CNRGH
Vulin A et al.
Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity
International Journal of Radiation Oncology*Biology*Physics 2018 102(2)
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Wang-Renault SF et al.
Deregulation of microRNA expression in purified T and B lymphocytes from patients with primary Sjögren's syndrome
Annals of the Rheumatic Diseases 2017 77(1)
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Weber A et al.
Epigenome-wide DNA methylation profiling in Progressive Supranuclear Palsy reveals major changes at DLX1
Nature Communications 2018 9(1)
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Yauy K et al.
B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation
Genetics in Medicine 2017 20(2)
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Brucato N et al.
The Comoros Show the Earliest Austronesian Gene Flow into the Swahili Corridor
The American Journal of Human Genetics 2018 102(1)
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Jaquiéry J et al.
Disentangling the Causes for Faster-X Evolution in Aphids
Genome Biology and Evolution 2018 10(2)
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Nadjet Belbachir et al.
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome
European Heart Journal 2019, vol. 40, issue 37
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Angela Bellini et al.
Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma
International Journal of Cancer 2019, vol. 145, issue 10
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Christel Thauvin-Robinet et al.
Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests
European Journal of Human Genetics 2019, vol. 27, issue 8
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Willem De Ridder et al.
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in BVES
Neurology Genetics 2019, vol. 5, issue 2
doi: 10.1212/nxg.0000000000000321