Epstein-Barr Virus and Helicobacter pylori as Two Main Risk Factors in Gastric Cancer
Abstract
(ISSN 2577-5790)
OBM Genetics is an international Open Access journal published quarterly online by LIDSEN Publishing Inc. It accepts papers addressing basic and medical aspects of genetics and epigenetics and also ethical, legal and social issues. Coverage includes clinical, developmental, diagnostic, evolutionary, genomic, mitochondrial, molecular, oncological, population and reproductive aspects. It publishes a variety of article types (Original Research, Review, Communication, Opinion, Comment, Conference Report, Technical Note, Book Review, etc.). There is no restriction on the length of the papers and we encourage scientists to publish their results in as much detail as possible.
Publication Speed (median values for papers published in 2023): Submission to First Decision: 5.1 weeks; Submission to Acceptance: 17.0 weeks; Acceptance to Publication: 7 days (1-2 days of FREE language polishing included)
Epstein-Barr Virus and Helicobacter pylori as Two Main Risk Factors in Gastric Cancerby
Parisa Zeynali
,
Hossein Teimouri
,
Seyed Mohammad Ali Hashemi
,
Arefeh Ebrahimian
,
Seyed Nooreddin Faraji
,
Shahriar Sakhaei
and
Emad Behboudi
Abstract Microbial and viral pathogens have emerged as pivotal agents in oncogenesis. Research conducted in the last twenty years has significantly enhanced our comprehension of the cancer-causing capabilities of infectious agents. An illustrative instance is gastric cancer (GC), which is closely associated with Helicobacter pylori (H. pylori) and Epstein-Barr [...] |
External Validation and Modification of a New Score for Predicting Mortality in Patients with COVID-19 in High Altitude Patients. A Peruvian Studyby
Walter Calderón-Gerstein
,
Gabriela Torres-Samaniego
,
Kevin Pazos-Sovero
and
Mirella Calderón-Anyosa
Abstract This study aims to validate two predictive mortality scores for patients with COVID-19 to support clinical decision-making in those who require hospitalization. The tomographic patterns found can be added to the original scores to increase their predictive power. Retrospective, analytical, observational, and cross-sectional studies were carried out [...] |
Phenotypic Characterization of Advanced Breeding Lines of Rice (Oryza sativa L.) for Drought and Low Phosphorus Stress Toleranceby
Sopnil Ahmed Jahin
,
Biswajit Das
,
Adrita Abdullah
,
Sadia Akter
,
Mohammad Abu Kawsar Sarower Siddique
and
Mohammad Anwar Hossain
Abstract Drought and phosphorus (P) deficiency stress are two significant natural abiotic stresses restricting rice growth and yield worldwide. Developing rice varieties tolerant to drought and low P stress is crucial for sustainable agricultural production. To address these issues, two separate experiments were conducted using selected advanced rice breeding [...] |
Cytogenetic and ISSR-Markers Polymorphism in the Population of Local Ukrainian Lebedyn CowsAbstract Preservation of the fund of local breeds of agricultural animals, which are breeding material for the creation of new ones and the improvement of existing ones, meets the requirements of the FAO - the protection of biological diversity. The study of the genetic structure of cows of the local Lebedyn breed, which was bred in Ukraine, with the use of [...] |
Synergistic Effect of Resveratrol and Paclitaxel in the Treatment of Malignant Pleural MesotheliomaAbstract Malignant pleural mesothelioma (MPM) is a lethal and aggressive cancer due to exposure to asbestos since this carcinogen is still being used in industrial buildings and housing in several countries. Untreated MPM has a median survival time of 12 months, and most people die within 24 months after diagnosis. If caught early, surgery may be performed. [...] |
Effect of Drought Stress on Agronomic Traits and Total Leaf Proteins in Different Bottle Gourd [Lagenaria siceraria (Molina) Standl.] Genotypesby
Phumzile Mkhize
and
Phetole Mangena
Abstract Breeding drought-tolerant genotypes using genetic and biochemical tools is an important mitigation strategy to improve stress response and yields in bottle gourd [Lagenaria siceraria (Molina) Standl.]. This current study evaluated the variations among bottle gourd genotypes for potential breeding purposes by establishing the relationship between agronom [...] |
Novel FLNC Gene Variant Associated with Hypertrophic Cardiomyopathyby
José A. Cedeño-Escudero.
