A citation-based method for searching scientific literature

Hashem A Shihab, Julian Gough, David N Cooper, Peter D Stenson, Gary L A Barker, Keith J Edwards, Ian N M Day, Tom R Gaunt. Hum Mutat 2013
Times Cited: 716



Sung Chun, Justin C Fay. Genome Res 2009
Times Cited: 663




List of shared articles



Times cited



Comprehensive Analysis of Co-Mutations Identifies Cooperating Mechanisms of Tumorigenesis.
Limin Jiang, Hui Yu, Scott Ness, Peng Mao, Fei Guo, Jijun Tang, Yan Guo. Cancers (Basel) 2022
3

Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines.
Emily G Baxi, Terri Thompson, Jonathan Li, Julia A Kaye, Ryan G Lim, Jie Wu, Divya Ramamoorthy, Leandro Lima, Vineet Vaibhav, Andrea Matlock,[...]. Nat Neurosci 2022
12

Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicity.
Mathieu Quinodoz, Virginie G Peter, Katarina Cisarova, Beryl Royer-Bertrand, Peter D Stenson, David N Cooper, Sheila Unger, Andrea Superti-Furga, Carlo Rivolta. Am J Hum Genet 2022
5

Potential Involvement of NSD1, KRT24 and ACACA in the Genetic Predisposition to Colorectal Cancer.
Isabel Quintana, Pilar Mur, Mariona Terradas, Sandra García-Mulero, Gemma Aiza, Matilde Navarro, Virginia Piñol, Joan Brunet, Victor Moreno, Rebeca Sanz-Pamplona,[...]. Cancers (Basel) 2022
0

Identifying Actionable Variants Using Capture-Based Targeted Sequencing in 563 Patients With Non-Small Cell Lung Carcinoma.
Haiping Jiang, Yinan Wang, Hanlin Xu, Wei Lei, Xiaoyun Yu, Haiying Tian, Cong Meng, Xueying Wang, Zicheng Zhao, Xiangfeng Jin. Front Oncol 2022
0


Case Report: Next-Generation Sequencing Identified a Novel Pair of Compound-Heterozygous Mutations of LPL Gene Causing Lipoprotein Lipase Deficiency.
Yakun Li, Man Hu, Lin Han, Lifang Feng, Luhong Yang, Xiaoqian Chen, Tingting Du, Hui Yao, Xiaohong Chen. Front Genet 2022
0

A CTNNB1-altered medulloblastoma shows the immunophenotypic, DNA methylation and transcriptomic profiles of SHH-activated, and not WNT-activated, medulloblastoma.
Jason Chiang, Daniel C Moreira, Nicholas J Pytel, Yen-Chun Liu, Patrick R Blackburn, Zonggao Shi, Maria Cardenas, David A Wheeler, Larissa V Furtado. Neuropathol Appl Neurobiol 2022
0

Machine learning methods for prediction of cancer driver genes: a survey paper.
Renan Andrades, Mariana Recamonde-Mendoza. Brief Bioinform 2022
1

OGDHL Variant rs2293239: A Potential Genetic Driver of Chinese Familial Depressive Disorder.
Zhi Pan, Hongjun Tian, Tao Fang, Zhidong Liu, Xiangdong Liu, Guangqian Dou, Guoyong Huang, Zhenqing Zhang, Guangdong Chen, Wenqiang Wang,[...]. Front Psychiatry 2022
1

AmazonForest: In Silico Metaprediction of Pathogenic Variants.
Helber Gonzales Almeida Palheta, Wanderson Gonçalves Gonçalves, Leonardo Miranda Brito, Arthur Ribeiro Dos Santos, Marlon Dos Reis Matsumoto, Ândrea Ribeiro-Dos-Santos, Gilderlanio Santana de Araújo. Biology (Basel) 2022
0

Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine.
Neven Maksemous, Claire D Blayney, Heidi G Sutherland, Robert A Smith, Rod A Lea, Kim Ngan Tran, Omar Ibrahim, Jeffrey R McArthur, Larisa M Haupt, M Zameel Cader,[...]. Front Mol Neurosci 2022
1

Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies.
Ionut-Florin Iancu, Irene Perea-Romero, Gonzalo Núñez-Moreno, Lorena de la Fuente, Raquel Romero, Almudena Ávila-Fernandez, María José Trujillo-Tiebas, Rosa Riveiro-Álvarez, Berta Almoguera, Inmaculada Martín-Mérida,[...]. Int J Mol Sci 2022
1

m6A-TSHub: Unveiling the Context-specific m6A Methylation and m6A-affecting Mutations in 23 Human Tissues.
Bowen Song, Daiyun Huang, Yuxin Zhang, Zhen Wei, Jionglong Su, João Pedro de Magalhães, Daniel J Rigden, Jia Meng, Kunqi Chen. Genomics Proteomics Bioinformatics 2022
1

An additive destabilising effect of compound T60I and V122I substitutions in ATTRv amyloidosis.
Tatiana Prokaeva, Elena S Klimtchuk, Polina Feschenko, Brian Spencer, Haili Cui, Eric J Burks, Roshanak Aslebagh, Khaja Muneeruddin, Scott A Shaffer, Elizabeth Varghese,[...]. Amyloid 2022
0

Genome sequencing data analysis for rare disease gene discovery.
Umm-Kulthum Ismail Umlai, Dhinoth Kumar Bangarusamy, Xavier Estivill, Puthen Veettil Jithesh. Brief Bioinform 2022
2

Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource.
Lisa Dressler, Michele Bortolomeazzi, Mohamed Reda Keddar, Hrvoje Misetic, Giulia Sartini, Amelia Acha-Sagredo, Lucia Montorsi, Neshika Wijewardhane, Dimitra Repana, Joel Nulsen,[...]. Genome Biol 2022
6

PirePred: An Accurate Online Consensus Tool to Interpret Newborn Screening-Related Genetic Variants in Structural Context.
Juan José Galano-Frutos, Helena García-Cebollada, Alfonso López, Mireia Rosell, Xavier de la Cruz, Juan Fernández-Recio, Javier Sancho. J Mol Diagn 2022
0


Computational Resources for the Interpretation of Variations in Cancer.
Grete Francesca Privitera, Salvatore Alaimo, Alfredo Ferro, Alfredo Pulvirenti. Adv Exp Med Biol 2022
0

Filamin A Is a Potential Driver of Breast Cancer Metastasis via Regulation of MMP-1.
Jie Zhou, Lvying Wu, Pengyan Xu, Yue Li, Zhiliang Ji, Xinmei Kang. Front Oncol 2022
3

Machine-learning of complex evolutionary signals improves classification of SNVs.
Sapir Labes, Doron Stupp, Naama Wagner, Idit Bloch, Michal Lotem, Ephrat L Lahad, Paz Polak, Tal Pupko, Yuval Tabach. NAR Genom Bioinform 2022
1

Genome interpretation using in silico predictors of variant impact.
Panagiotis Katsonis, Kevin Wilhelm, Amanda Williams, Olivier Lichtarge. Hum Genet 2022
2

Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID-19.
Rosario López-Rodríguez, Marta Del Pozo-Valero, Marta Corton, Pablo Minguez, Javier Ruiz-Hornillos, María Elena Pérez-Tomás, María Barreda-Sánchez, Esther Mancebo, Cristina Villaverde, Gonzalo Núñez-Moreno,[...]. Sci Rep 2022
0


RMDisease V2.0: an updated database of genetic variants that affect RNA modifications with disease and trait implication.
Bowen Song, Xuan Wang, Zhanmin Liang, Jiongming Ma, Daiyun Huang, Yue Wang, João Pedro de Magalhães, Daniel J Rigden, Jia Meng, Gang Liu,[...]. Nucleic Acids Res 2022
1

Roles of neuroligins in central nervous system development: focus on glial neuroligins and neuron neuroligins.
Xing Liu, Fuzhou Hua, Danying Yang, Yue Lin, Lieliang Zhang, Jun Ying, Hongguang Sheng, Xifeng Wang. J Transl Med 2022
0