Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome AJMH Verkerk, M Pieretti, JS Sutcliffe, YH Fu, DPA Kuhl, A Pizzuti, ... Cell 65 (5), 905-914, 1991 | 4282 | 1991 |
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox YH Fu, DPA Kuhl, A Pizzuti, M Pieretti, JS Sutcliffe, S Richards, ... Cell 67 (6), 1047-1058, 1991 | 2599 | 1991 |
The mGluR theory of fragile X mental retardation MF Bear, KM Huber, ST Warren Trends in neurosciences 27 (7), 370-377, 2004 | 1891 | 2004 |
Absence of expression of the FMR-1 gene in fragile X syndrome M Pieretti, F Zhang, YH Fu, ST Warren, BA Oostra, CT Caskey, DL Nelson Cell 66 (4), 817-822, 1991 | 1753 | 1991 |
Altered synaptic plasticity in a mouse model of fragile X mental retardation KM Huber, SM Gallagher, ST Warren, MF Bear Proceedings of the National Academy of Sciences 99 (11), 7746-7750, 2002 | 1547 | 2002 |
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome V Brown, P Jin, S Ceman, JC Darnell, WT O'Donnell, SA Tenenbaum, ... Cell 107 (4), 477-487, 2001 | 1383 | 2001 |
Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function GJ Bassell, ST Warren Neuron 60 (2), 201-214, 2008 | 1242 | 2008 |
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p (CCG) n EJ Kremer, M Pritchard, M Lynch, S Yu, K Holman, E Baker, ST Warren, ... Science 252 (5013), 1711-1714, 1991 | 1135 | 1991 |
Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function JC Darnell, KB Jensen, P Jin, V Brown, ST Warren, RB Darnell Cell 107 (4), 489-499, 2001 | 1126 | 2001 |
Fragile X genotype characterized by an unstable region of DNA S Yu, M Pritchard, E Kremer, M Lynch, J Nancarrow, E Baker, K Holman, ... Science 252 (5009), 1179-1181, 1991 | 1015 | 1991 |
FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding CT Ashley Jr, KD Wilkinson, D Reines, ST Warren Science 262 (5133), 563-566, 1993 | 991 | 1993 |
DNA methylation represses FMR-1 transcription in fragile X syndrome JS Sutcliffe, DL Nelson, F Zhang, M Pieretti, CT Caskey, D Saxe, ... Human molecular genetics 1 (6), 397-400, 1992 | 857 | 1992 |
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway P Jin, DC Zarnescu, S Ceman, M Nakamoto, J Mowrey, TA Jongens, ... Nature neuroscience 7 (2), 113-117, 2004 | 811 | 2004 |
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence HH Chou, H Takematsu, S Diaz, J Iber, E Nickerson, KL Wright, ... Proceedings of the National Academy of Sciences 95 (20), 11751-11756, 1998 | 754 | 1998 |
Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes Y Feng, CA Gutekunst, DE Eberhart, H Yi, ST Warren, SM Hersch Journal of neuroscience 17 (5), 1539-1547, 1997 | 680 | 1997 |
Molecular mechanisms of fragile X syndrome: a twenty-year perspective MR Santoro, SM Bray, ST Warren Annual Review of Pathology: Mechanisms of Disease 7 (1), 219-245, 2012 | 642 | 2012 |
FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association Y Feng, D Absher, DE Eberhart, V Brown, HE Malter, ST Warren Molecular cell 1 (1), 109-118, 1997 | 629 | 1997 |
A decade of molecular studies of fragile X syndrome WT O'Donnell, ST Warren Annual review of neuroscience 25 (1), 315-338, 2002 | 623 | 2002 |
Fragile X syndrome KB Garber, J Visootsak, ST Warren European journal of human genetics 16 (6), 666-672, 2008 | 593 | 2008 |
The fragile X mental retardation protein inhibits translation via interacting with mRNA Z Li, Y Zhang, L Ku, KD Wilkinson, ST Warren, Y Feng Nucleic acids research 29 (11), 2276-2283, 2001 | 557 | 2001 |