Default: Clinical Genetics

ISSN: 0009-9163

Journal Home

Journal Guideline

Clinical Genetics Q1 Unclaimed

Wiley-Blackwell Publishing Ltd United Kingdom
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

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: -

Price

3650 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

Clinical Genetics

1,241

SJR Impact factor

112

H Index

159

Total Docs (Last Year)

570

Total Docs (3 years)

4213

Total Refs

1975

Total Cites (3 years)

471

Citable Docs (3 years)

3.1

Cites/Doc (2 years)

26.5

Ref/Doc

Comments

No comments ... Be the first to comment!

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

View more

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

View more

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

View more

Estrogen receptor mutation in a girl with primary amenorrhea

View more

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

View more

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

View more

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

View more

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

View more

A locus for autosomal recessive achromatopsia on human chromosome 8q

View more

MEFVmutations in Iranian Azeri Turkish patients with familial Mediterranean fever

View more

Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype

View more

Novel mutations in the CHST6 gene causing macular corneal dystrophy

View more
SHOW MORE ARTICLES

Cortical dysgenesis in 2 patients with chromosome 22q11 deletion

View more

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

View more

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

View more

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

View more

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

View more

Omphalocele in trisomy 3q: further delineation of phenotype

View more

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

View more

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

View more

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

View more

Postaxial polydactyly and Dandy-Walker malformation. Further nosological comments

View more

Timing is everything: especially with loss of tumor suppressor genes

View more

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

View more

FAQS