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Inhoud geleverd door BlogTalkRadio.com and In Short Order. Alle podcastinhoud, inclusief afleveringen, afbeeldingen en podcastbeschrijvingen, wordt rechtstreeks geüpload en geleverd door BlogTalkRadio.com and In Short Order of hun podcastplatformpartner. Als u denkt dat iemand uw auteursrechtelijk beschermde werk zonder uw toestemming gebruikt, kunt u het hier beschreven proces https://nl.player.fm/legal volgen.
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In Short Order -- Dr. Mansoor S. Mohammed, BSc (Hons Mol Gen), PhD

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Manage episode 313453006 series 3271372
Inhoud geleverd door BlogTalkRadio.com and In Short Order. Alle podcastinhoud, inclusief afleveringen, afbeeldingen en podcastbeschrijvingen, wordt rechtstreeks geüpload en geleverd door BlogTalkRadio.com and In Short Order of hun podcastplatformpartner. Als u denkt dat iemand uw auteursrechtelijk beschermde werk zonder uw toestemming gebruikt, kunt u het hier beschreven proces https://nl.player.fm/legal volgen.
Dr. Mansoor S. Mohammed is a recognized authority in the fields of medical genomics and personalized medicine.Prior to cofounding Younique Genomics, Dr. Mohammed served as the President and CEO of CombiMatrix Diagnostics where he oversaw the development of one of the most comprehensive genomics testing menus in the diagnostic industry. Prior to his tenure at CombiMatrix Diagnostics, Dr. Mohammed was the Director of Advanced Technologies at Quest Diagnostics, North America's largest reference laboratory. At Quest Diagnostics, he was honored with the Medical Innovation Award, the highest accolade given for excellence in medical research. Prior to his role at Quest Diagnostics, Dr. Mohammed was a co-founder and Director of Research and Development at Spectral Genomics. Dr. Mohammed pioneered the development of commercial Comparative Genomic Hybridization (CGH) array technologies and was responsible for the design and launch of the industry's first commercially available CGH arrays. He was the co-primary author of the first peer-reviewed study utilizing CGH arrays in the clinical diagnosis of developmental abnormalities (2002) and later (2008) was the senior author of the first peer-reviewed study utilizing CGH arrays for clinical oncology purposes. Moreover, the CGH array technologies Dr. Mohammed helped to innovate became the basis for the discovery of genome copy number variations (CNVs). The latter has fundamentally altered and improved the way the human genome is viewed and interpreted, and has spawned thousands of studies and publications worldwide. Most recently, Dr. Mohammed has worked with leading medical practitioners to become one of the first in the world to incorporate genome CNV analyses into a comprehensive approach to personalized medicine. http://youniquegenomics.com/
  continue reading

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Artwork
iconDelen
 
Manage episode 313453006 series 3271372
Inhoud geleverd door BlogTalkRadio.com and In Short Order. Alle podcastinhoud, inclusief afleveringen, afbeeldingen en podcastbeschrijvingen, wordt rechtstreeks geüpload en geleverd door BlogTalkRadio.com and In Short Order of hun podcastplatformpartner. Als u denkt dat iemand uw auteursrechtelijk beschermde werk zonder uw toestemming gebruikt, kunt u het hier beschreven proces https://nl.player.fm/legal volgen.
Dr. Mansoor S. Mohammed is a recognized authority in the fields of medical genomics and personalized medicine.Prior to cofounding Younique Genomics, Dr. Mohammed served as the President and CEO of CombiMatrix Diagnostics where he oversaw the development of one of the most comprehensive genomics testing menus in the diagnostic industry. Prior to his tenure at CombiMatrix Diagnostics, Dr. Mohammed was the Director of Advanced Technologies at Quest Diagnostics, North America's largest reference laboratory. At Quest Diagnostics, he was honored with the Medical Innovation Award, the highest accolade given for excellence in medical research. Prior to his role at Quest Diagnostics, Dr. Mohammed was a co-founder and Director of Research and Development at Spectral Genomics. Dr. Mohammed pioneered the development of commercial Comparative Genomic Hybridization (CGH) array technologies and was responsible for the design and launch of the industry's first commercially available CGH arrays. He was the co-primary author of the first peer-reviewed study utilizing CGH arrays in the clinical diagnosis of developmental abnormalities (2002) and later (2008) was the senior author of the first peer-reviewed study utilizing CGH arrays for clinical oncology purposes. Moreover, the CGH array technologies Dr. Mohammed helped to innovate became the basis for the discovery of genome copy number variations (CNVs). The latter has fundamentally altered and improved the way the human genome is viewed and interpreted, and has spawned thousands of studies and publications worldwide. Most recently, Dr. Mohammed has worked with leading medical practitioners to become one of the first in the world to incorporate genome CNV analyses into a comprehensive approach to personalized medicine. http://youniquegenomics.com/
  continue reading

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