A citation-based method for searching scientific literature

Rebecca E Graff, Taylor B Cavazos, Khanh K Thai, Linda Kachuri, Sara R Rashkin, Joshua D Hoffman, Stacey E Alexeeff, Maruta Blatchins, Travis J Meyers, Lancelote Leong, Caroline G Tai, Nima C Emami, Douglas A Corley, Lawrence H Kushi, Elad Ziv, Stephen K Van Den Eeden, Eric Jorgenson, Thomas J Hoffmann, Laurel A Habel, John S Witte, Lori C Sakoda. Nat Commun 2021
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction.
Linda Kachuri, Rebecca E Graff, Karl Smith-Byrne, Travis J Meyers, Sara R Rashkin, Elad Ziv, John S Witte, Mattias Johansson. Nat Commun 2020
28
40

Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks.
Lars G Fritsche, Snehal Patil, Lauren J Beesley, Peter VandeHaar, Maxwell Salvatore, Ying Ma, Robert B Peng, Daniel Taliun, Xiang Zhou, Bhramar Mukherjee. Am J Hum Genet 2020
24
40

The UK Biobank resource with deep phenotyping and genomic data.
Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band, Lloyd T Elliott, Kevin Sharp, Allan Motyer, Damjan Vukcevic, Olivier Delaneau, Jared O'Connell,[...]. Nature 2018
33

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
26

Tutorial: a guide to performing polygenic risk score analyses.
Shing Wan Choi, Timothy Shin-Heng Mak, Paul F O'Reilly. Nat Protoc 2020
257
26

Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Sara R Rashkin, Rebecca E Graff, Linda Kachuri, Khanh K Thai, Stacey E Alexeeff, Maruta A Blatchins, Taylor B Cavazos, Douglas A Corley, Nima C Emami, Joshua D Hoffman,[...]. Nat Commun 2020
48
20

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.
Nasim Mavaddat, Kyriaki Michailidou, Joe Dennis, Michael Lush, Laura Fachal, Andrew Lee, Jonathan P Tyrer, Ting-Huei Chen, Qin Wang, Manjeet K Bolla,[...]. Am J Hum Genet 2019
334
20

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers.
Yan Dora Zhang, Amber N Hurson, Haoyu Zhang, Parichoy Pal Choudhury, Douglas F Easton, Roger L Milne, Jacques Simard, Per Hall, Kyriaki Michailidou, Joe Dennis,[...]. Nat Commun 2020
36
20

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
20

Discovery of common and rare genetic risk variants for colorectal cancer.
Jeroen R Huyghe, Stephanie A Bien, Tabitha A Harrison, Hyun Min Kang, Sai Chen, Stephanie L Schmit, David V Conti, Conghui Qu, Jihyoun Jeon, Christopher K Edlund,[...]. Nat Genet 2019
195
20

Improving reporting standards for polygenic scores in risk prediction studies.
Hannah Wand, Samuel A Lambert, Cecelia Tamburro, Michael A Iacocca, Jack W O'Sullivan, Catherine Sillari, Iftikhar J Kullo, Robb Rowley, Jacqueline S Dron, Deanna Brockman,[...]. Nature 2021
80
20

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
660
20

Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.
Joshua N Sampson, William A Wheeler, Meredith Yeager, Orestis Panagiotou, Zhaoming Wang, Sonja I Berndt, Qing Lan, Christian C Abnet, Laufey T Amundadottir, Jonine D Figueroa,[...]. J Natl Cancer Inst 2015
106
20

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
20

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
538
20


Developing and evaluating polygenic risk prediction models for stratified disease prevention.
Nilanjan Chatterjee, Jianxin Shi, Montserrat García-Closas. Nat Rev Genet 2016
339
13

Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
J L Mega, N O Stitziel, J G Smith, D I Chasman, M Caulfield, J J Devlin, F Nordio, C Hyde, C P Cannon, F Sacks,[...]. Lancet 2015
363
13

