Publications - Mariza de Andrade, Ph.D.

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1. Couch FJ, Wang X, McWilliams RR, Bamlet WR, de Andrade M, Petersen GM. Association of breast cancer susceptibility variants with risk of pancreatic cancer. Cancer Epidemiol Biomarkers Prev 2009 Nov; 18(11):3044-8. Epub 2009 Oct 20.
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2. Liu Y, Liu PY, Wen WD, James MA, Wang Y, Bailey-Wilson JE, Amos CI, Pinney SM, Yang P, de Andrade M, Petersen GM, Wiest JS, Fain PR, Schwartz AG, Gazdar A, Gaba C, Rothschild H, Mandal D, Kupert E, Lee J, Seminara D, Minna J, Anderson MW, You M. Haplotype and cell proliferation analyses of candidate lung cancer susceptibility genes on chromosome 15q24-25.1. Cancer Res 2009 Oct 1; 69(19):7844-50.
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3. Lindor NM, Yang P, Evans I, Schowalter K, De Andrade M, Li J, Jeavons E, Peterson G, Gallinger S, Bapat B, Hopper J, Jass J, Jenkins M, Templeton A, Potter J, Newcomb PA, Lemarchand L, Grove J, Haile R, Baron J, Seminara D, Limburg P, Thibodeau SN. Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: A study from the colon cancer family registry. Mol Genet Metab 2009 Sep 27. [Epub ahead of print]
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4. Brauch KM, Karst ML, Herron KJ, de Andrade M, Pellikka PA, Rodeheffer RJ, Michels VV, Olson TM. Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy. J Am Coll Cardiol 2009 Sep 1; 54(10):930-41.
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5. Pannala R, Leibson CL, Rabe KG, Timmons LJ, Ransom J, de Andrade M, Petersen GM, Chari ST. Temporal association of changes in fasting blood glucose and body mass index with diagnosis of pancreatic cancer. Am J Gastroenterol 2009 Sep; 104(9):2318-25. Epub 2009 Jun 09.
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6. Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, Fuchs CS, Petersen GM, Arslan AA, Bueno-De-Mesquita HB, Gross M, Helzlsouer K, Jacobs EJ, LaCroix A, Zheng W, Albanes D, Bamlet W, Berg CD, Berrino F, Bingham S, Buring JE, Bracci PM, Canzian F, Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat Genet 2009 Sep; 41(9):986-NIL_47.
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7. Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, Fuchs CS, Petersen GM, Arslan AA, Bueno-de-Mesquita HB, Gross M, Helzlsouer K, Jacobs EJ, LaCroix A, Zheng W, Albanes D, Bamlet W, Berg CD, Berrino F, Bingham S, Buring JE, Bracci PM, Canzian F, Clavel-Chap Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat Genet 2009 Sep; 41(9):986-90 Epub 2009 Aug 2.
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8. Pannala R, Leibson CL, Rabe KG, Timmons LJ, Ransom J, de Andrade M, Petersen GM, Chari ST. Temporal association of changes in fasting blood glucose and body mass index with diagnosis of pancreatic cancer. Am J Gastroenterol 2009 Sep; 104(9):2318-25 Epub 2009 Jun 9.
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9. McWilliams RR, Bamlet WR, de Andrade M, Rider DN, Couch FJ, Cunningham JM, Matsumoto ME, Rabe KG, Hammer TJ, Petersen GM. Polymorphic variants in hereditary pancreatic cancer genes are not associated with pancreatic cancer risk. Cancer Epidemiol Biomarkers Prev 2009 Sep; 18(9):2549-52. Epub 2009 Aug 18.
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10. Brighina L, Schneider NK, Lesnick TG, de Andrade M, Cunningham JM, Mrazek D, Rocca WA, Maraganore DM. Alpha-synuclein, alcohol use disorders, and Parkinson disease: a case-control study. Parkinsonism Relat Disord 2009 Jul; 15(6):430-4. Epub 2009 Feb 04.
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11. Brighina L, Schneider NK, Lesnick TG, de Andrade M, Cunningham JM, Mrazek D, Rocca WA, Maraganore DM. Alpha-synuclein, alcohol use disorders, and Parkinson disease: a case-control study. Parkinsonism Relat Disord 2009 Jul; 15(6):430-4. Epub 2009 Feb 04.
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12. Turner ST, Fornage M, Jack CR Jr, Mosley TH, Knopman DS, Kardia SL, Boerwinkle E, de Andrade M. Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships. Arch Neurol 2009 Jul; 66(7):847-57.
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13. You M, Wang D, Liu P, Vikis H, James M, Lu Y, Wang Y, Wang M, Chen Q, Jia D, Liu Y, Wen W, Yang P, Sun Z, Pinney SM, Zheng W, Shu XO, Long J, Gao YT, Xiang YB, Chow WH, Rothman N, Petersen GM, de Andrade M, Wu Y, Cunningham JM, Wiest JS, Fain PR, Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene. Clin Cancer Res 2009 Apr 15; 15(8):2666-74. Epub 2009 Apr 07.
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14. You M, Wang DL, Liu PY, Vikis H, James M, Lu Y, Wang Y, Wang M, Chen QO, Jia DM, Wen WD, Yang P, Sun ZF, Pinney SM, Zheng W, Shu XO, Long J, Gao YT, Xiang YB, Chow WH, Rothman N, Petersen GM, de Andrade M, Wu YH, Cunningham JM, et al. Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene. Clin Cancer Res 2009 Apr 15; 15(8):2666-74.
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15. McWilliams RR, Bamlet WR, de Andrade M, Rider DN, Cunningham JM, Petersen GM. Nucleotide excision repair pathway polymorphisms and pancreatic cancer risk: evidence for role of MMS19L. Cancer Epidemiol Biomarkers Prev 2009 Apr; 18(4):1295-302. Epub 2009 Mar 24.
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16. Brighina L, Schneider NK, Lesnick TG, de Andrade M, Cunningham JM, Mrazek D, Rocca WA, Maraganore DM. alpha-Synuclein, alcohol use disorders, and Parkinson disease: A case-control study. Parkinsonism Relat Disord 2009 Feb 2 Epub 2009 Feb 2.
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17. Giolo SR, Pereira AC, de Andrade M, de Oliveira CM, Krieger JE, Soler JM. Genetic analysis of age-at-onset for cardiovascular risk factors in a Brazilian family study. Hum Hered 2009; 68(2):131-8 Epub 2009 May 11.
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18. Ruiz Giolo S, Pereira AC, de Andrade M, de Oliveira CM, Krieger JE, Soler JM. Genetic analysis of age-at-onset for cardiovascular risk factors in a Brazilian family study. Hum Hered 2009; 68(2):131-8. Epub 2009 May 11.
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19. Giolo SR, Pereira AC, de Andrade M, de Oliveira CM, Krieger JE, Soler JMP. Genetic analysis of age-at-onset for cardiovascular risk factors in a Brazilian family study. Hum Hered 2009; 68(2):131-8.
