A citation-based method for searching scientific literature

Leila Jamal, Julie C Sapp, Katie Lewis, Tatiane Yanes, Flavia M Facio, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2014
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


Genomic research and wide data sharing: views of prospective participants.
Susan Brown Trinidad, Stephanie M Fullerton, Julie M Bares, Gail P Jarvik, Eric B Larson, Wylie Burke. Genet Med 2010
132
35

Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.
J M Oliver, M J Slashinski, T Wang, P A Kelly, S G Hilsenbeck, A L McGuire. Public Health Genomics 2012
70
35

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.
Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V Pearson, Dietrich A Stephan, Stanley F Nelson, David W Craig. PLoS Genet 2008
448
25

A systematic literature review of individuals' perspectives on broad consent and data sharing in the United States.
Nanibaa' A Garrison, Nila A Sathe, Armand H Matheny Antommaria, Ingrid A Holm, Saskia C Sanderson, Maureen E Smith, Melissa L McPheeters, Ellen W Clayton. Genet Med 2016
81
25

To share or not to share: a randomized trial of consent for data sharing in genome research.
Amy L McGuire, Jill M Oliver, Melody J Slashinski, Jennifer L Graves, Tao Wang, P Adam Kelly, William Fisher, Ching C Lau, John Goss, Mehmet Okcu,[...]. Genet Med 2011
65
25

Public and biobank participant attitudes toward genetic research participation and data sharing.
A A Lemke, W A Wolf, J Hebert-Beirne, M E Smith. Public Health Genomics 2010
165
25

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Saskia C Sanderson, Kyle B Brothers, Nathaniel D Mercaldo, Ellen Wright Clayton, Armand H Matheny Antommaria, Sharon A Aufox, Murray H Brilliant, Diego Campos, David S Carrell, John Connolly,[...]. Am J Hum Genet 2017
87
21

Public perspectives regarding data-sharing practices in genomics research.
S B Haga, J O'Daniel. Public Health Genomics 2011
29
17

Public opinion about the importance of privacy in biobank research.
David J Kaufman, Juli Murphy-Bollinger, Joan Scott, Kathy L Hudson. Am J Hum Genet 2009
169
17

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
469
17

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
17

Public preferences regarding informed consent models for participation in population-based genomic research.
Jodyn Platt, Juli Bollinger, Rachel Dvoskin, Sharon L R Kardia, David Kaufman. Genet Med 2014
53
17

De-identified genomic data sharing: the research participant perspective.
Deborah Goodman, Catherine O Johnson, Deborah Bowen, Megan Smith, Lari Wenzel, Karen Edwards. J Community Genet 2017
22
22


GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N Engl J Med 2015
98
14

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
216
14

Ethical, legal, and social implications of incorporating genomic information into electronic health records.
Ribhi Hazin, Kyle B Brothers, Bradley A Malin, Barbara A Koenig, Saskia C Sanderson, Mark A Rothstein, Marc S Williams, Ellen W Clayton, Iftikhar J Kullo. Genet Med 2013
60
10

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
201
10

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
47
10

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
10

Routes for breaching and protecting genetic privacy.
Yaniv Erlich, Arvind Narayanan. Nat Rev Genet 2014
138
10

Demographic differences in willingness to provide broad and narrow consent for biobank research.
Altovise T Ewing, Lori A H Erby, Juli Bollinger, Eva Tetteyfio, Luisel J Ricks-Santi, David Kaufman. Biopreserv Biobank 2015
25
12

Broad Consent for Research With Biological Samples: Workshop Conclusions.
Christine Grady, Lisa Eckstein, Ben Berkman, Dan Brock, Robert Cook-Deegan, Stephanie M Fullerton, Hank Greely, Mats G Hansson, Sara Hull, Scott Kim,[...]. Am J Bioeth 2015
138
10

A vision for the future of genomics research.
Francis S Collins, Eric D Green, Alan E Guttmacher, Mark S Guyer. Nature 2003
997
10

Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
51
10

A Survey of U.S Adults' Opinions about Conduct of a Nationwide Precision Medicine Initiative® Cohort Study of Genes and Environment.
David J Kaufman, Rebecca Baker, Lauren C Milner, Stephanie Devaney, Kathy L Hudson. PLoS One 2016
51
10


