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Papers authored by Destefano AL

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Genomewide association studies of stroke.

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Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, Debette S, Lumley T, Folsom AR, van den Herik EG, Bos MJ, Beiser A, Cushman M, Launer LJ, Shahar E, Struchalin M,

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The New England journal of medicine 360(17):1718-28, 2009 Apr 23 - Who cited this? | PubMed ID: 19369658 | Fulltext

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

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Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH, and PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories

Human genetics 124(6):593-605, 2009 Jan - Who cited this? | PubMed ID: 18985386 | Fulltext

Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis.

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Cui J, Taylor KE, Destefano AL, Criswell LA, Izmailova ES, Parker A, Roubenoff R, Plenge RM, Weinblatt ME, Shadick NA, and Karlson EW

Molecular medicine (Cambridge, Mass.) 15(5-6):136-43, 2009 - Who cited this? | PubMed ID: 19287509 | Fulltext

Genomewide association study for onset age in Parkinson disease.

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Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T, PROGENI Investigators, Coordinators and Molecular Genetic Laboratories, and GenePD Investigators, Coordinators and Molecular Genetic Laboratories

BMC medical genetics 10:98, 2009 - Who cited this? | PubMed ID: 19772629 | Fulltext

Bivariate heritability of total and regional brain volumes: the Framingham Study.

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DeStefano AL, Seshadri S, Beiser A, Atwood LD, Massaro JM, Au R, Wolf PA, and DeCarli C

Alzheimer disease and associated disorders 23(3):218-23, 2009 - Who cited this? | PubMed ID: 19812462 | Fulltext

Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study.

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McNicoll CF, Latourelle JC, MacDonald ME, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA,

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Movement disorders : official journal of the Movement Disorder Society 23(11):1596-601, 2008 Aug 15 - Who cited this? | PubMed ID: 18649400 | Fulltext

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

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Guo CY, Lunetta KL, Destefano AL, and Cupples LA

Genetic epidemiology, 2008 Jul 17 - Who cited this? | PubMed ID: 18636528 | Fulltext

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.

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Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, Goldwurm S,

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Neurology 71(1):28-34, 2008 Jul 1 - Who cited this? | PubMed ID: 18509094 | Fulltext

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

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Destefano AL, Latourelle J, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts R, Guttman M, Racette BA, Perlmutter JS, Marlor L, Shill HA, Singer C,

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Human genetics, 2008 Jun 29 - Who cited this? | PubMed ID: 18587682 | Fulltext

The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.

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Latourelle JC, Sun M, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA, Singer C,

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BMC medicine 6:32, 2008 - Who cited this? | PubMed ID: 18986508 | Fulltext

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

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Laramie JM, Wilk JB, DeStefano AL, and Myers RH

Bioinformatics (Oxford, England) 23(16):2190-2, 2007 Aug 15 - Who cited this? | PubMed ID: 17586827 | Fulltext

Sepiapterin reductase expression is increased in Parkinson's disease brain tissue.

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Tobin JE, Cui J, Wilk JB, Latourelle JC, Laramie JM, McKee AC, Guttman M, Karamohamed S, DeStefano AL, and Myers RH

Brain research 1139:42-7, 2007 Mar 30 - Who cited this? | PubMed ID: 17270157 | Fulltext

Informative-transmission disequilibrium test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring.

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Guo CY, Lunetta KL, DeStefano AL, Ordovas JM, and Cupples LA

Genetic epidemiology 31(2):115-33, 2007 Feb - Who cited this? | PubMed ID: 17123304 | Fulltext

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.

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Cupples LA, Arruda HT, Benjamin EJ, D'Agostino RB, Demissie S, Destefano AL, Dupuis J, Falls KM, Fox CS, Gottlieb DJ, Govindaraju DR, Guo CY, Heard-Costa NL, Hwang SJ, Kathiresan S, Kiel DP,

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BMC medical genetics 8 Suppl 1, 2007 - Who cited this? | PubMed ID: 17903291 | Fulltext

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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Seshadri S, Destefano AL, Au R, Massaro JM, Beiser AS, Kelly-Hayes M, Kase CS, D'Agostino RB, DeCarli C, Atwood LD, and Wolf PA

BMC medical genetics 8 Suppl 1, 2007 - Who cited this? | PubMed ID: 17903297 | Fulltext

Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks.

