A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Genomic medicine--an updated primer.
W Gregory Feero, Alan E Guttmacher, Francis S Collins. N Engl J Med 2010
280
1

Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan.
Mio Tsuchiya, Takahiro Yamada, Rina Akaishi, Haruka Hamanoue, Akira Hirasawa, Maki Hyodo, Issei Imoto, Tomoki Kosho, Kenji Kurosawa, Hiromi Murakami,[...]. J Hum Genet 2020
1
100

Disclosure of genetic research results to members of a founder population.
Rebecca L Anderson, Kathleen Murray, Jessica X Chong, Rebecca Ouwenga, Marina Antillon, Peixian Chen, Lorena Diaz de Leon, Kathryn J Swoboda, Lucille A Lester, Soma Das,[...]. J Genet Couns 2014
4
25

jMorp updates in 2020: large enhancement of multi-omics data resources on the general Japanese population.
Shu Tadaka, Eiji Hishinuma, Shohei Komaki, Ikuko N Motoike, Junko Kawashima, Daisuke Saigusa, Jin Inoue, Jun Takayama, Yasunobu Okamura, Yuichi Aoki,[...]. Nucleic Acids Res 2021
5
20

A training and education program for genome medical research coordinators in the genome cohort study of the Tohoku Medical Megabank Organization.
Mika Sakurai-Yageta, Hiroshi Kawame, Shinichi Kuriyama, Atsushi Hozawa, Naoki Nakaya, Fuji Nagami, Naoko Minegishi, Soichi Ogishima, Takako Takai-Igarashi, Inaho Danjoh,[...]. BMC Med Educ 2019
3
33

Security controls in an integrated Biobank to protect privacy in data sharing: rationale and study design.
Takako Takai-Igarashi, Kengo Kinoshita, Masao Nagasaki, Soichi Ogishima, Naoki Nakamura, Sachiko Nagase, Satoshi Nagaie, Tomo Saito, Fuji Nagami, Naoko Minegishi,[...]. BMC Med Inform Decis Mak 2017
16
6

Cohort Profile: Tohoku Medical Megabank Project Birth and Three-Generation Cohort Study (TMM BirThree Cohort Study): rationale, progress and perspective.
Shinichi Kuriyama, Hirohito Metoki, Masahiro Kikuya, Taku Obara, Mami Ishikuro, Chizuru Yamanaka, Masato Nagai, Hiroko Matsubara, Tomoko Kobayashi, Junichi Sugawara,[...]. Int J Epidemiol 2020
32
3

A comparison of genome cohort participants' genetic knowledge and preferences to receive genetic results before and after a genetics workshop.
Kayono Yamamoto, Atsushi Shimizu, Fumie Aizawa, Hiroshi Kawame, Tomoharu Tokutomi, Akimune Fukushima. J Hum Genet 2018
7
14

Identification and molecular characterisation of Lausanne Institutional Biobank participants with familial hypercholesterolaemia - a proof-of-concept study.
Fabienne Maurer, Sylvain Pradervand, Isabelle Guilleret, David Nanchen, Ali Maghraoui, Laurence Chapatte, Karolina Bojkowska, Zahurul Alam Bhuiyan, Nathalie Jacquemont, Keith Harshman,[...]. Swiss Med Wkly 2016
4
25

Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals.
Masao Nagasaki, Jun Yasuda, Fumiki Katsuoka, Naoki Nariai, Kaname Kojima, Yosuke Kawai, Yumi Yamaguchi-Kabata, Junji Yokozawa, Inaho Danjoh, Sakae Saito,[...]. Nat Commun 2015
229
1

Establishment of Integrated Biobank for Precision Medicine and Personalized Healthcare: The Tohoku Medical Megabank Project.
Nobuo Fuse, Mika Sakurai-Yageta, Fumiki Katsuoka, Inaho Danjoh, Ritsuko Shimizu, Gen Tamiya, Fuji Nagami, Hiroshi Kawame, Shinichi Higuchi, Kengo Kinoshita,[...]. JMA J 2019
7
14

Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.
Emilie S Zoltick, Michael D Linderman, Molly A McGinniss, Erica Ramos, Madeleine P Ball, George M Church, Debra G B Leonard, Stacey Pereira, Amy L McGuire, C Thomas Caskey,[...]. Genome Med 2019
17
5


