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Journal of Clinical & Medical Genomics

ISSN: 2472-128X

Open Access

Citations Report

Below are the list of articles published in Journal of Clinical & Medical Genomics that have been cited by eminent researchers all around the world.

Genetic Bleeding Risk Score (GBRS) for Patients on Oral Anticoagulant Therapy

NRP1 Activates NF-κB Signaling Pathway and Initiates Proliferation in Keratinocytes

Thrombosis Therapy: Focus on Antiplatelet Agents

IRE-1 Dependent Expression of Phosphoribosyl Pyrophosphate Synthetase Genes in U87 Glioma Cells: Effect of Glucose or Glutamine Deprivation

Making Use of Aberrant and Nonsense: Aberrant Splicing and Nonsense-Mediated Decay as Targets for Personalized Medicine

Noonan Syndrome and Systemic Lupus Erythematosus: Association or Risk Factor?

Reverse Direction Method: A Possible Tool to Link Animal Models with Corresponding Human Diseases and Disorders

Mitochondrial Genomes and Frameshift Mutations: Hidden Stop Codons, their Functional Consequences and Disease Associations

Establishment of Simple and Efficient Methods for Plant Material Harvesting and Storage to Allow DNA Extraction from a Myrtaceae Species with Medicinal Potential

Present and Future RNA-based Approaches to Medical Genomics

Statin Muscle Toxicity and Genetic Risk Factors

The Crosstalk between Micro RNA and Iron Homeostasis

Meta-Analysis of Interleukin Polymorphisms and NSAID Usage Indicates Correlations to the Risk of Developing Cancer

Trapping Enhancers by Transgenic Expression of BACs Engineered in Bacteria with loxP Transposons

Targeting Cancer Related Genes by Multiplex PCR Followed by High Throughput Parallel Sequencing

Detection of Jak2 V617f Mutation, Secondary to the Presence of Bcr-Abl1 Translocation in a Patient with Chronic Myeloid Leukemia: Report of a Case and Review of the Literature

Does Resistin Gene Polymorphisms +299 (G>A) Participate in Insulin Resistance in Egyption Non-obese Type 2 Diabetes?

Cardiac Resynchronization Therapy and Left Ventricular Diastolic Function

Genetic Mutations in Human Esophageal and Gastric Cardia Cancers Detected by Ampliseq Sequencing

SNPs, Linkage Disequilibrium and Transcriptional Factor Binding Sites Associated with Acute Mountain Sickness among Han Chinese at the Qinghai-Tibetan Plateau

Mutation Profiling in Mitochondrial D-Loop Associated with Stomach Cancer and Tobacco Consumers

The Power of Knowledge Facing the Power of Position: Case Study about the Conflict of Power

Epigenetics in Clinical Practice: Characterizing Patient and Provider Experiences with MTHFR Polymorphisms and Methylfolate

Cytogenomic Delineation and Clinical Characterization of Three Cases of MECP2 Duplication Syndrome

Burden and Determinants of Hypertension in Rural Pondicherry India

Eukaryotic Plasmids with Toxoplasma gondii Dense Granule Antigen (GRA 5) and Microneme 3 (MIC3) Genes as a Cocktail DNA Vaccine and Evaluation of Immune Responses in BALB/C Mice

Variants of PGIS and PPARγ in Idiopathic Pulmonary Arterial Hypertension

Human Papillomavirus: Flow Cytometry Detection and PCR Analysis, A Comparison Study

Phenotyping and 16S rDNA Analysis after Biofield Treatment on Citrobacter braakii: A Urinary Pathogen

Association of P2X7R Functional Expression and Gene Polymorphisms with Systemic Lupus Erythematosus

Genetic Markers Association in Autism Spectrum Disorder

Gene Variability between Perineural-Positive and Perineural-Negative Squamous Cell Skin Cancers

Design and Analysis of Ensemble Classifier for Gene Expression Data of Cancer

Association of Protein Tyrosine Phosphatase 1B (PTPN1) Gene Polymorphisms (1023C>A and 467T>C) With Type 2 Diabetes: A Case-Control Study

The Impact of Parental Separation and Divorce on the Health Status of Children, and the Ways to Improve it

Ethical Perceptions with Regard to Pre-implantation Genetic Diagnosis (PGD) from the Perspective of Selected Medical Professionals in Malaysia

Dermoscopic-pathologic Correlation of Bowen Disease: A Case Series and Review of the Literatures

Which Skin Lupus Criteria are of More Value in Determining the Disease: A Greater View with the Help of Direct Immune Fluorescent (DIF)

Extending Life: From Stem Cells to Gene Therapy

TCF7L2 rs7903146 Gene Variation Is Associated with Risk of Type 2 Diabetes in Turkish Population

Rejuvenation of Aged Hematopoietic Stem Cells

Obesity Kills: Can Genetics Help in the Targeting of Obesity Prevention?

Chromosomal Microarray Genetic Testing – A Qualitative Investigation among Parents of Children with Autism Spectrum Disorders in Rural North Carolina

Autism Spectrum Disorders are not linked to β-2-Adrenergic Receptor Agonists Treatment for Preterm Labor/Asthma

Severe Phenotype of De Barsy Syndrome in Two Siblings with Novel Mutations in the ALDH18A1 Gene

Applications of Next-Generation Sequencing in Cancer Research and Molecular Diagnosis

Re: Autism Spectrum Disorders are not Linked to β2 Adrenergic Receptor Agonists Treatment for Preterm Labour/Asthma - Still should be Administered <72 h

Polymorphisms of Cytochrome P450 2E1 Gene and Gastric Cancer Risk: A Case Control Study from West Bengal, India

Usefulness of Fetopathological Examination in the Diagnosis of Skeletal Dysplasias

Evaluation of ApoE Genotyping Using Saliva-Derived DNA

Congenital Multicystic Renal Dysplasia as Part of Caudal Regression Syndrome: Complixities and Considerations

Inherited Cardiomyopathies: From Genotype to Phenotype

Retrotransposons as a Genomic Risk Factor in Psychiatric Diseases

ONCOTARGET (ONCOALVO), a Custom NGS Panel for Therapeutic Decision in Solid Tumors Refractory to Conventional Therapy

Vitamin D Receptor Genetic Variants among CKD Patients of South Indian Population

Association between Vitamin D Receptor (VDR) Gene Polymorphisms and Type-2 Diabetes Mellitus in Population of Pakistan

Henna-Induced Haemolysis in an Un-diagnosed G6PD Deficient Arabian Baby-Case Report

Hypomelanosis of Ito and De novo Interstitial 15q11.2q13.3 Triplication in Bulgarian Family

Relationship between Human Papillomavirus and Tumor Markers Expression among Women in Two Tertiary Hospitals in Bayelsa State, Nigeria

Social Determinants of Diabetes.

Three Novel CYP1B1 Mutations (p.L480P, p.S476P, p.R175P) in Primary Congenital Glaucoma Cases Residing in Eastern Iran

overview of journal of clinical and medical genomics

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