Evidence map›Paper›PMID 37469269›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2023

X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.

Thiago P Leal, Shilpa C Rao, Jennifer N French-Kwawu, Mateus H Gouveia, Victor Borda, Sara Bandres-Ciga, Miguel Inca-Martinez, Emily A Mason, Andrea R V R Horimoto, Douglas P Loesch and 40 more

Open access · hybridAbstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Genetic Analysis of the X Chromosome Associates Loci with Progression of Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Epidemiology of Parkinson's Disease: An Update.Current neurology and neuroscience reports · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. X-chromosome variants and PD in Latin America.Nature reviews. Neurology · 2023
    Article
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

50 authors at 20 institutions in 6 countries.

Thiago P LealLerner Research Institute, Genomic Medicine, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0002-5829-6452
Shilpa C RaoThe Parkinson's Foundation, Miami, Florida, USA.
Jennifer N French-KwawuInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Mateus H GouveiaCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Victor BordaInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Sara Bandres-CigaCenter for Alzheimer's and Related Dementias, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0003-0056-1361
Miguel Inca-MartinezLerner Research Institute, Genomic Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Emily A MasonUniversity of South Carolina School of Medicine, Columbia, South Carolina, USA.
Andrea R V R HorimotoDivision of Aging, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Douglas P LoeschInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Elif I SarihanLerner Research Institute, Genomic Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Mario R Cornejo-OlivasNeurogenetics Working Group, Universidad Científica del Sur, Lima, Peru.ORCID 0000-0001-6313-5680
Luis E TorresMovement Disorders Unit, Instituto Nacional de Ciencias Neurologicas, Lima, Peru.
Pilar E Mazzetti-SolerNeurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru.
Carlos CosentinoMovement Disorders Unit, Instituto Nacional de Ciencias Neurologicas, Lima, Peru.ORCID 0000-0003-3677-9856
Elison H Sarapura-CastroNeurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru.ORCID 0000-0002-1562-3062
Andrea Rivera-ValdiviaNeurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru.
Angel C MedinaUniversidad Nacional del Altiplano, Puno, Peru.
Elena M DieguezNeurology Institute, Universidad de la República, Montevideo, Uruguay.
Víctor E RaggioDepartment of Genetics, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Andrés LescanoNeurology Institute, Universidad de la República, Montevideo, Uruguay.
Vitor TumasRibeirão Preto Medical School, Universidade de São Paulo, Ribeirão Preto, Brazil.
Vanderci BorgesMovement Disorders Unit, Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, Brazil.
Henrique B FerrazMovement Disorders Unit, Department of Neurology and Neurosurgery, Universidade Federal de São Paulo, São Paulo, Brazil.
Carlos R RiederDepartamento de Neurologia, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil.
Artur Schumacher SchuhServiço de Neurologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.ORCID 0000-0002-8722-0908
Bruno L Santos-LobatoInstituto de Ciências da Saúde, Universidade Federal do Pará, Belém, Brazil.ORCID 0000-0001-9321-5710
Carlos Velez-PardoNeuroscience Research Group, Medical Research Institute, Faculty of Medicine, Universidad de Antioquia, Medellín, Colombia.
Marlene Jimenez-Del-RioNeuroscience Research Group, Medical Research Institute, Faculty of Medicine, Universidad de Antioquia, Medellín, Colombia.
Francisco LoperaNeuroscience Research Group, Medical Research Institute, Faculty of Medicine, Universidad de Antioquia, Medellín, Colombia.
Sonia MorenoNeuroscience Research Group, Medical Research Institute, Faculty of Medicine, Universidad de Antioquia, Medellín, Colombia.
Pedro Chana-CuevasCETRAM, Facultad de Ciencias Médicas, Universidad de Santiago de Chile, Santiago, Chile.
William FernandezNeuroscience and Cell Death Research Groups, Medical School and Genetic Institute, Universidad Nacional de Colombia, Bogotá, Colombia.
Gonzalo ArboledaNeuroscience and Cell Death Research Groups, Medical School and Genetic Institute, Universidad Nacional de Colombia, Bogotá, Colombia.
Humberto ArboledaNeuroscience and Cell Death Research Groups, Medical School and Genetic Institute, Universidad Nacional de Colombia, Bogotá, Colombia.
Carlos E Arboleda BustosNeuroscience and Cell Death Research Groups, Medical School and Genetic Institute, Universidad Nacional de Colombia, Bogotá, Colombia.
Dora YearoutVeterans Affairs Puget Sound Health Care System, Seattle, Washington, USA.
Maira T BarbosaBehavioral and Cognitive Neurology Unit, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Francisco E C CardosoMovement Disorders Unit, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Paulo CaramelliBehavioral and Cognitive Neurology Unit, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Mauro C Q CunninghamBehavioral and Cognitive Neurology Unit, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Débora P MaiaMovement Disorders Unit, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Maria F Lima-CostaInstituto René Rachou da Fundação Oswaldo Cruz, Belo Horizonte, Brazil.
Eduardo Tarazona-SantosDepartment of Genetics, Ecology and Evolution, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Cyrus P ZabetianVeterans Affairs Puget Sound Health Care System, Seattle, Washington, USA.ORCID 0000-0002-7739-4306
International Parkinson Disease Genomics Consortium (IPDGC)
Timothy A ThorntonDepartment of Biostatistics, University of Washington, Seattle, Washington, USA.
Timothy D O'ConnorInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Ignacio F MataLerner Research Institute, Genomic Medicine, Cleveland Clinic, Cleveland, Ohio, USA.
Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD)
Universidade Federal de Minas Gerais · BRCleveland Clinic Lerner College of Medicine · USUniversidad de Antioquia · COUniversidad Nacional de Colombia · COUniversity of Maryland, Baltimore · USUniversidad de la República de Uruguay · UYUniversity of Washington · USInstitute of Peruvian Studies · PEInstituto Nacional de Ciencias NeurológicasNational Institutes of Health · USUniversidade Federal de São Paulo · BRBrigham and Women's Hospital · USFundação Oswaldo Cruz · BRNational University of San Marcos · PEParkinson's Foundation · USUniversidad Científica del Sur · PEUniversidad de Santiago de Chile · CLUniversidade de Ribeirão Preto · BRUniversidade Federal de Ciências da Saúde de Porto Alegre · BRUniversidade Federal do Pará · BR

