Aims and Scope

Aim of the Journal

The potentiality of Gene Therapy is enormous. Therefore, the Journal works with the aim to publish manuscripts concentrating on developing gene therapeutic mechanisms for diseases whose backgrounds have been genetically established and for other diseases that can be cured or improved by using the substances genes produce.

Scope of the Journal

The manuscripts published in Journal of Genetic Medicine and Gene Therapy are important sources of research results to discover the biological role of genes. Heighten Science encourages the doctors, researchers and scientists to develop manuscripts and send to the Journal for publication in the following, but not limited to, disciplines of genetic medicine and gene therapy:

  • Clinical Genetics
  • Abnormality in Gene Expression
  • Cancer Cytogenetics
  • Chromosome Abnormalities
  • Classical and Developmental Genetics
  • Conservation and Ecological Genetics
  • Cytogenetics
  • DNA damage Repair
  • Epigenetics
  • Evolutionary and Population Genetics
  • Forward and Reverse Genetics
  • Gene expression and Regulation
  • Gene Therapy
  • 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
  • Hereditary Genetic Disorders
  • Human Evolution
  • Human Genetic Disorders
  • Human Genetics
  • Human Genome Analysis
  • Immunogenetics
  • Medical Genetics
  • Molecular Genetics
  • Mutational Analysis
  • 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
  • Gene Therapy
  • Genetic Diseases
  • 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