,
Luis A. Sotillo-Bent.
,
Carolina Vega- Cuellar.
,
Rolando González-Angulo
,
Evelyn Medina-Batista
,
José Sotillo-Lindo
and
Luis A. Méndez-Rosado.
Abstract Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiomyopathy, affecting approximately 1 in 500 people. It is the most common genetic cardiomyopathy inherited as a Mendelian trait in approximately 50% of patients, mainly due to pathogenic variants in genes encoding sarcomeric proteins. Mutations in the sarcomeric protein filamin C (FLNC [...] |
Status of Azoospermia in Saudi Arabia: A Retrospective Narrative Mini-Reviewby
Meshari A. Alzahrani
,
Mohammad A. Alghafees
,
Lama H. Aldosari
,
Abdulaziz K. Almaymuni
,
Abdulltaif M. Altalhah
,
Mohammed M. Abualgasem
and
Basel O. Hakami
Abstract The total lack of spermatozoa in the ejaculate is known as Azoospermia. It is the most severe and significant contributor to male infertility. Therefore, the purpose of this study is to assess the status of Azoospermia and its etiologic factors that contribute to male infertility in Saudi Arabia. This study included all published studies written in [...] |
Polyploidy Induction by Sodium Azide and Ethyl Methane Sulfonate in Grape Genotypesby
Zeki Kara
and
Ahmet Beyatlı
Abstract Continuous improvement of vine rootstocks and grape varieties is necessary for the sustainability of viticulture. In this context, grapevine breeding and especially the development of polyploid grapevine genotypes offer opportunities. This study investigated the effectiveness of sodium azide (SA, five dozes and two treatment duration) and ethyl methane [...] |
DNA-Based Variability of Length Polymorphism of Plant Allergens Coding Genes Homologs in Selected Lamiaceae Herbsby
Lucia Urbanová
,
Silvia Farkasova
,
Ivana Speváková
,
Matúš Kyseľ
,
Veronika Šimora
,
Miroslava Kacaniova
and
Jana Žiarovská
Abstract Medicinal plants have been a part of human life from a very early age. In the field of plant genetics, they are still widely investigated for their genomic variability. This study used two DNA marker techniques to obtain polymorphic profiles in selected species from Lamiaceae. Both are based on the variability of plant genes that code for allergens [...] |
Becker Phenotype Muscular Dystrophy in a Man with Klinefelter Syndrome: A Rare Associationby
Arianne Llamos-Paneque
,
Isabel Echevarria-Frutos.
,
Amaury León-Siosa
,
Tanja Herrmann
and
Thomas Liehr
Abstract To present a rare clinical case of a man affected simultaneously by Becker phenotype Muscular Dystrophy (MD) and Klinefelter syndrome and the way how he was diagnosed. A 35-year-old man was evaluated in the context of hospitalization for respiratory failure. Since childhood, he had a clinical and muscle biopsy diagnosis of muscular dystrophy, possibl [...] |
Clinical Features, Genetic Landscape and Management of Behçet's Syndrome: A Comprehensive Reviewby
Edoardo Masiello
,
Sebastiano Caruso
,
Salvatore Lavalle
,
Roberta Foti
,
Caterina Gagliano
,
Ignazio La Mantia
,
Salvatore Giuseppe Cocuzza
,
Luigi La Via
,
Federica Maria Parisi
,
Christian Calvo-Henriquez
,
Miguel Mayo-Yanez
,
Jerome R. Lechien
,
Claudia Di Napoli
and
Antonino Maniaci
Abstract Behçet's syndrome is a systemic inflammatory disorder of unknown origin, presenting with diverse symptoms such as recurrent oral and genital ulcers, skin lesions, and uveitis, and can impact multiple organ systems. Diagnosis relies primarily on clinical evaluation due to the lack of specific diagnostic tests. Management requires a multidisciplinar [...] |
Molecular Marker Applications in the Selection of Elite Genotypes for Plant Stress Tolerance and Genetic FidelityAbstract Molecular markers play a crucial role in accelerating crop production for sustainable agriculture by identifying resistant traits and enhancing genetic diversity. In this review, we examine the impact of the molecular markers on advancing our understanding of stress tolerance mechanisms in plants, addressing the pressing imperative to bolster global [...] |
Unique Female Patient with de novo 6q22.31q27 Duplication and Xq28 Deletion: Case Report and Brief Literature Reviewby
Lamiae Afif
,
Zhour El Amrani
,
Aziza Sbiti
,
Ilham Ratbi
,
Imane Cherkaoui Jaouad
,
Youssef El Kadiri
,
Thomas Liehr
,
Abdelaziz Sefiani
and
Abdelhafid Natiq
