Impact Factor
2.85
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
1.87
189 total citations
h5-index
27
h5 depth signal
Cited share
51.5%
53 of 103
Total citations
189
Citation footprint
Metric signal
1.43
External metric anchor
Self-citation
1.6%
3 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United States
382
Canada
61
Italy
46
United Kingdom
40
Brazil
24
Citing Fields of Research
Cytogenetics
256
Genetics & Genomics
175
Congenital Disorders
152
Musculoskeletal Disorders
67
Neurodevelopmental Disorders
58
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
1,215
Articles tracked across the journal lifetime
Indexed publication set
103
53 cited publications
Last 12 months
29
2.6 publications/month
Open access share
48.3%
14 OA publications in the last year
Leading citing country
United States
382 citing publications
Leading citing field
Cytogenetics
256 citing publications
Latest tracked publication
9 September 2026
10 recent records available
Coverage & Indexing History
v117Cn1, Feb. 15, 2003-
v117Cn1, Feb. 15, 2003-
Active Coverage
Research Focus & Classification
Indexed Subjects
Cytogenetics
Congenital Disorders
Genetics & Genomics
Musculoskeletal Disorders
Broad Categories
Genetics, Medical
Cytogenetics
Neurodevelopmental Disorders
Genetics & Genomics
Cell Differentiation & Development
MeSH Descriptors
Genetics, Medical
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1002/ajmg.c.70024
Open DOI
Arthrogryposis Multiplex Congenita in Pediatric Age: Correlation Between MUScular MRI and Functional Evaluation ( AMUSE ), Toward a Biomechanical Model
Arthrogryposis Multiplex Congenita (AMC) is a group of diseases with joint limitations at two or more distinct joint levels at birth. Joint limitations are not progressive, but the functional consequences have a lifelong impact on patien...
02
DOI 10.1002/ajmg.c.70020
Open DOI
Understanding Arthrogryposis Multiplex Congenita ( AMC ) Across the Lifespan: An Integrative Review of the Adult AMC Registry's Contributions With Lived Experience Partnerships
This reflective essay explores how collaborative work between researchers and adults living with Arthrogryposis Multiplex Congenita (AMC) has deepened and broadened our understanding of what it means to live with this rare condition. By ...
03
DOI 10.1002/ajmg.c.70021
Open DOI
Pain and Health: Sex‐Specific Differences From a Survey Study of Adults With Arthrogryposis Multiplex Congenita
Arthrogryposis Multiplex Congenita (AMC), a rare congenital condition characterized by joint contractures in two or more body regions, is often accompanied by pain. Understanding pain and its relationship to health outcomes among adults ...
04
DOI 10.1002/ajmg.c.70018
Open DOI
Upper Extremity Entrapment Neuropathies in Adults With Arthrogryposis Multiplex Congenita: A National Database Study
Adults with arthrogryposis multiplex congenita (AMC) experience lifelong disability from joint contractures, yet susceptibility to upper extremity compressive neuropathy remains unevaluated. Using the TriNetX US Collaborative Network, we...
05
DOI 10.1002/ajmg.c.70014
Open DOI
Posthumously Diagnosed Myhre Syndrome Presenting With Pleural Remodeling and Endometrial Cancer
Myhre syndrome (OMIM 139210) is a genetic condition defined by neurodevelopmental disability, characteristic facial features, and multisystem proliferative fibrosis. While various types of lung disease have been reported, pleural remodel...
06
DOI 10.1002/ajmg.c.70013
Open DOI
The International Consortium for Arthrogryposis: A Collaborative Framework for Early Detection, Care, Research, and Education
Arthrogryposis multiplex congenita (AMC) is a group of rare congenital conditions, characterized by multiple joint contractures but may involve any body system including central nervous system. AMC is etiologically heterogeneous, with ov...
07
DOI 10.1002/ajmg.c.70016
Open DOI
Apical Ectodermal Ridge Disruption and Hypoplastic Digits in Amyoplasia
The cause of Amyoplasia remains controversial, with the predominant theory being loss of anterior horn cells secondary to vascular disruption as the primary insult. Disruption of the apical ectodermal ridge (AER) is extremely rare, occur...
08
DOI 10.1002/ajmg.c.70015
Open DOI
Caring for Pediatric Clients With Arthrogryposis Multiplex Congenita: The Development of an Occupational Therapy Continuing Education Course
Occupational therapy practitioners (OTPs) are vital members of the multidisciplinary team involved in caring for pediatric clients diagnosed with arthrogryposis multiplex congenita (AMC). However, a shortage of educational resources on A...
09
DOI 10.1002/ajmg.c.70011
Open DOI
Psychotic Features in Myhre Syndrome: Evidence for Broader Neuropsychiatric Surveillance
Myhre syndrome is a rare genetic disorder caused by pathogenic variants in SMAD4 . The neurocognitive profile may include intellectual disability and developmental delay across a wide spectrum of domains. Four individuals with Myhre synd...
10
DOI 10.1002/ajmg.c.70010
Open DOI
Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research
Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, d...
Bibliographical & Catalog Notes
Founded by: John M. Opitz.
Each vol. complete in one no.; even numbered vols. skipped in numbering.
Also issued online.