Programme at a Glance

Pre-conference courses

(separate registration needed)

Thursday, June 11, 2026

09:00 – 17:00 Clinical NGS Data Interpretation Course

Friday, June 12, 2026

09:00 – 17:00 Clinical NGS Data Interpretation Course

Conference programme

Saturday, June 13, 2026

08:30 – 10:00	Educational Session E01 E01 Curation of the clinical genome (Variant classification)	Interactive Sessions I01-I02 I01 Episignatures: Clinical utility beyond binary classification and future applications (LRS and prenatal) I02 Dysmorphology 1	Concurrent Symposia S01-S04 S01 Hunting for effector genes from GWAS studies S02 What’s new on chromosome X: Comparative views across species S03 Uncovering the Uncommon: Rare Cancers S04 Empowering Patient in research and clinical practice.
10:00 – 10:30	Coffee Break – Poster Mounting – Exhibition
10:00 – 11:15	Corporate Sessions
10:30 – 12:00	Concurrent Sessions C01-C07
12:00 – 12:15	Time to change rooms
12:15 – 13:15	Poster Viewing with Authors and Best Poster 1 & Lunch & Exhibition (Group A) – Only for in-person participants
12:15 – 13:15	ESHG Podcast “Genetic Sounds” Live – Click here to listen to previous episodes
12:15 – 13:15	G01 & G02 Get2Gether
12:15 – 12:45	Corporate Presentations
12:15 – 13:30	Corporate Sessions
13:00 – 13:30	Corporate Presentations
13:15 – 13:30	Time to change rooms
13:40 – 16:00	PL1-2 13:40-14:00 Welcoming addresses 14:00-14:15 Leena Peltonen Award Lecture 14:15-15:45 Opening Plenary
15:45 – 16:00	Time to change rooms
16:00 – 17:00	Poster Viewing with Authors and Best Poster 2 & Exhibition & coffee (Group B) – Only for in-person participants
16:00 – 17:00	G03 Get2Gether
17:00 – 18:30	PL3 What’s New? Highlight Session from submitted abstracts
18:30 – 18:45	Time to change rooms
18:45 – 20:15	Concurrent Sessions C08-C14
20:15-21:45	Opening Networking Mixer

Sunday, June 14, 2026

17:00 – 17:15 Time to change rooms

15:30 – 15:45Fruit Break – Free Poster Viewing – Exhibition

08:30 – 10:00	Educational Sessions E02-E03 E02 AI for functional genomics and genetic associations E03 Modelling disease with fish and chips	Interactive Sessions I03-I05 I03 Let’s debate: genomic newborn screening I04Long-read sequencing for beginners I05 Nonsense-mediated mRNA decay; a double-edged sword of mRNA variant classification and biology	Concurrent Symposia S05-S06 S05 Rrrrrrrrepeat-expansions — underestimated source of disease S06 Mechanisms of Chromatic Disorders (EpiGenRare)
08:30 – 09:45	Corporate Sessions
10:00 – 12:00	G04 Get2Gether: Ensuring Quality in Pharmacogenomics: Lessons Learned and the Future of Patient‑Centred Precision Medicine by EMQN
10:00 – 10:30	Coffee Break – Free Poster Viewing – Exhibition
10:30 -11:30	Corporate Sessions
10:30 – 12:00	Concurrent Sessions C15-C21
12:00 – 12:45	Lunch Break – Free Poster Viewing – Exhibition
12:15 – 13:30	Corporate Sessions
12:15 – 12:45	Corporate Presentations
12:15 – 13:15	G05 Get2Gether: The Genome of Europe initiative
12:15 – 13:45	I06 The new ethics of publishing
12:45 – 13:45	Poster Viewing with Authors and Best Poster 3 & Exhibition & coffee (Group C) – Only for in-person participants
13:00 – 13:30	Corporate Presentations
13:45 – 14:00	Time to change rooms
14:00 – 15:30	Concurrent Symposia S07-S11 S07 Polygenic scores: are we there yet for clinical implementation S08 Genome architecture: From disease to therapy S09 Digging into evolution and molecular archeology cancer S10 Education for and by First Nations genomics researchers S11 High-throughput perturbation methods to study disease	Interactive Sessions I07-I09 I07 UCSC and ENSEMBL genome browsers I08 (Digital) Tools and Service Models to Enhance the Delivery and Efficiency of Genetic Counseling I09 Pharmacogenomics and Population Health: From Biobank to Bedside
14:15 – 15:45	Corporate Sessions
15:45 – 16:45	Poster Viewing with Authors and Best Poster 4 & Exhibition & coffee (Group D) – Only for in-person participants
16:45 – 17:00	Time to change rooms
17:00 – 18:30	Concurrent Sessions C22-C28