Abstract 6q22.31q27 duplication and Xq28 deletion lead to two specific different rare chromosomal disorders. Partial trisomy 6q22.31q27 is a recognizable syndrome with a distinctive phenotype, and the most common finding in girls with Xqter deletions has been premature ovarian failure (POF) and secondary amenorrhea. To our knowledge, neither abnormality in one [...] |
Case Studies in the Ethics of Assisted Reproduction, by Louise P. King & Isabelle C. Band, Switzerland: Springer Cham, 152 Pages, Ebook, 978-3-031-41215-8Abstract "Case Studies in the Ethics of Assisted Reproduction" explores the moral and ethical implications of assisted reproductive technologies (ART), such as in vitro fertilization (IVF), surrogacy, and genetic screening. These findings outline ethical dilemmas, including the importance of informed consent, and highlight a multidisciplinary approach involving [...] |
A Child Carrying a Large Deletion in the 10p.15.3-p12.31 RegionAbstract Partial deletion of 10p is a rare disorder. Common features of this disorder include intellectual disability, developmental delay, dysmorphic features, hypoparathyroidism, deafness, and renal anomalies, but the phenotypes can vary between patients. We report an infant girl presented with global developmental delay, distinctive facial features with cleft [...] |
Phenylketonuria—Past, Present, and Future Directionsby
Nicole A. Bailey
and
Laura Mackay
Abstract Phenylketonuria (PKU) is an autosomal recessive inborn error of metabolism with an incidence that varies throughout the world. PKU is caused by loss of function variants in the phenylalanine hydroxylase gene. This loss of function leads to the accumulation of an amino acid, phenylalanine (Phe), that can reach toxic levels in the blood. PKU is managed [...] |
Miscarriages after Natural Conception & IVF: Comparative Study of Genetic Analysis of Products of Conceptionby
Elena V. Kudryavtseva
,
Sergey N. Fedenev
,
Ilia V. Kanivets
,
Anastasiya N. Troitskaya
and
Vladislav V. Kovalev
Abstract Assisted reproductive technologies (ART), including in vitro fertilization (IVF), are modern medical technologies widely used in developed countries. A frequent complication of pregnancy resulting from ART is miscarriage. The leading cause of miscarriage, both sporadic and recurrent, is chromosomal abnormalities (CA) of the embryo. To compare the freque [...] |
Exploring Multitargets Treatment for Diabetesby
Bolanle Adenike Akinsanola
,
Matthew Iyobhebhe
,
Tobiloba Christianah Maduakolam-Aniobi
,
Tomilola Debby Olaolu
,
Damilare Emmanuel Rotimi
and
Oluwafemi Adeleke Ojo
Abstract Diabetes Mellitus (DM) is a degenerative disease that modifies the body’s glucose metabolism. Although glucose is a vital energy source for body cells, individuals with diabetes can either not use insulin efficiently or do not create enough of this hormone, which controls blood sugar. This review aimed to explore the multi-target treatment for diabete [...] |
Blinatumomab vs Chemotherapy for Pediatric and Adult Acute Lymphoblastic LeukemiaAbstract Several therapeutic methods are used to cure acute lymphoblastic leukemia (ALL). Relapsed/refractory B-cell ALL (R/R B-ALL) remains the primary cause of death worldwide due to the limitation of cure. Blinatumomab is a bispecific T-cell engaging antibody used to treat R/R B-ALL. The use of blinatumomab for treating R/R B-ALL has shown to be very efficien [...] |
Potential Use of Human Mesenchymal Stem Cells (hMSCs) in Pancreatic Damage/CancerAbstract Pancreatic damage and pancreatic cancer pose significant challenges due to their complex pathogenesis, limited treatment options, and poor prognosis. In recent years, the potential use of human Mesenchymal Stem Cells (hMSCs) has been explored to address these complex pancreatic conditions and develop novel therapeutics. hMSCs, known for their regenerati [...] |
A Narrative Review on the Use of Eye-Tracking in Rett Syndrome: Implications for Diagnosis and TreatmentAbstract Rett syndrome (RTT) is a rare neurodevelopmental disorder primarily affecting females, characterized by a spectrum of debilitating symptoms that impact neurological, cognitive, and motor functions. Eye-tracking technology (ETT) has emerged as a prominent tool in Augmentative and Alternative Communication (AAC) systems, particularly for neurological [...] |
Causes of Chromosome Breakage and Mis-segregation Affecting Pregnancy and Newborn Health: An Insight into Developing Reproductive Health Preventive Strategiesby