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20. Rocca WA, Grossardt BR, Geda YE, Gostout BS, Bower JH, Maraganore DM, de Andrade M, Melton LJ 3rd. Long-term risk of depressive and anxiety symptoms after early bilateral oophorectomy. Menopause 2008 Nov-Dec; 15(6):1050-9.
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21. Facheris MF, Schneider NK, Lesnick TG, de Andrade M, Cunningham JM, Rocca WA, Maraganore DM. Coffee, caffeine-related genes, and Parkinson's disease: a case-control study. Mov Disord 2008 Oct 30; 23(14):2033-40.
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22. Liu P, Vikis HG, Wang D, Lu Y, Wang Y, Schwartz AG, Pinney SM, Yang P, de Andrade M, Petersen GM, Wiest JS, Fain PR, Gazdar A, Gaba C, Rothschild H, Mandal D, Coons T, Lee J, Kupert E, Seminara D, Minna J, Bailey-Wilson JE, Wu X, Spitz MR, Eisen T, Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. J Natl Cancer Inst 2008 Sep 17; 100(18):1326-30. Epub 2008 Sep 09.
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23. Halfdanarson TR, Wang L, Bamlet WR, de Andrade M, McWilliams RR, Cunningham JM, Petersen GM. Mitochondrial genetic polymorphisms do not predict survival in patients with pancreatic cancer. Cancer Epidemiol Biomarkers Prev 2008 Sep; 17(9):2512-3.
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24. Xing J, Chen M, Wood CG, Lin J, Spitz MR, Ma J, Amos CI, Shields PG, Benowitz NL, Gu J, de Andrade M, Swan GE, Wu X. Mitochondrial DNA content: its genetic heritability and association with renal cell carcinoma. J Natl Cancer Inst 2008 Aug 6; 100(15):1104-12. Epub 2008 Jul 29.
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25. Xing JL, Chen M, Wood CG, Lin J, Spitz MR, Ma JZ, Amos CI, Shields PG, Benowitz NL, Gu J, de Andrade M, Swan GE, Wu XF. Mitochondrial DNA content: Its genetic heritability and association with renal cell carcinoma. J Natl Cancer Inst 2008 Aug 6; 100(15):1104-12.
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26. Hodgson-Zingman DM, Karst ML, Zingman LV, Heublein DM, Darbar D, Herron KJ, Ballew JD, de Andrade M, Burnett JC Jr, Olson TM. Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation. N Engl J Med 2008 Jul 10; 359(2):158-65.
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27. Saito YA, Zimmerman JM, Harmsen WS, De Andrade M, Locke GR 3rd, Petersen GM, Talley NJ. Irritable bowel syndrome aggregates strongly in families: a family-based case-control study. Neurogastroenterol Motil 2008 Jul; 20(7):790-7.
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28. Hodgson-Zingman DM, Karst ML, Zingman LV, Heublein DM, Darbar D, Herron KJ, Ballew JB, de Andrade M, Burnett JC, Olson TM. Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation. New Engl J Med 2008 Jul; 359(2):158-65.
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29. McWilliams RR, Bamlet WR, Petersen GM, Goode EL, Boardman LA, de Andrade M, Cunningham JM. Polymorphisms in DNA repair genes smoking, and pancreatic adenocarcinoma risk. Cancer Research 2008 Jun 15; 68(12). Epub 2008 Jun 10.
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30. McWilliams RR, Bamlet WR, Cunningham JM, Goode EL, de Andrade M, Boardman LA, Petersen GM. Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk. Cancer Res 2008 Jun 15; 68(12):4928-35. Epub 2008 Jun 10.
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31. Yang P, Sun Z, Krowka MJ, Aubry MC, Bamlet WR, Wampfler JA, Thibodeau SN, Katzmann JA, Allen MS, Midthun DE, Marks RS, de Andrade M. Alpha1-antitrypsin deficiency carriers, tobacco smoke, chronic obstructive pulmonary disease, and lung cancer risk. Arch Intern Med 2008 May 26; 168(10):1097-103.
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32. Yang P, Sun Z, Krowka MJ, Aubry MC, Bamlet WR, Wampfler JA, Thibodeau SN, Katzmann JA, Allen MS, Midthun DE, Marks RS, de Andrade M. Alpha1-antitrypsin deficiency carriers, tobacco smoke, chronic obstructive pulmonary disease, and lung cancer risk. Arch Intern Med 2008 May 26; 168(10):1097-103.
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33. Brighina L, Frigerio R, Schneider NK, Lesnick TG, de Andrade M, Cunningham JM, Farrer MJ, Lincoln SJ, Checkoway H, Rocca WA, Maraganore DM. Alpha-synuclein, pesticides, and Parkinson disease: a case-control study. Neurology 2008 Apr 15; 70(16 Pt 2):1461-9. Epub 2008 Mar 05.
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34. Kantarci OH, Hebrink DD, Schaefer-Klein J, Sun Y, Achenbach S, Atkinson EJ, Heggarty S, Cotleur AC, de Andrade M, Vandenbroeck K, Pelfrey CM, Weinshenker BG. Interferon gamma allelic variants: sex-biased multiple sclerosis susceptibility and gene expression. Arch Neurol 2008 Mar; 65(3):349-57.
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35. Ding K, Feng D, de Andrade M, Mosley TH Jr, Turner ST, Boerwinkle E, Kullo IJ. Genomic regions that influence plasma levels of inflammatory markers in hypertensive sibships. J Hum Hypertens 2008 Feb; 22(2):102-10. Epub 2007 Oct 25.
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36. Ding K, Feng D, de Andrade M, Mosley TH Jr, Turner ST, Boerwinkle E, Kullo IJ. Genomic regions that influence plasma levels of inflammatory markers in hypertensive sibships. J Hum Hypertens 2008 Feb; 22(2):102-10. Epub 2007 Oct 25.
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37. Rocca WA, Bower JH, Maraganore DM, Ahlskog JE, Grossardt BR, de Andrade M, Melton LJ 3rd. Increased risk of parkinsonism in women who underwent oophorectomy before menopause. Neurology 2008 Jan 15; 70(3):200-9. Epub 2007 Aug 29.
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38. Chari ST, Leibson CL, Rabe KG, Timmons LJ, Ransom J, de Andrade M, Petersen GM. Pancreatic cancer-associated diabetes mellitus: prevalence and temporal association with diagnosis of cancer. Gastroenterology 2008 Jan; 134(1):95-101 Epub 2007 Oct 26.
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39. Fridley BL, de Andrade M. Missing phenotype data imputation in pedigree data analysis. Genet Epidemiol 2008 Jan; 32(1):52-60.
