ISSN: 0009-9163
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Clinical Genetics Q1 Unclaimed
Clinical Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 115. It has a price of 3650 €. It has an SJR impact factor of 1,236 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,236.
Clinical Genetics focuses its scope in these topics and keywords: genetic, syndrome, overgrowth, mutation, ring, syndromic, patients, brca, x, molecular, ...
Type: Journal
Type of Copyright:
Languages: English
Open Access Policy: Open Choice
Type of publications:
Publication frecuency: -
3650 €
Inmediate OANPD
Embargoed OA0 €
Non OAMetrics
1,236
SJR Impact factor115
H Index188
Total Docs (Last Year)548
Total Docs (3 years)4900
Total Refs1587
Total Cites (3 years)445
Citable Docs (3 years)2.67
Cites/Doc (2 years)26.06
Ref/DocOther journals with similar parameters
Signal Transduction and Targeted Therapy Q1
Nature Microbiology Q1
Nature Protocols Q1
Annual Review of Genetics Q1
Genome Biology Q1
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Aims and Scope
Best articles by citations
Familial Down syndrome: evidence supporting cytoplasmic inheritance
View moreFounder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families
View morePrenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells
View moreEstrogen receptor mutation in a girl with primary amenorrhea
View moreBilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1
View moreThe locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23
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 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 moreA locus for autosomal recessive achromatopsia on human chromosome 8q
View moreMEFVmutations in Iranian Azeri Turkish patients with familial Mediterranean fever
View moreGenetic susceptibility to neural tube defect pregnancy varies with offspring phenotype
View moreNovel mutations in the CHST6 gene causing macular corneal dystrophy
View moreCortical dysgenesis in 2 patients with chromosome 22q11 deletion
View moreOverlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis
View moreHomozygous C4A deficiency in systemic lupus erythematosus: analysis of patients from a defined population
View moreHomozygous deficiency of C4 in a child with a lupus erythematosus syndrome
View moreEvaluation for sleep apnea in patients with Ehlers-Danlos syndrome and Marfan: a questionnaire study
View moreOmphalocele in trisomy 3q: further delineation of phenotype
View moreHardly a stroke of luck! (Uncovering a gene for stroke is hard work)
View moreAtypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis
View moreAssociation of a single nucleotide polymorphism in CPB2 encoding the thrombin-activable fibrinolysis inhibitor (TAFI) with blood pressure
View morePostaxial polydactyly and Dandy-Walker malformation. Further nosological comments
View moreTiming is everything: especially with loss of tumor suppressor genes
View morePCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype
View more
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