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1.
VarCards2: an integrated genetic and clinical database for ACMG-AMP variant-interpretation guidelines in the human whole genome.
Nucleic Acids Res
; 52(D1): D1478-D1489, 2024 Jan 05.
Article
in English
| MEDLINE | ID: mdl-37956311
2.
Genetic landscape of human mitochondrial genome using whole-genome sequencing.
Hum Mol Genet
; 31(11): 1747-1761, 2022 06 04.
Article
in English
| MEDLINE | ID: mdl-34897451
3.
Performance evaluation of differential splicing analysis methods and splicing analytics platform construction.
Nucleic Acids Res
; 50(16): 9115-9126, 2022 09 09.
Article
in English
| MEDLINE | ID: mdl-35993808
4.
Association between ovarian reserve and spontaneous miscarriage and their shared genetic architecture.
Hum Reprod
; 38(11): 2247-2258, 2023 11 02.
Article
in English
| MEDLINE | ID: mdl-37713654
5.
Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.
Nucleic Acids Res
; 48(D1): D913-D926, 2020 01 08.
Article
in English
| MEDLINE | ID: mdl-31642496
6.
The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 143(7): 2220-2234, 2020 07 01.
Article
in English
| MEDLINE | ID: mdl-32613234
7.
Verbal-spatial IQ discrepancies impact brain activation associated with the resolution of cognitive conflict in children and adolescents.
Dev Sci
; 21(2)2018 03.
Article
in English
| MEDLINE | ID: mdl-28198067
8.
PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Brain
; 144(3): e25, 2021 04 12.
Article
in English
| MEDLINE | ID: mdl-33793763
9.
A Delay-Aware and Reliable Data Aggregation for Cyber-Physical Sensing.
Sensors (Basel)
; 17(2)2017 Feb 17.
Article
in English
| MEDLINE | ID: mdl-28218668
10.
ATP10B variants in Parkinson's disease: a large cohort study in Chinese mainland population.
Acta Neuropathol
; 141(5): 805-806, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33599816
11.
Establishment of machine learning-based tool for early detection of pulmonary embolism.
Comput Methods Programs Biomed
; 244: 107977, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38113803
12.
Risk factors associated with age at onset of Parkinson's disease in the UK Biobank.
NPJ Parkinsons Dis
; 10(1): 3, 2024 Jan 02.
Article
in English
| MEDLINE | ID: mdl-38167894
13.
Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders.
EBioMedicine
; 99: 104928, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-38113761
14.
A comprehensive perspective of Huntington's disease and mitochondrial dysfunction.
Mitochondrion
; 70: 8-19, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36906250
15.
Interactions of genetic risks for autism and the broad autism phenotypes.
Front Psychiatry
; 14: 1110080, 2023.
Article
in English
| MEDLINE | ID: mdl-37102084
16.
Severity of Autism Spectrum Disorder Symptoms Associated with de novo Variants and Pregnancy-Induced Hypertension.
J Autism Dev Disord
; 2022 Nov 29.
Article
in English
| MEDLINE | ID: mdl-36445517
17.
Revealing a novel contributing landscape of ferroptosis-related genes in Parkinson's disease.
Comput Struct Biotechnol J
; 20: 5218-5225, 2022.
Article
in English
| MEDLINE | ID: mdl-36187920
18.
Performance comparison of computational methods for the prediction of the function and pathogenicity of non-coding variants.
Genomics Proteomics Bioinformatics
; 2022 Mar 07.
Article
in English
| MEDLINE | ID: mdl-35272052
19.
Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.
J Autism Dev Disord
; 52(3): 1299-1313, 2022 Mar.
Article
in English
| MEDLINE | ID: mdl-33970367
20.
Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing.
Front Genet
; 13: 810595, 2022.
Article
in English
| MEDLINE | ID: mdl-35601492