Stephanie Tuminello | Genetic Epidemiology | Innovative Research Award

Published on by Global Genetics Award

 

Innovative Research Award

Stephanie Tuminello
Icahn School of Medicine at Mount Sinai

Stephanie Tuminello
Affiliation Icahn School of Medicine at Mount Sinai
Country United States
Scopus ID 57193871243
Documents 60
Citations 1,069
h-index 15
Subject Area Genetic Epidemiology
Event Global Genetics Awards

Stephanie Tuminello is affiliated with the Icahn School of Medicine at Mount Sinai, where her scholarly work contributes to the advancement of genetic epidemiology and related biomedical research. Her publication record, citation performance, and sustained research activity demonstrate continued engagement in understanding genetic determinants of disease, epidemiological methodologies, and translational biomedical science. Bibliometric indicators from Scopus show a substantial scholarly contribution supported by peer-reviewed publications and academic citations, reflecting the influence of her research within the international scientific community.[1]

Abstract

Stephanie Tuminello’s research portfolio focuses on genetic epidemiology through the integration of population-based investigation, molecular genetics, and clinical data analysis. Her scientific work contributes to understanding disease susceptibility, inherited genetic variation, and risk prediction using evidence-based epidemiological methodologies. The body of published literature demonstrates interdisciplinary collaboration and continued scientific productivity across multiple areas of biomedical research.[1]

Keywords

Genetic Epidemiology; Population Genetics; Human Genetics; Disease Susceptibility; Precision Medicine; Genomic Medicine; Epidemiological Research; Translational Medicine.

Introduction

Genetic epidemiology combines principles from genetics, epidemiology, and biostatistics to evaluate inherited and environmental influences on disease occurrence. Researchers working within this discipline investigate genetic risk factors, gene-environment interactions, and population-level disease patterns to improve healthcare outcomes. Stephanie Tuminello’s scholarly activities align with these objectives through peer-reviewed research that contributes to the broader understanding of genetic determinants of human health.[2]

Research Profile

According to publicly available bibliometric information, Stephanie Tuminello has authored 60 indexed publications that have collectively received more than one thousand citations, resulting in an h-index of 15. These indicators suggest sustained scholarly productivity and measurable research influence within biomedical sciences and genetic epidemiology.[1]

  • Affiliation: Icahn School of Medicine at Mount Sinai
  • Primary discipline: Genetic Epidemiology
  • Scopus-indexed publications: 60
  • Scopus citations: 1,069
  • Scopus h-index: 15

Research Contributions

The available publication record indicates contributions involving genetic risk assessment, epidemiological analysis, disease association studies, clinical research methodologies, and collaborative biomedical investigations. Such work supports improved understanding of disease mechanisms and facilitates evidence generation for future precision medicine initiatives.[1][3]

  • Population-based genetic investigations.
  • Clinical and translational epidemiological research.
  • Genetic susceptibility and disease association studies.
  • Interdisciplinary collaboration across biomedical sciences.

Publications

The author’s publication portfolio consists of peer-reviewed journal articles indexed by major scholarly databases. These publications collectively address topics within genetics, epidemiology, biomedical science, and translational research, demonstrating continued scientific productivity over multiple years.[1]

  • Research articles indexed in Scopus.
  • Collaborative multidisciplinary publications.
  • Biomedical and genetic epidemiology studies.

Research Impact

Bibliometric evidence indicates measurable academic influence through citations, publication output, and scholarly visibility. Citation metrics suggest that the published work has contributed to ongoing scientific discussions and has been referenced by researchers working in related biomedical disciplines. Such indicators are commonly employed in evaluating scientific productivity and research influence.[1]

Award Suitability

Stephanie Tuminello demonstrates characteristics generally considered during evaluation for an Innovative Research Award, including sustained publication activity, measurable citation impact, interdisciplinary collaboration, and contributions to genetic epidemiology. Recognition within an academic awards program would appropriately acknowledge continued scientific engagement while reflecting objective scholarly indicators rather than subjective assessments of scientific merit alone.[1]

Conclusion

Stephanie Tuminello has established an active academic profile through contributions to genetic epidemiology, peer-reviewed publications, and collaborative biomedical research. Publicly available bibliometric indicators demonstrate sustained scholarly productivity and research visibility, supporting recognition within academic and professional award programs dedicated to scientific excellence and innovation.[1]

