Defining personal utility in genomics: A Delphi study
Kohler, J.N., Turbitt, E., Lewis, K.L., Wilfond, B.S., Jamal, L., Peay, H.L., Biesecker, L.G., Biesecker, B.B.
Published in Clinical genetics (01.09.2017)
Published in Clinical genetics (01.09.2017)
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Patient actions and reactions after receiving negative results from expanded carrier screening
Kraft, S.A., Schneider, J.L., Leo, M.C., Kauffman, T.L., Davis, J.V., Porter, K.M., McMullen, C.K., Wilfond, B.S., Goddard, K.A.B.
Published in Clinical genetics (01.05.2018)
Published in Clinical genetics (01.05.2018)
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Integrating neurocritical care approaches into neonatology: should all infants be treated equitably?
Mann, P C, Gospe, S M, Steinman, K J, Wilfond, B S
Published in Journal of perinatology (01.12.2015)
Published in Journal of perinatology (01.12.2015)
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Hereditary Hemochromatosis: Gene Discovery and Its Implications for Population-Based Screening
Burke, Wylie, Thomson, Elizabeth, Khoury, Muin J, McDonnell, Sharon M, Press, Nancy, Adams, Paul C, Barton, James C, Beutler, Ernest, Brittenham, Gary, Buchanan, Allen, Clayton, Ellen Wright, Cogswell, Mary E, Meslin, Eric M, Motulsky, Arno G, Powell, Lawrie W, Sigal, Elliott, Wilfond, Benjamin S, Collins, Francis S
Published in JAMA : the journal of the American Medical Association (08.07.1998)
Published in JAMA : the journal of the American Medical Association (08.07.1998)
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Patient Perspectives on Group Benefits and Harms in Genetic Research
Goldenberg, A.J., Hull, S.C., Wilfond, B.S., Sharp, R.R.
Published in Community genetics (01.01.2011)
Published in Community genetics (01.01.2011)
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Characterisation of organisational issues in paediatric clinical ethics consultation: a qualitative study
Opel, D J, Wilfond, B S, Brownstein, D, Diekema, D S, Pearlman, R A
Published in Journal of medical ethics (01.08.2009)
Published in Journal of medical ethics (01.08.2009)
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Ethical issues with genetic testing in pediatrics
Published in Pediatrics (Evanston)
(01.06.2001)
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Cystic fibrosis newborn screening: impact on reproductive behavior and implications for genetic counseling
Mischler, E H, Wilfond, B S, Fost, N, Laxova, A, Reiser, C, Sauer, C M, Makholm, L M, Shen, G, Feenan, L, McCarthy, C, Farrell, P M
Published in Pediatrics (Evanston) (01.07.1998)
Published in Pediatrics (Evanston) (01.07.1998)
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Application of DNA analysis in a population-screening program for neonatal diagnosis of cystic fibrosis (CF) : comparison of screening protocols
GREGG, R. G, WILFOND, B. S, FARRELL, P. M, LAXOVA, A, HASSEMER, D, MISCHLER, E. H
Published in American journal of human genetics (01.03.1993)
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Published in American journal of human genetics (01.03.1993)
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The cystic fibrosis gene: medical and social implications for heterozygote detection
Wilfond, B S, Fost, N
Published in JAMA : the journal of the American Medical Association (23.05.1990)
Published in JAMA : the journal of the American Medical Association (23.05.1990)
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481 The ENVISION study: creating a values-oriented approach platform to informed consent for genetic therapy research
McNamara, S., Buckingham, R., Fogarty, B., Galinas, L., Mueller, R., Taylor, H., George, C., Krishnamurti, T., Mazuera, S., Hudson, J., Znidarsic, M., Duenas, D., Kelsh, A., Porter, K., Tsing, J., Wilfond, B., Kraft, S.
Published in Journal of cystic fibrosis (01.09.2024)
Published in Journal of cystic fibrosis (01.09.2024)
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