Monday, June 15, 2026

08:30 – 10:00	Educational Session E04 E04 ELSI in AI genomics	Interactive Sessions I10-I12 I10 Cancer cases I11 Addressing challenges in scaling up genomic newborn screening I12 The art of writing, reading and interpreting genomic reports	Concurrent Symposia S12-S14 S12 Blood as a window: genetic insights into health, aging, and immune function S13 Cytogenetics 2.0 – long-read genomes S14 Advancing genomics around the world
08:30 – 09:45	Corporate Sessions
10:00 – 10:30	Coffee Break – Free Poster Viewing – Exhibition
10:30 – 11:30	Corporate Sessions
10:30 – 12:00	Concurrent Sessions C29-C35
12:00 – 12:45	Lunch Break – Free Poster Viewing – Exhibition – Lunch
12:15 – 13:30	Corporate Sessions
12:15 – 12:45	Corporate Presentations
12:15 – 13:15	ESHG General Assembly
12:15 – 13:15	G06 Get2Gether
12:45 – 13:45	Poster Viewing with Authors and Best Poster 5 & Exhibition & coffee (Group E) – Only for in-person participants
13:00 – 13:30	Corporate Presentations
13:45 – 14:00	Time to change rooms
14:00 – 15:30	Educational Session E05 E05 Long-read RNAsequencing and epitranscriptomics	Interactive Sessions I13-I16 I13 Mutations we almost missed I14 Dysmorphology 2 I15 Predictive testing in neurodegenerative disease: Future directions I16 Social media in Genetics: a tool for building community, visibility and impact	Concurrent Symposia S15-S17 S15 Tracing human history through genetics: migration, adaptation, and evolution S16 Translational therapies S17 From Variants to Function: GWAS, CRISPR, and Organoids for Therapeutic Discovery
14:15 – 15:45	Corporate Sessions
15:30 – 15:45	Fruit Break – Free Poster Viewing – Exhibition
15:45 – 16:45	Poster Viewing with Authors and Best Poster 6 & Exhibition & coffee (Group F) – Only for in-person participants
16:45 – 17:00	Time to change rooms
17:00 – 18:30	Educational Session E06 E06 AI: From clinical applications to digital twins	Interactive Sessions I17-I18 I17 Structural chromosomal variants I18 Reproductive carrier screening: impact and follow-up	Concurrent Symposia S18-S21 S18 Evolutionary Shaping of the Human Regulome S19 Behavioral Genetics and assortative mating S20 Health economics in genomic medicine – maximising value, minimising waste S21 Visible difference and hidden information about genetic conditions: the impact of stigma on family life and reproduction
20:00	ESHG Networking Evening

Tuesday, June 16, 2026

09:00 – 10:30	Concurrent Symposia S22-S26 S22 Solving complex cases with multi-omics S23 The future of prenatal testing S24 Genetic subtypes of complex traits S25 Gene editing reaches the clinic S26 Who owns your genome?	Educational Session E07 E07 ecDNA: the extrachromosomal life
10:30 – 11:00	Coffee Break
11:00 – 12:30	Concurrent Sessions C36-C41
12:30 – 13:30	Lunch Break
13:30 – 13:50	PL4 ELPAG Award Lecture
13:50 – 14:35	PL5 ESHG Award Lecture
14:35 – 15:20	PL6 Mendel Award Lecture
15:20 – 16:00	PL7 Awards Session EJHG Citation Awards ESHG Early Career Awards Dian Donnai and Jill Clayton-Smith Award European DNA Day Contest Closing Address

Programme and speakers are subject to change.

Click on the session titles to access details.

