CCTS Biobank

Publications

2014

  1. López-Isac E, Bossini-Castillo L, Simeon CP, Egurbide MV, Alegre-Sancho JJ, Callejas JL, Roman-Ivorra JA, Freire M, Beretta L, Santaniello A, Airó P, Lunardi C, Hunzelmann N, Riemekasten G, Witte T, Kreuter A, Distler JHW, Schuerwegh AJ, Vonk MC, Voskuyl AE, Shiels PG, van Laar JM, Fonseca C, Denton C, Herrick A, Worthington J, Assassi S, Koeleman BP, Mayes MD, Radstake TRDJ, Martin J. A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility. Arthritis Res Ther. 2014 Jan 9;16(1):R6. PMID:24401602
  2. Mayes MD, Bossini-Castillo L, Gorlova O, Martin JE, Zhou X, Chen WV, Assassi S, Ying J, Tan K, Arnett FC, Reveille JD, Guerra S, Teruel M, Carmona FD, Gregersen PK, Lee AT, López-Isac E, Ochoa E, Carreira P, Simeón CP, Castellvi I, González-Gay MA, the Spanish Scleroderma Group, Koeleman BP, Zhernakova A, Padyukov L, Alarcón-Requelme M, Wijmengz C, Brown M, Beretta L, Riemekasten G, Witte T, Hunzelmann N, Kreuter A, Distler JHW, Voskuyl AE, Scherwegh AJ, Hesselstrand R, Nordin A, Airó P, Lunardi C, Shiels P, van Laar PM, Herrick A, Worthington J, Denton C, Wigley FM, Hummers LK, Varga J, Hinchcliff ME, Baron M, Hudson M, Pope JE, Furst ED, Khanna D, Phillips K, Schiopu E, Segal BM, Molitor JA, Silver RM, Steen FD, Simms RW, Lafyatis RA, Fessler BJ, Frech TM, AlKassab F, Docherty P, Kaminska E. Khalidi N, Jones HN, Markland J, Robinson D, Broen J, Radstake TRDJ, Fonseca C, Martin J.  Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis.  Am J Hum Genet. 2014 Jan 2;94(1):47-61. Doi: 10.1016/j.alhg.2013.12.002. PMID 24387989  PMCID: PMC3882906
  3. Zhou XD, Wang JC, Zou H, Jin L, Mayes MD, Lin Y, He D. Association of HLA-DPB1 with scleroderma and its clinical features in Chinese population.  PLoS One 2014 Jan 31;9(1):e87363. doi: 10.1371 PMID 24498086  PMCID: PMC3909094

