Abstracts from the 51st European Society of Human Genetics (ESHG) Conference, in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)

Abstract

s from the 51st European Society of Human Genetics Conference: Oral PresentationsPlenary SessionsPL1 Opening plenary lecture (PL1.1-PL1.2)PL2 What’s New (PL2.1-2.6, LB1-LB3)PL3 Mendel Lecture (PL3.1)Concurrent SymposiaS01 Prenatal Genetics-joint with EMPAG (S01.1-S01.3)S02 DNA damage and repair in cancer (S02.1-S02.2)S03 Genome Organization and Function (S03.2)S04 Genetics of dizziness (S04.2-S04.3)S05 Large-scale genetic studies in complex diseases (S05.2-S05.3)S06 Liquid biopsies in cancer (S06.3)S07 Drug repurposing for treating genetic disorders (S07.1-S07.2)S08 Microbiome and Virome (S08.1)S09 New Genomic Technologies (S09.1-S09.3)S11 Epigenetics of the brain (S11.1-S11.3)S12 Retinal diseases (S12.1-S12.3)S13 Genome editing (S13.1, S13.3)S14 Cellular heterogeneity in health and disease (S14.2-S14.3)S15 Understanding non-coding variants (S15.2)S16 Human epigenome dynamics (S16.1-S16.3)S17 ESHG-ASHG Building Bridges Debate: Germline genome editing-joint with EMPAG (S17.1-S17.2, S17.4)S18 Regulatory sequence functions and elements (S18.1-S18.3)S19 New nanotechnologies: the DNA Origami (S19.2)Educational SessionsE02 Hereditary cancer (E02.1-E2.2)E03 Resources for gene function analysis (E03.1-E3.2)E04 Pharmacogenomics (E04.1-E4.2)E05 Bone Density: High and Low (E05.1)E06 Statistics in Genetic Research and Diagnostics (E06.1-E06.2)E07 Organoids (E07.1-E07.2)E08 Congenital vasculopathies (E08.1-E08.2)E09 Iron in the brain-joint session with the European Society of Neurology (E09.2)E10 Genetics of infertility (E10.1)E12 Undiagnosed disease and matchmaking initiatives (E12.2)E13 Brain abnormalities in fetal life (E13.1-E13.2)E15 Disorders of sexual development (E15.1-E15.2)E16 Genetics with a Bite (E16.1-E16.2)Concurrent SessionsC01 Precision and Predictive Medicine (C01.1-C01.6)C02 Syndrome updates 1 (C02.1-C02.6)C03 Multi-omics 1 (C03.1-C03.6)C04 Epigenetics and Gene Regulation (C04.1-C04.6)C05 Neurological and Neuromuscular Disorders (C05.1-C05.6)C06 Internal Organs (C06.1-C06.6)C07 NGS diagnostics (C07.1-C07.6)C08 Population Genetics (C08.1-C08.6)C09 Mendelian chromatin disorders (C09.1-C09.6)C10 Best Posters 1 (P15.05A, P15.27C, P15.03C, P15.11C, P15.41A, P17.06B, P11.017A, P17.58B, P17.22B, P18.34B, P18.12D, P18.25A, P18.48D, P18.77A)C11 Metabolic and Mitochondrial Disorder (C11.1-C11.6)C12 Skin and Bones (C12.1-C12.6)C13 Prenatal and Reproductive Genetics (C13.1-C13.6)C14 Cancer genetics (C14.1-C14.6)C15 Syndrome updates 2 (C15.1-C15.6)C16 Multi-omics 2 (C16.1-C16.6)C17 Intellectual disability 1 (C17.1-C17.6)C18 Cardiovascular disorders (C18.1-C18.6)C19 Advanced sequencing technologies (C19.1-C19.6)C20 Intellectual Disability 2 (C20.1-C20.6)C21 Statistical Genetics (C21.1-C21.6)C22 Best Posters 2 (P02.48C, P04.05A, P06.64D, P06.72D, P06.35C. P06.36D, P09.001A, P09.98B, P09.139C, P12.214B, P19.24D, P20.05A, P16.40D)C23 Sensory disorders (C23.1-C23.6)