I'm pleased to announce the appointment of Dr Gregory Stuart to the position of Editor in Chief of Substance Abuse: Research and Treatment. Dr Stuart replaces Dr John Curtin who was forced to step down owing to pressure of other work commitments, and who has taken a position on the journal's Editorial Board.
Dr Stuart joined the Department of Psychology at the University of Tennessee-Knoxville in 2008. Previously he worked in the Department of Psychiatry and Human Behavior at the Alpert Medical School of Brown University. He maintains an affiliation there, and he is also the Director of Family Violence Research at Butler Hospital. He serves as an adjunct faculty member at the Brown University Center for Alcohol and Addiction Studies.
Dr. Stuart’s research has a particular emphasis on the role of substance use and abuse in intimate partner violence perpetration and victimization. His research has shown that intimate partner violence perpetration and victimization are overrepresented in populations of individuals in treatment for substance abuse, and that substance abuse is overrepresented in men and women court mandated to attend batterer intervention programs. His work examines the impact of substance abuse treatment on the prevalence and frequency of intimate partner violence and psychological aggression, as well as the effects of substance abuse treatment on other domains of relationship and family functioning. Dr. Stuart’s work also examines whether incorporating substance use treatments into batterer intervention programs improves outcomes for men and women arrested for domestic violence.
Joining Dr Stuart as the journal's first Associate Editor is Dr Susan Ramsey. Dr. Ramsey is an Assistant Professor (Research) in the Department of Psychiatry and Human Behavior and the Department of Medicine at the Warren Alpert Medical School of Brown University. She serves as coordinator of the seminar series for the Adult Psychopathology Track of the Brown University Clinical Psychology Training Consortium. Dr. Ramsey’s research focuses on the confluence of substance abuse, psychiatric disorders, and medical issues.
Friday, September 26, 2008
Friday, September 19, 2008
An interview with Dr James Willey

This is the first of an occasional series of blog entries interviewing Editors in Chief and Editorial Board members of Libertas Academica journals.
This interview is with Dr James Willey, Editor in Chief of Gene Regulation and Systems Biology and Professor of Medicine and Pathology at the University of Toledo Medical Center, Toledo.
Tom: What would you say is the primary focus of your research effort (and how do you refer to your 'sub-area')?
Dr Willey: The study of human inter-individual variation in gene regulatory pathways related to complex genetic disease risk. More specifically:
- Development of methods to identify individuals that have inherited sufficient alteration in regulation of a sufficient number of key genes to result in a detectable increase in disease risk.
- Application of these methods to identify the 10-15% of the population that is at highest risk if they smoke cigarettes.
Dr Willey: The recognition that genome wide association studies (GWAS) of interindividual variation in SNP allelotype are insufficient alone to identify individuals with particular complex genetic disease determinants. Rather:
- SNP analysis must be combined with phenotype analysis (e.g. transcript abundance analysis).
- Focus on SNP analysis of genes with high prior likelihood of association with phenotype markedly increases chance for success in determining association. Otherwise, when one compounds the number of SNPS assessed (now greater than 1,000,000) x the number of potential models to explain the phenotype, the number of models becomes cosmological.
- The role of rare SNPs may be much more important than initially recognized and this raises the priority of sequencing key gene areas, rather than simply performing SNP analysis and relying on hapblock estimates to locate disease determining SNPs.
- High frequency of recombination in CpG islands, which are common in promoters of important genes, leads to high recombination which renders haplotype block estimates inaccurate.
Dr Willey: Improvement in ability to compare transcript abundance data across experiments and laboratories. Up to this point, the basic analytical tools widely in use simply don't have the performance characteristics necessary to enable data comparison. For this reason, gene ontology efforts have been severely impaired. The software structure is there, but the suitable raw data are not.
Tom: Tell us about your collaborative research. Who else do you directly work with and what are the aims of your collaboration?
Dr Willey:
- Food and Drug Administration (FDA): Through the MicroArray Quality Control Consortium. The purpose of this effort is to improve ability to compare data across labs and experiments to facilitate drug discovery and development.