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2013

  1. Bossini-Castillo L, Martin JE, Broen J, Simeon CP, Beretta L, Gorlova OY, Vonk MC, Ortego-Centeno N, Espinosa G, Carreira P, García de la Peña P, Oreiro N, Román-Ivorra JA, Castillo MJ, González-Gay MA, Sáez-Comet L, Castellví I, Schuerwegh AJ, Voskuyl AE, Hoffmann-Vold AM, Hesselstrand R, Nordin A, Lunardi C, Scorza R, van Laar JM, Shiels PG, Herrick A, Worthington J, Fonseca C, Denton C, Tan FK, Arnett FC, Assassi S, Koeleman BP, Mayes MD, Radstake TR, Martin J., the Spanish Scleroderma Group.  Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factor in a large independent replication study. Ann Rheum Dis. 2013 Apr;72(4):602-7.  Doi: 10.1136/annrheumdis-2012-201888.  PMID 22896740  NIHMS ID: NIHMS541717
  2. Liu X, Mayes MD, Tan FK, Wu M, Reveille JD, Harper BE, Draeger HT, Gonzalez B, Assassi S.  Correlation of interferon-inducible chemokine plasma levels with disease severity in systemic sclerosis. Arthritis Rheum. 2013 Jan;65(1):226-35. doi: 10.1002/art.37742.  PMID 23055137 PMCID: PMC3687352
  3. Diaz-Gallo LM, Simeon CP, Broen JC, Orego-Centeno N, Beretta L, Vonk MC, Carreira PE, Vargas S, Román-Ivorra JA, González-Gay MA, Tolosa C, López-Longo FJ, Espinosa G, Vicente EF, Hesslestrand R, Riemekasten G, Witte T, Distler JH, Voskuyl AE, Schuerwegh AJ, Shiels PG, Nordin A, Padyukov L, Hoffmann-Vold AM, Scorza R, Lunardi C, Airó P, van Laar JM, Hunzelmann N, Gathof BS, Kreuter A, Herrick A, Worthington J, Denton CP, Zhou X, Arnett FC, Fonseca C, Koeleman BP, Assassi S, Radstake TR, Mayes MD, Martin J, the Spanish Scleroderma Group.  Implication of IL-2/IL-21 region in systemic sclerosis genetic susceptibility.  Ann Rheum Dis. 2013 Jul;72(7):1233-8. PMID 23172754 NIHMS ID: NIHMS541710
  4. Wang J, Assassi S, Guo G, Tu W, Wu W, Yang L, Xiao R, Zhao Y, Chu H, Liu J, Ma Y, Kim SJ, Jin L, Mayes MD, Zou H, Zhou X. Clinical and serological features of systemic sclerosis in a Chinese cohort. Clin Rheumatol. 2013 May;32(5):617-21. PMID 23271609 PMCID PMC3734856
  5. Elhaj M, Charles J, Pedroza C, Liu X, Zhou X, Estrada-Y-Martin RM, Gonzalez E, Lewis DE, Draeger HT, Kim S, Arnett FC, Mayes MD, Assassi S. Can serum surfactant protein D or CC chemokine ligand 18 predict outcome of interstitial lung disease in patients with early systemic sclerosis? J Rheumatol. 2013 Jul;40(7):1114-20. PMID 23588945  PMCID 3728890
  6. Liu X, Mayes MD, Pedroza C, Draeger HT, Gonzalez EB, Harper BE, Reveille JD, Assassi S. Does C-reactive protein predict the long-term progression of interstitial lung disease and survival in patients with early systemic sclerosis? Arthritis Care Res. 2013 Aug;65(8):1375-80. Doi: 10.10002/acr.21968. PMID 23401350  PMCID PMC3816494
  7. Carmona FD, Cénit MC, Diaz-Gallo LM, Broen JC, Simeón CP, Carreria PE, Callejas-Rubio JL, Fonollosa V, López-Longo FJ, González-Gay MA, Hunzelmann N, Riemekasten G, Witte T, Kreuter A, Distler JH, Madhok R, Shiels P, van Laar JM, Schuerwegh AJ, Vonk MC, Voskuyl AE, Fonseca C, Denton CP, Herrick A, Worthington J, Arnett FC, Tan FK, Assassi S, Radstake TR, Mayes MD, Martin J; Spanish Scleroderma Group.  New insight on the Xq28 association with systemic sclerosis.  Ann Rheum Dis 2013 Dec 1;72(12):2032-8.  Doi: 10.1136/annrheumdis-2012-202742.  PMID 23444193  PMCID PMC3818491
