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Multidrug and Mupirocin Resistance in Environmental Methicillin-Resistant Staphylococcus aureus (MRSA) Isolates from Homes of People Diagnosed with Community-Onset MRSA Infection.

Applied and environmental microbiology

Shahbazian JH, Hahn PD, Ludwig S, Ferguson J, Baron P, Christ A, Spicer K, Tolomeo P, Torrie AM, Bilker WB, Cluzet VC, Hu B, Julian K, Nachamkin I, Rankin SC, Morris DO, Lautenbach E, Davis MF.
PMID: 28939607
Appl Environ Microbiol. 2017 Oct 31;83(22). doi: 10.1128/AEM.01369-17. Print 2017 Nov 15.

Patients with community-onset (CO) methicillin-resistant

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Shahbazian JH, Hahn PD, Ludwig S, et al. Multidrug and Mupirocin Resistance in Environmental Methicillin-Resistant Staphylococcus aureus (MRSA) Isolates from Homes of People Diagnosed with Community-Onset MRSA Infection. Appl Environ Microbiol. 2017;83(22)doi: 10.1128/AEM.01369-17.
Shahbazian, J. H., Hahn, P. D., Ludwig, S., Ferguson, J., Baron, P., Christ, A., Spicer, K., Tolomeo, P., Torrie, A. M., Bilker, W. B., Cluzet, V. C., Hu, B., Julian, K., Nachamkin, I., Rankin, S. C., Morris, D. O., Lautenbach, E., & Davis, M. F. (2017). Multidrug and Mupirocin Resistance in Environmental Methicillin-Resistant Staphylococcus aureus (MRSA) Isolates from Homes of People Diagnosed with Community-Onset MRSA Infection. Applied and environmental microbiology, 83(22), . https://doi.org/10.1128/AEM.01369-17
Shahbazian, J H, et al. "Multidrug and Mupirocin Resistance in Environmental Methicillin-Resistant Staphylococcus aureus (MRSA) Isolates from Homes of People Diagnosed with Community-Onset MRSA Infection." Applied and environmental microbiology vol. 83,22 (2017). doi: https://doi.org/10.1128/AEM.01369-17
Shahbazian JH, Hahn PD, Ludwig S, Ferguson J, Baron P, Christ A, Spicer K, Tolomeo P, Torrie AM, Bilker WB, Cluzet VC, Hu B, Julian K, Nachamkin I, Rankin SC, Morris DO, Lautenbach E, Davis MF. Multidrug and Mupirocin Resistance in Environmental Methicillin-Resistant Staphylococcus aureus (MRSA) Isolates from Homes of People Diagnosed with Community-Onset MRSA Infection. Appl Environ Microbiol. 2017 Oct 31;83(22). doi: 10.1128/AEM.01369-17. Print 2017 Nov 15. PMID: 28939607; PMCID: PMC5666133.
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Early Life Metabolism of Bisphenol A: A Systematic Review of the Literature.

Current environmental health reports

Nachman RM, Hartle JC, Lees PS, Groopman JD.
PMID: 25838989
Curr Environ Health Rep. 2014 Mar;1(1):90-100. doi: 10.1007/s40572-013-0003-7.

When a comprehensive report on BPA was published in 2008, few data were available to assess the extent to which known poor glucuronidation capacity impacts BPA internal dose in infants and young children. In this paper, evidence that has...

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Nachman RM, Hartle JC, Lees PS, et al. Early Life Metabolism of Bisphenol A: A Systematic Review of the Literature. Curr Environ Health Rep. 2014;1(1):90-100doi: 10.1007/s40572-013-0003-7.
Nachman, R. M., Hartle, J. C., Lees, P. S., & Groopman, J. D. (2014). Early Life Metabolism of Bisphenol A: A Systematic Review of the Literature. Current environmental health reports, 1(1), 90-100. https://doi.org/10.1007/s40572-013-0003-7
Nachman, Rebecca M, et al. "Early Life Metabolism of Bisphenol A: A Systematic Review of the Literature." Current environmental health reports vol. 1,1 (2014): 90-100. doi: https://doi.org/10.1007/s40572-013-0003-7
Nachman RM, Hartle JC, Lees PS, Groopman JD. Early Life Metabolism of Bisphenol A: A Systematic Review of the Literature. Curr Environ Health Rep. 2014 Mar;1(1):90-100. doi: 10.1007/s40572-013-0003-7. PMID: 25838989; PMCID: PMC4380326.
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Hydroxymethylation as a Novel Environmental Biosensor.

