Sentences with phrase «human genomic medicine»

«Martin Pera brings an unparalleled depth of expertise in embryonic and pluripotent stem cell biology to our faculty, complementing and broadening our emerging research emphasis on human genomic medicine,» said Edison Liu, M.D., president and CEO of The Jackson Laboratory.

Not exact matches

«They are developing the clinical genomics necessary to foster and support the Precision Medicine Initiative of the National Institutes of Health, and generating the genomics data that further drives human genome research.»
«We feel it's critical that the scientific community consider the potential hazards of all off - target mutations caused by CRISPR, including single nucleotide mutations and mutations in non-coding regions of the genome,» says co-author Stephen Tsang, MD, PhD, the Laszlo T. Bito Associate Professor of Ophthalmology and associate professor of pathology and cell biology at Columbia University Medical Center, and in Columbia's Institute of Genomic Medicine and the Institute of Human Nutrition.
But now «the approach can be reset using the bacterial and human genomic data,» says immunologist Steven Schutzer of the University of Medicine and Dentistry of New Jersey.
The U.S. National Human Genome Research Institute and the National Academy of Medicine recently brought together 25 of these groups to compare projects, to examine the current state of implementation and desired near - term capabilities, and to identify opportunities for collaboration that promote the responsible practice of genomic mMedicine recently brought together 25 of these groups to compare projects, to examine the current state of implementation and desired near - term capabilities, and to identify opportunities for collaboration that promote the responsible practice of genomic medicinemedicine.
Human - genomics programs work together worldwide to speed the translation of genomic medicine to the clinic.
So our focus will be to study the genome through the transcripts in biological systems, to understand the genetic architecture of Pan-Asian populations, and finally to focus on the intersect between genomics and human medicine.
«Artificial intelligence (AI) has huge potential to revolutionize disease diagnosis and management by doing analyses and classifications involving immense amounts of data that are difficult for human experts — and doing them rapidly,» said senior author Kang Zhang, MD, PhD, professor of ophthalmology at Shiley Eye Institute and founding director of the Institute for Genomic Medicine at UC San Diego School of Medicine.
«This is the first systematic comparison of the mouse and human at the genomic level,» said Bing Ren, Ph.D., co-senior author on the Consortium's main Nature study and professor of cellular and molecular medicine at the University of California, San Diego.
Through his role in the UM Center for Genome Technology, part of the Miller School of Medicine, Dr. Hedges is actively involved in the incorporation of novel genomic technologies into the process of searching for the genetic variation underlying human disease risk.
Hotspots in the Human Genome The study, led by Joel Dudley, a genomics professor at the Icahn School of Medicine at Mount Sinai, proposes that because schizophrenia is relatively prevalent in humans, it perhaps has a complex evolutionary backstory that would explain its persistence and apparent exclusivity to humans.
The Global Alliance for Genomics and Health (Global Alliance, or GA4GH) was formed to help accelerate the potential of genomic medicine to advance human health.
In the post-genomic era, we are witnessing significant advances in the functional decipherment of the human genome sequence that have been made possible by new technological developments in the field of genomic medicine.
Research interests: primate comparative genomics, adaptive evolution, human brain evolution, infectious diseases in primate hosts, HIV / SIV and AIDS, evolutionary medicine, colobines
An international team of scientists, led by researchers at University of California, San Diego School of Medicine and the J. Craig Venter Institute (JCVI), have created the first comprehensive, cross-species genomic comparison of all 20 known species of Leptospira, a bacterial genus that can cause disease and death in livestock and other domesticated mammals, wildlife and humans.
He recently moved back to academia as an associate professor in the departments of Neuroscience and Human Genetics & Genomic Sciences at the Icahn School of Medicine at Mount Sinai in New York, where he continues his basic research and translational efforts in AD using a state - of - the - art experimental and computational toolkit, in collaboration with Drs. Alison Goate and Anne Schaefer within the Ronald M. Loeb Center for Alzheimer's Disease.
