A citation-based method for searching scientific literature

Angela R Bradbury, Linda Patrick-Miller, Brian Egleston, Colleen Burke Sands, Tianyu Li, Helen Schmidheiser, Maia Feigon, Comfort N Ibe, Fay J Hlubocky, Kisha Hope, Sarah Jackson, Melanie Corbman, Olufunmilayo I Olopade, Mary Daly, Christopher K Daugherty. J Clin Oncol 2010
Times Cited: 14

List of co-cited articles
67 articles co-cited >1

Times Cited
  Times     Co-cited

Parental preferences for CDKN2A/p16 testing of minors.
Jennifer M Taber, Lisa G Aspinwall, Wendy Kohlmann, Reed Dow, Sancy A Leachman. Genet Med 2010

Parents' attitudes toward pediatric genetic testing for common disease risk.
Kenneth P Tercyak, Sharon Hensley Alford, Karen M Emmons, Isaac M Lipkus, Benjamin S Wilfond, Colleen M McBride. Pediatrics 2011

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.
D Ford, D F Easton, M Stratton, S Narod, D Goldgar, P Devilee, D T Bishop, B Weber, G Lenoir, J Chang-Claude,[...]. Am J Hum Genet 1998

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.
A Antoniou, P D P Pharoah, S Narod, H A Risch, J E Eyfjord, J L Hopper, N Loman, H Olsson, O Johannsson, A Borg,[...]. Am J Hum Genet 2003

Parental communication of BRCA1/2 genetic test results to children.
K P Tercyak, C Hughes, D Main, C Snyder, J F Lynch, H T Lynch, C Lerman. Patient Educ Couns 2001

How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults.
Angela R Bradbury, James J Dignam, Comfort N Ibe, Sogyong L Auh, Fay J Hlubocky, Shelly A Cummings, Melody White, Olufunmilayo I Olopade, Christopher K Daugherty. J Clin Oncol 2007

Psychological issues among children of hereditary breast cancer gene (BRCA1/2) testing participants.
K P Tercyak, B N Peshkin, R Streisand, C Lerman. Psychooncology 2001

Predictive genetic testing in minors for adult-onset genetic diseases.
Pascal Borry, Tom Goffin, Herman Nys, Kris Dierickx. Mt Sinai J Med 2008

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
Flavia M Facio, Haley Eidem, Tyler Fisher, Stephanie Brooks, Amy Linn, Kimberly A Kaphingst, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2013

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

When parents disclose BRCA1/2 test results: their communication and perceptions of offspring response.
Angela R Bradbury, Linda Patrick-Miller, Brian L Egleston, Olufunmilayo I Olopade, Mary B Daly, Cynthia W Moore, Colleen B Sands, Helen Schmidheiser, Preethi K Kondamudi, Maia Feigon,[...]. Cancer 2012

Consumers' use of web-based information and their decisions about multiplex genetic susceptibility testing.
Kimberly A Kaphingst, Colleen M McBride, Christopher Wade, Sharon Hensley Alford, Lawrence C Brody, Andreas D Baxevanis. J Med Internet Res 2010

From genetics to genomics: ethics, policy, and parental decision-making.
Benjamin Wilfond, Lainie Friedman Ross. J Pediatr Psychol 2009

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011

Brief assessment of parents' attitudes toward testing minor children for hereditary breast/ovarian cancer genes: development and validation of the Pediatric BRCA1/2 Testing Attitudes Scale (P-TAS).
Beth N Peshkin, Tiffani A DeMarco, Judy E Garber, Heiddis B Valdimarsdottir, Andrea F Patenaude, Katherine A Schneider, Marc D Schwartz, Kenneth P Tercyak. J Pediatr Psychol 2009

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.
Mary-Claire King, Joan H Marks, Jessica B Mandell. Science 2003

Parent-child factors and their effect on communicating BRCA1/2 test results to children.
Kenneth P Tercyak, Beth N Peshkin, Tiffani A DeMarco, Barbara M Brogan, Caryn Lerman. Patient Educ Couns 2002

Meta-analysis of BRCA1 and BRCA2 penetrance.
Sining Chen, Giovanni Parmigiani. J Clin Oncol 2007

Controversies in communication of genetic risk for hereditary breast cancer.
Amy Mackenzie, Linda Patrick-Miller, Angela R Bradbury. Breast J 2009

Advances in breast cancer: pathways to personalized medicine.
Olufunmilayo I Olopade, Tatyana A Grushko, Rita Nanda, Dezheng Huo. Clin Cancer Res 2008

Learning of your parent's BRCA mutation during adolescence or early adulthood: a study of offspring experiences.
Angela R Bradbury, Linda Patrick-Miller, Kimberly Pawlowski, Comfort N Ibe, Shelly A Cummings, Fay Hlubocky, Olufunmilayo I Olopade, Christopher K Daugherty. Psychooncology 2009

Personalized medicine in the era of genomics.
Wylie Burke, Bruce M Psaty. JAMA 2007

Why test children for adult-onset genetic diseases?
Rosamond Rhodes. Mt Sinai J Med 2006

Whole-genome sequencing for optimized patient management.
Matthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, Jennifer Friedman, Claudia Gonzaga-Jauregui, Irene Newsham, Jeffrey G Reid, John K Fink, Margaret B Morgan, Marie-Claude Gingras,[...]. Sci Transl Med 2011

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.
Susanne B Haga, Madeline M Carrig, Julianne M O'Daniel, Lori A Orlando, Ley A Killeya-Jones, Geoffrey S Ginsburg, Alex Cho. J Gen Intern Med 2011

Exome sequencing identifies the cause of a mendelian disorder.
Sarah B Ng, Kati J Buckingham, Choli Lee, Abigail W Bigham, Holly K Tabor, Karin M Dent, Chad D Huff, Paul T Shannon, Ethylin Wang Jabs, Deborah A Nickerson,[...]. Nat Genet 2010

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.
Holly K Tabor, Jacquie Stock, Tracy Brazg, Margaret J McMillin, Karin M Dent, Joon-Ho Yu, Jay Shendure, Michael J Bamshad. Am J Med Genet A 2012

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
Elizabeth A Worthey, Alan N Mayer, Grant D Syverson, Daniel Helbling, Benedetta B Bonacci, Brennan Decker, Jaime M Serpe, Trivikram Dasu, Michael R Tschannen, Regan L Veith,[...]. Genet Med 2011

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy.
James R Lupski, Jeffrey G Reid, Claudia Gonzaga-Jauregui, David Rio Deiros, David C Y Chen, Lynne Nazareth, Matthew Bainbridge, Huyen Dinh, Chyn Jing, David A Wheeler,[...]. N Engl J Med 2010

Personalized medicine: progress and promise.
Isaac S Chan, Geoffrey S Ginsburg. Annu Rev Genomics Hum Genet 2011

Attitudes towards predictive genetic testing in minors for familial breast cancer: a systematic review.
Pascal Borry, Louise StultiĆ«ns, Herman Nys, Kris Dierickx. Crit Rev Oncol Hematol 2007

Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013

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.