Maura Pieretti

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe et al. · Cell · 1991 · 3.5K citations

Life Sciences, Genetics, Molecular Genetics +12

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Ying‐Hui Fu, Derek P.A. Kuhl, Antonio Pizzuti et al. · Cell · 1991 · 2.1K citations

Life Sciences, Genetics, Molecular Genetics +8

Absence of expression of the FMR-1 gene in fragile X syndrome

Maura Pieretti, Ying‐Hui Fu, Stephen T. Warren et al. · Cell · 1991 · 1.5K citations

Life Sciences, Genetics, Molecular Genetics +11

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Brunella Franco, Silvana Guioli, Antonella Pragliola et al. · Nature · 1991 · 851 citations

Life Sciences, Genetics, Molecular Genetics +13

DNA methylation represses <i>FMR-1</i> transcription in fragile X syndrome

James S. Sutcliffe, David L. Nelson, Fuping Zhang et al. · Human Molecular Genetics · 1992 · 681 citations

Life Sciences, Genetics, Molecular Genetics +15