Oyovwi Mega Obukohwo
,
Peggy Ejiro Ohwin
,
Rotu Arientare Rume
,
Olowe Gideon Temitope
,
Oyelere Abosede Oreoluwa
and
Adelowo Joy Motunrayo
Abstract Chromosome abnormalities are a leading cause of pregnancy loss, developmental delays, and birth defects. These abnormalities arise from errors in chromosome structure (breakage) or number (missegregation) during cell division. Understanding the causes of these errors is crucial for developing effective preventive strategies to improve reproductive healt [...] |
Hormonal and Physiological Manipulation Methods to Induce Polycystic Ovary in Rodents: A Review of the New FindingsAbstract Polycystic ovary syndrome (PCOS) is the most common endocrinopathy causing non-ovulation infertility in women. Women with PCOS have higher levels of luteinizing hormone (LH), testosterone, cholesterol and triglycerides but, in contrast, lower levels of follicular stimulating hormone (FSH) and sex hormone-binding globulin (SHBG) compared with health [...] |
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Takeshige Otoi from Tokushima University, Japan, to join the Editorial Board of OBM Genetics. He has more than 250 publications. We appreciate Dr. Takeshige Otoi for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Prof. Dr. Apostolos Zaravinos from European University Cyprus, Cyprus, to join the Editorial Board of OBM Genetics. He has more than 130 publications. We appreciate Prof. Dr. Apostolos Zaravinos for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Vishnu D Rajput from Southern Federal University, Russia, to join the Editorial Board of OBM Genetics. He has more than 400 publications. We appreciate Dr. Vishnu D Rajput for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Giuseppe Murdaca from the University of Genoa, Italy, to join the Editorial Board of OBM Genetics. Dr. Giuseppe Murdaca has received his PhD in Science and Space Engineering at the University of Genova (Italy) during the period of 2000-2003. Currently, he is working as an Assistant professor in the Internal Medicine University of Genova (Italy). His research has included Immunodeficiency, Autoimmunity, Neuro-endocrino-immunology, and Pharmacogenomics. Based on this research and fellowship training he has received several awards and honors, such as: Prize for young researchers of the study, assigned by the GILS, with the following motivation: "Standardization of a method to assess impairment by skinfold thickness skin", delivered on the occasion of the "Day VII Italian to fight Scleroderma" (Milan, 17/3 / 2001). Award for one of the three best oral presentations at the Ninth Congress of the Inter-SIMI Piemonte and Valle D'Aosta, Liguria (Genoa, 06.17.2004): Murdaca G., Fenoglio D., M. Setti, Brenci S., Villa R., Pontali E., A. Kunkl, Indiveri F., Puppo F. "Generation of CD4 + lines specific for Pneumocystis carinii and Candida albicans obtained from HIV + patients. Meaning of the coexpression of IFN-? and IL-4 ". He is serving as an editorial member of several reputed journals. We appreciate Dr. Giuseppe Murdaca for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Alexandr Sember from the Czech Academy of Sciences, Czech Republic, to join the Editorial Board of OBM Genetics. His main research interests are: sex chromosomes, phylogenetic context; use of laser microdissection, and comparative genomic hybridization (CGH) methods in (not only) fish cytotaxonomy. We appreciate Dr. Alexandr Sember for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Prof. Dr. Rouben Aroutiounian from Yerevan State University, Armenia, to join the Editorial Board of OBM Genetics. Prof. Dr. Rouben Aroutiounian is an expert in molecular genetics. He is responsible for research in molecular cytogenetics and genetic toxicology. He has more than 60 publications. We appreciate Prof. Dr. Rouben Aroutiounian for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Corrado Angelini from the Padova University School of Medicine, Italy, to join the Editorial Board of OBM Genetics. Dr. Corrado Angelini is an expert in molecular genetics. He is a member of the InterERN Neurometabolic Disease work group. He has served as an EB Member in several journals. He has more than 590 publications. We appreciate Dr. Corrado Angelini for his participation and support.