Funding

iPSC Neurodegenerative Diseasses InitiativeZIAAG000535 · NIA · NATIONAL INSTITUTE ON AGING · PI COOKSON, MARK · 2019 to 2025
$48.2M
NPGH LEADERs YR12: OBSSR (Greenberg, Ngwafong Mukere) & NIBIB (Lee)D43TW009345 · FIC · UNIVERSITY OF WASHINGTON · PI Dibyadyuti Datta, Chandy C. John · 2017 to 2026
$15.2M
Genome wide SNP analysis in Parkinson's diseaseZIAAG000949 · NIA · NATIONAL INSTITUTE ON AGING · PI SINGLETON, ANDREW · 2009 to 2024
$12.6M
Vascular Biology Training ProgramT32HL007698 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI Rosemary A Kozar, Dudley K. Strickland · 1991 to 2026
$8.7M
RESEARCH TRAINING IN THE EPIDEMIOLOGY OF AGINGT32AG000262 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI ANN L GRUBER-BALDINI, DENISE L ORWIG · 1998 to 2026
$8.2M
Modeling the impact of Women's Specific Health Factors in PD outcomes in LatinasR01NS112499 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI FERNANDEZ MATA, IGNACIO · 2020 to 2024
$3.3M
Genome wide SNP analysis in Parkinson's diseaseZ01AG000949 · NIA · NATIONAL INSTITUTE ON AGING · PI SINGLETON, ANDREW B · 2006 to 2008
$2.6M
Rapid Evolution of Genomic Architecture and Multi-omics TraitsR35HG010692 · NHGRI · UNIVERSITY OF MARYLAND BALTIMORE · PI O'CONNOR, TIMOTHY DAVID · 2019 to 2023
$2.3M
MIDCAREER AWARD IN PATIENT ORIENTED RESEARCH ON AGINGK24AG000949 · NIA · YALE UNIVERSITY · PI INOUYE, SHARON K. · 1999 to 2009
$1.4M
FIC NIH HHS D43 TW009345Intramural NIH HHS Z01 AG000949Intramural NIH HHS ZIA AG000535Intramural NIH HHS ZIA AG000949NHGRI NIH HHS R35 HG010692NHLBI NIH HHS T32 HL007698NIA NIH HHS K24 AG000949NIA NIH HHS T32 AG000262NINDS NIH HHS R01 NS112499
6 · The paper itself

Abstract

backgroundSex differences in Parkinson's disease (PD) risk are well-known. However, the role of sex chromosomes in the development and progression of PD is still unclear.

objectiveThe objective of this study was to perform the first X-chromosome-wide association study for PD risk in a Latin American cohort.

methodsWe used data from three admixed cohorts: (1) Latin American Research consortium on the Genetics of Parkinson's Disease (n = 1504) as discover cohort, and (2) Latino cohort from International Parkinson Disease Genomics Consortium (n = 155) and (3) Bambui Aging cohort (n = 1442) as replication cohorts. We also developed an X-chromosome framework specifically designed for admixed populations.

resultsWe identified eight linkage disequilibrium regions associated with PD. We replicated one of these regions (top variant rs525496; discovery odds ratio [95% confidence interval]: 0.60 [0.478-0.77], P = 3.13 × 10

conclusionsOur results reinforce the importance of including X-chromosome and diverse populations in genetic studies. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Chromosomes, Human, XParkinson DiseaseFemaleGenome-Wide Association StudyHispanic or LatinoHumansLatin AmericaLinkage DisequilibriumMaleSex Factorsadmixed populationshipanic/latinoParkinson's diseaseunderrepresented populationsx-chromosome wide association study

Identifiers

PMID37469269
PMCPMC10524402
OpenAlexW4384820035

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.