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GLOBAL MEDICAL GENETICS : Impact Factor & More

eISSN: 2699-9404pISSN: 2699-9404
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GLOBAL MEDICAL GENETICS Journal Specifications

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Overview
Publisher THIEME MEDICAL PUBL INC
Language English
Frequency Quarterly
Publication Time14
Editorial Review ProcessAnonymous peer review
General Details
LanguageEnglish
FrequencyQuarterly
Publication Start Year2020
Publisher URLVisit website
Website URLVisit website
Publication Details
Publication Time 14
Editorial Review Detail
Editorial TeamVisit website
Review ProcessAnonymous peer review
Review UrlVisit website
Information for authors
Author instructionsVisit website
Copyright DetailsVisit website
Deposit PolicySherpa/Romeo
License typeCC BY, CC BY-NC-ND
OA statementVisit website
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Recently Published Papers in GLOBAL MEDICAL GENETICS

CD73 targeted combination therapy reverses PD-1 inhibitor resistance in CD73-high PD-L1-negative NSCLC: Evidence from pleural effusion organoids.
  • 1 Dec 2026
  • Global medical genetics
Premature Pubarche in an Infant with CHD4-Neurodevelopmental Disorder (Sifrim-Hitz-Weiss Syndrome): Expanding the Endocrine Phenotype
  • 1 Oct 2026
  • Global Medical Genetics
Epstein\u2013Barr virus-associated T/NK-cell lymphoproliferative diseases with heterozygous IL10RA variants: two cases with pedigree analysis and a literature review
  • 1 Oct 2026
  • Global Medical Genetics
Toe walking in children with variants in myopathy-associated genes: A retrospective descriptive cohort study.
  • 1 Sep 2026
  • Global medical genetics
Toe Walking: A Descriptive Comparison of Clinical Characteristics Across Sensorimotor and Sensory Neuropathy-Associated Genes
  • 1 Sep 2026
  • Global Medical Genetics
Corrigendum to “Global comprehensive transcriptomic and proteomic analyses of murine terminal erythroid differentiation” [Glob. Med. Genet. 12 (2025) 100083
  • 1 Sep 2026
  • Global Medical Genetics
CD73 targeted combination therapy reverses PD-1 inhibitor resistance in CD73-high PD-L1-negative NSCLC: Evidence from pleural effusion organoids.
  • 1 Dec 2026
  • Global medical genetics
Premature Pubarche in an Infant with CHD4-Neurodevelopmental Disorder (Sifrim-Hitz-Weiss Syndrome): Expanding the Endocrine Phenotype
  • 1 Oct 2026
  • Global Medical Genetics
Epstein\u2013Barr virus-associated T/NK-cell lymphoproliferative diseases with heterozygous IL10RA variants: two cases with pedigree analysis and a literature review
  • 1 Oct 2026
  • Global Medical Genetics
Toe walking in children with variants in myopathy-associated genes: A retrospective descriptive cohort study.
  • 1 Sep 2026
  • Global medical genetics
Toe Walking: A Descriptive Comparison of Clinical Characteristics Across Sensorimotor and Sensory Neuropathy-Associated Genes
  • 1 Sep 2026
  • Global Medical Genetics
Corrigendum to “Global comprehensive transcriptomic and proteomic analyses of murine terminal erythroid differentiation” [Glob. Med. Genet. 12 (2025) 100083
  • 1 Sep 2026
  • Global Medical Genetics

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