References

  1. Elsevier. (n.d.). Scopus author details: Stephanie Tuminello, Author ID 57193871243.
    Scopus.https://www.scopus.com/authid/detail.uri?authorId=57193871243
  2. Disparities in COVID-19 testing and positivity in New York City
    https://www.sciencedirect.com/science/article/pii/S0749379720302634
  3. Lkb1 inactivation drives lung cancer lineage switching governed by Polycomb Repressive Complex 2
    https://www.nature.com/articles/ncomms14922
  4. Male sex, severe obesity, older age, and chronic kidney disease are associated with COVID-19 severity and mortality in New York City
    https://journal.chestnet.org/article/S0012-3692(20)34288-4/fulltext
  5. The impact of asthma on mortality in patients with COVID-19
    https://journal.chestnet.org/article/S0012-3692(20)31645-7/fulltext

 

 Andrea Manica | Population genetics software | Innovative Research Award

Published on by Global Genetics Award

Innovative Research Award

Andrea Manica
Affiliation University of Cambridge
Country United Kingdom
Scopus ID 6603416293
Documents 187
Citations 17,182
h-index 67
Subject Area Population genetics software
Event Global Genetics Awards
ORCID 0000-0003-1895-450X

 Andrea Manica

University of Cambridge, United Kingdom

The Innovative Research Award recognizes sustained scholarly excellence and significant contributions to scientific advancement. Andrea Manica, a researcher at the University of Cambridge, has established an internationally recognized research profile in evolutionary biology, population genetics, human migration, ecological modelling, and computational approaches to biodiversity research. His scholarly publications, extensive citation record, and interdisciplinary collaborations demonstrate continued influence across genetics and evolutionary sciences.[1]

Abstract

Andrea Manica’s research integrates population genetics, ecology, anthropology, computational biology, and evolutionary theory to investigate biological diversity and human evolutionary history. His work combines large-scale genomic datasets, ecological modelling, and statistical methods to improve understanding of species distributions, migration processes, adaptation, and conservation. His scholarly achievements have resulted in a substantial international research profile with extensive citations and broad interdisciplinary impact.[1][2]

Keywords

Population genetics, evolutionary biology, ecological modelling, biodiversity, human migration, computational biology, conservation genetics, statistical ecology, genomics, species distribution modelling.

Introduction

Modern genetics increasingly relies upon interdisciplinary analytical approaches capable of integrating molecular, ecological, and computational evidence. Andrea Manica’s research exemplifies this trend by combining quantitative analysis with evolutionary theory to address questions concerning biodiversity, adaptation, and demographic history. His work has contributed to both methodological development and biological discovery while supporting evidence-based conservation research.[2]

Research Profile

Andrea Manica is affiliated with the University of Cambridge and maintains an internationally visible publication record indexed in Scopus. His documented scholarly metrics include 187 indexed publications, over 17,000 citations, and an h-index of 67, reflecting consistent scientific influence across multiple research disciplines.[1]

  • Population genetics and demographic inference.
  • Human evolutionary history.
  • Ecological and environmental modelling.
  • Biodiversity and conservation science.
  • Statistical and computational biology.

Research Contributions

His investigations have improved scientific understanding of how evolutionary processes, environmental factors, and migration shape genetic diversity. By integrating computational simulations with empirical observations, his studies have informed research concerning adaptation, population structure, climate influences, and conservation planning.[2][3]

  • Development of computational approaches for population genetics.
  • Analysis of human migration and demographic history.
  • Research supporting biodiversity conservation.
  • Integration of ecological and genomic datasets.
  • Interdisciplinary collaboration across genetics and ecology.

Publications

Andrea Manica has authored numerous peer-reviewed publications appearing in internationally recognized scientific journals. His research articles are frequently cited within genetics, ecology, anthropology, conservation biology, and evolutionary science, reflecting sustained scholarly relevance.[1]

  • Population genetic analyses.
  • Evolutionary modelling studies.
  • Human demographic history research.
  • Biodiversity conservation publications.

Research Impact

The documented citation metrics indicate extensive international recognition of Andrea Manica’s scholarly work. His publications continue to support research across genetics, ecology, anthropology, and environmental sciences while influencing computational methodologies and conservation strategies. The breadth of citations reflects continued relevance across diverse scientific communities.[1]

Award Suitability

Based on publicly available scholarly indicators, Andrea Manica demonstrates characteristics consistent with recognition through an Innovative Research Award. These include a sustained publication record, internationally recognized citation impact, interdisciplinary scientific contributions, methodological innovation, and continued advancement of population genetics and evolutionary biology research. Such accomplishments align with common evaluation criteria used in academic recognition programs.[1]

Conclusion

Andrea Manica’s scholarly career reflects substantial contributions to population genetics, computational biology, biodiversity research, and evolutionary science. Through interdisciplinary collaboration and quantitative innovation, his work has strengthened scientific understanding of biological diversity and evolutionary processes. His documented academic achievements support recognition within international research award programs dedicated to scientific excellence and innovation.[2]

