Evidence map›Paper›PMID 32007754›Full record

ArticleJournal of the neurological sciences2020

A novel variant in the spatacsin gene causing SPG11 in a Malian family.

Guida Landouré, Kékouta Dembélé, Salimata Diarra, Lassana Cissé, Oumar Samassékou, Abdoulaye Bocoum, Abdoulaye Yalcouyé, Moussa Traoré, Kenneth H Fischbeck, Cheick O Guinto and 1 more

Open access · greenAbstract readCase ReportsLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of the neurological sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Novel variant inBrain communications · 2023
    Article
  5. Article
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

11 authors at 3 institutions in 2 countries.

Guida LandouréFaculté de Médecine et d'Odontostomatologie, USTTB, Bamako, Mali; Service de Neurologie, Centre Hospitalier Universitaire du Point "G", Bamako, Mali; Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD. Electronic address: guida@icermali.org.
Kékouta DembéléService de Neurologie, Centre Hospitalier Universitaire du Point "G", Bamako, Mali.
Salimata DiarraFaculté de Médecine et d'Odontostomatologie, USTTB, Bamako, Mali; Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD.
Lassana CisséService de Neurologie, Centre Hospitalier Universitaire du Point "G", Bamako, Mali.
Oumar SamassékouFaculté de Médecine et d'Odontostomatologie, USTTB, Bamako, Mali.
Abdoulaye BocoumFaculté de Médecine et d'Odontostomatologie, USTTB, Bamako, Mali.
Abdoulaye YalcouyéFaculté de Médecine et d'Odontostomatologie, USTTB, Bamako, Mali.
Moussa TraoréFaculté de Médecine et d'Odontostomatologie, USTTB, Bamako, Mali; Service de Neurologie, Centre Hospitalier Universitaire du Point "G", Bamako, Mali.
Kenneth H FischbeckNeurogenetics Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD.
Cheick O GuintoFaculté de Médecine et d'Odontostomatologie, USTTB, Bamako, Mali; Service de Neurologie, Centre Hospitalier Universitaire du Point "G", Bamako, Mali.
H3Africa Consortium
University of Bamako · MLUniversité des Sciences, des Techniques et des Technologies de Bamako · MLNational Institute of Neurological Disorders and Stroke · US

Funding

Studies Of Hereditary Neurological Disease: Disease Gene IdentificationZIANS002974 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI FISCHBECK, KENNETH · 2009 to 2023
$9.8M
Clinical and genetic studies of hereditary neurological disorders in MaliU01HG007044 · NHGRI · UNIV OF SCIENCES, TECH & TECH OF BAMAKO · PI LANDOURE, GUIDA · 2013 to 2022
$3.1M
NHGRI NIH HHS U01 HG007044
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Spastic Paraplegia, HereditaryHumansMutationProteinsProteinsSPG11 protein, human

Identifiers

PMID32007754
PMCPMC8312886
OpenAlexW3000334269

What OpenQuestion holds

Textmetadata
LicenceTDM
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.