Clinical Genetics
Clinical Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 121. It has a price of 3650 €. It has an SJR impact factor of 1,093 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 1,093.
Clinical Genetics focuses its scope in these topics and keywords: syndrome, genetic, molecular, patients, overgrowth, ring, syndromic, mutation, x, brca, ...
Unclaimed profile — some fields may be incomplete.
Metrics
Campos Scimago / CoP — sin series inventadas
SJR Impact
1,093
H-index
121
Docs (year)
188
Docs 3y
537
Total refs
5603
Cites 3y
1461
Citable 3y
434
Cites/Doc 2y
2.35
Ref/Doc
29.8
Immediate OA
3650 €
Embargoed OA
NPD
Non OA / Submission
0 €
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Best articles by citations
Association between polymorphism of the cholecystokinin gene and idiopathic Parkinson's disease
View moreVietnamese sisters with Grebe syndrome on a TV program in Japan
View moreCo-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome
View moreClinical teratology: identifying teratogenic risks in humans
View moreChromosome studies in IgA-deficient patients
View moreCentromere-telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy 1
View moreBroadening the spectrum of genetic disease mechanisms: making (anti)sense out of a-thalassemia
View moreBilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1
View moreAutosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmed
View moreAtypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis
View moreAttenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations
View moreAssociation of EDNRA, but not WNK4 or FKBP1B, polymorphisms with essential hypertension
View moreAssociation of a single nucleotide polymorphism in CPB2 encoding the thrombin-activable fibrinolysis inhibitor (TAFI) with blood pressure
View moreA de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificansprogressiva patient
View moreAnother gene to screen in polyposis disorders?
View moreAn interaction between the TaqIB polymorphism of cholesterol ester transfer protein and smoking is associated with changes in plasma high-density lipoprotein cholesterol levels in Turks
View moreAdult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene
View moreA systematic search for single nucleotide polymorphisms (SNPs) in the insulin receptor gene: association of an SNP with hyperlipidemia in Japanese type 2 diabetic subjects
View moreA reversal of fate? Left-right asymmetry, the inversin gene and childhood renal cystic disease
View moreA Reply
View moreA putative E3 ubiquitin ligase is deficient in progressive myoclonus epilepsy
View moreA PCR-based method for detecting known mutations in the human UDP galactose-4'-epimerase gene associated with epimerase-deficiency galactosemia
View moreA logistic regression model for measuring gene-longevity associations
View moreA locus for autosomal recessive achromatopsia on human chromosome 8q
View more