Works matching AU DeStefano, Anita L.

Results: 88

Evaluation of population stratification adjustment using genome‐wide or exonic variants.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 7, p. 702, doi. 10.1002/gepi.22332

By:

Chen, Yuning;
Peloso, Gina M.;
Liu, Ching‐Ti;
DeStefano, Anita L.;
Dupuis, Josée

Publication type:

Article

Incorporating biological information into association studies of sequencing data.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S29, doi. 10.1002/gepi.20646

By:

Chen, Gary;
Wei, Peng;
DeStefano, Anita L.

Publication type:

Article

Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.

Published in:

Genetic Epidemiology, 2009, v. 33, n. 1, p. 54, doi. 10.1002/gepi.20356

By:

Guo, Chao-Yu;
Lunetta, Kathryn L.;
DeStefano,, Anita L.;
Cupples, L. Adrienne

Publication type:

Article

Informative-Transmission Disequilibrium Test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring.

Published in:

Genetic Epidemiology, 2007, v. 31, n. 2, p. 115, doi. 10.1002/gepi.20195

By:

Guo, Chao-Yu;
Lunetta, Kathryn L.;
DeStefano, Anita L.;
Ordovas, Jose M.;
Adrienne Cupples, L.

Publication type:

Article

Data mining, neural nets, trees - Problems 2 and 3 of Genetic Analysis Workshop 15.

Published in:

Genetic Epidemiology, 2007, v. 31, n. S1, p. S51, doi. 10.1002/gepi.20280

By:

Ziegler, Andreas;
DeStefano, Anita L.;
König, Inke R.

Publication type:

Article

Influence of Marker Heterozygosity and Genetic Heterogeneity on Fine Mapping.

Published in:

Genetic Epidemiology, 2001, v. 21, p. S467, doi. 10.1002/gepi.2001.21.s1.s467

By:

Heard-Costa, Nancy L.;
Demissie, Serkalem;
DeStefano, Anita L.;
Knowlton, Beth A.;
Maher, Nancy E.;
Myers, Richard H.;
Volcjak, Jeanine S.;
Wilk, Jemma B.;
Cupples, L. Adrienne

Publication type:

Article

Family-Based Association Tests for Qualitative and Quantitative Traits Using Single-Nucleotide Polymorphism and Microsatellite Data.

Published in:

Genetic Epidemiology, 2001, v. 21, p. S364, doi. 10.1002/gepi.2001.21.s1.s364

By:

Wilk, Jemma B.;
Volcjak, Jeannine S.;
Myers, Richard H.;
Maher, Nancy E.;
Knowlton, Beth A.;
Heard-Costa, Nancy L.;
Demissie, Serkalem;
Cupples, L. Adrienne;
DeStefano, Anita L.

Publication type:

Article

Power of concordant versus discordant sib pairs at different penetrance levels.

Published in:

Genetic Epidemiology, 1999, v. 17, p. S679, doi. 10.1002/gepi.13701707111

By:

Nicolaou, Michael;
Premkumar, Smita;
Destefano, Anita L.;
Farrer, Lindsay A.;
Cupples, L. Adrienne

Publication type:

Article

Detecting linkage for a complex disease using simulated extended pedigrees.

Published in:

Genetic Epidemiology, 1997, v. 14, n. 6, p. 981, doi. 10.1002/(SICI)1098-2272(1997)14:6<981::AID-GEPI70>3.0.CO;2-G

By:

DeStefano, Anita L.;
Cupples, L. Adrienne;
Myers, Richard H.;
Farrer, Lindsay A.

