A citation-based method for searching scientific literature

Yonatan A Cooper, Qiuyu Guo, Daniel H Geschwind. Hum Mol Genet 2022
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Xueya Zhou, Pamela Feliciano, Chang Shu, Tianyun Wang, Irina Astrovskaya, Jacob B Hall, Joseph U Obiajulu, Jessica R Wright, Shwetha C Murali, Simon Xuming Xu,[...]. Nat Genet 2022
4
100

Systematic localization of common disease-associated variation in regulatory DNA.
Matthew T Maurano, Richard Humbert, Eric Rynes, Robert E Thurman, Eric Haugen, Hao Wang, Alex P Reynolds, Richard Sandstrom, Hongzhu Qu, Jennifer Brody,[...]. Science 2012
100




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
409
100

Scalable approaches for functional analyses of whole-genome sequencing non-coding variants.
Pavel P Kuksa, Emily Greenfest-Allen, Jeffrey Cifello, Matei Ionita, Hui Wang, Heather Nicaretta, Po-Liang Cheng, Wan-Ping Lee, Li-San Wang, Yuk Yee Leung. Hum Mol Genet 2022
1
100

From genome-wide associations to candidate causal variants by statistical fine-mapping.
Daniel J Schaid, Wenan Chen, Nicholas B Larson. Nat Rev Genet 2018
307
100

Functional genomic assays to annotate enhancer-promoter interactions genome wide.
Alden King-Yung Leung, Li Yao, Haiyuan Yu. Hum Mol Genet 2022
1
100

New insights into the genetic etiology of Alzheimer's disease and related dementias.
Céline Bellenguez, Fahri Küçükali, Iris E Jansen, Luca Kleineidam, Sonia Moreno-Grau, Najaf Amin, Adam C Naj, Rafael Campos-Martin, Benjamin Grenier-Boley, Victor Andrade,[...]. Nat Genet 2022
109
100

Non-coding RNAs in Alzheimer's disease: perspectives from omics studies.
Erming Wang, Mariana Lemos Duarte, Lauren E Rothman, Dongming Cai, Bin Zhang. Hum Mol Genet 2022
1
100


Bridging the splicing gap in human genetics with long-read RNA sequencing: finding the protein isoform drivers of disease.
Peter J Castaldi, Abdullah Abood, Charles R Farber, Gloria M Sheynkman. Hum Mol Genet 2022
2
100

Comprehensive characterization of protein-protein interactions perturbed by disease mutations.
Feixiong Cheng, Junfei Zhao, Yang Wang, Weiqiang Lu, Zehui Liu, Yadi Zhou, William R Martin, Ruisheng Wang, Jin Huang, Tong Hao,[...]. Nat Genet 2021
47
100

Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay.
Ryan Tewhey, Dylan Kotliar, Daniel S Park, Brandon Liu, Sarah Winnicki, Steven K Reilly, Kristian G Andersen, Tarjei S Mikkelsen, Eric S Lander, Stephen F Schaffner,[...]. Cell 2016
204
100

Functional regulatory variants implicate distinct transcriptional networks in dementia.
Yonatan A Cooper, Noam Teyssier, Nina M Dräger, Qiuyu Guo, Jessica E Davis, Sydney M Sattler, Zhongan Yang, Abdulsamie Patel, Sarah Wu, Sriram Kosuri,[...]. Science 2022
10
100

Building integrative functional maps of gene regulation.
Jinrui Xu, Henry E Pratt, Jill E Moore, Mark B Gerstein, Zhiping Weng. Hum Mol Genet 2022
2
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.