Current environmental health reports

Dao T, Cheng RY, Revelo MP, Mitzner W, Tang W.
PMID: 24860723
Curr Environ Health Rep. 2014 Mar 01;1(1):1-10. doi: 10.1007/s40572-013-0005-5.

Beyond the genome, epigenetics has become a promising approach in understanding the interactions between the gene and the environment. Epigenetic regulation includes DNA methylation, histone modifications, and non-coding RNAs. Among these, DNA methylation, which is the addition of a...

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Dao T, Cheng RY, Revelo MP, et al. Hydroxymethylation as a Novel Environmental Biosensor. Curr Environ Health Rep. 2014;1(1):1-10doi: 10.1007/s40572-013-0005-5.
Dao, T., Cheng, R. Y., Revelo, M. P., Mitzner, W., & Tang, W. (2014). Hydroxymethylation as a Novel Environmental Biosensor. Current environmental health reports, 1(1), 1-10. https://doi.org/10.1007/s40572-013-0005-5
Dao, T, et al. "Hydroxymethylation as a Novel Environmental Biosensor." Current environmental health reports vol. 1,1 (2014): 1-10. doi: https://doi.org/10.1007/s40572-013-0005-5
Dao T, Cheng RY, Revelo MP, Mitzner W, Tang W. Hydroxymethylation as a Novel Environmental Biosensor. Curr Environ Health Rep. 2014 Mar 01;1(1):1-10. doi: 10.1007/s40572-013-0005-5. PMID: 24860723; PMCID: PMC4029614.
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Differences in estimates of size distribution of beryllium powder materials using phase contrast microscopy, scanning electron microscopy, and liquid suspension counter techniques.

Particle and fibre toxicology

Stefaniak AB, Hoover MD, Dickerson RM, Day GA, Breysse PN, Scripsick RC.
PMID: 17328812
Part Fibre Toxicol. 2007 Feb 28;4:3. doi: 10.1186/1743-8977-4-3.

Accurate characterization of the physicochemical properties of aerosols generated for inhalation toxicology studies is essential for obtaining meaningful results. Great emphasis must also be placed on characterizing particle properties of materials as administered in inhalation studies. Thus, research is...

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Stefaniak AB, Hoover MD, Dickerson RM, et al. Differences in estimates of size distribution of beryllium powder materials using phase contrast microscopy, scanning electron microscopy, and liquid suspension counter techniques. Part Fibre Toxicol. 2007;4:3doi: 10.1186/1743-8977-4-3.
Stefaniak, A. B., Hoover, M. D., Dickerson, R. M., Day, G. A., Breysse, P. N., & Scripsick, R. C. (2007). Differences in estimates of size distribution of beryllium powder materials using phase contrast microscopy, scanning electron microscopy, and liquid suspension counter techniques. Particle and fibre toxicology, 43. https://doi.org/10.1186/1743-8977-4-3
Stefaniak, Aleksandr B, et al. "Differences in estimates of size distribution of beryllium powder materials using phase contrast microscopy, scanning electron microscopy, and liquid suspension counter techniques." Particle and fibre toxicology vol. 4 (2007): 3. doi: https://doi.org/10.1186/1743-8977-4-3
Stefaniak AB, Hoover MD, Dickerson RM, Day GA, Breysse PN, Scripsick RC. Differences in estimates of size distribution of beryllium powder materials using phase contrast microscopy, scanning electron microscopy, and liquid suspension counter techniques. Part Fibre Toxicol. 2007 Feb 28;4:3. doi: 10.1186/1743-8977-4-3. PMID: 17328812; PMCID: PMC1810321.
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Digital Inverter Amine Sensing via Synergistic Responses by n and p Organic Semiconductors.