References

    1. Elsevier. (n.d.). Scopus author details: Andrea Manica, Author ID 6603416293. Scopus.https://www.scopus.com/authid/detail.uri?authorId=6603416293
    2. ORCID. (n.d.). Andrea Manica
      ORCID Profile.      https://orcid.org/0000-0003-1895-450X
    3. Manica, A., et al. Representative research publication. Nature.
      DOI:
      https://doi.org/10.1038/nature06258
    4. Elsevier. (n.d.). Google scholar details: Andrea Manica.
      Google scholar. https://scholar.google.com/citations?user=v8V058QAAAAJ&hl=en
    5. An African origin for the intimate association between humans and Helicobacter pylori
       https://www.nature.com/articles/nature05562

Wei Li | Gene Therapy | Research Excellence Award

Published on by Global Genetics Award

Prof. Dr. Wei Li | Gene Therapy | Research Excellence Award

Department of Hematology, the First Affiliated Hospital of Zhengzhou University | China

Dr. Wei Li is an Associate Professor and Lab Director at the Department of Hematology, the First Affiliated Hospital of Zhengzhou University. He holds a PhD in Bioinformatics and completed postdoctoral training in clinical medicine. His research centers on erythroid development, hematological malignancies, and disease genomics, with a strong emphasis on genetic mechanisms underlying red cell disorders and cancer. Dr. Li has published 17 peer-reviewed articles in leading journals such as Blood and Journal of Hematology & Oncology, and has an H-index of 22. He leads multiple national research projects, serves as Associate Editor of the Journal of Translational Medicine, and maintains international collaborations, notably with the New York Blood Center.

Citation Metrics (Scopus)

3000
2000
1000
100
0

Citations
1,394

Documents
63

h-index
21

Citations

Documents

h-index


View Scopus Profile
 View Orcid Profile

Featured Publications

Jacob Raber | Cancer Genetics | Research Excellence Award

Published on by Global Genetics Award

Prof. Jacob Raber | Cancer Genetics | Research Excellence Award

OHSU | United States

Prof. Jacob Raber, Ph.D., is a distinguished Professor with interdisciplinary expertise spanning Behavioral Neuroscience, Neurology, Psychiatry, and Radiation Medicine. He serves as an Affiliated Scientist in the Division of Neuroscience at the Oregon National Primate Research Center (ONPRC), Oregon Health & Science University (OHSU), and holds a courtesy appointment as Professor of Pharmaceutical Sciences at Oregon State University. Dr. Raber earned his BSc in Chemistry and MSc in Pharmacochemistry from the Free University of Amsterdam, where his early research focused on β2-adrenergic receptor desensitization, complemented by training in immunochemistry and Yiddish language and literature. He completed his Ph.D. in Molecular Genetics and Virology at the Weizmann Institute of Science in Israel, investigating interferon-regulated pathways under the mentorship of Dr. Michel Revel. His work integrates molecular genetics with translational neuroscience to advance understanding of brain function and disease.

Citation Metrics (Scopus)

20000
15000
10000
500
0

Citations
15,411

Documents
304

h-index
63

Citations

Documents

h-index


View Scopus Profile
 View Orcid Profile

Featured Publications

Hanyurwumutima Egide | Molecular Genetics | Best Scholar Award

Published on by Global Genetics Award

Dr. Hanyurwumutima Egide | Molecular Genetics | Best Scholar Award

Graduate School of Chinese Academy of Agricultural Sciences/ Burundi Institute of Agricultral Sciences | Burundi

Dr. Hanyurwumutima Egide, a Veterinary Doctor of Burundian and Rwandan nationality, is an accomplished researcher and animal health professional with extensive experience in veterinary services, food safety, and livestock development. Since January 2016, he has served as a Researcher and National Animal Health Officer at the Burundi Institute of Agricultural Sciences and Research (ISABU), where he leads research initiatives, supports animal health management, provides extension services, and contributes to food safety programs. He also acted as the Burundi Facilitator for the Healthy Animal–Safe Food Program (ITP) supported by the Swedish International Cooperation Development Agency from 2018 to 2023, organizing regional activities and training participants in Sweden. As Chef of ISABU in the PADAIGL and LEAF (ADRA) projects, he established 200 bee and goat cooperatives, created 100 Farmer Field Schools, and trained farmers in livestock and environmental adaptation practices. His earlier roles include serving as Adviser in the Direction de la Promotion des Filières Animales, focusing on animal genetic resource improvement, fish production, and apiculture; Chef of Animal Health for Kayanza Province; and field veterinary officer at Cibitoke Ambulatory Veterinary Pharmacy.

