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      Peertechz Publisher ID: 10.17352
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    Editorial Board

    Daniele Fanale
    Department of Medical Oncology
    University Hospital Policlinico,
    Italy
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    Research Interest: Cancer biology, Cancer biomarkers, Cancer cells, Cancer research, Copy number variants, Epigenetics, Gene expression, Genomics, Gene regulation, Human genetics, Microarray analysis, microRNA, Molecular Oncology, Transcriptomics





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    Claudio Toma
    Senior Research Officer
    University of New South Wales (Neuroscience Research Australia (NeuRA))
    Australia
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    Dr Toma is senior research officer at Neuroscience Research Australia (NeuRA) and holds a conjoint lecturer position at School of Medical science (University of New South Wales). He obtained his PhD in human genetics at the University of Bologna (Italy) and carried out research projects in the genetics of neurodevelopmental disorders at the Wellcome Trust Centre for Human Genetics (University of Oxford, UK) and in the genetics of psychiatric and Mendelian diseases at the University of Barcelona (Spain).  Dr Toma has extensive experience in association studies, linkage studies, copy number variant (CNV) analyses and whole exome/genome sequencing. He has identified novel candidate genes for autism spectrum disorder and bipolar disorder, and suggested new genetic mechanisms.

    Research Interest: Genetics of psychiatric diseases

    Number of Publications: 31


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    Guangwen Long
    Huazhong University of Science and Technology
    China
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    Alessandro Pezzini
    Associate Professor
    Department of Clinical Sciences
    University of Brescia,
    Italy
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    Lin Zhou
    Associate Professor
    Department of Laboratory Medicine
    Second Military Medical University
    China
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    Research Interest: Experienced in Molecular Biologic, Cellular Biologic, and Immunologic Techniques; Expert at Flow Cytometry, ELISA, Real-Time PCR, and Luciferase Reporter Gene Assay.

    Current Research is focused on the Diagnostic and Therapeutic Role of B-Cell-Activating Factor (BAFF) in Autoimmune Disorders


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    Valentina Gatta
    Associate Professor
    University of Chieti
    Italy
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    Current position:
    2011- present : Associate Professor of Medical Genetics (Area A1/06- SSD MED03), University of Chieti-Pescara  Italy On April  2017, VG obtained the National Scientific Qualification as Full Professor  in Medical Genetics  (SSD MED/03)

    Previous positions:

    2005-2011:  University Researcher (Medical Genetics - MED 03) University of Chieti-Pescara ( Italy)
    2002-2005: Post-Phd Fellowship supported by University of Chieti.
    1995- Fellowship supported by European Structural Funds. Research area:  Biological and Medical Science carried out at the  Centro di Genetica Evoluzionistica- CNR Rome

    Research Interest: During the course of her scientific activity, VG  worked in the field of molecular genetics, using the most recent techniques for the study of gene mutations causing pathologies such as male infertility, short stature (linked to mutations of the SHOX gene), familiar breast cancer (due to mutations of the BRCA1 and BRCA2 genes), Van Der Woude syndrome (IRF6 gene), and several neuromuscular diseases (Duchenne Muscular Dystrohpy, distal SMA, and others).
     She is head of a research team, working in the CAST research Centre of Chieti University specialized in molecular genetics.
     During these years VG primary interest was the study of the molecular basis of human reproduction and  she is currently investigating molecular mechanisms involved in oocyte competence and male infertility.
     These studies have been carried out by VG using a variety of molecular genetics technique like PCR, Southern Blot, DNA sequencing, as well as Multiple Ligation-Dependent Probe Amplification (MLPA). In the last few years, she has employed Real Time PCR, microarray , HRM, pyrosequencing and NGS technologies to investigate the modulation of gene expression profile in  different  models and SNPs (oocyte mitochondrial DNA, sperm, cumulus cells, oocyte, Transgenic Mouse Models of AD, stem cells).

    URL: https://www.unich.it/ugov/person/1475

    Number of publications: 10


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    Boren Lin
    University of Toledo
    USA
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    Research Interest: Inflammatory responses, bone regeneration, bone metabolism, osteoclast, osteoblast, mesenchymal stem cell, signal transduction, cancer-induced bone diseases.

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    Chand Sourabh
    Department of Nephrology
    Royal Wolverhampton NHS Trust
    UK
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    Research Interest: Clinical research is in caveolin-1 (and related candidate gene) single nucleotide polymorphism in kidney disease, transplantation, patient related morbidity as well as basic science research of caveolin-1, its knockout, pericytes in models of renal fibrosis and methods to reintroduce caveolin-1 using viromimetic vectors. Other research interests include cytomegalovirus risk, allograft outcome prediction, medications effects in transplantation.

