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Jennifer Adamson

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Mariely DeJesus-Hernandez; Dennis W Dickson; Howard Feldman; NiCole A Finch; Heather Flynn; Daniel Geschwind; Neill R Graff-Radford; Ging-Yuek R Hsiung; Keith A Josephs; Anna Karydas; David S Knopman; Naomi Kouri; Ian R A Mackenzie; Bruce L Miller; Alexandra M Nicholson; Ronald C Petersen; Jennifer Adamson; Matt Baker; Bradley F Boeve; Adam L Boxer; Kevin B Boylan; Giovanni Coppola; Nicola J Rutherford; William W Seeley; Pheth Sengdy; Aleksandra Wojtas; Zbigniew K Wszolek; Rosa Rademakers
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Brendan J Kelley; Wael Haidar; Bradley F Boeve; Matt Baker; Maria M Shiung; David S. Knopman; Rosa Rademakers; Michael Hutton; Jennifer Adamson; Karen M Kuntz; dennis dickson; Joseph E Parisi; Glenn Smith; Ronald C. Petersen
Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin.
Brendan J Kelley; Wael Haidar; Bradley Boeve; Matt Baker; Neill R Graff-Radford; Thomas Krefft; Andrew R Frank; Clifford R Jack; Maria M Shiung; David S. Knopman; Keith A Josephs; Sotirios A Parashos; Rosa Rademakers; Michael Hutton; Stuart Pickering-Brown; Jennifer Adamson; Karen M Kuntz; dennis dickson; Joseph E Parisi; Glenn Smith; Robert J Ivnik; Ronald C. Petersen
Prominent phenotypic variability associated with mutations in Progranulin.

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All Publications

2011: Mariely DeJesus-Hernandez; Dennis W Dickson; Howard Feldman; NiCole A Finch; Heather Flynn; Daniel Geschwind; Neill R Graff-Radford; Ging-Yuek R Hsiung; Keith A Josephs; Anna Karydas; David S Knopman; Naomi Kouri; Ian R A Mackenzie; Bruce L Miller; Alexandra M Nicholson; Ronald C Petersen; Jennifer Adamson; Matt Baker; Bradley F Boeve; Adam L Boxer; Kevin B Boylan; Giovanni Coppola; Nicola J Rutherford; William W Seeley; Pheth Sengdy; Aleksandra Wojtas; Zbigniew K Wszolek; Rosa Rademakers
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Neuron 2011;72(2):245-56.
2010: Brendan J Kelley; Wael Haidar; Bradley F Boeve; Matt Baker; Maria M Shiung; David S. Knopman; Rosa Rademakers; Michael Hutton; Jennifer Adamson; Karen M Kuntz; dennis dickson; Joseph E Parisi; Glenn Smith; Ronald C. Petersen
Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin.
Archives of neurology 2010;67(2):171-7.
2009: Brendan J Kelley; Wael Haidar; Bradley Boeve; Matt Baker; Neill R Graff-Radford; Thomas Krefft; Andrew R Frank; Clifford R Jack; Maria M Shiung; David S. Knopman; Keith A Josephs; Sotirios A Parashos; Rosa Rademakers; Michael Hutton; Stuart Pickering-Brown; Jennifer Adamson; Karen M Kuntz; dennis dickson; Joseph E Parisi; Glenn Smith; Robert J Ivnik; Ronald C. Petersen
Prominent phenotypic variability associated with mutations in Progranulin.
Neurobiology of aging 2009;30(5):739-51.
2008: Leslie A Rudzinski; Rita M Fletcher; dennis dickson; Richard Crook; Michael Hutton; Jennifer Adamson; Neill R Graff-Radford
Early onset familial Alzheimer Disease with spastic paraparesis, dysarthria, and seizures and N135S mutation in PSEN1.
Alzheimer disease and associated disorders 2008;22(3):299-307.
2007: S Davion; N Johnson; Sandra Weintraub; Marek-Marsel Mesulam; A Engberg; M Mishra; M Baker; Jennifer Adamson; Michael Hutton; Rosa Rademakers; Eileen H Bigio
Clinicopathologic correlation in PGRN mutations.
Neurology 2007;69(11):1113-21.
2007: Justus C Dächsel; Owen A Ross; Ignacio Mata; Jennifer Kachergus; Mathias Toft; Ashley Cannon; Matt Baker; Jennifer Adamson; Michael Hutton; dennis dickson; Matthew J Farrer
Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions.
Acta neuropathologica 2007;113(5):601-6.