Profiles: Scopus 

Featured Publications

"Prevalence of pathogenic bacteria and their antimicrobial patterns analysis of clinical samples from free-range chickens raised in forest farms in Zhouqu county of Gansu Province, China", Hanyurwumutima Egide ,2025.

Dongli Pan | Herpesvirus Infection | Best Researcher Award

Published on by Global Genetics Award

Prof. Dr. Dongli Pan | Herpesvirus Infection | Best Researcher Award

Zhejiang University School of Medicine | China

Dr. Prof. Dongli Pan is a distinguished biochemist whose research has significantly advanced the understanding of viral pathogenesis and host-virus interactions. She earned her Ph.D. in Biochemistry from the University of Pennsylvania, Philadelphia (2001–2007), where her dissertation focused on the fast kinetics of tRNA movement on the ribosome during bacterial translation elongation, following a B.S. in Chemistry from Peking University, Beijing (1997–2001). Currently a Professor at the Zhejiang University School of Medicine, Dr. Pan’s major research interests center on the mechanisms of herpes simplex virus (HSV) infection and pathogenesis, HSV-host interactions, and anti-HSV drug development. Her research excellence has been recognized through several competitive national grants, including major projects funded by the National Key R&D Project of China and the National Natural Science Foundation of China, with total funding exceeding several million RMB. Dr. Pan has led and contributed to groundbreaking studies on viral latency, host microRNAs, and innate immune responses to DNA viruses. Before joining Zhejiang University, she conducted postdoctoral research at Harvard Medical School and the University of Pennsylvania, deepening her expertise in molecular virology. In addition to her research, Dr. Pan is a dedicated educator, actively involved in undergraduate and graduate teaching at Zhejiang University and the Zhejiang University–University of Edinburgh Institute, where she organizes and lectures in courses such as Infection 3, Pathogens, and Medical Microbiology and Parasitology, fostering the next generation of biomedical scientists through her bilingual instruction and mentorship.

Profiles: Scopus

Featured Publications

"Inhibitory effect of Alantolactone against varicella-zoster virus in vitro", Virology JournalThis link is disabled., 2025.

"A potent protective bispecific nanobody targeting Herpes simplex virus gD reveals vulnerable epitope for neutralizing",Nature CommunicationsThis link is disabled., 2025.

"Discovery of Novel Piperazinone-Fused Hydroxypyridinones Inhibiting Herpes Simplex Virus Gene Transcription and Viral Replication", Journal of Medicinal Chemistry, 2025.

"Quantification and analysis of thymidine kinase expression from acyclovir-resistant G-string insertion and deletion mutants in herpes simplex virus-infected cells", J. Virol, 2025.

Giulia Pascolini | Neurodevelopmental Disorders | Best Researcher Award 

Published on by Global Genetics Award

Dr. Giulia Pascolini | Neurodevelopmental Disorders | Best Researcher Award 

Dermopathic Institute of the Immaculate, IDI-IRCC | Italy 

Author Profile

Scopus 

Orcid ID

Google Scholar

🌟 Biography of Giulia Pascolini, MD, PhD

🎓 EARLY ACADEMIC PURSUITS

Giulia Pascolini's journey in medical science began with a Degree in Medicine from Sapienza University of Rome in 2008, which she completed with honors. Following this, she pursued specialization in Medical Genetics at Tor Vergata University of Rome, graduating with honors in 2015 after five years of in-depth study. Driven by her passion for genetics, Dr. Pascolini went on to earn her Ph.D. in Medical Genetics from Sapienza University in 2019, establishing her expertise in a rapidly advancing field. In 2022, she further expanded her knowledge with a Master of II level in Rare Diseases, also from Sapienza University, solidifying her role as a leading expert in rare genetic disorders.

🩺 PROFESSIONAL ENDEAVORS

Dr. Pascolini's professional career is marked by extensive experience across multiple prestigious institutions. Currently, she is a Clinical Geneticist and head of the Clinical Genetics Service at the Istituto Dermopatico dell'Immacolata (IDI-IRCCS) in Rome, Italy. Since September 2023, she also holds a position as Professor of Medical Genetics at the Faculty of Medicine and Surgery at Tor Vergata University of Rome. Over the years, she has held various roles, including serving as a clinical geneticist at Bambino Gesù Children’s Hospital and a researcher at San Camillo-Forlanini Hospital. Her long-standing commitment to clinical genetics spans over 15 years, with a focus on intellectual disability syndromes, dysmorphology, and developmental disorders.

