Stefan J. Green

Dr. Stefan J. Green

Rush University Medical Center
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 July 2015 in Movement Disorders
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Journal Article
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AKAli Keshavarzian
Ali Keshavarzian
SGStefan J. Green
Stefan J. Green
PEPhillip A. Engen
Phillip A. Engen
RVRobin M. Voigt
Robin M. Voigt
ANAnkur Naqib
Ankur Naqib
KSKathleen M. Shannon
Kathleen M. Shannon

12 April 2019 in Science
Verified
Journal Article
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FGFrancine E. Garrett-Bakelman
Francine E. Garrett-Bakelman
MDManjula Darshi
Manjula Darshi
SGStefan J. Green
Stefan J. Green
RGRuben C. Gur
Ruben C. Gur
LLLing Lin
Ling Lin
FTFred Turek
Fred Turek
What to expect after a year in space: Space is the final frontier for understanding how extreme environments affect human physiology. Following twin astronauts, one of which spent a year-long mission on the International Space Station, Garrett-Bakelman et al. examined molecular and physiological traits that may be affected by time in space (see the Perspective by Löbrich and Jeggo). Sequencing the components of whole blood revealed that the length of telomeres, which is important to maintain in dividing cells and may be related to human aging, changed substantially during space flight and again upon return to Earth. Coupled with changes in DNA methylation in immune cells and cardiovascular and cognitive effects, this study provides a basis to assess the hazards of long-term space habitation. Science , this issue p. eaau8650 ; see also p. 127

15 November 2011 in Applied and Environmental Microbiology
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Journal Article
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JKJoel E. Kostka
Joel E. Kostka
OPOm Prakash
Om Prakash
WOWill A. Overholt
Will A. Overholt
SGStefan J. Green
Stefan J. Green
GFGina Freyer
Gina Freyer
MHMarkus Huettel
Markus Huettel
A significant portion of oil from the recent Deepwater Horizon (DH) oil spill in the Gulf of Mexico was transported to the shoreline, where it may have severe ecological and economic consequences. The objectives of this study were (i) to identify and characterize predominant oil-degrading taxa that may be used as model hydrocarbon degraders or as microbial indicators of contamination and (ii) to characterize the in situ response of indigenous bacterial communities to oil contamination in beach ecosystems. This study was conducted at municipal Pensacola Beach, FL, where chemical analysis revealed weathered oil petroleum hydrocarbon (C 8 to C 40 ) concentrations ranging from 3.1 to 4,500 mg kg −1 in beach sands. A total of 24 bacterial strains from 14 genera were isolated from oiled beach sands and confirmed as oil-degrading microorganisms. Isolated bacterial strains were primarily Gammaproteobacteria , including representatives of genera with known oil degraders ( Alcanivora x, Marinobacter , Pseudomonas , and Acinetobacter ). Sequence libraries generated from oiled sands revealed phylotypes that showed high sequence identity (up to 99%) to rRNA gene sequences from the oil-degrading bacterial isolates. The abundance of bacterial SSU rRNA gene sequences was ∼10-fold higher in oiled (0.44 × 10 7 to 10.2 × 10 7 copies g −1 ) versus clean (0.024 × 10 7 to 1.4 × 10 7 copies g −1 ) sand. Community analysis revealed a distinct response to oil contamination, and SSU rRNA gene abundance derived from the genus Alcanivorax showed the largest increase in relative abundance in contaminated samples. We conclude that oil contamination from the DH spill had a profound impact on the abundance and community composition of indigenous bacteria in Gulf beach sands, and our evidence points to members of the Gammaproteobacteria ( Alcanivorax , Marinobacter ) and Alphaproteobacteria ( Rhodobacteraceae ) as key players in oil degradation there.

21 May 2014 in PLOS ONE
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Journal Article
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RVRobin Michelle Voigt-Zuwala
Robin Michelle Voigt-Zuwala
CFChristopher B. Forsyth
Christopher B. Forsyth
SGStefan J. Green
Stefan J. Green
EMEce Mutlu
Ece Mutlu
PEPhillip Engen
Phillip Engen
AKAli Keshavarzian
Ali Keshavarzian
Intestinal dysbiosis and circadian rhythm disruption are associated with similar diseases including obesity, metabolic syndrome, and inflammatory bowel disease. Despite the overlap, the potential relationship between circadian disorganization and dysbiosis is unknown; thus, in the present study, a model of chronic circadian disruption was used to determine the impact on the intestinal microbiome. Male C57BL/6J mice underwent once weekly phase reversals of the light:dark cycle (i.e., circadian rhythm disrupted mice) to determine the impact of circadian rhythm disruption on the intestinal microbiome and were fed either standard chow or a high-fat, high-sugar diet to determine how diet influences circadian disruption-induced effects on the microbiome. Weekly phase reversals of the light:dark (LD) cycle did not alter the microbiome in mice fed standard chow; however, mice fed a high-fat, high-sugar diet in conjunction with phase shifts in the light:dark cycle had significantly altered microbiota. While it is yet to be established if some of the adverse effects associated with circadian disorganization in humans (e.g., shift workers, travelers moving across time zones, and in individuals with social jet lag) are mediated by dysbiosis, the current study demonstrates that circadian disorganization can impact the intestinal microbiota which may have implications for inflammatory diseases.

19 September 2011 in Environmental Microbiology
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TGThomas M. Gihring
Thomas M. Gihring
SGStefan J. Green
Stefan J. Green
CSChristopher W. Schadt
Christopher W. Schadt
Summary: Technologies for massively parallel sequencing are revolutionizing microbial ecology and are vastly increasing the scale of ribosomal RNA (rRNA) gene studies. Although pyrosequencing has increased the breadth and depth of possible rRNA gene sampling, one drawback is that the number of reads obtained per sample is difficult to control. Pyrosequencing libraries typically vary widely in the number of sequences per sample, even within individual studies, and there is a need to revisit the behaviour of richness estimators and diversity indices with variable gene sequence library sizes. Multiple reports and review papers have demonstrated the bias in non‐parametric richness estimators (e.g. Chao1 and ACE) and diversity indices when using clone libraries. However, we found that biased community comparisons are accumulating in the literature. Here we demonstrate the effects of sample size on Chao1, ACE, CatchAll, Shannon, Chao–Shen and Simpson's estimations specifically using pyrosequencing libraries. The need to equalize the number of reads being compared across libraries is reiterated, and investigators are directed towards available tools for making unbiased diversity comparisons.

18 September 2014 in Nature Communications
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MOMaya Ofek-Lalzar
Maya Ofek-Lalzar
NSNoa Sela
Noa Sela
MGMilana Goldman-Voronov
Milana Goldman-Voronov
SGStefan J. Green
Stefan J. Green
YHYitzhak Hadar
Yitzhak Hadar
DMDror Minz
Dror Minz