Linh Ngo - Concepedia

Author

Linh Ngo

Australian Regenerative Medicine Institute

Also Known As

L. Ngo, Linh Bao Ngo, Linh Ngo, Ngo, Linh

Publications

494

Citations

H-Index

Concepts

All Affiliations

Australian Regenerative Medicine Institute Monash University EMBL Australia Harry Perkins Institute of Medical Research The University of Western Australia

About

Linh Ngo is an author at Australian Regenerative Medicine Institute specializing in developmental biology, medicine, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	320
2	Social Sciences	5	5	320
3	Cell Biology	3	3	264
4	Cellular Physiology	2	2	239
5	Molecular Biology	1	1	25

Linh Ngo

Publications

493

Citations

H-Index

Page 1

	Year	Citations
Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities Martin W. Breuss, Julian Ik‐Tsen Heng, Karine Poirier, Cell Reports Brain DevelopmentCytoskeletonStructural Brain AbnormalitiesCellular NeurobiologyMammalian Cortex	2012	199
Age‐related changes in climbing behavior and neural circuit physiology in <i>Drosophila</i> Vicente Martínez, C.S. Javadi, E. Ngo, Developmental Neurobiology	2007	81
TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons Linh Ngo, Matilda Haas, Zhengdong Qu, Human Molecular Genetics Brain DevelopmentSynaptic TransmissionNeurodevelopmentCytoskeletonCellular Neurobiology	2014	40
De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation Matilda Haas, Linh Ngo, Shanshan Li, Cell Reports Brain DevelopmentGeneticsDe Novo MutationsCellular NeurobiologyDevelopmental Neuroscience	2016	37
Bacurd1/Kctd13 and Bacurd2/Tnfaip1 are interacting partners to Rnd proteins which influence the long-term positioning and dendritic maturation of cerebral cortical neurons Ivan Gladwyn‐Ng, Lieven Huang, Linh Ngo, Neural Development	2016	30
The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome Shanshan Li, Zhengdong Qu, Matilda Haas, Scientific Reports	2016	26
Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway Simon Edvardson, Guoling Tian, Hayley Cullen, Human Molecular Genetics NeurogenomicsGeneticsRadial MigrationMolecular BiologyMolecular Genetics	2016	25
Bacurd2 is a novel interacting partner to Rnd2 which controls radial migration within the developing mammalian cerebral cortex Ivan Gladwyn‐Ng, Shanshan Li, Zhengdong Qu, Neural Development	2015	21
Disease‐associated missense variants in ZBTB18 disrupt DNA binding and impair the development of neurons within the embryonic cerebral cortex Isabel Hemming, Olivier Clément, Ivan Gladwyn‐Ng, Human Mutation Brain DevelopmentGeneticsGenomic MechanismDisease Gene IdentificationEpigenetics	2019	19
mRNA export factors store nascent transcripts within nuclear speckles as an adaptive response to transient global inhibition of transcription Tobias Williams, Ewa M. Michalak, Kirstyn T. Carey, Molecular Cell	2025	15

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