🔬 CONTRIBUTIONS AND RESEARCH FOCUS ON NEURODEVELOPMENTAL DISORDERS 

Dr. Pascolini's research primarily centers around Developmental Disorders of Chromatin Remodeling (DDCRs), intellectual disability (ID) syndromes, and genodermatoses. She has played a crucial role in the study of the skin phenotype in rare genetic diseases, and her work on deep learning technologies for diagnosing genetic syndromes using facial phenotype recognition is groundbreaking. Her involvement with FDNA Inc. and the DeepGestalt technology is a testament to her contributions to advancing medical genetics through innovative platforms. She is also a principal investigator for multiple research projects, including studies on rare cutaneous tumors and familial melanoma, with funding of over €47,000 for these projects.

🌍 IMPACT AND INFLUENCE

As a Scientific Board Member of the ADNP Syndrome Italian Association and an editorial board member of the Journal of Pediatric Genetics, Dr. Pascolini has made significant contributions to the broader medical community. Her work has helped shape new approaches to the clinical understanding of complex genetic disorders, particularly in rare diseases and neurodevelopmental syndromes. Through her collaborative efforts with international organizations and her academic roles, she continues to influence both current medical practices and future research directions.

📚 ACADEMIC CITES AND PUBLICATIONS

Dr. Pascolini has authored several impactful works, including her involvement in the DeepGestalt technology article on SETD5-associated intellectual disability published in the Journal of Translational Genetics and Genomics. Her contributions to book chapters, such as her writing on Genomic Copy Number Variants (CNVs) and Autism Spectrum Disorder (ASD), have added substantial value to academic literature. Her expertise has also been recognized through invitations to write for special issues in leading journals, enhancing her standing as a key voice in her field.

🏅 AWARDS AND RECOGNITION

In 2019, Dr. Pascolini was awarded the Franca Dagna Bricarelli Award for her clinical research on genetic mutations associated with the BAF complex. This prestigious award highlights her excellence in medical genetics and clinical research. Her contributions to the field, recognized by peers and institutions alike, reflect her profound impact on the study and treatment of genetic disorders.

🌟 LEGACY AND FUTURE CONTRIBUTIONS

With her leadership in clinical genetics, active research on rare skin diseases, and innovative work in genetic syndrome diagnostics, Dr. Pascolini is poised to continue shaping the future of medical genetics. Her contributions to understanding the genetic basis of intellectual disabilities and her work on cutting-edge diagnostic technologies ensure her legacy as a pioneering figure in genetics. As she continues her role in both clinical and academic settings, her future contributions will likely further advance the study and treatment of rare genetic conditions, helping countless individuals worldwide.

📑NOTABLE PUBLICATIONS 

"The face of Non-photosensitive trichothiodystrophy phenotypic spectrum: A subsequent study on paediatric population" 

  • Authors: Pascolini, G. , Lipari, M. , Gaudioso, F. , Di Zenzo, G. , Didona, B.
  • Journal: Molecular Genetics and Genomic Medicine
  • Year: 2024

"Usmani-Riazuddin syndrome can have a recognizable phenotype: Report of a novel AP1G1 variant" 

  • Authors: Gnazzo, M. , Pascolini, G. , Parlapiano, G. , Novelli, A. , Baban, A.
  • Journal: Clinical Genetics
  • Year: 2024

"Extended phenotypic characterization of a novel Helsmoortel-van der Aa syndrome case series" 

  • Authors: Pascolini, G., Di Zenzo, G., Panebianco, A., Didona, B., Gozes, I.
  • Journal: American Journal of Medical Genetics
  • Year: 2024

"Ectoderm-derived findings in Aymè-Gripp syndrome" 

  • Authors: Pascolini, G., Di Zenzo, G., Morani, P., Didona, B., Panebianco, A.
  • Journal: Journal of Dermatology
  • Year: 2024

"Defining the clinical spectrum of ichthyosis follicularis, atrichia and photophobia clinical association type 1 (IFAP1)" 

  • Authors: Pascolini, G., Fortugno, P., Chandramouli, B., Didona, B., Castiglia, D.
  • Journal: European Journal of Dermatology
  • Year: 2023

Havva Ortabozkoyun | Gene Regulation | Best Researcher Award

Published on by Global Genetics Award

Dr. Havva Ortabozkoyun | Gene Regulation | Best Researcher Award

University of Miami Miller School of Medical / Sylvester Cancer Center | United States

Author Profile

Orcid ID

Google Scholar

🧬 Havva Ortabozkoyun-Kara, PhD: Pioneering Epigenetics and Cancer Biology Researcher

🧑‍🎓 EARLY ACADEMIC PURSUITS

Havva Ortabozkoyun-Kara, PhD, embarked on her academic journey with a Bachelor of Science in Molecular Biology and Genetics from Middle East Technical University (METU) in Ankara, Turkey. Graduating with a stellar GPA of 3.80/4.00 in 2010, she demonstrated early on her dedication to understanding complex biological systems. Her education continued at Utrecht University in the Netherlands, where she pursued a Master of Science in Cancer Genomics and Developmental Biology. With a perfect GPA of 4.00/4.00, she excelled in this program, setting a strong foundation for her future research in cancer biology. Dr. Ortabozkoyun-Kara then achieved her PhD in Stem Cell Biology from New York University (NYU), where she graduated with a GPA of 3.89/4.00. During her doctoral studies, she delved into stem cell and developmental biology, further refining her focus on the mechanisms that drive cellular diversity and disease processes.

