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Pregnancy Hypertension|November 18, 2023
The significance of mitochondrial haplogroups in preeclampsia riskKristina Wendelboe Olsen, Paula L Hedley, Christian M Hagen, et al.
Human Molecular Genetics|October 5, 2013
The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potentialPaul M Smith, Joanna L Elson, Laura C Greaves, et al.
Plos One|January 10, 2013
Physically-induced cytoskeleton remodeling of cells in three-dimensional cultureSheng-Lin Lee, Ali Nekouzadeh, Boyd Butler, et al.
Archives of Neurology|March 14, 2012
Relationship between mitochondria and α-synuclein: a study of single substantia nigra neuronsAmy K Reeve, Tae-Kyung Park, Evelyn Jaros, et al.
BMC Medical Genetics|March 18, 2017
Clinically proven mtDNA mutations are not common in those with chronic fatigue syndromeElizna M Schoeman, Francois H Van Der Westhuizen, Elardus Erasmus, et al.
Nature Neuroscience|January 10, 2019
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Carcinogenesis|April 8, 2020
Mitochondrial DNA mutations induce mitochondrial biogenesis and increase the tumorigenic potential of Hodgkin and Reed-Sternberg cellsSophie Haumann, Julia Boix, Jana Knuever, et al.
Nature Neuroscience|May 13, 2018
Publisher Correction: Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Nature Neuroscience|December 13, 2017
Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestrySandra Sanchez-Roige, Pierre Fontanillas, Sarah L Elson, et al.
Breast Cancer Research and Treatment|July 27, 2013
The Athena Breast Health Network: developing a rapid learning system in breast cancer prevention, screening, treatment, and careSarah L Elson, Robert A Hiatt, Hoda Anton-Culver, et al.
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