Ariane Chapgier

University College London — United Kingdom

Immunology and Microbiology · Life Sciences

30h-index7.1kcitations46works0.02yr avg
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Research Topics

Immunodeficiency and Autoimmune Disorders(26), Mycobacterium research and diagnosis(14), Tuberculosis Research and Epidemiology(8), Immune Response and Inflammation(7), Immune Cell Function and Interaction(6)

Publications45 total

HIRA directly targets the enhancers of selected cardiac transcription factors during in vitro differentiation of mouse embryonic stem cells
Molecular Biology Reports·2018· 10 citedOpen Access
HIRA Is Required for Heart Development and Directly Regulates Tnni2 and Tnnt3
PLoS ONE·2016· 34 citedOpen Access
The kinetochore protein, <i>CENPF</i>, is mutated in human ciliopathy and microcephaly phenotypes
Journal of Medical Genetics·2015· 81 citedOpen Access
The Fine Tuning Role of HIRA in The Differentiation Of Mouse Embryonic Stem Cells Into A Cardiogenic Mesoderm
UCL Discovery (University College London)·2015
HIRA Is Required for Heart Development and Directly Regulates Tnni2 and Tnnt3
UCL Discovery (University College London)·2015Open Access
Hira-Dependent Histone H3.3 Deposition Facilitates PRC2 Recruitment at Developmental Loci in ES Cells
Cell·2013· 279 citedOpen Access
Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease
Human Molecular Genetics·2012· 63 citedOpen Access
Human Stat1 Deficiencies
OpenGrey (Institut de l'Information Scientifique et Technique)·2011
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease
Nature Immunology·2011· 282 citedOpen Access
Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds
Human Molecular Genetics·2011· 95 citedOpen Access
Revisiting Human IL-12Rβ1 Deficiency
Medicine·2010· 379 citedOpen Access
THE CLINICAL SPECTRUM OF PATIENTS WITH DEFICIENCY OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION-1
The Pediatric Infectious Disease Journal·2010· 62 cited
Distinct Factors Control Histone Variant H3.3 Localization at Specific Genomic Regions
Cell·2010· 1.3k citedOpen Access
Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN‐γ receptor 1 deficiency
American Journal of Medical Genetics Part A·2010· 22 citedOpen Access
Disseminated Mycobacterium scrofulaceum infection in a child with interferon-γ receptor 1 deficiency
International Journal of Infectious Diseases·2009· 31 citedOpen Access
A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon
Human Molecular Genetics·2009· 36 citedOpen Access
SUCCESSFUL HEMATOPOIETIC STEM CELL TRANSPLANTATION FROM AN UNRELATED DONOR IN A CHILD WITH INTERFERON GAMMA RECEPTOR DEFICIENCY
The Pediatric Infectious Disease Journal·2009· 16 cited
A partial form of recessive STAT1 deficiency in humans
Journal of Clinical Investigation·2009· 183 citedOpen Access
Inborn errors of interferon (IFN)‐mediated immunity in humans: insights into the respective roles of IFN‐α/β, IFN‐γ, and IFN‐λ in host defense
Immunological Reviews·2008· 313 cited
Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation
Journal of Biotechnology·2008· 1 cited
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Frequent Co-authors

Jean‐Laurent Casanova(36), Stéphanie Boisson‐Dupuis(21), Jacqueline Feinberg(21), Jacinta Bustamante(20), Guillaume Vogt(19), Capucine Pïcard(18), Laurent Abel(14), Orchidée Filipe‐Santos(13), Ludovic de Beaucoudrey(13), Claire Fieschi(11), Emmanuelle Jouanguy(10), Anne Puel(7), Xiao‐Fei Kong(7), Alexandre Alcaïs(7), Peter Scambler(5), Shen‐Ying Zhang(5), Steven M. Holland(5), Cheng‐Lung Ku(4), Sami Al-Hajjar(4), Robert D. Schreiber(4)