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      • Publication lead time3 - 4 weeks
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    • Permanent article identifier We provide DOI to all published papers to facilitate higher citation and classification of articles.
      Peertechz Publisher ID: 10.17352
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    Editorial Board

    Zihui Tang
    Department of Endocrinology and Metabolism
    Tongji University
    China
    dr_zhtang@yeah.net
    SJGGT

    Research Interest: Diabetes and its Complications, Osteoporosis, Cardiovascular Disease, Neuropathy; Mathematical Modelling for Human Complex Disease; Policy and Clinical Decision Analysis in Medical Science; Stochastic Process Analysis and Bayesian Analysis for Clinical Medicine; Mathematical Methodology Development for Clinical Science; Gene Mapping and Identification of Human Complex Disease; Data Analysis for Results of Experiment

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    Maria Piccione
    Director
    University of Palermo,
    Italy
    piccionemaria@libero.it
    SJGGT

    Research Interest: Genetics

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    Zhang Jianzhong
    Department of Communicable Disease Diagnostics
    State Key Laboratory for Infectious Disease Prevention & Control
    China
    Helico99@sina.com
    SJGGT

    Research Interest: My Research Focuses on the Bacterial Pathogens Analysis. It includes: Pathogen Identification (Including MALDI-TOF MS/MS Analysis); Bacteria GWAS Analysis; Infectious Disease Diagnosis; Vaccine Development

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    Jacinto da Costa Silva Neto
    Professor
    Department of Histology and Embryology
    Federal University of Pernambuco,
    Brazil
    jacintocosta@hotmail.com
    SJGGT

    Research Interest: Processos carcinogênicos e progressão de lesão. Invasão e metastáse. Processos patológicos envolvendo Papilomavirus humano (HPV) Estudos envolvendo análises citológicas e histopatológicos.


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    Moritz Caspar Franz Oberstadt
    Department of Pharmacology
    University of Greifswald,
    Germany
    mocafrob@gmx.de
    SJGGT

    Research Interest: Epigenetics in glioma, especially methylation patterns, Stem cell research in glioma

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    Chand Sourabh
    Department of Nephrology
    Royal Wolverhampton NHS Trust
    UK
    sourabh.chand@nhs.net
    SJGGT

    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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    Claudio Toma
    Senior Research Officer
    University of New South Wales (Neuroscience Research Australia (NeuRA))
    Australia
    c.toma@neura.edu.au
    SJGGT

    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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    Lin Zhou
    Associate Professor
    Department of Laboratory Medicine
    Second Military Medical University
    China
    lynnzhou36@163.com
    SJGGT

    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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    Yong-yi Yuan
    Department of Otolaryngology
    Chinese PLA General Hospital
    China
    yyymzh@163.com
    SJGGT

    Research Interest: Identification of the Gene Responsible for Hereditary Deafness and Onycodystrophy Syndrome and Functional Study on the Gene

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    Paulo Sarmanho da Costa Lima
    Agricultural Research
    Agricultural Research Centre,
    Brazil
    paulo.costa-lima@embrapa.br
    SJGGT

    Research Interest: Biological Sciences, Genetics, Subarea: Molecular Genetics of Microorganisms and Major Agrarian Sciences, Agronomy, Plant, Specialty: Vegetable Improvement  Major, Agrarian Sciences, Agronomy, Subarea: Plant, Specialty: Management and Cultural Abuse






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    Katarzyna Anna Starska
    Professor
    Medical Univeristy,
    Poland
    katarzyna.starska@umed.lodz.pl
    SJGGT

    Research Interest: Oncology, Genetics and Gene Therapy, Signaling Pathways, Molecular Research, Cell Biology, Signal transduction.

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    Daniele Fanale
    Department of Medical Oncology
    University Hospital Policlinico,
    Italy
    fandan@libero.it
    SJGGT

    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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    Zhongzhou Chen
    Professor,
    Department of Biological Sciences
    Agricultural University,
    PR China
    chenzhongzhou@cau.edu.cn
    SJGGT

    Research Interest: Protein expression, purification, crystallization and structure determination Sign a transaction and transcription regulation Chemistry, drug design, origin of life and quantum chemistry

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    Xiaosheng Wang
    Department of Genetics, Cell Biology & Anatomy
    University of Nebraska Medical Center
    USA
    xiaosheng.wang@unmc.edu
    SJGGT

    Research Interest: Analysis of genomic data including next-generation sequencing, microarrays data etc.; development of algorithms for discovery of predictive biomarkers for cancer such as gene mutation signatures and gene expression signatures; systems and computational biology for elucidating the nature of oncogenesis; inference of molecular interaction networks relevant to specific disease; inference of cancer genomic evolution based on gene mutation information; identification of synthetic lethal genes for cancer therapy.

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    Anna Grandone
    Second University of Naples
    Italy
    agrandone@gmail.com
    SJGGT

    Research Interest: Pediatrics, endocrinology, short stature, puberty, obesity, genetics

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    mendeley

    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
    mendeley

    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
    mendeley

    Triplet with Dicephalus Twins: A Case Report

    DOI Logo 10.17352/sjggt.000012

    Published On: November 11, 2017 | Pages: 001 - 003

    Author(s): Adeku MA, Ajayi GO*, Adegbola O and Adeyemi A
    Abstract View Full Article View
    mendeley

    Role of Molecular Markers in Assessing Genetic Diversity in Mentha: A Review

    DOI Logo 10.17352/sjggt.000011

    Published On: December 30, 2016 | Pages: 022 - 026

    Author(s): Nidaf khan and Sunita Singh Dhawan*
    Abstract View Full Article View
    mendeley

    Transcription Factors in Schizophrenia: A Current View of Genetic Aspects

    DOI Logo 10.17352/sjggt.000010

    Published On: December 30, 2016 | Pages: 017 - 021

    Author(s): Roksana Zakharyan*
    Abstract View Full Article View
    mendeley

    Identification of Novel TMC1 Compound Heterozygous Mutations Related to Autosomal Recessive Hearing Loss by Targeted Capture Sequencing

    DOI Logo 10.17352/sjggt.000009

    Published On: July 08, 2016 | Pages: 013 - 016

    Author(s): Xue Gao, Sha-Sha Huang, Yu Su, Jin-Cao Xu and Pu Dai*
    Abstract View Full Article View

     

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