受强制性开放获取政策约束的文章 - Pei-Lung Chen了解详情
无法在其他位置公开访问的文章：3 篇
Linkage and association on 8p21. 2‐p21. 1 in schizophrenia
MD Fallin, VK Lasseter, Y Liu, D Avramopoulos, J McGrath, PS Wolyniec, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 …, 2011
强制性开放获取政策： US National Institutes of Health
Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing
YH Lin, CC Wu, TY Hsu, WY Chiu, CJ Hsu, PL Chen
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 771, 1-5, 2015
强制性开放获取政策： US National Institutes of Health
A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration
HY Chen, HI Lin, CL Hsu, PL Chen, CY Huang, SC Teng, CH Lin
Parkinsonism & Related Disorders 109, 105353, 2023
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：14 篇
Tuberous sclerosis complex diagnostic criteria update: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
H Northrup, DA Krueger, S Roberds, K Smith, J Sampson, B Korf, ...
Pediatric neurology 49 (4), 243-254, 2013
强制性开放获取政策： US National Institutes of Health
Tuberous sclerosis complex surveillance and management: recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
DA Krueger, H Northrup, S Roberds, K Smith, J Sampson, B Korf, ...
Pediatric neurology 49 (4), 255-265, 2013
强制性开放获取政策： US National Institutes of Health
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
PL Chen, SR Shih, PW Wang, YC Lin, CC Chu, JH Lin, SC Chen, ...
Nature communications 6 (1), 7633, 2015
强制性开放获取政策： US National Institutes of Health
Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia
PL Chen, D Avramopoulos, VK Lasseter, JA McGrath, MD Fallin, KY Liang, ...
The American Journal of Human Genetics 84 (1), 21-34, 2009
强制性开放获取政策： US National Institutes of Health
Familiality of novel factorial dimensions of schizophrenia
JA McGrath, D Avramopoulos, VK Lasseter, PS Wolyniec, MD Fallin, ...
Archives of general psychiatry 66 (6), 591-600, 2009
强制性开放获取政策： US National Institutes of Health
Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women
Y Liu, PL Chen, J McGrath, P Wolyniec, D Fallin, G Nestadt, KY Liang, ...
Psychiatric genetics 20 (4), 184-186, 2010
强制性开放获取政策： US National Institutes of Health
Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling
Y Liu, X Pham, L Zhang, P Chen, G Burzynski, DM McGaughey, S He, ...
G3: Genes, Genomes, Genetics 5 (1), 61-72, 2015
强制性开放获取政策： US National Institutes of Health
Neuregulin 3 knockout mice exhibit behaviors consistent with psychotic disorders
LN Hayes, A Shevelkin, M Zeledon, G Steel, PL Chen, C Obie, A Pulver, ...
Molecular neuropsychiatry 2 (2), 79-87, 2016
强制性开放获取政策： US National Institutes of Health
KCNN2 polymorphisms and cardiac tachyarrhythmias
CC Yu, T Chia-Ti, PL Chen, CK Wu, FC Chiu, FT Chiang, PS Chen, ...
Medicine 95 (29), e4312, 2016
强制性开放获取政策： US National Institutes of Health
Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes
CJ Lee, TH Chen, AMW Lim, CC Chang, JJ Sie, PL Chen, SW Chang, ...
Communications Biology 5 (1), 1175, 2022
强制性开放获取政策： UK Medical Research Council
Identification and functional studies of regulatory variants responsible for the association of NRG3 with a delusion phenotype in schizophrenia
M Zeledón, N Eckart, M Taub, H Vernon, M Szymanski, R Wang, PL Chen, ...
Molecular neuropsychiatry 1 (1), 36-46, 2015
强制性开放获取政策： US National Institutes of Health
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct
YH Lin, CC Wu, YH Lin, YC Lu, CS Chen, TC Liu, PL Chen, CJ Hsu
The Journal of Molecular Diagnostics 21 (1), 138-148, 2019
强制性开放获取政策： US National Institutes of Health
Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population
YH Lee, CY Tsai, YS Lu, PH Lin, YT Chiang, TH Yang, JSJ Hsu, CJ Hsu, ...
Genes 14 (4), 880, 2023
强制性开放获取政策： US National Institutes of Health
Functional Variants in DPYSL2 Sequence Increase Schizophrenia Risk and Suggest a Link To mTOR Signaling
Y Liu, X Pham, L Zhang, P Chen, G Burzynski, DM McGaughey, S He, ...
强制性开放获取政策： US National Institutes of Health
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