The ESHG 2017 marks the 50th Anniversary of the first ESHG Conference which took place in Copenhagen in 1967. Additional information about the event may be found on the conference website: https://2017.eshg.org/

Sponsorship: Publication of this supplement is sponsored by the European Society of Human Genetics.

ORAL PRESENTATIONS

Plenary Sessions

      PL1 50 years of ESHG

PL2 What's New? Highlights Session

PL3 "ESHG-ASHG Building Bridges Debate: Ethical and Legal Discussions—Past, Present & Future"

PL4 Mendel Lecture

PL5 ESHG Award Lecture

Concurrent Symposia

      S01 Single cell studies: From technology to biology

S02 "One gene, many phenotypes"

S03 Novel Treatment Options

S04 From Association to Causality in complex diseases

S05 3D genome architecture: non-coding variants and human disease

S06 Treatment-Focused Genetic Testing in Cancer

S07 Still the golden age of chromosomes

S08 New technologies in Neurogenetics

S09 Explaining phenotypic variability

S10 Population and evolutionary genetics

S11 Cancer immunogenetics

S12 Genetics and Microbiome

S13 Next generation clinical genetics

S14 Organoid models: The Maxi Impact Of Mini Organs

S15 ESHG / ESC JOINT Symposium: Polygenic Cardiovascular traits

S16 Autophagy in health and disease

Educational Sessions

      E01 "Sequencing, Sponsored by Illumina"

E02 CRISPR/Cas9 genome editing to model disease

E03 50 Shades of Cancer Genetics

E04 Channelopathies

E05 Imprinting-related disorders

E06 Bioethics for 'dummies'

E07 Pharmacogenomics in the clinic

E08 Multi-omics data integration

E09 Phakomatosis Update

E10 Whole-genome haplotyping methods for human embryo selection

E11 Strategies to avoid sudden cardiac death

E12 The evolution of genetic counseling: Lessons learned from psychotherapy

E13 Network Medicine

Concurrent Sessions

      C01 Personalized Medicine and Pharmacogenomics

C02 Neurogenetics 1

C03 Best Posters Session

C04 Epigenetics and Gene Regulation

C05 Skin and Bones

C06 ELSI genomics

C07 Novel genomics technologies

C08 Neuromuscular Disorders

C09 Molecular Mechanisms of Disease

C10 GWAS: Resolving Missing Causality

C11 Sensory disorders

C12 Engaging Patients in Genomics

C13 Innovative Variant Interpretation

C14 Population Genetics and Ancient DNA

C15 Reproductive Genetics

C16 Intellectual Disability

C17 Hereditary Cancer

C18 Internal organs

C19 Diagnostic variant interpretation and quality control

C20 Molecular syndromology

C21 Cardiovascular disorders

C22 Systems Genetics

C23 Neurogenetics 2

POSTERS

      P01 Reproductive Genetics/Prenatal Genetics

P02 "Sensory disorders (eye, ear, pain)"

P03 "Internal organs & endocrinology (lung, kidney, liver, gastrointestinal)"

P04 "Skeletal, connective tissue, ectodermal and skin disorders"

P05 Cardiovascular disorders

P06 Metabolic and mitochondrial disorders

P07 Immunology and hematopoietic system

P08 Intellectual Disability

P09 Neurogenetic and psychiatric disorders

P10 Neuromuscular disorders

P11 Multiple Malformation/anomalies syndromes

P12 Cancer genetics

P13 Basic mechanisms in molecular and cytogenetics

P14 "New diagnostic approaches, technical aspects & quality control"

P15 Personalized/Predictive Medicine and Pharmacogenomics

P16 Omics/Bioinformatics

P17 Epigenetics and Gene Regulation

P18 Genetic epidemiology/Population genetics/Statistical methodology and evolutionary genetics

P19 Genetic counselling/Education/public services

P20 Psychological/Ethical/legal issues

ELECTRONIC POSTERS

      E-P01 Reproductive Genetics/Prenatal Genetics

E-P02 "Sensory disorders (eye, ear, pain)"

E-P03 "Internal organs & endocrinology (lung, kidney, liver, gastrointestinal)"

E-P04 "Skeletal, connective tissue, ectodermal and skin disorders"

E-P05 Cardiovascular disorders

E-P06 Metabolic and mitochondrial disorders

E-P07 Immunology and hematopoietic system

E-P08 Intellectual Disability

E-P09 Neurogenetic and psychiatric disorders

E-P10 Neuromuscular disorders

E-P11 Multiple Malformation/anomalies syndromes

E-P12 Cancer genetics

E-P13 Basic mechanisms in molecular and cytogenetics

E-P14 "New diagnostic approaches, technical aspects & quality control"

E-P15 Personalized/Predictive Medicine and Pharmacogenomics

E-P16 Omics/Bioinformatics

E-P17 Epigenetics and Gene Regulation

E-P18 Genetic epidemiology/Population genetics/Statistical methodology and evolutionary genetics

E-P19 Genetic counselling/Education/public services

E-P20 Psychological/Ethical/legal issues