Advanced functional materials

Tremblay NJ, Jung BJ, Breysse P, Katz HE.
PMID: 23754969
Adv Funct Mater. 2011 Nov 22;21(22):4314-4319. doi: 10.1002/adfm.201101324.

Chemiresistors and sensitive OFETs have been substantially developed as cheap, scalable, and versatile sensing platforms. While new materials are expanding OFET sensing capabilities, the device architectures have changed little. Here we report higher order logic circuits utilizing OFETs sensitive...

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Tremblay NJ, Jung BJ, Breysse P, et al. Digital Inverter Amine Sensing via Synergistic Responses by n and p Organic Semiconductors. Adv Funct Mater. 2011;21(22):4314-4319doi: 10.1002/adfm.201101324.
Tremblay, N. J., Jung, B. J., Breysse, P., & Katz, H. E. (2011). Digital Inverter Amine Sensing via Synergistic Responses by n and p Organic Semiconductors. Advanced functional materials, 21(22), 4314-4319. https://doi.org/10.1002/adfm.201101324
Tremblay, Noah J, et al. "Digital Inverter Amine Sensing via Synergistic Responses by n and p Organic Semiconductors." Advanced functional materials vol. 21,22 (2011): 4314-4319. doi: https://doi.org/10.1002/adfm.201101324
Tremblay NJ, Jung BJ, Breysse P, Katz HE. Digital Inverter Amine Sensing via Synergistic Responses by n and p Organic Semiconductors. Adv Funct Mater. 2011 Nov 22;21(22):4314-4319. doi: 10.1002/adfm.201101324. PMID: 23754969; PMCID: PMC3676732.
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BPA Alters Estrogen Receptor Expression in the Heart After Viral Infection Activating Cardiac Mast Cells and T Cells Leading to Perimyocarditis and Fibrosis.

Frontiers in endocrinology

Bruno KA, Mathews JE, Yang AL, Frisancho JA, Scott AJ, Greyner HD, Molina FA, Greenaway MS, Cooper GM, Bucek A, Morales-Lara AC, Hill AR, Mease AA, Di Florio DN, Sousou JM, Coronado AC, Stafford AR, Fairweather D.
PMID: 31551929
Front Endocrinol (Lausanne). 2019 Sep 04;10:598. doi: 10.3389/fendo.2019.00598. eCollection 2019.

Myocarditis is an inflammatory heart disease that leads to dilated cardiomyopathy (DCM) and heart failure. Sex hormones play an important role in the development of myocarditis with testosterone driving disease in males and estrogen being cardioprotective in females. The...

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Bruno KA, Mathews JE, Yang AL, et al. BPA Alters Estrogen Receptor Expression in the Heart After Viral Infection Activating Cardiac Mast Cells and T Cells Leading to Perimyocarditis and Fibrosis. Front Endocrinol (Lausanne). 2019;10:598doi: 10.3389/fendo.2019.00598.
Bruno, K. A., Mathews, J. E., Yang, A. L., Frisancho, J. A., Scott, A. J., Greyner, H. D., Molina, F. A., Greenaway, M. S., Cooper, G. M., Bucek, A., Morales-Lara, A. C., Hill, A. R., Mease, A. A., Di Florio, D. N., Sousou, J. M., Coronado, A. C., Stafford, A. R., & Fairweather, D. (2019). BPA Alters Estrogen Receptor Expression in the Heart After Viral Infection Activating Cardiac Mast Cells and T Cells Leading to Perimyocarditis and Fibrosis. Frontiers in endocrinology, 10598. https://doi.org/10.3389/fendo.2019.00598
Bruno, Katelyn Ann, et al. "BPA Alters Estrogen Receptor Expression in the Heart After Viral Infection Activating Cardiac Mast Cells and T Cells Leading to Perimyocarditis and Fibrosis." Frontiers in endocrinology vol. 10 (2019): 598. doi: https://doi.org/10.3389/fendo.2019.00598
Bruno KA, Mathews JE, Yang AL, Frisancho JA, Scott AJ, Greyner HD, Molina FA, Greenaway MS, Cooper GM, Bucek A, Morales-Lara AC, Hill AR, Mease AA, Di Florio DN, Sousou JM, Coronado AC, Stafford AR, Fairweather D. BPA Alters Estrogen Receptor Expression in the Heart After Viral Infection Activating Cardiac Mast Cells and T Cells Leading to Perimyocarditis and Fibrosis. Front Endocrinol (Lausanne). 2019 Sep 04;10:598. doi: 10.3389/fendo.2019.00598. eCollection 2019. PMID: 31551929; PMCID: PMC6737078.
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Weighted Gene Correlation Network Analysis (WGCNA) Reveals Novel Transcription Factors Associated With Bisphenol A Dose-Response.

