Ronald Davis
Ronald Wayne Davis, PhD., is a Professor of Biochemistry & Genetics and the Director of the Stanford Genome Technology Center at Stanford University. In 1983, he was bestowed the honor of being elected a member of the National Academy of Sciences.[1]
His son, Whitney Dafoe, is severely ill with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Professor Davis leads the End ME/CFS Project with the Open Medicine Foundation whose first project was the ME/CFS Severely Ill, Big Data Study.[2]
Committees and boards[edit | edit source]
Open Medicine Foundation[edit | edit source]
Director of the Scientific Advisory Board at Open Medicine Foundation, which is committed to research for ME/CFS and related chronic complex diseases.[3]
Institute of Medicine report[edit | edit source]
Dr. Davis was one of the experts on the "Committee on the Diagnostic Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome" that was convened as per US government request for the 2015 Institute of Medicine.[4] The Institute of Medicine has since changed its name to the National Academy of Medicine.[5]
ME/CFS Common Data Element (CDE) Project[edit | edit source]
Member of the Biomarkers Working Group of the Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Common Data Element (CDE) Project sponsored by the National Institute of Neurological Disorders and Stroke and the Centers for Disease Control and Prevention.[6]
Advocacy[edit | edit source]
Open Letters[edit | edit source]
- 2016 and 2018, Dr. Davis was one of the signatories of the Open letter to the Lancet urging its editor to commission a fully independent review of the PACE trial as published in its journal.[7][8][9]
- 2017, Dr. Davis was one of the signatories of An open letter to Psychological Medicine about “recovery” and the PACE trial[10]
Millions Missing protest[edit | edit source]
Dr. Ron Davis and his wife, Dr. Janet Dafoe, protested with #MillionsMissing at the San Francisco satellite protest on May 25, 2016.[11] Dr. Davis gave a speech about the challenges ME patients face, and his hopes for the future of ME research.[12]
ME/CFS research[edit | edit source]
- March 2016, it was announced that the ME/CFS Severely Ill, Big Data Study had a significant result in the area of mitochondria. This lead to the addition of Dr. Robert Naviaux (a mitochondrial expert) to the research team.[13]
- February 2017, Dr. Davis explained in a video that the development of new nanofabricated technology allows rapid drug screening via measurement of electrical impedance. This technology may be able to determine which medications could be most effective in treating myalgic encephalomyelitis/chronic fatigue syndrome. Experimentation is also being carried out to test if this same nanofabricated technology could be used in developing a simple diagnostic test for myalgic encephalomyelitis/chronic fatigue syndrome.[14]
- June 2018, Dr. Davis and the Stanford Genome Center received a grant award for the research study 'Molecular and Single-cell Immunology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome' "to investigate the immunological basis of ME/CFS using cutting-edge technologies to understand the role of infection and autoimmunity in the behavior of single immune cells from patients – offering precise insights into how this complex illness originates and persists that may lead to new strategies for treatment."[15] This is a five-year study that will receive $745,000 a year.[16]
- Nov 2018, Erythrocyte Deformability As a Potential Biomarker for Chronic Fatigue Syndrome[17]
- Feb 2019, Red blood cell deformability is diminished in patients with Chronic Fatigue Syndrome[18] - (Full text)
- Apr 2019, A nanoelectronics-blood-based diagnostic biomarker for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)[19] - (Full text)
Talks and interviews[edit | edit source]
2016
- 21 May 2016, Short Story of a Family's Struggle with ME/CFS[20]
- 3 Jun 2016, Speaker at the 11th Invest in ME International ME Conference - Big Data Approach: Severely Ill ME Patient Cohort DVD available
- Dr. Davis's interview at the San Francisco #MillionsMissing protest
- 13 Dec 2016, Getting Answers to ME/CFS Faster through Collaboration and Openness[21]
2017
- 3 Feb 2017, Scientist Ron Davis Tells How We Are "Fast-Tracking" ME/CFS Research[22]
- 20 Feb 2017, Chronic Fatigue: Missing Millions (Carte Blanche DSTV)
- 21 Feb 2017, "An Update on ME/CFS Research with Dr. Ronald W. Davis"
- 7 Mar 2017, Q&A on ME/CFS Research with Dr. Ron Davis[23]
- Jun, Ron Davis is optimistic at the 2017 Invest in ME Research Conference[24]
- 2 Jun 2017, Speaker at the 12th Invest in ME International ME Conference on "Big Data Approach: Severely ill ME Patient Cohort"[25] DVD available
- 15 Jun 2017, "The Last Major Disease To Be Studied? Ron Davis of Stanford Thinks So"
- 12 Aug 2017, Community Symposium on the Molecular Basis of ME/CFS - 2017: Speech title - Establishing new mechanistic and diagnostic paradigms for ME/CFS[26]
2018
- 3-5 May 2018, ME/CFS Canadian Collaborative Team Conference - Speech titles: The Future of ME/CFS Research in the Multiomic and Big Data Era and An Integrative, Molecular, Data and Technology-Driven Approach to ME/CFS[27]
- 3 Jun 2018, Speaker at the 13th Invest in ME Conference 2018; Speech title: Establishing new mechanistic and diagnostic paradigms for ME/CFS[28] - (Video)
- Sep 2018, Dr. Ron Davis Presents ME/CFS Research at the 2018 IIMEC Conference[29] Patients' gene expression profiles most closely resembles Trypanosome infection (African sleeping sickness) variant suspected.
