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Alexis Proust

The ribosomal basis of diamond-blackfan anemia: mutation and database update
2010 · Ilenia Boria, Emanuela Garelli, et al. · Human Mutation · 240
Decreased B cell activating factor receptor expression on peripheral lymphocytes associated with increased disease activity in primary Sjögren's syndrome and systemic lupus erythematosus
2006 · Jérémie Sellam, Corinne Miceli-Richard, et al. · Annals of the Rheumatic Diseases · 95
Clinical and molecular variability in congenital dyserythropoietic anaemia type I
2005 · Hannah Tamary, Orly Dgany, et al. · British Journal of Haematology · 61
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Different impacts of alleles αLEPRA and αLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in trans
2004 · J. Delaunay, V. Nouyrigat, et al. · British Journal of Haematology · 51
No evidence for an association between the -871 T/C promoter polymorphism in the B-cell-activating factor gene and primary Sjögren's syndrome
2006 · Jacques-Eric Gottenberg, Jérémie Sellam, et al. · Arthritis Research & Therapy · 48
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Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis
2014 · Véronique Picard, Alexis Proust, et al. · Blood · 43
No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome
2005 · M Ittah, J-E Gottenberg, et al. · Genes and Immunity · 43
Enhanced modifications of low-density lipoproteins (LDL) by endothelial cells from smokers: a possible mechanism of smoking-related atherosclerosis
1996 · M.A. Pech-Amsellem, I. Myara, et al. · Cardiovascular Research · 41
Default in plasma and intestinal IgA responses during acute infection by simian immunodeficiency virus
2012 · Nada Chaoul, Chantal Burelout, et al. · Retrovirology · 34
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Ten novel Diamond–Blackfan anemia mutations and three polymorphisms within the rps19 gene
2003 · Alexis Proust, Lydie Da Costa, et al. · The Hematology Journal · 34
Occurrence of Aortic Aneurysms in 5 Cases of Wiskott-Aldrich Syndrome
2011 · Isabelle Pellier, Sophie Dupuis Girod, et al. · PEDIATRICS · 25
Galaxy Is a Suitable Bioinformatics Platform for the Molecular Diagnosis of Human Genetic Disorders Using High-Throughput Sequencing Data Analysis: Five Years of Experience in a Clinical Laboratory
2021 · Kenneth Chappell, Bruno Francou, et al. · Clinical Chemistry · 23
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NF-κB-Mediated Modulation of Inducible Nitric Oxide Synthase Activity Controls Induction of the Epstein-Barr Virus Productive Cycle by Transforming Growth Factor Beta 1
2011 · Lassad Oussaief, Vanessa Ramírez, et al. · Journal of Virology · 23
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Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia
2008 · A. Cretien, C. Hurtaud, et al. · Haematologica · 23
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Whole-genome analysis reveals unexpected dynamics of mutant subclone development in a patient with JAK2-V617F-positive chronic myeloid leukemia
2017 · Ivan Sloma, Maria Teresa Mitjavila-Garcia, et al. · Experimental Hematology · 19
Clinical profile and genetic basis of Wiskott-Aldrich syndrome at Chandigarh, North India.
2012 · Deepti Suri, Surjit Singh, et al. · PubMed · 17
KDM1A genotyping and expression in 146 sporadic somatotroph pituitary adenomas
2024 · Fanny Chasseloup, Daniela Regazzo, et al. · European Journal of Endocrinology · 14
Identification by high-throughput sequencing of HPV variants and quasispecies that are untypeable by linear reverse blotting assay in cervical specimens
2019 · Lucie Molet, Delphine Girlich, et al. · Papillomavirus Research · 14
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Neonatal sepsis due to NDM-1 and VIM-2 co-producing Pseudomonas aeruginosa in Morocco
2024 · Dina Daaboul, Marwan Osman, et al. · Journal of Antimicrobial Chemotherapy · 13
Undetectable Production of the VIM-1 Carbapenemase in an Atlantibacter hermannii Clinical Isolate
2021 · Delphine Girlich, Rémy A. Bonnin, et al. · Frontiers in Microbiology · 13
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Is Inhibitor of differentiation 3 involved in human primary Sjögren's syndrome?
2008 · J. Sellam, C. Miceli-Richard, et al. · Rheumatology · 13
AKAP9-Related Channelopathy: Novel Pathogenic Variant and Review of the Literature
2022 · Minh-Tuan Huynh, Alexis Proust, et al. · Genes · 11
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Genetic variants in the noncoding region of RPS19 gene in Diamond‐Blackfan anemia: Potential implications for phenotypic heterogeneity
2009 · Aurore Crétien, Alexis Proust, et al. · American Journal of Hematology · 11
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Detection of 28 novel mutations in the Wiskott–Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR
2007 · Alexis Proust, Benoît Guillet, et al. · Blood Cells Molecules and Diseases · 10
Recurrent V75M mutation within the Wiskott–Aldrich syndrome protein: description of a homozygous female patient
2005 · Alexis Proust, Benoît Guillet, et al. · European Journal Of Haematology · 9
Works count: 61
Citation count: 986
H-index: 16
I10-index: 24
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