A citation-based method for searching scientific literature

Katrina A B Goddard, K Sabina Smith, Chuhe Chen, Carmit McMullen, Cheryl Johnson. Biopreserv Biobank 2009
Times Cited: 29







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



Times Cited
  Times     Co-cited
Similarity



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
184
37

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
177
31

Potential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?
J L Ridgeway, L C Han, J E Olson, K A Lackore, B A Koenig, T J Beebe, J Y Ziegenfuss. Public Health Genomics 2013
32
31

Factors influencing public participation in biobanking.
Mamoun Ahram, Areej Othman, Manal Shahrouri, Ebtihal Mustafa. Eur J Hum Genet 2014
43
31

Willingness to donate blood samples for genetic research: a survey from a community in Singapore.
M L Wong, K S Chia, W M Yam, G R Teodoro, K W Lau. Clin Genet 2004
57
27

Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
109
27

Biobanking for research: a survey of patient population attitudes and understanding.
Alanna Kulchak Rahm, Michelle Wrenn, Nikki M Carroll, Heather Spencer Feigelson. J Community Genet 2013
60
27

Public attitudes regarding the donation and storage of blood specimens for genetic research.
S S Wang, F Fridinger, K M Sheedy, M J Khoury. Community Genet 2001
99
24

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
57
24

Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study.
Philippe A Melas, Louise K Sjöholm, Tord Forsner, Maigun Edhborg, Niklas Juth, Yvonne Forsell, Catharina Lavebratt. J Med Ethics 2010
48
20

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
138
20

Assessing the understanding of biobank participants.
K E Ormond, A L Cirino, I B Helenowski, R L Chisholm, W A Wolf. Am J Med Genet A 2009
108
20

Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns.
Aaro Tupasela, Sinikka Sihvo, Karolna Snell, Pa Jallinoja, Arja R Aro, Elina Hemminki. Scand J Public Health 2010
50
20

Hypothetical and factual willingness to participate in biobank research.
Linus Johnsson, Gert Helgesson, Thorunn Rafnar, Ingibjorg Halldorsdottir, Kee-Seng Chia, Stefan Eriksson, Mats G Hansson. Eur J Hum Genet 2010
60
20

Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.
Klaus Hoeyer, Bert-Ove Olofsson, Tom Mjörndal, Niels Lynöe. Scand J Public Health 2004
141
17

DNA data sharing: research participants' perspectives.
Amy L McGuire, Jennifer A Hamilton, Rebecca Lunstroth, Laurence B McCullough, Alica Goldman. Genet Med 2008
78
17

Veterans' attitudes regarding a database for genomic research.
David Kaufman, Juli Murphy, Lori Erby, Kathy Hudson, Joan Scott. Genet Med 2009
38
17

Public's attitudes on participation in a biobank for research: an Italian survey.
Corinna Porteri, Patrizio Pasqualetti, Elena Togni, Michael Parker. BMC Med Ethics 2014
35
17

Factors that influence characteristics of genetic biobanks.
Jennifer E Sanner, Lorraine Frazier. J Nurs Scholarsh 2007
33
13

Research on stored biological samples: views of African American and White American cancer patients.
Rebecca D Pentz, Laurent Billot, David Wendler. Am J Med Genet A 2006
66
13

Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study.
Samantha A Streicher, Saskia C Sanderson, Ethylin Wang Jabs, Michael Diefenbach, Meg Smirnoff, Inga Peter, Carol R Horowitz, Barbara Brenner, Lynne D Richardson. J Community Genet 2011
61
13

Consent for genetic research in a general population: the NHANES experience.
Geraldine M McQuillan, Kathryn S Porter, Maria Agelli, Raynard Kington. Genet Med 2003
125
13

Consent to the use of stored DNA for genetics research: a survey of attitudes in the Jewish population.
M D Schwartz, K Rothenberg, L Joseph, J Benkendorf, C Lerman. Am J Med Genet 2001
48
13