Publication type:

Article

Association of genetic risk of Alzheimer’s disease and cognitive function in two European populations.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-90277-9

By:

Wang, Biqi;
Chibnik, Lori B.;
Choi, Seung Hoan;
Blacker, Deborah;
DeStefano, Anita L.;
Lin, Honghuang

Publication type:

Article

The role of common structural variants in Alzheimer's disease.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.092501

By:

Lee, Songmi;
Xia, Rui;
English, Adam C;
Peloso, Gina M.;
Bis, Josh;
Lin, Honghuang;
Choi, Seung Hoan;
Heard‐Costa, Nancy;
DeStefano, Anita L.;
Sedlazeck, Fritz J;
Fornage, Myriam

Publication type:

Article

Multi‐ancestry whole genome sequencing analysis of 36,361 individuals from the Alzheimer's Disease Sequencing Project (ADSP).

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.092063

By:

Kunkle, Brian W.;
Farrell, John J.;
Akgun, Bilcag;
Wang, Dongyu;
Zhu, Congcong;
Hamilton‐Nelson, Kara L.;
Dietrich, Sven‐Thorsten;
Zhang, Xiaoling;
Rampersaud, Andy;
Yang, Jiemin;
Naj, Adam C.;
Martin, Eden R.;
DeStefano, Anita L.;
Choi, Seung Hoan

Publication type:

Article

Whole Genome Sequencing Analysis of Cognitively Wellderly Individuals Identifies Potential Protective Genetic Variants for Alzheimer's Disease.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.088478

By:

Wang, Dongyu;
Choi, Seung Hoan;
Abbruzzese, Sabrina;
Rosser, Morgan A;
Bis, Joshua C;
Fornage, Myriam;
Boerwinkle, Eric;
Satizabal, Claudia L;
Psaty, Bruce M.;
Lopez, Oscar L.;
Mosley, Thomas H.;
Wang, Yanbing;
Dupuis, Josée;
DeStefano, Anita L.;
Seshadri, Sudha;
Peloso, Gina M.

Publication type:

Article

The plasma miRNAome in ADNI: Signatures to aid the detection of at‐risk individuals.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 11, p. 7479, doi. 10.1002/alz.14157

By:

Krüger, Dennis M.;
Pena‐Centeno, Tonatiuh;
Liu, Shiwei;
Park, Tamina;
Kaurani, Lalit;
Pradhan, Ranjit;
Huang, Yen‐Ning;
Risacher, Shannon L.;
Burkhardt, Susanne;
Schütz, Anna‐Lena;
Wan, Yang;
Shaw, Leslie M.;
Brodsky, Alexander S.;
DeStefano, Anita L.;
Lin, Honghuang;
Schroeder, Robert;
Krunic, Andre;
Hempel, Nina;
Sananbenesi, Farahnaz;
Blusztajn, Jan Krzysztof

Publication type:

Article

Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 5, p. 3290, doi. 10.1002/alz.13705

By:

Wang, Yanbing;
Sarnowski, Chloé;
Lin, Honghuang;
Pitsillides, Achilleas N.;
Heard‐Costa, Nancy L.;
Choi, Seung Hoan;
Wang, Dongyu;
Bis, Joshua C.;
Blue, Elizabeth E.;
Boerwinkle, Eric;
De Jager, Philip L.;
Fornage, Myriam;
Wijsman, Ellen M.;
Seshadri, Sudha;
Dupuis, Josée;
Peloso, Gina M.;
DeStefano, Anita L.

Publication type:

Article

Genetic analyses of longitudinal phenotype data: a comparison of univariate methods and a multivariate approach.

Published in:

BMC Genetics, 2003, v. 4, p. S29, doi. 10.1186/1471-2156-4-S1-S29

By:

Qiong Yang;
Chazaro, Irmarie;
Jing Cui;
Chao-Yu Guo;
Demissie, Serkalem;
Larson, Martin;
Atwood, Larry D.;
Cupples, L. Adrienne;
DeStefano, Anita L.

Publication type:

Article

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.

Published in:

Movement Disorders, 2011, v. 26, n. 11, p. 2039, doi. 10.1002/mds.23781

By:

Latourelle, Jeanne C.;
Hendricks, Audrey E.;
Pankratz, Nathan;
Wilk, Jemma B.;
Halter, Cheryl;
Nichols, William C.;
Gusella, James F.;
Destefano, Anita L.;
Myers, Richard H.;
Foroud, Tatiana

Publication type:

Article

Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype.

