Publicaciones en colaboración con investigadores/as de University Hospital of Lausanne (24)

2024

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

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

  3. 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

  4. 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

  5. Pulse Wave Amplitude Drops Index: A Biomarker of Cardiovascular Risk in Obstructive Sleep Apnea

    American Journal of Respiratory and Critical Care Medicine, Vol. 207, Núm. 12, pp. 1620-1632

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. Respiratory Polygraphy Patterns and Risk of Recurrent Cardiovascular Events in Patients With Acute Coronary Syndrome

    Frontiers in Medicine, Vol. 9

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. 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. Global Survey of Outcomes of Neurocritical Care Patients: Analysis of the PRINCE Study Part 2

    Neurocritical Care, Vol. 32, Núm. 1, pp. 88-103

  2. Worldwide Organization of Neurocritical Care: Results from the PRINCE Study Part 1

    Neurocritical Care, Vol. 32, Núm. 1, pp. 172-179

2019

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

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

  2. Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study

    Neuroepidemiology, Vol. 53, Núm. 3-4, pp. 169-179

  3. Epidemiology of achondroplasia: A population-based study in Europe

    American Journal of Medical Genetics, Part A, Vol. 179, Núm. 9, pp. 1791-1798

  4. Epidemiology of congenital cerebral anomalies in Europe: A multicentre, population-based EUROCAT study

    Archives of Disease in Childhood, Vol. 104, Núm. 12, pp. 1181-1187

  5. Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

    Nature Genetics, Vol. 51, Núm. 5, pp. 804-814

  6. Rising rural body-mass index is the main driver of the global obesity epidemic in adults

    Nature