A citation-based method for searching scientific literature

Katherine S Pollard, Melissa J Hubisz, Kate R Rosenbloom, Adam Siepel. Genome Res 2010
Times Cited: 1263



Gregory M Cooper, Eric A Stone, George Asimenos, Eric D Green, Serafim Batzoglou, Arend Sidow. Genome Res 2005
Times Cited: 922




List of shared articles



Times cited

Clinical manifestations of patients with GDF2 mutations associated with hereditary hemorrhagic telangiectasia type 5.
Ahmed Farhan, Frank Yuan, Elizabeth Partan, Clifford R Weiss. Am J Med Genet A 2022
3

The GRN concept as a guide for evolutionary developmental biology.
Charles Feigin, Sha Li, Jorge Moreno, Ricardo Mallarino. J Exp Zool B Mol Dev Evol 2022
1

Microbiome-associated human genetic variants impact phenome-wide disease risk.
Robert H George Markowitz, Abigail Leavitt LaBella, Mingjian Shi, Antonis Rokas, John A Capra, Jane F Ferguson, Jonathan D Mosley, Seth R Bordenstein. Proc Natl Acad Sci U S A 2022
2

Inferring mammalian tissue-specific regulatory conservation by predicting tissue-specific differences in open chromatin.
Irene M Kaplow, Daniel E Schäffer, Morgan E Wirthlin, Alyssa J Lawler, Ashley R Brown, Michael Kleyman, Andreas R Pfenning. BMC Genomics 2022
0

Classification of non-coding variants with high pathogenic impact.
Lambert Moyon, Camille Berthelot, Alexandra Louis, Nga Thi Thuy Nguyen, Hugues Roest Crollius. PLoS Genet 2022
1

Integrating convolution and self-attention improves language model of human genome for interpreting non-coding regions at base-resolution.
Meng Yang, Lichao Huang, Haiping Huang, Hui Tang, Nan Zhang, Huanming Yang, Jihong Wu, Feng Mu. Nucleic Acids Res 2022
0

Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer.
Diamanto Skopelitou, Aayushi Srivastava, Beiping Miao, Abhishek Kumar, Dagmara Dymerska, Nagarajan Paramasivam, Matthias Schlesner, Jan Lubinski, Kari Hemminki, Asta Försti,[...]. Mol Genet Genomics 2022
0

Whole genome sequencing and inheritance-based variant filtering as a tool for unraveling missing heritability in pediatric cancer.
Charlotte Derpoorter, Ruben Van Paemel, Katrien Vandemeulebroecke, Jolien Vanhooren, Bram De Wilde, Geneviève Laureys, Tim Lammens. Pediatr Hematol Oncol 2022
0

The noncoding genome and hearing loss.
Karen B Avraham, Lama Khalaily, Yael Noy, Lara Kamal, Tal Koffler-Brill, Shahar Taiber. Hum Genet 2022
1

ESC: a comprehensive resource for SARS-CoV-2 immune escape variants.
Mercy Rophina, Kavita Pandhare, Afra Shamnath, Mohamed Imran, Bani Jolly, Vinod Scaria. Nucleic Acids Res 2022
6

Genetic load: genomic estimates and applications in non-model animals.
Giorgio Bertorelle, Francesca Raffini, Mirte Bosse, Chiara Bortoluzzi, Alessio Iannucci, Emiliano Trucchi, Hernán E Morales, Cock van Oosterhout. Nat Rev Genet 2022
4