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Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of CTTNBP2 in a Quad Family Affected by Autism Spectrum Disorder.
Xie Y et al.
Children (basel, Switzerland), 2022
36670631 (PubMed )
Supplement: children-10-00080-s001.zip › children-2044403-supplementary › children-2044403-Supplementary › Supplementary_Tables-R1.xlsx › STS5
Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.
Sebate B et al.
Plos One, 2021
33770142 (PubMed )
Supplement: pone.0249324.s003.xlsx › 8772__III-8__
Tumor mutation burden and recurrent tumors in hereditary lung cancer.
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Cancer Medicine, 2019
30941903 (PubMed )
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PRIMA-1MET-induced neuroblastoma cell death is modulated by p53 and mycn through glutathione level.
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Journal of Experimental & Clinical Cancer Research : Cr, 2019
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Supplement: 13046_2019_1066_MOESM1_ESM.xlsx › BE-2C
Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing.
Kim YC et al.
Plos One, 2017
28076423 (PubMed )
Supplement: pone.0167581.s003.xlsx › Egyptian-specific
Molecular Guided Therapy Provides Sustained Clinical Response in Refractory Choroid Plexus Carcinoma.
Cornelius A et al.
Frontiers in Pharmacology, 2017
28993730 (PubMed )
Supplement: Table3.xlsx › Germline
Single-cell mRNA sequencing identifies subclonal heterogeneity in anti-cancer drug responses of lung adenocarcinoma cells.
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Genome Biology, 2015
26084335 (PubMed )
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XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
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Plos One, 2015
25905921 (PubMed )
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