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40. Barahmani N, de Andrade M, Slusser JP, Wei Q, Hordinsky M, Price VH, Christiano A, Norris D, Reveille J, Duvic M. Human Leukocyte antigen class II alleles are associated with risk of alopecia areata. J Invest Dermatol 2008 Jan; 128(1):240-3 Epub 2007 Jul 19.
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41. Fridley BL, de Andrade M. Missing phenotype data imputation in pedigree data analysis. Genet Epidemiol 2008 Jan; 32(1):52-60.
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42. Chari ST, Leibson CL, Rabe KG, Timmons LJ, Ransom J, de Andrade M, Petersen GM. Pancreatic cancer-associated diabetes mellitus: prevalence and temporal association with diagnosis of cancer. Gastroenterology 2008 Jan; 134(1):95-101. Epub 2007 Oct 26.
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43. de Oliveira CM, Pereira AC, de Andrade M, Soler JM, Krieger JE. Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study. BMC Med Genet 2008; 9:32. Epub 2008 Apr 22.
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44. de Oliveira CM, Pereira AC, de Andrade M, Soler JM, Krieger JE. Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study. BMC Med Genet 2008; 9:32. Epub 2008 Apr 22.
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45. Pongprasobchai S, Pannala R, Smyrk TC, Bamlet W, Pitchumoni S, Ougolkov A, de Andrade M, Petersen GM, Chari ST. Long-term survival and prognostic indicators in small (View PubMed
46. Goode EL, Cherny SS, Christian JC, Jarvik GP, de Andrade M. Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins. Twin Res Hum Genet 2007 Oct; 10(5):703-11.
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47. Lin J, Swan GE, Shields PG, Benowitz NL, Gu J, Amos CI, de Andrade M, Spitz MR, Wu X. Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: genotype-phenotype correlation. Cancer Epidemiol Biomarkers Prev 2007 Oct; 16(10):2065-71.
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48. Goode EL, Cherny SS, Christian JC, Jarvik GP, de Andrade M. Longitudinal changes in heritability of body mass index and lipid and lipoprotein levels in aging twins. Twin Research and Human Genetics 2007 Oct; 10(5):703-11.
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49. Lin J, Swan GE, Shields PG, Benowitz NL, Gu J, Amos CI, de Andrade M, Spitz MR, Wu X. Mutagen sensitivity and genetic variants in nucleotide excision repair pathway: genotype-phenotype correlation. Cancer Epidemiol Biomarkers Prev 2007 Oct; 16(10):2065-71.
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50. Rocca WA, Bower JH, Maraganore DM, Ahlskog JE, Grossardt BR, de Andrade M, Melton LJ 3rd. Increased risk of cognitive impairment or dementia in women who underwent oophorectomy before menopause. Neurology 2007 Sep 11; 69(11):1074-83. Epub 2007 Aug 29.
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51. Saunders CL, Chiodini BD, Sham P, Lewis CM, Abkevich V, Adeyemo AA, de Andrade M, Arya R, Berenson GS, Blangero J, Boehnke M, Borecki IB, Chagnon YC, Chen W, Comuzzie AG, Deng HW, Duggirala R, Feitosa MF, Froguel P, Hanson RL, Hebebrand J, Huezo-Dias P, K Meta-analysis of genome-wide linkage studies in BMI and obesity. Obesity (Silver Spring) 2007 Sep; 15(9):2263-75.
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52. Lazaridis KN, Juran BD, Boe GM, Slusser JP, de Andrade M, Homburger HA, Ghosh K, Dickson ER, Lindor KD, Petersen GM. Increased prevalence of antimitochondrial antibodies in first-degree relatives of patients with primary biliary cirrhosis. Hepatology 2007 Sep; 46(3):785-92.
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53. Rocca WA, Bower JH, Maraganore DM, Ahlskog JE, Grossardt BR, de Andrade M, Melton LJ. Increased risk of Parkinson in women who underwent oophorectomy before menopause. Neurology. Epub ahead of print. 2007 Aug 29.
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54. Wang L, Bamlet WR, de Andrade M, Boardman LA, Cunningham JM, Thibodeau SN, Petersen GM. Mitochondrial genetic polymorphisms and pancreatic cancer risk. Cancer Epidemiol Biomarkers Prev 2007 Jul; 16(7):1455-9.
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55. Brighina L, Okubadejo NU, Schneider NK, Lesnick TG, de Andrade M, Cunningham JM, Farrer MJ, Lincoln SJ, Rocca WA, Maraganore DM. Beta-synuclein gene variants and Parkinson's disease: a preliminary case-control study. Neurosci Lett 2007 Jun 15; 420(3):229-34. Epub 2007 May 21.
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56. Lesnick TG, Papapetropoulos S, Mash DC, Ffrench-Mullen J, Shehadeh L, de Andrade M, Henley JR, Rocca WA, Ahlskog JE, Maraganore DM. A genomic pathway approach to a complex disease: axon guidance and Parkinson's disease. PLoS Genet 2007 Jun; 3(6):e98.
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57. Lesnick TG, Papapetropoulos S, Mash DC, Ffrench-Mullen J, Shehadeh L, de Andrade M, Henley JR, Rocca WA, Ahlskog JE, Maraganore DM. A genomic pathway approach to a complex disease: axon guidance and Parkinson disease. PLoS Genet 2007 Jun; 3(6):e98.
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58. Saito YA, Locke GR 3rd, Zimmerman JM, Holtmann G, Slusser JP, de Andrade M, Petersen GM, Talley NJ. A genetic association study of 5-HTT LPR and GNbeta3 C825T polymorphisms with irritable bowel syndrome. Neurogastroenterol Motil 2007 Jun; 19(6):465-70.
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59. Vikis H, Sato M, James M, Wang D, Wang Y, Wang M, Jia D, Liu Y, Bailey-Wilson JE, Amos CI, Pinney SM, Petersen GM, de Andrade M, Yang P, Wiest JS, Fain PR, Schwartz AG, Gazdar A, Gaba C, Rothschild H, Mandal D, Kupert E, Seminara D, Viswanathan A, Govinda EGFR-T790M is a rare lung cancer susceptibility allele with enhanced kinase activity. Cancer Res 2007 May 15; 67(10):4665-70.
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60. Frigerio R, Breteler MM, de Lau LM, Sanft KR, Bower JH, Ahlskog JE, Grossardt BR, de Andrade M, Maraganore DM, Rocca WA. Number of children and risk of Parkinson's disease. Mov Disord 2007 Apr 15; 22(5):632-9.
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61. Frigerio R, Breteler MM, de Lau LM, Sanft KR, Bower JH, Ahlskog JE, Grossardt BR, de Andrade M, Maraganore DM, Rocca WA. Number of children and risk of Parkinson's disease. Mov Disord 2007 Apr 15; 22(5):632-9.
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62. Klein AP, de Andrade M, Hruban RH, Bondy M, Schwartz AG, Gallinge SGr, Lynch HT, Syngal S, Rabe KG, Goggins MG, Petersen GM. Linkage analysis of chromosome 4 in families with familial pancreatic cancer. Cancer Biology and Therapy 2007 March; 6(3):320-323.
