Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics

Por Bombard, Yvonne, Miller, Fiona A
Publicado em 2012

Understanding relevance of health research: considerations in the context of research impact assessment

Por Dobrow, Mark J., Miller, Fiona A., Frank, Cy, Brown, Adalsteinn D.
Publicado no Health Res Policy Syst (2017)

When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results

Por Miller, Fiona A, Giacomini, Mita, Ahern, Catherine, Robert, Jason S, de Laat, Sonya
Publicado em 2008

Resources and population served: a description of the Ontario Paediatric Diabetes Network

Por Shulman, Rayzel, Miller, Fiona A., Stukel, Therese A., Daneman, Denis, Guttmann, Astrid
Publicado no CMAJ Open (2016)

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

Por Bombard, Yvonne, Miller, Fiona A, Hayeems, Robin Z, Avard, Denise, Knoppers, Bartha M
Publicado em 2010

Postal survey of physicians and laboratories: Practices and perceptions of molecular oncology testing

Por Miller, Fiona A, Krueger, Paul, Christensen, Robert J, Ahern, Catherine, Carter, Ronald F, Kamel-Reid, Suzanne
Publicado em 2009

Examining the ethical and social issues of health technology design through the public appraisal of prospective scenarios: a study protocol describing a multimedia-based deliberati...

Por Lehoux, Pascale, Gauthier, Philippe, Williams-Jones, Bryn, Miller, Fiona A, Fishman, Jennifer R, Hivon, Myriam, Vachon, Patrick
Publicado no Implement Sci (2014)

Low socioeconomic status is associated with adverse events in children and teens on insulin pumps under a universal access program: a population-based cohort study

Por Shulman, Rayzel, Stukel, Therese A, Miller, Fiona A, Newman, Alice, Daneman, Denis, Wasserman, Jonathan D, Guttmann, Astrid
Publicado no BMJ Open Diabetes Res Care (2016)

Primary care role in expanded newborn screening: After the heel prick test

Por Hayeems, Robin Z., Miller, Fiona A., Carroll, June C., Little, Julian, Allanson, Judith, Bytautas, Jessica P., Chakraborty, Pranesh, Wilson, Brenda J.
Publicado em 2013

Understanding sickle cell carrier status identified through newborn screening: a qualitative study

Por Miller, Fiona A, Paynter, Martha, Hayeems, Robin Z, Little, Julian, Carroll, June C, Wilson, Brenda J, Allanson, Judith, Bytautas, Jessica P, Chakraborty, Pranesh
Publicado em 2010

Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders

Por Bombard, Yvonne, Miller, Fiona A, Hayeems, Robin Z, Wilson, Brenda J, Carroll, June C, Paynter, Martha, Little, Julian, Allanson, Judith, Bytautas, Jessica P, Chakraborty, Pranesh
Publicado em 2012

Expectations and values about expanded newborn screening: a public engagement study

Por Hayeems, Robin Z., Miller, Fiona A., Bombard, Yvonne, Avard, Denise, Carroll, June, Wilson, Brenda, Little, Julian, Chakraborty, Pranesh, Bytautas, Jessica, Giguere, Yves, Allanson, Judith, Axler, Renata
Publicado no Health Expect (2013)

Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care

Por Miller, Fiona A, Hayeems, Robin Z, Bytautas, Jessica P, Bedard, Philippe L, Ernst, Scott, Hirte, Hal, Hotte, Sebastien, Oza, Amit, Razak, Albiruni, Welch, Stephen, Winquist, Eric, Dancey, Janet, Siu, Lillian L
Publicado em 2014

Public views on participating in newborn screening using genome sequencing

Por Bombard, Yvonne, Miller, Fiona A, Hayeems, Robin Z, Barg, Carolyn, Cressman, Celine, Carroll, June C, Wilson, Brenda J, Little, Julian, Avard, Denise, Painter-Main, Michael, Allanson, Judith, Giguere, Yves, Chakraborty, Pranesh
Publicado em 2014

A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis

Por Bombard, Yvonne, Miller, Fiona A., Barg, Carolyn J., Patton, Sarah J., Carroll, June C., Chakraborty, Pranesh, Potter, Beth K., Tam, Karen, Taylor, Louise, Kerr, Elizabeth, Davies, Christine, Milburn, Jennifer, Ratjen, Felix, Guttmann, Astrid, Hayeems, Robin Z.
Publicado no Genet Med (2016)

Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups

Por Khangura, Sara D., Tingley, Kylie, Chakraborty, Pranesh, Coyle, Doug, Kronick, Jonathan B., Laberge, Anne-Marie, Little, Julian, Miller, Fiona A, Mitchell, John J., Prasad, Chitra, Siddiq, Shabnaz, Siriwardena, Komudi, Sparkes, Rebecca, Speechley, Kathy N., Stockler, Sylvia, Trakadis, Yannis, Wilson, Brenda J., Wilson, Kumanan, Potter, Beth K.
Publicado no J Inherit Metab Dis (2015)

The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study

Por Karaceper, Maria D., Chakraborty, Pranesh, Coyle, Doug, Wilson, Kumanan, Kronick, Jonathan B., Hawken, Steven, Davies, Christine, Brownell, Marni, Dodds, Linda, Feigenbaum, Annette, Fell, Deshayne B., Grosse, Scott D., Guttmann, Astrid, Laberge, Anne-Marie, Mhanni, Aizeddin, Miller, Fiona A., Mitchell, John J., Nakhla, Meranda, Prasad, Chitra, Rockman-Greenberg, Cheryl, Sparkes, Rebecca, Wilson, Brenda J., Potter, Beth K.
Publicado no Orphanet J Rare Dis (2016)

Reflections on the Cost of "Low-Cost" Whole Genome Sequencing: Framing the Health Policy Debate

Por Caulfield, Timothy, Evans, Jim, McGuire, Amy, McCabe, Christopher, Bubela, Tania, Cook-Deegan, Robert, Fishman, Jennifer, Hogarth, Stuart, Miller, Fiona A., Ravitsky, Vardit, Biesecker, Barbara, Borry, Pascal, Cho, Mildred K., Carroll, June C., Etchegary, Holly, Joly, Yann, Kato, Kazuto, Lee, Sandra Soo-Jin, Rothenberg, Karen, Sankar, Pamela, Szego, Michael J., Ossorio, Pilar, Pullman, Daryl, Rousseau, Francois, Ungar, Wendy J., Wilson, Brenda
Publicado em 2013