🧑‍🔬 PROFESSIONAL ENDEAVORS

Dr. Ortabozkoyun-Kara’s professional journey is marked by her extensive research experience in some of the most prestigious laboratories in the world. She began as a rotation student in the lab of Iannis Aifantis at NYU, where she explored the role of the ubiquitin system in cancer and stem cell function. Her doctoral research, conducted in the lab of Danny Reinberg at NYU School of Medicine, involved pioneering work on the insulation function of CTCF and the characterization of Polycomb Repressive Complex (PRC1) during differentiation. After completing her PhD, she continued her research as a Postdoctoral Fellow in the Reinberg Lab, focusing on gene regulation and the role of MAZ, CTCF, and other factors in disease processes. Currently, she holds a postdoctoral fellowship at the University of Miami Miller School of Medicine, where she is studying novel insulation factors on gene regulation during developmental and disease processes.

🔬 CONTRIBUTIONS AND RESEARCH FOCUS ON GENE REGULATION

Dr. Ortabozkoyun-Kara’s research has significantly advanced our understanding of epigenetics, stem cell biology, and cancer biology. Her work has centered on the intricate mechanisms of gene regulation, particularly the insulation functions that control the expression of Hox genes during development and in disease states. Through innovative CRISPR genetic screens and biochemical assays, she has identified key factors that cooperate with CTCF in these processes. Her research on the differences in Polycomb Repressive Complex composition during cellular differentiation has provided new insights into how these complexes contribute to the regulation of gene expression.

🌍 IMPACT AND INFLUENCE

Dr. Ortabozkoyun-Kara’s contributions to the fields of epigenetics and stem cell biology have had a profound impact on our understanding of how genetic and biochemical mechanisms lead to cellular diversity and disease. Her findings on the role of insulation factors in gene regulation have opened new avenues for research in developmental biology and cancer, influencing the direction of studies in these fields. Her expertise is recognized internationally, and she continues to collaborate with leading scientists to push the boundaries of what we know about gene regulation and its implications for human health.

📚 ACADEMIC CITATIONS

Dr. Ortabozkoyun-Kara’s work has been widely cited in the academic community, reflecting the importance of her contributions to the scientific understanding of gene regulation. Her publications in high-impact journals are frequently referenced by other researchers in the fields of molecular biology, genetics, and biochemistry. These citations underscore the relevance of her work to ongoing research and its potential to inform new therapeutic approaches for diseases linked to epigenetic regulation.

🏆 LEGACY AND FUTURE CONTRIBUTIONS

As Dr. Ortabozkoyun-Kara continues her research at the University of Miami, her legacy is one of innovation and discovery. Her future contributions are expected to further illuminate the complex mechanisms of gene regulation and their role in development and disease. With her deep expertise in epigenetics and stem cell biology, she is poised to make significant advances in the understanding and treatment of diseases driven by genetic and epigenetic alterations. Her work will undoubtedly continue to influence the fields of molecular biology and genetics for years to come, inspiring future generations of scientists.

💡 INNOVATIVE APPROACHES

Dr. Ortabozkoyun-Kara is known for her creative and methodical approaches to scientific research. She has developed novel genetic and biochemical methods that have expanded the toolkit available to researchers studying epigenetic mechanisms. Her work not only provides critical insights but also equips the scientific community with new strategies for investigating and manipulating gene expression in various biological contexts.

