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Arnaud Maillard

Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder
2021 · Jonathan Lévy, Guillaume Cogan, et al. · Clinical Genetics · 14
An AluYa5 Insertion in the 3′UTR of COL4A1 and Cerebral Small Vessel Disease
2024 · Chaker Aloui, Lisa Neumann, et al. · JAMA Network Open · 12
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Short-term evolution under copper stress increases probability of plasmid uptake
2019 · Uli Klümper, Arnaud Maillard, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 5
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Correspondence on “De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females” by Polla et al.
2021 · Florence Riccardi, Alexandre Astier, et al. · Genetics in Medicine · 4
A WAS promoter variant underlying Wiskott-Aldrich syndrome in two kindreds
2025 · Pauline Ober, Christelle Lenoir, et al. · Journal of Human Immunity · 2
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Heterozygous truncating variants in BICC1 are a novel cause of autosomal-dominant tubulointerstitial kidney disease
2026 · Naomi Eylath, Kendrah O. Kidd, et al. · medRxiv
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BARD1 and breast cancer genetic predisposition: case–control study and HRD signature analysis
2026 · Marie-Florence Reveneau, Antoine De Pauw, et al. · Breast Cancer
Objective clinical scoring system and diagnostic variability in idiopathic pulmonary fibrosis
2026 · Charlotte Abecassis, Jean Pastre, et al. · BMC Pulmonary Medicine
Identity-by-Descent Analysis Uncovering a Founder Event in a Novel Hereditary Small Vessel Cerebral Disease
2025 · Arnaud Maillard, Eva Pipiras, et al. · Stroke
Author response for "Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder"
2021 · Jonathan Lévy, Guillaume Cogan, et al.
Works count: 10
Citation count: 36
H-index: 4
I10-index: 2
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