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D

Daniel Rochefort

mcgill university
H指数:32
被引数:4,991

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Transcriptomic and epigenomic consequences of heterozygous loss-of-function mutations in AKAP11, a shared risk gene for bipolar disorder and schizophrenia

AKAP11(一种共享双相情感障碍和精神分裂症风险基因)杂合失活突变引起的转录组学和表观基因组学后果

2025-05-020
PRE
Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes
2024-08-010
OAAI
FOXP1-related intellectual disability syndrome: a recognisable entity
2017-07-2258
OAAI
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia (vol 98, pg 1038, 2016)
2016-06-018
OAAI
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
2016-05-0190
OAAI
Inhibition of the kinase WNK1/HSN2 ameliorates neuropathic pain by restoring GABA inhibition
2016-03-2941
OAAI
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
2014-10-24120
OAAI