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Hongyu Long

7PUBLICATIONS

12CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsElectrochemical energy storage and conversionGlycoconjugatesNeonatology

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Publications (7)

Sort by Publication Date:

|Sep 23, 2022

Clinical features of <i>NOTCH2NLC</i>-related neuronal intranuclear inclusion disease.

Yun Tian, Lu Zhou, Jing Gao

|Sep 08, 2022

Cohen syndrome in two patients from China.

Jiaoe Gong, Lily Zhang, Yanwei Long

|Jul 20, 2022

A de novo inframe deletion variant in CAPZA2 tentacle domain with global developmental delay and secondary microcephaly.

Shanyu Pi, Xiao Mao, Hongyu Long

|Aug 31, 2021

The second DDOST-CDG patient with lactose intolerance, developmental delay, and situs inversus totalis.

Shanyu Pi, Jiaoe Gong, Wenbiao Xiao

|Jul 11, 2020

A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy.

Hongjun Fang, Xi Zhang, Bo Xiao

|Jun 11, 2020

CpG methylation signature defines human temporal lobe epilepsy and predicts drug-resistant.

Wenbiao Xiao, Chaorong Liu, Kuo Zhong

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Frequent Collaborators

1 joint publications

Chenhui Mao

1 joint publications

Liling Dong

1 joint publications

Guohua Zhao

1 joint publications

Yacen Hu

1 joint publications

Li Feng

1 joint publications

Lili Long

1 joint publications

Ji-Feng Guo

1 joint publications

Hong Jiang

1 joint publications

Lu Shen

1 joint publications

Wenbiao Xiao

Frequent Collaborators

1 joint publications

Chenhui Mao

1 joint publications

Liling Dong

1 joint publications

Guohua Zhao

1 joint publications

Yacen Hu

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