I., Cavero-Carbonell, C., García-Villodre, L., Given, J., Jordan, S., Loane, M., Lutke, L. R., Neville, A. J., Santoro, M., Scanlon, I., Tan, J., de Walle, H. E. K., Kiuru-Kuhlefelt, S. & Gissler, M., jun.-2024, In: Maternal and child health journal. 28, 6, blz. 1020-1030 11 blz.

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3 Downloads (Pure)

2023

Accuracy of congenital anomaly coding in live birth children recorded in European health care databases, a EUROlinkCAT study

Bakker, M. K., Loane, M., Garne, E., Ballardini, E., Cavero-Carbonell, C., García, L., Gissler, M., Given, J., Heino, A., Jamry-Dziurla, A., Jordan, S., Urhoj, S. K., Latos-Bieleńska, A., Limb, E., Lutke, R., Neville, A. J., Pierini, A., Santoro, M., Scanlon, I. & Tan, J. & 3 anderen, Wellesley, D., de Walle, H. E. K. & Morris, J. K., mrt.-2023, In: European Journal of Epidemiology. 38, 3, blz. 325-334 10 blz.

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6 Citaten (Scopus)

39 Downloads (Pure)

Causes of death in children with congenital anomalies up to age 10 in eight European countries

Rissmann, A., Tan, J., Glinianaia, S. V., 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, H. E. K., Gatt, M., Gissler, M. & Heino, A. & 11 anderen, Jordan, S., Urhoj, S. K., Klungsøyr, K., Lutke, R., Mokoroa, O., Neville, A. J., Thayer, D. S., Wellesley, D. G., Yevtushok, L., Zurriaga, O. & Morris, J., 23-jun.-2023, In: BMJ Paediatrics Open. 7, 1, 11 blz., e001617.

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3 Citaten (Scopus)

22 Downloads (Pure)

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

Loane, M., Given, J. E., 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, A. J., Odak, L., Puccini, A., Santoro, M., Scanlon, I., Urhoj, S. K. & de Walle, H. E. K. & 2 anderen, Wellesley, D. & Morris, J. K., aug.-2023, In: PLoS ONE. 18, 8, 16 blz., e0290711.

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4 Citaten (Scopus)

45 Downloads (Pure)

Maternal first trimester COVID-19 vaccination and risk of major non-genetic congenital anomalies

Woestenberg, P. J., de Feijter, M., Bergman, J. E. H., Lutke, L. R., Passier, A. J. L. M. & Kant, A. C., 1-nov.-2023, In: Birth Defects Research. 115, 18, blz. 1746-1757 12 blz.

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2 Citaten (Scopus)

41 Downloads (Pure)

Risk factors for mortality in infancy and childhood in children with major congenital anomalies: A European population-based cohort study

Tan, J., Glinianaia, S. V., Rankin, J., Pierini, A., Santoro, M., Coi, A., Garne, E., Loane, M., Given, J. E., Brigden, J., Ballardini, E., Cavero-Carbonell, C., de Walle, H. E. K., García-Villodre, L., Gatt, M., Gissler, M., Heino, A., Jordan, S., Khoshnood, B. & Klungsoyr, K. & 7 anderen, Lelong, N., Lutke, R. L., Neville, A. J., Tucker, D., Urhoj, S. K., Wellesley, D. & Morris, J. K., nov.-2023, In: Paediatric and Perinatal Epidemiology. 37, 8, blz. 679-690 12 blz.

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1 Citaat (Scopus)

35 Downloads (Pure)

2022

COVID-19 and children with congenital anomalies: a European survey of parents' experiences of healthcare services

Latos-Bieleńska, A., Marcus, E., Jamry-Dziurla, A., Rankin, J., Barisic, I., Cavero-Carbonell, C., Den Hond, E., Garne, E., Genard, L., João Santos, A., Lutke, L. R., Matias Dias, C., Neergaard Pedersen, C., Neville, A., Niemann, A., Odak, L., Páramo-Rodríguez, L., Pierini, A., Rissmann, A. & Morris, J. K., 19-jul.-2022, In: BMJ Open. 12, 7, 13 blz., e061428.

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Hospital length of stay among children with and without congenital anomalies across 11 European regions-A population-based data linkage study

Urhoj, S. K., Tan, J., Morris, J. K., Given, J., Astolfi, G., Baldacci, S., Barisic, I., Brigden, J., Cavero-Carbonell, C., Evans, H., Gissler, M., Heino, A., Jordan, S., Lutke, R., Odak, L., Puccini, A., Santoro, M., Scanlon, I., de Walle, H. E. K. & Wellesley, D. & 3 anderen, Zurriaga, Ó., Loane, M. & Garne, E., 22-jul.-2022, In: PLoS ONE. 17, 7, 17 blz., e0269874.

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16 Citaten (Scopus)

42 Downloads (Pure)

Information needs of parents of children with congenital anomalies across Europe: a EUROlinkCAT survey

Marcus, E., Latos-Bielenska, A., Jamry-Dziurla, A., Barišić, I., Cavero-Carbonell, C., Den Hond, E., Garne, E., Genard, L., Santos, A. J., Lutke, L. R., Matias Dias, C., Neergaard Pedersen, C., Neville, A. J., Niemann, A., Odak, L., Pierini, A., Rico, J., Rissmann, A., Rankin, J. & Morris, J. K., dec.-2022, In: BMC Pediatrics. 22, 13 blz., 657.

