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Relative calibration of the LIGO and Virgo detectors using astrophysical events from their third observing run

Classical and quantum gravity, 2022-10, Vol.39 (19), p.195019

2022

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Pathogenic mechanisms in genetically defined Ehlers–Danlos syndromes

Trends in molecular medicine, 2024-09, Vol.30 (9), p.824-843

2024

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The Implication of Early Chromatin Changes in X Chromosome Inactivation

Cell, 2019-01, Vol.176 (1-2), p.182-197.e23

2019

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Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation

eLife, 2016-02, Vol.5

2016

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Locus specific epigenetic modalities of random allelic expression imbalance

Nature communications, 2021-09, Vol.12 (1), p.5330-5330, Article 5330

2021

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Xist-dependent imprinted X inactivation and the early developmental consequences of its failure

Nature structural & molecular biology, 2017-03, Vol.24 (3), p.226-233

2017

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Microarray analyses of the dorsal root ganglia support a role for innate neuro-immune pathways in persistent pain in experimental osteoarthritis

Osteoarthritis and cartilage, 2020-05, Vol.28 (5), p.581-592

2020

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Contribution of epigenetic landscapes and transcription factors to X-chromosome reactivation in the inner cell mass

Nature communications, 2017-11, Vol.8 (1), p.1297-14, Article 1297

2017

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The role of Xist‐mediated Polycomb recruitment in the initiation of X‐chromosome inactivation

EMBO reports, 2019-10, Vol.20 (10), p.e48019-n/a

2019

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Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria

Human mutation, 2012-10, Vol.33 (10), p.1485-1493

2012

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Kinetics of Xist -induced gene silencing can be predicted from combinations of epigenetic and genomic features

Genome research, 2019-07, Vol.29 (7), p.1087-1099

2019

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Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers–Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix

Genetics in medicine, 2020, Vol.22 (1), p.112-123

2020

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Hypermobility, the Ehlers-Danlos syndromes and chronic pain

Clinical and experimental rheumatology, 2017-09, Vol.35 Suppl 107 (5), p.116

2017

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Editorial: Ehlers-Danlos syndrome: from bedside to bench

Frontiers in genetics, 2024, Vol.15, p.1399386-1399386

2024

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Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome

Matrix biology, 2020-07, Vol.89, p.59-75

2020

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MATRISOME GENE CHANGES IN DORSAL ROOT GANGLIA IN MOUSE MODELS OF OSTEOARTHRITIS PAIN SUGGEST A ROLE FOR FIBROBLAST-NOCICEPTOR COMMUNICATION IN CHRONIC PAIN

Osteoarthritis and cartilage, 2024-04, Vol.32, p.S517

2024

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756 - MATRISOME GENE CHANGES IN DORSAL ROOT GANGLIA IN MOUSE MODELS OF OSTEOARTHRITIS PAIN SUGGEST A ROLE FOR FIBROBLAST-NOCICEPTOR COMMUNICATION IN CHRONIC PAIN

Osteoarthritis and cartilage, 2024-04, Vol.32, p.S517-S517

2024

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Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers–Danlos syndrome

Human mutation, 2021-10, Vol.42 (10), p.1294-1306

2021

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Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen

Genetics in medicine, 2021-12, Vol.23 (12), p.2378-2385

2021

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa

American journal of human genetics, 2017-02, Vol.100 (2), p.216-227

2017

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Bi-allelic AEBP1 mutations in two patients with Ehlers–Danlos syndrome

Human molecular genetics, 2019-06, Vol.28 (11), p.1853-1864

2019

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Animal Models of Ehlers-Danlos Syndromes: Phenotype, Pathogenesis, and Translational Potential

Frontiers in genetics, 2021-10, Vol.12, p.726474

2021

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Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder

American journal of human genetics, 2013-06, Vol.92 (6), p.935-945

2013

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The Virgo Newtonian calibration system for the O4 observing run

Classical and quantum gravity, 2024-10

2024

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The case of the electronic cigarette in the EU

European journal of health law, 2014-01, Vol.21 (2), p.161-175

Syx, Eugenie

2014

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Relative calibration of the LIGO and Virgo detectors using astrophysical events from their third observing run

Pathogenic mechanisms in genetically defined Ehlers–Danlos syndromes

The Implication of Early Chromatin Changes in X Chromosome Inactivation

Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation

Locus specific epigenetic modalities of random allelic expression imbalance

Xist-dependent imprinted X inactivation and the early developmental consequences of its failure

Microarray analyses of the dorsal root ganglia support a role for innate neuro-immune pathways in persistent pain in experimental osteoarthritis

Contribution of epigenetic landscapes and transcription factors to X-chromosome reactivation in the inner cell mass

The role of Xist‐mediated Polycomb recruitment in the initiation of X‐chromosome inactivation

Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria

Kinetics of Xist -induced gene silencing can be predicted from combinations of epigenetic and genomic features

Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers–Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix

Hypermobility, the Ehlers-Danlos syndromes and chronic pain

Editorial: Ehlers-Danlos syndrome: from bedside to bench

Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome

MATRISOME GENE CHANGES IN DORSAL ROOT GANGLIA IN MOUSE MODELS OF OSTEOARTHRITIS PAIN SUGGEST A ROLE FOR FIBROBLAST-NOCICEPTOR COMMUNICATION IN CHRONIC PAIN

756 - MATRISOME GENE CHANGES IN DORSAL ROOT GANGLIA IN MOUSE MODELS OF OSTEOARTHRITIS PAIN SUGGEST A ROLE FOR FIBROBLAST-NOCICEPTOR COMMUNICATION IN CHRONIC PAIN

Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers–Danlos syndrome

Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen

Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa

Bi-allelic AEBP1 mutations in two patients with Ehlers–Danlos syndrome

Animal Models of Ehlers-Danlos Syndromes: Phenotype, Pathogenesis, and Translational Potential

Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder

The Virgo Newtonian calibration system for the O4 observing run

The case of the electronic cigarette in the EU

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