A citation-based method for searching scientific literature

Mackenzie Graham, Nina Hallowell, Berge Solberg, Ari Haukkala, Joanne Holliday, Angeliki Kerasidou, Thomas Littlejohns, Elizabeth Ormondroyd, John-Arne Skolbekken, Marleena Vornanen. J Med Ethics 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


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
122
100

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study.
Michael P Mackley, Edward Blair, Michael Parker, Jenny C Taylor, Hugh Watkins, Elizabeth Ormondroyd. Eur J Hum Genet 2018
14
100

Direct-to-consumer genetic testing.
Rachel Horton, Gillian Crawford, Lindsey Freeman, Angela Fenwick, Caroline F Wright, Anneke Lucassen. BMJ 2019
24
100

Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population.
Anna Fry, Thomas J Littlejohns, Cathie Sudlow, Nicola Doherty, Ligia Adamska, Tim Sprosen, Rory Collins, Naomi E Allen. Am J Epidemiol 2017
711
100

What is the clinical utility of genetic testing?
Scott D Grosse, Muin J Khoury. Genet Med 2006
176
100

Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study.
Lisa M Ballard, Rachel H Horton, Sandi Dheensa, Angela Fenwick, Anneke M Lucassen. Eur J Hum Genet 2020
5
100

Legislation of direct-to-consumer genetic testing in Europe: a fragmented regulatory landscape.
L Kalokairinou, H C Howard, S Slokenberga, E Fisher, M Flatscher-Thöni, M Hartlev, R van Hellemondt, J Juškevičius, J Kapelenska-Pregowska, P Kováč,[...]. J Community Genet 2018
32
100

Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists.
Julia El Mecky, Lennart Johansson, Mirjam Plantinga, Angela Fenwick, Anneke Lucassen, Trijnie Dijkhuizen, Annemieke van der Hout, Kate Lyle, Irene van Langen. BMC Med Genomics 2019
9
100

Measuring clinical utility in the context of genetic testing: a scoping review.
Shantel E Walcott, Fiona A Miller, Kourtney Dunsmore, Tanya Lazor, Brian M Feldman, Robin Z Hayeems. Eur J Hum Genet 2021
2
100

Identity inference of genomic data using long-range familial searches.
Yaniv Erlich, Tal Shor, Itsik Pe'er, Shai Carmi. Science 2018
92
100


Direct-to-consumer raw genetic data and third-party interpretation services: more burden than bargain?
Tia Moscarello, Brittney Murray, Chloe M Reuter, Erin Demo. Genet Med 2019
23
100

Internet-Based Direct-to-Consumer Genetic Testing: A Systematic Review.
Loredana Covolo, Sara Rubinelli, Elisabetta Ceretti, Umberto Gelatti. J Med Internet Res 2015
60
100

Population testing for cancer predisposing BRCA1/BRCA2 mutations in the Ashkenazi-Jewish community: a randomized controlled trial.
Ranjit Manchanda, Kelly Loggenberg, Saskia Sanderson, Matthew Burnell, Jane Wardle, Sue Gessler, Lucy Side, Nyala Balogun, Rakshit Desai, Ajith Kumar,[...]. J Natl Cancer Inst 2014
109
100

Should UK primary care be an early adopter of genomic medicine?
Donna Dickenson, Imran Rafi, John Spicer, Andrew Papanikitas. Br J Gen Pract 2019
1
100

Personal utility in genomic testing: is there such a thing?
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. J Med Ethics 2015
61
100

Direct-to-consumer genetic testing: where and how does genetic counseling fit?
Anna Middleton, Álvaro Mendes, Caroline M Benjamin, Heidi Carmen Howard. Per Med 2017
27
100


Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, Miranda L G Hallquist, Janet L Williams, Alanna Kulchak Rahm, Heather Rocha, Juliann M Savatt, Alyson E Evans, Loren M Butry,[...]. JAMA Netw Open 2018
79
100

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Cathie Sudlow, John Gallacher, Naomi Allen, Valerie Beral, Paul Burton, John Danesh, Paul Downey, Paul Elliott, Jane Green, Martin Landray,[...]. PLoS Med 2015
100


Weaving the Strands of Life (Iiná Bitł'ool): History of Genetic Research Involving Navajo People.
Rene L Begay, Nanibaa' A Garrison, Franklin Sage, Mark Bauer, Ursula Knoki-Wilson, David H Begay, Beverly Becenti-Pigman, Katrina G Claw. Hum Biol 2020
3
100