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63. Klein AP, de Andrade M, Hruban RH, Bondy M, Schwartz AG, Gallinger S, Lynch HT, Syngal S, Rabe KG, Goggins MG, Petersen GM. Linkage analysis of chromosome 4 in families with familial pancreatic cancer. Cancer Biol Ther 2007 Mar; 6(3):320-3. Epub 2007 Mar 15.
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64. Couch FJ, Johnson MR, Rabe KG, Brune K, de Andrade M, Goggins M, Rothenmund H, Gallinger S, Klein A, Petersen GM, Hruban RH. The prevalence of BRCA2 mutations in familial pancreatic cancer. Cancer Epidemiol Biomarkers Prev 2007 Feb; 16(2):342-6.
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65. Wang M, Vikis HG, Wang Y, Jia DM, Wang DL, Bierut LJ, Bailey-Wilson JE, Amos CI, Pinney SM, Petersen GM, de Andrade M, Yang P, Wiest JS, Fain PR, Schwartz AG, Gazdar A, Minna J, Gaba C, Rothschild H, Mandal D, Kupert E, Seminara D, Liu Y, Viswanathan A, Identification of a novel tumor suppressor gene p34 on human chromosome 6q25.1. Cancer Res 2007 Jan 1; 67(1):93-9.
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66. Fornage M, Mosley TH, Jack CR, de Andrade M, Kardia SLR, Boerwinkle E, Turner ST. Family-based association study of matrix metalloproteinase-3 and-9 haplotypes with susceptibility to ischemic white matter injury. Hum Genet 2007 Jan; 120(5):671-80.
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67. de Andrade M, Allen AS. Summary of contributions to GAW15 Group 13: Candidate gene association studies. Genet Epidemiol 2007; 31(Suppl 1):S110-7.
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68. Cordell HJ, de Andrade M, Babron MC, Bartlett CW, Beyene J, Bickeboller H, Culverhouse R, Cupples LA, Daw EW, Dupuis J, Falk CT, Ghosh S, Goddard KA, Goode EL, Hauser ER, Martin LJ, Martinez M, North KE, Saccone NL, Schmidt S, Tapper W, Thomas D, Tritchle Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc 2007; 1 Suppl 1:S1 Epub 2007 Dec 18.
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69. de Andrade M, Atkinson EJ, Fridley BL, Goode EL, McDonnell S, Liu-Mares W, Rabe KG, Sun Z, Slager SL. The genetics of gene expression: comparison of linkage scans using two phenotype normalization methods. BMC Proc 2007; 1 Suppl 1:S151. Epub 2007 Dec 18.
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70. Ye Z, Atkinson EJ, Fridley BL, de Andrade M. Comparison of variable and model selection methods for genetic association studies using the GAW15 simulated data. BMC Proc 2007; 1 Suppl 1:S34. Epub 2007 Dec 18.
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71. Atkinson EJ, Fridley BL, Goode EL, McDonnell SK, Liu-Mares W, Rabe KG, Sun Z, Slager SL, de Andrade M. Linkage analysis using principal components of gene expression data. BMC Proc 2007; 1(Suppl 1):S79 Epub 2007 Dec 18.
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72. Goode EL, Fridley BL, Sun Z, Atkinson EJ, Nord AS, McDonnell SK, Jarvik GP, de Andrade M, Slager SL. Comparison of tagging single-nucleotide polymorphism methods in association analyses. BMC Proc 2007; 1 Suppl 1:S6 Epub 2007 Dec 18.
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73. Cordell HJ, de Andrade M, Babron MC, Bartlett CW, Beyene J, Bickeböller H, Culverhouse R, Cupples LA, Daw EW, Dupuis J, Falk CT, Ghosh S, Goddard KA, Goode EL, Hauser ER, Martin LJ, Martinez M, North KE, Saccone NL, Schmidt S, Tapper W, Thomas D, Tri Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci. BMC Proc 2007; 1(Suppl 1):S1 Epub 2007 Dec 18.
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74. Liu-Mares W, Sun Z, Bamlet WR, Atkinson EJ, Fridley BL, Slager SL, de Andrade M, Goode EL. Analysis of variation in NF-kappaB genes and expression levels of NF-kappaB-regulated molecules. BMC Proc 2007; 1 Suppl 1:S126. Epub 2007 Dec 18.
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75. de Andrade M, Allen AS, Brinza D, Cheng R, Da Y, de Vries AR, Ewhida A, Feng Z, Jung H, Hsieh HJ, Kohler K, Liu Y, Liu-Mares W, Luan J, Marquard V, Nolte IM, Oh S, Platt A, Qin X, Yoo YJ, Yuan A, Tian X, Won S. Summary of contributions to GAW15 Group 13: candidate gene association studies. Genet Epidemiol 2007; 31 Suppl 1:S110-7.
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76. Frigerio R, Sanft KR, Grossardt BR, Peterson BJ, Elbaz A, Bower JH, Ahlskog JE, de Andrade M, Maraganore DM, Rocca WA. Chemical exposures and Parkinson's disease: a population-based case-control study. Mov Disord 2006 Oct; 21(10):1688-92.
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77. Rocca WA, Grossardt BR, de Andrade M, Malkasian GD, Melton LJ 3rd. Survival patterns after oophorectomy in premenopausal women: a population-based cohort study. Lancet Oncol 2006 Oct; 7(10):821-8.
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78. McWilliams RR, Bamlet WR, Rabe KG, Olson JE, de Andrade M, Petersen GM. Association of family history of specific cancers with a younger age of onset of pancreatic adenocarcinoma. Clin Gastroenterol Hepatol 2006 Sep; 4(9):1143-7. Epub 2006 Jul 24.
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79. Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Kruger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, Ferrarese C, Hadjigeorgiou G, Hattori N, Kawakami H, Lambert JC, Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. JAMA 2006 Aug 9; 296(6):661-70.
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80. Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Kruger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, Ferrarese C, Hadjigeorgiou G, Hattori N, Kawakami H, Lambert JC, Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. JAMA 2006 Aug 9; 296(6):661-70.
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81. Kullo IJ, Turner ST, Kardia SL, Mosley TH Jr, Boerwinkle E, de Andrade M. A genome-wide linkage scan for ankle-brachial index in African American and non-Hispanic white subjects participating in the GENOA study. Atherosclerosis 2006 Aug; 187(2):433-8. Epub 2005 Nov 08.
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82. Kantarci OH, Barcellos LF, Atkinson EJ, Ramsay PP, Lincoln R, Achenbach SJ, De Andrade M, Hauser SL, Weinshenker BG. Men transmit MS more often to their children vs women: the Carter effect. Neurology 2006 Jul 25; 67(2):305-10.
