Egyptian Journal of Medical Human Genetics
SpringerOpen
About the journal
Egyptian Journal of Medical Human Genetics is an open-access journal published by SpringerOpen in United Kingdom, publishing in english. It is listed in DOAJ according to the sources read. Declared review time at DOAJ: 18 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- SpringerOpen
- ISSN
- 1110-8630 · 2090-2441
- Country
- United Kingdom
- Languages
- english
- Access
- Open access
- Articles in DOAJ
- 1215
- Declared review time
- 18 weeks
- Declared peer-review model
- double_blind
- Official website
- https://jmhg.springeropen.com
Index listings
- DOAJ · 2016-05-25
- Indexing
- DOAJ
- APC
- —
- Declared review time (DOAJ)
- 18 weeks — journal-declared only (not measured)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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- Choose your university and rank below ↓
Methodology signals (dated facts from their sources)
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Articles in DOAJ
1215
Most recent article
last month
Average review time (journal-declared via DOAJ)
18weeks
Works in OpenAlex
1447
Last recorded publication year
2026
h-index
36
i10-index
281
From OpenAlex open data (CC0).
Editorial & policy10
- Last DOAJ review date
- 2026-03-17
- Added to DOAJ
- 2016-05-25
- Declared plagiarism screening
- Declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Open references deposited at Crossref
- 0%
- ORCID iDs in current deposits
- 0%
- Peer-review policy
- View policy
Identity & continuity3
- Alternate titles
- Al-Maǧallaẗ al-Miṣriyyaẗ al-’ilmiyyaẗ lil-amrāḍ al-wirāṯiyyaẗ
- Source type
- journal
- NLM unique ID (PubMed)
- 101151137
Classification4
Subjects (DOAJ)
LCC codes
Subject areas
- Cancer-related molecular mechanisms research
- Cancer-related molecular mechanisms research
- RNA modifications and cancer
- RNA modifications and cancer
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Hemoglobinopathies and Related Disorders
- MicroRNA in disease regulation
Show all subjects (50)
- Hemoglobinopathies and Related Disorders
- MicroRNA in disease regulation
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Folate and B Vitamins Research
- Folate and B Vitamins Research
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Iron Metabolism and Disorders
- Metabolism and Genetic Disorders
- Iron Metabolism and Disorders
- Metabolism and Genetic Disorders
- Circular RNAs in diseases
- Circular RNAs in diseases
- Epigenetics and DNA Methylation
- Congenital heart defects research
- Congenital heart defects research
- Epigenetics and DNA Methylation
- Acute Myeloid Leukemia Research
- Diabetes and associated disorders
- Acute Myeloid Leukemia Research
- Genetic Associations and Epidemiology
- Liver Disease Diagnosis and Treatment
- Diabetes and associated disorders
- Liver Disease Diagnosis and Treatment
- RNA Research and Splicing
- Blood groups and transfusion
- Blood groups and transfusion
- RNA Research and Splicing
- Genetic Associations and Epidemiology
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Computational Drug Discovery Methods
- Mitochondrial Function and Pathology
- Mitochondrial Function and Pathology
- Computational Drug Discovery Methods
- Autism Spectrum Disorder Research
- Autism Spectrum Disorder Research
Keywords (DOAJ)
- biochemistry
- cell biology
- molecular genetics
- structural biology
- protein deficiencies
- hereditary pathogenesis
Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.
The journal's record in other sources:Web of Science MJLDOAJ