Douglas E. V. Pires - Concepedia

Concepedia

Author

Douglas E. V. Pires

The University of Melbourne

Also Known As

D.E.V. Pires, Douglas E V Pires, Douglas E. V. Pires, Douglas E.V. Pires, Douglas Pires, Pires, Douglas, Pires, Douglas E. V., Pires, Douglas EV

31

Publications

1.1K

Citations

9

H-Index

35

Concepts

All Affiliations

The University of Melbourne Baker Heart and Diabetes Institute The University of Queensland University of Cambridge Fundação Oswaldo Cruz

DE

About

Douglas E. V. Pires is an author at The University of Melbourne specializing in medicine, genetics, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	243
2	Engineering	1	1	16
3	Public Health	1	1	16
4	Biochemistry	1	1	124
5	Biostatistics	1	1	61

Douglas E. V. Pires

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9

Publications

1.1K

Citations

9

H-Index

	Year	Citations
A structural biology community assessment of AlphaFold2 applications Mehmet Akdel, Douglas E. V. Pires, Eduard Porta‐Pardo, Nature Structural & Molecular Biology	2022	655
Prediction and Optimization of Pharmacokinetic and Toxicity Properties of the Ligand Douglas E. V. Pires, Lisa M. Kaminskas, David B. Ascher Methods in molecular biology Pharmacokinetic ModelingBiochemistryToxicity PropertiesDrug DiscoveryMedicine	2018	124
Widespread remodeling of proteome solubility in response to different protein homeostasis stresses Xiaojing Sui, Douglas E. V. Pires, Angelique R. Ormsby, Proceedings of the National Academy of Sciences	2020	68
Exploring the structural distribution of genetic variation in SARS-CoV-2 with the COVID-3D online resource Stephanie Portelli, Moshe Olshansky, Carlos H. M. Rodrigues, Nature Genetics Viral EvolutionCovid-19 PandemicCovid-3d Online ResourceVirologyBiostatistics	2020	61
A Family of Dual-Activity Glycosyltransferase-Phosphorylases Mediates Mannogen Turnover and Virulence in Leishmania Parasites M. Fleur Sernee, Julie E. Ralton, Tracy L. Nero, Cell Host & Microbe	2019	39
Distinguishing between PTEN clinical phenotypes through mutation analysis Stephanie Portelli, Lucy Barr, Alex G. C. de Sá, Computational and Structural Biotechnology Journal Somatic VariantMedicineGeneticsProteomicsPathology	2021	29
CSM‐peptides: A computational approach to rapid identification of therapeutic peptides Carlos H. M. Rodrigues, Anjali Garg, David W. Keizer, Protein Science	2022	29
A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism Shridhar Parthasarathy, Sarah M. Ruggiero, A. Gélot, The American Journal of Human Genetics Epileptic EncephalopathyNeurogenomicsSplice Site VariantGenetic DisorderGenetics	2022	29
Preventing Digital Overdiagnosis Daniel Capurro, Simon Coghlan, Douglas E. V. Pires JAMA EngineeringDatabasesDiagnosisMedical DiagnosisData Science	2022	16

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