A citation-based method for searching scientific literature

Yang Luo, Xinyi Li, Xin Wang, Steven Gazal, Josep Maria Mercader, Benjamin M Neale, Jose C Florez, Adam Auton, Alkes L Price, Hilary K Finucane, Soumya Raychaudhuri. Hum Mol Genet 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
66

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
66

A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains.
Christy L Avery, Qianchuan He, Kari E North, Jose L Ambite, Eric Boerwinkle, Myriam Fornage, Lucia A Hindorff, Charles Kooperberg, James B Meigs, James S Pankow,[...]. PLoS Genet 2011
68
33

Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Chani J Hodonsky, Antoine R Baldassari, Stephanie A Bien, Laura M Raffield, Heather M Highland, Colleen M Sitlani, Genevieve L Wojcik, Ran Tao, Marielisa Graff, Weihong Tang,[...]. BMC Genomics 2020
7
33


Powerful Genetic Association Analysis for Common or Rare Variants with High-Dimensional Structured Traits.
Xiang Zhan, Ni Zhao, Anna Plantinga, Timothy A Thornton, Karen N Conneely, Michael P Epstein, Michael C Wu. Genetics 2017
18
33


Multi-trait analysis of genome-wide association summary statistics using MTAG.
Patrick Turley, Raymond K Walters, Omeed Maghzian, Aysu Okbay, James J Lee, Mark Alan Fontana, Tuan Anh Nguyen-Viet, Robbee Wedow, Meghan Zacher, Nicholas A Furlotte,[...]. Nat Genet 2018
231
33

Methods for meta-analysis of multiple traits using GWAS summary statistics.
Debashree Ray, Michael Boehnke. Genet Epidemiol 2018
23
33

Implications of pleiotropy: challenges and opportunities for mining Big Data in biomedicine.
Can Yang, Cong Li, Qian Wang, Dongjun Chung, Hongyu Zhao. Front Genet 2015
24
33

Pleiotropy in complex traits: challenges and strategies.
Nadia Solovieff, Chris Cotsapas, Phil H Lee, Shaun M Purcell, Jordan W Smoller. Nat Rev Genet 2013
534
33

PLEIO: a method to map and interpret pleiotropic loci with GWAS summary statistics.
Cue Hyunkyu Lee, Huwenbo Shi, Bogdan Pasaniuc, Eleazar Eskin, Buhm Han. Am J Hum Genet 2021
1
100


SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes.
Reedik Mägi, Yury V Suleimanov, Geraldine M Clarke, Marika Kaakinen, Krista Fischer, Inga Prokopenko, Andrew P Morris. BMC Bioinformatics 2017
11
33

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Michael J Gandal, Jillian R Haney, Neelroop N Parikshak, Virpi Leppa, Gokul Ramaswami, Chris Hartl, Andrew J Schork, Vivek Appadurai, Alfonso Buil, Thomas M Werge,[...]. Science 2018
428
33


Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.
Michael Inouye, Samuli Ripatti, Johannes Kettunen, Leo-Pekka Lyytikäinen, Niku Oksala, Pirkka-Pekka Laurila, Antti J Kangas, Pasi Soininen, Markku J Savolainen, Jorma Viikari,[...]. PLoS Genet 2012
107
33

MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS.
Paul F O'Reilly, Clive J Hoggart, Yotsawat Pomyen, Federico C F Calboli, Paul Elliott, Marjo-Riitta Jarvelin, Lachlan J M Coin. PLoS One 2012
210
33


Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension.
Xiaofeng Zhu, Tao Feng, Bamidele O Tayo, Jingjing Liang, J Hunter Young, Nora Franceschini, Jennifer A Smith, Lisa R Yanek, Yan V Sun, Todd L Edwards,[...]. Am J Hum Genet 2015
154
33


Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.
Antoine R Baldassari, Colleen M Sitlani, Heather M Highland, Dan E Arking, Steve Buyske, Dawood Darbar, Rahul Gondalia, Misa Graff, Xiuqing Guo, Susan R Heckbert,[...]. Circ Genom Precis Med 2020
3
33

The implications of the shared genetics of psychiatric disorders.
Michael C O'Donovan, Michael J Owen. Nat Med 2016
76
33


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
984
33



Genetic analyses of diverse populations improves discovery for complex traits.
Genevieve L Wojcik, Mariaelisa Graff, Katherine K Nishimura, Ran Tao, Jeffrey Haessler, Christopher R Gignoux, Heather M Highland, Yesha M Patel, Elena P Sorokin, Christy L Avery,[...]. Nature 2019
199
33

