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    "143371-21892958":
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        "datetime_modified":"20260107T120418",
        "datetime_start":"20260413T110000",
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        "has_end_time":1,
        "date_start":"2026-04-13",
        "date_end":"2026-04-13",
        "time_start":"11:00:00",
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        "time_zone":"America\/Detroit",
        "event_title":"Human Genetics Research Seminar Series",
        "occurrence_title":"",
        "combined_title":"Human Genetics Research Seminar Series: presenting Jacy Wagnon, PhD, Assistant Professor Department of Neuroscience The Ohio State University College of Medicine",
        "event_subtitle":"presenting Jacy Wagnon, PhD, Assistant Professor Department of Neuroscience The Ohio State University College of Medicine",
        "event_type":"Lecture \/ Discussion",
        "event_type_id":"13",
        "description":"Monday, April 13, 2026\r\n11:00am - 12:00pm\r\n1020 Kahn Auditorium, BSRB\r\n\r\nJacy Wagnon, PhD\r\nAssistant Professor\r\nDepartment of Neuroscience\r\nThe Ohio State University College of Medicine\r\n\u201cSeminar Title TBD\u201d\r\n\r\nHosted By: Miriam Meisler, PhD, Department of Human Genetics\r\n___\r\nDevelopmental and epileptic encephalopathies (DEE) are a genetically heterogeneous group of neurological disorders characterized by early-onset seizures along with cognitive, motor, and behavioral impairments. The Wagnon laboratory is interested in understanding genetic and molecular mechanisms underlying DEE and identifying new treatment strategies for these severe disorders. Our current studies focus on DEE caused by variants in the neuronal voltage-gated sodium channel gene SCN8A. We are developing mouse models of SCN8A encephalopathy to study pathogenesis of seizures and related comorbidities. A second focus of the lab is to investigate the role of regulation of gene expression in seizure pathology. Changes in mRNA and microRNA levels represent a general transcriptional response to seizures that may implicate new therapeutic targets.",
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    {
        "datetime_modified":"20260107T120429",
        "datetime_start":"20260420T110000",
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        "date_start":"2026-04-20",
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        "event_title":"Human Genetics Research Seminar Series",
        "occurrence_title":"",
        "combined_title":"Human Genetics Research Seminar Series: presenting Aaron Ragsdale, PhD Assistant Professor Integrative Biology University of Wisconsin-Madison",
        "event_subtitle":"presenting Aaron Ragsdale, PhD Assistant Professor Integrative Biology University of Wisconsin-Madison",
        "event_type":"Lecture \/ Discussion",
        "event_type_id":"13",
        "description":"Monday, April 20, 2026\r\n11:00am - 12:00pm\r\n1020 Kahn Auditorium, BSRB\r\n\r\nAaron Ragsdale, PhD\r\nAssistant Professor\r\nIntegrative Biology\r\nUniversity of Wisconsin-Madison\r\n\u201cSeminar Title TBD\u201d\r\n\r\nHosted By: Jeffrey Kidd, PhD, Department of Human Genetics\r\n___\r\nOur research aims to understand how evolutionary forces are expected to shape genetic diversity within populations, and then uses this understanding to learn about demographic and selective histories and processes from genome sequencing data. One focus of our research is on developing population genetic theory that lets us predict patterns of diversity and genetic structure under varying models of demography and selection. Another focus is on turning that theory into computational tools to compare model predictions to observations from natural populations. Finally, we have a strong interest in inferring (mostly) human evolutionary history from genetic data, including both ancient history and population structure as well as more recent migrations, movements, and dynamics.",
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    {
        "datetime_modified":"20260107T120451",
        "datetime_start":"20260504T110000",
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        "date_start":"2026-05-04",
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        "time_zone":"America\/Detroit",
        "event_title":"Human Genetics Research Seminar Series",
        "occurrence_title":"",
        "combined_title":"Human Genetics Research Seminar Series: presenting Alex Pollen, PhD, Assistant Professor Neurobiology Developmental & Stem Cell Biology University of California, San Francisco",
        "event_subtitle":"presenting Alex Pollen, PhD, Assistant Professor Neurobiology Developmental & Stem Cell Biology University of California, San Francisco",
