% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{BandresCiga:272954,
author = {Bandres-Ciga, Sara and Faghri, Faraz and Majounie, Elisa
and Koretsky, Mathew J and Kim, Jeffrey and Levine, Kristin
S and Leonard, Hampton and Makarious, Mary B and Iwaki,
Hirotaka and Crea, Peter Wild and Hernandez, Dena G and
Arepalli, Sampath and Billingsley, Kimberley and Lohmann,
Katja and Klein, Christine and Lubbe, Steven J and Jabbari,
Edwin and Saffie-Awad, Paula and Narendra, Derek and
Reyes-Palomares, Armando and Quinn, John P and Schulte,
Claudia and Morris, Huw R and Traynor, Bryan J and Scholz,
Sonja W and Houlden, Henry and Hardy, John and Dumanis,
Sonya and Riley, Ekemini and Blauwendraat, Cornelis and
Singleton, Andrew and Nalls, Mike and Jeff, Janina and
Vitale, Dan},
collaboration = {Dementias, Related},
othercontributors = {Alzheimer's, Global Parkinson's Genetics Program and the
Center for},
title = {{N}euro{B}ooster {A}rray: {A} {G}enome-{W}ide {G}enotyping
{P}latform to {S}tudy {N}eurological {D}isorders {A}cross
{D}iverse {P}opulations.},
journal = {Movement disorders},
volume = {39},
number = {11},
issn = {0885-3185},
address = {New York, NY},
publisher = {Wiley},
reportid = {DZNE-2024-01333},
pages = {2039 - 2048},
year = {2024},
abstract = {Commercial genome-wide genotyping arrays have historically
neglected coverage of genetic variation across
populations.We aimed to create a multi-ancestry genome-wide
array that would include a wide range of neuro-specific
genetic content to facilitate genetic research in
neurological disorders across multiple ancestral groups,
fostering diversity and inclusivity in research studies.We
developed the Illumina NeuroBooster Array (NBA), a custom
high-throughput and cost-effective platform on a backbone of
1,914,934 variants from the Infinium Global Diversity Array
and added custom content comprising 95,273 variants
associated with more than 70 neurological conditions or
traits, and we further tested its performance on more than
2000 patient samples. This novel platform includes
approximately 10,000 tagging variants to facilitate
imputation and analyses of neurodegenerative disease-related
genome-wide association study loci across diverse
populations.In this article, we describe NBA's potential as
an efficient means for researchers to assess known and novel
disease genetic associations in a multi-ancestry framework.
The NBA can identify rare genetic variants and accurately
impute more than 15 million common variants across
populations. Apart from enabling sample prioritization for
further whole-genome sequencing studies, we envisage that
NBA will play a pivotal role in recruitment for
interventional studies in the precision medicine space.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.},
keywords = {Humans / Genome-Wide Association Study: methods / Nervous
System Diseases: genetics / Genotype / Genetic Variation:
genetics / Genotyping Techniques: methods / Polymorphism,
Single Nucleotide: genetics / Genetic Predisposition to
Disease: genetics / Centre for Alzheimer's and Related
Dementias (Other) / Global Parkinson's Genetics Program
(Other) / NeuroBooster array (Other) / diversity (Other) /
genetic screening (Other) / genotyping (Other) /
neurological diseases (Other)},
cin = {AG Gasser},
ddc = {610},
cid = {I:(DE-2719)1210000},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39283294},
pmc = {pmc:PMC11568947},
doi = {10.1002/mds.29902},
url = {https://pub.dzne.de/record/272954},
}