Paper · 9506542

Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH Consortium.

Tawil R and 3 others. Ann Neurol, 1998. Cited by 81 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Cite this record

ConductScience Library. Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH Consortium. Papers, record 9506542. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/9506542

On this page

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH Consortium.; PubMed
Journal: Ann Neurol; PubMed
Year: 1998; PubMed
Publication types: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S., Review; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/9506542/; PubMed
DOI: https://doi.org/10.1002/ana.410430303; PubMed
The journal: https://conductscience.org/library/journal-index/7707449; PubMed
Citations, by iCite: 81; iCite
Relative citation ratio, by iCite: 1.67; iCite
Revised in PubMed: 2007-11-14; PubMed

Authors4

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename
1	Tawil R	R
2	Figlewicz DA	D A
3	Griggs RC	R C
4	Weiffenbach B	B

Source PubMed

Topics9

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
Muscular Dystrophies	Major topic
Animals
Chromosome Mapping
Disease Models, Animal
Gene Deletion
Genotype
Humans
Muscular Dystrophy, Animal
Phenotype

Source PubMed

Grants2

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes it	Agency	Country	NIH project	Stated by	Source
1 R13 NS35435-01A1	NINDS NIH HHS	United States	R13NS354350	PubMed	NIH RePORTER
			R13NS035435	NIH	NIH RePORTER

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References0

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

None in this release.

Cited by32

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 81 citations.

PMID	Title	Journal	Year	In Papers	Source
41,652,446	DUCKS4: a comprehensive workflow for Nanopore sequencing analysis of facioscapulohumeral muscular dystrophy (FSHD).	Hum Genomics	2026	https://conductscience.org/library/papers/41652446	PubMed
39,501,809	Dominantly inherited muscle disorders: understanding their complexity and exploring therapeutic approaches.	Dis Model Mech	2024	https://conductscience.org/library/papers/39501809	PubMed
37,511,653	Molecular and Phenotypic Changes in FLExDUX4 Mice.	J Pers Med	2023	https://conductscience.org/library/papers/37511653	PubMed
36,475,552	Management of scapular dysfunction in facioscapulohumeral muscular dystrophy: the biomechanics of winging, arthrodesis indications, techniques and outcomes.	EFORT Open Rev	2022	https://conductscience.org/library/papers/36475552	PubMed
35,121,673	Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With SMCHD1 Variants.	Neurology	2022	https://conductscience.org/library/papers/35121673	PubMed
34,131,248	CRISPR mediated targeting of DUX4 distal regulatory element represses DUX4 target genes dysregulated in Facioscapulohumeral muscular dystrophy.	Sci Rep	2021	https://conductscience.org/library/papers/34131248	PubMed
29,328,515	Magnetic resonance imaging in facioscapulohumeral muscular dystrophy.	Muscle Nerve	2018	https://conductscience.org/library/papers/29328515	PubMed
27,722,032	PARP1 Differentially Interacts with Promoter region of DUX4 Gene in FSHD Myoblasts.	J Genet Syndr Gene Ther	2016	https://conductscience.org/library/papers/27722032	PubMed
26,184,877	ZNF555 protein binds to transcriptional activator site of 4qA allele and ANT1: potential implication in Facioscapulohumeral dystrophy.	Nucleic Acids Res	2015	https://conductscience.org/library/papers/26184877	PubMed
26,063,958	Serum Enzyme Profiles Differentiate Five Types of Muscular Dystrophy.	Dis Markers	2015	https://conductscience.org/library/papers/26063958	PubMed

1 to 10 of 32

See all 32 cited by

Genes1

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes
FSHMD1A	2,489	PubTator's text mining	https://conductscience.org/library/genes/2489

Source NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this paper from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/papers/v1/9506542

GET https://conductscience.org/api/papers/v1/9506542/cited_by?page=2

API reference For AI assistants