        "event_type":"Lecture \/ Discussion",
        "event_type_id":"13",
        "description":"Monday, May 4, 2026\r\n11:00am - 12:00pm\r\n1020 Kahn Auditorium, BSRB\r\n\r\nAlex Pollen, PhD\r\nAssistant Professor\r\nNeurobiology\r\nDevelopmental & Stem Cell Biology\r\nUniversity of California, San Francisco\r\n\u201cSeminar Title TBD\u201d\r\n\r\nHosted By: Xander Nuttle, PhD, Department of Human Genetics\r\n___\r\nWe study how genetic changes that accumulated over the last 6 million years of human evolution influence specialized features of brain development using single cell genomics, cerebral organoid models of ape brain development, and genome engineering.\r\n\r\nOver the last six million years, human cognition has changed in remarkable ways to support symbolic language, long-term planning, cooperation on vast scales, and the rapid cultural accumulation of technology. During this time, patterns of brain development and life history changed to triple the number of neurons produced prenatally, extend synaptic plasticity through a prolonged phase of development, and restructure connectivity between brain regions. At the same time tens of millions of mutations accumulated as fixed changes in the human genome through the processes of selection and drift. A portion of this new genomic information guides the development of uniquely human traits and contributes to disease vulnerabilities shared by all humans. However, connecting human-specific mutations to recently evolved traits remains a major challenge because we lack experimental systems for comparative and functional studies of great ape cortical development. To identify genomic differences underlying unique features or vulnerabilities of the human brain, we are incorporating advances in single cell genomics and genome engineering with great ape cerebral organoid models of brain development. We are enthusiastic for new graduate students to join the team, and the lab is well suited for those with an interest in evolution, neuropsychiatric disorders, neuronal cell diversity, stem cell models, or bioinformatics.",
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    {
        "datetime_modified":"20260107T120504",
        "datetime_start":"20260511T110000",
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        "has_end_time":1,
        "date_start":"2026-05-11",
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        "time_zone":"America\/Detroit",
        "event_title":"Human Genetics Research Seminar Series",
        "occurrence_title":"",
        "combined_title":"Human Genetics Research Seminar Series: presenting Tony Capra, PhD, Professor Bakar Computational Health Sciences Institute Department of Epidemiology and Biostatistics University of California, San Francisco",
        "event_subtitle":"presenting Tony Capra, PhD, Professor Bakar Computational Health Sciences Institute Department of Epidemiology and Biostatistics University of California, San Francisco",
        "event_type":"Lecture \/ Discussion",
        "event_type_id":"13",
        "description":"Monday, May 11, 2026\r\n11:00am - 12:00pm\r\n1020 Kahn Auditorium, BSRB\r\n\r\nTony Capra, PhD\r\nProfessor\r\nBakar Computational Health Sciences Institute\r\nDepartment of Epidemiology and Biostatistics\r\nUniversity of California, San Francisco\r\n\u201cSeminar Title TBD\u201d\r\n\r\nHosted By: Xinjun Zhang, PhD, Department of Human Genetics\r\n___\r\nWe use the tools of computer science and statistics to address problems in genetics, evolution, and biomedicine. For a summary of our major research foci, see Research.\r\n\r\nOur group is located in the Bakar Computational Health Sciences Institute and the Department of Epidemiology and Biostatistics at the University of California, San Francisco. Prior to coming to UCSF, Tony spent 7 wonderful years at Vanderbilt University.\r\n\r\nHumans differ from one another and our closest living relatives, the chimpanzees, in a wide range of traits, including our susceptibility to many diseases. We model the evolutionary processes that have produced these novel traits and develop algorithms that compare genomes to predict the functional relevance of specific genetic differences between individuals and species.",
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        "datetime_modified":"20260107T120515",
        "datetime_start":"20260518T110000",
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        "has_end_time":1,
        "date_start":"2026-05-18",
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        "event_title":"Human Genetics Research Seminar Series",
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        "combined_title":"Human Genetics Research Seminar Series: presenting Arneet Saltzman, PhD, Assistant Professor Department of Cell & Systems Biology University of Toronto",
