Publicaciones en colaboración con investigadores/as de University of Groningen (33)

2024

  1. Exploring the genetics of airflow limitation in lung function across the lifespan – a polygenic risk score study

    eClinicalMedicine, Vol. 75

  2. Surveillance of multiple congenital anomalies; searching for new associations

    European Journal of Human Genetics, Vol. 32, Núm. 4, pp. 407-412

2023

  1. Amniotic band syndrome and limb body wall complex in Europe 1980–2019

    American Journal of Medical Genetics, Part A, Vol. 191, Núm. 4, pp. 995-1006

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

    BMJ Paediatrics Open, Vol. 7, Núm. 1

  3. Diminishing benefits of urban living for children and adolescents’ growth and development

    Nature, Vol. 615, Núm. 7954, pp. 874-883

  4. Epidemiology of aplasia cutis congenita: A population-based study in Europe

    Journal of the European Academy of Dermatology and Venereology, Vol. 37, Núm. 3, pp. 581-589

  5. Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies

    BMJ Open, Vol. 13, Núm. 7

  6. Gestational age at birth and body size from infancy through adolescence: An individual participant data meta-analysis on 253,810 singletons in 16 birth cohort studies

    PLoS medicine, Vol. 20, Núm. 1, pp. e1004036

  7. Maternal age and the prevalence of congenital heart defects in Europe, 1995–2015: A register-based study

    Birth Defects Research, Vol. 115, Núm. 6, pp. 583-594

2022

  1. Prevalence of congenital heart defects in Europe, 2008–2015: A registry-based study

    Birth Defects Research, Vol. 114, Núm. 20, pp. 1404-1416

  2. Prevalence of vascular disruption anomalies and association with young maternal age: A EUROCAT study to compare the United Kingdom with other European countries

    Birth Defects Research, Vol. 114, Núm. 20, pp. 1417-1426

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

    Paediatric and Perinatal Epidemiology, Vol. 36, Núm. 6, pp. 792-803

2021

  1. Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT study

    Paediatric and Perinatal Epidemiology, Vol. 35, Núm. 5, pp. 530-539

  2. Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight

    eLife, Vol. 10

  3. Integration of gene expression and DNA methylation identifies epigenetically controlled modules related to PM2.5 exposure

    Environmental International, Vol. 146

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

    Drug Safety, Vol. 44, Núm. 7, pp. 765-785

2020

  1. A novel whole blood gene expression signature for asthma, dermatitis, and rhinitis multimorbidity in children and adolescents

    Allergy: European Journal of Allergy and Clinical Immunology, Vol. 75, Núm. 12, pp. 3248-3260

  2. Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

    PLoS Genetics, Vol. 16, Núm. 10

2019

  1. Association of Gestational Weight Gain With Adverse Maternal and Infant Outcomes

    JAMA, Vol. 321, Núm. 17, pp. 1702-1715

  2. Congenital clubfoot in Europe: A population-based study

    American Journal of Medical Genetics, Part A, Vol. 179, Núm. 4, pp. 595-601