Saturday, June 6, 2020

	Live Sessions	On-demand Sessions – Always Available
09:00 – 11:00	Education Sessions E01 E01 New Technologies	Education Sessions E02-E16 E02 Statistical Rigor and Reproducibility in Genetic Research E03 Pharmacogenomics in the Clinic E04 Hypermobility and the Ehlers Danlos Syndromes E05 Interpreting Variation Outside of Protein-coding Sequence E06 Brain Size Matters! E07 Genome Editing: Multiple Tools and their Applications E08 Does Genetic Counselling Work? E09 Updates on Mitochondrial Diagnostics E10 Therapy for Rare Disorders E11 Heritability Estimations E12 Artificial Intelligence in Biomedicine E13 Mainstreaming Mitochondrial Replacement Techniques? E14 Repeat Expansions: From Detection to Treatment E15 Variant Interpretation in Hereditary Cancer: Lessons learned from Big International Consortia E16 Revisiting Consanguinity in the Era of Improved Genomic Diagnosis
		Workshops Wxx-Wxx W01 NGS in the Clinic – Mistakes and Quality Assurance – To be confirmed W04 ESHG-Y – To be confirmed
11:00 – 11:15	Break
11:15 – 12:45	Concurrent Sessions C01 – C07 C01 From Carrier Screening to Infertility and Fetal Diagnostics C02 Intellectual Disability C03 Novel Bioinformatic and Machine-Learning Methods	Corporate Satellites
12:45 – 13:00	Break
13:00 – 14:30	Corporate Satellites
14:30 – 14:45	Break
14:45 – 16:15	PL1 Opening Plenary Session
14:30 – 14:45	Break
16:30 – 18:00	PL2 What’s New? Highlight Session from submitted abstracts
18:00 – 18:15	Break
18:15 – 19:45	Concurrent Sessions C04 – C07 C04 Basic Research in Cancer C05 Elucidating the Function of Cardiac Genes C06 Sensory Disorders C07 Impact of Genomic Medicine on Public and Patients

Sunday, June 7, 2020

	Live Sessions	On-demand Sessions – Always Available
08:30 – 10:00	Concurrent Symposia S01 – S04 S01 What to Expect from Prenatal Diagnosis S02 Liquid Biopsy for early Detection of Cancer S03 Our Ancestry S04 Public and Patient Engagement	Education Sessions E02-E16 E02 Statistical Rigor and Reproducibility in Genetic Research E03 Pharmacogenomics in the Clinic E04 Hypermobility and the Ehlers Danlos Syndromes E05 Interpreting Variation Outside of Protein-coding Sequence E06 Brain Size Matters! E07 Genome Editing: Multiple Tools and their Applications E08 Does Genetic Counselling Work? E09 Updates on Mitochondrial Diagnostics E10 Therapy for Rare Disorders E11 Heritability Estimations E12 Artificial Intelligence in Biomedicine E13 Mainstreaming Mitochondrial Replacement Techniques? E14 Repeat Expansions: From Detection to Treatment E15 Variant Interpretation in Hereditary Cancer: Lessons learned from Big International Consortia E16 Revisiting Consanguinity in the Era of Improved Genomic Diagnosis
	Corporate Satellites
10:00 – 10:15	Break
10:15 – 11:45	Concurrent Sessions C08 – C12 C08 Impact of Diagnostics Improvements in Healthcare C09 Metabolic and Mitochondrial Disorders C10 Rare and Common Variants in Personalized Medicine C11 Multiple Malformation Syndromes I C12 Neuropsychiatry
11:45 – 12:00	Break
12:00 – 13:00	Corporate Satellites
13:00 – 13:45	Poster Viewing with Authors
14:15 – 15:45	Workshops Wxx – Wxx	Workshops W05 – W11 W05 Exome and Genome Variant Interpretation W06 Prenatal Diagnosis – To be confirmed W07 “Treatabolome”: A Treatment Awareness Project for Rare Diseases W08 European Reference Networks – What is in it for me? – To be confirmed W09 UCSC Genome Browser – To be confirmed W11 Pharmacogenomics in Practice – To be confirmed
14:45 – 15:15	Break
15:15 – 16:45	Concurrent Symposia S05 – S08 S05 Development and Disease at Single Cell Resolution S06 Making Sense out of Nonsense S07 Strategies and Applications in Translating GWAS to Function S07 Cardiovascular Genetics
16:45 – 17:00	Break
17:00 – 18:30	Concurrent Sessions C13-C16 C13 3D Genome Architecture C14 Internal Organs C15 Best Posters Session 1 C16 The Interplay of Law, Policy and Genomics
18:30 – 18:45	Break
18:45 – 20:15	Corporate Satellites