        "event_subtitle":"presenting Arneet Saltzman, PhD, Assistant Professor Department of Cell & Systems Biology University of Toronto",
        "event_type":"Lecture \/ Discussion",
        "event_type_id":"13",
        "description":"Monday, May 18, 2026\r\n11:00am - 12:00pm\r\n1020 Kahn Auditorium, BSRB\r\n\r\nArneet Saltzman, PhD\r\nAssistant Professor\r\nDepartment of Cell & Systems Biology\r\nUniversity of Toronto\r\n\u201cSeminar Title TBD\u201d\r\n\r\nHosted By: Stephanie Bielas, PhD, Department of Human Genetics\r\n___\r\nMost of the cells in an organism share the same genome sequence, yet they are able to carry out many distinct functions. Along with other layers of gene regulation, chromatin modification plays a key role in this cellular specialization. Our research focuses on histone modifications such as lysine methylation, and the proteins that recognize these modifications, which are often referred to as chromatin \u2018readers\u2019. Chromatin readers can recruit and act as part of diverse chromatin modifying protein complexes to mediate the silencing of many genes with important functions in cell proliferation and differentiation. We will use a combination of genetic, biochemical and genome-wide sequencing approaches to investigate the striking regulatory complexity of chromatin readers. Our research will contribute to a better understanding of how cells acquire and maintain different fates during development, how chromatin readers contribute to epigenetic inheritance, and how aberrant regulation of histone methylation contributes to the pathogenesis of several human diseases, including cancers.",
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    {
        "datetime_modified":"20260107T102207",
        "datetime_start":"20260522T120000",
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        "has_end_time":1,
        "date_start":"2026-05-22",
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        "time_start":"12:00:00",
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        "time_zone":"America\/Detroit",
        "event_title":"James V. Neel, MD, PhD Lecture in Human Genetics & Award",
        "occurrence_title":"",
        "combined_title":"James V. Neel, MD, PhD Lecture in Human Genetics & Award: presenting Eric S. Lander, PhD, Professor of Biology & Professor of Systems Biology at Harvard Medical School and Founding Director Emeritus at the Broad Institute of MIT",
        "event_subtitle":"presenting Eric S. Lander, PhD, Professor of Biology & Professor of Systems Biology at Harvard Medical School and Founding Director Emeritus at the Broad Institute of MIT",
        "event_type":"Conference \/ Symposium",
        "event_type_id":"5",
        "description":"Join us as Eric S. Lander, PhD, Professor of Biology & Professor of Systems Biology at Harvard Medical School and Founding Director Emeritus at the Broad Institute of MIT, presents their research at The Department of Human Genetics 25th Annual James V. Neel Lecture.  We will have presentations from our student awardees, a poster session, and a light reception. \r\n\r\n12:00-2:00 Award Presentations & Keynote Seminar | 1020 Kahn Auditorium, BSRB\r\n2:00-3:00 Reception & Poster Session | ABC Seminar Rooms, BSRB\r\n\r\nReady to share your research? Present your poster at the 25th Annual Neel Lectureship. Submit your poster information no later than Friday, May 8, 2026 @midnight.\r\n\r\n12:00 \u2013 Lectureship Begins\r\n12:15 \u2013 Graduate Student Neel Award Presentation (PhD)\r\n12:30 \u2013 Graduate Student Neel Award Presentation (MS\/GC)\r\n1:00 \u2013 Keynote Address\r\n2:00 \u2013 Reception Begins\/ Poster Session Begins\r\n3:00 \u2013 Conclude",
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        "website":"https:\/\/medschool.umich.edu\/events\/james-v-neel-md-phd-lecture-human-genetics-award\/2026-05-22",
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    {
        "datetime_modified":"20260107T120530",
        "datetime_start":"20260914T110000",
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        "date_start":"2026-09-14",
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        "event_title":"Human Genetics Research Seminar Series",
        "occurrence_title":"",
        "combined_title":"Human Genetics Research Seminar Series: presenting Yang Shi, PhD Professor of Epigenetics Ludwig Institute for Cancer Research, Oxford University, Oxford, England",
        "event_subtitle":"presenting Yang Shi, PhD Professor of Epigenetics Ludwig Institute for Cancer Research, Oxford University, Oxford, England",
        "event_type":"Lecture \/ Discussion",
        "event_type_id":"13",