Published in:

JAMA Neurology, 2019, v. 76, n. 9, p. 1099, doi. 10.1001/jamaneurol.2019.1456

By:

Ma, Yiyi;
Jun, Gyungah R.;
Zhang, Xiaoling;
Chung, Jaeyoon;
Naj, Adam C.;
Chen, Yuning;
Bellenguez, Celine;
Hamilton-Nelson, Kara;
Martin, Eden R.;
Kunkle, Brian W.;
Bis, Joshua C.;
Debette, Stéphanie;
DeStefano, Anita L.;
Fornage, Myriam;
Nicolas, Gaël;
van Duijn, Cornelia;
Bennett, David A.;
De Jager, Philip L.;
Mayeux, Richard;
Haines, Jonathan L

Publication type:

Article

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke.

Published in:

JAMA Neurology, 2015, v. 72, n. 7, p. 781, doi. 10.1001/jamaneurol.2015.0582

By:

Auer, Paul L.;
Nalls, Mike;
Meschia, James F.;
Worrall, Bradford B.;
Longstreth Jr., W. T.;
Seshadri, Sudha;
Kooperberg, Charles;
Burger, Kathleen M.;
Carlson, Christopher S.;
Carty, Cara L.;
Wei-Min Chen;
Cupples, Adrienne;
DeStefano, Anita L.;
Fornage, Myriam;
Hardy, John;
Li Hsu;
Jackson, Rebecca D.;
Jarvik, Gail P.;
Kim, Daniel S.;
Lakshminarayan, Kamakshi

Publication type:

Article

Serum Brain-Derived Neurotrophic Factor and the Risk for Dementia.

Published in:

JAMA Neurology, 2014, v. 71, n. 1, p. 55, doi. 10.1001/jamaneurol.2013.4781

By:

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

Publication type:

Article

Is DFNA5 a susceptibility gene for age-related hearing impairment?

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 12, p. 883, doi. 10.1038/sj.ejhg.5200878

By:

Van Laer, Lut;
DeStefano, Anita L;
Myers, Richard H;
Flothmann, Kris;
Thys, Sofie;
Fransen, Erik;
Gates, George A;
Van Camp, Guy;
Baldwin, Clinton T

Publication type:

Article

Network analysis of drug effect on triglyceride-associated DNA methylation.

Published in:

BMC Proceedings, 2018, v. 12, n. 9, p. N.PAG, doi. 10.1186/s12919-018-0130-0

By:

Lim, Elise;
Xu, Hanfei;
Wu, Peitao;
Posner, Daniel;
Wu, Jiayi;
Peloso, Gina M.;
Pitsillides, Achilleas N.;
DeStefano, Anita L.;
Adrienne Cupples, L.;
Liu, Ching-Ti

Publication type:

Article

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

Published in:

BMC Proceedings, 2018, v. 12, n. 9, p. N.PAG, doi. 10.1186/s12919-018-0125-x

By:

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

Publication type:

Article

Pathway analysis following association study.

Published in:

BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S18

By:

Ngwa, Julius S.;
Manning, Alisa K.;
Grimsby, Jonna L.;
Chen Lu;
Zhuang, Wei V.;
DeStefano, Anita L.

Publication type:

Article

Identifying rare variants from exome scans: the GAW17 experience.

Published in:

2011

By:

Ghosh, Saurabh;
Bickeböller, Heike;
Bailey, Julia;
Bailey-Wilson, Joan E.;
Cantor, Rita;
Culverhouse, Robert;
Daw, Warwick;
DeStefano, Anita L.;
Engelman, Corinne D.;
Hinrichs, Anthony;
Houwing-Duistermaat, Jeanine;
König, Inke R.;
Kent, Jr., Jack;
Laird, Nan;
Pankratz, Nathan;
Paterson, Andrew;
Pugh, Elizabeth;
Suarez, Brian;
Sun, Yan;
Thomas, Alun

Publication type:

Conference Paper/Materials

Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume.