Frontiers in genetics

Maertens A, Tran V, Kleensang A, Hartung T.
PMID: 30483308
Front Genet. 2018 Nov 12;9:508. doi: 10.3389/fgene.2018.00508. eCollection 2018.

Despite Bisphenol-A (BPA) being subject to extensive study, a thorough understanding of molecular mechanism remains elusive. Here we show that using weighted gene correlation network analysis (WGCNA), which takes advantage of a graph theoretical approach to understanding correlations amongst...

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Maertens A, Tran V, Kleensang A, et al. Weighted Gene Correlation Network Analysis (WGCNA) Reveals Novel Transcription Factors Associated With Bisphenol A Dose-Response. Front Genet. 2018;9:508doi: 10.3389/fgene.2018.00508.
Maertens, A., Tran, V., Kleensang, A., & Hartung, T. (2018). Weighted Gene Correlation Network Analysis (WGCNA) Reveals Novel Transcription Factors Associated With Bisphenol A Dose-Response. Frontiers in genetics, 9508. https://doi.org/10.3389/fgene.2018.00508
Maertens, Alexandra, et al. "Weighted Gene Correlation Network Analysis (WGCNA) Reveals Novel Transcription Factors Associated With Bisphenol A Dose-Response." Frontiers in genetics vol. 9 (2018): 508. doi: https://doi.org/10.3389/fgene.2018.00508
Maertens A, Tran V, Kleensang A, Hartung T. Weighted Gene Correlation Network Analysis (WGCNA) Reveals Novel Transcription Factors Associated With Bisphenol A Dose-Response. Front Genet. 2018 Nov 12;9:508. doi: 10.3389/fgene.2018.00508. eCollection 2018. PMID: 30483308; PMCID: PMC6240694.
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Intrauterine Inflammation and Maternal Exposure to Ambient PM2.5 during Preconception and Specific Periods of Pregnancy: The Boston Birth Cohort.

Environmental health perspectives

Nachman RM, Mao G, Zhang X, Hong X, Chen Z, Soria CS, He H, Wang G, Caruso D, Pearson C, Biswal S, Zuckerman B, Wills-Karp M, Wang X.
PMID: 27120296
Environ Health Perspect. 2016 Oct;124(10):1608-1615. doi: 10.1289/EHP243. Epub 2016 Apr 27.

BACKGROUND: Prenatal exposure to ambient PM2.5, (i.e., fine particulate matter, aerodynamic diameter ≤ 2.5 μm) has been associated with preterm birth and low birth weight. The association between prenatal PM2.5 exposure and intrauterine inflammation (IUI), an important risk factor...

