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In Silico Discrimination of Single Nucleotide Polymorphisms and Pathological Mutations in Human Gene Promoter Regions by Means of Local DNA Sequence Context and Regularity.

I. Khan, M. Mort, P. Buckland, M. O'Donovan, D. Cooper, and N. Chuzhanova. In Silico Biology, 6 (1-2): 23-34 (2006)

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Matthew E Gordley

Manfred Mört

Susanne Elisabeth Florentine Mortsch

Zahn- und Kieferveränderungen bei AkromegalieS. Mortsch. Uni Duisburg-Essen, (2009)

Matthew Mellon

Matthew David

Other publications of authors with the same name

DDIG-in: detecting disease-causing genetic variations due to frameshifting indels and nonsense mutations employing sequence and structural properties at nucleotide and protein levels.L. Folkman, Y. Yang, Z. Li, B. Stantic, A. Sattar, M. Mort, D. Cooper, Y. Liu, and Y. Zhou. Bioinform., 31 (10): 1599-1606 (2015)When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.K. Pagel, V. Pejaver, G. Lin, H. Nam, M. Mort, D. Cooper, J. Sebat, L. Iakoucheva, S. Mooney, and P. Radivojac. Bioinform., 33 (14): i389-i398 (2017)regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions.M. Teng, S. Ichikawa, L. Padgett, Y. Wang, M. Mort, D. Cooper, D. Koller, T. Foroud, H. Edenberg, M. Econs and 1 other author(s). Bioinform., 28 (14): 1879-1886 (2012)In Silico Discrimination of Single Nucleotide Polymorphisms and Pathological Mutations in Human Gene Promoter Regions by Means of Local DNA Sequence Context and Regularity.I. Khan, M. Mort, P. Buckland, M. O'Donovan, D. Cooper, and N. Chuzhanova. In Silico Biology, 6 (1-2): 23-34 (2006)The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited Disease.J. Lugo-Martinez, V. Pejaver, K. Pagel, S. Jain, M. Mort, D. Cooper, S. Mooney, and P. Radivojac. PLoS Comput. Biol., (2016)Automated inference of molecular mechanisms of disease from amino acid substitutions.B. Li, V. Krishnan, M. Mort, F. Xin, K. Kamati, D. Cooper, S. Mooney, and P. Radivojac. Bioinform., 25 (21): 2744-2750 (2009)Gain and loss of phosphorylation sites in human cancer.P. Radivojac, P. Baenziger, M. Kann, M. Mort, M. Hahn, and S. Mooney. ECCB, page 241-247. (2008)Overview of the interactive task in BioCreative V.Q. Wang, S. Abdul, L. Almeida, S. Ananiadou, Y. Balderas-Martínez, R. Batista-Navarro, D. Campos, L. Chilton, H. Chou, G. Contreras and 46 other author(s). Database J. Biol. Databases Curation, (2016)Mining clinical attributes of genomic variants through assisted literature curation in Egas.S. Matos, D. Campos, R. Pinho, R. Silva, M. Mort, D. Cooper, and J. Oliveira. Database J. Biol. Databases Curation, (2016)Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome.K. Pagel, D. Antaki, A. Lian, M. Mort, D. Cooper, J. Sebat, L. Iakoucheva, S. Mooney, and P. Radivojac. PLoS Comput. Biol., (2019)

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Disambiguation of "Mort, Matthew E."