- 29 Sep 2018, Biomarkers, given at Second Annual Community Symposium on the Molecular Basis of ME/CFS, sponsored by Open Medicine Foundation - (Video)
2019
- 14 Mar 2019, Establishing New Mechanistic & Diagnostic Paradigms for ME/CFS given at the International Research Symposium, Geelong, Australia, sponsored by Emerge Australia
- 29 Apr 2019, What does the nanoneedle research mean for ME/CFS patients?
- 31 May 2019, Speaker at the 14th Invest in ME International ME Conference; Speech title: Establishing new mechanistic and diagnostic paradigms for ME/CFS - (Video)
- 8 June 2019, Stanford Experiences with ME/CFS: Update on Stanford activities, given at the Inaugural Harvard ME/CFS Collaboration Symposium sponsored by Open Medicine Foundation
Book[edit | edit source]
- 2021, The Puzzle Solver: A Scientist's Desperate Quest to Cure the Illness that Stole his Son By Tracie White with Ronald W. Davis[30]
Online presence[edit | edit source]
See also[edit | edit source]
Learn more[edit | edit source]
- Wikipedia - Ronald Davis
- 2016, Happy 75th Birthday to Scientist Ronald W. Davis, PhD[31]
- 2016, Tackling chronic fatigue syndrome[32]
- 2016, The puzzle solver: A researcher changes course to help his son[33]
References[edit | edit source]
- ↑ http://www.nasonline.org, National Academy of Sciences -. "Ronald Davis". www.nasonline.org. Retrieved August 16, 2018.
- ↑ "End ME/CFS Project | Open Medicine Foundation". Open Medicine Foundation. Retrieved August 16, 2018.
- ↑ "Scientific Advisory Board | Open Medicine Foundation". Open Medicine Foundation. Retrieved August 16, 2018.
- ↑ Syndrome, Committee on the Diagnostic Criteria for Myalgic Encephalomyelitis/Chronic Fatigue; Populations, Board on the Health of Select; Medicine, Institute of (February 10, 2015). Biographical Sketches of Committee Members, Consultants, and Staff. National Academies Press (US).
- ↑ "Home - National Academy of Medicine". National Academy of Medicine. Retrieved August 16, 2018.
- ↑ "Complete Myalgic Encephalomyelitis/Chronic Fatigue Syndrome CDE Roster". NIH. Retrieved October 11, 2019. Cite has empty unknown parameter:
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(help) - ↑ "An open letter to Dr. Richard Horton and The Lancet". www.virology.ws. Retrieved August 18, 2018.
- ↑ "An open letter to The Lancet, again". www.virology.ws. Retrieved August 18, 2018.
- ↑ "Trial By Error: An Open Letter to The Lancet, Two Years On". www.virology.ws. Retrieved August 18, 2018.
- ↑ "An open letter to Psychological Medicine about "recovery" and the PACE trial". www.virology.ws. Retrieved August 18, 2018.
- ↑ "#MillionsMissing - #MillionsMissing". millionsmissing.meaction.net. Retrieved August 16, 2018.
- ↑ "Speeches from the Front Lines of #MillionsMissing: Ron Davis | #MEAction". www.meaction.net. Retrieved August 16, 2018.
- ↑ "End ME/CFS Severe Patient Study Turns to the Mitochondria". Health Rising's Chronic Fatigue Syndrome (ME/CFS) and Fibromyalgia Forums. Retrieved September 12, 2019.
