Consultant Clinical Geneticist, responsible of Prenatal Genetics Department at the Institute of Pathology and Genetics (IPG), Gosselies, Belgium
Belgium
Dr. Julie Désir is a leading Belgian Consultant Clinical Geneticist specializing in prenatal, preimplantation, and postnatal genetic diagnostics. Currently heading the Prenatal Genetics Department at the Institute of Pathology and Genetics in Gosselies, Belgium, she brings over two decades of expertise in neurodevelopmental disorders, oncogenetics, and rare genetic conditions. With a PhD in Medical Sciences and extensive research contributions in cutting-edge prenatal genetics and neurogenetics, Dr. Désir is recognized for her role in advancing genetic diagnostics and treatment through innovative technologies like NIPT and Next-Generation Sequencing.
Dr. Julie Désir is a prominent Belgian Consultant Clinical Geneticist, currently leading the Prenatal Genetics Department at the Institute of Pathology and Genetics (IPG) in Gosselies, Belgium, since 2019. Her career spans over two decades, during which she has been responsible for prenatal, preimplantation, and postnatal genetic consultations, both in outpatient settings and as a consultant in various hospitals across Belgium. Her expertise encompasses a wide range of genetic conditions, including neurodevelopmental and neurological disorders, oncogenetics, fertility issues, neuromuscular diseases, and cardiological pathologies. Dr. Désir is also heavily involved in the validation of molecular genetics reports, including Non-Invasive Prenatal Testing (NIPT) and Next-Generation Sequencing (NGS), showcasing her commitment to integrating cutting-edge technologies into clinical practice.
With a robust academic foundation, Dr. Désir earned her PhD in Medical Sciences from the Free University of Brussels (ULB) in 2009 and holds dual specialties in Clinical Genetics and Pediatrics. Throughout her career, she has supervised numerous Master’s and Doctoral theses, contributing significantly to advancements in the diagnosis of brain malformations and the development of prenatal genomic databases. Her involvement in several European research projects, such as the neuro-MIG network and EUROMICRO, reflects her deep engagement with the latest research in neurogenetics and rare diseases, making her a leading voice in the field of fetal medicine and congenital malformations.
Dr. Désir's contributions to genetics research have been widely recognized through her numerous publications in high-impact journals, particularly on topics related to rare neurodevelopmental syndromes, microcephalies, and prenatal genetic diagnostics. Her recent work includes groundbreaking studies on genetic mutations linked to conditions such as lissencephaly, Sturge-Weber syndrome, and primary microcephalies. In addition to her clinical and research work, Dr. Désir actively participates in multiple working groups within the Belgian Society of Human Genetics, focusing on prenatal and preimplantation genetic testing, as well as ethical, legal, and social implications of genetic research.
Her dedication to education and mentorship is further evidenced by her teaching roles at Belgian universities, where she imparts her knowledge in human genetics, obstetrics, and perinatal care. Dr. Désir's leadership in both clinical practice and academic research continues to shape the field of clinical genetics, making her an authority in genetic diagnostics and prenatal care.
Department at the Institute of Pathology and Genetics (IPG), Gosselies, Belgium.
Department at the Center of Human Genetics of Free University of Brussels - ULB
Belgian French Community
2019
INAMI
2011
ULB - Free University of Brussels
2009
ULB
2007
ULB
2000