2007: Stacey Melquist; David Craig; Matthew Huentelman; Richard Crook; John Pearson; Matt Baker; Victoria L Zismann; Jennifer Gass; Jennifer Adamson; Szabolcs Szelinger; Jason Corneveaux; Ashley Cannon; Keith D Coon; Sarah J Lincoln; Charles H Adler; Paul Tuite; Donald B Calne; Eileen H Bigio; Ryan Uitti; Zbigniew K Wszolek; Lawrence I Golbe; Richard Caselli; Neill R Graff-Radford; Irene Litvan; Matthew J Farrer; dennis dickson; Michael Hutton; Dietrich A Stephan
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
American journal of human genetics 2007;80(4):769-78.
2007: Jennifer L Whitwell; Clifford R Jack; Matthew Baker; Rosa Rademakers; Jennifer Adamson; Bradley Boeve; David S. Knopman; Joseph E Parisi; Ronald C. Petersen; dennis dickson; Michael Hutton; Keith A Josephs
Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations.
Archives of neurology 2007;64(3):371-6.
2007: Keith A Josephs; Zeshan Ahmed; Omi Katsuse; Joseph E Parisi; Bradley Boeve; David S. Knopman; Ronald C. Petersen; Peter Davies; Ranjan Duara; Neill R Graff-Radford; Ryan Uitti; Rosa Rademakers; Jennifer Adamson; Matthew Baker; Michael Hutton; dennis dickson
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations.
Journal of neuropathology and experimental neurology 2007;66(2):142-51.
2006: Jennifer Gass; Ashley Cannon; Ian R A Mackenzie; Bradley Boeve; Matt Baker; Jennifer Adamson; Richard Crook; Stacey Melquist; Karen Kuntz; Ronald C. Petersen; Keith A Josephs; Stuart Pickering-Brown; Neill R Graff-Radford; Ryan Uitti; dennis dickson; Zbigniew K Wszolek; John Gonzalez; Thomas Beach; Eileen H Bigio; Nancy Johnson; Sandra Weintraub; Marek-Marsel Mesulam; Charles L White; Bryan Woodruff; Richard Caselli; Ging-Yuek Hsiung; Howard Feldman; David S. Knopman; Michael Hutton; Rosa Rademakers
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
Human molecular genetics 2006;15(20):2988-3001.
2006: Matt Baker; Ian R A Mackenzie; Stuart Pickering-Brown; Jennifer Gass; Rosa Rademakers; Caroline Lindholm; Julie Snowden; Jennifer Adamson; A Dessa Sadovnick; Sara Rollinson; Ashley Cannon; Emily Dwosh; David Neary; Stacey Melquist; Anna Richardson; dennis dickson; Zdenek Berger; Jason Eriksen; Todd Robinson; Cynthia Zehr; Chad A Dickey; Richard Crook; Eileen McGowan; D M A Mann; Bradley Boeve; Howard Feldman; Michael Hutton
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
Nature 2006;442(7105):916-9.
2006: Ashley Cannon; Matthew Baker; Bradley Boeve; Keith A Josephs; David S. Knopman; Ronald C. Petersen; Joseph E Parisi; Dennis Dickison; Jennifer Adamson; Julie Snowden; David Neary; D M A Mann; Michael Hutton; Stuart Pickering-Brown
CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.
Neuroscience letters 2006;398(1-2):83-4.
2006: Ian R A Mackenzie; Matthew Baker; Gemma West; John Woulfe; Najeeb Qadi; Jennifer Gass; Ashley Cannon; Jennifer Adamson; Howard Feldman; Caroline Lindholm; Stacey Melquist; Rachel Pettman; A Dessa Sadovnick; Emily Dwosh; Sidney W Whiteheart; Michael Hutton; Stuart Pickering-Brown
A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17.
Brain : a journal of neurology 2006;129(Pt 4):853-67.
2006: Parastoo Momeni; Jennifer C Schymick; Shushant Jain; Mark Cookson; Nigel J Cairns; Elisa Greggio; Matthew J Greenway; Stephen Berger; Stuart Pickering-Brown; Adriano Chio; Hon-Chung Fung; David M Holtzman; Edward D Huey; Eric M Wassermann; Jennifer Adamson; Michael Hutton; Ekaterina Rogaeva; Peter St George-Hyslop; Jeffrey rothstein; Orla Hardiman; Jordan Grafman; Andrew Singleton; John Hardy; Bryan Joseph Traynor
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD.
BMC neurology 2006;6():44.
2005: Rosa Rademakers; Stacey Melquist; Marc Cruts; Jessie Theuns; Jurgen Del-Favero; Parvoneh Poorkaj-Navas; Matt Baker; Kristel Sleegers; Richard Crook; Tim De Pooter; Samira Bel Kacem; Jennifer Adamson; Dirk Van den Bossche; Marleen Van den Broeck; Jennifer Gass; Ellen Corsmit; Peter De Rijk; Natalie Thomas; Sebastiaan Engelborghs; Michael G Heckman; Irene Litvan; Julia Crook; Peter Paul De Deyn; dennis dickson; Gerard D Schellenberg; Christine Van Broeckhoven; Michael Hutton
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
Human molecular genetics 2005;14(21):3281-92.
