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European Journal of Neurology|March 10, 2025
Genetic Etiology Influences the Low-Frequency Components of Globus Pallidus Internus Electrophysiology in DystoniaAhmet Kaymak, Luigi M Romito, Fabiana Colucci, et al.
Health Policy (Amsterdam, Netherlands)|August 23, 2023
Challenges facing mental health systems arising from the COVID-19 pandemic: Evidence from 14 European and North American countriesJanet R Cummings, Xinyue Zhang, Coralie Gandré, et al.
Biology Letters|July 25, 2019
Long-term fire resilience of the Ericaceous Belt, Bale Mountains, EthiopiaGraciela Gil-Romera, Carole Adolf, Blas M Benito, et al.
Medrxiv : the Preprint Server for Health Sciences|September 25, 2023
Clinical actionability of genetic findings in cerebral palsySara A Lewis, Maya Chopra, Julie S Cohen, et al.
JAMA Pediatrics|December 2, 2024
Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-AnalysisSara A Lewis, Maya Chopra, Julie S Cohen, et al.
Nature Genetics|June 13, 2017
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traitsAnke R Hammerschlag, Sven Stringer, Christiaan A de Leeuw, et al.
Sleep|June 7, 2022
The genetic etiology of periodic limb movement in sleepJacob L Edelson, Logan D Schneider, David Amar, et al.
BMC Oral Health|March 9, 2022
Exploring variation of coverage and access to dental care for adults in 11 European countries: a vignette approachJuliane Winkelmann, Jesús Gómez Rossi, Falk Schwendicke, et al.
American Journal of Human Genetics|October 11, 2011
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulationMonika B Hartig, Arcangela Iuso, Tobias Haack, et al.
Cells|April 13, 2023
Loss-of-Function Variants in DRD1 in Infantile Parkinsonism-DystoniaKimberley M Reid, Dora Steel, Sanjana Nair, et al.
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