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Egyptian Journal of Medical Human Genetics : Impact Factor & More

eISSN: 2090-2441pISSN: 1110-8630
JournalOpen Access

Key Metrics

CiteScore
1.4
SNIP
0.55
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Topics Covered on Egyptian Journal of Medical Human Genetics

Egyptian Journal of Medical Human Genetics Journal Specifications

Overview
Publisher SPRINGERNATURE
Language English
Frequency Continuous publication
Publication Time18
Editorial Review ProcessDouble anonymous peer review
General Details
LanguageEnglish
Society/Institute/SponsorThe Egyptian Societies of Medical Human Genetics
FrequencyContinuous publication
Publication Start Year2010
Publisher URLVisit website
Website URLVisit website
Publication Details
PlagiarismVisit website
Publication Time 18
Editorial Review Detail
Editorial TeamVisit website
Review ProcessDouble anonymous peer review
Review UrlVisit website
Information for authors
Author instructionsVisit website
Copyright DetailsVisit website
Deposit PolicySherpa/Romeo
License typeCC BY
OA statementVisit website
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Recently Published Papers in Egyptian Journal of Medical Human Genetics

Unveiled SOX2 disorder in a child initially diagnosed as cerebral palsy
  • 23 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Impact of GATA2 gene polymorphism (rs2335052 A > G) on coronary artery disease susceptibility
  • 22 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Bioinformatic analysis of missense SNPs in the KCNJ10 gene associated with neurological disorders
  • 19 Oct 2025
  • Egyptian Journal of Medical Human Genetics
A study on UGT1A1 and ABCG8 gene polymorphism: meta-analysis and bioinformatics approach in the etiology of gallstone disease
  • 18 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Prenatal diagnosis of chromosome 21q homologous rearrangement: integrated cytogenetic and molecular characterization
  • 17 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Late-onset mitochondrial complex IV deficiency, nuclear type 1 associated with the SURF1 gene: a case report
  • 14 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Unveiled SOX2 disorder in a child initially diagnosed as cerebral palsy
  • 23 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Impact of GATA2 gene polymorphism (rs2335052 A > G) on coronary artery disease susceptibility
  • 22 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Bioinformatic analysis of missense SNPs in the KCNJ10 gene associated with neurological disorders
  • 19 Oct 2025
  • Egyptian Journal of Medical Human Genetics
A study on UGT1A1 and ABCG8 gene polymorphism: meta-analysis and bioinformatics approach in the etiology of gallstone disease
  • 18 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Prenatal diagnosis of chromosome 21q homologous rearrangement: integrated cytogenetic and molecular characterization
  • 17 Oct 2025
  • Egyptian Journal of Medical Human Genetics
Late-onset mitochondrial complex IV deficiency, nuclear type 1 associated with the SURF1 gene: a case report
  • 14 Oct 2025
  • Egyptian Journal of Medical Human Genetics

FAQs on Egyptian Journal of Medical Human Genetics