Saturday, June 1, 2024

08:30 – 10:00 Concurrent Symposia S01 – S03
S01 Paleogenomics as a tool to elucidate the genetic basis of modern diseases
S02 The place of non-directiveness in genetic counselling revisited
S03 The urinary bladder: from discovery to treatment
10:00 – 10:30 Coffee Break – Poster Mounting – Exhibition
10:00 – 11:30 Corporate Satellites
10:30 – 12:00 Educational Sessions E01 – E02
E01 Telomeres in cancer
E02 Germline mosaicism: contribution to disease, diagnostics options and counselling
Workshop W01 – W04
W01 Exome sequencing for beginners
W02 Dysmorphology 1
W03 How to make the most of your clinical database and other large-scale biomedical databases
W04 Promoting research in the field of genetic counseling
Concurrent Symposia S04
S04 Understanding the non coding genome
12:00 – 13:45 Lunch Break – Free Poster Viewing – Exhibition
12:15 – 13:15 ESHG Podcast “Genetic Sounds” Live – Click here to listen to previous episodes
12:15 – 13:45 G1 Meet the next generation – Get2Gether ESHG-Y & Junge Humangenetik
12:00 – 13:30 Corporate Satellites
13:45 – 14:15 PL0 Welcoming addresses
14:15 – 14:30 PL1 ELPAG Award Lecture
14:30 – 16:00 PL2 Opening Plenary
16:00 – 16:30 Fruit Break – Free Poster Viewing – Exhibition
16:30 – 18:00 PL3 What’s New? Highlight Session
from submitted abstracts
18:00 – 18:30 Coffee Break – Free Poster Viewing – Exhibition
18:30 – 20:00 Concurrent Sessions C01 – C07
20:00-21:30 Opening Networking Mixer

Sunday, June 2, 2024

08:30 – 10:00 Concurrent Symposia S05 – S11
S05 GWAS of disease progression: are we there yet?
S06 Genetic Infertility
S07 Editing in cardiovascular disease
S08 Precision Oncology
S09 Assessing variants at scale
S10 Expanding newborn screening towards genomics
S11 Epilepsy genetics
08:30 – 10:00 Corporate Satellites
10:00 – 10:30 Coffee Break – Free Poster Viewing – Exhibition
10:30 – 12:00 Concurrent Sessions C08 – C15
12:00 – 13:00 Lunch Break – Free Poster Viewing – Exhibition
12:00 – 13:00 Corporate Satellites
12:15 – 13:15 G2 Get2gether European Reference Networks (ERN)
12:15 – 13:45 Workshops W05
W05 How to publish your genomics research
13:00 – 14:00 Poster Viewing with Authors and coffee
(Group A) – Only for in-person participants
14:00 – 15:30 Workshops W06 – W12
W06 Fairness in medical genomics
W07 Mutations we almost missed
W08 Prenatal reporting of carrier status
W09 Dysmorphology 2
W10 UCSC Genome Browser
W11 GenEthics
W12 Family communication of genetic information
14:00 – 15:30 Corporate Satellites
15:30 – 15:45 Fruit Break – Free Poster Viewing – Exhibition
15:45 – 16:45 Poster Viewing with Authors and coffee
(Group B) – Only for in-person participants
16:45 – 17:00 Time to change rooms
17:00 – 18:30 Concurrent Symposia S12 – S16
S12 Things that RNAs can do that we did not know about
S13 Integrative genomics: opportunities for disease prevention
S14 Long-read sequencing in the clinic
S15 Preimplantation genetic testing for polygenic conditions
S16 Sex and the Single Cell
Educational Sessions E03-E04
E03 AI meets genomics
E04 Genetic Skeletal Disorders (GSD): from diagnosis to treatment
18:45 – 20:15 Corporate Satellites

Monday, June 3, 2024

08:30 – 10:00 Concurrent Symposia S17 – S21
S17 Next generation functional genomics: variant effects at the single cell level
S18 Advanced statistical methods in human genetics
S19 Genomics in Africa
S20 Who owns your genome?
S21 Inherited Metabolic Diseases
Educational Sessions E05 – E06
E05 Next generation cytogenetics
E06 Genetics of Speech Disorders
08:30 – 10:00 Corporate Satellites
10:00 – 10:30 Coffee Break – Free Poster Viewing – Exhibition
10:30 – 12:00 Concurrent Sessions C16 – C23
12:00 – 13:00 Lunch Break – Free Poster Viewing – Exhibition – Lunch
12:00 – 13:00 Corporate Satellites
12:15 – 13:15 ESHG General Assembly
12:15 – 13:15 G3 Get2gether EBMG/Human genetic professionals: how can we fit future requirements?
13:00 – 14:00 Poster Viewing with Authors and coffee
(Group C) – Only for in-person participants
14:00 – 15:30 Workshops W13 – W19
W13 FAIRIFICATION of genomic research
W14 Clinical Genome: a German perspective
W15 Structural chromosomal variants
W16 The science, guidance and experience of informed consent
W17 Software tools for the sharing & use of GWAS summary statistics and polygenic scores
W18 Implementing pharmacogenetic testing into de clinics: let’s debate
W19 Interpreting NGS variants in prenatal and/or complex settings
14:00 – 15:30 Corporate Satellites
15:30 – 15:45 Fruit Break – Free Poster Viewing – Exhibition
15:45 – 16:45 Poster Viewing with Authors and coffee
(Group D) – Only for in-person participants
16:45 – 17:00 Time to change rooms
17:00 – 18:30 Concurrent Symposia S22 – S26
S22 Dosage sensitivity of human genetic disorders – clinical implications and therapeutic avenues
S23 Predisposition, Molecular signatures and Treatment in Cancer
S24 From single cell maps to function: disentangling the heterogeneity of complex diseases
S25 Biogeographical definitions of population groups
S26 Complete genomes
Educational Session E07 – E08
E07 Mental Health in Academia and Healthcare
E08 FADS – from phenotype to genotype
20:00 ESHG Networking Evening

Tuesday, June 4, 2024

09:00 – 10:30 Concurrent Symposia S27 – S30
S27 Psychiatric Genomics
S28 Proteomics in human genetics and precision medicine
S29 AI genomics: uses, ethics and regulatory issues
S30 Repeat expansion diseases: progress and puzzles
Educational Sessions E09 – E10
E09 Understanding variant penetrance in the era of large-scale population-based sequencing studies
E10 Crosstalk between germline variants and cancer treatment
10:30 – 11:00 Coffee Break
11:00 – 12:30 Concurrent Sessions C24 – C29
12:30 – 13:30 Lunch Break
13:30 – 14:15 PL4 Mendel Lecture
14:15 – 15:00 PL5 ESHG Award Lecture
15:00 – 16:00 PL6 Awards Session
EJHG Citation Awards
ESHG Early Career Awards
European DNA Day Contest
Closing Address