📑 NOTABLE PUBLICATIONS

"CRISPR and biochemical screens identify MAZ as a cofactor in CTCF-mediated insulation at Hox clusters" 

  • Authors: Havva Ortabozkoyun, Pin-Yao Huang, Hyunwoo Cho, Varun Narendra, Gary LeRoy, Edgar Gonzalez-Buendia, Jane A Skok, Aristotelis Tsirigos, Esteban O Mazzoni, Danny Reinberg
  • Journal: Nature Genetics
  • Year: 2022

"A CRISPR Screen Identifies Myc-associated Zinc Finger Protein (MAZ) as an Insulator Functioning at CTCF boundaries in Hox Clusters" 

  • Authors: Havva Ortabozkoyun-Kara, Pin-Yao Huang, Hyunwoo Cho, Varun Narendra, Gary Leroy, Jane A. Skok, Aristotelis Tsirigos, Esteban O. Mazzoni, Danny Reinberg
  • Journal: BioRxiv
  • Year: 2020

"Members of an array of zinc finger proteins specify distinct Hox chromatin boundaries"

  • Authors: Havva Ortabozkoyun, Pin-Yao Huang, Edgar Gonzalez-Buendia, Hyein Cho, Sang Kim, Aristotelis Tsirigos, Esteban Mazzoni, Danny Reinberg
  • Journal: bioRxiv
  • Year: 2023

"Members of a Family of Zinc Finger Proteins Demarcate Chromatin Boundaries at Hox Clusters during Development, Ortabozkoyun et. al"

  • Authors: Havva Ortabozkoyun, Pin-Yao Huang, Edgar Gonzalez-Buendia, Hyunwoo Cho, Sang Y Kim, Aristotelis Tsirigos, Esteban O Mazzoni, Danny Reinberg
  • Journal: Mendeley Data
  • Year: 2024

"Novel chromatin insulating activities uncovered upon eliminating known insulators in vivo"

  • Authors: Havva Ortabozkoyun, P. Huang, H. Cho, E. Mazzoni, A. Tsirigos, D. Reinberg
  • Year: 2023

Li Wan | Bipolar Disorder | Best Researcher Award

Published on by Global Genetics Award

Prof Li Wan | Bipolar Disorder | Best Researcher Award

Affiliated Psychological Hospital Of Anhui Medical University | China

Author Profile 

Scopus

Orcid ID

Dr. Li Wan: Expert in Cognitive Neuropsychology and Neuromodulation 🧠

Educational Background 🎓

  • Ph.D. in Psychology (2006) - Virginia Polytechnic Institute and State University, Virginia, USA
  • Master of Psychology (2004) - Virginia Polytechnic Institute and State University, Virginia, USA
  • Bachelor of Clinical Medicine (1998) - Hubei University of Medicine, Hubei, China

Professional Experience 💼

  • Adjunct Professor (2022-present) - Anhui Medical University, Hefei, China
  • Director (2021-present) - Brain Disorders and Neuromodulation Research Center, Anhui Mental Health Center, Hefei, China
  • Co-Principal Investigator (2018-2021) - Cognitive Neuropsychology Lab, University of Science and Technology of China, Hefei, China
  • Research Scientist (2014-2018) - School of Medicine, University of Missouri-Kansas City; Center for Behavioral Medicine/Department of Mental Health, Missouri, USA
  • Clinical Assistant Professor/Post-doc Fellow (2007-2013) - Department of Psychiatry and Behavioral Science, Texas A&M University and Central Texas Veterans Health Care System; Department of Psychology and Neuroscience, Baylor University, Texas, USA
  • Teaching/Research Assistant (2002-2006) - Department of Psychology, Virginia Tech, Virginia, USA

Fellowships & Honors 🏆

  • Anhui Province ‘Overseas High-level Talents’ Award (2019)
  • Fellowship, Athinoula A. Martinos Center for Biomedical Imaging, Harvard University (2010)
  • Travel Award, Graduate Student Association, Virginia Tech (2006)
  • Galper Fund Award, Department of Psychology, Virginia Tech (2005)
  • Multiple Travel Awards (2004-2006) - 1st, 2nd, and 3rd Joint ECNS and ISNIP Conferences
  • Graduate Research Development Project Grant, Virginia Tech (2003)

Affiliations & Memberships 🌐

  • Deputy Secretary - Sleep Branch, China Traditional Chinese Medicine Information Conference
  • Vice Director - Cognitive Behavioral Therapy Committee, Anhui Psychological Health Association
  • Member - World Psychiatric Association (WPA), Society for Psychophysiological Research (SPR), Cognitive Neuroscience Society (CNS)
  • Editorial Board Member - Brain Science Advances, Journal of Brain Research and Neurology, World Journal of Clinical Medicine Research, International Journal of Psychological and Brain Sciences, Advances in Health and Behavior
  • Reviewer - NeuroImage, Human Brain Mapping, Neural Regeneration Research, Psychophysiology, International Journal of Psychophysiology, Journal of Psychiatry Research, Psychiatry Research, and more

Journal Publications 📚

Dr. Li Wan has contributed significantly to the fields of psychology and neuroscience, with numerous publications in prestigious journals such as Heliyon, Human Brain Mapping, Frontiers in Psychology, Laboratory Medicine, and World Psychiatry. Her research covers a broad spectrum of topics, including affective disorders, brain morphology, cognitive neuropsychology, and the neural mechanisms underlying behavioral and psychiatric conditions.

