S Elias, G J Annas. N Engl J Med 1994
Times Cited: 111
Times Cited: 111
Times Cited
Times Co-cited
Similarity
Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time.
Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
12
Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine.
Janice G Edwards, Gerald Feldman, James Goldberg, Anthony R Gregg, Mary E Norton, Nancy C Rose, Adele Schneider, Katie Stoll, Ronald Wapner, Michael S Watson. Obstet Gynecol 2015
Janice G Edwards, Gerald Feldman, James Goldberg, Anthony R Gregg, Mary E Norton, Nancy C Rose, Adele Schneider, Katie Stoll, Ronald Wapner, Michael S Watson. Obstet Gynecol 2015
9
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
9
Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consent.
G Geller, J R Botkin, M J Green, N Press, B B Biesecker, B Wilfond, G Grana, M B Daly, K Schneider, M J Kahn. JAMA 1997
G Geller, J R Botkin, M J Green, N Press, B B Biesecker, B Wilfond, G Grana, M B Daly, K Schneider, M J Kahn. JAMA 1997
8
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
10
Informed consent for genetic research on stored tissue samples.
E W Clayton, K K Steinberg, M J Khoury, E Thomson, L Andrews, M J Kahn, L M Kopelman, J O Weiss. JAMA 1995
E W Clayton, K K Steinberg, M J Khoury, E Thomson, L Andrews, M J Kahn, L M Kopelman, J O Weiss. JAMA 1995
7
Genetic counseling for families with inherited susceptibility to breast and ovarian cancer.
B B Biesecker, M Boehnke, K Calzone, D S Markel, J E Garber, F S Collins, B L Weber. JAMA 1993
B B Biesecker, M Boehnke, K Calzone, D S Markel, J E Garber, F S Collins, B L Weber. JAMA 1993
7
Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
7
Challenges in the clinical application of whole-genome sequencing.
Kelly E Ormond, Matthew T Wheeler, Louanne Hudgins, Teri E Klein, Atul J Butte, Russ B Altman, Euan A Ashley, Henry T Greely. Lancet 2010
Kelly E Ormond, Matthew T Wheeler, Louanne Hudgins, Teri E Klein, Atul J Butte, Russ B Altman, Euan A Ashley, Henry T Greely. Lancet 2010
7
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
7
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
7
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
7
Physicians' knowledge of genetics and genetic tests.
K J Hofman, E S Tambor, G A Chase, G Geller, R R Faden, N A Holtzman. Acad Med 1993
K J Hofman, E S Tambor, G A Chase, G Geller, R R Faden, N A Holtzman. Acad Med 1993
6
Non-invasive prenatal testing: ethical issues explored.
Antina de Jong, Wybo J Dondorp, Christine E M de Die-Smulders, Suzanne G M Frints, Guido M W R de Wert. Eur J Hum Genet 2010
Antina de Jong, Wybo J Dondorp, Christine E M de Die-Smulders, Suzanne G M Frints, Guido M W R de Wert. Eur J Hum Genet 2010
6
A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
12
16
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
5
ASHG statement. Professional disclosure of familial genetic information. The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure.
. Am J Hum Genet 1998
. Am J Hum Genet 1998
5
Psychological issues in genetic testing for breast cancer susceptibility.
C Lerman, R Croyle. Arch Intern Med 1994
C Lerman, R Croyle. Arch Intern Med 1994
5
The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
5
Two models of implementing informed consent.
C W Lidz, P S Appelbaum, A Meisel. Arch Intern Med 1988
C W Lidz, P S Appelbaum, A Meisel. Arch Intern Med 1988
5
What do patients prefer: informed consent models for genetic carrier testing.
K E Ormond, M Iris, S Banuvar, J Minogue, G J Annas, S Elias. J Genet Couns 2007
K E Ormond, M Iris, S Banuvar, J Minogue, G J Annas, S Elias. J Genet Couns 2007
16
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood.
H Christina Fan, Yair J Blumenfeld, Usha Chitkara, Louanne Hudgins, Stephen R Quake. Proc Natl Acad Sci U S A 2008
H Christina Fan, Yair J Blumenfeld, Usha Chitkara, Louanne Hudgins, Stephen R Quake. Proc Natl Acad Sci U S A 2008
5
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
7
Clinical assessment incorporating a personal genome.