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Meng Y, Yang Q, Cuenco KT, Cupples LA, Destefano AL, and Lunetta KL

BMC proceedings 1 Suppl 1, 2007 - Who cited this? | PubMed ID: 18466556 | Fulltext

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

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Ziegler A, Destefano AL, König IR, Bardel C, Brinza D, Bull S, Cai Z, Glaser B, Jiang W, Lee KE, Li CX, Li J, Li X, Majoram P, Meng Y, Nicodemus KK,

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Genetic epidemiology 31 Suppl 1, 2007 - Who cited this? | PubMed ID: 18046765 | Fulltext

Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study.

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Wilk JB, Tobin JE, Suchowersky O, Shill HA, Klein C, Wooten GF, Lew MF, Mark MH, Guttman M, Watts RL, Singer C, Growdon JH, Latourelle JC, Saint-Hilaire MH, DeStefano AL, Prakash R,

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Neurology 67(12):2206-10, 2006 Dec 26 - Who cited this? | PubMed ID: 17190945 | Fulltext

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.

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Sun M, Latourelle JC, Wooten GF, Lew MF, Klein C, Shill HA, Golbe LI, Mark MH, Racette BA, Perlmutter JS, Parsian A, Guttman M, Nicholson G, Xu G, Wilk JB, Saint-Hilaire MH,

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Archives of neurology 63(6):826-32, 2006 Jun - Who cited this? | PubMed ID: 16769863 | Fulltext

Genome-wide scan for white matter hyperintensity: the Framingham Heart Study.

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Destefano AL, Atwood LD, Massaro JM, Heard-Costa N, Beiser A, Au R, Wolf PA, and DeCarli C

Stroke; a journal of cerebral circulation 37(1):77, 2006 Jan - Who cited this? | PubMed ID: 16322484 | Fulltext

BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study.

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Karamohamed S, Latourelle JC, Racette BA, Perlmutter JS, Wooten GF, Lew M, Klein C, Shill H, Golbe LI, Mark MH, Guttman M, Nicholson G, Wilk JB, Saint-Hilaire M, DeStefano AL, Prakash R,

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Neurology 65(11):1823-5, 2005 Dec 13 - Who cited this? | PubMed ID: 16344533 | Fulltext

Association of NEDD4L ubiquitin ligase with essential hypertension.

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Russo CJ, Melista E, Cui J, DeStefano AL, Bakris GL, Manolis AJ, Gavras H, and Baldwin CT

Hypertension 46(3):488-91, 2005 Sep - Who cited this? | PubMed ID: 16103266 | Fulltext

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study.

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Karamohamed S, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Liu J, Shoemaker CM, Wilk JB, DeStefano AL,

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Movement disorders : official journal of the Movement Disorder Society 20(9):1188-91, 2005 Sep - Who cited this? | PubMed ID: 15966003 | Fulltext

Heritability and a genome-wide linkage scan for arterial stiffness, wave reflection, and mean arterial pressure: the Framingham Heart Study.

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Mitchell GF, DeStefano AL, Larson MG, Benjamin EJ, Chen MH, Vasan RS, Vita JA, and Levy D

Circulation 112(2):194-9, 2005 Jul 12 - Who cited this? | PubMed ID: 15998672 | Fulltext

Sequence variation of bradykinin receptors B1 and B2 and association with hypertension.

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Cui J, Melista E, Chazaro I, Zhang Y, Zhou X, Manolis AJ, Baldwin CT, Destefano AL, and Gavras H

Journal of hypertension 23(1):55-62, 2005 Jan - Who cited this? | PubMed ID: 15643125 | Fulltext

Polymorphisms in the promoter region of catalase gene and essential hypertension.

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Zhou XF, Cui J, DeStefano AL, Chazaro I, Farrer LA, Manolis AJ, Gavras H, and Baldwin CT

Disease markers 21(1):3-7, 2005 - Who cited this? | PubMed ID: 15735318 | Fulltext

Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios.