Omics research project on prospective cohort studies from the Tohoku Medical Megabank Project.
Seizo Koshiba, Ikuko Motoike, Daisuke Saigusa, Jin Inoue, Matsuyuki Shirota, Yasutake Katoh, Fumiki Katsuoka, Inaho Danjoh, Atsushi Hozawa, Shinichi Kuriyama,[...]. Genes Cells 2018
21
4

jMorp: Japanese Multi Omics Reference Panel.
Shu Tadaka, Daisuke Saigusa, Ikuko N Motoike, Jin Inoue, Yuichi Aoki, Matsuyuki Shirota, Seizo Koshiba, Masayuki Yamamoto, Kengo Kinoshita. Nucleic Acids Res 2018
51
1

Clinical application of exome sequencing in undiagnosed genetic conditions.
Anna C Need, Vandana Shashi, Yuki Hitomi, Kelly Schoch, Kevin V Shianna, Marie T McDonald, Miriam H Meisler, David B Goldstein. J Med Genet 2012
273
1

Guidelines for Diagnosis and Treatment of Familial Hypercholesterolemia 2017.
Mariko Harada-Shiba, Hidenori Arai, Yasushi Ishigaki, Shun Ishibashi, Tomonori Okamura, Masatsune Ogura, Kazushige Dobashi, Atsushi Nohara, Hideaki Bujo, Katsumi Miyauchi,[...]. J Atheroscler Thromb 2018
71
1

The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting.
Peter D Stenson, Matthew Mort, Edward V Ball, Molly Chapman, Katy Evans, Luisa Azevedo, Matthew Hayden, Sally Heywood, David S Millar, Andrew D Phillips,[...]. Hum Genet 2020
40
2

Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare.
Jun Yasuda, Kengo Kinoshita, Fumiki Katsuoka, Inaho Danjoh, Mika Sakurai-Yageta, Ikuko N Motoike, Yoko Kuroki, Sakae Saito, Kaname Kojima, Matsuyuki Shirota,[...]. J Biochem 2019
23
4

ClinVar: public archive of interpretations of clinically relevant variants.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Jeffrey Hoover,[...]. Nucleic Acids Res 2016
1

Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients.
Yasue Horiuchi, Hiroyuki Matsubayashi, Yoshimi Kiyozumi, Seiichiro Nishimura, Satomi Higashigawa, Nobuhiro Kado, Takeshi Nagashima, Maki Mizuguchi, Sumiko Ohnami, Makoto Arai,[...]. Hum Genet 2021
1
100

Returning incidental findings in African genomics research.
Ambroise Wonkam, Jantina de Vries. Nat Genet 2020
11
9

Assessing the Costs and Cost-Effectiveness of Genomic Sequencing.
Kurt D Christensen, Dmitry Dukhovny, Uwe Siebert, Robert C Green. J Pers Med 2015
58
1

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.
C Alexander Valencia, Ammar Husami, Jennifer Holle, Judith A Johnson, Yaping Qian, Abhinav Mathur, Chao Wei, Subba Rao Indugula, Fanggeng Zou, Haiying Meng,[...]. Front Pediatr 2015
105
1

Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate.
Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
10
10

Progress on impoverishing health spending in 122 countries: a retrospective observational study.
Adam Wagstaff, Gabriela Flores, Marc-François Smitz, Justine Hsu, Kateryna Chepynoga, Patrick Eozenou. Lancet Glob Health 2018
64
1

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.
Dean A Regier, Stuart J Peacock, Reka Pataky, Kimberly van der Hoek, Gail P Jarvik, Jeffrey Hoch, David Veenstra. CMAJ 2015
49
2

Assessing risk of bias in prevalence studies: modification of an existing tool and evidence of interrater agreement.
Damian Hoy, Peter Brooks, Anthony Woolf, Fiona Blyth, Lyn March, Chris Bain, Peter Baker, Emma Smith, Rachelle Buchbinder. J Clin Epidemiol 2012
833
1

What are people willing to pay for whole-genome sequencing information, and who decides what they receive?
Deborah A Marshall, Juan Marcos Gonzalez, F Reed Johnson, Karen V MacDonald, Amy Pugh, Michael P Douglas, Kathryn A Phillips. Genet Med 2016
20
5

