2013 Publications

Glurich I, Chyou PH, Engel JM, Cross DS, Onitilo AA. Tamoxifen-induced venothromboembolic events: exploring validation of putative genetic association. CLIN MED RES 2013;11:16-25.
PubMed ID: 23411630

Pan N, Frome WL, Dart RA, Tewksbury D, Luo J. Expression of the renin-angiotensin system in a human placental cell line. CLIN MED RES 2013;11:1-6.
PubMed ID: 22997355

Webster J, Kauffman TL, Feigelson HS, Pawloski PA, Onitilo AA, Potosky AL, Cross D, Meier PR, Mirabedi AS, Delate T, Daida Y, Williams AE, Alexander GL, McCarty CA, Honda S, Kushi LH, Goddard KA; CERGEN study team. KRAS testing and epidermal growth factor receptor inhibitor treatment for colorectal cancer in community settings. CANCER EPIDEMIOL BIOMARKERS PREV 2013;22:91-101.
PubMed ID: 23155138

Manolio TA, Chisholm RL, Ozenberger B, Roden DM, Williams MS, Wilson R, Bick D, Bottinger EP, Brilliant MH, Eng C, Frazer KA, Korf B, Ledbetter DH, Lupski JR, Marsh C, Mrazek D, Murray MF, O'Donnell PH, Rader DJ, Relling MV, Shuldiner AR, Valle D, Weinshilboum R, Green ED, Ginsburg GS. Implementing genomic medicine in the clinic: the future is here. GENET MED 2013;15(4):258-67.
PubMed ID: 23306799

Hebbring SJ, Slager SL, Epperla N, Mazza JJ, Ye Z, Zhou Z, Achenbach SJ, Vasco DA, Call TG, Rabe KG, Kay NE, Caporaso NE, Lanasa MC, Camp NJ, Strom SS, Goldin LR, Cerhan JR, Brilliant MH, Schrodi SJ. Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia. BLOOD 2013;121:237-8.
PubMed ID: 23287625

McPherson E. Discovering the cause of stillbirth. CURR OPIN OBSTET GYNECOL 2013;25:152-6.
PubMed ID: 23354074

Ritchie MD, Denny JC, Zuvich RL, Crawford DC, Schildcrout JS, Bastarache L, Ramirez AH, Mosley JD, Pulley JM, Basford MA, Bradford Y, Rasmussen LV, Pathak J, Chute CG, Kullo IJ, McCarty CA, Chisholm RL, Kho AN, Carlson CS, Larson EB, Jarvik GP, Sotoodehnia N; Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) QRS Group, Manolio TA, Li R, Masys DR, Haines JL, Roden DM. Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. CIRCULATION 2013;127(13):1377-85.
PubMed ID: 23463857

Pendergrass SA, Verma SS, Holzinger ER, Moore CB, Wallace J, Dudek SM, Huggins W, Kitchner T, Waudby C, Berg R, McCarty CA, Ritchie MD. Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using biofilter, and gene-environment interactions using the phenx toolkit. PAC SYMP BIOCOMPUT 2013:147-58.
PubMed ID: 23424120

Glurich I, Acharya A, Shukla SK, Nycz GR, Brilliant MH. The oral-systemic personalized medicine model at Marshfield Clinic. ORAL DIS 2013 Jan;19(1):1-17.
PubMed ID: 22458294



2012 Publications

Cross DS, Ritter M, Reding DJ. Historical prostate cancer screening and treatment outcomes from a single institution. CLIN MED RES 2012;10:97-105.
PubMed ID: 22537761

Kawaler E, Cobian A, Peissig P, Cross D, Yale S, Craven M. Learning to predict post-hospitalization VTE risk from EHR data. AMIA ANNU SYMP PROC 2012;2012:436-45.
PubMed ID: 23304314

Foth W, Waudby C, Brilliant MH. Certificates of confidentiality and the Marshfield Clinic's Personalized Medicine Research Project. VIRTUAL MENTOR 2012;14(8):653-6.
PubMed ID: 23351322

