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A Call for Papers

Catherine D. DeAngelis, MD, MPH; Phil B. Fontanarosa, MD, MBA; Mary-Claire King, PhD; Boris Pasche, MD, PhD

JAMA. 2007;298:228.

The October 15, 1997, issue of JAMA¹ was devoted to genetics and featured articles on genomic screening in late-onset familial Alzheimer disease, BRCA1 sequence analysis, hereditary prostate cancer 1 locus, chromosome 19 single locus, and multilocus haplotype associations with multiple sclerosis, cancer incidence after retinoblastoma, prenatal genetic carrier testing, molecular diagnosis and carrier screening for -thalassemia, genetic testing in hereditary colorectal cancer, molecular neurogenetics, family history and genetic risk factors, and preparing health professionals for the genetic revolution.

During the past decade, there has been an explosion of progress in genetics and genomics including the sequencing of the human genome.^2-3 In March 2008, JAMA will devote an entire theme issue to practical applications of genetics and genomics that are or might become clinically important. We invite authors to submit manuscripts reporting the results of original research, especially clinical trials; systematic reviews including meta-analyses; special communications; and commentaries. Evidence-based articles will be given priority.

Topics of particular interest include genetic diagnosis including prenatal tests, genetic testing especially for illnesses for which presymptomatic intervention is possible, pharmacogenomics, gene therapy, evolutionary medicine such as genotypes with proven adaptive responses to emerging infections, genetic counseling, and ethical issues surrounding genetics.

Manuscripts received by November 1, 2007, will have the best chance for consideration for this theme issue. All manuscripts will undergo our usual rigorous editorial review process. High-quality submissions not accepted for the theme issue may be considered for other issues of JAMA or, with the authors' permission, for consideration by one of our Archives specialty journals, which are also devoting a March theme issue to this topic.

Authors are encouraged to consult the JAMA Instructions for Authors⁴ for guidelines on preparing and submitting manuscripts.

AUTHOR INFORMATION

Financial Disclosures: None reported.

Editorials represent the opinions of the authors and JAMA and not those of the American Medical Association.

Author Affiliations: Dr DeAngelis is Editor in Chief (cathy.deangelis{at}jama-archives.org), Dr Fontanarosa is Executive Deputy Editor, Dr King is on the Editorial Board, and Dr Pasche is Contributing Editor, JAMA. Departments of Genome Sciences and Medicine (Medical Genetics), University of Washington, Seattle (Dr King); and Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois (Dr Pasche).

REFERENCES
1. Genetics. JAMA. 1997;278(15, theme issue):1212-1287. FULL TEXT | PUBMED 2. Venter JC, Adams MD, Myers EW, et al. The sequence of human genome. Science. 2001;291(5507):1304-1351. FREE FULL TEXT 3. Lander ES, Linton LM, Birren B, et al, International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome. Nature. 2001;409(6822):860-921. FULL TEXT | PUBMED 4. JAMA Instructions for Authors. http://jama.ama-assn.org/misc/ifora.dtl. Accessed June 7, 2007.