A citation-based method for searching scientific literature

Yasue Horiuchi, Hiroyuki Matsubayashi, Yoshimi Kiyozumi, Seiichiro Nishimura, Satomi Higashigawa, Nobuhiro Kado, Takeshi Nagashima, Maki Mizuguchi, Sumiko Ohnami, Makoto Arai, Kenichi Urakami, Masatoshi Kusuhara, Ken Yamaguchi. Hum Genet 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
947
75

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
25
50

The return of unexpected research results in a biobank study and referral to health care for heritable long QT syndrome.
A Haukkala, E Kujala, P Alha, V Salomaa, S Koskinen, H Swan, H Kääriäinen. Public Health Genomics 2013
24
50

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
50

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
69
50

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Wendy K Chung, Adam S Gordon, Gail E Herman, Teri E Klein, Douglas R Stewart, Laura M Amendola, Kathy Adelman, Sherri J Bale,[...]. Genet Med 2021
91
50

Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot.
Julie C Sapp, Jennifer J Johnston, Kate Driscoll, Alexis R Heidlebaugh, Ane Miren Sagardia, D Nadine Dogbe, Kendall L Umstead, Erin Turbitt, Ilias Alevizos, Jeffrey Baron,[...]. Am J Hum Genet 2018
23
50

Ethics of future disclosure of individual risk information in a genetic cohort study: a survey of donor preferences.
Kenji Matsui, Reidar K Lie, Yoshikuni Kita, Hirotsugu Ueshima. J Epidemiol 2008
22
25

Healthcare Utilization and Patients' Perspectives After Receiving a Positive Genetic Test for Familial Hypercholesterolemia.
Laney K Jones, Alanna Kulchak Rahm, Kandamurugu Manickam, Loren Butry, Amanda Lazzeri, Timothy Corcoran, Daniel Komar, Navya S Josyula, Sarah A Pendergrass, Amy C Sturm,[...]. Circ Genom Precis Med 2018
15
25

Medicine. Whole-genome sequencing: the new standard of care?
Liam R Brunham, Michael R Hayden. Science 2012
51
25


Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals.
Yumi Yamaguchi-Kabata, Jun Yasuda, Osamu Tanabe, Yoichi Suzuki, Hiroshi Kawame, Nobuo Fuse, Masao Nagasaki, Yosuke Kawai, Kaname Kojima, Fumiki Katsuoka,[...]. J Hum Genet 2018
22
25

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur J Hum Genet 2016
116
25

3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome.
Shu Tadaka, Fumiki Katsuoka, Masao Ueki, Kaname Kojima, Satoshi Makino, Sakae Saito, Akihito Otsuki, Chinatsu Gocho, Mika Sakurai-Yageta, Inaho Danjoh,[...]. Hum Genome Var 2019
58
25

Study Profile of the Tohoku Medical Megabank Community-Based Cohort Study.
Atsushi Hozawa, Kozo Tanno, Naoki Nakaya, Tomohiro Nakamura, Naho Tsuchiya, Takumi Hirata, Akira Narita, Mana Kogure, Kotaro Nochioka, Ryohei Sasaki,[...]. J Epidemiol 2021
31
25

The Tohoku Medical Megabank Project: Design and Mission.
Shinichi Kuriyama, Nobuo Yaegashi, Fuji Nagami, Tomohiko Arai, Yoshio Kawaguchi, Noriko Osumi, Masaki Sakaida, Yoichi Suzuki, Keiko Nakayama, Hiroaki Hashizume,[...]. J Epidemiol 2016
135
25

Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?
Isabelle Budin-Ljøsne, Deborah Mascalzoni, Sirpa Soini, Helena Machado, Jane Kaye, Heidi Beate Bentzen, Emmanuelle Rial-Sebbag, Flavio D'Abramo, Michał Witt, Geneviève Schamps,[...]. Biopreserv Biobank 2016
15
25

Biobank Establishment and Sample Management in the Tohoku Medical Megabank Project.
Naoko Minegishi, Ichiko Nishijima, Takahiro Nobukuni, Hisaaki Kudo, Noriko Ishida, Takahiro Terakawa, Kazuki Kumada, Riu Yamashita, Fumiki Katsuoka, Soichi Ogishima,[...]. Tohoku J Exp Med 2019
24
25

Genomic medicine--an updated primer.
W Gregory Feero, Alan E Guttmacher, Francis S Collins. N Engl J Med 2010
283
25

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

Population-based biobank participants' preferences for receiving genetic test results.
Kayono Yamamoto, Tsuyoshi Hachiya, Akimune Fukushima, Naoki Nakaya, Akira Okayama, Kozo Tanno, Fumie Aizawa, Tomoharu Tokutomi, Atsushi Hozawa, Atsushi Shimizu. J Hum Genet 2017
16
25

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
92
25

The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
David J Carey, Samantha N Fetterolf, F Daniel Davis, William A Faucett, H Lester Kirchner, Uyenlinh Mirshahi, Michael F Murray, Diane T Smelser, Glenn S Gerhard, David H Ledbetter. Genet Med 2016
184
25

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
5
25

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
356
25

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
6
25

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
306
25

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
20
25

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
46
25

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
8
25

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
258
25

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
11
25


Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Saskia C Sanderson, Michael D Linderman, Sabrina A Suckiel, George A Diaz, Randi E Zinberg, Kadija Ferryman, Melissa Wasserstein, Andrew Kasarskis, Eric E Schadt. Eur J Hum Genet 2016
60
25

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
26
25

The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.
Leslie G Biesecker, James C Mullikin, Flavia M Facio, Clesson Turner, Praveen F Cherukuri, Robert W Blakesley, Gerard G Bouffard, Peter S Chines, Pedro Cruz, Nancy F Hansen,[...]. Genome Res 2009
204
25


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
25
25

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
63
25

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
290
25

The legal risks of returning results of genomics research.
Ellen Wright Clayton, Amy L McGuire. Genet Med 2012
89
25

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
103
25

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
121
25

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
29
25

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
257
25

LOVD v.2.0: the next generation in gene variant databases.
Ivo F A C Fokkema, Peter E M Taschner, Gerard C P Schaafsma, J Celli, Jeroen F J Laros, Johan T den Dunnen. Hum Mutat 2011
620
25

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
25

Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing.
Dominik S Westphal, Gloria S Leszinski, Esther Rieger-Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner. Clin Genet 2019
17
25

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17
25


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.