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Guo CY, DeStefano AL, Lunetta KL, Dupuis J, and Cupples LA

Human heredity 59(3):125-35, 2005 - Who cited this? | PubMed ID: 15867473 | Fulltext

APOE epsilon4 is associated with obstructive sleep apnea/hypopnea: the Sleep Heart Health Study.

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Gottlieb DJ, DeStefano AL, Foley DJ, Mignot E, Redline S, Givelber RJ, and Young T

Neurology 63(4):664-8, 2004 Aug 24 - Who cited this? | PubMed ID: 15326239 | Fulltext

Genome-wide scan for pulse pressure in the National Heart, Lung and Blood Institute's Framingham Heart Study.

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DeStefano AL, Larson MG, Mitchell GF, Benjamin EJ, Vasan RS, Li J, Corey D, and Levy D

Hypertension 44(2):152-5, 2004 Aug - Who cited this? | PubMed ID: 15210652 | Fulltext

Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study.

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Jiang Y, Wilk JB, Borecki I, Williamson S, DeStefano AL, Xu G, Liu J, Ellison RC, Province M, and Myers RH

American journal of human genetics 75(2):220-30, 2004 Aug - Who cited this? | PubMed ID: 15197684 | Fulltext

A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study.

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Karamohamed S, DeStefano AL, Wilk JB, Shoemaker CM, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Sullivan KM,

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Neurology 61(11):1557-61, 2003 Dec 9 - Who cited this? | PubMed ID: 14663042 | Fulltext

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

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Wilk JB, DeStefano AL, Joost O, Myers RH, Cupples LA, Slater K, Atwood LD, Heard-Costa NL, Herbert A, O'Connor GT, and Gottlieb DJ

Human molecular genetics 12(21):2745-51, 2003 Nov 1 - Who cited this? | PubMed ID: 12966033 | Fulltext

Association of polymorphisms in the promoter region of the PNMT gene with essential hypertension in African Americans but not in whites.

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Cui J, Zhou X, Chazaro I, DeStefano AL, Manolis AJ, Baldwin CT, and Gavras H

American journal of hypertension : journal of the American Society of Hypertension 16(10):859-63, 2003 Oct - Who cited this? | PubMed ID: 14553966 | Fulltext

Genetic variants of WNK4 in whites and African Americans with hypertension.

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Erlich PM, Cui J, Chazaro I, Farrer LA, Baldwin CT, Gavras H, and DeStefano AL

Hypertension 41(6):1191-5, 2003 Jun - Who cited this? | PubMed ID: 12719438 | Fulltext

A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study.

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Wilk JB, DeStefano AL, Arnett DK, Rich SS, Djousse L, Crapo RO, Leppert MF, Province MA, Cupples LA, Gottlieb DJ, and Myers RH

American journal of respiratory and critical care medicine 167(11):1528-33, 2003 Jun 1 - Who cited this? | PubMed ID: 12637344 | Fulltext

Genomewide linkage analysis to presbycusis in the Framingham Heart Study.

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DeStefano AL, Gates GA, Heard-Costa N, Myers RH, and Baldwin CT

Archives of otolaryngology--head & neck surgery 129(3):285-9, 2003 Mar - Who cited this? | PubMed ID: 12622536 | Fulltext

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

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Yang Q, Chazaro I, Cui J, Guo CY, Demissie S, Larson M, Atwood LD, Cupples LA, and DeStefano AL

BMC genetics 4 Suppl 1:S29, 2003 - Who cited this? | PubMed ID: 14975097 | Fulltext

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

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Van Laer L, DeStefano AL, Myers RH, Flothmann K, Thys S, Fransen E, Gates GA, Van Camp G, and Baldwin CT

European journal of human genetics : EJHG 10(12):883-6, 2002 Dec - Who cited this? | PubMed ID: 12461698 | Fulltext

PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study.

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Destefano AL, Lew MF, Golbe LI, Mark MH, Lazzarini AM, Guttman M, Montgomery E, Waters CH, Singer C, Watts RL, Currie LJ, Wooten GF, Maher NE, Wilk JB, Sullivan KM, Slater KM,

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American journal of human genetics 70(5):1089, 2002 May - Who cited this? | PubMed ID: 11920285 | Fulltext

Genome-wide scan for Parkinson's disease: the GenePD Study.

