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Genomewide association study for susceptibility genes contributing to familial Parkinson disease
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Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Pankratz, Nathan ; Wilk, Jemma B ; Latourelle, Jeanne C ; DeStefano, Anita L ; Halter, Cheryl ; Pugh, Elizabeth W ; Doheny, Kimberly F ; Gusella, James F ; Nichols, William C ; Foroud, Tatiana ; Myers, Richard H

Human genetics, 2009-01, Vol.124 (6), p.593-605 [Periódico revisado por pares]

Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag

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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

French, Curtis R ; Seshadri, Sudha ; Destefano, Anita L ; Fornage, Myriam ; Arnold, Corey R ; Gage, Philip J ; Skarie, Jonathan M ; Dobyns, William B ; Millen, Kathleen J ; Liu, Ting ; Dietz, William ; Kume, Tsutomu ; Hofker, Marten ; Emery, Derek J ; Childs, Sarah J ; Waskiewicz, Andrew J ; Lehmann, Ordan J

The Journal of clinical investigation, 2014-11, Vol.124 (11), p.4877-4881 [Periódico revisado por pares]

United States: American Society for Clinical Investigation

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3
Copy number variation in familial Parkinson disease
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Artigo
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Copy number variation in familial Parkinson disease

Pankratz, Nathan ; Dumitriu, Alexandra ; Hetrick, Kurt N ; Sun, Mei ; Latourelle, Jeanne C ; Wilk, Jemma B ; Halter, Cheryl ; Doheny, Kimberly F ; Gusella, James F ; Nichols, William C ; Myers, Richard H ; Foroud, Tatiana ; DeStefano, Anita L Roberts, Roland G.

PloS one, 2011-08, Vol.6 (8), p.e20988 [Periódico revisado por pares]

United States: Public Library of Science

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4
Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study
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Artigo
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Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study

Seshadri, Sudha ; DeStefano, Anita L ; Au, Rhoda ; Massaro, Joseph M ; Beiser, Alexa S ; Kelly-Hayes, Margaret ; Kase, Carlos S ; D'Agostino, Sr, Ralph B ; Decarli, Charles ; Atwood, Larry D ; Wolf, Philip A

BMC medical genetics, 2007-09, Vol.8 Suppl 1 (S1), p.S15-S15, Article S15 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Integrative methylation score to identify epigenetic modifications associated with lipid changes resulting from fenofibrate treatment in families
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Artigo
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Integrative methylation score to identify epigenetic modifications associated with lipid changes resulting from fenofibrate treatment in families

Wang, Biqi ; DeStefano, Anita L ; Lin, Honghuang

BMC proceedings, 2018-09, Vol.12 (Suppl 9), p.28-28, Article 28 [Periódico revisado por pares]

England: BioMed Central

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6
Genomewide association study for onset age in Parkinson disease
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Artigo
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Genomewide association study for onset age in Parkinson disease

Latourelle, Jeanne C ; Pankratz, Nathan ; Dumitriu, Alexandra ; Wilk, Jemma B ; Goldwurm, Stefano ; Pezzoli, Gianni ; Mariani, Claudio B ; DeStefano, Anita L ; Halter, Cheryl ; Gusella, James F ; Nichols, William C ; Myers, Richard H ; Foroud, Tatiana

BMC medical genetics, 2009-09, Vol.10 (1), p.98-98, Article 98 [Periódico revisado por pares]

England: BioMed Central Ltd

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7
Cardiovascular health, genetic risk, and risk of dementia in the Framingham Heart Study
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Artigo
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Cardiovascular health, genetic risk, and risk of dementia in the Framingham Heart Study

Peloso, Gina M ; Beiser, Alexa S ; Satizabal, Claudia L ; Xanthakis, Vanessa ; Vasan, Ramachandran S ; Pase, Matthew P ; Destefano, Anita L ; Seshadri, Sudha

Neurology, 2020-09, Vol.95 (10), p.e1341-e1350 [Periódico revisado por pares]

United States: American Academy of Neurology

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8
Serum Brain-Derived Neurotrophic Factor and the Risk for Dementia: The Framingham Heart Study
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Artigo
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Serum Brain-Derived Neurotrophic Factor and the Risk for Dementia: The Framingham Heart Study

Weinstein, Galit ; Beiser, Alexa S ; Choi, Seung Hoan ; Preis, Sarah R ; Chen, Tai C ; Vorgas, Demetrios ; Au, Rhoda ; Pikula, Aleksandra ; Wolf, Philip A ; DeStefano, Anita L ; Vasan, Ramachandran S ; Seshadri, Sudha

JAMA neurology, 2014-01, Vol.71 (1), p.55-61 [Periódico revisado por pares]

United States: American Medical Association

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9
Exploiting family history in aggregation unit-based genetic association tests
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Artigo
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Exploiting family history in aggregation unit-based genetic association tests

Wang, Yanbing ; Chen, Han ; Peloso, Gina M ; DeStefano, Anita L ; Dupuis, Josée

European journal of human genetics : EJHG, 2022-12, Vol.30 (12), p.1355-1362 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease
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Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease

Xue, Diane ; Bush, William S. ; Renton, Alan E. ; Marcora, Edoardo A. ; Bis, Joshua C. ; Kunkle, Brian W. ; Boerwinkle, Eric ; DeStefano, Anita L. ; Farrer, Lindsay ; Goate, Alison ; Mayeux, Richard ; Pericak‐Vance, Margaret ; Schellenberg, Gerard ; Seshadri, Sudha ; Wijsman, Ellen ; Haines, Jonathan L. ; Blue, Elizabeth E.

Alzheimer's & dementia : diagnosis, assessment & disease monitoring, 2021, Vol.13 (1), p.e12255-n/a [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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