Case Reports in Genetics : Impact Factor & More
eISSN: 2090-6552pISSN: 2090-6544
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Topics Covered on Case Reports in Genetics
Case Reports in Genetics Journal Specifications
| Overview | |
| Publisher | Hindawi Limited |
| Language | English |
| Article Processing Charges | USD 725 |
| Publication Time | 13 |
| Editorial Review Process | Anonymous peer review |
| General Details | |
| Language | English |
| Website URL | Visit website |
| Publication Details | |
| Editorial Review Detail | |
| Information for authors | |
| Author instructions | Visit website |
| Copyright Details | Visit website |
| Deposit Policy | Sherpa/Romeo |
| License type | CC BY |
| OA statement | Visit website |
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Recently Published Papers in Case Reports in Genetics
Phenotypic Spectrum of Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS) in Denmark: A Case Series Characterizing the First Danish Families With the APC Promotor 1B Variant c.‐191T > C
- 8 Jan 2026
- Case Reports in Genetics
Identification of a Novel DNAAF3 Variant in a 54‐Year‐Old Patient With Newly Diagnosed Primary Ciliary Dyskinesia (PCD)
- 6 Jan 2026
- Case Reports in Genetics
Hypokalemic Periodic Paralysis Associated With a Rare CACNA1S Variant (p.Leu1243Val): Expanding the Mutational Spectrum
- 1 Jan 2026
- Case Reports in Genetics
Title not available
- 1 Jan 2026
- Case Reports in Genetics
Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra‐Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature
- 26 Dec 2025
- Case Reports in Genetics
Identification of a Mosaic BMPR1A Pathogenic Variant in Juvenile Polyposis Syndrome: A Case Study and Its Impact on Cancer Screening
- 9 Nov 2025
- Case Reports in Genetics
Phenotypic Spectrum of Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS) in Denmark: A Case Series Characterizing the First Danish Families With the APC Promotor 1B Variant c.‐191T > C
- 8 Jan 2026
- Case Reports in Genetics
Identification of a Novel DNAAF3 Variant in a 54‐Year‐Old Patient With Newly Diagnosed Primary Ciliary Dyskinesia (PCD)
- 6 Jan 2026
- Case Reports in Genetics
Hypokalemic Periodic Paralysis Associated With a Rare CACNA1S Variant (p.Leu1243Val): Expanding the Mutational Spectrum
- 1 Jan 2026
- Case Reports in Genetics
Title not available
- 1 Jan 2026
- Case Reports in Genetics
Rare Presentation of Homozygous SLC20A2 Mutations Causing Intra‐Arterial Cerebral Vasculopathy and Stroke in Infancy: Case Report and Review of the Literature
- 26 Dec 2025
- Case Reports in Genetics
Identification of a Mosaic BMPR1A Pathogenic Variant in Juvenile Polyposis Syndrome: A Case Study and Its Impact on Cancer Screening
- 9 Nov 2025
- Case Reports in Genetics
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