Felicity Kate Boardman. Soc Sci Med 2014
Times Cited: 32
Times Cited: 32
Times Cited
Times Co-cited
Similarity
How do genetically disabled adults view selective reproduction? Impairment, identity, and genetic screening.
Felicity K Boardman, Rachel Hale. Mol Genet Genomic Med 2018
Felicity K Boardman, Rachel Hale. Mol Genet Genomic Med 2018
40
Choosing not to choose: reproductive responses of parents of children with genetic conditions or impairments.
Susan E Kelly. Sociol Health Illn 2009
Susan E Kelly. Sociol Health Illn 2009
21
Attitudes toward genetic counseling and prenatal diagnosis among a group of individuals with physical disabilities.
E A Chen, J F Schiffman. J Genet Couns 2000
E A Chen, J F Schiffman. J Genet Couns 2000
31
Knowledge is power? The role of experiential knowledge in genetically 'risky' reproductive decisions.
Felicity K Boardman. Sociol Health Illn 2014
Felicity K Boardman. Sociol Health Illn 2014
46
The relationship between the genetic counseling profession and the disability community: a commentary.
Anne C Madeo, Barbara B Biesecker, Campbell Brasington, Lori H Erby, Kathryn F Peters. Am J Med Genet A 2011
Anne C Madeo, Barbara B Biesecker, Campbell Brasington, Lori H Erby, Kathryn F Peters. Am J Med Genet A 2011
18
Disability rights critique of prenatal genetic testing: reflections and recommendations.
Erik Parens, Adrienne Asch. Ment Retard Dev Disabil Res Rev 2003
Erik Parens, Adrienne Asch. Ment Retard Dev Disabil Res Rev 2003
18
Having a son or daughter with Down syndrome: perspectives from mothers and fathers.
Brian G Skotko, Susan P Levine, Richard Goldstein. Am J Med Genet A 2011
Brian G Skotko, Susan P Levine, Richard Goldstein. Am J Med Genet A 2011
15
With new prenatal testing, will babies with Down syndrome slowly disappear?
Brian G Skotko. Arch Dis Child 2009
Brian G Skotko. Arch Dis Child 2009
15
Attitudes of mothers of children with down syndrome towards noninvasive prenatal testing.
Gregory Kellogg, Leah Slattery, Louanne Hudgins, Kelly Ormond. J Genet Couns 2014
Gregory Kellogg, Leah Slattery, Louanne Hudgins, Kelly Ormond. J Genet Couns 2014
15
What constitutes 'balanced' information in the practitioners' portrayals of Down's syndrome?
Clare Williams, Priscilla Alderson, Bobbie Farsides. Midwifery 2002
Clare Williams, Priscilla Alderson, Bobbie Farsides. Midwifery 2002
15
Negotiating desires and options: how mothers who carry the fragile X gene experience reproductive decisions.
Kelly Amanda Raspberry, Debra Skinner. Soc Sci Med 2011
Kelly Amanda Raspberry, Debra Skinner. Soc Sci Med 2011
16
Disability advocacy and reproductive choice: engaging with the expressivist objection.
Madelyn Peterson. J Genet Couns 2012
Madelyn Peterson. J Genet Couns 2012
62
Choosing who will be disabled: genetic intervention and the morality of inclusion.
Allen Buchanan. Soc Philos Policy 1996
Allen Buchanan. Soc Philos Policy 1996
15
The best experts: the narratives of those who have a genetic condition.
Alan Petersen. Soc Sci Med 2006
Alan Petersen. Soc Sci Med 2006
15
Perceptions and Discourses Relating to Genetic Testing: Interviews with People with Down Syndrome.
Barbara Barter, Richard Patrick Hastings, Rebecca Williams, Jaci C Huws. J Appl Res Intellect Disabil 2017
Barbara Barter, Richard Patrick Hastings, Rebecca Williams, Jaci C Huws. J Appl Res Intellect Disabil 2017
41
Impairment Experiences, Identity and Attitudes Towards Genetic Screening: the Views of People with Spinal Muscular Atrophy.
Felicity K Boardman, Philip J Young, Frances E Griffiths. J Genet Couns 2018
Felicity K Boardman, Philip J Young, Frances E Griffiths. J Genet Couns 2018
41
Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening.
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat Diagn 2013
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat Diagn 2013
12
The disability rights critique of prenatal genetic testing. Reflections and Recommendations.