Identity inference of genomic data using long-range familial searches.
Yaniv Erlich, Tal Shor, Itsik Pe'er, Shai Carmi. Science 2018
84
10

'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research.
Pauline McCormack, Anna Kole, Sabina Gainotti, Deborah Mascalzoni, Caron Molster, Hanns Lochmüller, Simon Woods. Eur J Hum Genet 2016
35
10

IRB chairs' perspectives on genotype-driven research recruitment.
Laura M Beskow, Emily E Namey, Patrick R Miller, Daniel K Nelson, Alexandra Cooper. IRB 2012
10
20

Integrating genomics into clinical oncology: ethical and social challenges from proponents of personalized medicine.
Michelle L McGowan, Richard A Settersten, Eric T Juengst, Jennifer R Fishman. Urol Oncol 2014
25
8

Ethical, legal, and counseling challenges surrounding the return of genetic results in oncology.
Martijn P Lolkema, Christa G Gadellaa-van Hooijdonk, Annelien L Bredenoord, Peter Kapitein, Nancy Roach, Edwin Cuppen, Nine V Knoers, Emile E Voest. J Clin Oncol 2013
62
7

Framing genomics, public health research and policy: points to consider.
Bartha Maria Knoppers, T Leroux, H Doucet, B Godard, C Laberge, M Stanton-Jean, S Fortin, J Cousineau, C Monardes, N Girard,[...]. Public Health Genomics 2010
23
8

Community engagement with genetics: public perceptions and expectations about genetics research.
Holly Etchegary, Jane Green, Patrick Parfrey, Catherine Street, Daryl Pullman. Health Expect 2015
15
13

Community perceptions of genomic research: implications for addressing health disparities.
Malika Roman Isler, Karey Sutton, R Jean Cadigan, Giselle Corbie-Smith. N C Med J 2013
11
18

Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health.
Daniel B Thiel, Tevah Platt, Jodyn Platt, Susan B King, Sharon L R Kardia. J Community Genet 2014
24
8

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
122
7

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
809
7

Motivators for participation in a whole-genome sequencing study: implications for translational genomics research.
Flavia M Facio, Stephanie Brooks, Johanna Loewenstein, Susannah Green, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2011
96
7

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Jason L Vassy, Denise M Lautenbach, Heather M McLaughlin, Sek Won Kong, Kurt D Christensen, Joel Krier, Isaac S Kohane, Lindsay Z Feuerman, Jennifer Blumenthal-Barby, J Scott Roberts,[...]. Trials 2014
102
7

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants.
S E Gollust, E S Gordon, C Zayac, G Griffin, M F Christman, R E Pyeritz, L Wawak, B A Bernhardt. Public Health Genomics 2012
110
7

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
336
7

Informing family members about a hereditary predisposition to cancer: attitudes and practices among clinical geneticists.
Yrrah H Stol, Fred H Menko, Marjan J Westerman, Rien M J P A Janssens. J Med Ethics 2010
18
11

Attitudes of parents toward the return of targeted and incidental genomic research findings in children.
Conrad V Fernandez, Eric Bouffet, David Malkin, Nada Jabado, Colleen O'Connell, Denise Avard, Bartha M Knoppers, Meghan Ferguson, Kym M Boycott, Poul H Sorensen,[...]. Genet Med 2014
63
7

Researcher and institutional review board chair perspectives on incidental findings in genomic research.
Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Nancy Downing, Laura Shinkunas, Debra Brandt, Christian Simon. Genet Test Mol Biomarkers 2012
26
7

Research ethics and the challenge of whole-genome sequencing.
Amy L McGuire, Timothy Caulfield, Mildred K Cho. Nat Rev Genet 2008
141
7

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research.
Holly K Tabor, Benjamin E Berkman, Sara Chandros Hull, Michael J Bamshad. Am J Med Genet A 2011
93
7

Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.
Susan M Wolf, Rebecca Branum, Barbara A Koenig, Gloria M Petersen, Susan A Berry, Laura M Beskow, Mary B Daly, Conrad V Fernandez, Robert C Green, Bonnie S LeRoy,[...]. J Law Med Ethics 2015
57
7

Public access to genome-wide data: five views on balancing research with privacy and protection.
George Church, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington, Jane Kaye, Martin Bobrow, Bruce Weir. PLoS Genet 2009
57
7

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
213
7


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.