Ying‐Hui Fu

ORCID：0000-0003-4748-4498

发表论文 48 篇 · 总被引 10136 次 · h-index 22

代表论文

• Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome (1991 · Cell · 被引 3541)
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox (1991 · Cell · 被引 2104)
• Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein (2001 · The American Journal of Human Genetics · 被引 1018)
• Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome (2001 · Cell · 被引 1009)
• Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) (2002 · Journal of Clinical Investigation · 被引 541)
• Preferential electrical coupling regulates neocortical lineage-dependent microcircuit assembly (2012 · Nature · 被引 229)