Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Times Cited: 48
Times Cited: 48
Times Cited
Times Co-cited
Similarity
Multiplex genetic testing for cancer susceptibility: out on the high wire without a net?
Susan M Domchek, Angela Bradbury, Judy E Garber, Kenneth Offit, Mark E Robson. J Clin Oncol 2013
Susan M Domchek, Angela Bradbury, Judy E Garber, Kenneth Offit, Mark E Robson. J Clin Oncol 2013
4
Anticipate and communicate: Ethical management of incidental and secondary findings in the clinical, research, and direct-to-consumer contexts (December 2013 report of the Presidential Commission for the Study of Bioethical Issues).
Christine Weiner. Am J Epidemiol 2014
Christine Weiner. Am J Epidemiol 2014
4
Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment.
B A Bernhardt, B B Biesecker, C L Mastromarino. Am J Med Genet 2000
B A Bernhardt, B B Biesecker, C L Mastromarino. Am J Med Genet 2000
4
Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing.
Megan Allyse, Marsha Michie. Trends Biotechnol 2013
Megan Allyse, Marsha Michie. Trends Biotechnol 2013
4
Knowledge and attitudes regarding expanded genetic carrier screening among women's healthcare providers.
Kaylene Ready, Imran S Haque, Balaji S Srinivasan, John R Marshall. Fertil Steril 2012
Kaylene Ready, Imran S Haque, Balaji S Srinivasan, John R Marshall. Fertil Steril 2012
6
A universal carrier test for the long tail of Mendelian disease.
Balaji S Srinivasan, Eric A Evans, Jason Flannick, A Scott Patterson, Christopher C Chang, Tuan Pham, Sharon Young, Amit Kaushal, James Lee, Jessica L Jacobson,[...]. Reprod Biomed Online 2010
Balaji S Srinivasan, Eric A Evans, Jason Flannick, A Scott Patterson, Christopher C Chang, Tuan Pham, Sharon Young, Amit Kaushal, James Lee, Jessica L Jacobson,[...]. Reprod Biomed Online 2010
4
ACMG position statement on prenatal/preconception expanded carrier screening.
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
4
ACOG Committee Opinion No. 486: Update on carrier screening for cystic fibrosis.
. Obstet Gynecol 2011
. Obstet Gynecol 2011
4
Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011
4
Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience.
Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2012
Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski, Michael Parker. BMC Med Ethics 2012
4
Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents.
Nchangwi Syntia Munung, Patricia Marshall, Megan Campbell, Katherine Littler, Francis Masiye, Odile Ouwe-Missi-Oukem-Boyer, Janet Seeley, D J Stein, Paulina Tindana, Jantina de Vries. J Med Ethics 2016
Nchangwi Syntia Munung, Patricia Marshall, Megan Campbell, Katherine Littler, Francis Masiye, Odile Ouwe-Missi-Oukem-Boyer, Janet Seeley, D J Stein, Paulina Tindana, Jantina de Vries. J Med Ethics 2016
7
Scrutinizing the Right Not to Know.
Benjamin E Berkman, Sara Chandros Hull, Leslie G Biesecker. Am J Bioeth 2015
Benjamin E Berkman, Sara Chandros Hull, Leslie G Biesecker. Am J Bioeth 2015
50
Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Marcia Van Riper, Rebecca L Walker, Eric T Juengst. Am J Bioeth 2015
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Marcia Van Riper, Rebecca L Walker, Eric T Juengst. Am J Bioeth 2015
7
Attitudes of non-African American focus group participants toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am J Med Genet A 2014
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am J Med Genet A 2014
5
Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing.
Angela R Bradbury, Linda J Patrick-Miller, Brian L Egleston, Laura DiGiovanni, Jamie Brower, Diana Harris, Evelyn M Stevens, Kara N Maxwell, Abha Kulkarni, Tyler Chavez,[...]. Genet Med 2016
Angela R Bradbury, Linda J Patrick-Miller, Brian L Egleston, Laura DiGiovanni, Jamie Brower, Diana Harris, Evelyn M Stevens, Kara N Maxwell, Abha Kulkarni, Tyler Chavez,[...]. Genet Med 2016
5
Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
4
Genetic counselors' views and experiences with the clinical integration of genome sequencing.
Kalotina Machini, Jessica Douglas, Alicia Braxton, Judith Tsipis, Kate Kramer. J Genet Couns 2014
Kalotina Machini, Jessica Douglas, Alicia Braxton, Judith Tsipis, Kate Kramer. J Genet Couns 2014
5
Informed consent for medical treatment and research: a review.
Marcela G del Carmen, Steven Joffe. Oncologist 2005
Marcela G del Carmen, Steven Joffe. Oncologist 2005
4
Practices and policies of clinical exome sequencing providers: analysis and implications.
Seema M Jamal, Joon-Ho Yu, Jessica X Chong, Karin M Dent, Jessie H Conta, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
Seema M Jamal, Joon-Ho Yu, Jessica X Chong, Karin M Dent, Jessie H Conta, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
4
Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
4
Blurring lines. The research activities of direct-to-consumer genetic testing companies raise questions about consumers as research subjects.
Heidi C Howard, Bartha Maria Knoppers, Pascal Borry. EMBO Rep 2010
Heidi C Howard, Bartha Maria Knoppers, Pascal Borry. EMBO Rep 2010
7
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
. Genet Med 2015
. Genet Med 2015
4
Informed consent in direct-to-consumer personal genome testing: the outline of a model between specific and generic consent.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Bioethics 2014
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Bioethics 2014
13
Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
4
Attitudes of pregnant women regarding termination of pregnancy for fetal abnormality.
