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Results: 16

Cited In for PubMed (Select 18310190)


Implementing risk-stratified screening for common cancers: a review of potential ethical, legal and social issues.

Hall AE, Chowdhury S, Hallowell N, Pashayan N, Dent T, Pharoah P, Burton H.

J Public Health (Oxf). 2014 Jun;36(2):285-91. doi: 10.1093/pubmed/fdt078. Epub 2013 Aug 28. Review.


Developmental and behavioral pediatricians' attitudes toward screening for fragile X.

Acharya K, Schindler A.

Am J Intellect Dev Disabil. 2013 Jul;118(4):284-93. doi: 10.1352/1944-7558-188.4.284.


What research ethics should learn from genomics and society research: lessons from the ELSI Congress of 2011.

Henderson GE, Juengst ET, King NM, Kuczynski K, Michie M.

J Law Med Ethics. 2012 Winter;40(4):1008-24. doi: 10.1111/j.1748-720X.2012.00728.x.


Obtaining consent from both parents for pediatric research: what does "reasonably available" mean?

Nelson DK, Skinner D, Guarda S, Choudhury S, Sideris J, Barnum L, Ten Haagen K, Heyward Q, Bailey DB Jr.

Pediatrics. 2013 Jan;131(1):e223-9. doi: 10.1542/peds.2012-1278. Epub 2012 Dec 24.


Newborn screening and cascade testing for FMR1 mutations.

Sorensen PL, Gane LW, Yarborough M, Hagerman RJ, Tassone F.

Am J Med Genet A. 2013 Jan;161A(1):59-69. doi: 10.1002/ajmg.a.35680. Epub 2012 Dec 13.


Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.

Downing NR, Williams JK, Daack-Hirsch S, Driessnack M, Simon CM.

Patient Educ Couns. 2013 Jan;90(1):133-8. doi: 10.1016/j.pec.2012.09.010. Epub 2012 Oct 12.


Early negative affect predicts anxiety, not autism, in preschool boys with fragile X syndrome.

Tonnsen BL, Malone PS, Hatton DD, Roberts JE.

J Abnorm Child Psychol. 2013 Feb;41(2):267-80. doi: 10.1007/s10802-012-9671-2.


Cell-free fetal DNA testing for fetal aneuploidy and beyond: clinical integration challenges in the US context.

Allyse M, Sayres LC, King JS, Norton ME, Cho MK.

Hum Reprod. 2012 Nov;27(11):3123-31. doi: 10.1093/humrep/des286. Epub 2012 Aug 3.


Caregiver opinions about fragile X population screening.

Bailey DB Jr, Bishop E, Raspa M, Skinner D.

Genet Med. 2012 Jan;14(1):115-21. doi: 10.1038/gim.0b013e31822ebaa6. Epub 2011 Sep 13.


Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project.

Skinner D, Choudhury S, Sideris J, Guarda S, Buansi A, Roche M, Powell C, Bailey DB Jr.

Pediatrics. 2011 Jun;127(6):e1455-63. doi: 10.1542/peds.2010-3078. Epub 2011 May 29.


Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.

Bombard Y, Miller FA, Hayeems RZ, Avard D, Knoppers BM.

Eur J Hum Genet. 2010 Jul;18(7):751-60. doi: 10.1038/ejhg.2010.13. Epub 2010 Mar 3. Review.


High-risk fragile x screening in Guatemala: use of a new blood spot polymerase chain reaction technique.

Yuhas J, Walichiewicz P, Pan R, Zhang W, Casillas EM, Hagerman RJ, Tassone F.

Genet Test Mol Biomarkers. 2009 Dec;13(6):855-9. doi: 10.1089/gtmb.2009.0108.


Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

Coffee B, Keith K, Albizua I, Malone T, Mowrey J, Sherman SL, Warren ST.

Am J Hum Genet. 2009 Oct;85(4):503-14. doi: 10.1016/j.ajhg.2009.09.007.


Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population.

Fernandez-Carvajal I, Walichiewicz P, Xiaosen X, Pan R, Hagerman PJ, Tassone F.

J Mol Diagn. 2009 Jul;11(4):324-9. doi: 10.2353/jmoldx.2009.080173. Epub 2009 May 21.


Advances in the treatment of fragile X syndrome.

Hagerman RJ, Berry-Kravis E, Kaufmann WE, Ono MY, Tartaglia N, Lachiewicz A, Kronk R, Delahunty C, Hessl D, Visootsak J, Picker J, Gane L, Tranfaglia M.

Pediatrics. 2009 Jan;123(1):378-90. doi: 10.1542/peds.2008-0317. Review.


Supporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screening.

Bailey DB Jr, Armstrong FD, Kemper AR, Skinner D, Warren SF.

J Pediatr Psychol. 2009 Jul;34(6):648-61. doi: 10.1093/jpepsy/jsn032. Epub 2008 Mar 30.

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