ArticlemedRxiv : the preprint server for health sciences2024
Differential Tractography: A Biomarker for Neuronal Function in Neurodegenerative Disease.
Connor J Lewis, Zeynep Vardar, Anna Luisa Kühn, Jean M Johnston, Precilla D'Souza, William A Gahl, Mohammed Salman Shazeeb, Cynthia J Tifft, Maria T Acosta
Abstract readPreprint
In one paragraphArticle in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
5 · Who and what moneyAuthors and funding
9 authors.
Connor J LewisOffice of the Clinical Director and Medical Genetics Branch, National Human Genome Research Institute, 10 Center Drive, Bethesda MD USA.ORCID 0000-0002-8204-5848 Zeynep VardarDepartment of Radiology, University of Massachusetts Chan Medical School, 55 N Lake Ave, Worcester MA USA.
Anna Luisa KühnDepartment of Radiology, University of Massachusetts Chan Medical School, 55 N Lake Ave, Worcester MA USA.
Jean M JohnstonOffice of the Clinical Director and Medical Genetics Branch, National Human Genome Research Institute, 10 Center Drive, Bethesda MD USA.
Precilla D'SouzaOffice of the Clinical Director and Medical Genetics Branch, National Human Genome Research Institute, 10 Center Drive, Bethesda MD USA.
William A GahlMedical Genetics Branch, National Human Genome Research Institute, 10 Center Drive, Bethesda MD USA.
Mohammed Salman ShazeebDepartment of Radiology, University of Massachusetts Chan Medical School, 55 N Lake Ave, Worcester MA USA.
Cynthia J TifftOffice of the Clinical Director and Medical Genetics Branch, National Human Genome Research Institute, 10 Center Drive, Bethesda MD USA.
Maria T AcostaOffice of the Clinical Director and Medical Genetics Branch, National Human Genome Research Institute, 10 Center Drive, Bethesda MD USA.ORCID 0000-0001-8914-7401 Funding
Pathogenesis informs therapy in the GM1 and GM2 GangliosidosesZIAHG200409 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI TIFFT, CYNTHIA · 2020 to 2025
$4.1MLONKAGE ANALYSIS OF PROSTATE CANCERZ01HG000107 · NHGRI · HUMAN GENOME RESEARCH · PI BAILEY-WILSON, JOAN E. · 1997 to 2004
–Intramural NIH HHS Z01 HG000107Intramural NIH HHS ZIA HG200409
6 · The paper itselfAbstract
GM1 gangliosidosis is an ultra-rare inherited neurodegenerative lysosomal storage disorder caused by biallelic mutations in the
Indexed as
Differential TractographyGM1 GangliosidosisImaging Biomarkers
Identifiers
PMID39371116
PMCPMC11451749
What OpenQuestion holds
Textmetadata
LicenceCC0
Read underepoch 390