It is our pleasure to announce that LIDSEN has joined the ORCID community. ORCID (Open Researcher and Contributor ID), a global, not-for-profit organization, provides a free, unique, and persistent digital identifier (an ORCID iD), which can automatically link researchers to their own contributions, so as to disambiguate researchers from one another. Authors who publish with OBM Genetics are greatly encouraged to register for a unique iD to ensure proper attribution.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Prof. Dr. Pedro Martínez-Gómez, from CEBAS-CSIC, Spain, to join the Editorial Board of OBM Genetics. He is an international reference in Prunus Breeding and Biotechnology including Genetics, Genomics, Transcriptomics and epigenetics with more than 150 papers published in international journals included in the Web of Science. He also has 5 new apricot varieties, 4 new almond varieties and 1 new Japanese plum variety widely cultivated in Spain and Southern Europe where more than 5 M trees from these varieties are grown at this moment. In addition, he has been coordinator of 22 projects at the regional, national and international levels, as well as participating in 30 other projects and agreements with companies as a member of the research team. Throughout his research career he has participated in the scientific training of more than 70 students and researchers from 20 different nationalities. He has supervised 18 PhD Theses. Most of their former graduate doctors are, at this moment, junior and senior researchers around the world. In August 2006 received in Seoul (Korea) the "Miklos Faust International Award", an International Award of the American Society for Horticultural Science (ASHS) and the International Society for Horticultural Science (ISHS) for its contribution to the international fruit science research. In January 2012 he received in Teheran (Iran) the “Khwarizmi International Award” organized by the Iranian Research Organization for Science and Technology (IROST) and the “FAO Medal Award” from the Food and Agriculture Organization for his contribution to the application of biotechnology tolls in the development of the fruit research in developing countries. In January of 2019, received in La Havana (Cuba), the “CITMA Award 2018” for their collaboration in the conservation of plant genetic resources in Cuba. We appreciate Prof. Martínez-Gómez for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Prof. Bruce O'Hara, from the University of Kentucky, USA, to join the Editorial Board of OBM Genetics. He obtained his PhD in Human and Mammalian Genetics from The Johns Hopkins School of Medicine, and later spent twelve years at the Stanford University Center for Sleep and Circadian Neurobiology where he established a research program directed towards an understanding of sleep using higher throughput behavioral and genomic methodologies. He currently has over 35 years of experience in mammalian genetics and especially mouse models of human disease, and has over 95 publications in areas ranging from the effects of drugs to large-scale genetic screens and models of neurodegenerative disorders. We appreciate Dr. O'Hara for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Prof. Yuri Shavrukov, from Flinders University, Australia, to join the Editorial Board of OBM Genetics. Originally, Prof. Shavrukov worked at the Institute of Cytology and Genetics, Russian Academy of Sciences, Novosibirsk (Russia), where he received his PhD degree (1991). In 2001, he was selected and employed by CSIRO (Commonwealth Scientific and Industrial Research Organisation), Adelaide, Australia. After CSIRO, he received a position at the University of Adelaide, Plant Genomics Centre (2005-2016), and since that he moved to Flinders University, Adelaide. Currently, Prof. Yuri Shavrukov is working at Flinders University with some collaborative international research projects. His research interests include plant genetics and genomics, gene structure and expression analysis in plants, development and application of molecular markers in plant biology. We appreciate Prof. Shavrukov for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Mohan Shri Jain from University of Helsinki, Finland, to join the Editorial Board of OBM Genetics. He received his M. Phil, 1973 and Ph.D., 1978, Jawaharlal Nehru University, New Delhi, India. He was a postdoctoral fellow in Israel, USA, and visiting Professor in Japan, Malaysia, Germany, and Italy. He was a Technical Officer at, International Atomic Energy Agency (IAEA), Vienna, Austria, from 1999-to 2005. He is on the Editorial Board and a reviewer in several well-reputed journals. His publications are over 170 in peer-reviewed journals, book chapters, and conference proceedings, and edited 68 books; invited speakers, and acted as a chairperson in several international conferences worldwide. In commemoration of the awarding IAEA of the Nobel Peace Prize in 2005, as a team member, he received this certificate; consultant to IAEA, the European Union, The Government of Grenada, and the Egyptian Government. His current research interests are on in vitro techniques, mutagenesis, transgenics, genetic diversity and conservation, climate change, and food security. We appreciate Dr. Jain for his participation and support.
