Impact Factor
2.15
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
0.87
51 total citations
h5-index
7
h5 depth signal
Cited share
54.3%
38 of 70
Total citations
51
Citation footprint
Metric signal
0.55
External metric anchor
Self-citation
0.0%
0 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
United Kingdom
89
India
71
Turkey
70
United States
68
China
28
Citing Fields of Research
Cytogenetics
288
Genetics & Genomics
184
Congenital Disorders
178
Cell Differentiation & Development
46
Neurodevelopmental Disorders
36
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
1,973
Articles tracked across the journal lifetime
Indexed publication set
70
38 cited publications
Last 12 months
36
3.6 publications/month
Open access share
5.6%
2 OA publications in the last year
Leading citing country
United Kingdom
89 citing publications
Leading citing field
Cytogenetics
288 citing publications
Latest tracked publication
8 October 2026
10 recent records available
Coverage & Indexing History
v1n1,Jan. 1992-
v1n1,Jan. 1992-
Active Coverage
Research Focus & Classification
Indexed Subjects
Cytogenetics
Genetics & Genomics
Congenital Disorders
Cell Differentiation & Development
Neurodevelopmental Disorders
Issuing & Sponsoring Bodies
Contributor
UK Dysmorphology Club
Broad Categories
Teratology
Cytogenetics
Cell Differentiation & Development
Cancer & Development
Hematology
Musculoskeletal & Nerve Cancer
Lysosomal Storage Disorders
MeSH Descriptors
Congenital Abnormalities
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1097/mcd.0000000000000581
Open DOI
Application of deep learning and explainable AI-supported medical decision-making for facial phenotyping in genetic syndromes
Objective: To conduct a pilot study to assess whether saliency-based explainable artificial intelligence (XAI) affects the recognition of genetic conditions from facial images. Methods: Forty-four medical geneticists, divided into AI-onl...
02
DOI 10.1097/mcd.0000000000000583
Open DOI
A prenatal-onset severe phenotype of SLC35A2-related congenital disorder of glycosylation associated with a mosaic hemizygous intronic variant
Was not provided for this article.
03
DOI 10.1097/mcd.0000000000000582
Open DOI
Expanding the phenotype of GDI1-related neurodevelopmental disorder: report of the fifth family
Was not provided for this article.
04
DOI 10.1097/mcd.0000000000000578
Open DOI
Second-trimester prenatal phenotype of complete trisomy 10 with combined encephalocele and myelomeningocele
Was not provided for this article.
05
DOI 10.1097/mcd.0000000000000580
Open DOI
Marbach–Rustad progeroid syndrome caused by a hotspot LEMD2 variant: expanding the phenotypic spectrum with skeletal, cutaneous, and renal findings
Was not provided for this article.
06
DOI 10.1097/mcd.0000000000000577
Open DOI
Nonimmune hydrops fetalis with skeletal dysplasia due to a novel homozygous recessive TAPT1 splice-donor variant
Was not provided for this article.
07
DOI 10.1097/mcd.0000000000000579
Open DOI
A novel homozygous frameshift variant in DYM causing Dyggve–Melchior–Clausen syndrome: expansion of the mutational spectrum
Was not provided for this article.
08
DOI 10.1097/mcd.0000000000000576
Open DOI
Omphalocele–exstrophy–imperforate anus–spinal defects complex associated with a very rare limb anomaly mimicking polymelia
Was not provided for this article.
09
DOI 10.1097/mcd.0000000000000575
Open DOI
Monochorionic dizygotic twins with discordant genetic findings and congenital malformations
Objective: To describe prenatal evaluation and postnatal outcome of monochorionic diamniotic twins with discordant anomalies and genetic findings after intracytoplasmic sperm injection and double-embryo transfer. Methods: A 36-year-old g...
10
DOI 10.1097/mcd.0000000000000573
Open DOI
Generalized overgrowth in CDC42BPB-related Chilton-Okur-Chung neurodevelopmental syndrome: expanding the phenotypic spectrum
Was not provided for this article.
Bibliographical & Catalog Notes
Title from cover.
Includes abstracts and summaries from the UK Dysmorphology Club.
Also issued online.
Vol. 4, no. 1 (JAN 1995)19940124 Notice not published Printed on acid-free paper