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Zhu, Wenmiao
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1

A recurrent single‐exon deletion inTBCKmight be under‐recog..:

Dai, Hongzheng ; Zhu, Wenmiao ; Yuan, Bo...
Human Mutation.  43 (2022)  12 - p. 1816-1823 , 2022
Link: https://doi.org/10.1002/..
 
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2

Sequencing individual genomes with recurrent genomic disord..:

Yuan, Bo ; Schulze, Katharina V. ; Assia Batzir, Nurit...
Genome Medicine.  14 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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3

Retrospective analysis of a clinical exome sequencing cohor..:

Chen, Chun-An ; Lattier, John ; Zhu, Wenmiao...
Genetics in Medicine.  24 (2022)  2 - p. 364-373 , 2022
Link: https://doi.org/10.1016/..
 
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4

Barth syndrome caused by a novel TAZ deletion through an al..:

Vossaert, Liesbeth ; Lattier, John ; Zhu, Wenmiao...
Molecular Genetics and Metabolism.  132 (2021)  - p. S93-S95 , 2021
Link: https://doi.org/10.1016/..
 
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5

Combined Genome Sequencing and RNA Analysis Reveals and Cha..:

Bodle, Ethan E. ; Zhu, Wenmiao ; Velez-Bartolomei, Frances...
Pediatric Neurology.  114 (2021)  - p. 16-20 , 2021
Link: https://doi.org/10.1016/..
 
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6

PPP3CAtruncating variants clustered in the regulatory domai..:

Panneerselvam, Sugi ; Wang, Julia ; Zhu, Wenmiao...
Clinical Genetics.  100 (2021)  2 - p. 227-233 , 2021
Link: https://doi.org/10.1111/..
 
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7

CNVs cause autosomal recessive genetic diseases with or wit..:

Yuan, Bo ; Wang, Lei ; Liu, Pengfei...
Genetics in Medicine.  22 (2020)  10 - p. 1633-1641 , 2020
Link: https://doi.org/10.1038/..
 
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8

Correction to: De novo and inherited TCF20 pathogenic varia..:

The DDD study ; Vetrini, Francesco ; McKee, Shane...
Genome Medicine.  11 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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9

De novo and inherited TCF20 pathogenic variants are associa..:

The DDD study ; Vetrini, Francesco ; McKee, Shane...
Genome Medicine.  11 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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10

Biallelic mutation ofFBXL7suggests a novel form of Hennekam..:

Boone, Philip M. ; Paterson, Scott ; Mohajeri, Kiana...
American Journal of Medical Genetics Part A.  182 (2019)  1 - p. 189-194 , 2019
Link: https://doi.org/10.1002/..
 
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11

Two de novo novel mutations in one SHANK3 allele in a patie..:

Zhu, Wenmiao ; Li, Jianli ; Chen, Stella...
American Journal of Medical Genetics Part A.  176 (2018)  4 - p. 973-979 , 2018
Link: https://doi.org/10.1002/..
 
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12

Haploinsufficiency of the E3 ubiquitin-protein ligase gene ..:

Zhang, Jing ; Gambin, Tomasz ; Yuan, Bo...
Human Genetics.  136 (2017)  4 - p. 377-386 , 2017
Link: https://doi.org/10.1007/..
 
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13

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ..:

Zhang, Jing ; Gambin, Tomasz ; Yuan, Bo...
Human Genetics.  136 (2017)  8 - p. 1009-1011 , 2017
Link: https://doi.org/10.1007/..
 
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14

CRIPT exonic deletion and a novel missense mutation in a fe..:

Leduc, Magalie S. ; Niu, Zhiyv ; Bi, Weimin...
American Journal of Medical Genetics Part A.  170 (2016)  8 - p. 2206-2211 , 2016
Link: https://doi.org/10.1002/..
 
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15

Mutations in PURA Cause Profound Neonatal Hypotonia, Seizur..:

Lalani, Seema R. ; Zhang, Jing ; Schaaf, Christian P....
The American Journal of Human Genetics.  95 (2014)  5 - p. 579-583 , 2014
Link: https://doi.org/10.1016/..
 
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