A 29 Mainland Chinese cohort of patients with Phelan–McDermid syndrome: genotype–phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes

Na Xu, Hui Lv, Tingting Yang, +9

Orphanet Journal of Rare Diseases

Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study

Yu Sun, Jing Peng, Desheng Liang, +26

Human Mutation

Family MedicineGenetic Testing/Intellectual DisabilityGeneticsGenetic Epidemiology +24

Novel and de novo point and large microdeletion mutation in <i>PRRT2</i> ‐related epilepsy

Yang Li, Cuiping You, Shiyan Qiu, +11

Brain and Behavior

Urea hydrolysis in different farmland soils as affected by long-term biochar application

Rui Zhao, Juying Liu, Na Xu, +3

Frontiers in Environmental Science

BiocharEngineeringBioenergyEnvironmental EngineeringUrea Hydrolysis +13

Time‐ordering <i>japonica/geng</i> genomes analysis indicates the importance of large structural variants in rice breeding

Yu Wang, Fengcheng Li, Fan Zhang, +22

Plant Biotechnology Journal

Dissecting the genetic basis of heterosis in elite super-hybrid rice

Zhizhong Sun, Jianxiang Peng, Qiming Lv, +20

PLANT PHYSIOLOGY

Breeding value estimation of the application of IPA1 and DEP1 to improvement of Oryza sativa L. ssp. japonica in early hybrid generations

Quan Xu, Na Xu, Hai Xu, +4

Molecular Breeding

BiologyQuantitative GeneticsHybridisationMedicineGenetics +10

Genetic and clinical characteristics of 24 mainland Chinese patients with <i>CTNNB1</i> loss‐of‐function variants

Dan Yan, Yu Sun, Na Xu, +2

Molecular Genetics & Genomic Medicine

Multiple nucleotide polymorphism DNA markers for the accurate evaluation of genetic variations

Zhiwei Fang, Lun Li, Junfei Zhou, +16

A novel composition of two heterozygous <i>GFM1</i> mutations in a Chinese child with epilepsy and mental retardation

Cuiping You, Na Xu, Shiyan Qiu, +4

Brain and Behavior