Precision Medicine in Internal Medicine.
Krzysztof Kiryluk, David B Goldstein, John W Rowe, Ali G Gharavi, Ronald Wapner, Wendy K Chung. Ann Intern Med 2019
5
20

Economic evidence on identifying clinically actionable findings with whole-genome sequencing: a scoping review.
Michael P Douglas, Uri Ladabaum, Mark J Pletcher, Deborah A Marshall, Kathryn A Phillips. Genet Med 2016
16
6


Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial.
Kurt D Christensen, Jason L Vassy, Kathryn A Phillips, Carrie L Blout, Danielle R Azzariti, Christine Y Lu, Jill O Robinson, Kaitlyn Lee, Michael P Douglas, Jennifer M Yeh,[...]. Genet Med 2018
17
5

Assessing the quality of published genetic association studies in meta-analyses: the quality of genetic studies (Q-Genie) tool.
Zahra N Sohani, David Meyre, Russell J de Souza, Philip G Joseph, Mandark Gandhi, Brittany B Dennis, Geoff Norman, Sonia S Anand. BMC Genet 2015
47
2

How to prepare a systematic review of economic evaluations for informing evidence-based healthcare decisions: data extraction, risk of bias, and transferability (part 3/3).
Bfm Wijnen, Gapg Van Mastrigt, W K Redekop, Hjm Majoie, Rja De Kinderen, Smaa Evers. Expert Rev Pharmacoecon Outcomes Res 2016
53
1

Patients' views on incidental findings from clinical exome sequencing.
Kristin E Clift, Colin M E Halverson, Alexander S Fiksdal, Ashok Kumbamu, Richard R Sharp, Jennifer B McCormick. Appl Transl Genom 2015
57
1

Dissecting in silico Mutation Prediction of Variants in African Genomes: Challenges and Perspectives.
Christian Domilongo Bope, Emile R Chimusa, Victoria Nembaware, Gaston K Mazandu, Jantina de Vries, Ambroise Wonkam. Front Genet 2019
7
14

When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing.
Leila Jamal, Jill O Robinson, Kurt D Christensen, Jennifer Blumenthal-Barby, Melody J Slashinski, Denise Lautenbach Perry, Jason L Vassy, Julia Wycliff, Robert C Green, Amy L McGuire. AJOB Empir Bioeth 2017
24
4



Racial and Ethnic Disparities in the Quality of Health Care.
Kevin Fiscella, Mechelle R Sanders. Annu Rev Public Health 2016
131
1

Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project.
Sabrina A Suckiel, Michael D Linderman, Saskia C Sanderson, George A Diaz, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt, Randi E Zinberg. J Genet Couns 2016
11
9

Moral concerns and the willingness to donate to a research biobank.
Tom Tomlinson, Raymond De Vries, Kerry Ryan, Hyungjin Myra Kim, Nicole Lehpamer, Scott Y H Kim. JAMA 2015
36
2


Omics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism Investigations.
Abdellah Tebani, Carlos Afonso, Stéphane Marret, Soumeya Bekri. Int J Mol Sci 2016
67
1

Return of individual genetic results in a high-risk sample: enthusiasm and positive behavioral change.
Sarah M Hartz, Emily Olfson, Robert Culverhouse, Patricia Cavazos-Rehg, Li-Shiun Chen, James DuBois, Sherri Fisher, Kimberly Kaphingst, David Kaufman, Andrew Plunk,[...]. Genet Med 2015
19
5

How, who, and when: preferences for delivery of genome sequencing results among women diagnosed with breast cancer at a young age.
Kimberly A Kaphingst, Jennifer Ivanovich, Ashley Elrick, Rebecca Dresser, Cindy Matsen, Melody S Goodman. Mol Genet Genomic Med 2016
5
20

Alzheimer's disease in the omics era.
Giulia M Sancesario, Sergio Bernardini. Clin Biochem 2018
31
3

Racial differences in trust in health care providers.
Chanita Hughes Halbert, Katrina Armstrong, Oscar H Gandy, Lee Shaker. Arch Intern Med 2006
235
1

Distrust of the health care system and self-reported health in the United States.
Katrina Armstrong, Abigail Rose, Nikki Peters, Judith A Long, Suzanne McMurphy, Judy A Shea. J Gen Intern Med 2006
106
1


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.