Neurodevelopment: parental influences, in utero exposures, and genetics, volume II

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CASE REPORT

Published on 04 Feb 2026

Case Report: Prenatal imaging and genetic integrated diagnosis of SCN2A encephalopathy—a case of cryptical cortical dysplasia caused by a loss-of-function frameshift genetic variant

Linyan Zhu
Mei Chen
Huiqing Ding
Minyue Dong

doi 10.3389/fnins.2026.1698102

555 views

ORIGINAL RESEARCH

Published on 07 Jan 2026

A novel variant in SIAH1 associated with autosomal dominant Buratti-Harel syndrome

Hong Zheng
Lan Zhang
Fuwei Li

doi 10.3389/fnins.2025.1677646

857 views

ORIGINAL RESEARCH

Published on 12 Aug 2025

Oxytocin enhances oligodendrocyte development and improves social deficits in autistic rats

Min Wen
Shuang Zheng
Hongbo Luo
Yi Zhang
Bo Zhou

doi 10.3389/fnins.2025.1624932

2,856 views

ORIGINAL RESEARCH

Published on 22 Jul 2025

Clinical and genetic characteristics associated with dual-positive gene variations

Li Wang
Jinghe Shi
Xiaojing Yin
Pingyun Qiao
Fuwei Li
Weixing Feng

doi 10.3389/fnins.2025.1516589

1,974 views

ORIGINAL RESEARCH

Published on 03 Jun 2025

Association of genetic variants, protein domains, and phenotypes in the ZMIZ1 syndromic neurodevelopmental disorder

Kendall E. Cormier
Belle L. Kantor
Rajan K C
Xabier Blanco-Fernandez
Maria J. Galazo

doi 10.3389/fnins.2025.1605762

3,013 views
1 citation

ORIGINAL RESEARCH

Published on 16 Apr 2025

Pregnant maternal brain dorsal anterior cingulate cortex choline/creatine ratios on 1H-MR spectroscopy in opioid exposure

Jonathan A. Class
Ramana V. Vishnubhotla
Yi Zhao
Nathan Ooms
David M. Haas
Senthilkumar Sadhasivam
Rupa Radhakrishnan

doi 10.3389/fnins.2025.1569558

2,239 views

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