- National Institutes of Standards and Technology (NIST): External RNA Control Consortium. This is a cooperative effort to develop standards that will facilitate development of transcript abundance measurement methods that generate data that may be compared across labs and experiments.
- Gene Express, Inc.. This is a company that I co-founded and that licenses standardized and quality controlled transcript abundance measurement technology developed in my NIH-funded laboratory. It also licenses new diagnostic tests developed in my laboratory for further development into commercial products.
- Biotrove, Inc. and University of Rochester. I am Co-PI, along with Tom Morrison of Biotrove, Inc. and Tony Godfrey of the University of Rochester on a recently awarded NCI grant to support development of the Standardized Nanoarray PCR Platform (SNAP). The press release is posted at the Biotrove website).
Dr Willey: Yes. Surround myself with highest quality colleagues. Stay informed regarding latest developments in my field. Think ahead, anticipate demands on my time.
Tom: What do you consider to be the most significant developments or advancements to have occurred in your field of research?
Dr Willey:
- Recognition that any meaningful understanding of phenotype depends on analysis of regulation and function of many genes.
- Development of tools and knowledge to assess the function and regulation of many genes and integrate the data.
Dr Willey: Early 1990's. Even at this early point in the Human Genome Project, there was sequence information on a sufficient number of genes to begin the process of evaluating expression of many genes simultaneously.
Tom: What resources do you find indispensible for your research work?
Dr Willey: NCBI databases, inexpensive sequencing and oligonucleotide synthesis services, NIH funding, electronic publishing.
Tom: What do you think about the development of open access publishing and open access development? How has it changed your perspective on research or development practices?
Essential component of what I do today. Markedly increases the efficiency of information transfer. Electronic submission, review, and publishing are all important.
Tom: What books do you think should be required reading for researchers working in your area?
Dr Willey: At this point, text books have a difficult time keeping up. Researchers almost need to jump on treadmill that is already moving at high speed.
Tom: What books are current on your reading list?
Dr Willey:
- A Guinea Pig's History of Biology, Jim Endersby (Amazon.com)
- Darwin, The Life of a Tormented Evolutionist, Adrian Desmond and James Moore (Amazon.com)
Dr Willey: Genetic Predisposition to Lung cancer lectures in the graduate school course entitled "Systems Pathophysiology II: Cancer Biology".
Tom: Which historical research figures do you think have most influenced you in how you think about research? Why are they significant?
Dr Willey:
- Socrates: Always question conventional wisdom.
- Aristotle: Develop hypotheses consistent with high quality empiric data, rather than developing empiric data to support high quality hypotheses.
- Darwin: For obvious reasons
Dr Willey:
- American Association for Cancer Research
- NIH sponsored meetings: NCI IMAT, NIH study sections to review grants.
Dr Willey: Will keep you posted, expect developments over the next couple of years.
Tom: If you could change three things about how research in your area is conducted, used, perceived, or resourced, what would they be?
Dr Willey:
- Researchers need to inquire with greater rigor regarding the performance characteristics of the transcript abundance, protein measurement methods they purchase and/or use.
- Researchers need to focus more on the ability to compare data across labs and experiments.
Monday, September 8, 2008
Two journals now in EBSCO Academic Search Complete
Analytical Chemistry Insights and Evolutionary Bioinformatics have been accepted for indexing in EBSCO's Academic Search Complete database.
Academic Search Complete is a multi-disciplinary full-text database containing over 4,500 peer reviewed journals, abstracts of 9,500 and more than 10,000 other publications including monographs, conference proceedings etc.
Academic Search Complete is a multi-disciplinary full-text database containing over 4,500 peer reviewed journals, abstracts of 9,500 and more than 10,000 other publications including monographs, conference proceedings etc.
Thursday, September 4, 2008
More new introductory editorials
Introductory Editorials have just been published for these new open access journals:
Please register to receive these journals' RSS feeds and email notifications.
Please register to receive these journals' RSS feeds and email notifications.
Tuesday, September 2, 2008
More journals accepted for DOAJ
These open access journals, published by Libertas Academica, have now been added to DOAJ today:
We will add existing articles appearing in these journals to DOAJ over the coming week.
We will add existing articles appearing in these journals to DOAJ over the coming week.
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