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83. Turner ST, Kardia SL, Mosley TH, Rule AD, Boerwinkle E, de Andrade M. Influence of genomic loci on measures of chronic kidney disease in hypertensive sibships. J Am Soc Nephrol 2006 Jul; 17(7):2048-55. Epub 2006 Jun 14.
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84. Kullo IJ, Ding K, Boerwinkle E, Turner ST, de Andrade M. Quantitative trait loci influencing low density lipoprotein particle size in African Americans. J Lipid Res 2006 Jul; 47(7):1457-62. Epub 2006 Apr 19.
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85. Kullo IJ, Ding K, Boerwinkle E, Turner ST, Mosley TH Jr, Kardia SL, de Andrade M. Novel genomic loci influencing plasma homocysteine levels. Stroke 2006 Jul; 37(7):1703-9. Epub 2006 Jun 01.
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86. Wu X, Spitz MR, Amos CI, Lin J, Shao L, Gu J, de Andrade M, Benowitz NL, Shields PG, Swan GE. Mutagen sensitivity has high heritability: evidence from a twin study. Cancer Res 2006 Jun 15; 66(12):5993-6.
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87. Saito YA, Talley NJ, de Andrade M, Petersen GM. Case-control genetic association studies in gastrointestinal disease: review and recommendations. Am J Gastroenterol 2006 Jun; 101(6):1379-89.
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88. Petersen GM, de Andrade M, Goggins M, Hruban RH, Bondy M, Korczak JF, Gallinger S, Lynch HT, Syngal S, Rabe KG, Seminara D, Klein AP. Pancreatic cancer genetic epidemiology consortium. Cancer Epidemiol Biomarkers Prev 2006 Apr; 15(4):704-10.
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89. Turner ST, Peyser PA, Kardia SL, Bielak LF, Sheedy PF 3rd, Boerwinkle E, de Andrade M. Genomic loci with pleiotropic effects on coronary artery calcification. Atherosclerosis 2006 Apr; 185(2):340-6. Epub 2005 Jul 27.
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90. Burnett MS, Strain KJ, Lesnick TG, de Andrade M, Rocca WA, Maraganore DM. Reliability of self-reported ancestry among siblings: implications for genetic association studies. Am J Epidemiol 2006 Mar 1; 163(5):486-92. Epub 2006 Jan 18.
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91. Barahmani N, de Andrade M, Slusser JP, Zhang Q, Duvic M. Major histocompatibility complex class I chain-related gene A polymorphisms and extended haplotypes are associated with familial alopecia areata. J Invest Dermatol 2006 Jan; 126(1):74-8.
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92. Rocca WA, Grossardt BR, Peterson BJ, Bower JH, Trenerry MR, Ahlskog JE, Sanft KR, de Andrade M, Maraganore DM. The Mayo Clinic cohort study of personality and aging: design and sampling, reliability and validity of instruments, and baseline description. Neuroepidemiology 2006; 26(3):119-29. Epub 2006 Jan 17.
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93. Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeboller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, Rice J, Satten G, Suarez B, Vieland V, Wilcox M, Zhang H, Ziegler A, MacCluer Genetic analysis workshop 14: Microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans. BMC Genetics 2005 Dec 30; 6(Suppl 1).
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94. Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeboller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, Rice J, Satten G, Suarez B, Vieland V, Wilcox M, Zhang H, Ziegler A, Maccluer Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans. BMC Genet 2005 Dec 30; 6 Suppl 1:S1. [Epub ahead of print]
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95. de Andrade M, Olswold CL, Slusser JP, Tordsen LA, Atkinson EJ, Rabe KG, Slager SL. Identification of genes involved in alcohol consumption and cigarettes smoking. BMC Genet 2005 Dec 30; 6(Suppl 1):S112.
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96. Kantarci OH, Morales Y, Ziemer PA, Hebrink DD, Mahad DJ, Atkinson EJ, Achenbach SJ, De Andrade M, Mack M, Ransohoff RM, Lassmann H, Bruck W, Weinshenker BG, Lucchinetti CF. CCR5 Delta 32 polymorphism effects on CCR5 expression, patterns of immunopathology and disease course in multiple sclerosis. J Neuroimmunol 2005 Dec; 169(1-2):137-43 Epub 2005 Sep 22.
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97. Frigerio R, Elbaz A, Sanft KR, Peterson BJ, Bower JH, Ahlskog JE, Grossardt BR, de Andrade M, Maraganore DM, Rocca WA. Education and occupations preceding Parkinson disease - A population-based case-control study. Neurology 2005 Nov 22; 65(10):1575-83.
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98. Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PVK, Frazer KA, Cox DR, Ballinger DG. High-resolution whole-genome association study of Parkinson disease. Am J Hum Genet 2005 Nov; 77(5):685-93.
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99. Kraja AT, Rao DC, Weder AB, Cooper R, Curb JD, Hanis CL, Turner ST, de Andrade M, Hsiung CA, Quertermous T, Zhu XF, Province MA. Two major QTLs and several others relate to factors of metabolic syndrome in the family blood pressure program. Hypertension 2005 Oct; 46(4):751-7.
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100. Chari ST, Leibson CL, Rabe KG, Ransom J, De Andrade M, Petersen GM. Probability of pancreatic cancer following diabetes: A population-based study. Gastroenterology 2005 Aug; 129(2):504-11.
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101. Kullo IJ, Turner ST, Boerwinkle E, Kardia SL, de Andrade M. A novel quantitative trait locus on chromosome 1 with pleiotropic effects on HDL-cholesterol and LDL particle size in hypertensive sibships. Am J Hypertens 2005 Aug; 18(8):1084-90.
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102. McWilliams RR, Rabe KG, Olsold C, De Andrade M, Petersen GM. Risk of malignancy in first-degree relatives of patients with pancreatic carcinoma. Cancer 2005 Jul 15; 104(2):388-94.
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103. Yang P, Bamlet WR, Sun Z, Ebbert JO, Aubry MC, Krowka MJ, Taylor WR, Marks RS, Deschamps C, Swensen SJ, Wieben ED, Cunningham JM, Melton LJ, de Andrade M. Alpha1-antitrypsin and neutrophil elastase imbalance and lung cancer risk. Chest 2005 Jul; 128(1):445-52.
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104. Yang P, Bamlet WR, Sun Z, Ebbert JO, Aubry MC, Taylor WR, Marks RS, Deschamps C, Swensen SJ, Wieben ED, Cunningham JM, Melton LJ, de Andrade M. Alpha1-antitrypsin and neutrophil elastase imbalance and lung cancer risk. Chest 2005 Jul; 128(1):445-52.
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105. Facheris M, Strain KJ, Lesnick TG, de Andrade M, Bower JH, Ahlskog JE, Cunningham JM, Lincoln S, Farrer MJ, Rocca WA, Maraganore DM. UCHL1 is associated with Parkinson's disease: A case-unaffected sibling and case-unrelated control study. Neurosci Lett 2005 Jun 10; 381(1-2):131-4.