Euan A Ashley, Atul J Butte, Matthew T Wheeler, Rong Chen, Teri E Klein, Frederick E Dewey, Joel T Dudley, Kelly E Ormond, Aleksandra Pavlovic, Alexander A Morgan,[...]. Lancet 2010
Euan A Ashley, Atul J Butte, Matthew T Wheeler, Rong Chen, Teri E Klein, Frederick E Dewey, Joel T Dudley, Kelly E Ormond, Aleksandra Pavlovic, Alexander A Morgan,[...]. Lancet 2010
5
Letting the genome out of the bottle--will we get our wish?
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N Engl J Med 2008
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N Engl J Med 2008
5
Genetic testing in asymptomatic minors: Recommendations of the European Society of Human Genetics.
. Eur J Hum Genet 2009
. Eur J Hum Genet 2009
5
Serious genetic disorders: can or should they be defined?
Dorothy C Wertz, Bartha Maria Knoppers. Am J Med Genet 2002
Dorothy C Wertz, Bartha Maria Knoppers. Am J Med Genet 2002
10
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent.
Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
11
Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
5
Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
5
DNA sequencing versus standard prenatal aneuploidy screening.
Diana W Bianchi, R Lamar Parker, Jeffrey Wentworth, Rajeevi Madankumar, Craig Saffer, Anita F Das, Joseph A Craig, Darya I Chudova, Patricia L Devers, Keith W Jones,[...]. N Engl J Med 2014
Diana W Bianchi, R Lamar Parker, Jeffrey Wentworth, Rajeevi Madankumar, Craig Saffer, Anita F Das, Joseph A Craig, Darya I Chudova, Patricia L Devers, Keith W Jones,[...]. N Engl J Med 2014
5
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
16
Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
5
Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels.
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS One 2014
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS One 2014
10
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families.
E H Corder, A M Saunders, W J Strittmatter, D E Schmechel, P C Gaskell, G W Small, A D Roses, J L Haines, M A Pericak-Vance. Science 1993
E H Corder, A M Saunders, W J Strittmatter, D E Schmechel, P C Gaskell, G W Small, A D Roses, J L Haines, M A Pericak-Vance. Science 1993
4
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.
R Wooster, S L Neuhausen, J Mangion, Y Quirk, D Ford, N Collins, K Nguyen, S Seal, T Tran, D Averill. Science 1994
R Wooster, S L Neuhausen, J Mangion, Y Quirk, D Ford, N Collins, K Nguyen, S Seal, T Tran, D Averill. Science 1994
4
4
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.
W J Strittmatter, A M Saunders, D Schmechel, M Pericak-Vance, J Enghild, G S Salvesen, A D Roses. Proc Natl Acad Sci U S A 1993
W J Strittmatter, A M Saunders, D Schmechel, M Pericak-Vance, J Enghild, G S Salvesen, A D Roses. Proc Natl Acad Sci U S A 1993
4
Genetic testing for children and adolescents. Who decides?
D C Wertz, J H Fanos, P R Reilly. JAMA 1994
D C Wertz, J H Fanos, P R Reilly. JAMA 1994
4
Shattuck lecture--medical and societal consequences of the Human Genome Project.
F S Collins. N Engl J Med 1999
F S Collins. N Engl J Med 1999
4
The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing.
S Wiggins, P Whyte, M Huggins, S Adam, J Theilmann, M Bloch, S B Sheps, M T Schechter, M R Hayden. N Engl J Med 1992
S Wiggins, P Whyte, M Huggins, S Adam, J Theilmann, M Bloch, S B Sheps, M T Schechter, M R Hayden. N Engl J Med 1992
4
Ethical issues in genetic research: disclosure and informed consent.
P R Reilly, M F Boshar, S H Holtzman. Nat Genet 1997
P R Reilly, M F Boshar, S H Holtzman. Nat Genet 1997
5
BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.
C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, G Bonney, K Gold, B Trock, D Main, J Lynch,[...]. JAMA 1996
C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, G Bonney, K Gold, B Trock, D Main, J Lynch,[...]. JAMA 1996
4
"Decoding" informed consent. Insights from women regarding breast cancer susceptibility testing.
G Geller, M Strauss, B A Bernhardt, N A Holtzman. Hastings Cent Rep 1997
G Geller, M Strauss, B A Bernhardt, N A Holtzman. Hastings Cent Rep 1997
10
Tiered disclosure options promote the autonomy and well-being of research subjects.
Mark A Rothstein. Am J Bioeth 2006
Mark A Rothstein. Am J Bioeth 2006
10
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
Trilochan Sahoo, Sau Wai Cheung, Patricia Ward, Sandra Darilek, Ankita Patel, Daniela del Gaudio, Sung Hae L Kang, Seema R Lalani, Jiangzhen Li, Sallie McAdoo,[...]. Genet Med 2006
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.