Conference Description
The Functional Genomics of Human Brain Development and Disease GRC is a premier, international scientific conference focused on advancing the frontiers of science through the presentation of cutting-edge and unpublished research, prioritizing time for discussion after each talk and fostering informal interactions among scientists of all career stages. The conference program includes a diverse range of speakers and discussion leaders from institutions and organizations worldwide, concentrating on the latest developments in the field. The conference is five days long and held in a remote location to increase the sense of camaraderie and create scientific communities, with lasting collaborations and friendships. In addition to premier talks, the conference has designated time for poster sessions from individuals of all career stages, and afternoon free time and communal meals allow for informal networking opportunities with leaders in the field.
In its second iteration, this conference seeks to bring together a multidisciplinary group of geneticists, molecular biologists, neuroscientists, computational experts, and stem cell biologists endeavoring to improve diagnostics, prognostics, and treatment of brain disease. The conference will explore (1) emerging molecular mechanisms in brain development and responses, (2) recent efforts in atlases and other resources to enhance knowledge generation (3) advances in linking genetics to brain function; (4) new insights into human brain development and disordersobtained through investigations that span across scales; and (5) progress towards novel therapeutic targets and interventions, including regulatory and ethical aspects. Whereas large-scale genomic studies are uncovering the complex genetic architecture of gene regulation and disease risk, the causal cellular mechanisms of disease risk and progression remain unclear. While the generation of patient-specific neurons, glia, and organoids facilitate the study of human brain development, CRISPR-based engineering approaches facilitate single or genome-wide perturbations in DNA sequence or epigenetic activity; their integration makes it possible to investigate the molecular mechanisms of disease-associated variations. Together, these approaches translate the myriad advances from large-scale genetic studies into clinically actionable information. This GRC will contribute to improving our understanding the cellular and molecular mechanisms involved in regulating human brain development in health and disease The main goal is to bring together communities with synergistic approaches, from large-scale genomic studies uncovering the complex genetic architecture of gene regulation and disease risk to cellular and molecular modeling through stem cell differentiation, organoids, screens, and transcriptomics to investigate the molecular mechanisms of disease-associated variations. This GRC will contribute to improving our understanding of the cellular and molecular mechanisms involved in regulating human brain development in health and disease.
The conference will consist of nine sessions, on the topics listed below. The conference chair is currently developing their preliminary program, which will include the names of the invited speakers and discussion leaders for each of these sessions. The preliminary program will be available by July 10, 2024. Please check back for updates.