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Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children.
Kemper AR, Green NS, Calonge N, Lam WK, Comeau AM, Goldenberg AJ, Ojodu J, Prosser LA, Tanksley S, Bocchini JA Jr. Kemper AR, et al. Among authors: green ns. Genet Med. 2014 Feb;16(2):183-7. doi: 10.1038/gim.2013.98. Epub 2013 Aug 1. Genet Med. 2014. PMID: 23907646 Free article.
A framework for key considerations regarding point-of-care screening of newborns.
Kemper AR, Kus CA, Ostrander RJ, Comeau AM, Boyle CA, Dougherty D, Mann MY, Botkin JR, Green NS; United States Secretary of Health and Human Services Advisory Committee. Kemper AR, et al. Among authors: green ns. Genet Med. 2012 Dec;14(12):951-4. doi: 10.1038/gim.2012.89. Epub 2012 Aug 16. Genet Med. 2012. PMID: 22899090 Free PMC article.
A framework for assessing outcomes from newborn screening: on the road to measuring its promise.
Hinton CF, Homer CJ, Thompson AA, Williams A, Hassell KL, Feuchtbaum L, Berry SA, Comeau AM, Therrell BL, Brower A, Harris KB, Brown C, Monaco J, Ostrander RJ, Zuckerman AE, Kaye C, Dougherty D, Greene C, Green NS; Follow-up and Treatment Sub-committee of the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC). Hinton CF, et al. Among authors: green ns. Mol Genet Metab. 2016 Aug;118(4):221-9. doi: 10.1016/j.ymgme.2016.05.017. Epub 2016 May 31. Mol Genet Metab. 2016. PMID: 27268406 Free PMC article.
An evidence development process for newborn screening.
Perrin JM, Knapp AA, Browning MF, Comeau AM, Green NS, Lipstein EA, Metterville DR, Prosser L, Queally D, Kemper AR. Perrin JM, et al. Among authors: green ns. Genet Med. 2010 Mar;12(3):131-4. doi: 10.1097/GIM.0b013e3181d28eb1. Genet Med. 2010. PMID: 20154629 Free article. Review. No abstract available.
120 results