Published in:

2012

By:

Ikram, M Arfan;
Fornage, Myriam;
Smith, Albert V;
Seshadri, Sudha;
Schmidt, Reinhold;
Debette, Stéphanie;
Vrooman, Henri A;
Sigurdsson, Sigurdur;
Ropele, Stefan;
Taal, H Rob;
Mook-Kanamori, Dennis O;
Coker, Laura H;
Longstreth, W T;
Niessen, Wiro J;
DeStefano, Anita L;
Beiser, Alexa;
Zijdenbos, Alex P;
Struchalin, Maksim;
Jack, Clifford R;
Rivadeneira, Fernando

Publication type:

Erratum

Common variants at 6q22 and 17q21 are associated with intracranial volume.

Published in:

Nature Genetics, 2012, v. 44, n. 5, p. 539, doi. 10.1038/ng.2245

By:

Ikram, M Arfan;
Fornage, Myriam;
Smith, Albert V;
Seshadri, Sudha;
Schmidt, Reinhold;
Debette, Stéphanie;
Vrooman, Henri A;
Sigurdsson, Sigurdur;
Ropele, Stefan;
Taal, H Rob;
Mook-Kanamori, Dennis O;
Coker, Laura H;
Longstreth, W T;
Niessen, Wiro J;
DeStefano, Anita L;
Beiser, Alexa;
Zijdenbos, Alex P;
Struchalin, Maksim;
Jack, Clifford R;
Rivadeneira, Fernando

Publication type:

Article

Common variants at 12q14 and 12q24 are associated with hippocampal volume.

Published in:

Nature Genetics, 2012, v. 44, n. 5, p. 545, doi. 10.1038/ng.2237

By:

Bis, Joshua C;
DeCarli, Charles;
Smith, Albert Vernon;
van der Lijn, Fedde;
Crivello, Fabrice;
Fornage, Myriam;
Debette, Stephanie;
Shulman, Joshua M;
Schmidt, Helena;
Srikanth, Velandai;
Schuur, Maaike;
Yu, Lei;
Choi, Seung-Hoan;
Sigurdsson, Sigurdur;
Verhaaren, Benjamin F J;
DeStefano, Anita L;
Lambert, Jean-Charles;
Jack, Clifford R;
Struchalin, Maksim;
Stankovich, Jim

Publication type:

Article

Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database.

Published in:

PLoS Genetics, 2012, v. 8, n. 3, p. 1, doi. 10.1371/journal.pgen.1002548

By:

M. Lill, Christina;
Roehr, Johannes T.;
McQueen, Matthew B.;
Kavvoura, Fotini K.;
Bagade, Sachin;
Schjeide, Brit-Maren M.;
Schjeide, Leif M.;
Meissner, Esther;
Zauft, Ute;
Allen, Nicole C.;
Liu, Tian;
Schilling, Marcel;
Anderson, Kari J.;
Beecham, Gary;
Berg, Daniela;
Biernacka, Joanna M.;
Brice, Alexis;
DeStefano, Anita L.;
Do, Chuong B.;
Eriksson, Nicholas

Publication type:

Article

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

Published in:

2014

By:

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.;
Ting Liu;
Dietz, William;
Tsutomu Kume;
Hofker, Marten;
Emery, Derek J.;
Childs, Sarah J.;
Waskiewicz, Andrew J.;
Lehmann, Ordan J.;
Liu, Ting;
Kume, Tsutomu

Publication type:

journal article

Expectation Maximization Algorithm Based Haplotype Relative Risk (EM-HRR): Test of Linkage Disequilibrium Using Incomplete Case-Parents Trios.