The Post-GWAS Era: From Association to Function.
Michael D Gallagher, Alice S Chen-Plotkin. Am J Hum Genet 2018
301
13

Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Kazuyoshi Ishigaki, Masato Akiyama, Masahiro Kanai, Atsushi Takahashi, Eiryo Kawakami, Hiroki Sugishita, Saori Sakaue, Nana Matoba, Siew-Kee Low, Yukinori Okada,[...]. Nat Genet 2020
94
13

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
Freddie Bray, Jacques Ferlay, Isabelle Soerjomataram, Rebecca L Siegel, Lindsey A Torre, Ahmedin Jemal. CA Cancer J Clin 2018
13

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.
Christopher A Haiman, Gary K Chen, Celine M Vachon, Federico Canzian, Alison Dunning, Robert C Millikan, Xianshu Wang, Foluso Ademuyiwa, Shahana Ahmed, Christine B Ambrosone,[...]. Nat Genet 2011
238
13

GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
Tatsuo Masuda, Siew-Kee Low, Masato Akiyama, Makoto Hirata, Yutaka Ueda, Koichi Matsuda, Tadashi Kimura, Yoshinori Murakami, Michiaki Kubo, Yoichiro Kamatani,[...]. Eur J Hum Genet 2020
15
13

Is Type 2 Diabetes Causally Associated With Cancer Risk? Evidence From a Two-Sample Mendelian Randomization Study.
Shuai Yuan, Siddhartha Kar, Paul Carter, Mathew Vithayathil, Amy M Mason, Stephen Burgess, Susanna C Larsson. Diabetes 2020
35
13

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
13

Genome-wide association studies of cancer: current insights and future perspectives.
Amit Sud, Ben Kinnersley, Richard S Houlston. Nat Rev Cancer 2017
164
13

A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese.
Tatsuo Masuda, Kotaro Ogawa, Yoichiro Kamatani, Yoshinori Murakami, Tadashi Kimura, Yukinori Okada. Cancer Sci 2020
12
16

Identification of nine new susceptibility loci for endometrial cancer.
Tracy A O'Mara, Dylan M Glubb, Frederic Amant, Daniela Annibali, Katie Ashton, John Attia, Paul L Auer, Matthias W Beckmann, Amanda Black, Manjeet K Bolla,[...]. Nat Commun 2018
77
13

Most common 'sporadic' cancers have a significant germline genetic component.
Yi Lu, Weronica E Ek, David Whiteman, Thomas L Vaughan, Amanda B Spurdle, Douglas F Easton, Paul D Pharoah, Deborah J Thompson, Alison M Dunning, Nicholas K Hayward,[...]. Hum Mol Genet 2014
61
13

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.
Maria Teresa Landi, D Timothy Bishop, Stuart MacGregor, Mitchell J Machiela, Alexander J Stratigos, Paola Ghiorzo, Myriam Brossard, Donato Calista, Jiyeon Choi, Maria Concetta Fargnoli,[...]. Nat Genet 2020
48
13

Multiplex melanoma families are enriched for polygenic risk.
Matthew H Law, Lauren G Aoude, David L Duffy, Georgina V Long, Peter A Johansson, Antonia L Pritchard, Kiarash Khosrotehrani, Graham J Mann, Grant W Montgomery, Mark M Iles,[...]. Hum Mol Genet 2020
4
50

Genomic Risk Score for Melanoma in a Prospective Study of Older Individuals.
Andrew Bakshi, Mabel Yan, Moeen Riaz, Galina Polekhina, Suzanne G Orchard, Jane Tiller, Rory Wolfe, Amit Joshi, Yin Cao, Aideen M McInerney-Leo,[...]. J Natl Cancer Inst 2021
9
22

Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.
Hyuna Sung, Jacques Ferlay, Rebecca L Siegel, Mathieu Laversanne, Isabelle Soerjomataram, Ahmedin Jemal, Freddie Bray. CA Cancer J Clin 2021
13


