Yonatan A Cooper, Qiuyu Guo, Daniel H Geschwind. Hum Mol Genet 2022
Times Cited: 1
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
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
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
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
Demystifying non-coding GWAS variants: an overview of computational tools and methods.
Marijn Schipper, Danielle Posthuma. Hum Mol Genet 2022
Marijn Schipper, Danielle Posthuma. Hum Mol Genet 2022
100
A practical view of fine-mapping and gene prioritization in the post-genome-wide association era.
R V Broekema, O B Bakker, I H Jonkers. Open Biol 2020
R V Broekema, O B Bakker, I H Jonkers. Open Biol 2020
100
High-throughput CRISPRi and CRISPRa technologies in 3D genome regulation for neuropsychiatric diseases.
Ian R Jones, Xingjie Ren, Yin Shen. Hum Mol Genet 2022
Ian R Jones, Xingjie Ren, Yin Shen. Hum Mol Genet 2022
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
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
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
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
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
Daniel J Schaid, Wenan Chen, Nicholas B Larson. Nat Rev Genet 2018
100
Functional genomic assays to annotate enhancer-promoter interactions genome wide.
Alden King-Yung Leung, Li Yao, Haiyuan Yu. Hum Mol Genet 2022
Alden King-Yung Leung, Li Yao, Haiyuan Yu. Hum Mol Genet 2022
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
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
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
Erming Wang, Mariana Lemos Duarte, Lauren E Rothman, Dongming Cai, Bin Zhang. Hum Mol Genet 2022
100
From bugs to bedside: functional annotation of human genetic variation for neurological disorders using invertebrate models.
Melanie Mew, Kim A Caldwell, Guy A Caldwell. Hum Mol Genet 2022
Melanie Mew, Kim A Caldwell, Guy A Caldwell. Hum Mol Genet 2022
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
Peter J Castaldi, Abdullah Abood, Charles R Farber, Gloria M Sheynkman. Hum Mol Genet 2022
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
Feixiong Cheng, Junfei Zhao, Yang Wang, Weiqiang Lu, Zehui Liu, Yadi Zhou, William R Martin, Ruisheng Wang, Jin Huang, Tong Hao,[...]. Nat Genet 2021
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
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
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
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
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
Jinrui Xu, Henry E Pratt, Jill E Moore, Mark B Gerstein, Zhiping Weng. Hum Mol Genet 2022
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.