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106. Facheris M, Strain KJ, Lesnick TG, de Andrade M, Bower JH, Ahlskog JE, Cunningham JM, Lincoln S, Farrer MJ, Rocca WA, Maraganore DM. Discordant sibling analyses confirm the association of UCHL1 with Parkinson's Disease. Neurosci Lett 2005 Jun 10-17; 381(1-2):131-4.
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107. Lindor NM, Rabe K, Petersen GM, Haile R, Casey G, Baron J, Gallinger S, Bapat B, Aronson M, Hopper J, Jass J, LeMarchand L, Grove J, Potter J, Newcomb P, Terdiman JP, Conrad P, Moslein G, Goldberg R, Ziogas A, Anton-Culver H, de Andrade M, Siegmund K, Thi Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency - Familial colorectal cancer type X. JAMA 2005 Apr 27; 293(16):1979-85.
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108. Liu QR, Walther D, Drgon T, Polesskaya O, Lesnick TG, Strain KJ, de Andrade M, Bower JH, Maraganore DM, Uhl GR. Human brain derived neurotrophic factor (BDNF) genes, splicing patterns, and assessments of associations with substance abuse and Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet 2005 Apr 5; 134B(1):93-103.
109. Turner ST, Fornage M, Jack CR, Mosley TH, Kardia SLR, Boerwinkle E, de Andrade M. Genomic susceptibility loci for brain atrophy in hypertensive sibships from the GENOA study. Hypertension 2005 Apr; 45(4):793-8.
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110. Heit JA, Petterson TM, Owen WG, Burke JP, DE Andrade M, Melton LJ 3rd. Thrombomodulin gene polymorphisms or haplotypes as potential risk factors for venous thromboembolism: a population-based case-control study. J Thromb Haemost 2005 Apr; 3(4):710-7.
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111. Mamah CE, Lesnick TG, Lincoln SJ, Strain KJ, de Andrade M, Bower JH, Ahlskog JE, Rocca WA, Farrer MJ, Maraganore DM. Interaction of alpha-synuclein and tau genotypes in Parkinson's disease. Ann Neurol 2005 Mar; 57(3):439-43.
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112. Kantarci OH, Goris A, Hebrink DD, Heggarty S, Cunningham S, Alloza I, Atkinson EJ, de Andrade M, McMurray CT, Graham CA, Hawkins SA, Billiau A, Dubois B, Weinshenker BG, Vandenbroeck K. IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosis. Genes Immun 2005 Mar; 6(2):153-61.
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113. Ertekin-Taner N, Ronald J, Feuk L, Prince J, Tucker M, Younkin L, Hella M, Jain S, Hackett A, Scanlin L, Kelly J, Kihiko-Ehman M, Neltner M, Hersh L, Kindy M, Markesbery W, Hutton M, de Andrade M, Petersen RC, Graff-Radford N, Estus S, Brookes AJ, Elevated amyloid beta protein (A beta 42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene. Hum Mol Genet 2005 Feb 1; 14(3):447-60.
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114. Pankratz VS, de Andrade M, Therneau TM. Random-effects cox proportional hazards model: General variance components methods for time-to-event data. Genet Epidemiol 2005 Feb; 28(2):97-109.
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115. Couch FJ, Johnson MR, Rabe K, Boardman L, McWilliams R, de Andrade M, Petersen G. Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Cancer Res 2005 Jan 15; 65(2):383-6.
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116. Kullo IJ, Andrade MC, Boerwinkle E, McConnell JP, Kardia SLR, Turner ST. Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships. Am J Hypertens 2005 Jan; 18(1):99-103.
117. Kullo IJ, de Andrade M, Boerwinkle E, McConnell JP, Kardia SL, Turner ST. Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships. Am J Hypertens 2005 Jan; 18(1):99-103.
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118. de Andrade M, Mendell NR. Summary of contributions to GAW group 12: Multivariate methods. Genet Epidemiol 2005; 29(Suppl 1):S91-5.
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119. Yang P, Bamlet WR, Ebbert JO, Taylor WR, de Andrade M. Glutathione pathway genes and lung cancer risk in young and old populations. Carcinogenesis 2004 Oct; 25(10):1935-44.
120. Bailey-Wilson JE, Amos CI, Pinney SM, Petersen GM, de Andrade M, Wiest JS, Fain P, Schwartz AG, You M, Franklin W, Klein C, Gazdar A, Rothschild H, Mandal D, Coons T, Slusser J, Lee J, Gaba C, Kupert E, Perez A, Zhou X, Zeng D, Liu Q, Zhang Q, Seminara A major lung cancer susceptibility locus maps to chromosome 6q23-25. Am J Hum Genet 2004 Sep; 75(3):460-74.
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121. Maraganore DM, Wilkes K, Lesnick TG, Strain KJ, de Andrade M, Rocca WA, Bower JH, Ahlskog JE, Lincoln S, Farrer MJ. A limited role for DJ1 in Parkinson disease susceptibility. Neurology 2004 Aug 10; 63(3):550-3.
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122. Turner ST, Kardia SLR, Boerwinkle E, de Andrade M. Multivariate linkage analysis of blood pressure and body mass index. Genet Epidemiol 2004 Jul; 27(1):64-73.
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123. Heit JA, Phelps MA, Ward SA, Slusser JP, Petterson TM, de Andrade M. Familial segregation of venous thromboembolism. J Thromb Haemost 2004 May; 2(5):731-6.
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124. Maraganore DM, Lesnick TG, Elbaz A, Chartier-Harlin MC, Gasser T, Kruger R, Hattori N, Mellick GD, Quattrone A, Satoh J, Toda T, Wang J, Ioannidis JPA, de Andrade M, Rocca WA. UCHL1 is a Parkinson's disease susceptibility gene. Ann Neurol 2004 Apr; 55(4):512-21.
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125. Kantarci OH, Hebrink DD, Achenbach SJ, Pittock SJ, Altintas A, Schaefer-Klein JL, Atkinson EJ, de Andrade M, McMurray CT, Rodriguez M, Weinshenker BG. Association of APOE polymorphisms with disease severity in MS is limited to women. Neurology 2004 Mar 9; 62(5):811-4.
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126. Turner ST, Jack CR, Fornage M, Mosley TH, Boerwinkle E, de Andrade M. Heritability of leukoaraiosis in hypertensive sibships. Hypertension 2004 Feb; 43(2 Part 2):483-7.
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127. de Andrade M, Ebbert JO, Wampfler JA, Miller DL, Marks RS, Croghan GA, Jatoi A, Finke EE, Sellers TA, Yang P. Environmental tobacco smoke exposure in women with lung cancer. Lung Cancer 2004 Feb; 43(2):127-34.
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128. Kantarci OH, Hebrink DD, Achenbach SJ, Atkinson EJ, de Andrade M, McMurray CT, Weinshenker BG. CD95 polymorphisms are associated with susceptibility to MS in women - A population-based study of CD95 and CD95L in MS. J Neuroimmunol 2004 Jan; 146(1-2):162-70.
