Sherin Devaskar | Gene Regulation Epigenetics | Best Researcher Award

Prof. Sherin Devaskar | Gene Regulation Epigenetics | Best Researcher Award

Prof. Sherin Devaskar | UCLA | United States

Dr. Sherin U. Devaskar is a Distinguished Professor of Pediatrics at UCLA and the Executive Director of the Children’s Discovery and Innovation Institute. Renowned for her work in neonatology and developmental biology, Dr. Devaskar has committed her scientific career to unraveling how intrauterine environments influence neonatal and long-term offspring outcomes. Her research spans cellular, molecular, genetic, epigenetic, and physiological mechanisms, specifically focusing on placental biology and metabolic programming. As a leader in her field, she combines clinical excellence with groundbreaking research, translating findings into improvements in pediatric care. She has been recognized nationally for her academic contributions, holding memberships in elite institutions like the National Academy of Medicine. Dr. Devaskar’s research has had a significant impact on public health, particularly in understanding how early life exposures affect lifelong health trajectories. Her translational work bridges laboratory insights with population-based outcomes, making her a respected authority in developmental and environmental health research.

Publication Profiles: 

Scopus
Google Scholar

Education:

Dr. Sherin Devaskar began her medical training at Madras Medical College, India, where she earned her M.B.B.S./M.D. in Medicine. She pursued an Internship in Pediatrics (PL1) at the Institute of Child Health, Madras, completing. Seeking advanced clinical training, she moved to the United States and completed a Residency in Pediatrics (PL1 & PL2) at Wayne State Affiliated Hospitals, Detroit, MI. This strong foundation in both Indian and American medical systems gave her a global perspective in pediatrics. Over time, she augmented her clinical training with postdoctoral research and academic development, evolving into a globally recognized expert in neonatal and pediatric medicine. Her education laid the groundwork for a lifelong pursuit of excellence in child health and developmental research, fostering interdisciplinary collaboration across medicine, epidemiology, nutrition, and molecular biology.

Experience:

Dr. Devaskar has more than four decades of experience in pediatric medicine, specializing in neonatology and developmental biology. She currently holds the title of Distinguished Professor of Pediatrics at UCLA and serves as the Executive Director of both the Children’s Discovery and Innovation Institute and the Neonatal Research Center. Throughout her career, she has bridged clinical practice with scientific inquiry, directing major NIH-funded projects and mentoring the next generation of physician-scientists. Her work spans bench-to-bedside research on maternal-fetal health, metabolic programming, and placental function. She has held leadership roles in various pediatric research networks and has served on advisory boards for national health agencies. Her professional experience is distinguished not just by volume but also by the interdisciplinary and translational nature of her work. Dr. Devaskar is also a committed educator, having trained countless medical students, residents, and fellows who now contribute meaningfully to pediatric research and care worldwide.

Awards and Honors:

Dr. Sherin Devaskar’s pioneering contributions to pediatric medicine and research have earned her numerous prestigious awards. Most notably, she received the American Pediatric Society John Howland Award, the highest honor in academic pediatrics, recognizing her lifetime achievements in research, education, and leadership. She was honored with the Outstanding Scientific Accomplishments Award by the ATMA Association. Her election to the National Academy of Medicine further highlights her stature among the leading medical scientists in the world. These accolades reflect her sustained commitment to advancing pediatric health through rigorous science, innovation, and mentorship. In addition to these national honors, she is regularly invited to speak at international conferences, review NIH grants, and contribute to influential scientific panels. Her recognition underscores a career dedicated not only to scientific discovery but also to improving the lives of children globally through compassionate, evidence-based care.

Research Focus:

Dr. Devaskar’s research centers on the impact of intrauterine and early-life exposures on fetal and neonatal development, with an emphasis on placental biology, metabolic imprinting, and epigenetic regulation. Her multidisciplinary approach integrates molecular biology, environmental health, physiology, and neonatology, making her a leader in unraveling how prenatal environments shape long-term health outcomes. She has investigated the effects of air pollutants, nutritional mismatches, and oxidative stress on pregnancy outcomes and infant development. Her studies incorporate animal models, human cohorts, and placental tissue analyses to uncover biomarkers and molecular pathways that could be targeted for interventions. Notably, she explores placental resilience, especially under extreme stressors like COVID-19 or urban pollution. Dr. Devaskar’s work has direct translational relevance, offering insight into preventative strategies and therapeutic solutions for adverse pregnancy outcomes, pre-eclampsia, and neonatal hypoglycemia. Her research is frequently published in top-tier journals and is influential in shaping maternal-child health policies.

Publications Top Notes: 

  1. Diet, polycyclic aromatic hydrocarbons, and oxidative stress biomarkers in pregnancy: A Los Angeles pregnancy cohort

  2. Pediatric subspecialty workforce: what is needed to secure its vitality and survival?

  3. Does Amsterdam criteria applied to largely unsubmitted term placentas with favorable fetal outcomes show significant maternal clinicopathologic correlation?