Published in:

Human Heredity, 2005, v. 59, n. 3, p. 125, doi. 10.1159/000085571

By:

Chao-Yu Guo;
DeStefano, Anita L.;
Lunetta, Kathryn L.;
Dupuis, Josée;
Cupples, L. Adrienne

Publication type:

Article

HaploBuild: an algorithm to construct non-contiguous associated haplotypes in family based genetic studies.

Published in:

Bioinformatics, 2007, v. 23, n. 16, p. 2190, doi. 10.1093/bioinformatics/btm316

By:

Jason M. Laramie;
Jemma B. Wilk;
Anita L. DeStefano;
Richard H. Myers

Publication type:

Article

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.

Published in:

Nature Genetics, 2014, v. 46, n. 9, p. 989, doi. 10.1038/ng.3043

By:

Nalls, Mike A;
Pankratz, Nathan;
Lill, Christina M;
Do, Chuong B;
Hernandez, Dena G;
Saad, Mohamad;
DeStefano, Anita L;
Kara, Eleanna;
Bras, Jose;
Sharma, Manu;
Schulte, Claudia;
Keller, Margaux F;
Arepalli, Sampath;
Letson, Christopher;
Edsall, Connor;
Stefansson, Hreinn;
Liu, Xinmin;
Pliner, Hannah;
Lee, Joseph H;
Cheng, Rong

Publication type:

Article

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.

Published in:

Nature Genetics, 2013, v. 45, n. 12, p. 1452, doi. 10.1038/ng.2802

By:

Lambert, Jean-Charles;
Ibrahim-Verbaas, Carla A;
Harold, Denise;
Naj, Adam C;
Sims, Rebecca;
Bellenguez, Céline;
Jun, Gyungah;
DeStefano, Anita L;
Bis, Joshua C;
Beecham, Gary W;
Grenier-Boley, Benjamin;
Russo, Giancarlo;
Thornton-Wells, Tricia A;
Jones, Nicola;
Smith, Albert V;
Chouraki, Vincent;
Thomas, Charlene;
Ikram, M Arfan;
Zelenika, Diana;
Vardarajan, Badri N

Publication type:

Article

Common variants at 6q22 and 17q21 are associated with intracranial volume.

Published in:

Nature Genetics, 2013, v. 45, n. 6, p. 713, doi. 10.1038/ng0613-713c

By:

Ikram, M Arfan;
Fornage, Myriam;
Smith, Albert V;
Seshadri, Sudha;
Schmidt, Reinhold;
Debette, Stéphanie;
Vrooman, Henri A;
Sigurdsson, Sigurdur;
Ropele, Stefan;
Taal, H Rob;
Mook-Kanamori, Dennis O;
Coker, Laura H;
Longstreth, W T;
Niessen, Wiro J;
DeStefano, Anita L;
Beiser, Alexa;
Zijdenbos, Alex P;
Struchalin, Maksim;
Jack, Clifford R;
Rivadeneira, Fernando

Publication type:

Article

Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels.

Published in:

Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03287-y

By:

Sarnowski, Chloé;
Ghanbari, Mohsen;
Bis, Joshua C.;
Logue, Mark;
Fornage, Myriam;
Mishra, Aniket;
Ahmad, Shahzad;
Beiser, Alexa S.;
Boerwinkle, Eric;
Bouteloup, Vincent;
Chouraki, Vincent;
Cupples, L Adrienne;
Damotte, Vincent;
DeCarli, Charles S.;
DeStefano, Anita L.;
Djoussé, Luc;
Fohner, Alison E.;
Franz, Carol E.;
Kautz, Tiffany F.;
Lambert, Jean-Charles

Publication type:

Article

Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart Study.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 21, p. 2745, doi. 10.1093/hmg/ddg311

By:

Wilk, Jemma B.;
DeStefano, Anita L.;
Joost, Oscar;
Myers, Richard H.;
Cupples, L. Adrienne;
Slater, Karen;
Atwood, Larry D.;
Heard-Costa, Nancy L.;
Herbert, Alan;
O'Connor, George T.;
Gottlieb, Daniel J.

