Publications (870)

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

    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, Öhman I, Bergvall T, Star K, Dolk H, Loane M, Addor MC, Barisic I, Cavero-Carbonell C, Garne E, Gatt M, Khoshnood B, Klungsøyr K, Latos-Bielenska A, Lelong N, Lutke R, Materna-Kiryluk A, Nelen V, Nevill A, O'Mahony M, Mokoroa O, Pierini A, Randrianaivo H, Rissmann A, Tucker D, Wiesel A, Yevtushok L, Morris JK
    Drug Safety, 2021 , 44: (7) 765 - 785

  • Sociodemographic Differences in Prenatal Diagnosis of Chromosomal Anomalies: A Population-Based Study

    Sociodemographic Differences in Prenatal Diagnosis of Chromosomal Anomalies: A Population-Based Study

    Michele Santoro, Lorena Mezzasalma, Alessio Coi, Silvia Baldacci, Lucia Pasquini and Anna Pierini
    Frontiers in Pediatrics, 2021 , 9:
    Subjects: chromosomal anomalies, prenatal diagnosis, socioeconomic status
    Anomalies: chromosomal anomalies, Down syndrome

  • Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs

    Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs

    Bell JC, Baynam G, Bergman JEH, Bermejo-Sánchez E, Botto LD, Canfield MA, Dastgiri S, Gatt M, Groisman B, Hurtado-Villa P, Kallen K, Khoshnood B, Konrad V, Landau D, Lopez-Camelo JS, Martinez L, Morgan M, Mutchinick OM, Nance AE, Nembhard W, Pierini A, Rissmann A, Shan X, Sipek A, Szabova E, Tagliabue G, Yevtushok LS, Zarante I, Nassar N
    Birth Defects Research, 2021 , 113: (12) 945 - 957

  • A multi-country study of prevalence and early childhood mortality among children with omphalocele

    A multi-country study of prevalence and early childhood mortality among children with omphalocele

    Nembhard WN, Bergman JEH, Politis MD, Arteaga-Vázquez J, Bermejo-Sánchez E, Canfield MA, Cragan JD, Dastgiri S, de Walle HEK, Feldkamp ML, Nance A, Gatt M, Groisman B, Hurtado-Villa P, Kallén K, Landau D, Lelong N, Lopez-Camelo J, Martinez L, Morgan M, Pierini A, Rissmann A, Šípek A, Szabova E, Tagliabue G, Wertelecki W, Zarante I, Bakker MK, Kancherla V, Mastroiacovo P
    BDR online , 2020 , October:
    Subjects: Omphalocele, associated anomalies, abdominal birth defect
    Anomalies: Omphalocele

  • Etiological diagnosis in limb reduction defects and the number of affected limbs: a population-based study in the Northern Netherlands

    Etiological diagnosis in limb reduction defects and the number of affected limbs: a population-based study in the Northern Netherlands

    Bergman JEH, Löhner K, van der Sluis CK, Rump P, de Walle HEK
    AJMG part A online , 2020 , Sept :
    Subjects: Limb reduction defects (LRDs)
    Anomalies: congenital anomalies

  • Lifestyle and Socio-Demographic Risk Factors for Gastroschisis: A Systematic Review and Meta-Analysis

    Lifestyle and Socio-Demographic Risk Factors for Gastroschisis: A Systematic Review and Meta-Analysis

    Baldacci S, Santoro M, Coi A, Mezzasalma L, Bianchi F, Pierini A
    Archives of Diseases in Childhood, 2020 , 105: (8) 756 - 764
    Subjects: prevention, lifestyle risk factors, socio-demographic risk factors
    Anomalies: Gastroschisis

  • Maternal occupational exposure to solvents and gastroschisis in offspring - National Birth Defects Prevention Study 1997–2011

    Maternal occupational exposure to solvents and gastroschisis in offspring - National Birth Defects Prevention Study 1997–2011

    Spinder N, Almli LM, Desrosiers TA, Arnold EA, Bergman JEH, Kromhout H, Boezen HM, de Walle HEK, Rocheleau C, Reefhuis J
    Occupational and Environmental Medicine , 2020 , Published Online First: 16 January 2020. doi: 10.1136/oemed-2019-106147:
    Subjects: maternal occupational exposure to solvents and gastroschisis in offspring
    Anomalies: gastroschisis

  • Maternal risk factors associated with the VACTERL association: a case-control study

    Maternal risk factors associated with the VACTERL association: a case-control study

    van de Putte R, de Walle HEK, van Hooijdonk KJM, de Blaauw I, Marcelis CLM, van Heijst A, Giltay JC, Renkema KY, Broens PMA, Brosens E, Sloots CEJ, Bergman JEH, Roeleveld N, van Rooij ALM
    Birth Defects Research, 2020 , July:
    Subjects: VACTERL, risk factors
    Anomalies: congenital anomalies: vertebral, anal, cardiac, tracheo‐esophageal, renal, limb anomalies

  • Maternal risk factors for the VACTERL association: a EUROCAT case-control study.

    Maternal risk factors for the VACTERL association: a EUROCAT case-control study.

    Van de Putte Romy, Van Rooij Iris A.L.M., Haanappel C, Marcelis Carlo, Brunner Han, Addor Marie-Claude, Cavero-Carbonell Clara, Dias Carlos Matias, Draper Elizabeth, Etxebarriarteum Larraitz, Gatt Miriam, Khoshnood Babak, Kinsner-Ovaskainen Agnieszka, Klungsoyr Kari, Kurinczuk Jennifer, Latos-Bielenska Anna, Luyt Karen, O'Mahony Mary T., Miller Nicola, Mullaney Carmel, Nelen Vera, Neville Amanda, Perthus Isabelle, Pierini Anna, Randrianaivo Hanitra, Rankin Judith, Rissmann Anke, Rouget Florence, Schaub Bruno, Tucker David, Wellesley Diana, Wiesel Awi, Zymak-Zakutnia Natalia, Loane Maria, Barisic Ingeborg, De Walle Hermien, Bergman Jorieke E.H., Roeleveld Nel.
    Birth Defect Research, 2020 , 112: 688 - 698
    Subjects: VACTERL assocation, maternal risk factors,
    Anomalies: VACTERL association

  • Methadone, Pierre Robin sequence and other congenital anomalies: case-control study

    Methadone, Pierre Robin sequence and other congenital anomalies: case-control study

    Cleary, B., Loane, M., Addor, M-C., Barisic, I., de Walle, H. E. K., Dias, C. M., Gatt, M., Klungsoyr, K., McDonnell, B., Neville, A., Pierini, A., Rissmann, A., Tucker, D. F., Zurriaga, O. & Dolk, H
    Archives of Disease in Childhood-Fetal and Neonatal, 2020 , Mar- edition 105: (2) F151 - F157
    Subjects: Methadone, Pierre Robin sequence, congenital anomalies
    Anomalies: congenital anomalies