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We sincerely welcome Dr. Paola Ungaro, from National Research Council, Italy, to join the Editorial Board of OBM Genetics. Dr. Ungaro is a Researcher at the National Research Council (CNR) in Institute for Experimental Endocrinology and Oncology “Gaetano Salvatore” of Naples, Italy. Dr Ungaro’s research interest includes epigenetic and transcriptional regulation of obesity and diabetes related genes and epigenetic regulation by natural compounds. The research activity includes three main research lines: 1. Evaluation of the effects of High-Fat Diet (HFD) on the expression of genes codifying for enzymes known to induce histone post-translational modifications (PTMs). 2. Study of the effects of Polyphenols on the epigenetic regulation of obesity-related genes and on the expression of key enzyme involved in chromatin remodelling. 3. Study of the effects of Polyphenols on the expression of genes involved in the browning of white adipose tissue. We appreciate Dr. Ungaro for her participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Prof. Dr. Yan Sanders, from University of Alabama at Birmingham, United States, to join the Editorial Board of OBM Genetics. Dr. Sanders is currently Associate Professor of Medicine. Her main research interests are epigenetic mechanisms in tissue injury, repair and aging. Her ongoing projects include exploring epigenetic alterations in pulmonary fibrosis, examining the effects of histone modifier on fibrotic lung fibroblasts, determining the epigenetic mechanisms of cellular senescence, aging, and age-related chronic diseases, specifically histone modifications and DNA methylation. We appreciate Prof. Sanders for her participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Shin Murakami from Touro University California, USA, to join the Editorial Board of OBM Genetics. Professor Murakami received his Ph.D. from Kyoto University, Japan. He then worked at the University of Colorado-Boulder, University of Michigan-Ann Arbor, University of Louisville, among others. Current research interest is to understand the transition of aging processes from normal aging to disease (including Alzheimer’s disease, AD), using semi-automated imaging systems (Machino et al., 2014) and big data analysis of dementia genes in humans and C. elegans (Vahdati et al., 2017). He has formulated the multiplex stress resistance theory of aging, which has now been extended to the middle-life crisis theory of aging. Importantly, the middle-life crisis theory predicted the outcome of one or more clinical trials in the Alzheimer's disease. Recently he accepted new national leadership roles, including Public Policy Representative of BS Section Executive Committee (Gerontology Society of America); and Committee and Task Force/New Comprehensive Foundational Sciences Examination (NBOME). We appreciate Professor Murakami for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Penna Suprasanna, former-Head of Nuclear Agriculture & Biotechnology Division, BARC, Mumbai & Homi Bhabha National Institute, India, to join the Editorial Board of OBM Genetics. Prof. Suprasanna obtained his MSc (Genetics) and Doctorate in Genetics from Osmania University, Hyderabad (India) and did his post-doc research in the Laboratory of Tropical Crop Improvement, Cathloic University of Leuven, Leuven, Belgium. His research interests include plant stress biology, biotechnology, plant mutagenesis and plant genomics. He has made concerted efforts to apply radiation mutagenesis techniques in plants in collaboration with International Atomic Energy Agency (IAEA), Vienna. He is the recipient of the “Award of Scientific and Technical Excellence” by the Department of Atomic Energy, Government of India, and is the Fellow of International Society of Environmental Botany. Dr. Suprasanna has a patent; published more than 300 research papers/articles in national and international journals, has edited special issues for journals & books. We appreciate Professor Suprasanna for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor John Marshall from Institute of Ophthalmology (UCL), United Kingdom to join the Editorial Board of OBM Genetics. Professor Marshall has extensive experience in ophthalmology, inherited retinal disease, diabetes, glaucoma, neurodegenerative diseases, etc. We are very grateful to Prof. Marshall for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Jaroslav Alois Hubáček, PhD, DSc., from Institute for Clinical and Experimental Medicine, Czech Republic, to join the Editorial Board of OBM Genetics. Dr. Hubáček has extensive experience in population population genetics, gene, diabetes, cardiovascular genetics, genetic predisposition of noncommunicable diseases, etc. We are very grateful to Prof. Hubáček for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Jose J. G. Marin from University of Salamanca, Spain, to join the