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  1. McGoldrick, Niall [Author]; Revie, Gavin [Author]; Groisman, Boris [Author]; Hurtado-Villa, Paula [Author]; Sipek, Antonin [Author]; Khoshnood, Babak [Author]; Rißmann, Anke [Author]; Dastgiri, Saeed [Author]; Landau, Danielle [Author]; Tagliabue, Giovanna [Author]; Pierini, Anna [Author]; Gatt, Miriam [Author]; Mutchinick, Osvaldo M. [Author]; Martinez, Laura [Author]; Walle, Hermein E. K. de [Author]; Szabova, Elena [Author]; Lopez Camelo, Jorge [Author]; Källén, Karin [Author]; Morgan, Margery [Author]; Wertelecki, Wladimir [Author]; Nance, Amy [Author]; Stallings, Erin B. [Author]; Nembhard, Wendy N. [Author]; Mossey, Peter [Author]

    A multi-program analysis of cleft lip with cleft palate prevalence and mortality using data from 22 International Clearinghouse for Birth Defects Surveillance and Research programs, 1974-2014

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    2023

    Published in: Birth defects research ; 115(2023), 10, Seite 980-997

  2. Bakker, Marian K. [Author]; Bergman, Jorieke E. H. [Author]; Krikov, Sergey [Author]; Amar, Emmanuelle [Author]; Cocchi, Guido [Author]; Cragan, Janet [Author]; Walle, Hermien E. K. de [Author]; Gatt, Miriam [Author]; Groisman, Boris [Author]; Liu, Shiliang [Author]; Nembhard, Wendy N. [Author]; Pierini, Anna [Author]; Rißmann, Anke [Author]; Chidambarathanu, Shanti [Author]; Sipek Jr, Antonin [Author]; Szabova, Elena [Author]; Tagliabue, Giovanna [Author]; Tucker, David [Author]; Mastroiacovo, Pierpaolo [Author]; Botto, Lorenzo D. [Author]

    Prenatal diagnosis and prevalence of critical congenital heart defects : an international retrospective cohort study

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    2019

    Published in: BMJ open ; Bd. 9.2019, 7, Art. e028139, insges. 12 S.

  3. Kancherla, Vijaya [Author]; Sundar, Manasvi [Author]; Tandaki, Lucita [Author]; Lux, Anke [Author]; Bakker, Marian K. [Author]; Bergman, Jorieke E. H. [Author]; Bermejo-Sánchez, Eva [Author]; Canfield, Mark A. [Author]; Dastgiri, Saeed [Author]; Feldkamp, Marcia L. [Author]; Gatt, Miriam [Author]; Groisman, Boris [Author]; Hurtado-Villa, Paula [Author]; Kallen, Kärin [Author]; Landau, Danielle [Author]; Lelong, Nathalie [Author]; Lopez-Camelo, Jorge [Author]; Martinez, Laura Elia [Author]; Mastroiacovo, Pierpaolo [Author]; Morgan, Margery [Author]; Mutchinick, Osvaldo M. [Author]; Nance, Amy E. [Author]; Nembhard, Wendy N. [Author]; Pierini, Anna [Author]; [...]

    Prevalence and mortality among children with anorectal malformation : a multi-country analysis

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    2023

    Published in: Birth defects research ; 115(2023), 3, Seite 390-404

  4. Bakker, Marian K. [Author]; Kancherla, Vijaya [Author]; Canfield, Mark A. [Author]; Bermejo-Sanchez, Eva [Author]; Cragan, Janet D. [Author]; Dastgiri, Saeed [Author]; Walle, Hermien E. K. de [Author]; Feldkamp, Marcia L. [Author]; Groisman, Boris [Author]; Gatt, Miriam [Author]; Hurtado-Villa, Paula [Author]; Kallen, Karin [Author]; Landau, Danielle [Author]; Lelong, Nathalie [Author]; Camelo, Jorge S. Lopez [Author]; Martínez, Laura [Author]; Morgan, Margery [Author]; Mutchinick, Osvaldo M. [Author]; Nembhard, Wendy N. [Author]; Pierini, Anna [Author]; Rißmann, Anke [Author]; Sipek, Antoni [Author]; Szabova, Elena [Author]; Tagliabue, Giovanna [Author]; [...]

    Analysis of mortality among neonates and children with spina bifida : an international registry-based study, 2001-2012

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    2019

    Published in: Paediatric and perinatal epidemiology ; 33(2019), 6, Seite 436-448

  10. Ercoli, Gabriel; Bidondo, María Paz; Senra, Blanca Cristina; Groisman, Boris

    Apert syndrome with omphalocele: A case report

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    Wiley, 2014

    Published in: Birth Defects Research Part A: Clinical and Molecular Teratology, 100 (2014) 9, Seite 726-729

  11. Brun, Paloma; Groisman, Boris; Bidondo, María Paz; Barbero, Pablo; Trotta, Marianela; Liascovich, Rosa

    Prevalence of congenital anomalies and prenatal diagnosis by birth institution (public vs. non-public): indicators of inequality in access to elective termination of pregnancy for fetal anomalies

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    Springer Science and Business Media LLC, 2024

    Published in: Journal of Community Genetics (2024)