The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.
Annalisa Buniello, Jacqueline A L MacArthur, Maria Cerezo, Laura W Harris, James Hayhurst, Cinzia Malangone, Aoife McMahon, Joannella Morales, Edward Mountjoy, Elliot Sollis,[...]. Nucleic Acids Res 2019
13

The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation.
Samuel A Lambert, Laurent Gil, Simon Jupp, Scott C Ritchie, Yu Xu, Annalisa Buniello, Aoife McMahon, Gad Abraham, Michael Chapman, Helen Parkinson,[...]. Nat Genet 2021
79
13

Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative.
Lars G Fritsche, Stephen B Gruber, Zhenke Wu, Ellen M Schmidt, Matthew Zawistowski, Stephanie E Moser, Victoria M Blanc, Chad M Brummett, Sachin Kheterpal, Gonçalo R Abecasis,[...]. Am J Hum Genet 2018
82
13

Polygenic risk scores: from research tools to clinical instruments.
Cathryn M Lewis, Evangelos Vassos. Genome Med 2020
202
13

Robust relationship inference in genome-wide association studies.
Ani Manichaikul, Josyf C Mychaleckyj, Stephen S Rich, Kathy Daly, Michèle Sale, Wei-Min Chen. Bioinformatics 2010
13

Association analysis identifies 65 new breast cancer risk loci.
Kyriaki Michailidou, Sara Lindström, Joe Dennis, Jonathan Beesley, Shirley Hui, Siddhartha Kar, Audrey Lemaçon, Penny Soucy, Dylan Glubb, Asha Rostamianfar,[...]. Nature 2017
596
13

Shared heritability and functional enrichment across six solid cancers.
Xia Jiang, Hilary K Finucane, Fredrick R Schumacher, Stephanie L Schmit, Jonathan P Tyrer, Younghun Han, Kyriaki Michailidou, Corina Lesseur, Karoline B Kuchenbaecker, Joe Dennis,[...]. Nat Commun 2019
43
13

Evaluating the Utility of Polygenic Risk Scores in Identifying High-Risk Individuals for Eight Common Cancers.
Guochong Jia, Yingchang Lu, Wanqing Wen, Jirong Long, Ying Liu, Ran Tao, Bingshan Li, Joshua C Denny, Xiao-Ou Shu, Wei Zheng. JNCI Cancer Spectr 2020
29
13

Evaluating polygenic risk scores in assessing risk of nine solid and hematologic cancers in European descendants.
Jungyoon Choi, Guochong Jia, Wanqing Wen, Jirong Long, Wei Zheng. Int J Cancer 2020
5
40

Guidelines for performing Mendelian randomization investigations.
Stephen Burgess, George Davey Smith, Neil M Davies, Frank Dudbridge, Dipender Gill, M Maria Glymour, Fernando P Hartwig, Michael V Holmes, Cosetta Minelli, Caroline L Relton,[...]. Wellcome Open Res 2020
184
13

An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
13

Second-generation PLINK: rising to the challenge of larger and richer datasets.
Christopher C Chang, Carson C Chow, Laurent Cam Tellier, Shashaank Vattikuti, Shaun M Purcell, James J Lee. Gigascience 2015
13

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Daniel Taliun, Daniel N Harris, Michael D Kessler, Jedidiah Carlson, Zachary A Szpiech, Raul Torres, Sarah A Gagliano Taliun, André Corvelo, Stephanie M Gogarten, Hyun Min Kang,[...]. Nature 2021
315
13

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Alicia R Martin, Christopher R Gignoux, Raymond K Walters, Genevieve L Wojcik, Benjamin M Neale, Simon Gravel, Mark J Daly, Carlos D Bustamante, Eimear E Kenny. Am J Hum Genet 2017
527
13

Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.
Roseann E Peterson, Karoline Kuchenbaecker, Raymond K Walters, Chia-Yen Chen, Alice B Popejoy, Sathish Periyasamy, Max Lam, Conrad Iyegbe, Rona J Strawbridge, Leslie Brick,[...]. Cell 2019
149
13

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
13


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.