Publications by authors named "Jennifer Adamson"

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Fragile X-associated tremor ataxia syndrome with co-occurrent progressive supranuclear palsy-like neuropathology.
Amanda N Sacino, Stefan Prokop, Meggen A Walsh, Jennifer Adamson, S H Subramony

Acta Neuropathol Commun· October 2019

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Association of cognition with functional trajectories in patients admitted to geriatric wards: A retrospective observational study.
Peter Hartley, Kerry Alexander, Jennifer Adamson, Carol Cunningham, Georgina Embleton

Geriatr Gerontol Int· October 2017

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Clinical frailty and functional trajectories in hospitalized older adults: A retrospective observational study.
Peter Hartley, Jennifer Adamson, Carol Cunningham, Georgina Embleton, Roman Romero-Ortuno

Geriatr Gerontol Int· July 2017

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Unbiased screen reveals ubiquilin-1 and -2 highly associated with huntingtin inclusions.
Nicola J Rutherford, Jada Lewis, Amy K Clippinger, Michael A Thomas, Jennifer Adamson

Brain Res· August 2013

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Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72.
Bradley F Boeve, Kevin B Boylan, Neill R Graff-Radford, Mariely DeJesus-Hernandez, David S Knopman, Jennifer Adamson

Brain· March 2012

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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
Rosa Rademakers, Matt Baker, Alexandra M Nicholson, Nicola J Rutherford, NiCole Finch, Jennifer Adamson

Nat Genet· December 2011

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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Jennifer Adamson

Neuron· October 2011

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Ataxin-2 repeat-length variation and neurodegeneration.
Owen A Ross, Nicola J Rutherford, Matt Baker, Alexandra I Soto-Ortolaza, Minerva M Carrasquillo, Jennifer Adamson

Hum Mol Genet· August 2011

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Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin.
Brendan J Kelley, Wael Haidar, Bradley F Boeve, Matt Baker, Maria Shiung, Jennifer Adamson

Arch Neurol· February 2010

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Prominent phenotypic variability associated with mutations in Progranulin.
Brendan J Kelley, Wael Haidar, Bradley F Boeve, Matt Baker, Neill R Graff-Radford, Jennifer Adamson

Neurobiol Aging· May 2009

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Early onset familial Alzheimer Disease with spastic paraparesis, dysarthria, and seizures and N135S mutation in PSEN1.
Leslie A Rudzinski, Rita M Fletcher, Dennis W Dickson, Richard Crook, Michael L Hutton, Jennifer Adamson

Alzheimer Dis Assoc Disord· November 2008

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Cholesterol-related genetic risk scores are associated with hypometabolism in Alzheimer's-affected brain regions.
Eric M Reiman, Kewei Chen, Richard J Caselli, Gene E Alexander, Daniel Bandy, Jennifer L Adamson

Neuroimage· April 2008

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New genes, new dilemmas: FTLD genetics and its implications for families.
Jill S Goldman, Jennifer Adamson, Anna Karydas, Bruce L Miller, Mike Hutton

Am J Alzheimers Dis Other Demen· March 2008

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Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Rosa Rademakers, Matt Baker, Jennifer Gass, Jennifer Adamson, Edward D Huey

Lancet Neurol· October 2007

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Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions.
Justus C Dächsel, Owen A Ross, Ignacio F Mata, Jennifer Kachergus, Mathias Toft, Jennifer Adamson

Acta Neuropathol· May 2007

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Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
Stacey Melquist, David W Craig, Matthew J Huentelman, Richard Crook, John V Pearson, Jennifer Adamson

Am J Hum Genet· April 2007

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Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations.
Jennifer L Whitwell, Clifford R Jack, Matthew Baker, Rosa Rademakers, Jennifer Adamson

Arch Neurol· March 2007

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Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations.
Keith A Josephs, Zeshan Ahmed, Omi Katsuse, Joseph F Parisi, Bradley F Boeve, Jennifer Adamson

J Neuropathol Exp Neurol· February 2007

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Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.
Marsel Mesulam, Nancy Johnson, Thomas A Krefft, Jennifer M Gass, Ashley D Cannon, Jennifer L Adamson

Arch Neurol· January 2007

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APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD).
Sarju G Mehta, Giles D J Watts, Jennifer L Adamson, Mike Hutton, Geanie Umberger

Genet Med· January 2007

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Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD.
Parastoo Momeni, Jennifer Schymick, Shushant Jain, Mark R Cookson, Nigel J Cairns, Jennifer Adamson

BMC Neurol· December 2006

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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
Jennifer Gass, Ashley Cannon, Ian R Mackenzie, Bradley Boeve, Matt Baker, Jennifer Adamson

Hum Mol Genet· October 2006

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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, Jennifer Gass, Rosa Rademakers, Jennifer Adamson

Nature· August 2006

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CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.
Ashley Cannon, Matthew Baker, Brad Boeve, Keith Josephs, David Knopman, Jennifer Adamson

Neurosci Lett· May 2006

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A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17.
Ian R Mackenzie, Matthew Baker, Gemma West, John Woulfe, Najeeb Qadi, Jennifer Adamson

Brain· April 2006

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