  8. Yi L, Wang JC, Guo XJ, Gu YH, Tu WZ, Guo G, Yang L, Xiao R, Yu L, Mayes MD, Assassi S, Zou HJ, Zhou XD.  STAT4 is a genetic risk factor for systemic sclerosis in Chinese population.  Int. J. Immunopathol. Pharmacol. 2013 Apr-Jun:26(6):473-8.  PMID: 23755762
  9. Martin JE, Assassi S, Diaz-Gallo LM, Broen JC, Simeón CP, Castellvi I, Vicente-Rabanda E, Fonollosa V, Ortego-Centeno N, González-Gay MA, Espinosa G, Carreira P; Spanish Scleroderma Group; SLEGEN consortium; U.S. Scleroderma GWAS group; BIOLUPUS, Camps M, Sabio JM, D’Alfonso S, Vonk MC, Voskuyl AE, Schuerwegh AJ, Kreuter A, Witte T, Riemakasten G, Hunzelmann N, Airo P, Beretta L, Scorza R, Lunardi C, vanLaar JM, Chee MM, Worthington J, Herrick A, Denton C, Fonseca C, Tan FK, Arnett F, Zhou X, Reveille JD, Gorlova O, Koeleman BP, Radstake TR, Vyse T, Mayes MD, Arlarcón-Requelme ME, Martin J. A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci, Hum Molec Genet 2013 Oct 1:22(19):4021-9.  Doi: 10.1093/hmg/ddt248.  PMID: 23740937 PMCID PMC3766185
  10. Zhou XD, Yi L, Guo XJ, Chen E, Zou HJ, Jin L, Mayes MD, Assassi S, Wang JC.  Association of HLA-DQB1*0501 with scleroderma and its clinical features in Chinese population.  Int J Immunopathol Pharmacol. 2013 Jul-Sept;26(3):747-51. PMID: 24067471
  11. Wu M 1, Pedroza M, Lafyatis R, George AT, Mayes MD, Assassi S, Tan FK, Brenner MB, Agarwal SK. Identification of cadherin-11 as a mediator of dermal fibrosis and possible role in systemic sclerosis. Arthritis Rheum. 2013 Nov 18. doi: 10.1002/art.38275. [Epub ahead of print] PMID: 24249394
  12. Go AS, Mozaffarian D, Roger VL, Benjamin EJ, Berry JD, Borden WB, Bravata DM, Dai S, Ford ES, Fox CS, Franco S, Fullerton HJ, Gillespie C, Hailpern SM, Heit JA, Howard VJ, Huffman MD, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Magid D, Marcus GM, Marelli A, Matchar DB, McGuire DK, Mohler ER, Moy CS, Mussolino ME, Nichol G, Paynter NP, Schreiner PJ, Sorlie PD, Stein J, Turan TN, Virani SS, Wong ND, Woo D, Turner MB; American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Heart disease and stroke statistics--2013 update: a report from the American Heart Association. Circulation. 2013 Jan 1;127(1):e6-e245. doi: 10.1161/CIR.0b013e31828124ad. Epub 2012 Dec 12 PMID 23239837
  13. Yammine L, Frazier L. Comparison of demographic, psychosocial, and clinical characteristics among younger and older persons with acute coronary syndrome. J Am Assoc Nurse Pract. 2013 Feb;25(2):103-8. doi: 10.1111/j.1745-7599.2012.00779.x. Epub 2012 Sep 24. PMID 23347246
  14. Williams PH1, Nemeth LS, Sanner JE, Frazier LQ. Thematic analysis of cardiac care patients' explanations for declining contribution to a genomic research-based biobank. Am J Crit Care. 2013 Jul;22(4):320-7. doi: 10.4037/ajcc2013838. PMID 23817821
  15. Frazier L, Sanner J, Yu E, Cron SG, Moeller FG. Using a Single Screening Question for Depressive Symptoms in Patients With Acute Coronary Syndrome. J Cardiovasc Nurs. 2013 Apr 30. [Epub ahead of print] PMID 23635808
  16. Sanner JE, Frazier L, Udtha M. The role of platelet serotonin and depression in the acute coronary syndrome population. Yale J Biol Med. 2013 Mar;86(1):5-13. Epub 2013 Mar 12. PMID 23482419
  17. Sanner JE, Frazier L, Udtha M. Effects of delayed laboratory processing on platelet serotonin levels. Biol Res Nurs. 2013 Jan;15(1):13-6. doi: 10.1177/1099800411416636. Epub 2011 Aug 22. PMID 21859747

