This list includes recent articles, authored or co-authored by Wisconsin healthcare providers and researchers, that are relevant to genetics and public health. It is not meant to be an exhaustive nor a complete list of all genetics-related articles with Wisconsin co-authors or authors.
Gottesman, O. et al. The Electronic Medical Records and Genomics (eMERGE) Network: Past, Present and Future. Genet Med. 2013 Oct;15(10):761-71. Note: Researchers from Marshfield Clinic are among the co-authors.
Jorgenson, M. et al. Stillbirth: the heart of the matter. Am J Med Gen A. 2014 Jan 23.
Kuhl, A. et al. Genetic Counseling Graduate Student Debt: Impact on Program, Career and Life Choices. J Genet Couns. 2014 Mar 1.
Kwan, A. et al. Newborn Screening for Severe Combined Immunodeficiency in 11 Newborn Screening Programs in the United States. JAMA August 20, 2014, Vol 312, No. 7. Note: there are multiple Wisconsin co-authors.
Lhost, JJ et al. Pulse Oximetry Screening for Critical Congenital Heart Disease in Planned Out-of-Hospital Births. J Pediatr. 2014 Jun 16.
MacArthur, D.G. et al. Guidelines for Investigating Causality of Sequence Variants in Human Disease. Nature. 2014 Apr 24; 508(7497): 469-76. Note: A Wisconsin geneticist is a co-author.
McPherson, E. et al. Neuroblastoma in a 17-week fetus: A Stimulus for Investigation of Tumors in a Series of 2786 Stillbirth and Late Miscarriages. Am J Med Genet A. 2014 Oct 22.
McPherson, E. et al. Radiographic evaluation of stillbirth: What does it contribute? Am J Med Genet A. 2014 Jul 10
May, T. An Adoptive Parental Perspective on Personal Genomic Screening. Pediatrics. 2015 Mar 9.
Ngui, EM et al. Perceptions of African-American Health Professionals and Community Members on the Participation of Children and Pregnant Women in Genetic Research. Public Health Genomics. 2013 Nov 6.
Ossorio, PN and Kelleher, JP. Why We Should Not Use the Affordable Care Act to Encourage Widespread Whole Genome Sequencing. J Health Polit Policy Law. 2013 Nov 5. Note: This article is in response to an article by Payne et al in the same issue.
Rasmussen-Torvik, L. et al. Design and Anticipated Outcomes of the e-MERGE-PGx Project: a Multicenter Pilot for Preemptive Pharmacogenomics in Electronic Health Record Systems. Clinical Pharmacology and Therapeutics. 20 August 2014. Note: this article includes Wisconsin co-authors.
Strong, K. et al. Views of Primary Care Providers Regarding the Return of Genome Sequencing Incidental Findings. Clin Genet. 2014 Mar 27.
Wintergerst, K. Congenital Hypothyroidism Long-Term Follow-Up Project: Navigating the Rough Waters of a Multi-Center, Multi-State Public Health Project. J Genet Couns. 2014 Nov 18.