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 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: -

Categories: Genetics (Q1) Genetics (clinical) (Q1) Genetics (clinical) (Q1)

Price

3650 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

1,236

SJR Impact factor

115

H Index

188

Total Docs (Last Year)

548

Total Docs (3 years)

4900

Total Refs

1587

Total Cites (3 years)

445

Citable Docs (3 years)

2.67

Cites/Doc (2 years)

26.06

Ref/Doc

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Aims and Scope

Best articles by citations

Familial Down syndrome: evidence supporting cytoplasmic inheritance

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

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

Estrogen receptor mutation in a girl with primary amenorrhea

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

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

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

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

A locus for autosomal recessive achromatopsia on human chromosome 8q

MEFVmutations in Iranian Azeri Turkish patients with familial Mediterranean fever

Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype

Novel mutations in the CHST6 gene causing macular corneal dystrophy

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Cortical dysgenesis in 2 patients with chromosome 22q11 deletion

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

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

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

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

Omphalocele in trisomy 3q: further delineation of phenotype

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

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

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

Postaxial polydactyly and Dandy-Walker malformation. Further nosological comments

Timing is everything: especially with loss of tumor suppressor genes

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