Terry Snell

Terry Snell's profile picture
terry.snell@biosci.gatech.edu

Terry Snell, an Emeritus Professor in the School of Biological Sciences, is a member of the Parker H. Petit Institute for Bioengineering and Bioscience.

Professor Emeritus
Phone
404-385-4498
Office
Cherry Emerson 201
Additional Research
Chemical ecology of zooplankton; mate recognition; evolutionary ecology; aquatic toxicology; gene expression in response to environmental stress; aquaculture. 
Research Focus Areas
Google Scholar
https://scholar.google.com/citations?user=_4PzVMEAAAAJ&hl=en

Kirill Lobachev

Kirill Lobachev's profile picture
kirill.lobachev@biology.gatech.edu

My laboratory investigates molecular mechanisms underlying eukaryotic genome stability. Chromosomal rearrangements create genetic variation that can have deleterious or advantageous consequences. Karyotypic abnormalities are a hallmark of many tumors and hereditary diseases in humans. Chromosome rearrangements can also be a part of the programmed genetic modifications during cellular differentiation and development. In addition, gross DNA rearrangements play a major role in the chromosome evolution of eukaryotic organisms. Therefore, elucidation of molecular mechanisms leading to chromosome instability is important for studying human pathology and also for our understanding of the fundamental processes that determine the architecture and dynamics of eukaryotic genomes. 

My overall contribution to the field of genome instability has been the demonstration of the phenomenon that repeats often found in eukaryotic genomes are potent sources of genome instability. Specifically, I have been investigating one of the most fundamental and enigmatic processes as to how repetitive sequences that adopt non-canonical DNA secondary structures, such as hairpins and cruciforms, cause replication arrest, double-strand breaks, and gross chromosomal rearrangements. Using molecular biology approaches, we investigate the instability of secondary structure-forming repeats in Saccharomyces cerevisiae, Schizosaccharomyces pombe, and human fibroblasts.

Associate Professor
Phone
404-385-6197
Office
Petit Biotechnology Building, Office 2303
Additional Research
Using yeastSaccharomyces cerevisiaeas a model, my laboratory investigates molecular mechanisms underlying eukaryotic genome stability. Chromosomal rearrangements create genetic variation that can have deleterious or advantageous consequences. Karyotypic abnormalities are a hallmark of many tumors and hereditary diseases in humans. Chromosome rearrangements can also be a part of the programmed genetic modifications during cellular differentiation and development. In addition, gross DNA rearrangements play a major role in chromosome evolution of eukaryotic organisms. Therefore, elucidation of molecular mechanisms leading to chromosome instability is important for studying the human pathology and also for our understanding of the fundamental processes that determine the architecture and dynamics of eukaryotic genomes. Myoverall contributionto the field of genome instability has been the demonstration of the phenomenon that repeats often found in higher eukaryotic genomes including the human genome are potent sources of double-strand breaks (DSB) and gross chromosomal rearrangements (GCR). Specifically, my lab, is investigating how repetitive sequences that can adopt non-B DNA secondary structures pose a threat to chromosomal integrity dictated by their size and arrangement. Currently three sequence motifs are studied in my laboratory: inverted repeats; Friedreich's ataxia GAA/TTC trinucleotide repeats and G-quadruplex-forming tracts. We also are collaborating with Dr. Malkova lab, University of Iowa, to study one of the outcomes of the DSB formation at unstable repeats - break-induced replication.
Research Focus Areas
Google Scholar
https://scholar.google.com/citations?user=SagVxawAAAAJ&hl=en

Roman Mezencev

Roman Mezencev's profile picture
roman.mezencev@biosci.gatech.edu

Roman Mezencev is an adjunct associate professor in the School of Biological Sciences at Georgia Tech and a scientist at the U.S. EPA’s National Center of Public Health and Environmental Assessment. His areas of research interest include cancer biology, pharmacology, toxicogenomics, protein misfolding diseases, and public health. In cancer biology, his main research focuses on using omics data to identify new cancer subtypes through molecular profiling, which can help enhance their diagnosis and treatment. Additionally, Mezencev explores the use of omics data to predict and understand chemically-induced cancer and other adverse outcomes to protect public health. He is also investigating the intriguing epidemiological associations and mechanistic connections between cancer and Alzheimer’s disease (AD), as well as other protein-misfolding diseases. By understanding these associations, we can identify shared risk factors and molecular mechanisms that can lead to the development of new anti-cancer and anti-AD drugs and enhance our understanding of these complex diseases.
 

Adjunct Associate Professor, School of Biological Sciences
Phone
404-992-0151

King Jordan

King Jordan's profile picture
king.jordan@biology.gatech.edu

King Jordan is Professor in the School of Biological Sciences and Director of the Bioinformatics Graduate Program at the Georgia Institute of Technology. He has a computational laboratory and his group works on a wide variety of research and development projects related to: (1) human clinical & population genomics, (2) computational genomics for public health, and (3) computational approaches to functional genomics. He is particularly interested in the relationship between human genetic ancestry and health. His lab is also actively engaged in capacity building efforts in genomics and bioinformatics in Latin America. 

