A citation-based method for searching scientific literature

Beate Leppert, Louise A C Millard, Lucy Riglin, George Davey Smith, Anita Thapar, Kate Tilling, Esther Walton, Evie Stergiakouli. PLoS Genet 2020
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Naomi R Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M Byrne, Abdel Abdellaoui, Mark J Adams, Esben Agerbo, Tracy M Air, Till M F Andlauer,[...]. Nat Genet 2018
895
50


Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems.
Amanda B Zheutlin, Jessica Dennis, Richard Karlsson Linnér, Arden Moscati, Nicole Restrepo, Peter Straub, Douglas Ruderfer, Victor M Castro, Chia-Yen Chen, Tian Ge,[...]. Am J Psychiatry 2019
39
40

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Joshua C Denny, Marylyn D Ritchie, Melissa A Basford, Jill M Pulley, Lisa Bastarache, Kristin Brown-Gentry, Deede Wang, Dan R Masys, Dan M Roden, Dana C Crawford. Bioinformatics 2010
540
30


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
30

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
562
30

Causal associations between risk factors and common diseases inferred from GWAS summary data.
Zhihong Zhu, Zhili Zheng, Futao Zhang, Yang Wu, Maciej Trzaskowski, Robert Maier, Matthew R Robinson, John J McGrath, Peter M Visscher, Naomi R Wray,[...]. Nat Commun 2018
240
30


Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
Mats Nagel, Philip R Jansen, Sven Stringer, Kyoko Watanabe, Christiaan A de Leeuw, Julien Bryois, Jeanne E Savage, Anke R Hammerschlag, Nathan G Skene, Ana B Muñoz-Manchado,[...]. Nat Genet 2018
171
30

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
885
30

From genome-wide associations to candidate causal variants by statistical fine-mapping.
Daniel J Schaid, Wenan Chen, Nicholas B Larson. Nat Rev Genet 2018
170
30

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
62
30

Characteristics Associated With Racial/Ethnic Disparities in COVID-19 Outcomes in an Academic Health Care System.
Tian Gu, Jasmine A Mack, Maxwell Salvatore, Swaraaj Prabhu Sankar, Thomas S Valley, Karandeep Singh, Brahmajee K Nallamothu, Sachin Kheterpal, Lynda Lisabeth, Lars G Fritsche,[...]. JAMA Netw Open 2020
53
20

Association of Interleukin 6 Receptor Variant With Cardiovascular Disease Effects of Interleukin 6 Receptor Blocking Therapy: A Phenome-Wide Association Study.
Tianxi Cai, Yichi Zhang, Yuk-Lam Ho, Nicholas Link, Jiehuan Sun, Jie Huang, Tianrun A Cai, Scott Damrauer, Yuri Ahuja, Jacqueline Honerlaw,[...]. JAMA Cardiol 2018
36
20

Hospitalization and Mortality among Black Patients and White Patients with Covid-19.
Eboni G Price-Haywood, Jeffrey Burton, Daniel Fort, Leonardo Seoane. N Engl J Med 2020
694
20

The COVID-19 Pandemic: a Call to Action to Identify and Address Racial and Ethnic Disparities.
Cato T Laurencin, Aneesah McClinton. J Racial Ethn Health Disparities 2020
273
20

Exploring and visualizing large-scale genetic associations by using PheWeb.
Sarah A Gagliano Taliun, Peter VandeHaar, Andrew P Boughton, Ryan P Welch, Daniel Taliun, Ellen M Schmidt, Wei Zhou, Jonas B Nielsen, Cristen J Willer, Seunggeun Lee,[...]. Nat Genet 2020
21
20

Accuracy of administrative coding for type 2 diabetes in children, adolescents, and young adults.
Erinn T Rhodes, Lori M B Laffel, Tessa V Gonzalez, David S Ludwig. Diabetes Care 2007
58
20


Air pollution, racial disparities, and COVID-19 mortality.
Eric B Brandt, Andrew F Beck, Tesfaye B Mersha. J Allergy Clin Immunol 2020
59
20


Patients with mental health disorders in the COVID-19 epidemic.
Hao Yao, Jian-Hua Chen, Yi-Feng Xu. Lancet Psychiatry 2020
471
20

Age, Comorbid Conditions, and Racial Disparities in COVID-19 Outcomes.
Zanthia Wiley, Julianne N Kubes, Jason Cobb, Jesse T Jacob, Nicole Franks, Laura Plantinga, Janice Lea. J Racial Ethn Health Disparities 2021
7
28

A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study.
Xueyan Zhao, Xin Geng, Vinodh Srinivasasainagendra, Ninad Chaudhary, Suzanne Judd, Virginia Wadley, Orlando M Gutiérrez, Henry Wang, Ethan M Lange, Leslie A Lange,[...]. BMC Med Genomics 2019
4
50

Understanding associations among race, socioeconomic status, and health: Patterns and prospects.
David R Williams, Naomi Priest, Norman B Anderson. Health Psychol 2016
300
20