Editorial Board of OBM Genetics. Professor Marin has extensive experience in physiology, pharmacology, liver cancer, chemotherapy, genetics, molecular, cell, etc. We are grateful to Professor Marin for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Tapan K Bera from National Cancer Institute, USA, to join the Editorial Board of OBM Genetics. Dr. Bera has extensive experience in antibody engineering; immunotherapy; recombinant immunotoxin; multiple myeloma; BCMA; mesothelin, etc. We are grateful to Dr. Bera for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Veena N Rao from Morehouse School of Medicine, USA, to join the Editorial Board of OBM Genetics. Professor Rao has extensive experience in triple negative breast cancers, ovarian cancers, tumor suppressor genes, biomarkers, cancer biology, epigenetics, protein-protein interactions, gene therapy, molecular biology, BRCA1, post translational modifications, precision medicine, etc. We are grateful to Professor Rao for her participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor James CS Chim from University of Hong Kong, Hong Kong, to join the Editorial Board of OBM Genetics. Professor Chim has extensive experience in DNA methylation of tumour suppressor genes, non-coding RNAs (micro-RNAs & long noncoding RNAs) in blood cancers including multiple myeloma, lymphoma and chronic lymphocytic leukemia, etc. We are grateful to Professor Chim for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Lunawati L Bennett from Union University, USA, to join the Editorial Board of OBM Genetics. Professor Bennett has extensive experience in pharmacotherapy, pharmacogenomics, genetic disease, cancer, apoptosis, endocrine, antioxidants, natural product, nutrition, etc. We are grateful to Professor Bennett for her participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Andrew Collins from University of Southampton, UK, to join the Editorial Board of OBM Genetics. Professor Collins has extensive experience in genetic epidemiology, next generation sequencing, bioinformatics, human genetics and cancer, etc. We are grateful to Professor Collins for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Michael R. Ladomery from University of the West of England, UK, to join the Editorial Board of OBM Genetics. Professor Ladomery has extensive experience in RNA biology, alternative splicing, noncoding RNA, RNA-based cancer therapies, etc. We are grateful to Professor Ladomery for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Katalin Csiszar from the University of Hawaii, USA, to join the Editorial Board of OBM Genetics. Professor Csiszar has extensive experience in molecular and medical genetics focused on heritable disorders associated with the extracellular matrix. We are grateful to Professor Csiszar for her participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Sergei G. Tevosian from University of Florida, USA, to join the Editorial Board of OBM Genetics. Professor Tevosian has extensive experience in reproductive genetics, developmental genetics, adrenal development; developmental biology, etc. We are grateful to Professor Tevosian for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Professor Juraj Gregan from Comenius University, Slovakia, to join the Editorial Board of OBM Genetics. Professor Gregan has extensive experience in chromosome biology, mitosis, meiosis, etc. We are grateful to Professor Gregan for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Dr. Xuehuo Zeng from Case Western Reserve University, USA, to join the Editorial Board of OBM Genetics. Dr. Zeng has extensive experience in DNA damage response, molecular genetics, autophagy, cancer, etc. We are grateful to Dr. Zeng for his participation and support.
OBM Genetics Welcomes New Editorial Board Member
We sincerely welcome Assistant Professor Kakoli Das from Duke-NUS Graduate Medical School, Singapore, to join the Editorial Board of OBM Genetics. Dr. Das has extensive experience in molecular genetics, genetic heterogeneity, mutant, genotype, genetic diseases, etc. We are grateful to Dr. Das for her participation and support.
Historical Announcements
Update: Article Processing Charge (Price Changes Effective January 1, 2025) | 2024-10-21 |
In memoriam prof. dr. Joep Geraedts | 2023-12-25 |
OBM Genetics welcomes the following types of articles: original research, review, communication, opinion, case report, comment, conference report, technical note, book review, etc. There is no restriction on the length of the papers, color figures, supplementary file types. More details please see Instructions for Authors.
2023 | ||
CiteScore | SJR | SNIP |
0.4 | 0.160 | 0.093 |
Update: Article Processing Charge (Price Changes Effective January 1, 2025)
The journal OBM Genetics (ISSN: 2577-5790) will have the new APCs (New APC, 950 USD) for manuscripts submitted after 31 December 2024.
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