This colourful chat is brought to you by the European Society of Human Genetics and the Witworth Group. Listen to the sound of our genomics podcast session talks with monthly guest speakers.
Our podcast, seeks to stimulate new conversations around human genetics and bring you some of the biggest stories in science that affects us all.
Every first Friday of the month, we will be discussing all things genetic, now that genomics has moved to the forefront of medicine. What does that mean for everyone? Genomic Sounds is the ESHG podcast exploring themes close to our mind and heart.
In the final episode of our second series, we discuss the wide topic of “What is the next ethical frontier in genetics?”. Recorded with a live audience in Glasgow, Scotland.
On the panel we have a wonderful range of guests including Professor Tara Clancy from The University of Manchester, Gemma Louise Chandratillake from the Institute of Continuing Education, and Masha Shabina, Assistant Professor in Privacy Law at Institute for International Research on Criminal Policy, Ghent, Belgium.
In this episode, we discuss reproductive genetics and choices.
In this conversation, we are joined by Director of The Raphael Recanati Genetics Institute, Lina Basel, and Dr Edith Coonen, Senior Clinical Embryologist at the department of Reproductive Medicine, and a Laboratory Specialist in Reproductive Genetics at the department of Clinical Genetics, Maastricht University Medical Centre.
In this episode, we discuss intellectual disability and consent in human genetics.
In this conversation, we are joined by two guests from The University of New South Wales in Sydney, Dr Elizabeth Emma Palmer and Professor Iva Strnadova.
In this episode, we discuss “What exactly is a centre for rare conditions?”
A conversation with Professor Siddharth Banka from the University of Manchester, Professor Gareth Baynam from Australian National University’s National Centre for Indigenous Genomics, and Dame Laura Lee, the first employee and now CEO of Maggie’s, a charity providing free cancer support and information in centres across the UK and online.
In this episode, we discuss the treatments of genetic conditions, exciting breakthroughs, and their costs. A conversation with Assistant Professor Roos van Westrhenen, Professors Katherine Payne and Graeme Black from the University of Manchester, and Wayne Thompson, a patient who took part in a gene therapy trial for Choroideremia.
As we return with our second series of Genetic Sounds, in this first episode we discuss the background of the African Society of Human Genetics, and Equity in African research. A conversation with Professor Ambroise Wonkam, President of the African Society of Human Genetics, Human Genetics Scientist Professor Michele Ramsay, based at the University of Witswatersrand, Johannesburg, Dr Rokhaya Ndiaye, from the Senegal Human Genetics Society, and Dr Vicky Nembaware, current secretory for the African Society of Human Genetics.
In this final episode, we discuss the wide topic of “What is the future in genetics?”
Recorded with a live audience as one of the sessions at the 2022 European Society of Human Genetics conference in Vienna where we take questions from the live and virtual audience.
On the panel we have a wonderful range of guests including; Gijs WE Santen a clinical geneticist from the Netherlands with a special interest in dysmorphology, in particular Coffin-Siris syndrome, and prenatal genetic testing. Professor Clara Gaff, an Executive Director for Melbourne Genomics who has worked in public health, government, academic and not-for-profit sectors. Khadijah Bakur, a Genetic counsellor with expertise in understanding the role of religion -specially the role of Islam - on decision making for patients. And Alexander Hoischen, who has expertise in the identification of rare disease genes using latest genomics tools.
In this episode, we debate “Is your genetic information just yours?”. We discuss where you find your genetic information if you need it, and who should have access to this. A conversation with Lawyer and bioethicist, Betina Cuñado, Associate Professor at the IHMPE in Toronto, Dr Yvonne Bombard, who specialises in the assessment and translation of genomic technologies in clinical care, and Dr Jantina de Vries, Associate Professor in Bioethics at the Department of Medicine of the University of Cape Town.
In this episode, we discuss "What is a genetic syndrome?". We ask whether we still need ‘conditions’, or can we just have genes? A conversation with Leslie Biesecker, NIH Distinguished Investigator at the Center for Precision Health Research and Izzy Rundle, Engagement and Support Manager at SWAN UK (Syndrome Without a Name). Sofia Douzgou, from the European Society of Human Genetics also joins the conversation.
Bringing together the debate on access to genetic services, and discussing what can be done to improve the experience for individuals in need of these services. A conversation with Professor Dame Elizabeth Anionwu, founder of the Romanian Prader Willi Association, Dorica Dan, and Celia Azevedo Soares, Medical Genetics resident at Porto Medical Center, and a member of the Education Committee of the European Society of Human Genetics.
Bringing together the debate on gender and advances in knowledge about sex biases in human genetics.A conversation with Prof Gareth Evans, Professor of Medical Genetics and Cancer Epidemiology at The University of Manchester, Reubs J Walsh, a PhD Candidate in the Department of Clinical, Neuro- and Developmental Psychology at the Vrije Universiteit Amsterdam, and Dr Can Ding, Vice Chair of the ESHG Young Geneticists Committee (ESHG-Y).
In our first episode, we are joined by Professor of Anatomy, Anne Spurkland from the Institute of Basic Medical Sciences in Oslo, Norway, Professor of Medical Genetics at The University of Bergen, Norway, Gunnar Douzgos-Houge, and Professor Milan Macek, Chairman of the National Coordination Centre for Rare Diseases in Prague, Czech Republic.
We discuss the impact of current events linked to Covid-19, and why it is important for everyone to have basic knowledge about genetics.