Stacey S. Cherny

The University of Hong Kong, San Francisco, Hong Kong Island, Hong Kong 
statistical genetics
"Stacey Cherny"
Mean distance: 18.48 (cluster 7)


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John C. DeFries grad student 1989-1995 CU Boulder
 (second supervisor)
David W. Fulker grad student 1989-2005 CU Boulder
 (Structural models for the development of specific cognitive abilities in the Colorado Adoption Project)
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Wong JKL, Gui H, Kwok M, et al. (2018) Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis. Neurology. Genetics. 4: e245
Tang CS, Zhuang X, Lam WY, et al. (2018) Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing. European Journal of Human Genetics : Ejhg
Hsu JSJ, So M, Tang CSM, et al. (2017) De novo mutations in Caudal Type Homeo Box Transcription Factor 2 (CDX2) in patients with persistent cloaca. Human Molecular Genetics
Gui H, Li M, Sham PC, et al. (2017) Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics
Tang CS, Dattani S, So MT, et al. (2017) Actionable secondary findings from whole-genome sequencing of 954 East Asians. Human Genetics
Gui H, Kwan JS, Sham PC, et al. (2017) Sharing of Genes and Pathways Across Complex Phenotypes: A Multilevel Genome-Wide Analysis. Genetics
Cheng G, Chung PH, Chan EK, et al. (2017) Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis. Bmc Medical Genomics. 10: 22
Cheung CY, Tang CS, Xu A, et al. (2017) An Exome-Chip Association Analysis in Chinese Reveals a Functional Missense Variant of Gckr that Regulates Fgf21 Levels. Diabetes
Gui H, Schriemer D, Cheng WW, et al. (2017) Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes. Genome Biology. 18: 48
Porsch RM, Merello E, De Marco P, et al. (2016) Sacral agenesis: a pilot whole exome sequencing and copy number study. Bmc Medical Genetics. 17: 98
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