Saturday, June 6, 2020

08:00 – 10:00	Educational Session E01 New Technologies
10:00 – 10:30	Coffee Break – Poster Mounting – Exhibition
10:00 – 11:30	Corporate Satellites
10:30 – 12:00	Education Sessions E02-E04 E02 Statistical Rigor and Reproducibility in Genetic Research E03 Pharmacogenomics in the Clinic E04 Hypermobility and the Ehlers Danlos Syndromes	Workshops W01-W04 W01 NGS in the Clinic – Mistakes and Quality Assurance W02 Dysmorphology I W03 Molecular Newborn Screening vs. Newborn Testing W04 GenEthics
12:00 – 14:00	Lunch Break – Free Poster Viewing – Exhibition
12:15 – 13:45	Corporate Satellites
14:00 – 14:30	PL0 Welcoming Addresses
14:30 – 16:00	PL1 Opening Plenary Session
16:00 – 16:30	Fruit Break – Free Poster Viewing – Exhibition
16:30 – 18:00	PL2 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 C01 From Carrier Screening to Infertility and Fetal Diagnostics C02 Intellectual Disability C03 Novel Bioinformatic and Machine-Learning Methods C04 Basic Research in Cancer C05 Elucidating the Function of Cardiac Genes C06 Sensory Disorders C07 Impact of Genomic Medicine on Public and Patients
20:00 – 22:00	Opening Networking Mixer

Sunday, June 7, 2020

08:30 – 10:00	Concurrent Symposia S01 – S05 S01 What to Expect from Prenatal Diagnosis S02 Multi-omics Approaches for Diagnosing Rare Diseases S03 Liquid Biopsy for early Detection of Cancer S04 Our Ancestry S05 Public and Patient Engagement	Educational Sessions E05-E06 E05 Interpreting Variation Outside of Protein-coding Sequence E06 Brain Size Matters!
08:30 – 10:00	Corporate Satellites
10:00 – 10:30	Coffee Break, Free Poster Viewing, Exhibition
10:30 – 12:00	Concurrent Sessions C08 – C15 C08 Impact of Diagnostics Improvements in Healthcare C09 Metabolic and Mitochondrial Disorders C10 Rare and Common Variants in Personalized Medicine C11 Multiple Malformation Syndromes I C12 Neuropsychiatry C13 3D Genome Architecture C14 Internal Organs C15 Best Posters 1
12:00 – 13:00	Concurrent Sessions C16 C16 The Interplay of Law, Policy and Genomics
12:00 – 13:00	Free Poster Viewing – Exhibition – Lunch
12:00 – 13:00	Corporate Satellites
13:00 – 14:00	Poster Viewing with Authors and coffee (Group A)
14:15 – 15:45	Workshops W05 – W11 W05 Exome and Genome Variant Interpretation W06 Prenatal Diagnosis W07 “Treatabolome”: A Treatment Awareness Project for Rare Diseases W08 Science Communication W09 UCSC Genome Browser W10 Community Genetics: Prospects for Curing Genetic Disorders W11 Pharmacogenomics in Practice
14:15 – 15:45	Corporate Satellites
15:45 – 16:00	Fruit Break – Free Poster Viewing – Exhibition
16:00 – 17:00	Poster Viewing with Authors and coffee (Group B)
17:15 – 18:45	Concurrent Symposia S06 – S09 S06 Development and Disease at Single Cell Resolution S07 Making Sense out of Nonsense S08 Strategies and Applications in Translating GWAS to Function S09 Cardiovascular Genetics	Educational Sessions E07-E09 E07 Genome Editing: Multiple Tools and their Applications E08 Does Genetic Counselling Work? E09 Updates on Mitochondria Diagnostics
19:00 – 20:00	ESHG Membership Meeting
19:00 – 20:30	Corporate Satellites