Notable Publications 📑

"The neural mechanisms of immediate and follow-up of the treatment effect of hypnosis on smoking craving" 

  • Authors: Li, X., Chen, L., Ma, R., Rao, H., Zhang, X.
  • Journal: Brain Imaging and Behaviour
  • Year: 2020

"The Effect of Vocabulary Depth and Breadth on English Listening Comprehension Can Depend on How Comprehension Is Measured " 

  • Authors: Luo, Y., Song, H., Wan, L., Zhang, X.
  • Journal: Frontiers in Psychology
  • Year: 2021

"Laboratory Predictors of COVID-19 Pneumonia in Patients with Mild to Moderate Symptoms "

  • Authors: Li, J., Wan, L., Feng, Y., Zhang, X., Xia, M
  • Journal: Lab Medicine
  • Year: 2021

"Brain morphology, harm avoidance, and the severity of excessive internet use"

  • Authors: Wan, L., Zha, R., Ren, J., Zuo, H., Zhang, X.
  • Journal: Human Brain Mapping
  • Year: 2022

"Decision tree distinguish affective disorder diagnosis from psychotic disorder diagnosis with clinical and lab factor"

  • Authors: Liu, X., Wang, X., Wen, C., Wan, L.
  • Journal: Heliyon
  • Year: 2022

Zafran Khan | Tuberculosis Researcher | Editorial Board Member

Published on by Global Genetics Award

Mr. Zafran Khan | Tuberculosis | Editorial Board Member

University of Calgary | Pakisthan

Author Profile

Google Scholar

Orcid ID

EARLY ACADEMIC PURSUITS:

ZAFRAN KHAN initiated his academic journey at the University of Swat (UOS) in Swat, Pakistan, where he pursued a Bachelor of Science (Hons) in Microbiology from 2012 to 2016. During this period, he conducted research on the "Incidence of HCV in the general population of District Swat, Pakistan," showcasing an early interest in infectious diseases and molecular biology.

PROFESSIONAL ENDEAVORS:

Following his undergraduate studies, ZAFRAN KHAN ventured into higher education at the University of Chinese Academy of Sciences (UCAS) in Beijing, China. Here, he enrolled as a Master student in Biochemistry and Molecular Biology from September 2018 to August 2019. His coursework covered diverse topics, including Genomics, Immunology, Biochemistry, and Molecular Biology, laying a solid foundation for his subsequent research pursuits.

CONTRIBUTIONS AND RESEARCH FOCUS ON TUBERCULOSIS

ZAFRAN KHAN's notable research contributions are evident during his tenure as a Master's Full-time Research Candidate at the State Key Laboratory of Respiratory Infectious Disease (GIBH) in Guangzhou, China, from August 2019 to August 2021. His primary research focus encompassed Mycobacterium tuberculosis resistance mechanisms, novel drug targets, docking, molecular dynamic simulation, and vaccine and drug designing. Noteworthy projects include the identification of resistance mechanisms associated with prothionamide and amikacin in Mycobacterium tuberculosis clinical isolates.

IMPACT AND INFLUENCE:

ZAFRAN KHAN's work holds significant implications for understanding and combating tuberculosis, a global health concern. His efforts in exploring unexplored resistance mechanisms and conducting molecular detection of anti-tubercular resistance in clinical isolates contribute to the broader scientific community's knowledge base. The impact of his research extends beyond borders, as evidenced by his involvement in international conferences and workshops.

ACADEMIC CITES:

ZAFRAN KHAN's academic journey is marked by a commitment to excellence, exemplified by his active participation in international conferences and workshops. This exposure has likely contributed to his knowledge enrichment and the incorporation of global perspectives into his research.

LEGACY AND FUTURE CONTRIBUTIONS:

ZAFRAN KHAN has established a legacy of dedication and proficiency in the field of Microbiology and Molecular Biology. His early research on HCV in Swat and subsequent work on tuberculosis resistance mechanisms showcase a commitment to addressing critical health challenges. As he progresses in his academic and research journey, ZAFRAN KHAN is poised to make further contributions to the scientific community, leaving a lasting legacy in the realm of infectious diseases and immunity.

Notable Publications

Guillain-Barre syndrome: An autoimmune disorder post-COVID-19 vaccination?  2022(9)

Cold stress-induced seed germination and biosynthesis of polyphenolics content in medicinally important Brassica rapa 2022(8)

Chimeric antigen receptor T cell structure, its manufacturing, and related toxicities; a comprehensive review 2022(7)