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Nachman RM, Mao G, Zhang X, et al. Intrauterine Inflammation and Maternal Exposure to Ambient PM2.5 during Preconception and Specific Periods of Pregnancy: The Boston Birth Cohort. Environ Health Perspect. 2016;124(10):1608-1615doi: 10.1289/EHP243.
Nachman, R. M., Mao, G., Zhang, X., Hong, X., Chen, Z., Soria, C. S., He, H., Wang, G., Caruso, D., Pearson, C., Biswal, S., Zuckerman, B., Wills-Karp, M., & Wang, X. (2016). Intrauterine Inflammation and Maternal Exposure to Ambient PM2.5 during Preconception and Specific Periods of Pregnancy: The Boston Birth Cohort. Environmental health perspectives, 124(10), 1608-1615. https://doi.org/10.1289/EHP243
Nachman, Rebecca Massa, et al. "Intrauterine Inflammation and Maternal Exposure to Ambient PM2.5 during Preconception and Specific Periods of Pregnancy: The Boston Birth Cohort." Environmental health perspectives vol. 124,10 (2016): 1608-1615. doi: https://doi.org/10.1289/EHP243
Nachman RM, Mao G, Zhang X, Hong X, Chen Z, Soria CS, He H, Wang G, Caruso D, Pearson C, Biswal S, Zuckerman B, Wills-Karp M, Wang X. Intrauterine Inflammation and Maternal Exposure to Ambient PM2.5 during Preconception and Specific Periods of Pregnancy: The Boston Birth Cohort. Environ Health Perspect. 2016 Oct;124(10):1608-1615. doi: 10.1289/EHP243. Epub 2016 Apr 27. PMID: 27120296; PMCID: PMC5047781.
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Big-data and machine learning to revamp computational toxicology and its use in risk assessment.

Toxicology research

Luechtefeld T, Rowlands C, Hartung T.
PMID: 30310652
Toxicol Res (Camb). 2018 May 01;7(5):732-744. doi: 10.1039/c8tx00051d. eCollection 2018 Sep 01.

The creation of large toxicological databases and advances in machine-learning techniques have empowered computational approaches in toxicology. Work with these large databases based on regulatory data has allowed reproducibility assessment of animal models, which highlight weaknesses in traditional

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Luechtefeld T, Rowlands C, Hartung T. Big-data and machine learning to revamp computational toxicology and its use in risk assessment. Toxicol Res (Camb). 2018;7(5):732-744doi: 10.1039/c8tx00051d.
Luechtefeld, T., Rowlands, C., & Hartung, T. (2018). Big-data and machine learning to revamp computational toxicology and its use in risk assessment. Toxicology research, 7(5), 732-744. https://doi.org/10.1039/c8tx00051d
Luechtefeld, Thomas, et al. "Big-data and machine learning to revamp computational toxicology and its use in risk assessment." Toxicology research vol. 7,5 (2018): 732-744. doi: https://doi.org/10.1039/c8tx00051d
Luechtefeld T, Rowlands C, Hartung T. Big-data and machine learning to revamp computational toxicology and its use in risk assessment. Toxicol Res (Camb). 2018 May 01;7(5):732-744. doi: 10.1039/c8tx00051d. eCollection 2018 Sep 01. PMID: 30310652; PMCID: PMC6116175.
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Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease.

Cell discovery

Martos SN, Li T, Ramos RB, Lou D, Dai H, Xu JC, Gao G, Gao Y, Wang Q, An C, Zhang X, Jia Y, Dawson VL, Dawson TM, Ji H, Wang Z.
PMID: 29387450
Cell Discov. 2017 Nov 14;3:17038. doi: 10.1038/celldisc.2017.38. eCollection 2017.

Imprinted genes are vulnerable to environmental influences during early embryonic development, thereby contributing to the onset of disease in adulthood. Monoallelic methylation at several germline imprints has been reported as DNMT1-dependent. However, which of these two epigenetic attributes, DNMT1-dependence...

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Martos SN, Li T, Ramos RB, et al. Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease. Cell Discov. 2017;3:17038doi: 10.1038/celldisc.2017.38.
Martos, S. N., Li, T., Ramos, R. B., Lou, D., Dai, H., Xu, J. C., Gao, G., Gao, Y., Wang, Q., An, C., Zhang, X., Jia, Y., Dawson, V. L., Dawson, T. M., Ji, H., & Wang, Z. (2017). Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease. Cell discovery, 317038. https://doi.org/10.1038/celldisc.2017.38
Martos, Suzanne N, et al. "Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease." Cell discovery vol. 3 (2017): 17038. doi: https://doi.org/10.1038/celldisc.2017.38
Martos SN, Li T, Ramos RB, Lou D, Dai H, Xu JC, Gao G, Gao Y, Wang Q, An C, Zhang X, Jia Y, Dawson VL, Dawson TM, Ji H, Wang Z. Two approaches reveal a new paradigm of 'switchable or genetics-influenced allele-specific DNA methylation' with potential in human disease. Cell Discov. 2017 Nov 14;3:17038. doi: 10.1038/celldisc.2017.38. eCollection 2017. PMID: 29387450; PMCID: PMC5787696.
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Arsenic and Chronic Kidney Disease: A Systematic Review.