  4. Exploring the long-term impacts of neonatal hypoglycemia to determine a safe threshold for glucose concentrations

  5. Hepatic and Pancreatic Cellular Response to Early Life Nutritional Mismatch

  6. Ambient exposure to fine particulate matter with oxidative potential affects oxidative stress biomarkers in pregnancy

  7. Placental Privilege: Evidence of organ resilience in severe COVID-19 in pregnancy

  8. Omega-3 reverses the metabolic and epigenetically regulated placental phenotype acquired from preconceptional and peri-conceptional exposure to air pollutants

  9. Urinary polycyclic aromatic hydrocarbon metabolites and their association with oxidative stress among pregnant women in Los Angeles

  10. Circulating extracellular vesicular microRNA signatures in early gestation show an association with subsequent clinical features of pre-eclampsia

Conclusion:

In conclusion, Dr. Sherin U. Devaskar is an outstanding candidate for the Best Researcher Award, with a remarkable blend of research excellence, leadership, and clinical relevance. Her contributions to understanding fetal and placental programming, particularly in the context of environmental exposures and metabolic health, have advanced the field in both depth and scope. Her dedication to interdisciplinary methods and translational science positions her as a thought leader in pediatric and perinatal research. Although greater global engagement and public science dissemination could enhance the reach of her work, these are growth areas rather than gaps. The breadth of her expertise, combined with her history of academic leadership and award-winning research, make her not only deserving of this recognition but also a role model for future generations of physician-scientists. Recognizing Dr. Devaskar with this award would honor a career built on scientific rigor, innovation, and a lifelong commitment to improving child and maternal health worldwide.

Raphael Borie | Gene Regulation Epigenetics | Best Researcher Award

Prof. Dr. Raphael Borie | Gene Regulation Epigenetics | Best Researcher Award

Prof. Dr. Raphael Borie, APHP, France

Dr. Raphaël Borie, born on August 15, 1977, in Paris, France, is a leading expert in pulmonology and genetic respiratory diseases. Currently a University Professor Hospital Practitioner at Bichat Hospital (Paris Cité University), he has consistently contributed to the advancement of respiratory medicine, particularly in the field of interstitial lung diseases (ILDs). His clinical insight, combined with a strong research portfolio, has positioned him as a prominent figure within the OrphaLung network. A dedicated family man with two children, Dr. Borie is widely respected for his integrity, leadership, and commitment to collaborative medicine. His career reflects a unique blend of academic excellence and impactful translational research, bridging the gap between genomics and clinical care in ILD. He is a registered member of the French Medical Council (Ordre des Médecins No. 75/71138), and his research has influenced European clinical guidelines and improved the understanding of rare genetic pulmonary conditions.

Publication Profile: 

Scopus

✅ Strengths for the Award:

  1. Robust Academic Background:
    Dr. Borie holds a PhD in Genetics, Master’s in Physiology, and HDR (habilitation to supervise doctoral research), which underlines his scientific credibility and ability to lead independent research.

  2. Clinical-Research Integration:
    As a University Professor and Hospital Practitioner, he merges frontline patient care with cutting-edge genetic and respiratory disease research.

  3. High Publication Impact:
    With 283 PubMed-indexed articles and an H-index of 60, Dr. Borie’s work demonstrates strong citation influence, indicating widespread recognition and utility in the scientific community.

  4. International Leadership:
    Active in multinational collaborations (e.g., OrphaLung, ERS), he has co-authored major position statements and clinical trials, influencing European respiratory care guidelines.

  5. Innovation in Rare Diseases:
    A recognized expert in familial interstitial lung disease and telomere disorders, his work has led to earlier diagnosis and targeted therapies—critical in fields where few experts exist.

  6. Recognition and Funding:
    He has secured prestigious mobility grants (ERS, Respirology Teachers College)—a marker of trust in his scientific mission and innovation.

🔍 Areas for Improvement:

  • Wider Public Health Translation: While Dr. Borie’s genomic research is exceptional, expanding into real-world health policy implementation could enhance systemic impact.

  • Patient Engagement & Advocacy: Developing patient-oriented tools or registries (e.g., digital apps or platforms for familial lung diseases) may broaden his outreach beyond academia and clinics.

  • Broader Visibility: Although highly cited in professional circles, participation in international keynote talks, editorial leadership, or mainstream health media could elevate his public and professional visibility.