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    2012

    1. Frazier L, Yu E, Sanner J, Liu F, Udtha M, Cron S, Coulter S, Bogaev RC. Gender Differences in Self-Reported Symptoms of Depression among Patients with Acute Coronary Syndrome. Nurs Res Pract. 2012;2012:109251. doi: 10.1155/2012/109251. Epub 2012 Mar 26. PMID 22567222
    2. Boileau C, Guo DC, Hanna N, Regalado ES, Detaint D, Gong L, Varret M, Prakash SK, Li AH, d'Indy H, Braverman AC, Grandchamp B, Kwartler CS, Gouya L, Santos-Cortez RL, Abifadel M, Leal SM, Muti C, Shendure J, Gross MS, Rieder MJ, Vahanian A, Nickerson DA, Michel JB; National Heart, Lung, and Blood Institute (NHLBI) Go Exome Sequencing Project, Jondeau G, Milewicz DM. TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome. Nat Genet. 2012 Jul 8;44(8):916-21. doi: 10.1038/ng.2348. PMID 22772371
    3. Roger VL, Go AS, Lloyd-Jones DM, Benjamin EJ, Berry JD, Borden WB, Bravata DM, Dai S, Ford ES, Fox CS, Fullerton HJ, Gillespie C, Hailpern SM, Heit JA, Howard VJ, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Makuc DM, Marcus GM, Marelli A, Matchar DB, Moy CS, Mozaffarian D, Mussolino ME, Nichol G, Paynter NP, Soliman EZ, Sorlie PD, Sotoodehnia N, Turan TN, Virani SS, Wong ND, Woo D, Turner MB; American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Executive summary: heart disease and stroke statistics--2012 update: a report from the American Heart Association. Circulation. 2012 Jan 3;125(1):188-97. doi: 10.1161/CIR.0b013e3182456d46 PMID 22215894
    4. Virani SS, Brautbar A, Davis BC, Nambi V, Hoogeveen RC, Sharrett AR, Coresh J, Mosley TH, Morrisett JD, Catellier DJ, Folsom AR, Boerwinkle E, Ballantyne CM. Associations between lipoprotein(a) levels and cardiovascular outcomes in black and white subjects: the Atherosclerosis Risk in Communities (ARIC) Study. Circulation. 2012 Jan 17;125(2):241-9. doi: 10.1161/CIRCULATIONAHA.111.045120. Epub 2011 Nov 29. PMID 22128224
    5. Virani SS, Brautbar A, Lee VV, MacArthur E, Morrison AC, Grove ML, Nambi V, Frazier L, Wilson JM, Willerson JT, Boerwinkle E, Ballantyne CM. Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease. Circ J. 2012;76(4):950-6. Epub 2012 Feb 9 PMID 22322877

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    2011

    1. Kuang SQ, Guo DC, Prakash SK, McDonald ML, Johnson RJ, Wang M, Regalado ES, Russell L, Cao JM, Kwartler C, Fraivillig K, Coselli JS, Safi HJ, Estrera AL, Leal SM, Lemaire SA, Belmont JW, Milewicz DM; GenTAC Investigators. Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections. PLoS Genet. 2011 Jun;7(6):e1002118. Epub 2011 Jun 16. PMID: 21698135
    2. Prakash SK, Haden-Pinneri K, Milewicz DM. Susceptibility to acute thoracic aortic dissections in patients dying outside the hospital: an autopsy study. Am Heart J. 2011 Sep;162(3):474-9. doi: 10.1016/j.ahj.2011.06.020. Epub 2011 Aug 9. PMID 21884863
    3. Regalado E, Medrek S, Tran-Fadulu V, Guo DC, Pannu H, Golabbakhsh H, Smart S, Chen JH, Shete S, Kim DH, Stern R, Braverman AC, Milewicz DM. Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial aneurysms. Am J Med Genet A. 2011 Sep;155A(9):2125-30. doi: 10.1002/ajmg.a.34050. Epub 2011 Aug 3. PMID 21815248
    4. Virani SS, Brautbar A, Lee VV, Elayda M, Sami S, Nambi V, Frazier L, Wilson JM, Willerson JT, Boerwinkle E, Ballantyne CM. Usefulness of single nucleotide polymorphism in chromosome 4q25 to predict in-hospital and long-term development of atrial fibrillation and survival in patients undergoing coronary artery bypass grafting. Am J Cardiol. 2011 May 15;107(10):1504-9. doi: 10.1016/j.amjcard.2011.01.026. Epub 2011 Mar 15. PMID 21414601
    5. Sanner JE, Frazier L. The role of serotonin in depression and clotting in the coronary artery disease population. J Cardiovasc Nurs. 2011 Sep-Oct;26(5):423-9. doi: 10.1097/JCN.0b013e3182076a81. PMID 21372736