Identification of Pleiotropic Cancer Susceptibility Variants from Genome-Wide Association Studies Reveals Functional Characteristics.
Yi-Hsuan Wu, Rebecca E Graff, Michael N Passarelli, Joshua D Hoffman, Elad Ziv, Thomas J Hoffmann, John S Witte. Cancer Epidemiol Biomarkers Prev 2018
16
33


Multivariate genome-wide analyses of the well-being spectrum.
Bart M L Baselmans, Rick Jansen, Hill F Ip, Jenny van Dongen, Abdel Abdellaoui, Margot P van de Weijer, Yanchun Bao, Melissa Smart, Meena Kumari, Gonneke Willemsen,[...]. Nat Genet 2019
73
33


An efficient Bayesian meta-analysis approach for studying cross-phenotype genetic associations.
Arunabha Majumdar, Tanushree Haldar, Sourabh Bhattacharya, John S Witte. PLoS Genet 2018
19
33

Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test.
Diptavo Dutta, Sarah A Gagliano Taliun, Joshua S Weinstock, Matthew Zawistowski, Carlo Sidore, Lars G Fritsche, Francesco Cucca, David Schlessinger, Gonçalo R Abecasis, Chad M Brummett,[...]. Genet Epidemiol 2019
6
33

A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Matthias Wuttke, Yong Li, Man Li, Karsten B Sieber, Mary F Feitosa, Mathias Gorski, Adrienne Tin, Lihua Wang, Audrey Y Chu, Anselm Hoppmann,[...]. Nat Genet 2019
177
33


edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.
Mark D Robinson, Davis J McCarthy, Gordon K Smyth. Bioinformatics 2010
33

Genetic effects on gene expression across human tissues.
Alexis Battle, Christopher D Brown, Barbara E Engelhardt, Stephen B Montgomery. Nature 2017
33

Anomalous collapses of Nares Strait ice arches leads to enhanced export of Arctic sea ice.
G W K Moore, S E L Howell, M Brady, X Xu, K McNeil. Nat Commun 2021
186
33

Genetic determinants of co-accessible chromatin regions in activated T cells across humans.
Rachel E Gate, Christine S Cheng, Aviva P Aiden, Atsede Siba, Marcin Tabaka, Dmytro Lituiev, Ido Machol, M Grace Gordon, Meena Subramaniam, Muhammad Shamim,[...]. Nat Genet 2018
51
33

LS-GKM: a new gkm-SVM for large-scale datasets.
Dongwon Lee. Bioinformatics 2016
41
33

chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data.
Alicia N Schep, Beijing Wu, Jason D Buenrostro, William J Greenleaf. Nat Methods 2017
244
33


GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach.
Ellen M Schmidt, Ji Zhang, Wei Zhou, Jin Chen, Karen L Mohlke, Y Eugene Chen, Cristen J Willer. Bioinformatics 2015
72
33

Metabolic memory and diabetic nephropathy: potential role for epigenetic mechanisms.
Stephen Tonna, Assam El-Osta, Mark E Cooper, Chris Tikellis. Nat Rev Nephrol 2010
74
33

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
Ayush Giri, Jacklyn N Hellwege, Jacob M Keaton, Jihwan Park, Chengxiang Qiu, Helen R Warren, Eric S Torstenson, Csaba P Kovesdy, Yan V Sun, Otis D Wilson,[...]. Nat Genet 2019
109
33

Cell type-specific genetic regulation of gene expression across human tissues.
Sarah Kim-Hellmuth, François Aguet, Meritxell Oliva, Manuel Muñoz-Aguirre, Silva Kasela, Valentin Wucher, Stephane E Castel, Andrew R Hamel, Ana Viñuela, Amy L Roberts,[...]. Science 2020
45
33

Genetic control of blood pressure and the angiotensinogen locus.
H S Kim, J H Krege, K D Kluckman, J R Hagaman, J B Hodgin, C F Best, J C Jennette, T M Coffman, N Maeda, O Smithies. Proc Natl Acad Sci U S A 1995
559
33

Fast and efficient QTL mapper for thousands of molecular phenotypes.
Halit Ongen, Alfonso Buil, Andrew Anand Brown, Emmanouil T Dermitzakis, Olivier Delaneau. Bioinformatics 2016
167
33

Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis.
Kazuyoshi Ishigaki, Yuta Kochi, Akari Suzuki, Yumi Tsuchida, Haruka Tsuchiya, Shuji Sumitomo, Kensuke Yamaguchi, Yasuo Nagafuchi, Shinichiro Nakachi, Rika Kato,[...]. Nat Genet 2017
62
33


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.