Monday, June 8, 2020

08:30 – 10:00	Concurrent Symposia S10- S14 S10 Beyond Mendelian Inheritance S11 Single Cell Cancer Genetics S12 Embryo and Placenta: Equal Partners S13 Where Science and Ethics Meet S14 Lysosomes in Health and Disease	Educational Sessions E10-E11 E10 Therapy for Rare Disorders E11 Heritability Estimations
08:30- 10:00	Corporate Satellites
10:00 – 10:30	Coffee Break, Free Poster Viewing, Exhibition
10:30 – 12:00	Concurrent Sessions C17 – C24 C17 New Therapeutic Approaches C18 Clinical Cancer Research C19 Multiple Malformation Syndromes II C20 Neurogenetics C21 Methods and Applications of Association Studies in Large Cohorts C22 Immunology and Hematology C23 Counselling, Communication and Deliberation C24 Best Posters 2
12:00 – 13:00	Free Poster Viewing – Exhibition – Lunch
12:00 – 13:00	Corporate Satellites
12:15 – 13:00	PL3 ELPAG Award Lecture
13:00 – 14:00	Poster Viewing with Authors and coffee (Group C)
14:15 – 15:45	Workshops W12 – W18 W12 Copy Number Variant Interpretation and Classification W13 Dysmorphology II W14 Exome Pipelines for Clinicians W15 Using the Ensembl VEP for analysing Variants in Rare and Common Disease W16 Genetic Counselling Models for Genomic Screening W17 European Reference Networks – What is in it for me? W18 Reproducible and transparent Analysis with Galaxy
14:15 – 15:45	Corporate Satellites
15:45 – 16:00	Fruit Break – Free Poster Viewing – Exhibition
16:00 – 17:00	Poster Viewing with Authors and coffee (Group D)
17:15 – 18:45	Concurrent Symposia S15 – S18 S15 ESHG-ASHG Building Bridges Session on Polygenic Risk Scores: Risky or Useful in the Clinic? S16 Detection of Structural Variation S17 Genetic Mechanisms in Haematological Neoplasias S18 Cornelia de Lange Syndrome and Cohesinopathies	Educational Sessions E12-E13 E12 Artificial Intelligence in Biomedicine E13 Mainstreaming Mitochondrial Replacement Techniques?
20:00	ESHG Networking Evening

Tuesday, June 9, 2020

09:00 – 10:30	Concurrent Symposia S19- S21 S19 Clonal Fitness of Somatic Mutations S20 Data-driven Genomic Care and its Implementation in the Clinic: A Paradigm Shift S21 Integrating Large-scale Functional Data into Genome-wide Association Studies	Educational Sessions E14-E16 E14 Repeat Expansions: From Detection to Treatment E15 Variant Interpretation in Hereditary Cancer: Lessons learned from Big International Consortia E15 Revisiting Consanguinity in the Era of Improved Genomic Diagnosis
11:00 – 12:30	Concurrent Sessions C25 – C31 C25 New Technologies and Approaches C26 Genome Variation and Architecture C27 Late Breaking Session C28 Neurodevelopment C29 Skin & Bones C30 Polygenic Risk Scores: From Tool to Practice C31 Shaping the Genomic Medicine Era
12:30 – 13:30	Lunch Break
13:30 – 14:30	PL4 Mendel Lecture
14:30 – 15:30	PL5 ESHG Award Lecture
15:30 – 16:15	PL6 Awards Session ESHG Education Award EJHG Citation Awards ESHG Awards for Best Presentations by Young Investigators Closing

Welcome to the European Human Genetics Conference
Hybrid Conference
Gothenburg, Sweden

June 13–16, 2026

Welcome to the European Human Genetics Conference
Hybrid Conference
Gothenburg, Sweden

June 13–16, 2026

Programme at a Glance

Pre-conference courses

Thursday, June 11, 2026

Friday, June 12, 2026

Conference programme

Saturday, June 13, 2026

Sunday, June 14, 2026

Monday, June 15, 2026

Tuesday, June 16, 2026

Click on the session titles to access details.

Saturday, June 6, 2020

Sunday, June 7, 2020

Saturday, June 6, 2020

Sunday, June 7, 2020

Monday, June 8, 2020

Tuesday, June 9, 2020

Welcome to the European Human Genetics Conference Hybrid Conference Gothenburg, Sweden

June 13–16, 2026

Programme at a Glance

Pre-conference courses

Thursday, June 11, 2026

Friday, June 12, 2026

Conference programme

Saturday, June 13, 2026

Sunday, June 14, 2026

Monday, June 15, 2026

Tuesday, June 16, 2026

Click on the session titles to access details.

Saturday, June 6, 2020

Sunday, June 7, 2020

Saturday, June 6, 2020

Sunday, June 7, 2020

Monday, June 8, 2020

Tuesday, June 9, 2020

Welcome to the European Human Genetics Conference
Hybrid Conference
Gothenburg, Sweden