S. Smemo

发表

DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.

Taylor J. Maxwell, M. Owen, J. Morris, 2006, Human molecular genetics.

Obesity-associated variants within FTO form long-range functional connections with IRX3

N. Cox, E. Gamazon, M. Nóbrega, 2014, Nature.

A common genetic variant within SCN10A modulates cardiac SCN5A expression.

J. Seidman, M. Nóbrega, C. Seidman, 2014, The Journal of clinical investigation.

Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function.

G. Wang, John M Westlund, M. Nóbrega, 2011, The Journal of clinical investigation.

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Taylor J. Maxwell, Peter Holmans, John Hardy, 2006, American journal of human genetics.

Variation in the urokinase‐plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD

M. Owen, J. Morris, M. Hamshere, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Taylor J. Maxwell, M. Owen, J. Morris, 2006, American journal of human genetics.

Catenin delta-1 (CTNND1) phosphorylation controls the mesenchymal to epithelial transition in astrocytic tumors.

M. Howard, A. Bassuk, S. Tsang, 2016, Human molecular genetics.

Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.

M. Nóbrega, J. Krieger, A. Pereira, 2012, Human molecular genetics.

TBX5 drives Scn5a expression to regulate cardiac conduction system function.

M. Nóbrega, Gene Kim, S. Smemo, 2012, The Journal of clinical investigation.

Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family.

M. Owen, J. Morris, P. Holmans, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Association studies testing for risk for late‐onset Alzheimer's disease with common variants in the β‐amyloid precursor protein (APP)

J. Morris, A. Goate, P. Nowotny, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Association studies between risk for late‐onset Alzheimer's disease and variants in insulin degrading enzyme

Taylor J. Maxwell, M. Owen, J. Morris, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

FTO-Mediated Formation of N6-Hydroxymethyladenosine and N6-Formyladenosine in Mammalian RNA

Chuan He, Marcelo A. Nobrega, Guifang Jia, 2013, Nature Communications.

Molecular Neurodegeneration Apolipoprotein E Levels in Cerebrospinal Fluid and the Effects of Abca1 Polymorphisms

Edu, A. Fagan, A. Shah, 2022 .

Redundancy in Genotyping Arrays

Justin O. Borevitz, J. Borevitz, S. Smemo, 2007, PloS one.

A multi-incident, Old-Order Amish family with PD

M. Farrer, S. Lincoln, M. Rundle, 2002, Neurology.

Ubiquilin 1 polymorphisms are not associated with late‐onset Alzheimer's disease

M. Owen, M. O’Donovan, J. Morris, 2006, Annals of neurology.

α-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer’s disease

M. Owen, J. Morris, P. Holmans, 2007, NeuroMolecular Medicine.