E. Audain

发表

Isoelectric point optimization using peptide descriptors and support vector machines.

Markus Müller, J. Vizcaíno, Rui Wang, 2012, Journal of proteomics.

In-depth Analysis of Protein Inference Algorithms using a Workflow Framework and Well-Defined Metrics

K. Reinert, H. Hermjakob, O. Kohlbacher, 2017 .

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

M. Hurles, A. McCallion, A. Franco‐Cereceda, 2019, Nature Genetics.

A proteomics sample metadata representation for multiomics integration and big data analysis

A. Brazma, Mathias Wilhelm, E. Deutsch, 2021, Nature Communications.

A proteomics sample metadata representation for multiomics integration and big data analysis

A. Brazma, Mathias Wilhelm, E. Deutsch, 2021, Nature Communications.

Sequence analysis Accurate estimation of isoelectric point of protein and peptide based on amino acid sequences

H. Hermjakob, D. Flower, Yasset Pérez-Riverol, 2016 .

The PRIDE database and related tools and resources in 2019: improving support for quantification data

Martin Eisenacher, Johannes Griss, Juan Antonio Vizcaíno, 2018, Nucleic Acids Res..

DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs

R. Siebert, O. Ammerpohl, H. Kramer, 2019, Clinical Epigenetics.

A survey of molecular descriptors used in mass spectrometry based proteomics.

Juan Antonio Vizcaíno, Yasset Perez-Riverol, Enrique Audain, 2014, Current topics in medicinal chemistry.

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

R. Siebert, J. Coselli, K. Devriendt, 2020, bioRxiv.

In-depth analysis of protein inference algorithms using multiple search engines and well-defined metrics.

Martin Eisenacher, Yasset Perez-Riverol, Knut Reinert, 2017, Journal of proteomics.

Bio-analytical method based on MALDI-MS analysis for the quantification of CIGB-300 anti-tumor peptide in human plasma.

Y. Perera, B. G. de la Torre, V. Besada, 2015, Journal of pharmaceutical and biomedical analysis.

Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

Tudor I. Oprea, Corey L. Reynolds, Denise G. Lanza, 2022, Nature Cardiovascular Research.

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

H. Mefford, I. Thiffault, T. Pastinen, 2021, Genetics in Medicine.

Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

S. Brunak, S. G. Ellesøe, J. Izarzugaza, 2019, bioRxiv.

Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

Tudor I. Oprea, Corey L. Reynolds, Denise G. Lanza, 2022, Nature Cardiovascular Research.

The omics discovery REST interface

Yasset Perez-Riverol, Henning Hermjakob, Gaurhari Dass, 2020, bioRxiv.

Accurate and fast feature selection workflow for high-dimensional omics data

Yasset Perez-Riverol, Juan Antonio Vizcaíno, Marc-Phillip Hitz, 2017, bioRxiv.

Accurate estimation of isoelectric point of protein and peptide based on amino acid sequences

Henning Hermjakob, Darren R. Flower, Enrique Audain, 2015, Bioinform..

Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

S. Brunak, S. G. Ellesøe, J. Izarzugaza, 2020, Genome Medicine.

Genetics of Congenitally Corrected Transposition of the Great Arteries: next generation sequencing shows a mutation load effect for 156 genes involved in cardiac patterning

A. Boland, J. Deleuze, S. Lyonnet, 2023, medRxiv.

Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

S. Brunak, S. G. Ellesøe, J. Izarzugaza, 2020, Genome Medicine.

STIGMA: Single-cell tissue-specific gene prioritization using machine learning

M. Spielmann, E. Audain, Saranya Balachandran, 2024, American journal of human genetics.