False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
Stephany Tandy-Connor, Jenna Guiltinan, Kate Krempely, Holly LaDuca, Patrick Reineke, Stephanie Gutierrez, Phillip Gray, Brigette Tippin Davis. Genet Med 2018
114
100

Whole-genome sequencing of patients with rare diseases in a national health system.
Ernest Turro, William J Astle, Karyn Megy, Stefan Gräf, Daniel Greene, Olga Shamardina, Hana Lango Allen, Alba Sanchis-Juan, Mattia Frontini, Chantal Thys,[...]. Nature 2020
91
100

Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results: a systematic review and meta-analysis.
Kelly F J Stewart, Anke Wesselius, Maartje A C Schreurs, Annemie M W J Schols, Maurice P Zeegers. J Community Genet 2018
34
100


Identifying Ashkenazi Jewish BRCA1/2 founder variants in individuals who do not self-report Jewish ancestry.
Ruth I Tennen, Sarah B Laskey, Bertram L Koelsch, Matthew H McIntyre, Joyce Y Tung. Sci Rep 2020
5
100

Overvaluing individual consent ignores risks to tribal participants.
Krystal S Tsosie, Joseph M Yracheta, Donna Dickenson. Nat Rev Genet 2019
23
100

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
34
100

From Expectations to Experiences: Consumer Autonomy and Choice in Personal Genomic Testing.
Jacqueline Savard, Chriselle Hickerton, Sylvia A Metcalfe, Clara Gaff, Anna Middleton, Ainsley J Newson. AJOB Empir Bioeth 2020
4
100

Regulating direct-to-consumer genetic tests: what is all the fuss about?
Caroline F Wright, Alison Hall, Ron L Zimmern. Genet Med 2011
22
100

Impact of detecting potentially serious incidental findings during multi-modal imaging.
Lorna M Gibson, Thomas J Littlejohns, Ligia Adamska, Steve Garratt, Nicola Doherty, Joanna M Wardlaw, Giles Maskell, Michael Parker, Roger Brownsword, Paul M Matthews,[...]. Wellcome Open Res 2017
16
100

Health system implications of direct-to-consumer personal genome testing.
Amy L McGuire, Wylie Burke. Public Health Genomics 2011
28
100

Perspectives on Achieving Institutional Trust in Personalized Medicine.
Gabrielle Samuel, Sandi Dheensa. Am J Bioeth 2018
2
100

Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study.
Saskia C Sanderson, Celine Lewis, Christine Patch, Melissa Hill, Maria Bitner-Glindzicz, Lyn S Chitty. Genet Med 2019
8
100

Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation.
Weedon Mn, Jackson L, Harrison Jw, Ruth Ks, Tyrrell J, Hattersley At, Wright Cf. BMJ 2021
6
100

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
422
100

Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting.
Caroline F Wright, Ben West, Marcus Tuke, Samuel E Jones, Kashyap Patel, Thomas W Laver, Robin N Beaumont, Jessica Tyrrell, Andrew R Wood, Timothy M Frayling,[...]. Am J Hum Genet 2019
64
100

Effect of co-payment on behavioral response to consumer genomic testing.
Wendy Liu, Jessica J Outlaw, Nathan Wineinger, Debra Boeldt, Cinnamon S Bloss. Transl Behav Med 2018
3
100

Third-Party Genetic Interpretation Tools: A Mixed-Methods Study of Consumer Motivation and Behavior.
Sarah C Nelson, Deborah J Bowen, Stephanie M Fullerton. Am J Hum Genet 2019
15
100

Toward better governance of human genomic data.
Kieran C O'Doherty, Mahsa Shabani, Edward S Dove, Heidi Beate Bentzen, Pascal Borry, Michael M Burgess, Don Chalmers, Jantina De Vries, Lisa Eckstein, Stephanie M Fullerton,[...]. Nat Genet 2021
4
100

The UK's 100,000 Genomes Project: manifesting policymakers' expectations.
Gabrielle Natalie Samuel, Bobbie Farsides. New Genet Soc 2017
19
100

Impact of direct-to-consumer genetic testing on Australian clinical genetics services.
Michael Millward, Jane Tiller, Michael Bogwitz, Helen Kincaid, Shelby Taylor, Alison H Trainer, Paul Lacaze. Eur J Med Genet 2020
5
100

Who's on third? Regulation of third-party genetic interpretation services.
Christi J Guerrini, Jennifer K Wagner, Sarah C Nelson, Gail H Javitt, Amy L McGuire. Genet Med 2020
15
100

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
100


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.