Hui Guo - Concepedia

Author

Hui Guo

Central South University ORCID

Also Known As

Guo Hui, Guo, Hui, H B Guo, H Guo, HUI GUO, Han, Jianjun, Huaiyong Guo, Hui Guo, Jackson, Amanda L, Jackson, Amanda L.

168

Publications

4.5K

Citations

H-Index

Concepts

All Affiliations

Central South University Second Xiangya Hospital of Central South University University of Washington Howard Hughes Medical Institute Chinese Academy of Sciences

About

Hui Guo is an author at Central South University specializing in medicine, genetics, and autism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	29	1.8K
2	Social Sciences	10	10	587
3	Health Sciences	2	2	41
4	Public Health	2	2	248
5	Natural Sciences	1	1	11

Hui Guo

Publications

4.2K

Citations

H-Index

Page 1

	Year	Citations
De novo genic mutations among a Chinese autism spectrum disorder cohort Tianyun Wang, Hui Guo, Bo Xiong, Nature Communications	2016	378
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders Vincenzo Salpietro, Christine L. Dixon, Hui Guo, Nature Communications	2019	236
<i>OsTTG1</i>, a WD40 repeat gene, regulates anthocyanin biosynthesis in rice Xinghai Yang, Junrui Wang, Xiuzhong Xia, The Plant Journal	2021	225
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Nature Communications GeneticsMost GenesDisease Gene IdentificationGenomicsNdd Cases	2020	204
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains Madeleine R. Geisheker, Gabriel Heymann, Tianyun Wang, Nature Neuroscience Neurodevelopmental DisordersNeurodevelopmental Disorder GenesFunctional DomainsDevelopmental BiologyGenetic Disorder	2017	176
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model Hui Guo, Tianyun Wang, Huidan Wu, Molecular Autism	2018	165
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders Holly A.F. Stessman, Marjolein H. Willemsen, Michaela Fencková, The American Journal of Human Genetics Neurodevelopmental DisordersDown SyndromeIntellectual ImpairmentDevelopmental DisabilityAutism Spectrum Disorders	2016	162
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes Hui Guo, Michael Duyzend, Bradley P. Coe, Genetics in Medicine Syndromic AutismMedicineGeneticsPsychiatric GeneticsSevere Phenotypes	2018	138
Recent ultra-rare inherited variants implicate new autism candidate risk genes Amy B. Wilfert, Tychele N. Turner, Shwetha C. Murali, Nature Genetics Syndromic AutismGenetic DisorderGeneticsPsychiatric GeneticsFragile X Spectrum	2021	137
Excessive UBE3A dosage impairs retinoic acid signaling and synaptic plasticity in autism spectrum disorders Xingxing Xu, Chuanyin Li, Xiaobo Gao, Cell Research	2017	128

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