A citation-based method for searching scientific literature

Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, Kushal K Dey, Joseph Nasser, Karthik A Jagadeesh, Daniel J Weiner, Huwenbo Shi, Charles P Fulco, Luke J O'Connor, Bogdan Pasaniuc, Jesse M Engreitz, Alkes L Price. Nat Genet 2022
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Partitioning heritability by functional annotation using genome-wide association summary statistics.
Hilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Farh,[...]. Nat Genet 2015
891
100

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus.
Kiran Musunuru, Alanna Strong, Maria Frank-Kamenetsky, Noemi E Lee, Tim Ahfeldt, Katherine V Sachs, Xiaoyu Li, Hui Li, Nicolas Kuperwasser, Vera M Ruda,[...]. Nature 2010
759
100

Genome-wide enhancer maps link risk variants to disease genes.
Joseph Nasser, Drew T Bergman, Charles P Fulco, Philine Guckelberger, Benjamin R Doughty, Tejal A Patwardhan, Thouis R Jones, Tung H Nguyen, Jacob C Ulirsch, Fritz Lekschas,[...]. Nature 2021
55
100

Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model.
Naomi R Wray, Cisca Wijmenga, Patrick F Sullivan, Jian Yang, Peter M Visscher. Cell 2018
116
100

Multiple causal variants underlie genetic associations in humans.
Nathan S Abell, Marianne K DeGorter, Michael J Gloudemans, Emily Greenwald, Kevin S Smith, Zihuai He, Stephen B Montgomery. Science 2022
3
100

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
100

Functionally informed fine-mapping and polygenic localization of complex trait heritability.
Omer Weissbrod, Farhad Hormozdiari, Christian Benner, Ran Cui, Jacob Ulirsch, Steven Gazal, Armin P Schoech, Bryce van de Geijn, Yakir Reshef, Carla Márquez-Luna,[...]. Nat Genet 2020
39
100

An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level.
Daniel E Bauer, Sophia C Kamran, Samuel Lessard, Jian Xu, Yuko Fujiwara, Carrie Lin, Zhen Shao, Matthew C Canver, Elenoe C Smith, Luca Pinello,[...]. Science 2013
383
100

Single-cell RNA-seq reveals cell type-specific molecular and genetic associations to lupus.
Richard K Perez, M Grace Gordon, Meena Subramaniam, Min Cheol Kim, George C Hartoularos, Sasha Targ, Yang Sun, Anton Ogorodnikov, Raymund Bueno, Andrew Lu,[...]. Science 2022
9
100

An Expanded View of Complex Traits: From Polygenic to Omnigenic.
Evan A Boyle, Yang I Li, Jonathan K Pritchard. Cell 2017
100

Single-cell eQTL mapping identifies cell type-specific genetic control of autoimmune disease.
Seyhan Yazar, Jose Alquicira-Hernandez, Kristof Wing, Anne Senabouth, M Grace Gordon, Stacey Andersen, Qinyi Lu, Antonia Rowson, Thomas R P Taylor, Linda Clarke,[...]. Science 2022
7
100

Exome sequencing and analysis of 454,787 UK Biobank participants.
Joshua D Backman, Alexander H Li, Anthony Marcketta, Dylan Sun, Joelle Mbatchou, Michael D Kessler, Christian Benner, Daren Liu, Adam E Locke, Suganthi Balasubramanian,[...]. Nature 2021
33
100

An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci.
Edward Mountjoy, Ellen M Schmidt, Miguel Carmona, Jeremy Schwartzentruber, Gareth Peat, Alfredo Miranda, Luca Fumis, James Hayhurst, Annalisa Buniello, Mohd Anisul Karim,[...]. Nat Genet 2021
24
100


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.