2003: Andrew Grover; Elisabet England; Mathew Baker; Naruhiko Sahara; Jennifer Adamson; Brian Granger; Henry Houlden; Ulla Passant; Shu-Hui C. Yen; Michael DeTure; Michael Hutton
A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy.
Experimental neurology 2003;184(1):131-40.
2003: Floyd B Willis; Neill R Graff-Radford; Martin Pinto; LaShaune Lawson; Jennifer Adamson; Dawn Epstein; Francine Parfitt; Michael Hutton; Peter C O'Brien
Apolipoprotein epsilon4 allele frequency in young Africans of Ugandan descent versus African Americans.
Journal of the National Medical Association 2003;95(1):71-6.
2002: Rodney A Short; Neill R Graff-Radford; Jennifer Adamson; Matt Baker; Michael Hutton
Differences in tau and apolipoprotein E polymorphism frequencies in sporadic frontotemporal lobar degeneration syndromes.
Archives of neurology 2002;59(4):611-5.
2001: WK Liu; T V Le; Jennifer Adamson; Matt Baker; Natalie Cookson; John Hardy; Michael Hutton; Shu-Hui C. Yen; dennis dickson
Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy.
Annals of neurology 2001;50(4):494-502.
2001: Nilüfer Ertekin-Taner; Neill R Graff-Radford; Linda Younkin; Christopher B Eckman; Jennifer Adamson; D J Schaid; John C Blangero; Michael Hutton; Steven G Younkin
Heritability of plasma amyloid beta in typical late-onset Alzheimer's disease pedigrees.
Genetic epidemiology 2001;21(1):19-30.
2001: Henry Houlden; M Baker; H R Morris; N MacDonald; S Pickering-Brown; Jennifer Adamson; Andrew J Lees; Martin N Rossor; Niall Quinn; A Kertesz; M N Khan; John Hardy; P L Lantos; P St George-Hyslop; David G Munoz; D M A Mann; Anthony E Lang; C Bergeron; Eileen H Bigio; Irene Litvan; K P Bhatia; dennis dickson; Nicholas W Wood; Michael Hutton
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.
Neurology 2001;56(12):1702-6.
2001: Eileen H Bigio; M B Vono; Sivapong Satumtira; Jennifer Adamson; Estelle Sontag; Linda Hynan; Charles L White; M Baker; Michael Hutton
Cortical synapse loss in progressive supranuclear palsy.
Journal of neuropathology and experimental neurology 2001;60(5):403-10.
2000: Nilüfer Ertekin-Taner; Neill R Graff-Radford; Linda Younkin; Christopher B Eckman; Matt Baker; Jennifer Adamson; James Ronald; John C Blangero; Michael Hutton; Steven G Younkin
Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees.
Science (New York, N.Y.) 2000;290(5500):2303-4.
1999: Henry Houlden; Matt Baker; Jennifer Adamson; Andrew Grover; S Waring; dennis dickson; Timothy Lynch; Bradley Boeve; Ronald C. Petersen; Stuart Pickering-Brown; F Owen; David Neary; David Craufurd; Julie Snowden; D M A Mann; Michael Hutton
Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia.
Annals of neurology 1999;46(2):243-8.
1999: Andrew Grover; Henry Houlden; Matt Baker; Jennifer Adamson; Jada Lewis; Guy Prihar; Stuart Pickering-Brown; karen duff; Michael Hutton
5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.
The Journal of biological chemistry 1999;274(21):15134-43.
1999: Matt Baker; Irene Litvan; Henry Houlden; Jennifer Adamson; dennis dickson; Jordi Perez-Tur; John Hardy; Timothy Lynch; Eileen H Bigio; Michael Hutton
Association of an extended haplotype in the tau gene with progressive supranuclear palsy.
Human molecular genetics 1999;8(4):711-5.
1999: Henry Houlden; Patrizia Rizzu; M Stevens; P de Knijff; C.M. Duijn; John C van Swieten; Peter Heutink; Jordi Perez-Tur; V Thomas; Matt Baker; H Morris; Martin N Rossor; J C Jannsen; Ronald C. Petersen; P Dodd; F Dark; Bradley Boeve; dennis dickson; Peter Davies; Stuart Pickering-Brown; D M A Mann; Jennifer Adamson; Timothy Lynch; Haydeh Payami; John Hardy
Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations.
Neuroscience letters 1999;260(3):193-5.