It should be noted that the 7th Pan Arab Human Genetics Conference will be held from 18 to 20 January 2018 at Conrad hotel in Dubai, and will discuss the Omics Era through 4 main topics: precision medicine, big data in human genetics, genomics of multifactorial disorders, and the current trend in human genetics scieHuman Genetics Conference will be held from 18 to 20 January 2018 at Conrad hotel in Dubai, and will discuss the Omics Era through 4 main topics: precision medicine, big data in human genetics, genomics of multifactorial disorders, and the current trend in human genetics sciehuman genetics, genomics of multifactorial disorders, and the current trend in human genetics sciehuman genetics sciences.
Participating institutions: Helmholtz Association • CNRS • Institute of Molecular Biotechnology • Research Center for Molecular Medicine of the Austrian Academy of Sciences • VIB - KU Leuven • Friedrich Miescher Institute for Biomedical Research • University of Basel • University of Zurich • Central European Institute of Technology • Max Planck Institute of Immunobiology and Epigenetics • Max Planck Institute for Molecular Genetics • German Cancer Research Center • Max Delbrück Center for Molecular Medicine • German Center for Neurodegenerative Diseases • Helmholtz Zentrum München • Max Planck Institute for Evolutionary Anthropology • Helmholtz Institute of RNA - based Infection Research • Saarland University • Technical University Munich • University of Würzburg • Biotech Research & Innovation Centre • Interdisciplinary Nanoscience Center • University of Copenhagen • Centre for Genomic Regulation • Institut Curie • Université de Montpellier • Inserm • Université Toulouse III — Paul Sabatier • École nationale supérieure des mines de Paris • Institute for Molecular Medicine Finland • The Biomedical Research Foundation, Academy of Athens • Weizmann Institute of Science • Hebrew University • Sapienza — University of Rome • Instituto Nazionale Genetica Molecolare • University of Napoli • University of Padua • University of Milan • European Institute of Oncology • Netherlands Cancer Institute • Radboud University • University Medical Center Utrecht • Hubrecht Institute • Instituto Gulbenkian de Ciência • Institute of Bioorganic Chemistry of the Polish Academy of Sciences • Romanian Center for Systems Immunology • Karolinska Institute • MRC Human Genetics Unit • University of Edinburgh • Wellcome Sanger Institute • The Babraham Institute • European Molecular Biology Laboratory — European Bioinformatics Institute
And now, Charis Eng, MD, PhD, the Director of our Genomic Medicine Institute, has been named to the U.S. Department of Health and Human Services Secretary's Advisory Committee on Genetics, Health and Society.
«This is the most comprehensive effort to do a genomic comparison between humans and mice at this level, including the regulatory elements and gene expression,» said Feng Yue, an assistant professor in the department of biochemistry and molecular biology at Penn State College of Medicine.
Improving human health by enabling safer, more effective cell and gene medicines through proprietary genomics, bioinformatics and intelligent data driven design
Teri Manolio, Director, Division of Genomic Medicine, National Human Genome Research Institute, USA
Aug 8, 2008 Two New Predisposition Genes For Breast, Thyroid And Kidney Cancers Could Lead to More Accurate Diagnosis and Earlier Detection of These Cancers Charis Eng, MD, PhD, Sondra J and Stephen R Hardis Endowed Chair of Cancer Genomic Medicine and Chair, GMI, and her team published in the Aug 8, 2008 issue of the American Journal of Human Genetics that germline mutations in SDHB and SDHD, which play key roles in the mitochondria (the cell's power houses), predispose to Cowden and Cowden - like syndromes.
Moderator: Teri Manolio, Director, Division of Genomic Medicine, National Human Genome Research Institute (USA)
Shimul Chowdhury, director of the clinical laboratory at the Rady Children's Institute for Genomic Medicine, presented data today (October 19) on six case studies of NICU infants at the annual meeting of the American Society of Human Genetics in Orlando.
The Genomic Medicine Institute (GMI) and the Center for Clinical Genomics are excited to announce a broad research collaboration with Human Longevity Inc., (HLI), Dr. J. Craig Venter's company in San Diego, CA.
