| Association of CAPN10 SNP-19 with Metabolic Traits in Mexican Patients with Type 2 Diabetes |
2 |
| Structural Similarity and Probabilistic Neural Network Based Human G-Band Chromosomes Classification |
2 |
| Association between Selected microRNA SNPs and Breast Cancer Risk in a Vietnamese Population |
2 |
| Analysis of Genetic Alterations in Colorectal Cancer (CRC) Patients in South Indian Population |
1 |
| Clinical Significance of PRR13 Expression in Colorectal Cancer and Its Correlation with Patients' Prognosis |
1 |
| In-Silico Target Prediction for hsa-mir-27a and Identification of Genes Involved in Breast Cancer |
1 |
| Predicting Potential Targets of miR-130a in Venous Thromboembolism Based on a Target Score Method |
1 |
| Frequency of Anaplastic Lymphoma Kinase (ALK) Rearrangement in Turkish Patients with Non-small Cell Lung Carcinoma |
0 |
| The GP Method can be Effective as a Screening Test Before STR Typing |
0 |
| Risk of Lung Cancer and Genetic Variations of TERT and CLPTM1L Genes: A Case-Control Study in an Iranian Population |
0 |
| High Frequency of Severe Phenylketonuria in Jalisco, Mexico |
0 |
| Investigation of IncRNA Biomarkers in Postmenopausal Osteoporosis Using an IncRNA-Mediated, Competitive Endogenous RNA Network |
0 |
| Gibbs Sampling Method Identifies Disrupted Pathways and Genes in Periodontitis |
0 |
| Identification of IncRNA-Mediated ceRNA Network Reveals Potential Biomarkers for Early Stage Acute Myocardial Infarction |
0 |
| Integrated Analyses of Gene Profile Digs out Suitable Biomarkers for Ankylosing Spondylitis using Three Different Methods |
0 |
| Identification of Hub Genes and Pathways in Acute Respiratory Distress Syndrome Based on Differential Expression Network |
0 |
| Characterization of miRNA-mRNA-Pathway Network Predicts Significant Biomarkers for Renal Injury in Kidney Biopsies from Patients with Lupus Nephritis |
0 |
| Altered DNA Methylations May Contribute to Rheumatoid Arthritis |
0 |
| Abnormal DNA Methylations Associated with Allergic Asthma Children |
0 |
| Expression Quantitative Trait Loci for ALMS1 and Their Influence on the Symptoms of Alstrom Syndrome |
0 |
| Incidental Finding of Lynch Syndrome Role of Genetic Counselling |
0 |
| Evaluation of Pregnancies in 25 Families with Balanced/Unbalanced Chromosomal Translocations |
0 |
| Matrilineal and Patrilineal Genetic Continuity of Two Iron Age Individuals from a Pazyryk Culture Burial |
0 |
| Selected ABCB1 Single Nucleotide Polymorphisms and its Haplotype - Connection with Development of Depression and Treatment Efficacy |
0 |
| Endothelial Nitric Oxide Synthase Gene Variants and Susceptibility to Chronic Myeloid Leukemia (Ph plus ) |
0 |
| Methylenetetrahydrofolate Reductase (MTHFR) and Angiotensin Converting Enzyme (ACE) Gene Variations in Link with Breast Cancer in Jammu Region of Jammu and Kashmir State |
0 |
| Mutational Analysis of TYR Gene Causing Oculocutaneous Albinism in Families from District Peshawar |
0 |
| Risk Assessment and Psychological Implications of Genetic Counselling |
0 |
| Identification of Novel Mutation delC336 and insC376 in Exon 4-of LDLR Gene in Vietnamese Patients with High-Blood-Cholesterol |
0 |
| Review of the Status of Knowledge on the Genetic Susceptibility of Indian Women for Polycystic Ovary Syndrome |
0 |
| Association of MTHFR C677T with Idiopathic Recurrent Pregnancy Loss in Anhui Province of China |
0 |
| Duplication of Isoderivative Ph Chromosome with Tp53 Deletion in a Case of Imatinib Resistant CML |
0 |
| Cytogenetics of Recurrent Spontaneous Abortions: A Study of 250 Products of Conception |
0 |
| Association of an Endothelial Nitric Oxide Synthase Gene Polymorphism with Diabetic Retinopathy |
0 |
| Non-invasive Prenatal Testing for Hemoglobin Bart's Hydrops Fetalis Syndrome (SEA Deletion) Using Cell-Free Fetal DNA in Maternal Plasma: Systematic Review and Meta-analysis |
0 |
| ITG alpha 4 Inhibition by miR-30d as a Potential Target in Relapsing Form of MS Therapy |
0 |
| Association between MTHFR C677/APOB G10708B Polymorphisms and Excess Body Weight in Blood Donors |
0 |
| Paternal Age: The Considerable Confounding Risk Factor in Chromosomal Aneuploidies |
0 |
| Melanocortin 2 Receptor Mutations and Clinical Significance in Case of Cushing Syndrome and Subclinical Cushing Syndrome and Primary Aldosteronism |
0 |
| Linkage Analysis of Autosomal Recessive Non-syndromic Mental Retardation Locus in Pakistani Families |
0 |
| Importance of Prenatal Diagnosis in Patients with History of Chromosomal Abnormalities |
0 |
| Roles of p53 Codon 72 and miR-502-binding Site in the 3 '-UTR of SET8 SNPs in Urinary Bladder Cancer Predisposition in Turkish Population |
0 |
| Quality Assessment of DNA Extraction Methods from Formalin-Fixed Paraffin-Embedded Tissues |
0 |
| The Identification of Sub-pathways in Juvenile Idiopathic Arthritis by Integrating Expression Profiles between IncRNA-mRNA and Pathway Topologies |
0 |
| Identification of Core Modules and Genes in Rheumatoid Arthritis Following Infliximab Therapy |
0 |
| The Prediction of miRNAs Target Genes Associated with Rheumatoid Arthritis by Using Novel Prediction Algorithm Called Targetscore |
0 |
| Targetscore used to Reveal Potential Targets of Mir-26a in Osteoporosis by Integrating MicroRNA Over-expression and Microarray Data |
0 |
| Subpathway Strategy used to Extract Significant Subpathways Competitively Regulated by IncRNAs in Atopic Dermatitis Treated by Cyclosporine A Based on IncRNA-mRNA Expression Data and Pathway Topologies |
0 |
| Revealing Dysregulated Modules and Genes for Postmenopausal Osteoporosis Based on Module Inference and Attract Method |
0 |
| Prediction of Key Transcription Facto rs-Genes Regulatory Network of Ankylosing Spondylitis Based on Transcription Factor Prognosis System |
0 |