        "description":"Monday, September 14, 2026\r\n11:00am - 12:00pm\r\nLocation TBD\r\n\r\nYang Shi, PhD\r\nProfessor of Epigenetics\r\nLudwig Institute for Cancer Research\r\nOxford University, Oxford, England\r\n\u201cSeminar Title TBD\u201d\r\n\r\nHosted By: Shigeki Iwase, PhD, Department of Human Genetics\r\n___\r\nBefore joining Ludwig Oxford in 2020, I was Professor of Cell Biology and C. H. Waddington Professor of Pediatrics at Harvard Medical School. I received my PhD from New York University and postdoctoral training at Princeton University. I joined Harvard Medical School as an Assistant Professor in 1991 and was appointed a Professor of Pathology in 2004. In 2009 I joined the Newborn Medicine Division of Boston Children\u2019s Hospital.\r\n\r\nI am interested in identifying key epigenetic regulators in cancer, elucidating their mechanism of action and providing the conceptual basis for translating our basic findings to the clinic via the development of new therapeutic strategies. With the discovery of the first histone methyl eraser, LSD1, in 2004, our group demonstrated that histone methylation is dynamically regulated, which overturned the long-held dogma that such modifications were static and irreversible. We have also discovered many additional histone demethylases with different specificities, and novel readers, including those that specifically recognize unmodified lysine and arginine and suggest that the unmodified states are not simply a ground neutral state of epigenetic information but rather likely code for epigenetic information as modified states. Importantly, many of these chromatin enzymes and readers have since been implicated in various types of human cancers, indicating an important role of chromatin regulation in tumorigenesis.\r\n\r\nMore recently, we have also been studying RNA modifications and how they impact gene expression regulation. In many ways this exciting field parallels the early days of chromatin biochemistry and biology, i.e., the nature and the biological and pathological functions of RNA modifications, as well as the enzymes responsible for writing, erasing and reading them, are just beginning to be understood.\r\n\r\nAt Ludwig Oxford, my lab is focusing on two questions. First, how to convert \u201ccold tumors to \u201chot\u201d and how to sustain durable responses to cancer immune checkpoint blockade therapy. Second, how to induce therapeutic differentiation of cancers, using acute myeloid leukemia and diffuse intrinsic pontine glioma as models where chromatin\/epigenetics have been shown to play a crucial role in the maintenance of a poorly differentiated state.",
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        "combined_title":"Human Genetics Research Seminar Series: presenting Ira Hall, PhD, Professor of Genetics Director of the Yale Center for Genomic Health Yale School of Medicine",
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        "combined_title":"Human Genetics Research Seminar Series: presenting Malia Fullerton, DPhil, University of Washington",
        "event_subtitle":"presenting Malia Fullerton, DPhil, University of Washington",
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        "description":"Monday, October 12, 2026\r\n11:00am - 12:00pm\r\nLocation TBD\r\n\r\nMalia Fullerton, DPhil\r\nAdjunct Professor, Epidemiology\r\nProfessor, Bioethics and Humanities\r\nAdjunct Professor, Genome Sciences\r\nAdjunct Professor, Medicine - Medical Genetics\r\nActing\/Interim Center\/Institute Director, School of Public Health\r\nUniversity of Washington\r\n\u201cSeminar Title TBD\u201d\r\n\r\nHosted By: Wendy R. Uhlmann, Department of Human Genetics\r\n___\r\nStephanie Malia Fullerton, DPhil, is Professor of Bioethics and Humanities at the University of Washington School of Medicine. She is also Adjunct Professor in the UW Departments of Epidemiology, Genome Sciences, and Medicine (Medical Genetics), as well as an affiliate investigator with the Public Health Sciences division of the Fred Hutchinson Cancer Research Center. She received a PhD in Human Population Genetics from the University of Oxford and later re-trained in Ethical, Legal, and Social Implications (ELSI) research with a fellowship from the NIH National Human Genome Research Institute.\r\n\r\nDr. Fullerton\u2019s work focuses on the ethical and social implications of genomic research and its equitable and safe translation for clinical and public health benefit. She serves as the ELSI lead for the Clinical Sequencing Evidence-Generating Research (CSER2) Consortium coordinating center, co-chairs the TOPMed Consortium ELSI Committee, and chairs the Bioethics Advisory Board of the Kaiser Permanente national Research Bank. She contributes to a range of empirical projects focused on clinical genomics translation and precision medicine approaches to the treatment and prevention of cancer and kidney disease in diverse patient populations.",
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