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Zhu, Wenmiao
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1

Retrospective analysis of a clinical exome sequencing cohor..:

Chen, Chun-An ; Lattier, John ; Zhu, Wenmiao...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957292/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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2

A recurrent single-exon deletion in TBCK might be under-rec..:

Dai, Hongzheng ; Zhu, Wenmiao ; Yuan, Bo...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772143/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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3

Sequencing individual genomes with recurrent genomic disord..:

Yuan, Bo ; Schulze, Katharina V ; Assia Batzir, Nurit...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9526336/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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4

Sequencing individual genomes with recurrent genomic disord..:

Yuan, Bo ; Schulze, Katharina V ; Assia Batzir, Nurit...
Yuan, Bo, Schulze, Katharina V., Assia Batzir, Nurit, et al. "Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits." Genome Medicine, 14, (2022) Springer Nature: https://doi.org/10.1186/s13073-022-01113-y..  , 2022
Link: https://hdl.handle.net/1..
 
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5

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

Yuan, Bo ; Wang, Lei ; Liu, Pengfei...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445517/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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6

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

Vetrini, Francesco ; McKee, Shane ; Rosenfeld, Jill A...
10.1186/s13073-019-0623-0.  , 2019
Link: https://hdl.handle.net/1..
 
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7

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

Vetrini, Francesco ; McKee, Shane ; Rosenfeld, Jill A...
10.1186/s13073-019-0630-1.  , 2019
Link: https://hdl.handle.net/1..
 
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8

Two De Novo Novel Mutations in One SHANK3 Allele in a Patie..:

Zhu, Wenmiao ; Li, Jianli ; Chen, Stella...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956516/.  , 2018
Link: http://www.ncbi.nlm.nih...
 
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9

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

Leduc, Magalie S ; Niu, Zhiyv ; Bi, Weimin...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725961/.  , 2016
Link: http://www.ncbi.nlm.nih...
 
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10

De Novo Truncating Mutations in AHDC1 in Individuals with S..:

Xia, Fan ; Bainbridge, Matthew N ; Tan, Tiong Yang...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC.  , 2014
Link: http://www.ncbi.nlm.nih...
 
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11

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

Lalani, Seema R ; Zhang, Jing ; Schaaf, Christian P...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225583/.  , 2014
Link: http://www.ncbi.nlm.nih...
 
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12

Deadenylation is prerequisite for P-body formation and mRNA..:

Zheng, Dinghai ; Ezzeddine, Nader ; Chen, Chyi-Ying A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447901.  , 2008
Link: http://www.ncbi.nlm.nih...
 
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13

Versatile applications of transcriptional pulsing to study ..:

Chen, Chyi-Ying A ; Yamashita, Yukiko ; Chang, Tsung-Cheng...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1986818.  , 2007
Link: http://www.ncbi.nlm.nih...
 
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14

Human TOB, an Antiproliferative Transcription Factor, Is a ..:

Ezzeddine, Nader ; Chang, Tsung-Cheng ; Zhu, Wenmiao...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2169145.  , 2007
Link: http://www.ncbi.nlm.nih...
 
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15

UNR, a new partner of poly(A)-binding protein, plays a key ..:

Chang, Tsung-Cheng ; Yamashita, Akio ; Chen, Chyi-Ying A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC514181.  , 2004
Link: http://www.ncbi.nlm.nih...
 
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