Default: Clinical Genetics

ISSN: 0009-9163

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Clinical Genetics Q1 Unclaimed

Wiley-Blackwell Publishing Ltd United Kingdom
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Clinical Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 112. It has a price of 3650 €. It has an SJR impact factor of 1,241 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,241.

Clinical Genetics focuses its scope in these topics and keywords: syndrome, genetic, brca, ring, syndromic, overgrowth, patients, molecular, mutation, x, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -


3650 €

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Clinical Genetics


SJR Impact factor


H Index


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Total Docs (3 years)


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Total Cites (3 years)


Citable Docs (3 years)


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Aims and Scope

syndrome, genetic, brca, ring, syndromic, overgrowth, patients, molecular, mutation, x, children, delineation, deletion, ctnnb, considerations, clustering, chromosomean, chromosomealumediated, additional, child, channelopathyfunding, cdsn, causative, calcification, biobank, bandlike, balanced, abnormal, dilemmafamilial, aspects, ambras,

Best articles by citations

Familial Down syndrome: evidence supporting cytoplasmic inheritance

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Founder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families

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Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells

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Estrogen receptor mutation in a girl with primary amenorrhea

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Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1

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The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23

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A systematic search for single nucleotide polymorphisms (SNPs) in the insulin receptor gene: association of an SNP with hyperlipidemia in Japanese type 2 diabetic subjects

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An 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

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A locus for autosomal recessive achromatopsia on human chromosome 8q

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MEFVmutations in Iranian Azeri Turkish patients with familial Mediterranean fever

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Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype

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Novel mutations in the CHST6 gene causing macular corneal dystrophy

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Cortical dysgenesis in 2 patients with chromosome 22q11 deletion

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Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis

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Homozygous C4A deficiency in systemic lupus erythematosus: analysis of patients from a defined population

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Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome

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Evaluation for sleep apnea in patients with Ehlers-Danlos syndrome and Marfan: a questionnaire study

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Omphalocele in trisomy 3q: further delineation of phenotype

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Hardly a stroke of luck! (Uncovering a gene for stroke is hard work)

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Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis

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Association of a single nucleotide polymorphism in CPB2 encoding the thrombin-activable fibrinolysis inhibitor (TAFI) with blood pressure

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Postaxial polydactyly and Dandy-Walker malformation. Further nosological comments

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Timing is everything: especially with loss of tumor suppressor genes

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PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype

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