Professor
Director, Bioinformatics Graduate Program
Phone
404-385-2224
Office
EBB 2109
Additional Research

Epigenetics ; Computational genomics for public health. We are broadly interested in the relationship between genome sequence variation and health outcomes. We study this relationship through two main lines of investigation - human and microbial.Human:we study how genetic ancestry and population structure impact disease prevalence and drug response. Our human genomics research is focused primarily on complex common disease and aims to characterize the genetic architecture of health disparities, in pursuit of their elimination.Microbial:we develop and apply genome-enabled approaches to molecular typing and functional profiling of microbial pathogens that cause infectious disease. The goal of our microbial genomics research is to empower public health agencies to more effectively monitor and counter infectious disease agents.

Google Scholar
https://scholar.google.com/citations?user=v1hVGqgAAAAJ&hl=en

Marc Weissburg

Marc Weissburg's profile picture
marc.weissburg@biology.gatech.edu
Professor, School of Biological Sciences
Brook Byers Professor
Phone
404.894.8433
Office
ES&T 2238
Additional Research

Bio-inspired materials

Research Focus Areas
Google Scholar
https://scholar.google.com/citations?hl=en&user=z5dzCHUAAAAJ&view_op=list_works&sortby=pubdate

Joel Kostka

Joel Kostka's profile picture
joel.kostka@biology.gatech.edu

Dr. Kostka is currently a professor of Biology at Georgia Institute of Technology (GT). Prior to GT, he was an Associate Professor at the Department of Oceanography, Florida State University. His research involves microorganism studies in geochemical cycles of pristine and contaminated ecosystems, from the oceans to the terrestrial subsurface.

Professor, School of Biological Sciences
Associate Chair of Research, School of Biological Sciences
Phone
(404) 385-3325
Research Focus Areas

Jennifer Leavey

Portrait of Jennifer Leavey
jennifer.leavey@cos.gatech.edu

Jennifer Leavey is a principal academic professional in the School of Biological Sciences and assistant dean for Faculty Mentoring for the College of Sciences. She also coordinates the College's educational programs related to science and sustainability including the Georgia Tech Urban Honey Bee Project and the Living Building Science Vertically Integrated Project Team.   

Assistant Dean for Faculty Mentoring, College of Sciences
Principal Academic Professional, School of Biological Sciences

Katherine Duchesneau

Katherine Duchesneau's profile picture
kduchesneau3@gatech.edu

Katherine Duchesneau is a Ph.D. student in the School of Biological Sciences at Georgia Tech. Her dissertation research closely couples biogeochemistry with metagenomics to elucidate the impacts of climate change on soil microbial communities that play an important role in greenhouse gas production and the global carbon cycle. Over the long term, she plans to pursue a career in academia, generating fundamental research that drives the development of climate change mitigation and adaptation strategies. Katherine strongly believes that substantive solutions for sustainability issues will only be achieved through multi-disciplinary and diverse collaborations that bring together scientists, policymakers, and the public. Before coming to Georgia Tech, Katherine completed a MSc at Queen’s University with Dr. Robert Colautti and Dr. Pedro Antunes researching the effects of Alliaria petiolata invasion on soil microbial communities. She also holds a bachelor’s degree in Environmental Biology, specializing in plant biology, from McGill University.

BBISS Graduate Fellow - First Cohort

Jeannette Yen

Jeannette Yen's profile picture
jeannette.yen@biology.gatech.edu
Professor, School of Biological Sciences
Phone
404.385.1596
Office
Cherry Emerson A116
Additional Research

Aquatic chemical communicationHydrodynamicsSmall-Scale Biological-Chemical-Physical Interactions in Marine Zooplankton 

Google Scholar
https://scholar.google.com/scholar?q=Jeannette+Yen&btnG=&hl=en&as_sdt=0,11

Matthew Torres

Matthew Torres's profile picture
matthew.torres@biology.gatech.edu

Matt is a former Tar Heel from UNC Chapel Hill. His training is in mass spectrometry-based proteomics and G protein signaling. He has been investigating PTMs since 2001. He is also a co-director of the Systems Mass Spectrometry Core (SYMS-C) facility at Georgia Tech.

Associate Professor
Phone
404-385-0401
Office
EBB 4009
Additional Research
Bioinformatics. My lab integrates mass spectrometry and experimental cell biology using the yeast model system to understand how networks of coordinated PTMs modulate biological function. Now well into the era of genomics and proteomics, it is widely appreciated that understanding individual genes or proteins, although necessary, is often not sufficient to explain the complex behavior observed in living organisms. Indeed, placing context on the dynamic network of relationships that exist between multiple proteins is now one of the greatest challenges in Biology. Post-translational modifications (PTMs, e.g. phosphorylation, ubiquitination and over 200 others), which can be readily quantified by mass spectrometry (MS), often mediate these dynamic relationships through enhancement or disruption of binding and/or catalytic properties that can result in changes in protein specificity, stability, or cellular localization. We use a combination of tools including quantitative mass spectrometry, yeast genetics, dose-response assays, in vitro biochemistry, and microscopy to explore testable systems-level hypotheses. My current research interests can be grouped into four main categories:(1)coordinated PTM-based regulation of dynamic signaling complexes, (2) cross-pathway coordination by PTMs, (3) PTM networks in stress adaptation, and (4) technology development for rapid PTM network detection.
Research Focus Areas
Google Scholar
https://scholar.google.com/citations?user=YU_CG7wAAAAJ&hl=en&oi=ao