Case Report
Accepted on 28 Aug 2024
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
540,312 articles related to "Polar Bear"
Articles
Case Report
Accepted on 28 Aug 2024
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
Original Research
Accepted on 28 Aug 2024
Exploring neural oscillations during speech perception via surrogate gradient spiking neural networks
in Neural Technology
Frontiers in Neuroscience
doi 10.3389/fnins.2024.1449181
Brief Research Report
Accepted on 28 Aug 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
Original Research
Accepted on 28 Aug 2024
Further validation of the association between MAPT haplotype-tagging polymorphisms and Alzheimer's disease: neuropsychological tests, cerebrospinal fluid biomarkers, and APOE genotype
in Brain Disease Mechanisms
Frontiers in Molecular Neuroscience
doi 10.3389/fnmol.2024.1456670
Editorial
Accepted on 28 Aug 2024
Editorial: [Feeding Difficulties in Newborn Infants and New Approaches in Practice]
in Neonatology
Frontiers in Pediatrics
doi 10.3389/fped.2024.1462493
Original Research
Accepted on 28 Aug 2024
A Combined Transcriptomics and Proteomics Approach Reveals S100A4 as Potential Biomarker for Graves' Orbitopathy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1342205
Brief Research Report
Accepted on 28 Aug 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
Review
Accepted on 28 Aug 2024
Genetic aetiology 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
Original Research
Accepted on 28 Aug 2024
Combination Effects of Environmental Tobacco Smoke Exposure and Nutrients Supplement during pregnancy on obesity in Chinese preschool children
in Pediatric Obesity
Frontiers in Pediatrics
doi 10.3389/fped.2024.1423556
Case Report
Accepted on 28 Aug 2024
Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency of newborn
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1464556
Original Research
Accepted on 28 Aug 2024
TFE3 and TP53 were novel diagnostic biomarkers related to mitochondrial autophagy in chronic rhinosinusitis with nasal polyps
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1423778
Original Research
Accepted on 28 Aug 2024
Identification of a Novel FERMT1 Variant Causing Kindler Syndrome and a Review of the Clinical and Molecular Genetic Features in Chinese Patients
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2024.1425030
Case Report
Accepted on 28 Aug 2024
Case report: Cerebral folate deficiency caused by FOLR1 variant
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2024.1434209
Clinical Trial
Accepted on 28 Aug 2024
Subjective experiences of an Acceptance and Mindfulness-Based Group Intervention (Feel-Good-Group) in young people with early psychosis
in Psychological Therapy and Psychosomatics
Frontiers in Psychiatry
doi 10.3389/fpsyt.2024.1369629
Original Research
Accepted on 28 Aug 2024
Screening of genes co-associated with osteoporosis and chronic HBV infection based on bioinformatics analysis and machine learning
in Cancer Immunity and Immunotherapy
Frontiers in Immunology
doi 10.3389/fimmu.2024.1472354