E Parens, A Asch. Hastings Cent Rep 1999
E Parens, A Asch. Hastings Cent Rep 1999
12
Self-perceptions from people with Down syndrome.
Brian G Skotko, Susan P Levine, Richard Goldstein. Am J Med Genet A 2011
Brian G Skotko, Susan P Levine, Richard Goldstein. Am J Med Genet A 2011
12
Screening for Fragile X Syndrome: parent attitudes and perspectives.
Debra Skinner, Karen L Sparkman, Donald B Bailey. Genet Med 2003
Debra Skinner, Karen L Sparkman, Donald B Bailey. Genet Med 2003
12
Anticipated stigma and blameless guilt: Mothers' evaluation of life with the sex-linked disorder, hypohidrotic ectodermal dysplasia (XHED).
Angus Clarke. Soc Sci Med 2016
Angus Clarke. Soc Sci Med 2016
33
Deciding against disability: does the use of reproductive genetic technologies express disvalue for people with disabilities?
Janet Malek. J Med Ethics 2010
Janet Malek. J Med Ethics 2010
25
Attitudes of deaf and hard of hearing subjects towards genetic testing and prenatal diagnosis of hearing loss.
S J Stern, K S Arnos, L Murrelle, K Oelrich Welch, W E Nance, A Pandya. J Med Genet 2002
S J Stern, K S Arnos, L Murrelle, K Oelrich Welch, W E Nance, A Pandya. J Med Genet 2002
12
Disability identity and attitudes toward cure in a sample of disabled activists.
Harlan D Hahn, Todd L Belt. J Health Soc Behav 2004
Harlan D Hahn, Todd L Belt. J Health Soc Behav 2004
14
Population screening for spinal muscular atrophy: A mixed methods study of the views of affected families.
Felicity K Boardman, Philip J Young, Frances E Griffiths. Am J Med Genet A 2017
Felicity K Boardman, Philip J Young, Frances E Griffiths. Am J Med Genet A 2017
12
What is a "balanced" description? Insight from parents of individuals with down syndrome.
Catriona Hippman, Angela Inglis, Jehannine Austin. J Genet Couns 2012
Catriona Hippman, Angela Inglis, Jehannine Austin. J Genet Couns 2012
26
Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake.
Reana Tischler, Louanne Hudgins, Yair J Blumenfeld, Henry T Greely, Kelly E Ormond. Prenat Diagn 2011
Reana Tischler, Louanne Hudgins, Yair J Blumenfeld, Henry T Greely, Kelly E Ormond. Prenat Diagn 2011
9
Will the introduction of non-invasive prenatal diagnostic testing erode informed choices? An experimental study of health care professionals.
Ananda van den Heuvel, Lyn Chitty, Elizabeth Dormandy, Ainsley Newson, Zuzana Deans, Sophie Attwood, Shelley Haynes, Theresa M Marteau. Patient Educ Couns 2010
Ananda van den Heuvel, Lyn Chitty, Elizabeth Dormandy, Ainsley Newson, Zuzana Deans, Sophie Attwood, Shelley Haynes, Theresa M Marteau. Patient Educ Couns 2010
9
ACMG statement on noninvasive prenatal screening for fetal aneuploidy.
Anthony R Gregg, S J Gross, R G Best, K G Monaghan, K Bajaj, B G Skotko, B H Thompson, M S Watson. Genet Med 2013
Anthony R Gregg, S J Gross, R G Best, K G Monaghan, K Bajaj, B G Skotko, B H Thompson, M S Watson. Genet Med 2013
9
9
Attitudes towards non-invasive prenatal testing for aneuploidy among US adults of reproductive age.
M Allyse, L C Sayres, T A Goodspeed, M K Cho. J Perinatol 2014
M Allyse, L C Sayres, T A Goodspeed, M K Cho. J Perinatol 2014
9
A disability critique of the new prenatal test for Down syndrome.
Chris Kaposy. Kennedy Inst Ethics J 2013
Chris Kaposy. Kennedy Inst Ethics J 2013
13
Genetic counseling for prenatal testing: where is the discussion about disability?
Ellyn Farrelly, Mildred K Cho, Lori Erby, Debra Roter, Anabel Stenzel, Kelly Ormond. J Genet Couns 2012
Ellyn Farrelly, Mildred K Cho, Lori Erby, Debra Roter, Anabel Stenzel, Kelly Ormond. J Genet Couns 2012
11
A single center's experience with noninvasive prenatal testing.
