Evidence map›Paper›PMID 38291851›Full record

ArticleMovement disorders clinical practice2024

Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities.

Ai Huey Tan, Mario Cornejo-Olivas, Njideka Okubadejo, Pramod Kumar Pal, Gerard Saranza, Paula Saffie-Awad, Azlina Ahmad-Annuar, Artur F Schumacher-Schuh, Kigocha Okeng'o, Ignacio F Mata and 2 more

Abstract read
In one paragraph

Article in Movement disorders clinical practice, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Collaborative Genomics for Dystonia in Central and Eastern Europe: Successes Achieved, New Frontiers Ahead.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Parkinson's Disease is Predominantly a Genetic Disease.Journal of Parkinson's disease · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Ai Huey TanDivision of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.ORCID 0000-0002-2979-3839
Mario Cornejo-OlivasNeurogenetics Working Group, Universidad Científica del Sur, Lima, Peru.ORCID 0000-0001-6313-5680
Njideka OkubadejoDepartment of Medicine, College of Medicine, University of Lagos, Lagos, Nigeria.ORCID 0000-0003-2975-8803
Pramod Kumar PalDepartment of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, India.ORCID 0000-0002-4085-2377
Gerard SaranzaMovement Disorders Service, Section of Neurology, Department of Internal Medicine, Chong Hua Hospital and Vicente Sotto Memorial Medical Center, Cebu, Philippines.ORCID 0000-0001-8322-4226
Paula Saffie-AwadCETRAM-Centro de Estudios de Transtornos del Movimiento, Clínica Santa María, Santiago, Chile.ORCID 0000-0002-8056-365X
Azlina Ahmad-AnnuarDepartment of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.ORCID 0000-0001-6329-4366
Artur F Schumacher-SchuhDepartamento de Farmacologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.ORCID 0000-0002-8722-0908
Kigocha Okeng'oT.M.J. Super Specialized Polyclinic, Dar es Salaam, Tanzania.ORCID 0000-0003-2615-9274
Ignacio F MataGenomic Medicine Institute, Lerner Research Institute, Genomic Medicine, Cleveland Clinic Foundation, Cleveland, Ohio, USA.ORCID 0000-0003-1198-0633
Emilia M GattoDepartment of Neurology, Hospital Sanatorio de la Trinidad Mitre, Instituto de Neurociencias Buenos Aires, School of Medicine, Buenos Aires University, Buenos Aires, Argentina.ORCID 0000-0002-1346-5443
Shen-Yang LimDivision of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.ORCID 0000-0002-6942-2522

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Parkinson DiseaseGenetic TestingHumansgenetic counsellinggeneticsgenomicslow and middle incomereturn-of-resultsunder-represented population

Identifiers

PMID38291851
PMCPMC10828609

What OpenQuestion holds

Textmetadata
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.