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Welcome to International Journal of Genetic Medicine and Gene Therapy

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International Journal of Genetic Medicine and Gene Therapy is an international, independent, peer reviewed journal that aim to publish original research articles and covers most up-to-date excellent quality research articles on genetics and gene therapy including molecular genetics, gene transfer and its application in gene and cell therapy. The journal focus on the application of genetic syndrome , human gene therapy, gene mapping & covering all biological, clinical and medical aspects of potential gene therapies , genetic disorders which includes treatment of arthritis, inherited diseases, cancers and various infectious disease and promise to unite the diverse organ based specialties.

The online peer reviewed journal which dedicate to publish the original submission of perspectives Articles, review, mini-review, case report, short communications, letters. IJGMGT provides excellent and latest and update information to online viewers in the field of Genetics, human and medical genetics, genetic engineering, functional genetics and gene therapy for diverse genetic disorders and genetic abnormalities.

  • Genetic Disorders
  • Single Gene Disorders
  • Common Complex Diseases
  • Metabolic Diseases
  • Gene-based prognostic
  • Design of novel synthetic
  • Genomics
  • Genetic diseases
  • Viral vectors
  • Genetic Mutations
  • Antisense
  • Exon-skipping agents
  • Refined genome editing tools
  • Nucleic acid
  • Protein combinations
  • Gene modulation
  • Pharmacological studies
  • Animal models
  • Human clinical trials
  • Novel therapeutic
  • Nucleic acids
  • mRNA
  • Population Genetics
  • Epigenetics
  • Disease-specific
  • Environmental Genetics
  • Gene Mapping
  • Regenerative Medicine
  • Gene Regulation
  • Autosomal recessive diseases
  • Charcot-Marie-Tooth disease
  • Myotonic dystrophy
  • Tuberous sclerosis
  • Diabetes mellitus and deafness
  • Encephalomyopathy
  • Lactic acidosis
  • Leber hereditary optic neuropathy
  • Leigh syndrome
  • Mitochondrial myopathy
  • Myoclonic epilepsy with ragged red fibers
  • Myoneurogenic gastrointestinal encephalopathy
  • Precision medicine
  • Adrenoleukodystrophy
  • Duchenne muscular dystrophy
  • Hemophilia
  • Rett syndrome
  • Genetic testing
  • Mitochondrial diseases
  • Personalized medicine
  • Stem cell therapy
  • X-linked traits
  • Y-linked traits
  • Weill-Marchesani syndrome
  • Wilson's disease
  • Wiskott-Aldrich syndrome
  • Maternally inherited diabetes and deafness
  • Facioscapulohumeral muscular dystrophy
  • Familial hypercholesterolemia
  • Hereditary nonpolyposis colorectal cancer
  • Huntington disease
  • Marfan syndrome
  • Neurofibromatosis type 1
  • Neurofibromatosis type 2
  • Polycystic kidney disease
  • Weill-Marchesani syndrome
  • Williams-Beuren syndrome
  • Autoimmune polyendocrine syndrome type 1
  • Cockayne syndrome
  • Congenital adrenal hyperplasia
  • Cystic fibrosis
  • Galactosemia
  • Gaucher's disease
  • Glycogen storage diseases
  • Mucopolysaccharidoses
  • Niemann-Pick disease
  • Phenylketonuria
  • Sickle cell disease
  • Spinal muscular atrophy
  • Tay-Sachs disease
  • Thalassemia
  • Alpha-thalassemia
  • Beta-thalassemia
  • Mutational analysis
  • Computational genetics
  • Regulation of gene expression
  • Immunogenetics
  • Chromosome biology
  • Stem cell Therapy
  • Cytogenetics
  • Cancer Genetics
  • Genetic Probes
  • Genetic epidemiology
  • Gene therapy
  • Recombinant Gene
  • Medical Genetics
  • Gene cloning and mapping
  • Reproductive Genetics
  • Gene chip technology
  • Clinical genetics
  • RNA Processing
  • Behavioral genetics
  • Ecological Genomics
  • Evolutionary Genetics
  • Genetics in Society
  • Chemical Genetics
  • Genetic Algorithms and Statistical Analysis
  • Novel mutations found in cancer cells
  • Neurogenetics
  • Psychiatrics Genetics. Transposes: jumping genes
  • Down syndrome
  • Edwards syndrome
  • Fragile X syndrome
  • Patau syndrome
  • Turner syndrome
  • Angelman syndrome
  • Beckwith-Wiedemann syndrome
  • Prader-Willi syndrome
  • Chromosomal disorders
  • Disorders of imprinting
  • Autosomal dominant diseases
  • Molecular Genetics
  • Human evolution
  • Human genetic disorders
  • Human Genetics
  • Human genome analysis
  • Genealogical Tracing
  • Genetic counseling
  • Genetic disorder therapies
  • Genetic Engineering
  • Genetic linkage and genetic maps
  • Genetic polymorphisms
  • Genetics of Infectious Diseases
  • Genetics of Plants and Animals in Agronomy Quantitative Genetics
  • DNA damage repair Epigenetics
  • Evolutionary and Population Genetics
  • Forward and Reverse genetics
  • Gene expression and Regulation
  • Abnormality in gene expression
  • Cancer Cytogenetics
  • Chromosome Abnormalities
  • Classical and Developmental Genetics
  • Conservation and Ecological Genetics

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