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Research on Congenital Anomalies

  • Postal address

    Colombia

Organization profile

Research fields

Epidemiological Research; Knowledge Socialization; Social Appropriation of Knowledge; Congenital Anomalies of Different Systems; Genetic Syndromes

Organization profile

Interest group in congenital anomalies that seeks the generation and appropriation of knowledge in the area through scientific production, participation in academic meetings and constant updating on the subject.

Área de conocimiento (OCDE)

  • Medical and Health Sciences

UN Sustainable Development Goals

In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. Our work contributes towards the following SDG(s):

  1. SDG 1 - No Poverty
    SDG 1 No Poverty
  2. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  3. SDG 10 - Reduced Inequalities
    SDG 10 Reduced Inequalities
  4. SDG 11 - Sustainable Cities and Communities
    SDG 11 Sustainable Cities and Communities

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Collaborations and top research areas from the last five years

Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
  • Gastroschisis prevalence patterns in 27 surveillance programs from 24 countries, International Clearinghouse for Birth Defects Surveillance and Research, 1980–2017

    Feldkamp, M. L., Canfield, M. A., Krikov, S., Prieto-Merino, D., Šípek, A., LeLong, N., Amar, E., Rissmann, A., Csaky-Szunyogh, M., Tagliabue, G., Pierini, A., Gatt, M., Bergman, J. E. H., Szabova, E., Bermejo-Sánchez, E., Tucker, D., Dastgiri, S., Bidondo, M. P., Canessa, A. & Zarante, I. & 12 others, Hurtado-Villa, P., Martinez, L., Mutchinick, O. M., Camelo, J. L., Benavides-Lara, A., Thomas, M. A., Liu, S., Nembhard, W. N., Gray, E. B., Nance, A. E., Mastroiacovo, P. & Botto, L. D., Feb 2024, In: Birth Defects Research. 116, 2, e2306.

    Research output: Contribution to journalArticlepeer-review

    21 Scopus citations
  • The Human Phenotype Ontology in 2024: phenotypes around the world

    Gargano, M. A., Matentzoglu, N., Coleman, B., Addo-Lartey, E. B., Anagnostopoulos, A. V., Anderton, J., Avillach, P., Bagley, A. M., Bakštein, E., Balhoff, J. P., Baynam, G., Bello, S. M., Berk, M., Bertram, H., Bishop, S., Blau, H., Bodenstein, D. F., Botas, P., Boztug, K. & Čady, J. & 156 others, Callahan, T. J., Cameron, R., Carbon, S. J., Castellanos, F., Caufield, J. H., Chan, L. E., Chute, C. G., Cruz-Rojo, J., Dahan-Oliel, N., Davids, J. R., Dieuleveult, M., Souza, V., de Vries, B. B. A., Vries, E., DePaulo, J. R., Derfalvi, B., Dhombres, F., Diaz-Byrd, C., Dingemans, A. J. M., Donadille, B., Duyzend, M., Elfeky, R., Essaid, S., Fabrizzi, C., Fico, G., Firth, H. V., Freudenberg-Hua, Y., Fullerton, J. M., Gabriel, D. L., Gilmour, K., Giordano, J., Goes, F. S., Moses, R. G., Green, I., Griese, M., Groza, T., Gu, W., Guthrie, J., Gyori, B., Hamosh, A., Hanauer, M., Hanušová, K., He, Y., Hegde, H., Helbig, I., Holasová, K., Hoyt, C. T., Huang, S., Hurwitz, E., Jacobsen, J. O. B., Jiang, X., Joseph, L., Keramatian, K., King, B., Knoflach, K., Koolen, D. A., Kraus, M. L., Kroll, C., Kusters, M., Ladewig, M. S., Lagorce, D., Lai, M. C., Lapunzina, P., Laraway, B., Lewis-Smith, D., Li, X., Lucano, C., Majd, M., Marazita, M. L., Martinez-Glez, V., McHenry, T. H., McInnis, M. G., McMurry, J. A., Mihulová, M., Millett, C. E., Mitchell, P. B., Moslerová, V., Narutomi, K., Nematollahi, S., Nevado, J., Nierenberg, A. A., Čajbiková, N. N., Nurnberger, J. I., Ogishima, S., Olson, D., Ortiz, A., Pachajoa, H., Nanclares, G. P., Peters, A., Putman, T., Rapp, C. K., Rath, A., Reese, J., Rekerle, L., Roberts, A. M., Roy, S., Sanders, S. J., Schuetz, C., Schulte, E. C., Schulze, T. G., Schwarz, M., Scott, K., Seelow, D., Seitz, B., Shen, Y., Similuk, M. N., Simon, E. S., Singh, B., Smedley, D., Smith, C. L., Smolinsky, J. T., Sperry, S., Stafford, E., Stefancsik, R., Steinhaus, R., Strawbridge, R., Sundaramurthi, J. C., Talapova, P., Castano, J. A. T., Tesner, P., Thomas, R. H., Thurm, A., Turnovec, M., van Gijn, M. E., Vasilevsky, N. A., Vlčková, M., Walden, A., Wang, K., Wapner, R., Ware, J. S., Wiafe, A. A., Wiafe, S. A., Wiggins, L. D., Williams, A. E., Wu, C., Wyrwoll, M. J., Xiong, H., Yalin, N., Yamamoto, Y., Yatham, L. N., Yocum, A. K., Young, A. H., Yüksel, Z., Zandi, P. P., Zankl, A., Zarante, I., Zvolský, M., Toro, S., Carmody, L. C., Harris, N. L., Munoz-Torres, M. C., Danis, D., Mungall, C. J., Köhler, S., Haendel, M. A. & Robinson, P. N., 05 Jan 2024, In: Nucleic Acids Research. 52, D1, p. D1333-D1346

    Research output: Contribution to journalArticlepeer-review

    252 Scopus citations
  • Asociación poco frecuente del complejo OEIS con un defecto diafragmático

    Translated title of the contribution: Infrequent association of OEIS complex with a diaphragmatic defectCatalina Torres, P., Montaña-Jiménez, L. P., Ramírez-Corredor, A., Vargas Vaca, Y. A., Zarante, I. & López Cruz, R. L., 01 Jul 2023, In: Andes Pediatrica. 94, 4, p. 536-541 6 p.

    Research output: Contribution to journalArticlepeer-review