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4 Citaten (Scopus)

57 Downloads (Pure)

Survival of children with rare structural congenital anomalies: a multi-registry cohort study

Coi, A., Santoro, M., Pierini, A., Rankin, J., Glinianaia, S. V., Tan, J., Reid, A.-K., Garne, E., Loane, M., Given, J., Ballardini, E., Cavero-Carbonell, C., de Walle, H. E. K., Gatt, M., García-Villodre, L., Gissler, M., Jordan, S., Kiuru-Kuhlefelt, S., Kjaer Urhoj, S. & Klungsøyr, K. & 7 anderen, Lelong, N., Lutke, L. R., Neville, A. J., Rahshenas, M., Scanlon, I., Wellesley, D. & Morris, J. K., 29-mrt.-2022, In: Orphanet journal of rare diseases. 17, 1, 11 blz., 142.

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9 Citaten (Scopus)

64 Downloads (Pure)

Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort study

Santoro, M., Coi, A., Pierini, A., Rankin, J., Glinianaia, S., Tan, J., Reid, A., Garne, E., Loane, M., Given, J., Aizpurua, A., Astolfi, G., Barisic, I., Cavero-Carbonell, C., de Walle, H. E. K., Den Hond, E., Garcia-Villodre, L., Gatt, M., Gissler, M. & Jordan, S. & 16 anderen, Khoshnood, B., Kiuru-Kuhlefelt, S., Klungsoyr, K., Lelong, N., Lutke, R., Mokoroa, O., Nelen, V., Neville, A. J., Odak, L., Rissmann, A., Scanlon, I., Urhoj, S. K., Wellesley, D., Wertelecki, W., Yevtushok, L. & Morris, J. K., nov.-2022, In: Paediatric and Perinatal Epidemiology. 36, 6, blz. 792-803 12 blz.

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8 Citaten (Scopus)

51 Downloads (Pure)

2021

Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records: A EUROlinkCAT study

Loane, M., Given, J. E., Tan, J., Reid, A., Akhmedzhanova, D., Astolfi, G., Barišić, I., Bertille, N., Bonet, L. B., Carbonell, C. C., Carollo, O. M., Coi, A., Densem, J., Draper, E., Garne, E., Gatt, M., Glinianaia, S. V., Heino, A., Hond, E. D. & Jordan, S. & 18 anderen, Khoshnood, B., Kiuru-Kuhlefelt, S., Klungsøyr, K., Lelong, N., Lutke, L. R., Neville, A. J., Ostapchuk, L., Puccini, A., Rissmann, A., Santoro, M., Scanlon, I., Thys, G., Tucker, D., Urhoj, S. K., de Walle, H. E. K., Wellesley, D., Zurriaga, O. & Morris, J. K., 27-aug.-2021, In: PLoS ONE. 16, 8, 15 blz., e0256535.

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21 Citaten (Scopus)

48 Downloads (Pure)

Signal Detection in EUROmediCAT: Identification and Evaluation of Medication-Congenital Anomaly Associations and Use of VigiBase as a Complementary Source of Reference

Cavadino, A., Sandberg, L., Ohman, I., Bergvall, T., Star, K., Dolk, H., Loane, M., Addor, M.-C., Barisic, I., Cavero-Carbonell, C., Garne, E., Gatt, M., Khoshnood, B., Klungsoyr, K., Latos-Bielenska, A., Lelong, N., Lutke, R., Materna-Kiryluk, A., Nelen, V. & Nevill, A. & 9 anderen, O'Mahony, M., Mokoroa, O., Pierini, A., Randrianaivo, H., Rissmann, A., Tucker, D., Wiesel, A., Yevtushok, L. & Morris, J. K., jul.-2021, In: Drug Safety. 44, 7, blz. 765-785 21 blz.

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12 Citaten (Scopus)

117 Downloads (Pure)

2018

Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study

Bergman, J. E. H., Lutke, L. R., Gans, R. O. B., Addor, M.-C., Barisic, I., Cavero-Carbonell, C., Garne, E., Gatt, M., Klungsoyr, K., Lelong, N., Lynch, C., Mokoroa, O., Nelen, V., Neville, A. J., Pierini, A., Randrianaivo, H., Rissmann, A., Tucker, D., Wiesel, A. & Dolk, H. & 2 anderen, Loane, M. & Bakker, M. K., apr.-2018, In: Drug Safety. 41, 4, blz. 415-427 13 blz.

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34 Citaten (Scopus)

289 Downloads (Pure)

1996

Isolation of two cyclotoxic diterpenes from the fern Pteris multifida

Woerdenbag, H. J., Lutke, L. R., Bos, R., Stevens, J. F., Hulst, R., Kruizinga, W. H., Zu, Y.-P., Elema, E. T., Hendriks, H., van Uden, W. & Pras, N., 1996, In: Zeitschrift fur Naturforschung. blz. 635 - 638 4 blz.

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Isolation of two cytotoxic diterpenes from the fern Pteris multifida

Woerdenbag, H., Lutke, L., Bos, R., Stevens, J., Hulst, R., Kruizinga, W., Elema, E., Hendriks, H., vanUden, W. & Pras, N., 1996, In: Zeitschrift fur naturforschung c-A journal of biosciences. 51, 9-10, blz. 635-638 4 blz.

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14 Citaten (Scopus)

Renée Lutke

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