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    Alejandro Iglesias-Linares
    Spain
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    Antonino Tuttolomondo
    Assistant Professor
    University of Palermo,
    Italy
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    Research Interest: Epidemiology and  pathophysiology of ischemic stroke Inflammatory  activation of the acute phase of acute ischemic stroke in relation of  subtypes of ischemic stroke,CD4+CD28- T cells in acute ischemic stroke  killer cell immunoglobulin-like receptors (KIR) receptors in acute clinical subtypes of acute ischemic stroke Treatment with  high-dose furosemide and small-volume hypertonic saline therapy in refractory heart failure Treatment with  high-dose furosemide and small-volume hypertonic saline therapy in refractory ascites diabetic foot as a cardiovascular risk marker Anderson-Fabry disease

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    Hung-Yun Lin
    Professor
    Institute of Cancer Biology and Drug Discovery
    Taipei Medical University,
    Taiwan
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    Shiwei Duan
    Professor
    Ningbo University,
    China
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    Research Interest: Epigenomics and pharmacogenomics in anti-cancer chemotherapy (Epi)Genetics and (epi)genomics for cancers and complex diseases

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    Maria Piccione
    Director
    University of Palermo,
    Italy
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    Research Interest: Genetics

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    Bo Wang
    Associate Professor
    Department of pathology
    University for the Nationalities
    China
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    Research Interest: Molecular Biology and Toxicology; Mainly on Liver Toxicity and Testis of Cadmium, he has Made a Great Contribution to Understand the Mechanisms and to Potentially Prevent these Diseases for Cadmium

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    Mateus Ferreira Santana
    Professor
    Federal University of Vicosa,
    Brazil
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    Research Interest: Molecular markers Genome, Evolutionary and Population, Genetics, Microbial Genetics

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    mendeley

    Exosome-driven epigenetic modulation of histone proteins: Pioneering anti-oncogenic and skin health applications

    DOI Logo 10.17352/sjggt.000022

    Published On: April 12, 2023 | Pages: 001 - 004

    Author(s): Ekta Yadav*, Niket Yadav, Katherine Vanta and Jagjit S Yadav
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    Voluntary Selection; Bringing Evolution at the Service of Humanity

    DOI Logo 10.17352/sjggt.000021

    Published On: December 28, 2022 | Pages: 009 - 015

    Author(s): Omid Sadeghi Fathabadi*

    ORCID Logo  0000-0002-7238-6235

    Abstract View Full Article View
    mendeley

    Potential effects of genetic polymorphism on anesthesia use for COVID-19 infected patients at intensive care unit

    DOI Logo 10.17352/sjggt.000020

    Published On: January 06, 2022 | Pages: 001 - 008

    Author(s): Sara AR, Mohamed Raslan, Eslam MS and Nagwa A Sabri*
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    Characterization of the complete chloroplast genome sequence of Vitis vinifera ‘Guifeimeigui’

    DOI Logo 10.17352/sjggt.000019

    Published On: December 04, 2021 | Pages: 001 - 003

    Author(s): Li Liu, Yang Yang, Xiujie Li* and Bo Li*
    Abstract View Full Article View    
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    Does human leukocyte antigen gene polymorphism affect management of COVID-19 Patients? A review article

    DOI Logo 10.17352/sjggt.000018

    Published On: August 29, 2020 | Pages: 001 - 003

    Author(s): Mohamed Ahmed Raslan, Mona Alshahawey, Eslam Mansour Shehata and Nagwa Ali Sabri*
    Abstract View Full Article View    
    mendeley

    Detection of new mutations in 3 cases de novo tuberous sclerosis

    DOI Logo 10.17352/sjggt.000017

    Published On: September 12, 2019 | Pages: 001 - 006

    Author(s): Carlos Andres Quintero Vasquez, Isabel Fernandez Gonzalez, Maria Luisa Quevedo Camera, Angelica Maria Garcia Ordonez and Luis Gustavo Celis Regalado*
    Abstract View Full Article View
    mendeley

    Caveolin-1 in renal disease

    DOI Logo 10.17352/sjggt.000016

    Published On: July 28, 2018 | Pages: 007 - 014

    Author(s): Sourabh Chand*
    Abstract View Full Article View    
    mendeley

    Strategies for investigating the genetics of chronic kidney disease

    DOI Logo 10.17352/sjggt.000015

    Published On: July 28, 2018 | Pages: 004 - 006

    Author(s): Sourabh Chand*
    Abstract View Full Article View    
    mendeley

    Lenalidomide as potential treatment in small cell neuroendocrine lung cancer with del 5q

    DOI Logo 10.17352/sjggt.000014

    Published On: July 11, 2018 | Pages: 002 - 003

    Author(s): Paul Hartel*
    Abstract View Full Article View    
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    First Treatment for Breast Cancer with certain Inherited Gene Mutation

    DOI Logo 10.17352/sjggt.000013

    Published On: February 15, 2018 | Pages: 001 - 001

    Author(s): Sulaiman Naseer*
    Abstract View Full Article View    

     

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