Publication type:

Article

Bone mineral density and the risk of incident dementia: A meta‐analysis.

Published in:

Journal of the American Geriatrics Society, 2024, v. 72, n. 1, p. 194, doi. 10.1111/jgs.18638

By:

Lary, Christine W.;
Ghatan, Samuel;
Gerety, Meghan;
Hinton, Alexandra;
Nagarajan, Archana;
Rosen, Clifford;
Ross, Ryan D.;
Bennett, David A.;
DeStefano, Anita L.;
Ikram, Mohammad A.;
Rivadeneira, Fernando;
Kiel, Douglas P.;
Seshadri, Sudha;
Beiser, Alexa

Publication type:

Article

A Genome-Wide Scan of Pulmonary Function Measures in the National Heart, Lung, and Blood Institute Family Heart Study.

Published in:

American Journal of Respiratory & Critical Care Medicine, 2003, v. 167, n. 11, p. 1528, doi. 10.1164/rccm.200207-755OC

By:

Wilk, Jemma B.;
DeStefano, Anita L.;
Arnett, Donna K.;
Rich, Stephen S.;
Djousse, Luc;
Crapo, Robert O.;
Leppert, Mark F.;
Province, Michael A.;
Cupples, L. Adrienne;
Gottlieb, Daniel J.;
Myers, Richard H.

Publication type:

Article

Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis.

Published in:

BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-017-1498-y

By:

Seung Hoan Choi;
Labadorf, Adam T.;
Myers, Richard H.;
Lunetta, Kathryn L.;
Dupuis, Josée;
DeStefano, Anita L.

Publication type:

Article

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.

Published in:

PLoS Genetics, 2016, v. 12, n. 10, p. 1, doi. 10.1371/journal.pgen.1006327

By:

Jakobsdottir, Johanna;
van der Lee, Sven J.;
Bis, Joshua C.;
Chouraki, Vincent;
Li-Kroeger, David;
Yamamoto, Shinya;
Grove, Megan L.;
Naj, Adam;
Vronskaya, Maria;
Salazar, Jose L.;
DeStefano, Anita L.;
Brody, Jennifer A.;
Smith, Albert V.;
Amin, Najaf;
Sims, Rebecca;
Ibrahim-Verbaas, Carla A.;
Choi, Seung-Hoan;
Satizabal, Claudia L.;
Lopez, Oscar L.;
Beiser, Alexa

Publication type:

Article

Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease.

Published in:

JAMA: Journal of the American Medical Association, 2010, v. 303, n. 18, p. 1832, doi. 10.1001/jama.2010.574

By:

Seshadri, Sudha;
Fitzpatrick, Annette L.;
Ikram, M. Arfan;
DeStefano, Anita L.;
Gudnason, Vilmundur;
Boada, Merce;
Bis, Joshua C.;
Smith, Albert V.;
Carassquillo, Minerva M.;
Lambert, Jean Charles;
Harold, Denise;
Schrijvers, Elisabeth M. C.;
Ramirez-Lorca, Reposo;
Debette, Stephanie;
Longstreth Jr., W. T.;
Janssens, A. Cecile J. W.;
Pankratz, V. Shane;
Dartigues, Jean François;
Hollingworth, Paul;
Aspelund, Thor

Publication type:

Article

Postmortem Interval Influences a-Synuclein Expression in Parkinson Disease Brain.

Published in:

2012

By:

Dumitriu, Alexandra;
Moser, Carlee;
Hadzi, Tiffany C.;
Williamson, Sally L.;
Pacheco, Christopher D.;
Hendricks, Audrey E.;
Latourelle, Jeanne C.;
Wilk, Jemma B.;
DeStefano, Anita L.;
Myers, Richard H.

Publication type:

Journal Article

Postmortem Interval Influences a-Synuclein Expression in Parkinson Disease Brain.

