Articles

The fragile X syndrome–autism comorbidity: what do we really know?

in Genetics of Common and Rare Diseases

• Leonard Abbeduto
• Andrea McDuffie
• Angela John Thurman

The Brain in Oral Clefting: A Systematic Review With Meta-Analyses

• Kinga A. Sándor-Bajusz
• Asaad Sadi
• Eszter Varga
• Györgyi Csábi
• Georgios N. Antonoglou
• Szimonetta Lohner

Case report: A novel nonsense mutation in the MARVELD2 gene causes nonsyndromic hearing loss in a China family

in Human and Medical Genomics

• Chuican Huang
• Zhenning Huang
• Ping Wang
• Xijing Wu
• Qiaomiao Zhou
• Jun Ding
• Qing Luo
• Weijia Wu
• Xialin Fan
• Lichun Fan

DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and Palate

in Developmental Epigenetics

• Juan I. Young
• Susan Slifer
• Jacqueline T. Hecht
• Susan H. Blanton

Integration of multimodal data in the developing tooth reveals candidate regulatory loci driving human odontogenic phenotypes

in Systems Integration

• Emma Wentworth Winchester
• Alexis Hardy
• Justin Cotney

A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype Correlation

in Cellular Neuropathology

• Thomas Parzefall
• Alexandra Frohne
• Martin Koenighofer
• Juergen Neesen
• Franco Laccone
• Julia Eckl-Dorna
• Jonathan J. Waters
• Markus Schreiner
• Sami Samir Amr
• Emma Ashton

A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability

in Behavioral and Psychiatric Genetics

• Babylakshmi Muthusamy
• Anikha Bellad
• Pramada Prasad
• Aravind K. Bandari
• G. Bhuvanalakshmi
• R. M. Kiragasur
• Satish Chandra Girimaji
• Akhilesh Pandey

Phenotypic and Genotypic Features of Thai Patients With Nonsyndromic Tooth Agenesis and WNT10A Variants

in Craniofacial Biology and Dental Research

• Charinya Kanchanasevee
• Kanokwan Sriwattanapong
• Thanakorn Theerapanon
• Sermporn Thaweesapphithak
• Wanna Chetruengchai
• Thantrira Porntaveetus
• Vorasuk Shotelersuk

Identification of Novel Variants in Cleft Palate-Associated Genes in Brazilian Patients With Non-syndromic Cleft Palate Only

in Molecular and Cellular Pathology

• Renato Assis Machado
• Hercílio Martelli-Junior
• Silvia Regina de Almeida Reis
• Erika Calvano Küchler
• Rafaela Scariot
• Lucimara Teixeira das Neves
• Ricardo D. Coletta

Case report: Expansion of phenotypic and genotypic data in TENM3-related syndrome: Report of two cases

in Genetics of Common and Rare Diseases

• Fen Lu
• Xin Xu
• Bixia Zheng
• Chunli Wang
• Wei Zhou
• Jian Tang
• Xiaoke Zhao

A review of the mechanisms underlying the role of the GIPC3 gene in hereditary deafness

• Xinxin Li
• Lin Shi
• Liang Wang

Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathy

in Pediatric Otolaryngology

• Lan Jiang
• Hongen Xu
• Danhua Liu
• Sen Zhang
• Ying Xu

Atypical cortical thickness and folding of language regions in Chinese nonsyndromic cleft lip and palate children after speech rehabilitation

in Applied Neuroimaging

• Shi Wang
• Lei Fang
• Guofu Miao
• Zhichao Li
• Bo Rao
• Hua Cheng

SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis

in Epilepsy

• Jiangwei Ding
• Xinxiao Li
• Haiyan Tian
• Lei Wang
• Baorui Guo
• Yangyang Wang
• Wenchao Li
• Feng Wang
• Tao Sun

Disruption of fos causes craniofacial anomalies in developing zebrafish

in Morphogenesis and Patterning

• Lorena Maili
• Bhavna Tandon
• Qiuping Yuan
• Simone Menezes
• Frankie Chiu
• S. Shahrukh Hashmi
• Ariadne Letra
• George T. Eisenhoffer
• Jacqueline T. Hecht

Research progress in delineating the pathological mechanisms of GJB2-related hearing loss

in Cellular Neuropathology

• Yujun Wang
• Yuan Jin
• Qiong Zhang
• Ying Xiong
• Xiang Gu
• Shan Zeng
• Wei Chen