Publications by authors named "Huidan Wu"

15Publications

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Nat Commun 2020 10 1;11(1):4932. Epub 2020 Oct 1.

Department of Genome Sciences, University of Washington, Seattle, WA, USA.

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http://dx.doi.org/10.1038/s41467-020-18723-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7530681PMC
October 2020

Excess of RALGAPB de novo variants in neurodevelopmental disorders.

Eur J Med Genet 2020 Nov 24;63(11):104041. Epub 2020 Aug 24.

Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School Of Life Sciences, Central South University, Changsha, Hunan, China; Hunan Key Laboratory of Animal Models for Human Diseases, Changsha 410078, China. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2020.104041DOI Listing
November 2020

Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders.

J Mol Neurosci 2020 Jun 10. Epub 2020 Jun 10.

Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.

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http://dx.doi.org/10.1007/s12031-020-01615-7DOI Listing
June 2020

Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.

Clin Genet 2020 02 14;97(2):338-346. Epub 2019 Nov 14.

Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, China.

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http://dx.doi.org/10.1111/cge.13665DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307605PMC
February 2020

Disruptive variants of associate with autism and interfere with neuronal development and synaptic transmission.

Sci Adv 2019 09 25;5(9):eaax2166. Epub 2019 Sep 25.

Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.

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http://dx.doi.org/10.1126/sciadv.aax2166DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6760934PMC
September 2019

POGZ de novo missense variants in neuropsychiatric disorders.

Mol Genet Genomic Med 2019 09 25;7(9):e900. Epub 2019 Jul 25.

Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/mgg3.900
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http://dx.doi.org/10.1002/mgg3.900DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732319PMC
September 2019

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.

Nat Commun 2019 07 12;10(1):3094. Epub 2019 Jul 12.

Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.

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http://dx.doi.org/10.1038/s41467-019-10910-wDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6626132PMC
July 2019

Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.

Mol Genet Genomic Med 2019 07 14;7(7):e00789. Epub 2019 Jun 14.

Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, China.

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http://dx.doi.org/10.1002/mgg3.789DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625093PMC
July 2019

Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development.

J Genet Genomics 2019 05 18;46(5):247-257. Epub 2019 May 18.

Center of Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, 410078, China; School of Life Sciences and Technology, Xinjiang University, Ürümqi, 830046, China; CAS Center for Excellence in Brain Science and Intelligence Technology (CEBSIT), Chinese Academy of Sciences, Shanghai, 200030, China. Electronic address:

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http://dx.doi.org/10.1016/j.jgg.2019.04.002DOI Listing
May 2019

Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders.

Am J Med Genet A 2018 12 9;176(12):2668-2676. Epub 2018 Dec 9.

Center for Medical Genetics & Hunan Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.a.40666
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http://dx.doi.org/10.1002/ajmg.a.40666DOI Listing
December 2018