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Author Details
Full Name
Weichen Zhou
Affiliation
Chengdu First People's Hospital
ORCID
Career Start Year
2011
Papers
32
H Index
14
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36778249
Somatic nuclear mitochondrial DNA insertions are prevalent in the human brain and accumulate over time in fibroblasts.
bioRxiv
2023
36626876
The Utility of the Ultrasound "Superimposed-Line" Sign at the Junction of the Vomer and Maxilla in First-Trimester Screening for Fetal Cleft Palate: A Case-Control Study.
Fetal Diagn Ther
2023
34117247
Cas9 targeted enrichment of mobile elements using nanopore sequencing.
Nat Commun
2021
33771168
Hypoxia modulation by dual-drug nanoparticles for enhanced synergistic sonodynamic and starvation therapy.
J Nanobiotechnology
2021
33632895
Haplotype-resolved diverse human genomes and integrated analysis of structural variation.
Science
2021
34706748
SquiggleNet: real-time, direct classification of nanopore signals.
Genome Biol
2021
34593003
Correction to: Hypoxia modulation by dual-drug nanoparticles for enhanced synergistic sonodynamic and starvation therapy.
J Nanobiotechnology
2021
33984634
Dual mitigation of immunosuppression combined with photothermal inhibition for highly effective primary tumor and metastases therapy.
Biomaterials
2021
32541955
A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
33575633
Characterization of nuclear mitochondrial insertions in the whole genomes of primates.
NAR Genom Bioinform
2020
31785024
Alleviation Effects and Mechanisms of Low-intensity Focused Ultrasound on Pain Triggered by Soft Tissue Injury.
J Ultrasound Med
2020
31853540
Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology.
Nucleic Acids Res
2020
33065790
Application of conventional ultrasound coupled with virtual touch tissue imaging and quantification in the assessment of muscle strength.
Ann Palliat Med
2020
32699374
Author Correction: A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
31087076
Treatment Effect of Low-Intensity Pulsed Ultrasound on Benzene- and Cyclophosphamide-Induced Aplastic Anemia in Rabbits.
Phys Ther
2019
30835868
Low-Intensity Pulsed Ultrasound Relieves Mild and Severe Myelosuppression Induced by Cyclophosphamide in Rabbits.
J Ultrasound Med
2019
30835554
Synergies of accelerating differentiation of bone marrow mesenchymal stem cells induced by low intensity pulsed ultrasound, osteogenic and endothelial inductive agent.
Artif Cells Nanomed Biotechnol
2019
29511625
A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models.
FEBS Open Bio
2018
30466390
knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable.
BMC Bioinformatics
2018
28804549
Treatment effect of low intensity pulsed ultrasound on leukopenia induced by cyclophosphamide in rabbits.
Am J Transl Res
2017
28334874
Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders.
Hum Mol Genet
2017
28328162
Predictive model for inflammation grades of chronic hepatitis B: Large-scale analysis of clinical parameters and gene expressions.
Liver Int
2017
25398944
CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis.
Hum Mol Genet
2015
26169839
Combination of low-intensity pulsed ultrasound and C3H10T1/2 cells promotes bone-defect healing.
Int Orthop
2015
25564734
TBX6 null variants and a common hypomorphic allele in congenital scoliosis.
N Engl J Med
2015
25324539
Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.
Hum Mol Genet
2015
24472662
Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity.
BMC Genomics
2014
25705150
Genome architecture and its roles in human copy number variation.
Genomics Inform
2014
23474816
Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms.
Hum Mol Genet
2013
21275653
Association of heme oxygenase-1 gene polymorphisms with essential hypertension and blood pressure in the Chinese Han population.
Genet Test Mol Biomarkers
2011
21309757
Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population.
Ann Hum Genet
2011
21721974
Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks.
Clin Exp Hypertens
2011
1 - 32 of 32
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The Broad Institute of MIT and Harvard
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Rice University
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