Name
Playground
About
FAQ
GitHub
Playground
Shortest Path Finder
Community Detector
Connected Papers
Author Trending
Farah-Ul-Ain
Daniel P. Kennedy
Emily Chia-Yu Su
Dan Graur
Barbara Aquilani
Roland Zumkeller
Maximilian Dürr
Liangliang Shang
Chen Ma
Haoyu Zhang
Home
/
Author
/
DAVID N COOPER
Author Info
Open Visualization
Name
Affiliation
Papers
DAVID N COOPER
Cardiff Univ, Sch Med, Inst Med Genet, Cardiff CF14 4XN, S Glam, Wales
17
Collaborators
Citations
PageRank
76
80
13.72
Referers
Referees
References
412
501
133
Search Limit
100
501
Publications (17 rows)
Collaborators (76 rows)
Referers (100 rows)
Referees (100 rows)
Title
Citations
PageRank
Year
SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing data
0
0.34
2019
RegulationSpotter: annotation and interpretation of extratranscriptic DNA variants.
0
0.34
2019
Mutational signatures and mutable motifs in cancer genomes.
0
0.34
2018
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.
3
0.46
2018
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.
0
0.34
2017
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.
0
0.34
2017
Mining clinical attributes of genomic variants through assisted literature curation in Egas.
3
0.40
2016
The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited Disease.
0
0.34
2016
Sequential data selection for predicting the pathogenic effects of sequence variation
0
0.34
2015
A probabilistic model to predict clinical phenotypic traits from genome sequencing.
0
0.34
2014
CRAVAT: cancer-related analysis of variants toolkit.
5
0.62
2013
Predicting the functional consequences of cancer-associated amino acid substitutions
8
1.89
2013
regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions.
3
0.49
2012
Structure-based kernels for the prediction of catalytic residues and their involvement in human inherited disease.
7
0.54
2010
Automated inference of molecular mechanisms of disease from amino acid substitutions.
30
1.62
2009
In Silico Discrimination of Single Nucleotide Polymorphisms and Pathological Mutations in Human Gene Promoter Regions by Means of Local DNA Sequence Context and Regularity.
0
0.34
2006
The Human Gene Mutation Database
21
4.65
1998
1