🎓 Education:

Dr. Borie has pursued an extensive and rigorous academic path focused on respiratory and genetic medicine. He obtained his medical degree with specialization in Allergology and Immunopathology in 2006. A year earlier, in 2005, he earned a Master’s degree in Biology and Physiology of Circulation and Respiration. Demonstrating deep interest in genetics, he completed a PhD in Genetics in 2017, contributing significantly to our understanding of genetic underpinnings in pulmonary fibrosis. In 2019, Dr. Borie achieved the prestigious Habilitation à Diriger des Recherches (HDR) from the University of Paris 7, enabling him to supervise doctoral research. His academic background illustrates a powerful integration of clinical expertise and molecular research—providing him with the tools to lead innovative research projects at the intersection of genomics and pulmonology.

🩺 Experience:

Dr. Raphaël Borie has over 15 years of experience in respiratory medicine. From July 2011 to August 2020, he served as a Hospital Practitioner in the Pneumology Department at Bichat Hospital under Professors Aubier and Crestani. Since September 2020, he has been a University Professor Hospital Practitioner in the same department, affiliated with Paris Cité University. He has contributed to patient care, education of medical students and residents, and cutting-edge research. As part of the OrphaLung network, he plays a critical role in advancing diagnostic tools and treatment approaches for rare lung diseases. He is recognized for his collaborative leadership and interdisciplinary contributions across genetics, immunology, and pulmonology. His international collaborations and authorship of over 280 PubMed-indexed publications demonstrate his ongoing commitment to improving patient outcomes through translational research.

🏆 Awards and Honors:

Dr. Borie’s research excellence has been recognized through several prestigious awards and scholarships. In 2017, he received the European Respiratory Society (ERS) Mobility Grant for his work on Identification of Preclinical Markers of Pulmonary Fibrosis, supporting international collaboration and advanced training. The same year, he was also honored with the Respirology Teachers College Mobility Grant, reinforcing his pioneering research on early detection of fibrotic lung disease. His selection for these awards highlights both scientific innovation and dedication to knowledge exchange. His leadership in multi-center studies and involvement in ERS guideline statements further reflect his status as a thought leader in interstitial lung disease. These honors are a testament to his influence in shaping the future of pulmonary genetics and translational respiratory medicine.

🔬 Research Focus:

Dr. Raphaël Borie’s research centers on familial and genetic interstitial lung diseases, particularly the molecular mechanisms behind pulmonary fibrosis, telomere biology, surfactant-related gene variants, and early detection strategies. He works extensively on identifying genetic risk variants (e.g., MUC5B, DSP) and their implications in idiopathic pulmonary fibrosis. Through his participation in the OrphaLung network, he supports genomic screening for hereditary lung disorders and contributes to developing European guidelines. His work bridges genomic medicine and clinical pulmonology, aiming for earlier diagnosis and personalized treatment approaches. He has led and co-authored critical studies on RTEL1 mutations, telomerase complex defects, and familial ILD phenotypes, helping clinicians globally understand the heterogeneity and systemic implications of genetic lung disorders. His collaborative international research ensures his findings are applied in practice to optimize long-term patient care.

📚Publications Top Notes:

  • 🧬 High risk of lung cancer in surfactant-related gene variant carriersEur Respir J, 2024

  • 📄 European Respiratory Society Statement on Familial Pulmonary FibrosisEur Respir J, 2022

  • 🧪 Colocalization of Gene Expression and DNA Methylation with Genetic Risk VariantsAm J Respir Crit Care Med, 2022

  • 🧬 RTEL1 mutations and their phenotypic variabilityEur Respir J, 2019

  • 💊 Safety and efficacy of pirfenidone in telomerase mutation carriersEur Respir J, 2018

  • 🌐 Diagnosis and follow-up of familial ILD: International surveyBMC Pulmonary Med, 2025

  • 🧬 New 2023 ACR/EULAR APS criteria performance in young patientsLetter, 2025

  • 🫁 A non-resolving cough: a case of familial pulmonary fibrosisBreathe, 2025

  • 🧬 PFMG2025: Genomic medicine in French healthcare systemReview, 2025

  • 💊 Efficacy of CFTR modulators in ABCA3-deficiency ILDOpen Access, 2025

  • 🧠 Neurological manifestations in VEXAS syndromeJournal of Neurology, 2025

  • 💉 Real-life use of PEXIVAS reduced-dose regimen in vasculitisAnn Rheum Dis, 2025

  • 🧫 Recurrent respiratory papillomatosis with lung involvementEur Respir J, 2025

  • 🔍 RA-ILD: genetics to clinical overviewReview, 2025

  • 👶 Childhood ILD survivors in adulthood: European studyEur Respir J, 2025

🧾 Conclusion:

Dr. Raphaël Borie exemplifies the ideal candidate for the Best Researcher Award. His excellence spans across clinical expertise, academic distinction, and international research leadership, especially in genetic and familial interstitial lung diseases—a field with enormous unmet need. His consistent scholarly output, impactful collaborations, and patient-focused studies highlight a unique blend of depth and innovation. While further expansion into public health frameworks and patient engagement tools would be valuable, his profile already reflects a world-class researcher with transformative contributions to pulmonary medicine.