Review
Published on 26 Sep 2024
Genetic etiology of autism spectrum disorder in the African population: a scoping review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1431093
- 3,144 views
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1,830 articles
Case Report
Published on 26 Sep 2024
Case report: Two siblings with very late onset of holocarboxylase synthase deficiency and a mini-review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1249480
- 799 views
Brief Research Report
Published on 25 Sep 2024
Whole-genome sequencing reveals rare variants associated with gout in Taiwanese males
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1423714
- 1,229 views
Original Research
Published on 25 Sep 2024
Integrating transcriptomics, eQTL, and Mendelian randomization to dissect monocyte roles in severe COVID-19 and gout flare
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1385316
- 2,080 views
Original Research
Published on 18 Sep 2024
A combined transcriptomics and proteomics approach reveals S100A4 as a potential biomarker for Graves’ orbitopathy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1342205
- 1,265 views
Brief Research Report
Published on 18 Sep 2024
Monozygotic triplets with juvenile-onset autoimmunity and 18p microdeletion involving PTPRM
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1437566
- 1,105 views
- 1 citation
Original Research
Published on 16 Sep 2024
Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1438375
- 1,523 views
Original Research
Published on 13 Sep 2024
Low prevalence of HIV in the northern Cameroon: contribution of some AIDS restriction genes and potential implications for gene therapy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1447971
- 1,282 views
Case Report
Published on 12 Sep 2024
Case report: Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency in newborns
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1464556
- 1,194 views
- 1 citation
Case Report
Published on 11 Sep 2024
Case report: Unveiling genetic and phenotypic variability in Nonketotic hyperglycinemia: an atypical early onset case associated with a novel GLRX5 variant
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1432272
- 1,380 views
Case Report
Published on 09 Sep 2024
Case report: Whole exome sequencing reveals a novel splicing variant of ANKRD17 gene in a Chinese male juvenile with developmental delay and transient tic disorder
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1422469
- 1,100 views
Brief Research Report
Published on 09 Sep 2024
De novo and inherited micro-CNV at 16p13.11 in 21 Chinese patients with defective cardiac left-right patterning
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1458953
- 1,322 views
Original Research
Published on 05 Sep 2024
Development and clinical validation of a novel detection kit for α-thalassemia in southern Chinese
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1457248
- 1,143 views
Case Report
Published on 04 Sep 2024
Case report: A novel TLK2 variant with a neuropsychiatric phenotype from a Chinese family
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1419027
- 1,152 views
Case Report
Published on 02 Sep 2024
Case report: Second report of neuromuscular syndrome caused by biallelic variants in ASCC3
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1382275
- 1,290 views
Correction
Published on 30 Aug 2024
Corrigendum: Evidence for a genetic contribution to the ossification of spinal ligaments in ossification of posterior longitudinal ligament and diffuse idiopathic skeletal hyperostosis: a narrative review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1477788
- 836 views