<scp>NeuroBooster</scp> Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

From a broader perspective, the NBA serves as a promising means to foster collaborative research endeavors in the field of neurological disorders worldwide. Ultimately, this carefully designed tool is poised to make a substantial contribution to uncovering the genetic etiology underlying these debilitating conditions. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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Institutions

Publication Details

Journal
Movement Disorders
Published
2024-09-16
DOI
https://doi.org/10.1002/mds.29902
Citations
35
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
19.26

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article

NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

Kimberley J. Billingsley, Katja Lohmann, Derek P. Narendra, Armando Reyes‐Palomares et al.
35 citations
Movement Disorders
Genomics and Rare Diseases
19.26
article

NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

Kimberley J. Billingsley, Katja Lohmann, Derek P. Narendra, Armando Reyes‐Palomares, Steven Lubbe, Kristin Levine, John Hardy, Christine Klein, Peter Wild Crea, Hampton L. Leonard, Paula Saffie Awad, Bryan J. Traynor, Edwin Jabbari, Sara Bandrés‐Ciga, Mathew J. Koretsky, Mary B. Makarious, Sonja W. Scholz, Sonya B. Dumanis, Faraz Faghri, John P. Quinn, Ekemini Riley, Claudia Schulte, Elisa Majounie, Cornelis Blauwendraat, Huw R. Morris, Henry Houlden, Dan Vitale, Hirotaka Iwaki, Andrew B. Singleton, Dena Hernández, Janina M. Jeff, Sampath Arepalli, Mike A. Nalls, Jeffrey Kim
article en
35 citations

Abstract

From a broader perspective, the NBA serves as a promising means to foster collaborative research endeavors in the field of neurological disorders worldwide. Ultimately, this carefully designed tool is poised to make a substantial contribution to uncovering the genetic etiology underlying these debilitating conditions. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

Movement DisordersVol. 39(11)
Northwestern University (US), National Institutes of Health (US), Universidade Federal do Rio Grande do Sul (BR), Johns Hopkins University (US), University of Liverpool (GB), Illumina (United States) (US), King's College London (GB), German Center for Neurodegenerative Diseases (DE), University Medical Center (US), Data Tecnica International (United States) (US), National Institute of Neurological Disorders and Stroke (US), National Institute on Aging (US), Clinica Santa Maria (CL), Hertie Institute for Clinical Brain Research (DE), National Hospital for Neurology and Neurosurgery (GB), Research Network (United States) (US), University College London (GB), Universidad de Málaga (ES), University of Lübeck (DE)
U.S. Department of Health and Human Services, Michael J. Fox Foundation for Parkinson's Research, Demensförbundet, Multiple System Atrophy Coalition, Parkinson's UK, National Institutes of Health, Medical Research Council, National Institute on Aging, National Human Genome Research Institute, National Institute of Neurological Disorders and Stroke
Partnerships for the goals
Openalex Percentile: Top 0%
Genomics and Rare Diseases
19.26
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