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    2010

    1. Brautbar A, LeMaire SA, Franco LM, Coselli JS, Milewicz DM, and Belmont JW. FBN1 mutations in patients with descending thoracic aortic dissections. Am J Med Genet A. 2010 Feb;152A(2):413-6. doi: 10.1002/ajmg.a.32856. PMID 20082464
    2. Prakash S.K., LeMaire S.A., Guo D.C., Russell L., Regaldo E.S., Golabbakhsh H., Johnson R.J., Safi H.J., Estrera A.L., Coselli J.S., Bray M.S., Leal S.M., Milewicz D.M., Belmont J.W..  Rare copy number variants disrupt genes regulating vascular smooth muscle cell adhesion and contractility in sporadic thoracic aortic aneurysms and dissections. American Journal of Human Genetics, 2010; 87: 743-56. PMID 21092924
    3. Prakash S., LeMaire S.A., Milewicz D.M., Bray M., Belmont J.W...  Large deletions and uniparental disomy detected by SNP arrays in adults with thoracic aortic aneurysms and dissections. American Journal of Medical Genetics, Part A 2010; 152A: 2399–405. PMID 20683997
    4. Villamizar C., Regalado E.S., Fadulu V.T., Hasham S.N., Gupta P., Willing M.C., Kuang S.Q., Guo D., Muilenburg A., Yee R.W., Fan Y., Towbin J., Coselli J.S., LeMaire S.A., Milewicz D.M. Paucity of skeletal manifestations in Hispanic families with FBN1 mutations. European Journal of Medical Genetics, 2010; 53: 80-4. PMID 19941982
    5. Wang L, Guo DC, Gong L, Regalado ES, Li L, Shete S, Gilchrist DM, Elefteriades JA, Milewicz DM. Mutations in myosin light chain kinase (MYLK) cause familial aortic dissections. Amer J Hum Genet 2010 Nov 12;87(5):701-7. PMC2978973 PMID 2105718
    6. Symes L, McFarlane J, Frazier L, Henderson-Everhardus MC, McGlory G, Watson KB, Liu Y, Rhodes CE, Hoogeveen RC. Exploring violence against women and adverse health outcomes in middle age to promote women's health. Crit Care Nurs Q. 2010 Jul-Sep;33(3):233-43. doi: 10.1097/CNQ.0b013e3181e6d7c4 PMID 20551737
    7. McFarlane J, Symes L, Frazier L, McGlory G, Henderson-Everhardus MC, Watson K, Liu Y. Connecting the dots of heart disease, poor mental health, and abuse to understand gender disparities and promote women's health: a prospective cohort analysis. Health Care Women Int. 2010 Apr;31(4):313-26. doi: 10.1080/07399330902893853 PMID 20390656
    8. Tai MK, Meininger JC,Frazier LQ, Chan W Ambulatory blood pressure and physical activity in heart failure. Biol Res Nurs. 2010 Jan;11(3):269-79. doi: 10.1177/1099800409337731. Epub 2009 Jul 17. PMID 19617234

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    2009

    1. Guo DC, Papke CL, Tran-Fadulu V, Regalado ES, Avidan N, Johnson RJ, Kim DH, Pannu H, Willing MC, Sparks E, Pyeritz RE, Singh MN, Dalman RL, Grotta JC, Marian AJ, Boerwinkle EA, Frazier LQ, LeMaire SA, Coselli JS, Estrera AL, Safi HJ, Veeraraghavan S, Muzny DM, Wheeler DA, Willerson JT, Yu RK, Shete SS, Scherer SE, Raman CS, Buja LM, Milewicz DM. Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.  Am J Hum Genet. 2009 May;84(5):617-27. doi: 10.1016/j.ajhg.2009.04.007. Epub 2009 Apr 30. PMID: 19409525 [PubMed - indexed for MEDLINE] PMCID: PMC2680995
    2. LeMaire SA, McDonald M-L, Guo D-L, Russell L, Miller III CC, Johnson RJ, Bekheirnia MR, Franco LM, Nguyen M, Pyeritz RE, Bavaria JE, Devereaux R, Maslen C, Holmes KW, Eagle K, Body SC, Seidman C, Seidman JG, Isselbacher EM, Bray M, Coselli JS, Estrera AL, Safi HJ, Belmont JW, Leal SM, Milewicz DM. Genome-wide association studies identify a major susceptibility locus for thoracic aortic aneurysms and aortic dissections at 15q21.1, encompassing FBN., Nature & Genetics, Sep 11;43(10):996-1000. doi: 10.1038/ng.934. 21909107.
    3. Frazier L, Wung SF, Sparks E, Eastwood C. Cardiovascular nursing on human genomics: what do cardiovascular nurses need to know about congestive heart failure? Prog Cardiovasc Nurs. 2009 Sep;24(3):80-5. doi: 10.1111/j.1751-7117.2009.00039.x. PMID 19737164
    4. Frazier L, Vaughn WK, Willerson JT, Ballantyne CM, Boerwinkle E. Inflammatory protein levels and depression screening after coronary stenting predict major adverse coronary events. Biol Res Nurs. 2009 Oct;11(2):163-73. doi: 10.1177/1099800409332801. Epub 2009 Feb 26. PMID 19251718

