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

Jing Chen
Shuo Yang
He Wang
Hongjing Wang
Yuanyuan Xiao
Shanling Liu

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

Alexandre Bittar
Philip N. Garner

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

Yu-Ping Tseng
Ya-Sian Chang
Venugopala R. Mekala
Ting-Yuan Liu
Jan-Gowth Chang
Grace S. Shieh

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

Mirjana Babić Leko
Ena Španić Popovački
Nanet Willumsen
Matea Nikolac Perković
Nikolina Pleić
Klara Zubčić
Lea Langer Horvat
Željka Vogrinc
Marina Boban
Fran Borovečki

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

Deniz Anuk Ince
Sahin Takci
Hasan Kilicdag
Ozden Turan

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

Chiaw Ling Chng
Oi Fah Lai
Lay-Leng Seah
Kai-Ling Yong
Yvonne Hsi-Wei Chung
Rochelle Goh
CHE KANG LIM

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

Kun Yu
Weicheng Chen
Yan Chen
Libing Shen
Boxuan Wu
Yuan Zhang
Xiangyu Zhou

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

Olivier HAKIZIMANA
Janvier Hitayezu
Jeanne Primitive Uyisenga
Hope ONOHUEAN
Leonor Palmeira
Vincent Bours
Abdullateef Alagbonsi
Annette UWINEZA

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

Wen-xuan Zhang
Esben Stig Strodl
Wei-Kang Yang
Xiao-Na Yin
Guo-Min Wen
Deng-Li Sun
Danxia Xian
Ya-Fen Zhao
Wei-Qing Chen

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

Patryk Lipiński
Katarzyna Wójcicka-Kowalczyk
Anna Bogdańska
Ewa Ehmke
Magdalena Pajdowska
Katarzyna Skrzypek
Agnieszka Charzewska
Dorota Hoffman

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

Ning Wang
Ying Yuan
Yanjun Jia
Yue Han
Xuemin Yu
Ying Fu
Xiao Li

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

Qiang Zhang
Qi Yang
Fei Shen
LIN LIN Wang
Jing si Luo

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

Qian Wang
Jie Yang
Chunmei Yu
Yao Deng
Qianhui Wen
Hua Yang
Hao Liu
Rong Luo

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

Laura von Hardenberg
Karolina Leopold
Andrea Pfennig
Céline Kuhn
Michèle Kallenbach
Navid Aliakbari
Stephanie Mehl
Andreas Bechdolf

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

Beibei Jiang
Jia Yang
Weiguang Yang
Yue Hu
Linjian Tong
Rui Liu
Lice Liu
Zhiming Sun

Frontiers in Immunology

doi 10.3389/fimmu.2024.1472354

Editorial

Accepted on 28 Aug 2024

Editorial: Domestic Violence and Abuse: increasing global and intersectional understanding

in Implementation Science

Michelle Myall
Sara Morgan
Steph Scott

Frontiers in Health Services

doi 10.3389/frhs.2024.1465688

Navigation group

Articles

Whole exome sequencing reveals a novel splicing variant of ANKRD17 gene in a Chinese male juvenile with developmental delay and transient tic disorder

Exploring neural oscillations during speech perception via surrogate gradient spiking neural networks

Whole-genome sequencing reveals rare variants associated with gout in Taiwanese males

Further validation of the association between MAPT haplotype-tagging polymorphisms and Alzheimer's disease: neuropsychological tests, cerebrospinal fluid biomarkers, and APOE genotype

Editorial: [Feeding Difficulties in Newborn Infants and New Approaches in Practice]

A Combined Transcriptomics and Proteomics Approach Reveals S100A4 as Potential Biomarker for Graves' Orbitopathy

De novo and inherited micro-CNV at 16p13.11 in 21 Chinese Patients with Defective Cardiac Left-right Patterning

Genetic aetiology of Autism Spectrum Disorder in the African population: A Scoping review

Combination Effects of Environmental Tobacco Smoke Exposure and Nutrients Supplement during pregnancy on obesity in Chinese preschool children

Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency of newborn

TFE3 and TP53 were novel diagnostic biomarkers related to mitochondrial autophagy in chronic rhinosinusitis with nasal polyps

Identification of a Novel FERMT1 Variant Causing Kindler Syndrome and a Review of the Clinical and Molecular Genetic Features in Chinese Patients

Case report: Cerebral folate deficiency caused by FOLR1 variant

Subjective experiences of an Acceptance and Mindfulness-Based Group Intervention (Feel-Good-Group) in young people with early psychosis

Screening of genes co-associated with osteoporosis and chronic HBV infection based on bioinformatics analysis and machine learning

Editorial: Domestic Violence and Abuse: increasing global and intersectional understanding