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129. Ertekin-Taner N, Ronald J, Asahara H, Younkin L, Hella M, Jain S, Gnida E, Younkin S, Fadale D, Ohyagi Y, Singleton A, Scanlin L, de Andrade M, Petersen R, Graff-Radford N, Hutton M. Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. Hum Mol Genet 2003 Dec 1; 12(23):3133-43.
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130. Maraganore DM, Farrer MJ, Lesnick TG, de Andrade M, Bower JH, Hernandez D, Hardy JA, Rocca WA. Case-control study of the alpha-synuclein interacting protein gene and Parkinson's disease. Mov Disord 2003 Nov; 18(11):1233-9.
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131. Lincoln SJ, Maraganore DM, Lesnick TG, Bounds R, de Andrade M, Bower JH, Hardy JA, Farrer MJ. Parkin variants in north American Parkinson's disease: Cases and controls. Mov Disord 2003 Nov; 18(11):1306-11.
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132. Maraganore DM, de Andrade M, Lesnick TG, Farrer MJ, Bower JH, Hardy JA, Rocca WA. Complex interactions in Parkinson's disease: A two-phased approach. Mov Disord 2003 Jun; 18(6):631-6.
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133. Kantarci OH, Hebrink DD, Achenbach SJ, Atkinson EJ, Waliszewska A, Buckle G, McMurray CT, de Andrade M, Hafler DA, Weinshenker BG. CTLA4 is associated with susceptibility to multiple sclerosis. J Neuroimmunol 2003 Jan; 134(1-2):133-41.
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134. Kraft P, de Andrade M. Group 6: Pleiotropy and multivariate analysis. Genet Epidemiol 2003; 25(Suppl 1):S50-6.
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135. de Andrade M, Olswold C. Comparison of longitudinal variance components and regression-based approaches for linkage detection on chromosome 17 for systolic blood pressure. BMC Genetics 2003; 4 Suppl 1:S17.
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136. Olswold C, de Andrade M. Localization of genes involved in the metabolic syndrome using multivariate linkage analysis. BMC Genetics 2003; 4 Suppl 1:S57.
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137. Atkinson EJ, de Andrade M. Screening the genome to detect an association with hypertension. BMC Genetics 2003; 4 Suppl 1:S63.
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138. de Andrade M, Gueguen R, Visvikis S, Sass C, Siest G, Amos CI. Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis. Genet Epidemiol 2002 Mar; 22(3):221-32.
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139. Kantarci OH, de Andrade M, Weinshenker BG. Identifying disease modifying genes in multiple sclerosis. J Neuroimmunol 2002 Feb; 123(1-2):144-59.
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140. Barahamani N, de Andrade M, Slusser J, Zhang Q, Duvic M. Interleukin-1 receptor antagonist allele 2 and familial alopecia areata. J Invest Dermatol 2002 Feb; 118(2):335-7.
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141. Barnholtz-Sloan JS, de Andrade M, Dyer TD, Chakraborty R. Admixture effects in the traditional linkage analysis of admixed families. Ethn Dis 2002; 12:411-9.
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142. Bondy ML, Wang LE, El-Zein R, de Andrade M, Selvan MS, Bruner JM, Levin VA, Yung WKA, Adatto P, Wei QY. gamma-radiation sensitivity and risk of glioma. J Natl Cancer Inst 2001 Oct 17; 93(20):1553-1557.
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143. Farrer M, Maraganore DM, Lockhart P, Singleton A, Lesnick TG, de Andrade M, West A, de Silva R, Hardy J, Hernandez D. Alpha-synuclein gene haplotypes are associated with Parkinson's disease. Hum Mol Genet 2001 Aug 15; 10(17):1847-1851.
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144. Duvic M, Nelson A, de Andrade M. The genetics of alopecia areata. Clin Dermatol 2001 Mar-Apr; 19(2):135-9.
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145. de Andrade M, Barnholtz JS, Amos CI, Adatto P, Spencer C, Bondy ML. Segregation analysis of cancer in families of glioma patients. Genet Epidemiol 2001 Feb; 20(2):258-70.
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146. Amos CI, de Andrade M. Genetic linkage methods for quantitative traits. Stat Methods Med Res 2001 Feb; 10(1):3-25.
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147. El-Zein R, Bondy ML, Wang LE, de Andrade M, Sigurdson AJ, Bruner JM, Kyritsis AP, Levin VA, Wei Q. Risk assessment for developing gliomas: A comparison of two cytogenetic approaches. Mutat Res/Genet Toxicol Environ Mutagenesis 2001; 490(1):35-44.
148. Barnholtz-Sloan JS, de Andrade M, Chakraborty R. The impact of population admixture on traditional linkage analysis. Ethn Dis 2001; 11(3):519-31.
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149. Amos CI, Zhu D, de Andrade M. Multivariate tests for genetic linkage. Hum Hered 2001; 51(3):133-44.
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150. Atkinson EJ, Hall D, de Andrade M. A comparison of software packages that assess linkage using a variance components approach. Genet Epidemiol 2001; 21(Suppl 1):S81-S88.
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151. Yoo B, Pankratz VS, de Andrade M. Practical application of residuals from survival models in quantitative trait linkage analysis. Genet Epidemiol 2001; 21(Suppl 1):S811-S816.
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152. Amos CI, de Andrade M, Zhu D. Comparison of multivariate tests for genetic linkage. Hum Hered 2001; 51(3):133-44.
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153. de Andrade M, Amos CI. Ascertainment issues in variance components models. Genet Epidemiol 2000 Dec; 19(4):333-44.
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154. de Andrade M, Spitz MR, Wu X, Liang JC, Strom SS. Statistical models for analysis of cytogenetic biomarkers. J Investig Med 2000 Jul; 48(4):281-6.
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155. Vulimiri SV, Wu X, Baer-Dubowska W, de Andrade M, Detry M, Spitz MR, DiGiovanni J. Analysis of aromatic DNA adducts and 7,8-dihydro-8-oxo- 2'-deoxyguanosine in lymphocyte DNA from a case-control study of lung cancer involving minority populations. Mol Carcinog. 2000 Jan;27(1):34-46 Erratum in: Mol Carcinog 2000 Apr; 27(4):330.
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156. Vulimiri SV, Wu X, Baer-Dubowska W, de Andrade M, Detry M, Spitz MR, Di Giovanni J. Analysis of aromatic DNA adducts and 7,8-dihydro-8-oxo-2'-deoxyguanosine in lymphocyte DNA from a case-control study of lung cancer involving minority populations. Mol Carcinog 2000 Jan; 27(1):34-46.
