Dorota Wicher

Scientific title: MD, PhD

Scientific position: assistant

Department: Department of Medical Genetics/Outpatient Clinic

OrcID No: 0000-0002-8360-0006

Biography:

  • graduated from The Medical University of Warsaw, First
    Faculty of Medicine
  • 2008-2013: specialization training in pediatrics
    (Department of Gastroenterology, Hepatology, Nutritional Disorders and
    Pediatrics)
  • since 2014: consultant at the Department of Medical
    Genetics (outpatient clinic)
  • member of the Polish Pediatric Society and the Polish
    Society of Human Genetics
  • author/co-author of polish and foreign medical
    publications, congressional reports and book chapters
  • co-researcher of scientific grants related to rare
    diseases (autosomal recessive polycystic kidney disease, Alport syndrome, Smith-Lemli-Opitz
    syndrome, neurofibromatosis type 1, Kabuki syndrome, hypertrophic
    cardiomyopathy, left ventricular noncompaction, cholestatic liver disorders)
  • participant in the first edition of the Polish Clinical Scholars Research Training (P-CSRT) program developed and implemented by Harvard Medical School Postgraduate Medical Education.

Qualifications and trainings:

  • specialist in pediatrics
  • specialist in clinical genetics
  • European Certificate in Medical Genetics and Genomics
  • certificate RESETHICSx: Research Ethics: a guide for responsible research with human subjects
  • certificate ICH E6 (R2) Good Clinical Practice ver. 1.0

Research interests:

Rare disorders: dysmorphic syndromes, ciliopathies, polycystic kidney disease, liver fibrosis, cholestasis, cardiomyopathies.

Contact: d.wicher@ipczd.pl