Editorial
Published on 17 Jul 2023
Editorial: Rare dyslipidemias
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1248435
- 2,602 views
- 5 citations
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1,758 articles
Articles
Editorial
Published on 17 Jul 2023
Editorial: Unravelling the basis of non-invasive prenatal screening results
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1247764
- 1,284 views
Original Research
Published on 13 Jul 2023
Clinical and mutational spectrum of paediatric Charcot-Marie-Tooth disease in a large cohort of Chinese patients
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1188361
- 2,684 views
- 3 citations
Editorial
Published on 12 Jul 2023
Editorial: Building capacity for sickle cell disease research and healthcare
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1226589
- 1,755 views
Original Research
Published on 12 Jul 2023
A novel IBA57 variant is associated with mitochondrial iron–sulfur protein deficiency and necrotizing myelopathy in dogs
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1190222
- 2,583 views
- 2 citations
Original Research
Published on 07 Jul 2023
Functional identification of two novel variants and a hypomorphic variant in ASS1 from patients with Citrullinemia type I
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1172947
- 3,058 views
- 2 citations
Original Research
Published on 05 Jul 2023
PCDH7 as the key gene related to the co-occurrence of sarcopenia and osteoporosis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1163162
- 4,784 views
- 5 citations
Original Research
Published on 04 Jul 2023
Myeloid lineage cells evince distinct steady-state level of certain gene groups in dependence on hereditary angioedema severity
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1123914
- 2,732 views
Review
Published on 03 Jul 2023
“HLA-C: evolution, epigenetics, and pathological implications in the major histocompatibility complex”
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1206034
- 5,469 views
- 7 citations
Brief Research Report
Published on 29 Jun 2023
Mitochondrial depletion syndrome type 3: the Lebanese variant
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1215083
- 2,694 views
- 4 citations
Original Research
Published on 29 Jun 2023
A chromosomal microarray analysis-based laboratory algorithm for the detection of genetic etiology of early pregnancy loss
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1203891
- 2,895 views
- 2 citations
Original Research
Published on 29 Jun 2023
A novel PKHD1 splicing variant identified in a fetus with autosomal recessive polycystic kidney disease
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1207772
- 2,713 views
- 2 citations
Case Report
Published on 27 Jun 2023
Parental gonadossomatic mosaicism in HIVEP2-related intellectual disability and impact on genetic counseling–case report
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1156847
- 2,891 views
Case Report
Published on 26 Jun 2023
Case report: Chorea and cognitive decline in a young woman: instrumental and genetic assessment of a case originally diagnosed as multiple sclerosis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1129289
- 2,421 views
Case Report
Published on 23 Jun 2023
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1174046
- 2,835 views
- 5 citations
Original Research
Published on 21 Jun 2023
Genotype and clinical characteristics of patients with Wolfram syndrome and WFS1-related disorders
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1198171
- 4,689 views
- 7 citations