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    2008

    1. Milewicz DM, Guo DC, Tran-Fadulu V, Lafont AL, Papke CL, Inamoto S, Pannu H. Genetic Basis of Thoracic Aortic Aneurysms and Dissections: Focus on Smooth Muscle Cell Contractile Dysfunction. 2008. Annu Rev Genomics Hum Genet, 2008 9:283-302. PMID 18544034
    2. Tai MK, Meininger JC, Frazier LQ. A systematic review of exercise interventions in patients with heart failure. Biol Res Nurs. 2008 Oct;10(2):156-82. doi: 10.1177/1099800408323217 PMID 18829599
    3. Frazier L, Sparks E, Sanner JE, Henderson M. Biobanks and biomarker research in cardiovascular disease. J Cardiovasc Nurs. 2008 Mar-Apr;23(2):153-8. doi: 10.1097/01.JCN.0000305075.51399.1c. PMID 18382258

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    2007

    1. Guo, D-C, Pannu, H, Fadulu, TV, Papke CL, Yu, RK, Avidan N, Bourgeois, S, Estrera AL, Safi, HJ, Sparks, E, Amor D, Ades, L, McConnell, V, Willoughby, CE, Abuelo, D, Willing, M, Lewis, RA, Kim, DH, Scherer, S, Pyee, PP, Aghn, C, Buja, M, Raman, CS, Shete SS, Milewicz, DM. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.  2007 Nature and Genetics, 39, 12, 1488-1492. PMID 17994018
    2. Pannu, H, Tran-Fadulu, V, Papke CL, Scherer, S, Yaozhong, L, Presley, C, Guo, DC, Estrera AL, Safi, HJ, Brasier, AL, Vick GW, Marian AJ, Raman, CS, Buja, M, and Milewicz, DM. MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II. 2007 Human Molecular Genetics, 16, 20, 2453-2462. PMID 17666408
    3. Gertz SD, Bodmann BG, Vela D, Papadakis M, Aboshady I, Cherukuri P, Alexander S, Kouri DJ, Baid S, Gittens AA, Gladish GW, Conyers JL, Cody DD, Gavish L, Mazraeshahi RM, Wilner WT, Frazier L, Madjid M, Zarrabi A, Lukovenkov S, Ahmed A, Willerson JT, Casscells SW Three-dimensional isotropic wavelets for post-acquisitional extraction of latent images of atherosclerotic plaque components from micro-computed tomography of human coronary arteries. Acad Radiol. 2007 Dec;14(12):1509-19. PMID 18035280
    4. Wilner WT, Mazraeshahi RM, Aboshady I, Bodmann BG, Papadakis M, Kouri D, Conyers JL, Cherukuri P, Vela D, Gladish G, Gavish L, Cody DD, Frazier L, Lukovenkov S, Madjid M, Zarrabi A, Ahmed A, Willerson JT, Casscells SW, Gertz SD. Quantification of roughness of calcific deposits in computed tomography scans of human coronary arteries. Invest Radiol. 2007 Nov;42(11):771-6. PMID 18030200
    5. Sanner JE, Frazier L. Factors that influence characteristics of genetic biobanks. J Nurs Scholarsh. 2007;39(1):25-9. PMID 17393962

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    2006

    1. Pannu H, Kim DH, Guo D, King TM, van Ginhoven G, Chin T, Chang K, Qi Y, Shete S, Milewicz DM. The role of MMP-2 and MMP-9 polymorphisms in sporadic intracranial aneurysms.  J Neurosurg. 2006 Sept; 105(3):418-23 PMID 16961137

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