Pei-Lung Chen
Affiliations: | 2009 | Johns Hopkins University, Baltimore, MD |
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"Pei-Lung Chen"Mean distance: 14.3 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentorRichard L. Huganir | grad student | 2009 | Johns Hopkins | |
(Genetic contributions to schizophrenia: Candidate genes on 10q.) |
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Publications
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Yeh HM, Liao MH, Chu CL, et al. (2020) Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermia. Journal of the Formosan Medical Association = Taiwan Yi Zhi |
Wu CC, Tsai CY, Lin YH, et al. (2019) Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population. Genes. 10 |
Lin CH, Chen PL, Tai CH, et al. (2019) A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing. Movement Disorders : Official Journal of the Movement Disorder Society |
Erdenechuluun J, Lin YH, Ganbat K, et al. (2018) Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations. Plos One. 13: e0209797 |
Hsiung YC, Lin PC, Chen CS, et al. (2018) Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan. Atherosclerosis. 277: 440-447 |
Lin YH, Wu CC, Lin YH, et al. (2018) Targeted next-generation sequencing facilitates genetic diagnosis and provides novel pathogenetic insights into deafness with enlarged vestibular aqueduct. The Journal of Molecular Diagnostics : Jmd |
Wu PC, Lin YH, Tsai LF, et al. (2018) ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies. Transfusion |
Chen YF, Chang YY, Lan MY, et al. (2017) Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review. Bmc Neurology. 17: 191 |
Lin HC, Lin CH, Chen PL, et al. (2017) Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: a case report and literature review. Bmc Neurology. 17: 186 |
Lin YH, Lin YH, Lu YC, et al. (2017) A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss. Scientific Reports. 7: 7551 |