| The PRIDE database and related tools and resources in 2019: improving support for quantification data Y Perez-Riverol, A Csordas, J Bai, M Bernal-Llinares, S Hewapathirana, ... Nucleic acids research 47 (D1), D442-D450, 2019 | 5628 | 2019 |
| Accurate and fast feature selection workflow for high-dimensional omics data Y Perez-Riverol, M Kuhn, JA Vizcaíno, MP Hitz, E Audain PloS one 12 (12), e0189875, 2017 | 74 | 2017 |
| Accurate estimation of isoelectric point of protein and peptide based on amino acid sequences E Audain, Y Ramos, H Hermjakob, DR Flower, Y Perez-Riverol Bioinformatics 32 (6), 821-827, 2016 | 65 | 2016 |
| In-depth analysis of protein inference algorithms using multiple search engines and well-defined metrics E Audain, J Uszkoreit, T Sachsenberg, J Pfeuffer, X Liang, H Hermjakob, ... Journal of proteomics 150, 170-182, 2017 | 57 | 2017 |
| Isoelectric point optimization using peptide descriptors and support vector machines Y Perez-Riverol, E Audain, A Millan, Y Ramos, A Sanchez, JA Vizcaíno, ... Journal of proteomics 75 (7), 2269-2274, 2012 | 44 | 2012 |
| Loss of ADAMTS19 causes progressive non-syndromic heart valve disease F Wünnemann, A Ta-Shma, C Preuss, S Leclerc, PP van Vliet, A Oneglia, ... Nature genetics 52 (1), 40-47, 2020 | 41 | 2020 |
| A proteomics sample metadata representation for multiomics integration and big data analysis C Dai, A Füllgrabe, J Pfeuffer, EM Solovyeva, J Deng, P Moreno, ... Nature Communications 12 (1), 5854, 2021 | 29 | 2021 |
| Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease E Audain, A Wilsdon, J Breckpot, JMG Izarzugaza, TW Fitzgerald, ... PLoS Genetics 17 (7), e1009679, 2021 | 14 | 2021 |
| Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease JMG Izarzugaza, SG Ellesře, C Doganli, NS Ehlers, MD Dalgaard, ... Genome medicine 12 (1), 1-13, 2020 | 11 | 2020 |
| DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs K Hoff, M Lemme, AK Kahlert, K Runde, E Audain, D Schuster, J Scheewe, ... Clinical Epigenetics 11 (1), 1-19, 2019 | 11 | 2019 |
| Generation of ENSEMBL-based proteogenomics databases boosts the identification of non-canonical peptides HM Umer, E Audain, Y Zhu, J Pfeuffer, T Sachsenberg, J Lehtiö, ... Bioinformatics 38 (5), 1470-1472, 2022 | 10 | 2022 |
| Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms ES van Walree, G Dombrowsky, IE Jansen, MU Mirkov, R Zwart, A Ilgun, ... Genetics in Medicine 23 (1), 103-110, 2021 | 8 | 2021 |
| Bio-analytical method based on MALDI-MS analysis for the quantification of CIGB-300 anti-tumor peptide in human plasma A Cabrales-Rico, BG de la Torre, HE Garay, YJ Machado, JA Gómez, ... Journal of Pharmaceutical and Biomedical Analysis 105, 107-114, 2015 | 8 | 2015 |
| Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy N Spielmann, G Miller, TI Oprea, CW Hsu, G Fobo, G Frishman, ... Nature Cardiovascular Research 1 (2), 157-173, 2022 | 6 | 2022 |
| Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot D Škorić-Milosavljević, N Lahrouchi, FM Bosada, G Dombrowsky, ... Genetics in Medicine 23 (10), 1952-1960, 2021 | 6 | 2021 |
| A survey of molecular descriptors used in mass spectrometry based proteomics E Audain, A Sanchez, J Antonio Vizcaíno, Y Perez-Riverol Current topics in medicinal chemistry 14 (3), 388-397, 2014 | 6 | 2014 |
| The omics discovery REST interface G Dass, MT Vu, P Xu, E Audain, MP Hitz, BA Grüning, H Hermjakob, ... Nucleic acids research 48 (W1), W380-W384, 2020 | 2 | 2020 |
| Competence Network For Congenital Heart Defects, Germany, Brook JD, Hitz MP, Larsen LA, Brunak S JM Izarzugaza, SG Ellesře, C Doganli, NS Ehlers, MD Dalgaard, ... Systems genetics analysis identifies calcium-signaling defects as novel …, 2020 | 2 | 2020 |
| Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy N Spielmann, G Miller, TI Oprea, CW Hsu, G Fobo, G Frishman, ... Nature Cardiovascular Research 1 (5), 529-531, 2022 | 1 | 2022 |
| Systems genetics analysis identify calcium signalling defects as novel cause of congenital heart disease JMG Izarzugaza, SG Ellesře, C Doganli, NS Ehlers, MD Dalgaard, ... bioRxiv, 2019 | 1 | 2019 |
Yasset Perez-RiverolTeam Coordinator, Proteomics Resources, EMBL-EBI, UKVerified email at ebi.ac.uk
