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Matthew E. Mort
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2010 – 2019
- 2019
- [j12]Kymberleigh A. Pagel
, Danny Antaki
, Aojie Lian
, Matthew E. Mort, David N. Cooper, Jonathan Sebat, Lilia M. Iakoucheva
, Sean D. Mooney
, Predrag Radivojac:
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome. PLoS Comput. Biol. 15(6) (2019) - 2018
- [j11]Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt
, Colin Campbell:
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features. Bioinform. 34(3): 511-513 (2018) - 2017
- [j10]Kymberleigh A. Pagel, Vikas Pejaver, Guan Ning Lin, Hyun-Jun Nam, Matthew E. Mort, David N. Cooper, Jonathan Sebat, Lilia M. Iakoucheva
, Sean D. Mooney
, Predrag Radivojac:
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants. Bioinform. 33(14): i389-i398 (2017) - [j9]Michael Ferlaino
, Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt
, Colin Campbell:
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome. BMC Bioinform. 18(1): 442:1-442:8 (2017) - 2016
- [j8]Sérgio Matos
, David Campos, Renato P. Pinho, Raquel M. Silva
, Matthew E. Mort, David N. Cooper, José Luís Oliveira
:
Mining clinical attributes of genomic variants through assisted literature curation in Egas. Database J. Biol. Databases Curation 2016 (2016) - [j7]Qinghua Wang, Shabbir Syed-Abdul
, Lara Almeida, Sophia Ananiadou, Yalbi I. Balderas-Martínez
, Riza Batista-Navarro
, David Campos, Lucy Chilton, Hui-Jou Chou, Gabriela Contreras, Laurel Cooper, Hong-Jie Dai, Barbra Ferrell, Juliane Fluck
, Socorro Gama-Castro, Nancy George, Georgios V. Gkoutos
, Afroza Khanam Irin, Lars Juhl Jensen
, Silvia Jimenez, Toni Rose Jue
, Ingrid M. Keseler, Sumit Madan, Sérgio Matos
, Peter McQuilton
, Marija Milacic
, Matthew E. Mort, Jeyakumar Natarajan, Evangelos Pafilis, Emiliano Pereira
, Shruti Rao
, Fabio Rinaldi
, Karen Rothfels, David Salgado
, Raquel M. Silva
, Onkar Singh, Raymund Stefancsik
, Chu-Hsien Su, Suresh Subramani, Hamsa D. Tadepally, Loukia Tsaprouni, Nicole A. Vasilevsky
, Xiaodong Wang, Andrew Chatr-aryamontri, Stanley J. F. Laulederkind, Sherri Matis-Mitchell, Johanna R. McEntyre
, Sandra E. Orchard
, Sangya Pundir
, Raul Rodriguez-Esteban
, Kimberly Van Auken, Zhiyong Lu, Mary L. Schaeffer, Cathy H. Wu
, Lynette Hirschman, Cecilia N. Arighi
:
Overview of the interactive task in BioCreative V. Database J. Biol. Databases Curation 2016 (2016) - [j6]Jose Lugo-Martinez
, Vikas Pejaver, Kymberleigh A. Pagel, Shantanu Jain
, Matthew E. Mort, David N. Cooper, Sean D. Mooney
, Predrag Radivojac:
The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited Disease. PLoS Comput. Biol. 12(8) (2016) - 2015
- [j5]Hashem A. Shihab, Mark F. Rogers, Julian Gough, Matthew E. Mort, David N. Cooper
, Ian N. M. Day, Tom R. Gaunt
, Colin Campbell:
An integrative approach to predicting the functional effects of non-coding and coding sequence variation. Bioinform. 31(10): 1536-1543 (2015) - [j4]Lukas Folkman
, Yuedong Yang
, Zhixiu Li, Bela Stantic, Abdul Sattar
, Matthew E. Mort, David N. Cooper
, Yunlong Liu, Yaoqi Zhou
:
DDIG-in: detecting disease-causing genetic variations due to frameshifting indels and nonsense mutations employing sequence and structural properties at nucleotide and protein levels. Bioinform. 31(10): 1599-1606 (2015) - [c2]Mark F. Rogers, Colin Campbell, Hashem A. Shihab, Tom R. Gaunt
, Matthew E. Mort, David N. Cooper:
Sequential data selection for predicting the pathogenic effects of sequence variation. BIBM 2015: 639-644 - 2012
- [j3]Mingxiang Teng
, Shoji Ichikawa, Leah R. Padgett, Yadong Wang, Matthew E. Mort, David N. Cooper
, Daniel L. Koller, Tatiana Foroud, Howard J. Edenberg
, Michael J. Econs
, Yunlong Liu:
regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions. Bioinform. 28(14): 1879-1886 (2012)
2000 – 2009
- 2009
- [j2]Biao Li, Vidhya G. Krishnan, Matthew E. Mort, Fuxiao Xin, Kishore K. Kamati, David N. Cooper
, Sean D. Mooney
, Predrag Radivojac:
Automated inference of molecular mechanisms of disease from amino acid substitutions. Bioinform. 25(21): 2744-2750 (2009) - 2008
- [c1]Predrag Radivojac, Peter H. Baenziger, Maricel G. Kann, Matthew E. Mort, Matthew W. Hahn, Sean D. Mooney
:
Gain and loss of phosphorylation sites in human cancer. ECCB 2008: 241-247 - 2006
- [j1]Imtiaz A. Khan, Matthew E. Mort, Paul R. Buckland, Michael C. O'Donovan, David N. Cooper, Nadia A. Chuzhanova:
In Silico Discrimination of Single Nucleotide Polymorphisms and Pathological Mutations in Human Gene Promoter Regions by Means of Local DNA Sequence Context and Regularity. Silico Biol. 6(1-2): 23-34 (2006)
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