- ↑ An Update on ME/CFS Research with Dr. Ronald W. Davis, retrieved September 12, 2019
- ↑ Molecular and Single-cell Immunology of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome - NIH RePORT Project Number 1R01AI139550-01
- ↑ HealthRising: Ron Davis (Finally) Gets His Big Grant! by Cort Johnson via Open Medicine Foundation
- ↑ Saha, Amit K; Schmidt, Brendan R; Wilhelmy, Julie; Nguyen, Vy; Do, Justin; Suja, Vineeth C; Nemat-Gorgani, Mohsen; Ramasubramanian, Anand K; Davis, Ronald W (November 2018). "Erythrocyte Deformability As a Potential Biomarker for Chronic Fatigue Syndrome". Blood (132): 4874. doi:10.1182/blood-2018-99-117260.
- ↑ Saha, Amit K.; Schmidt, Brendan R.; Wilhelmy, Julie; Nguyen, Vy; Abugherir, Abed; Do, Justin K.; Nemat-Gorgani, Mohsen; Davis, Ronald W.; Ramasubramanian, Anand K. (February 23, 2019). "Red blood cell deformability is diminished in patients with Chronic Fatigue Syndrome". Clinical Hemorheology and Microcirculation. 71 (1): 113–116. doi:10.3233/CH-180469.
- ↑ Esfandyarpour, R.; Kashi, A.; Nemat-Gorgani, M.; Wilhelmy, J.; Davis, R. W. (May 21, 2019). "A nanoelectronics-blood-based diagnostic biomarker for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)". Proceedings of the National Academy of Sciences. 116 (21): 10250–10257. doi:10.1073/pnas.1901274116. ISSN 0027-8424.
- ↑ Davis Family (May 21, 2016). "Short Story of a Family's Struggle with ME/CFS". YouTube. Cite has empty unknown parameter:
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(help) - ↑ Davis, Ronald; Tannenbaum, Linda (December 13, 2016). "Getting Answers to ME/CFS Faster through Collaboration and Openness". YouTube. Open Medicine Foundation - OMF. Cite has empty unknown parameter:
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(help) - ↑ Davis, Ronald (February 3, 2017). "Scientist Ron Davis Tells How We Are "Fast-Tracking" ME/CFS Research". YouTube. Open Medicine Foundation - OMF. Cite has empty unknown parameter:
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(help) - ↑ Davis, Ronald (March 7, 2017). "Q&A on ME/CFS Research with Dr. Ron Davis". YouTube. Open Medicine Foundation - OMF. Cite has empty unknown parameter:
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(help) - ↑ Davis, Ronald (June 20, 2017). "Ron Davis is optimistic at the 2017 Invest in ME Research Conference". YouTube. Open Medicine Foundation - OMF. Cite has empty unknown parameter:
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(help) - ↑ "Invest in ME Research - International ME Conferences and Colloquiums Home Page". investinme.org. Retrieved September 12, 2019.
- ↑ Davis, Ronald (September 28, 2017). "Ronald Davis, PhD, Speaking on ME/CFS Research Approach". YouTube. Open Medicine Foundation - OMF. Cite has empty unknown parameter:
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(help) - ↑ "ME/CFS Canadian Collaborative Team Conference program" (PDF). Retrieved March 6, 2019. Cite has empty unknown parameter:
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(help) - ↑ "Invest in ME Research - IIMEC13 International ME Conference 2018". www.investinme.org. Retrieved February 26, 2020.
- ↑ Davis, Ronald (September 17, 2018). "Dr. Ron Davis Presents ME/CFS Research at the 2018 IIMEC Conference". YouTube. Open Medicine Foundation - OMF. Cite has empty unknown parameter:
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(help) - ↑ White, Tracie; Davis, Ronald W. (May 5, 2020). The Puzzle Solver: A Scientist's Desperate Quest to Cure the Illness that Stole His Son (1st ed.). New York: Hachette Books. ISBN 9781549177545.
- ↑ Davis, Ronald (July 12, 2016). "Happy 75th Birthday to Scientist Ronald W. Davis, PhD". YouTube. Open Medicine Foundation - OMF. Cite has empty unknown parameter:
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(help) - ↑ Gu, Katie (January 4, 2016). "Tackling Chronic Fatigue Syndrome". The Stanford Daily. Retrieved September 17, 2018. Cite has empty unknown parameter:
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(help) - ↑ White, Tracie. "The puzzle solver". Stanford Medicine. Retrieved September 17, 2018. Cite has empty unknown parameter:
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