Re-analysis of Genetic Risks for Chronic Fatigue Syndrome From 23andMe Data Finds Few Remain
Main Authors: | Felice L. Bedford, Bastian Greshake Tzovaras |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-03-01
|
Series: | Frontiers in Pediatrics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fped.2021.590040/full |
Similar Items
-
Transparency, consent and trust in the use of customers' data by an online genetic testing company: an Exploratory survey among 23andMe users
by: Aviad E. Raz, et al.
Published: (2020-10-01) -
Medically Documenting Disability in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Cases
by: Barbara B. Comerford, et al.
Published: (2019-07-01) -
Why the Psychosomatic View on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Is Inconsistent with Current Evidence and Harmful to Patients
by: Manuel Thoma, et al.
Published: (2023-12-01) -
Evaluation of a Webinar to Increase Health Professionals’ Knowledge about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
by: Laura Froehlich, et al.
Published: (2023-08-01) -
Editorial: Advances in ME/CFS Research and Clinical Care
by: Kenneth J. Friedman, et al.
Published: (2019-09-01)