Jeffrey Neul
Jeffrey Neul
Director, Vanderbilt Kennedy Center, Vanderbilt University Medical Center
Verified email at
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Rett syndrome: revised diagnostic criteria and nomenclature
JL Neul, WE Kaufmann, DG Glaze, J Christodoulou, AJ Clarke, ...
Annals of neurology 68 (6), 944-950, 2010
Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes
HT Chao, H Chen, RC Samaco, M Xue, M Chahrour, J Yoo, JL Neul, ...
Nature 468 (7321), 263-269, 2010
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome
JL Neul, P Fang, J Barrish, J Lane, EB Caeg, EO Smith, H Zoghbi, A Percy, ...
Neurology 70 (16), 1313-1321, 2008
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males
D Del Gaudio, P Fang, F Scaglia, PA Ward, WJ Craigen, DG Glaze, ...
Genetics in Medicine 8 (12), 784-792, 2006
The Xenopus dorsalizing factor noggin ventralizes Drosophila embryos by preventing DPP from activating its receptor
SA Holley, JL Neul, L Attisano, JL Wrana, Y Sasai, MB O'Connor, ...
Cell 86 (4), 607-617, 1996
Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress
SL Fyffe, JL Neul, RC Samaco, HT Chao, S Ben-Shachar, P Moretti, ...
Neuron 59 (6), 947-958, 2008
Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities
RC Samaco, C Mandel-Brehm, HT Chao, CS Ward, SL Fyffe-Maricich, ...
Proceedings of the National Academy of Sciences 106 (51), 21966-21971, 2009
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome
VA Cuddapah, RB Pillai, KV Shekar, JB Lane, KJ Motil, SA Skinner, ...
Journal of medical genetics 51 (3), 152-158, 2014
Epilepsy and the natural history of Rett syndrome
DG Glaze, AK Percy, S Skinner, KJ Motil, JL Neul, JO Barrish, JB Lane, ...
Neurology 74 (11), 909-912, 2010
Neurologic complications associated with influenza A in children during the 2003–2004 influenza season in Houston, Texas
SM Maricich, JL Neul, TE Lotze, AC Cazacu, TM Uyeki, GJ Demmler, ...
Pediatrics 114 (5), e626-e633, 2004
A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
RC Samaco, JD Fryer, J Ren, S Fyffe, HT Chao, Y Sun, JJ Greer, ...
Human molecular genetics 17 (12), 1718-1727, 2008
Rett syndrome: a prototypical neurodevelopmental disorder
JL Neul, HY Zoghbi
The Neuroscientist 10 (2), 118-128, 2004
Preclinical research in Rett syndrome: setting the foundation for translational success
DM Katz, JE Berger-Sweeney, JH Eubanks, MJ Justice, JL Neul, ...
Disease models & mechanisms 5 (6), 733-745, 2012
Female Mecp2+/− mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies
RC Samaco, CM McGraw, CS Ward, Y Sun, JL Neul, HY Zoghbi
Human molecular genetics 22 (1), 96-109, 2013
Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome
KJ Motil, E Caeg, JO Barrish, S Geerts, JB Lane, AK Percy, F Annese, ...
Journal of pediatric gastroenterology and nutrition 55 (3), 292, 2012
Cerebral folate deficiency with developmental delay, autism, and response to folinic acid
P Moretti, T Sahoo, K Hyland, T Bottiglieri, S Peters, D Del Gaudio, B Roa, ...
Neurology 64 (6), 1088-1090, 2005
Spatially restricted activation of the SAX receptor by SCW modulates DPP/TKV signaling in Drosophila dorsal–ventral patterning
JL Neul, EL Ferguson
Cell 95 (4), 483-494, 1998
Breathing challenges in Rett syndrome: lessons learned from humans and animal models
JM Ramirez, CS Ward, JL Neul
Respiratory Physiology & Neurobiology 189 (2), 280-287, 2013
Rett syndrome diagnostic criteria: lessons from the Natural History Study
AK Percy, JL Neul, DG Glaze, KJ Motil, SA Skinner, O Khwaja, HS Lee, ...
Annals of neurology 68 (6), 951-955, 2010
Complexities of Rett syndrome and MeCP2
RC Samaco, JL Neul
Journal of Neuroscience 31 (22), 7951-7959, 2011
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