| Predicting drug response of tumors from integrated genomic profiles by deep neural networks |
19 |
| Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients |
18 |
| Application of Neural Networks for classification of Patau, Edwards, Down, Turner and Klinefelter Syndrome based on first trimester maternal serum screening data, ultrasonographic findings and patient demographics |
16 |
| GENT2: an updated gene expression database for normal and tumor tissues |
15 |
| HLA and proteasome expression body map |
15 |
| Identification of glioblastomagene prognosis modules based on weighted gene co-expression network analysis |
13 |
| Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics |
13 |
| Identification of biomarkers for amyotrophic lateral sclerosis by comprehensive analysis of exosomal mRNAs in human cerebrospinal fluid |
13 |
| Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes |
12 |
| Logistic regression model training based on the approximate homomorphic encryption |
12 |
| Placental microRNAs in pregnancies with early onset intrauterine growth restriction and preeclampsia: potential impact on gene expression and pathophysiology |
12 |
| The role of long non-coding RNAs in the pathogenesis of hereditary diseases |
12 |
| Genes CEP FOXD FOXF GNAO GRIA and KCNA5 as potential diagnostic biomarkers in colorectal cancer |
12 |
| Association between changes in gene signatures expression and disease activity among patients with systemic lupus erythematosus |
11 |
| Integration of genomic copy number variations and chemotherapy-response biomarkers in pediatric sarcoma |
10 |
| Computational identification of deleterious synonymous variants in human genomes using a feature-based approach |
10 |
| Integrative genomic analyses of APOBEC-mutational signature, expression and germline deletion of APOBEC3 genes, and immunogenicity in multiple cancer types |
10 |
| Genetic analysis of Wnt/PCP genes in neural tube defects |
10 |
| Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing |
10 |
| Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES) |
10 |
| Targeted next generation sequencing as a tool for precision medicine |
9 |
| Novel link prediction for large-scale miRNA-lncRNA interaction network in a bipartite graph |
9 |
| Early gut microbiota signature of aGvHD in children given allogeneic hematopoietic cell transplantation for hematological disorders |
9 |
| Identification of potential biomarkers related to glioma survival by gene expression profile analysis |
9 |
| MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip |
9 |
| A novel gene selection algorithm for cancer classification using microarray datasets |
8 |
| Predict drug sensitivity of cancer cells with pathway activity inference |
8 |
| DNA methylation in the APOE genomic region is associated with cognitive function in African Americans |
8 |
| Clinical providers' experiences with returning results from genomic sequencing: an interview study |
8 |
| Comprehensive analysis of key genes and microRNAs in radioresistant nasopharyngeal carcinoma |
8 |
| High-throughput RNA sequencing from paired lesional- and non-lesional skin reveals major alterations in the psoriasis circRNAome |
8 |
| Enhancer variants associated with Alzheimer's disease affect gene expression via chromatin looping |
8 |
| Mutational load in carotid body tumor |
7 |
| A meta-analysis of public microarray data identifies biological regulatory networks in Parkinson's disease |
7 |
| Exome analysis of carotid body tumor |
7 |
| Analysis of microbial sequences in plasma cell-free DNA for early-onset breast cancer patients and healthy females |
7 |
| Transcriptomic signatures reveal immune dysregulation in human diabetic and idiopathic gastroparesis |
7 |
| The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington's disease brain |
7 |
| Alternative cleavage and polyadenylation of genes associated with protein turnover and mitochondrial function are deregulated in Parkinson's, Alzheimer's and ALS disease |
7 |
| The added value of WES reanalysis in the field of genetic diagnosis: lessons learned from 200 exomes in the Lebanese population |
7 |
| Whole exome sequencing in three families segregating a pediatric case of sarcoidosis |
6 |
| Selecting precise reference normal tissue samples for cancer research using a deep learning approach |
6 |
| Defining housekeeping genes suitable for RNA-seq analysis of the human allograft kidney biopsy tissue |
6 |
| Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood |
6 |
| Hepatic transcriptomic signatures of statin treatment are associated with impaired glucose homeostasis in severely obese patients |
6 |
| Elevated neoantigen levels in tumors with somatic mutations in the HLA-A, HLA-B, HLA-C and B2M genes |
6 |
| Genomics of lipid-laden human hepatocyte cultures enables drug target screening for the treatment of non-alcoholic fatty liver disease |
6 |
| Pathway networks generated from human disease phenome |
5 |
| Min-redundancy and max-relevance multi-view feature selection for predicting ovarian cancer survival using multi-omics data |
5 |
| Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records |
5 |