A P Souka, V D Michalitsi, H Skentou, H Euripioti, G K Papadopoulos, D Kassanos, I E Messinis, E E Salamalekis. Prenat Diagn 2010
A P Souka, V D Michalitsi, H Skentou, H Euripioti, G K Papadopoulos, D Kassanos, I E Messinis, E E Salamalekis. Prenat Diagn 2010
8
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
4
What women want: lead considerations for current and future applications of noninvasive prenatal testing in prenatal care.
Ruth M Farrell, Patricia K Agatisa, Benjamin Nutter. Birth 2014
Ruth M Farrell, Patricia K Agatisa, Benjamin Nutter. Birth 2014
6
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
4
Public viewpoints on new non-invasive prenatal genetic tests.
Hannah R Farrimond, Susan E Kelly. Public Underst Sci 2013
Hannah R Farrimond, Susan E Kelly. Public Underst Sci 2013
6
Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
4
Advances in prenatal screening: the ethical dimension.
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat Rev Genet 2011
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat Rev Genet 2011
4
Prenatal whole genome sequencing: just because we can, should we?
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
5
From patients to partners: participant-centric initiatives in biomedical research.
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
4
Specific psychosocial issues of individuals undergoing genetic counseling for cancer - a literature review.
Willem Eijzenga, Daniela E E Hahn, Neil K Aaronson, Irma Kluijt, Eveline M A Bleiker. J Genet Couns 2014
Willem Eijzenga, Daniela E E Hahn, Neil K Aaronson, Irma Kluijt, Eveline M A Bleiker. J Genet Couns 2014
7
Potential Psychosocial Risks of Sequencing Newborns.
Leslie Ann Frankel, Stacey Pereira, Amy L McGuire. Pediatrics 2016
Leslie Ann Frankel, Stacey Pereira, Amy L McGuire. Pediatrics 2016
8
Testing an online, dynamic consent portal for large population biobank research.
Daniel B Thiel, Jodyn Platt, Tevah Platt, Susan B King, Nicole Fisher, Robert Shelton, Sharon L R Kardia. Public Health Genomics 2015
Daniel B Thiel, Jodyn Platt, Tevah Platt, Susan B King, Nicole Fisher, Robert Shelton, Sharon L R Kardia. Public Health Genomics 2015
8
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur J Hum Genet 2015
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur J Hum Genet 2015
4
NIPT-based screening for Down syndrome and beyond: what do pregnant women think?
Rachèl V van Schendel, Wybo J Dondorp, Danielle R M Timmermans, Eline J H van Hugte, Anne de Boer, Eva Pajkrt, Augusta M A Lachmeijer, Lidewij Henneman. Prenat Diagn 2015
Rachèl V van Schendel, Wybo J Dondorp, Danielle R M Timmermans, Eline J H van Hugte, Anne de Boer, Eva Pajkrt, Augusta M A Lachmeijer, Lidewij Henneman. Prenat Diagn 2015
4
The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.
S L van der Steen, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M I Srebniak, D Van Opstal, M Joosten, M F C M Knapen, A Tibben, K E M Diderich,[...]. J Genet Couns 2016
S L van der Steen, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M I Srebniak, D Van Opstal, M Joosten, M F C M Knapen, A Tibben, K E M Diderich,[...]. J Genet Couns 2016
8
The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing.
Sam Riedijk, Karin E M Diderich, Sanne L van der Steen, Lutgarde C P Govaerts, Marieke Joosten, Maarten F C M Knapen, Femke A T de Vries, Diane van Opstal, Aad Tibben, Robert-Jan H Galjaard. J Clin Med 2014
Sam Riedijk, Karin E M Diderich, Sanne L van der Steen, Lutgarde C P Govaerts, Marieke Joosten, Maarten F C M Knapen, Femke A T de Vries, Diane van Opstal, Aad Tibben, Robert-Jan H Galjaard. J Clin Med 2014
11
Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
6
Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. J Community Genet 2014
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. J Community Genet 2014
8
Qualitative content analysis in nursing research: concepts, procedures and measures to achieve trustworthiness.
U H Graneheim, B Lundman. Nurse Educ Today 2004
U H Graneheim, B Lundman. Nurse Educ Today 2004
4
Laboratory standards and guidelines for population-based cystic fibrosis carrier screening.
W W Grody, G R Cutting, K W Klinger, C S Richards, M S Watson, R J Desnick. Genet Med 2001
W W Grody, G R Cutting, K W Klinger, C S Richards, M S Watson, R J Desnick. Genet Med 2001
4
Changing trends in carrier screening for genetic disease in the United States.
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat Diagn 2015
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat Diagn 2015
5
Responsible implementation of expanded carrier screening.
Lidewij Henneman, Pascal Borry, Davit Chokoshvili, Martina C Cornel, Carla G van El, Francesca Forzano, Alison Hall, Heidi C Howard, Sandra Janssens, Hülya Kayserili,[...]. Eur J Hum Genet 2016
Lidewij Henneman, Pascal Borry, Davit Chokoshvili, Martina C Cornel, Carla G van El, Francesca Forzano, Alison Hall, Heidi C Howard, Sandra Janssens, Hülya Kayserili,[...]. Eur J Hum Genet 2016
4
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.