Current environmental health reports

Zheng L, Kuo CC, Fadrowski J, Agnew J, Weaver VM, Navas-Acien A.
PMID: 25221743
Curr Environ Health Rep. 2014 Sep 01;1(3):192-207. doi: 10.1007/s40572-014-0024-x.

In epidemiologic studies, high arsenic exposure has been associated with adverse kidney disease outcomes. We performed a systematic review of the epidemiologic evidence of the association between arsenic and various kidney disease outcomes. The search period was January 1966...

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Zheng L, Kuo CC, Fadrowski J, et al. Arsenic and Chronic Kidney Disease: A Systematic Review. Curr Environ Health Rep. 2014;1(3):192-207doi: 10.1007/s40572-014-0024-x.
Zheng, L., Kuo, C. C., Fadrowski, J., Agnew, J., Weaver, V. M., & Navas-Acien, A. (2014). Arsenic and Chronic Kidney Disease: A Systematic Review. Current environmental health reports, 1(3), 192-207. https://doi.org/10.1007/s40572-014-0024-x
Zheng, Laura, et al. "Arsenic and Chronic Kidney Disease: A Systematic Review." Current environmental health reports vol. 1,3 (2014): 192-207. doi: https://doi.org/10.1007/s40572-014-0024-x
Zheng L, Kuo CC, Fadrowski J, Agnew J, Weaver VM, Navas-Acien A. Arsenic and Chronic Kidney Disease: A Systematic Review. Curr Environ Health Rep. 2014 Sep 01;1(3):192-207. doi: 10.1007/s40572-014-0024-x. PMID: 25221743; PMCID: PMC4159179.
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A Scanning Transmission Electron Microscopy Method for Determining Manganese Composition in Welding Fume as a Function of Primary Particle Size.

Journal of aerosol science

Richman JD, Livi KJ, Geyh AS.
PMID: 21625364
J Aerosol Sci. 2011 Jun;42(6):408-418. doi: 10.1016/j.jaerosci.2011.03.004.

Increasing evidence suggests that the physicochemical properties of inhaled nanoparticles influence the resulting toxicokinetics and toxicodynamics. This report presents a method using scanning transmission electron microscopy (STEM) to measure the Mn content throughout the primary particle size distribution of...

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Richman JD, Livi KJ, Geyh AS. A Scanning Transmission Electron Microscopy Method for Determining Manganese Composition in Welding Fume as a Function of Primary Particle Size. J Aerosol Sci. 2011;42(6):408-418doi: 10.1016/j.jaerosci.2011.03.004.
Richman, J. D., Livi, K. J., & Geyh, A. S. (2011). A Scanning Transmission Electron Microscopy Method for Determining Manganese Composition in Welding Fume as a Function of Primary Particle Size. Journal of aerosol science, 42(6), 408-418. https://doi.org/10.1016/j.jaerosci.2011.03.004
Richman, Julie D, et al. "A Scanning Transmission Electron Microscopy Method for Determining Manganese Composition in Welding Fume as a Function of Primary Particle Size." Journal of aerosol science vol. 42,6 (2011): 408-418. doi: https://doi.org/10.1016/j.jaerosci.2011.03.004
Richman JD, Livi KJ, Geyh AS. A Scanning Transmission Electron Microscopy Method for Determining Manganese Composition in Welding Fume as a Function of Primary Particle Size. J Aerosol Sci. 2011 Jun;42(6):408-418. doi: 10.1016/j.jaerosci.2011.03.004. PMID: 21625364; PMCID: PMC3101895.
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