Sex differences in susceptibility, severity, and outcomes of coronavirus disease 2019: Cross-sectional analysis from a diverse US metropolitan area.
Farhaan S Vahidy, Alan P Pan, Hilda Ahnstedt, Yashasvee Munshi, Huimahn A Choi, Yordanos Tiruneh, Khurram Nasir, Bita A Kash, Julia D Andrieni, Louise D McCullough. PLoS One 2021
31
20

PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger.
Anurag Verma, Anastasia Lucas, Shefali S Verma, Yu Zhang, Navya Josyula, Anqa Khan, Dustin N Hartzel, Daniel R Lavage, Joseph Leader, Marylyn D Ritchie,[...]. Am J Hum Genet 2018
32
20

Accuracy of provider generated computerized problem lists in the Veterans Administration.
Carl Williams, Angelia Mosley-Williams, Clement McDonald. AMIA Annu Symp Proc 2007
5
40

Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb.
Lars G Fritsche, Lauren J Beesley, Peter VandeHaar, Robert B Peng, Maxwell Salvatore, Matthew Zawistowski, Sarah A Gagliano Taliun, Sayantan Das, Jonathon LeFaive, Erin O Kaleba,[...]. PLoS Genet 2019
14
20

An atlas of polygenic risk score associations to highlight putative causal relationships across the human phenome.
Tom G Richardson, Sean Harrison, Gibran Hemani, George Davey Smith. Elife 2019
67
20

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
488
20




Genome-wide association study identifies 30 loci associated with bipolar disorder.
Eli A Stahl, Gerome Breen, Andreas J Forstner, Andrew McQuillin, Stephan Ripke, Vassily Trubetskoy, Manuel Mattheisen, Yunpeng Wang, Jonathan R I Coleman, Héléna A Gaspar,[...]. Nat Genet 2019
461
20

Phenome-wide association studies across large population cohorts support drug target validation.
Dorothée Diogo, Chao Tian, Christopher S Franklin, Mervi Alanne-Kinnunen, Michael March, Chris C A Spencer, Ciara Vangjeli, Michael E Weale, Hannele Mattsson, Elina Kilpeläinen,[...]. Nat Commun 2018
45
20

Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.
Joshua C Denny, Lisa Bastarache, Dan M Roden. Annu Rev Genomics Hum Genet 2016
96
20

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
414
20

Pleiotropy in complex traits: challenges and strategies.
Nadia Solovieff, Chris Cotsapas, Phil H Lee, Shaun M Purcell, Jordan W Smoller. Nat Rev Genet 2013
521
20

An Expanded View of Complex Traits: From Polygenic to Omnigenic.
Evan A Boyle, Yang I Li, Jonathan K Pritchard. Cell 2017
999
20

Mendelian randomization: using genes as instruments for making causal inferences in epidemiology.
Debbie A Lawlor, Roger M Harbord, Jonathan A C Sterne, Nic Timpson, George Davey Smith. Stat Med 2008
20

Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD.
Evie Stergiakouli, Joanna Martin, Marian L Hamshere, Kate Langley, David M Evans, Beate St Pourcain, Nicholas J Timpson, Michael J Owen, Michael O'Donovan, Anita Thapar,[...]. J Am Acad Child Adolesc Psychiatry 2015
50
20

A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank.
Xueyi Shen, David M Howard, Mark J Adams, W David Hill, Toni-Kim Clarke, Ian J Deary, Heather C Whalley, Andrew M McIntosh. Nat Commun 2020
17
20

A global overview of pleiotropy and genetic architecture in complex traits.
Kyoko Watanabe, Sven Stringer, Oleksandr Frei, Maša Umićević Mirkov, Christiaan de Leeuw, Tinca J C Polderman, Sophie van der Sluis, Ole A Andreassen, Benjamin M Neale, Danielle Posthuma. Nat Genet 2019
174
20

Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan.
Barbara Franke, Giorgia Michelini, Philip Asherson, Tobias Banaschewski, Andrea Bilbow, Jan K Buitelaar, Bru Cormand, Stephen V Faraone, Ylva Ginsberg, Jan Haavik,[...]. Eur Neuropsychopharmacol 2018
139
20

Evidence for causal effects of lifetime smoking on risk for depression and schizophrenia: a Mendelian randomisation study.
Robyn E Wootton, Rebecca C Richmond, Bobby G Stuijfzand, Rebecca B Lawn, Hannah M Sallis, Gemma M J Taylor, Gibran Hemani, Hannah J Jones, Stanley Zammit, George Davey Smith,[...]. Psychol Med 2020
74
20

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Mengzhen Liu, Yu Jiang, Robbee Wedow, Yue Li, David M Brazel, Fang Chen, Gargi Datta, Jose Davila-Velderrain, Daniel McGuire, Chao Tian,[...]. Nat Genet 2019
348
20

Orienting the causal relationship between imprecisely measured traits using GWAS summary data.
Gibran Hemani, Kate Tilling, George Davey Smith. PLoS Genet 2017
162
20

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.
Joshua C Denny, Lisa Bastarache, Marylyn D Ritchie, Robert J Carroll, Raquel Zink, Jonathan D Mosley, Julie R Field, Jill M Pulley, Andrea H Ramirez, Erica Bowton,[...]. Nat Biotechnol 2013
444
20


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.