Shen Gu, Ph.D.

Affiliations: 
2013 The Chinese University of Hong Kong, Hong Kong, Hong Kong 
Area:
Biomedical Engineering, Epidemiology, General
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"Shen Gu"

Parents

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Chan W. Yee grad student 2013 Chinese University of Hong Kong
 (Regulation and Action of miRNA-199a in Health and Diseases.)
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Publications

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Robak LA, Du R, Yuan B, et al. (2020) Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease. Neurology. Genetics. 6: e498
Bahrambeigi V, Song X, Sperle K, et al. (2019) Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants. Genome Medicine. 11: 80
Gu S, Chen CA, Rosenfeld JA, et al. (2019) Truncating variants in UBAP1 associated with childhood-onset nonsyndromic hereditary spastic paraplegia. Human Mutation
Pehlivan D, Bayram Y, Gunes N, et al. (2019) The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance. American Journal of Human Genetics
Dharmadhikari AV, Ghosh R, Yuan B, et al. (2019) Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases. Genome Medicine. 11: 30
Li AH, Hanchard NA, Azamian M, et al. (2019) Genetic architecture of laterality defects revealed by whole exome sequencing. European Journal of Human Genetics : Ejhg
Song X, Beck CR, Du R, et al. (2018) Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements. Genome Research
Grochowski CM, Gu S, Yuan B, et al. (2018) Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes. Human Mutation
Gambin T, Akdemir ZC, Yuan B, et al. (2016) Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort. Nucleic Acids Research
Gu S, Szafranski P, Akdemir ZC, et al. (2016) Mechanisms for Complex Chromosomal Insertions. Plos Genetics. 12: e1006446
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