Subjects matter: a survey of public opinions about a large genetic cohort study.
David Kaufman, Juli Murphy, Joan Scott, Kathy Hudson. Genet Med 2008
163
13

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
210
13

Attitudes and perceptions of patients towards methods of establishing a DNA biobank.
Jill M Pulley, Margaret M Brace, Gordon R Bernard, Dan R Masys. Cell Tissue Bank 2008
76
13

Reconsidering the value of consent in biobank research.
Judy Allen, Beverley McNamara. Bioethics 2011
47
13

Cancer patient perceptions about biobanking and preferred timing of consent.
Kathryn L Braun, Joann U Tsark, Amy Powers, Kristen Croom, Robert Kim, Francine C Gachupin, Paul Morris. Biopreserv Biobank 2014
21
19

Informed consent for biorepositories: assessing prospective participants' understanding and opinions.
Laura M Beskow, Elizabeth Dean. Cancer Epidemiol Biomarkers Prev 2008
87
13

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
55
13


Predicting intention to biobank: a national survey.
Christine R Critchley, Dianne Nicol, Margaret F A Otlowski, Mark J A Stranger. Eur J Public Health 2012
46
13

Public perception towards biobanking in jordan.
Mamoun Ahram, Areej Othman, Manal Shahrouri. Biopreserv Biobank 2012
21
19

Understanding the Public's Reservations about Broad Consent and Study-By-Study Consent for Donations to a Biobank: Results of a National Survey.
Raymond Gene De Vries, Tom Tomlinson, Hyungjin Myra Kim, Chris Krenz, Diana Haggerty, Kerry A Ryan, Scott Y H Kim. PLoS One 2016
23
17

Assessment of knowledge about biobanking among healthcare students and their willingness to donate biospecimens.
Leena Merdad, Lama Aldakhil, Rawan Gadi, Mourad Assidi, Salina Y Saddick, Adel Abuzenadah, Jim Vaught, Abdelbaset Buhmeida, Mohammed H Al-Qahtani. BMC Med Ethics 2017
19
21

Community Perceptions of Biobanking Participation: A Qualitative Study among Mexican-Americans in Three Texas Cities.
Natalia I Heredia, Sarah Krasny, Larkin L Strong, Laura Von Hatten, Lynne Nguyen, Belinda M Reininger, Lorna H McNeill, María E Fernández. Public Health Genomics 2017
28
14

The role of race and trust in tissue/blood donation for genetic research.
Jada Bussey-Jones, Joanne Garrett, Gail Henderson, Mairead Moloney, Connie Blumenthal, Giselle Corbie-Smith. Genet Med 2010
79
10

An investigation of patients' motivations for their participation in genetics-related research.
N Hallowell, S Cooke, G Crawford, A Lucassen, M Parker, C Snowdon. J Med Ethics 2010
72
10

Patients attending tertiary referral urology clinics: willingness to participate in tissue banking.
Patricia E Fitzpatrick, Kenneth D McKenzie, Avril Beasley, John D Sheehan. BJU Int 2009
10
30

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
464
10


Parental Perspectives on a Pediatric Human Non-Subjects Biobank.
Kyle B Brothers, Ellen Wright Clayton. AJOB Prim Res 2012
20
15

Two large-scale surveys on community attitudes toward an opt-out biobank.
Kyle B Brothers, Daniel R Morrison, Ellen W Clayton. Am J Med Genet A 2011
53
10

Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
10


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
130
10

Glad you asked: participants' opinions of re-consent for dbGap data submission.
Evette J Ludman, Stephanie M Fullerton, Leslie Spangler, Susan Brown Trinidad, Monica M Fujii, Gail P Jarvik, Eric B Larson, Wylie Burke. J Empir Res Hum Res Ethics 2010
86
10

The privacy-reciprocity connection in biobanking: comparing German with UK strategies.
A Hobbs, J Starkbaum, U Gottweis, H E Wichmann, H Gottweis. Public Health Genomics 2012
28
10



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.