Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur. J. Hum. Genet. 2013
Times Cited: 46
Times Cited: 46
Times Cited
Citation Count
Similarity
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
9
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
6
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
6
The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J. Med. Genet. 2015
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J. Med. Genet. 2015
4
Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N. Engl. J. Med. 2013
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N. Engl. J. Med. 2013
4
Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet. Med. 2014
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet. Med. 2014
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
6
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
The challenge of informed consent and return of results in translational genomics: empirical analysis and recommendations.
Gail E Henderson, Susan M Wolf, Kristine J Kuczynski, Steven Joffe, Richard R Sharp, D Williams Parsons, Bartha M Knoppers, Joon-Ho Yu, Paul S Appelbaum. J Law Med Ethics 2014
Gail E Henderson, Susan M Wolf, Kristine J Kuczynski, Steven Joffe, Richard R Sharp, D Williams Parsons, Bartha M Knoppers, Joon-Ho Yu, Paul S Appelbaum. J Law Med Ethics 2014
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
14
Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur. J. Hum. Genet. 2013
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur. J. Hum. Genet. 2013
4
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
10
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
7
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
7
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
6
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
8
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
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
5
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
10
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. 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. 2014
13
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
7
Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. 2014
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. 2014
9
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
7
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
Factors affecting decisions to accept or decline cystic fibrosis carrier testing/screening: a theory-guided systematic review.
Lei-Shih Chen, Patricia Goodson. Genet. Med. 2007
Lei-Shih Chen, Patricia Goodson. Genet. Med. 2007
6
"Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening.
Jennifer L Schneider, Katrina A B Goddard, James Davis, Benjamin Wilfond, Tia L Kauffman, Jacob A Reiss, Marian Gilmore, Patricia Himes, Frances L Lynch, Michael C Leo,[...]. J Genet Couns 2016
Jennifer L Schneider, Katrina A B Goddard, James Davis, Benjamin Wilfond, Tia L Kauffman, Jacob A Reiss, Marian Gilmore, Patricia Himes, Frances L Lynch, Michael C Leo,[...]. J Genet Couns 2016
7
Expanded carrier screening: A review of early implementation and literature.
Gabriel A Lazarin, Imran S Haque. Semin. Perinatol. 2016
Gabriel A Lazarin, Imran S Haque. Semin. Perinatol. 2016
7
Attitudes of European Geneticists Regarding Expanded Carrier Screening.
Sandra Janssens, Davit Chokoshvili, Danya Vears, Anne De Paepe, Pascal Borry. J Obstet Gynecol Neonatal Nurs 2017
Sandra Janssens, Davit Chokoshvili, Danya Vears, Anne De Paepe, Pascal Borry. J Obstet Gynecol Neonatal Nurs 2017
16
Expanded carrier screening in reproductive healthcare: perspectives from genetics professionals.
D Cho, M L McGowan, J Metcalfe, R R Sharp. Hum. Reprod. 2013
D Cho, M L McGowan, J Metcalfe, R R Sharp. Hum. Reprod. 2013
6
The changing landscape of carrier screening: expanding technology and options?.
Michelle L McGowan, Deborah Cho, Richard R Sharp. Health Matrix Clevel 2013
Michelle L McGowan, Deborah Cho, Richard R Sharp. Health Matrix Clevel 2013
14
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.