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157. Spitz MR, Duphorne CM, Detry MA, Pillow PC, Amos CI, Lei L, de Andrade M, Gu XJ, Hong WK. Dietary intake of isothiocyanates: Evidence of a joint effect with glutathione S-transferase polymorphisms in lung cancer risk. Cancer Epidemiol Biomarkers Prev 2000; 9(10):1017-20.
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158. Wang LE, Bondy ML, de Andrade M, Strom SS, Wang X, Sigurdson A, Spitz MR, Wei Q. Gender difference in smoking effect on chromosome sensitivity to gamma radiation in a healthy population. Radiat Res 4 2000 15; 154(1):20-7.
159. de Andrade M, Jackow CM, Dahm N, Hordinsky M, Reveille JD, Duvic M. Alopecia areata in families: association with the HLA locus. J Investig Dermatol Symp Proc 1999 Dec; 4(3):220-3.
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160. El-Zein R, Bondy ML, Wang LE, de Andrade M, Sigurdson AJ, Bruner JM, Kyritsis AP, Levin VA, Wei Q. Increased chromosomal instability in peripheral lymphocytes and risk of human gliomas. Carcinogenesis 1999 May; 20(5):811-5.
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161. de Andrade M, Amos CI, Thiel TJ. Methods to estimate genetic components of variance for quantitative traits in family studies. Genet Epidemiol 1999; 17(1):64-76.
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162. Peterson LE, Barnholtz JS, Page GP, King TM, de Andrade M, Amos CI. A genome-wide search for susceptibility genes linked to alcohol dependence. Genet Epidemiol 1999; 17(Suppl 1):S295-300.
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163. Barnholtz JS, de Andrade M, Page GP, King TM, Peterson LE, Amos CI. Assessing linkage of monoamine oxidase B in a genome-wide scan using a univariate variance components approach. Genet Epidemiol 1999; 17(Suppl 1):S49-54.
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164. Page GP, King TM, Barnholtz JS, de Andrade M, Peterson LE, Amos CI. Genome scans for genetic predisposition to alcoholism by use of transmission disequilibrium test analyses. Genet Epidemiol 1999; 17(Suppl 1):S277-81.
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165. Wan Y, de Andrade M, Yu L, Cohen J, Amos CI. Genetic linkage analysis using lognormal variance components. Ann Hum Genet 1998 Nov; 62(Pt 6):521-30.
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166. de Andrade M, Amos CI, Foulkes WD. Segregation analysis of squamous cell carcinoma of the head and neck: evidence for a major gene determining risk. Ann Hum Genet 1998 Nov; 62(Pt 6):505-10.
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167. de Andrade M, Barnholtz JS, Amos CI, Lochmiller C, Scott A, Risman M, Hecht JT. Segregation analysis of idiopathic talipes equinovarus in a Texan population. Am J Med Genet 1998 Sep 1; 79(2):97-102.
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168. Trizna Z, de Andrade M, Kyritsis AP, Briggs K, Levin VA, Bruner JM, Wei Q, Bondy ML. Genetic polymorphisms in glutathione S-transferase mu and theta, N-acetyltransferase, and CYP1A1 and risk of gliomas. Cancer Epidemiol Biomarkers Prev 1998 Jun; 7(6):553-5.
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169. Amos CI, de Andrade M. Variance components models for linkage in quantitative traits: Multivariate modeling and ascertainment. Proceedings: American Statistical Association, Joint Statistical Meetings, Biometrics Section. 1998:170-175.
170. Evans SC, Mims B, McMasters KM, Foster CJ, deAndrade M, Amos CI, Strong LC, Lozano GDDD. Exclusion of p53 germline mutation in a classic Li-Fraumeni syndrome family. Hum Genet 1998; 102(6):681-686.
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171. Palomino H, Cerda-Flores RM, Blanco R, Palomino HM, Barton SA, de Andrade M, Chakraborty R. Complex segregation analysis of facial clefting in Chile. Journal of Craniofacial Genetics & Developmental Biology 1997 Apr-Jun; 17(2):57-64.
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172. Musher DM, Groover JE, Watson DA, Pandey JP, Rodriguez-Barradas MC, Baughn RE, Pollack MS, Graviss EA, de Andrade M, Amos CI. Genetic regulation of the capacity to make immunoglobulin G to pneumococcal capsular polysaccharides. J Investig Med 1997 Feb; 45(2):57-68.
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173. de Andrade M, Thiel TJ, Yu L, Amos CI. Assessing linkage on chromosome 5 using components of variance approach: univariate versus multivariate. Genet Epidemiol 1997; 14(6):773-8.
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174. Amos CI, Krushkal J, Thiel TJ, Young A, Zhu DK, Boerwinkle E, de Andrade M. Comparison of model-free linkage mapping strategies for the study of a complex trait. Genet Epidemiol 1997; 14(6):743-8.
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175. Wang M, Dhingra K, Hittelman WN, Liehr JG, de Andrade M, Li D. Lipid peroxidation-induced putative malondialdehyde-DNA adducts in human breast tissues. Cancer Epidemiol Biomarkers Prev 1996 Sep; 5(9):705-10.
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176. Bondy ML, Kyritsis AP, Gu J, de Andrade M, Cunningham J, Levin VA, Bruner JM, Wei Q. Mutagen sensitivity and risk of gliomas: a case-control analysis. Cancer Res 1996 Apr 1; 56(7):1484-6.
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177. de Andrade M, Thandi I, Brown S, Gotto A Jr, Patsch W, Boerwinkle E. Relationship of the apolipoprotein E polymorphism with carotid artery atherosclerosis. Am J Hum Genet 1995 Jun; 56(6):1379-90.
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178. de Andrade M. Estimation of quantitative genetic parameters under non-normal models. Ann Hum Genet 1995 Jan; 59(Pt 1):107-22.
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179. Chakraborty R, Zhong Y, de Andrade M, Clemens PR, Fenwick RG, Caskey CT. Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophies. Genomics 1994 Jun;21(3):567-70.
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180. Pena SD, de Souza KT, de Andrade M, Chakraborty R. Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene. Proc Natl Acad Sci U S A 1994 Jan 18; 91(2):723-7.
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181. Chakraborty R, Srinivasan MR, de Andrade M. Intraclass and interclass correlations of allele sizes within and between loci in DNA typing data. Genetics 1993 Feb; 133(2):411-9.
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182. Chakraborty R, de Andrade M, Daiger SP, Budowle B. Apparent heterozygote deficiencies observed in DNA typing data and their implications in forensic applications. Ann Hum Genet 1992 Jan; 56(Pt 1):45-57.
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183. Chakraborty R, Srinivasan MR, Jin L, de Andrade M. Effects of population subdivision and allele frequency differences on interpretation of DNA typing data for human identification. Proceedings from The Third International Symposium on Human Identification 1992; 205-222.
184. Clemens PR, Fenwick RG, Chamberlain JS, Gibbs RA, de Andrade M, Chakraborty R, Caskey CT. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. Am J Hum Genet 1991 Nov; 49(5):951-60.
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