Impact Factor
1.39
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
2.50
0 total citations
h5-index
2
h5 depth signal
Cited share
0.0%
0 of 4
Total citations
0
Citation footprint
Metric signal
0.00
External metric anchor
Self-citation
0.0%
0 self-citations
Citations Trend
Citing Geographic Demographics
China
42
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
214
Articles tracked across the journal lifetime
Indexed publication set
4
0 cited publications
Last 12 months
0
0.0 publications/month
Open access share
0.0%
0 OA publications in the last year
Leading citing country
China
42 citing publications
Leading citing field
N/A
No field analytics available
Latest tracked publication
10 June 2023
10 recent records available
Coverage & Indexing History
v15n1, 1998-
v15n1, 1998-
Active Coverage
Research Focus & Classification
Issuing & Sponsoring Bodies
Contributor
Zhonghua yi xue hui (China : 1949- )
Contributor
Hua xi yi ke da xue
Contributor
Sichuan da xue
Broad Categories
Genetics, Medical
Cytogenetics
Cardiology
Cell Differentiation & Development
Genetics & Genomics
Mitochondria
Hematology
MeSH Descriptors
Genetic Diseases, Inborn
Genetics, Medical
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.3760/cma.j.cn511374-20220930-00661
Open DOI
[Study of the unique cellular molecular characteristics of moderately intrauterine adhesion based on single-cell RNA sequencing].
To depict the cell landscape and molecular biological characteristics of human intrauterine adhesion (IUA) so as to better understand its immune microenvironment and provide new inspirations for clinical treatment. Four patients with IUA...
02
DOI 10.3760/cma.j.cn511374-20220830-00587
Open DOI
[Clinical and genetic analysis of a patient with Craniofrontonasal syndrome].
To explore the clinical feature and genetic etiology of a patient with Craniofacial nasal syndrome (CNFS). A patient with CNFS who had presented at the Guiyang Maternal and Child Health Care Hospital on November 13, 2021 was selected as ...
03
DOI 10.3760/cma.j.cn511374-20211027-00852
Open DOI
[Genetic analysis of a Chinese pedigree with 6q26q27 microduplication and 15q26.3 microdeletion].
To explore the genetic basis for a Chinese pedigree with 6q26q27 microduplication and 15q26.3 microdeletion. A fetus with a 6q26q27 microduplication and a 15q26.3 microdeletion diagnosed at the First Affiliated Hospital of Wenzhou Medica...
04
DOI 10.3760/cma.j.cn511374-20220406-00228
Open DOI
[Analysis of a Chinese pedigree affected with familial short stature due to 15q25.3q26.1 deletion involving the ACAN gene].
To analyze the genetic etiology of a Chinese pedigree affected with short stature. A child with familial short stature (FSS) who had presented at the Ningbo Women and Children's Hospital in July 2020 and his parents and paternal and mate...
05
DOI 10.3760/cma.j.cn511374-20220120-00046
Open DOI
[Clinical evaluation of true and false positive Z values among high-risk cases screened by non-invasive prenatal testing].
To analyze the Z values of true and false positive cases by non-invasive prenatal testing (NIPT) in order to improve its accuracy in clinical practice. Results of 24 384 NIPT tests were reviewed. For cases with high risks for trisomies 2...
06
DOI 10.3760/cma.j.cn511374-20211209-00978
Open DOI
[A multiplex PCR-based sensitive and specific method for detecting Y chromosome material in patients with Turner syndrome].
To develop a multiplex PCR method for a rapid detection of Y chromosome-specific sequences in patients with Turner syndrome. Nine genes were selected from various regions of the Y chromosome for designing the primers, which included SRY,...
07
DOI 10.3760/cma.j.cn511374-20211104-00880
Open DOI
[Genetic diagnosis of a child with Café-au-lait macules and juvenile xanthogranuloma].
To explore the genetic basis for a child with café-au-lait macules and juvenile xanthogranuloma. Clinical data and peripheral blood samples of the patient and her family members were collected and subjected to targeted capture and high-t...
08
DOI 10.3760/cma.j.cn511374-20201105-00779
Open DOI
[Analysis of a patient with Kallmann syndrome and a 45,X/46,XY karyotype].
To explore the etiology of a patient with Kallmann syndrome (congenital hypogonadism and anosmia) and a 45,X/46,XY karyotype. Peripheral venous blood samples were collected from the proband and his parents and subjected to whole exome se...
09
DOI 10.3760/cma.j.cn511374-20210304-00186
Open DOI
[Association of genomic instability of CDH1 gene with clinicopathological characteristics of gastric cancer].
To assess the association of genomic instability of epithelial cadherin 1 (CDH1) gene and clinicopathological characteristics of gastric cancer. In total 120 paraffin-embedded gastric cancer tissue specimen were prepared, and genomic DNA...
10
DOI 10.3760/cma.j.cn511374-20220103-00001
Open DOI
[Analysis of three Chinese pedigrees affected with recurrent hydatidiform mole due to variants of NLRP7 gene].
To explore the genetic etiology of recurrent hydatidiform mole (RHM) and provide accurate guidance for reproduction. Peripheral venous blood samples of the probands with RHM and members from 5 unrelated pedigrees were collected. Genomic ...
Bibliographical & Catalog Notes
Description based on: Di 9 juan, di 6 qi, published in 1992; title from cover.
Numbering continues that of earlier title.
Also issued online.
In Chinese; table of contents and summaries also in English.
Sponsored by: Zhonghua yi xue hui; <2004-> by Sichuan University.
Vol. 15, no. 1 (FEB 1998)19980205 Notice published Printed on acid-free paper