Associated Papers
Proteogenomic analysis reveals adaptive strategies for alleviating the consequences of aneuploidy in cancer.
Bökenkamp JE et al.
The Embo Journal, 2025
39930267 (PubMed )
Supplement: 44318_2025_372_MOESM8_ESM.xlsx › AADAPT_TCGA
IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta.
Hytönen MK et al.
Plos Genetics, 2025
39804930 (PubMed )
Supplement: pgen.1011328.s007.xlsx › ncbi_dataset_ROH_genes
Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement.
LaFlamme CW et al.
Nature Communications, 2024
39107278 (PubMed )
Supplement: 41467_2024_50159_MOESM6_ESM.xlsx › SupplementaryData3B
GATA6 coordinates cross-talk between BMP10 and oxidative stress axis in pulmonary arterial hypertension.
Toyama T et al.
Scientific Reports, 2023
37087509 (PubMed )
Supplement: 41598_2023_33779_MOESM3_ESM.xlsx › Suppl_Table_1
Characterization of methionine dependence in melanoma cells.
Garg S et al.
Biorxiv : the Preprint Server for Biology, 2023
37066392 (PubMed )
Supplement: media-2.xlsx › A101D
Complete sequencing of a cynomolgus macaque major histocompatibility complex haplotype.
Karl JA et al.
Genome Research, 2023
36854669 (PubMed )
Supplement: supp_gr.277429.122_Supplemental_Table_S1.xlsx › Supplemental_Table_S1
MondoA drives malignancy in B-ALL through enhanced adaptation to metabolic stress.
Sipol A et al.
Blood, 2022
33908607 (PubMed )
Supplement: mmc1.xlsx › 1kb
VPS39-deficiency observed in type 2 diabetes impairs muscle stem cell differentiation via altered autophagy and epigenetics.
Davegårdh C et al.
Nature Communications, 2021
33893273 (PubMed )
Supplement: 41467_2021_22068_MOESM8_ESM.xlsx › A._expression_data
Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes.
Skol AD et al.
Elife, 2020
33164750 (PubMed )
Supplement: elife-59980-fig2-data3.xlsx › delta_DwoC_DwC_pvalue_all_2017-
Tob2 phosphorylation regulates global mRNA turnover to reshape transcriptome and impact cell proliferation.
Chen CA et al.
Rna (new York, N.y.), 2020
32404348 (PubMed )
Supplement: supp_073528.119_Supplemental_Table_S4.xlsx › Control_or_vector_half-life
PWAS: proteome-wide association study-linking genes and phenotypes by functional variation in proteins.
Brandes N et al.
Genome Biology, 2020
32665031 (PubMed )
Supplement: 13059_2020_2089_MOESM3_ESM.xlsx › 12__Monocyte_count_
Integrating Gene and Protein Expression Reveals Perturbed Functional Networks in Alzheimer's Disease.
Canchi S et al.
Cell Reports, 2019
31340147 (PubMed )
Supplement: NIHMS1585244-supplement-2.xlsx › Table_S1_Full_DEG_List
Inositol trisphosphate receptor-mediated Ca2+ signalling stimulates mitochondrial function and gene expression in core myopathy patients.
Suman M et al.
Human Molecular Genetics, 2018
29701772 (PubMed )
Supplement: ddy149_supp.zip › ddy149-suppl_data › p3369__male_child__MmD_.xlsx › p3369_male_child_MmD_ALL
MEF2C transcription factor is associated with the genetic and epigenetic risk architecture of schizophrenia and improves cognition in mice.
Mitchell AC et al.
Molecular Psychiatry, 2018
28115742 (PubMed )
Supplement: NIHMS834845-supplement-Supplementary_Tables.xlsx › ST5
Sequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II.
Norman PJ et al.
Genome Research, 2017
28360230 (PubMed )
Supplement: supp_gr.213538.116_Supplemental_Table_S3.xlsx › A_CDS
GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells.
Livide G et al.
European Journal of Human Genetics : Ejhg, 2015
24916645 (PubMed )
Supplement: ejhg201481x4.xls › down-regulated
A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia.
Vemula SR et al.
Molecular Genetics & Genomic Medicine, 2014
24936516 (PubMed )
Supplement: mgg30002-0261-SD1.docx
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