Published in:

Parkinson's Disease (20420080), 2012, p. 1, doi. 10.1155/2012/614212

By:

Dumitriu, Alexandra;
Moser, Carlee;
Hadzi, Tiffany C.;
Williamson, Sally L.;
Pacheco, Christopher D.;
Hendricks, Audrey E.;
Latourelle, Jeanne C.;
Wilk, Jemma B.;
DeStefano, Anita L.;
Myers, Richard H.

Publication type:

Article

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

Published in:

Human Genetics, 2009, v. 124, n. 6, p. 593, doi. 10.1007/s00439-008-0582-9

By:

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.

Publication type:

Article

Replication of association between ELAVL4 and Parkinson disease: the GenePD study.

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Human Genetics, 2008, v. 124, n. 1, p. 95, doi. 10.1007/s00439-008-0526-4

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DeStefano, Anita L.;
Latourelle, Jeanne;
Lew, Mark F.;
Suchowersky, Oksana;
Klein, Christine;
Golbe, Lawrence I.;
Mark, Margery H.;
Growdon, John H.;
Wooten, G. Frederick;
Watts, Ray;
Guttman, Mark;
Racette, Brad A.;
Perlmutter, Joel S.;
Marlor, Lynn;
Shill, Holly A.;
Singer, Carlos;
Goldwurm, Stefano;
Pezzoli, Gianni;
Saint-Hilaire, Marie H.;
Hendricks, Audrey E.

Publication type:

Article

Association of HSP70 and its Co-Chaperones with Alzheimer's Disease.

Published in:

Journal of Alzheimer's Disease, 2011, v. 25, n. 1, p. 93, doi. 10.3233/JAD-2011-101560

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Broer, Linda;
Ikram, Mohammad Arfan;
Schuur, Maaike;
DeStefano, Anita L.;
Bis, Joshua C.;
Fan Liu;
Rivadeneira, Fernando;
Uitterlinden, Andre G.;
Beiser, Alexa S.;
Longstreth, William T.;
Hofman, Albert;
Aulchenko, Yurii;
Seshadri, Sudha;
Fitzpatrick, Annette L.;
Oostra, Ben A.;
Breteler, Monique M. B.;
van Duijn, Cornelia M.

Publication type:

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Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2.

Published in:

Annals of Neurology, 2012, v. 71, n. 3, p. 370, doi. 10.1002/ana.22687

By:

Pankratz, Nathan;
Beecham, Gary W.;
DeStefano, Anita L.;
Dawson, Ted M.;
Doheny, Kimberly F.;
Factor, Stewart A.;
Hamza, Taye H.;
Hung, Albert Y.;
Hyman, Bradley T.;
Ivinson, Adrian J.;
Krainc, Dmitri;
Latourelle, Jeanne C.;
Clark, Lorraine N.;
Marder, Karen;
Martin, Eden R.;
Mayeux, Richard;
Ross, Owen A.;
Scherzer, Clemens R.;
Simon, David K.;
Tanner, Caroline

Publication type:

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Genome-wide association studies of cerebral white matter lesion burden.

Published in:

Annals of Neurology, 2011, v. 69, n. 6, p. 928, doi. 10.1002/ana.22403

By:

Fornage, Myriam;
Debette, Stephanie;
Bis, Joshua C.;
Schmidt, Helena;
Ikram, M. Arfan;
Dufouil, Carole;
Sigurdsson, Sigurdur;
Lumley, Thomas;
DeStefano, Anita L.;
Fazekas, Franz;
Vrooman, Henri A.;
Shibata, Dean K.;
Maillard, Pauline;
Zijdenbos, Alex;
Smith, Albert V.;
Gudnason, Haukur;
de Boer, Renske;
Cushman, Mary;
Mazoyer, Bernard;
Heiss, Gerardo

Publication type:

Article

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

Published in:

BMC Medical Genetics, 2007, v. 8, p. S15, doi. 10.1186/1471-2350-8-S1-S15

By:

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.

Publication type:

Article