Carmen J Beamon, Emily E Hardisty, Sarah C Harris, Neeta L Vora. Genet Med 2014
Carmen J Beamon, Emily E Hardisty, Sarah C Harris, Neeta L Vora. Genet Med 2014
11
Disability training in the genetic counseling curricula: bridging the gap between genetic counselors and the disability community.
Erica Sanborn, Annette R Patterson. Am J Med Genet A 2014
Erica Sanborn, Annette R Patterson. Am J Med Genet A 2014
42
Kinscapes, timescapes and genescapes: families living with genetic risk.
Paul Atkinson, Katie Featherstone, Maggie Gregory. Sociol Health Illn 2013
Paul Atkinson, Katie Featherstone, Maggie Gregory. Sociol Health Illn 2013
12
Guilt, blame and responsibility: men's understanding of their role in the transmission of BRCA1/2 mutations within their family.
Nina Hallowell, Audrey Arden-Jones, Ros Eeles, Claire Foster, Anneke Lucassen, Clare Moynihan, Maggie Watson. Sociol Health Illn 2006
Nina Hallowell, Audrey Arden-Jones, Ros Eeles, Claire Foster, Anneke Lucassen, Clare Moynihan, Maggie Watson. Sociol Health Illn 2006
9
Growing up and living with neurofibromatosis1 (NF1): a British Bangladeshi case-study.
Santi Rozario. J Genet Couns 2007
Santi Rozario. J Genet Couns 2007
50
Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, Frances L Lynch, Jacob A Reiss, Marian J Gilmore, Patricia Himes, Tia L Kauffman, James V Davis, Gail P Jarvik,[...]. Am J Med Genet A 2016
Michael C Leo, Carmit McMullen, Benjamin S Wilfond, Frances L Lynch, Jacob A Reiss, Marian J Gilmore, Patricia Himes, Tia L Kauffman, James V Davis, Gail P Jarvik,[...]. Am J Med Genet A 2016
17
The role of disability self-concept in adaptation to congenital or acquired disability.
Kathleen R Bogart. Rehabil Psychol 2014
Kathleen R Bogart. Rehabil Psychol 2014
9
Perceptions of population cystic fibrosis prenatal and preconception carrier screening among individuals with cystic fibrosis and their family members.
Susannah J Maxwell, Gaenor Kyne, Caron Molster, Nigel M Barker, Jacqueline Ormsby, Peter O'Leary. Genet Test Mol Biomarkers 2011
Susannah J Maxwell, Gaenor Kyne, Caron Molster, Nigel M Barker, Jacqueline Ormsby, Peter O'Leary. Genet Test Mol Biomarkers 2011
15
Attitudes to carrier screening for cystic fibrosis: a survey of health care professionals, relatives of sufferers and other members of the public.
E K Watson, R Williamson, J Chapple. Br J Gen Pract 1991
E K Watson, R Williamson, J Chapple. Br J Gen Pract 1991
9
Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases.
Mirjam Plantinga, Erwin Birnie, Kristin M Abbott, Richard J Sinke, Anneke M Lucassen, Juliette Schuurmans, Seyma Kaplan, Marian A Verkerk, Adelita V Ranchor, Irene M van Langen. Eur J Hum Genet 2016
Mirjam Plantinga, Erwin Birnie, Kristin M Abbott, Richard J Sinke, Anneke M Lucassen, Juliette Schuurmans, Seyma Kaplan, Marian A Verkerk, Adelita V Ranchor, Irene M van Langen. Eur J Hum Genet 2016
9
Negotiating responsibility: case studies of reproductive decision-making and prenatal genetic testing in families facing Huntington disease.
Claudia Downing. J Genet Couns 2005
Claudia Downing. J Genet Couns 2005
9
9
Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study.
C Roadhouse, C Shuman, K Anstey, K Sappleton, D Chitayat, E Ignagni. J Genet Couns 2018
C Roadhouse, C Shuman, K Anstey, K Sappleton, D Chitayat, E Ignagni. J Genet Couns 2018
50
Living with achondroplasia: attitudes toward population screening and correlation with quality of life.
Sarah E Gollust, Richard E Thompson, Holly C Gooding, Barbara B Biesecker. Prenat Diagn 2003
Sarah E Gollust, Richard E Thompson, Holly C Gooding, Barbara B Biesecker. Prenat Diagn 2003
13
The disability paradox: high quality of life against all odds.
G L Albrecht, P J Devlieger. Soc Sci Med 1999
G L Albrecht, P J Devlieger. Soc Sci Med 1999
9
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.