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DeStefano AL, Golbe LI, Mark MH, Lazzarini AM, Maher NE, Saint-Hilaire M, Feldman RG, Guttman M, Watts RL, Suchowersky O, Lafontaine AL, Labelle N, Lew MF, Waters CH, Growdon JH, Singer C,

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Neurology 57(6):1124-6, 2001 Sep 25 - Who cited this? | PubMed ID: 11571351 | Fulltext

Maternal component in the familial aggregation of hypertension.

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DeStefano AL, Gavras H, Heard-Costa N, Bursztyn M, Manolis A, Farrer LA, Baldwin CT, Gavras I, and Schwartz F

Clinical genetics 60(1):13-21, 2001 Jul - Who cited this? | PubMed ID: 11531965 | Fulltext

Family-based association tests for qualitative and quantitative traits using single-nucleotide polymorphism and microsatellite data.

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Wilk JB, Volcjak JS, Myers RH, Maher NE, Knowlton BA, Heard-Costa NL, Demissie S, Cupples LA, and DeStefano AL

Genetic epidemiology 21 Suppl 1:S364-9, 2001 - Who cited this? | PubMed ID: 11793700 | Fulltext

Influence of marker heterozygosity and genetic heterogeneity on fine mapping.

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Heard-Costa NL, Demissie S, DeStefano AL, Knowlton BA, Maher NE, Myers RH, Volcjak JS, Wilk JB, and Cupples LA

Genetic epidemiology 21 Suppl 1:S467-72, 2001 - Who cited this? | PubMed ID: 11793720 | Fulltext

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study.

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Levy D, Destefano AL, Larson MG, O'Donnell CJ, Lifton RP, Gavras H, Cupples LA, and Myers RH

Hypertension 36(4):477, 2000 Oct - Who cited this? | PubMed ID: 11040222 | Fulltext

Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study.

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Shearman AM, Ordovas JM, Cupples LA, Schaefer EJ, Harmon MD, Shao Y, Keen JD, DeStefano AL, Joost O, Wilson PW, Housman DE, and Myers RH

Human molecular genetics 9(9):1315-20, 2000 May 22 - Who cited this? | PubMed ID: 10814713 | Fulltext

Genetic predisposition to stroke in relatives of hypertensives.

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Nicolaou M, DeStefano AL, Gavras I, Cupples LA, Manolis AJ, Baldwin CT, Gavras H, and Farrer LA

Stroke; a journal of cerebral circulation 31(2):487-92, 2000 Feb - Who cited this? | PubMed ID: 10657427 | Fulltext

Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension.

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Baldwin CT, Schwartz F, Baima J, Burzstyn M, DeStefano AL, Gavras I, Handy DE, Joost O, Martel T, Manolis A, Nicolaou M, Bresnahan M, Farrer L, and Gavras H

American journal of hypertension : journal of the American Society of Hypertension 12(9 Pt 1):853-7, 1999 Sep - Who cited this? | PubMed ID: 10509541 | Fulltext

Evidence for linkage between essential hypertension and a putative locus on human chromosome 17.

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Baima J, Nicolaou M, Schwartz F, Destefano AL, Manolis A, Gavras I, Laffer C, Elijovich F, Farrer L, Baldwin CT, and Gavras H

Hypertension 34(1):4, 1999 Jul - Who cited this? | PubMed ID: 10406815 | Fulltext

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

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Nicolaou M, Premkumar S, DeStefano AL, Farrer LA, and Cupples LA

Genetic epidemiology 17 Suppl 1:S679-84, 1999 - Who cited this? | PubMed ID: 10597513 | Fulltext

Stratification techniques to explore genotype environment interactions.

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Wilk JB, Premkumar S, Nicolaou M, Myers RH, Maher NE, Harmon MD, Farrer LA, DeStefano AL, Cupples LA, and Couropmitree NN

Genetic epidemiology 17 Suppl 1:S761-6, 1999 - Who cited this? | PubMed ID: 10597527 | Fulltext

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