Interface of Genomics Research and Genomic Medicine Recent advances in DNA sequencing technologies mean that it is now possible to conduct genomic analyses, including analysis of the entire genome of an individual human, that just a few years ago would have been too costly anGenomic Medicine Recent advances in DNA sequencing technologies mean that it is now possible to conduct genomic analyses, including analysis of the entire genome of an individual human, that just a few years ago would have been too costly angenomic analyses, including analysis of the entire genome of an individual human, that just a few years ago would have been too costly and slow.
This data sharing deepens our understanding of variability in the human genome and the genetic underpinnings of disease, leading to advances in genomics research and genomic medicine.
09:00 09:30 Teri Manolio, Director, Division of Genomic Medicine National Human Genome Research Institute, Baltimore, MA, USA
Jane E. Koehler, M.D. University of California - San Francisco School of Medicine Genomic and clinical correlates of human Bartonella quintana infection
The Co-Chairs for the 2018 AGBT General Meeting are: Eric Green (National Human Genome Research Institute / National Institute of Health) Elaine Mardis (The Institute for Genomic Medicine at Nationwide Children's Hospital) and Len Pennacchio (Lawrence Berkeley National Laboratory).
Our news coverage focuses on stories about genomics and human medicine, as well as the ways in which scientists are using genomics to find biological solutions to energy needs and environmental problems.
· Landmark study creates «user's guide» to the human genome; will aid in finalizing the assembly of the genome and in applying genomics to create better medicine.
The goal of her research is to realize the full potential of genomics to infer human history and evolution and to inform better models for clinical medicine.
In 2013 she formed Biome Healthcare with J. Craig Venter which was later acquired by «Human Longevity Inc.» a company dedicated to link genomic and clinical data with the goal of facilitating personalized medicine.
Tags: AACR 2017, aacr 2018, Breast Cancer, Christopher J Kemp, Clinical Research, Colorectal Cancer, Eddie Mendez, genomics, head neck cancers, Human Biology, Ovarian Cancer, Pancreatic Cancer, precision medicine, Public Health Sciences, solid tumors, uterine cancer, Vijayakrishna Gadi
«The new studies complement the current GTEx project in assessing genomic variation and gene expression,» explained Simona Volpi, Pharm.D., Ph.D., GTEx program director in the Division of Genomic Medicine at the National Human Genome Research Institute (NHGRI), which helps administer the pgenomic variation and gene expression,» explained Simona Volpi, Pharm.D., Ph.D., GTEx program director in the Division of Genomic Medicine at the National Human Genome Research Institute (NHGRI), which helps administer the pGenomic Medicine at the National Human Genome Research Institute (NHGRI), which helps administer the program.
The Genomic Medicine Institute is committed to performing translational and clinical human genetics and genomics investigation.
This centre has been devised as a space for excellence research in genomic medicine, focussing on the comprehensive study and understanding of the genetic basis of human diseases in general, placing special emphasis on cancer and its genetic disorders related to inheritance.
His research interests focus on the structural variations in the human genomes, medical genetics and genomics, pathogenesis of human diseases, molecular diagnosis and precision medicine.
Tags: cancer genomics, Carla Grandori, Christopher J Kemp, Clinical Research, Eddie Mendez, Good News, head neck cancers, Human Biology, Jerald P Radich, personalized treatment, precision medicine, Tumor specific translational research, Vijayakrishna Gadi
From our earliest research that established cancer as a genetic disease to today's work in precision medicine, our unswerving focus on genetics and genomics continues to generate advances that improve human health.
In 2013, together with colleagues, she founded the company «Human Longevity Inc.», which links genomic and clinical data to further the goal of personalized medicine.
In an unprecedented partnership with the Massachusetts Institute of Technology, Harvard University and its affiliated hospitals and the Whitehead Institute for Biomedical Research, the Broads committed $ 700 million to fund The Broad Institute, the world's leading genomic medicine research institute that is focused on using the power of genomics to understand human disease.
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