Abdul Murad N, Mohammad Noor Y, Mohd Rani Z, Sulaiman S, Chow Y, Abdullah N
Genes (Basel). 2023; 14(3).
PMID: 36980993
PMC: 10048611.
DOI: 10.3390/genes14030721.
Liu D, Meyer D, Fennessy B, Feng C, Cheng E, Johnson J
Nat Genet. 2023; 55(3):369-376.
PMID: 36914870
PMC: 10011128.
DOI: 10.1038/s41588-023-01305-1.
Clarelli F, Barizzone N, Mangano E, Zuccala M, Basagni C, Anand S
Front Genet. 2022; 12:800262.
PMID: 35047017
PMC: 8762330.
DOI: 10.3389/fgene.2021.800262.
Hao X, Pang J, Li R, Lv L, Liu G, Li Y
Mol Brain. 2020; 13(1):82.
PMID: 32450902
PMC: 7249693.
DOI: 10.1186/s13041-020-00620-6.
Borges M, Rocha C, Carvalho B, Lopes-Cendes I
Genet Mol Biol. 2020; 43(2):e20190270.
PMID: 32343762
PMC: 7198014.
DOI: 10.1590/1678-4685-GMB-2019-0270.
The Progress of CRISPR/Cas9-Mediated Gene Editing in Generating Mouse/Zebrafish Models of Human Skeletal Diseases.
Wu N, Liu B, Du H, Zhao S, Li Y, Cheng X
Comput Struct Biotechnol J. 2019; 17:954-962.
PMID: 31360334
PMC: 6639410.
DOI: 10.1016/j.csbj.2019.06.006.
Identification of rare variants of allergic rhinitis based on whole genome sequencing and gene expression profiling: A preliminary investigation in four families.
Zhang Y, Li J, Zhao Y, Wang C, Zhang L
World Allergy Organ J. 2019; 12(6):100038.
PMID: 31236190
PMC: 6581771.
DOI: 10.1016/j.waojou.2019.100038.
A novel frameshift mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome using targeted exome sequencing.
Zhang L, Peng Y, Ouyang P, Liang Y, Zeng H, Wang N
BMC Med Genet. 2019; 20(1):105.
PMID: 31185933
PMC: 6560744.
DOI: 10.1186/s12881-019-0840-9.
VCF/Plotein: visualization and prioritization of genomic variants from human exome sequencing projects.
Ossio R, Garcia-Salinas O, Anaya-Mancilla D, Garcia-Sotelo J, Aguilar L, Adams D
Bioinformatics. 2019; 35(22):4803-4805.
PMID: 31161195
PMC: 6853650.
DOI: 10.1093/bioinformatics/btz458.
Family-based association tests for rare variants with censored traits.
Qi W, Allen A, Li Y
PLoS One. 2019; 14(1):e0210870.
PMID: 30682063
PMC: 6347269.
DOI: 10.1371/journal.pone.0210870.
Whole exome sequencing for the identification of CYP3A7 variants associated with tacrolimus concentrations in kidney transplant patients.
Sohn M, Kim M, Han N, Kim I, Gim J, Min S
Sci Rep. 2018; 8(1):18064.
PMID: 30584253
PMC: 6305386.
DOI: 10.1038/s41598-018-36085-w.
Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia.
Geier E, Bourdenx M, Storm N, Cochran J, Sirkis D, Hwang J
Acta Neuropathol. 2018; 137(1):71-88.
PMID: 30382371
PMC: 6371791.
DOI: 10.1007/s00401-018-1925-9.
Novel Variants Identified in Multiple Sclerosis Patients From Southern China.
Wang H, Pardeshi L, Rong X, Li E, Wong K, Peng Y
Front Neurol. 2018; 9:582.
PMID: 30140248
PMC: 6094994.
DOI: 10.3389/fneur.2018.00582.
Informatics and machine learning to define the phenotype.
Basile A, Ritchie M
Expert Rev Mol Diagn. 2018; 18(3):219-226.
PMID: 29431517
PMC: 6080627.
DOI: 10.1080/14737159.2018.1439380.
Reconsidering the causality of TIA1 mutations in ALS.
van der Spek R, van Rheenen W, Pulit S, Kenna K, Ticozzi N, Kooyman M
Amyotroph Lateral Scler Frontotemporal Degener. 2017; 19(1-2):1-3.
PMID: 29235362
PMC: 6516059.
DOI: 10.1080/21678421.2017.1413118.
Benchmarking distributed data warehouse solutions for storing genomic variant information.
Wiewiorka M, Wysakowicz D, Okoniewski M, Gambin T
Database (Oxford). 2017; 2017.
PMID: 29220442
PMC: 5504537.
DOI: 10.1093/database/bax049.
Genetics of Spontaneous Intracerebral Hemorrhage.
Falcone G, Woo D
Stroke. 2017; 48(12):3420-3424.
PMID: 29114093
PMC: 5777521.
DOI: 10.1161/STROKEAHA.117.017072.
Lumbosacral stenosis in Labrador retriever military working dogs - an exomic exploratory study.
Mukherjee M, Jones J, Yao J
Canine Genet Epidemiol. 2017; 4:12.
PMID: 29085643
PMC: 5651560.
DOI: 10.1186/s40575-017-0052-6.
Multiple analyses indicate the specific association of NR1I3, C6 and TNN with low hip BMD risk.
Han Y, Zhao L, Lin Y, He H, Tian Q, Zhu W
J Genet Genomics. 2017; 44(6):327-330.
PMID: 28629900
PMC: 5822710.
DOI: 10.1016/j.jgg.2017.05.004.
PhredEM: a phred-score-informed genotype-calling approach for next-generation sequencing studies.
Liao P, Satten G, Hu Y
Genet Epidemiol. 2017; 41(5):375-387.
PMID: 28560825
PMC: 5564424.
DOI: 10.1002/gepi.22048.