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Simon Lovestone

Simon Lovestone

Verified

Editorial Board Member, International Journal of Geriatric Psychiatry

Oxford

Final Covers

Health environment technology and science policy

Doesn’t Cover

Adult items.

Journalist Type

-

Seniority Positions

Medium Formats

Content

Total articles 9

  • Association of blood-based transcriptional risk scores with biomarkers for Alzheimer disease

    By Angela Hodges, Andrew Simmons Verified, Simon Lovestone, Michael Weiner| Neurology Verified AbstractObjective To determine whether transcriptional risk scores (TRSs), a summation of polarized expression levels of functional genes, reflect the risk of Alzheimer disease (AD). Methods Blood transcriptome data were from Caucasian participants, which included AD, mild cognitive impairment, and cognitively normal controls (CN) in the Alzheimer's Disease Neuroimaging Initiative (ADNI, n = 661) and AddNeuroMed (n = 674) cohorts.

    By Angela Hodges, Andrew Simmons Verified, Simon Lovestone, Michael Weiner · Neurology

    Oct. 04, 2020

  • Publisher Correction: Pattern of Altered Plasma Elemental Phosphorus, Calcium, Zinc, and Iron in Alzheimer’s Disease

    By Magda Tsolaki, Bruno Vellas, Simon Lovestone, Hilkka Soinine| Nature Verified Correction to: Scientific Reports https://doi.org/10.1038/s41598-018-37431-8, published online 28 February 2019The original version of this Article contained an error in the title of the paper, where “Pattern of Altered Plasma Elemental Phosphorus, Calcium, Zinc, and Iron in Alzheimer’s Disease” was incorrectly given as “Pattern of Altered Plasma Elemental Phosphorus, Calcium, Selenium, Iron and Copper in Alzheimer’s Disease”.

    By Magda Tsolaki, Bruno Vellas, Simon Lovestone, Hilkka Soinine · Nature

    Apr. 16, 2019

  • Association of blood-based transcriptional risk scores with biomarkers for Alzheimer disease

    By Angela Hodges, Andrew Simmons Verified, Simon Lovestone, Michael Weiner| Neurology Verified AbstractObjective To determine whether transcriptional risk scores (TRSs), a summation of polarized expression levels of functional genes, reflect the risk of Alzheimer disease (AD). Methods Blood transcriptome data were from Caucasian participants, which included AD, mild cognitive impairment, and cognitively normal controls (CN) in the Alzheimer's Disease Neuroimaging Initiative (ADNI, n = 661) and AddNeuroMed (n = 674) cohorts.

    By Angela Hodges, Andrew Simmons Verified, Simon Lovestone, Michael Weiner · Neurology

    Oct. 04, 2020

As seen in

Company Info

International Journal of Geriatric Psychiatry

Oxford, England, United Kingdom

+44 1865 277227