Rose WE, Eickhoff JC, Shukla SK, Pantrangi M, Rooijakkers S, Cosgrove SE, Nizet V, Sakoulas G. Elevated serum interleukin-10 at time of hospital admission is predictive of mortality in patients with Staphylococcus aureus bacteremia. J INFECT DIS 2012;206:1604-11.
PubMed ID: 22966128

Cross DS, McCarty CA, Hytopoulos E, Beggs M, Nolan N, Harrington DS, Hastie T, Tibshirani R, Tracy RP, Psaty BM, McClelland R, Tsao PS, Quertermous T. Coronary risk assessment among intermediate risk patients using a clinical and biomarker based algorithm developed and validated in two population cohorts. CURR MED RES OPIN 2012;28(11):1819-30.
PubMed ID: 23092312

Drawz PE, Baraniuk S, Davis BR, Brown CD, Colon PJ Sr, Cujyet AB, Dart RA, Graumlich JF, Henriquez MA, Moloo J, Sakalayen MG, Simmons DL, Stanford C, Sweeney ME, Wong ND, Rahman M. Cardiovascular risk assessment: addition of CKD and race to the Framingham equation. AM HEART J 2012;164:925-31.
PubMed ID: 23194494

SPS3 Investigators (including Dart RA), Benavente OR, Hart RG, McClure LA, Szychowski JM, Coffey CS, Pearce LA. Effects of clopidogrel added to aspirin in patients with recent lacunar stroke. N ENGL J MED 2012;367:817-25.
PubMed ID: 22931315

Burmeister B, Zaleski C, Cold C, McPherson E. Wisconsin Stillbirth Service Program: analysis of large for gestational age cases. AM J MED GENET A 2012;158A:2493-8.
PubMed ID: 22965821

Collaborative Association Study of Psoriasis (including Schrodi SJ), Genetic Analysis of Psoriasis Consortium, Psoriasis Association Genetics Extension, Wellcome Trust Case Control Consortium 2. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. NAT GENET 2012; 44:1341-1348.
PubMed ID: 23143594

Shukla SK, Pantrangi M, Stahl B, Briska AM, Stemper ME, Wagner TK, Zentz EB, Callister SM, Lovrich SD, Henkhaus JK, Dykes CW. Comparative whole-genome mapping to determine Staphylococcus aureus genome size, virulence motifs, and clonality. J CLIN MICROBIOL 2012;50:3526-33.
PubMed ID: 22915603

Sacco JC, Abouraya M, Motsinger-Reif A, Yale SH, McCarty CA, Trepanier LA. Evaluation of polymorphisms in the sulfonamide detoxification genes NAT2, CYB5A, and CYB5R3 in patients with sulfonamide hypersensitivity. PHARMACOGENET GENOMICS 2012;22(10):733-40.
PubMed ID: 22850190

Ding K, Shameer K, Jouni H, Masys DR, Jarvik GP, Kho AN, Ritchie MD, McCarty CA, Chute CG, Manolio TA, Kullo IJ. Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. MAYO CLIN PROC 2012;87(5):461-74.
PubMed ID: 22560525

Zuvich RL, Armstrong LL, Bielinski SJ, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes MG, Jarvik GP, Jiang L, Kullo IJ, Li R, Ling H, Manolio TA, Matsumoto ME, McCarty CA, McDavid AN, Mirel DB, Olson LM, Paschall JE, Pugh EW, Rasmussen LV, Rasmussen-Torvik LJ, Turner SD, Wilke RA, Ritchie MD. Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality. GENET EPIDEMIOL 2011;35(8):887-98.
PubMed ID: 22125226

Rose WE, Schulz LT, Andes D, Striker R, Berti AD, Hutson PR, Shukla SK. Addition of ceftaroline to daptomycin after emergence of daptomycin-nonsusceptible Staphylococcus aureus during therapy improves antibacterial activity. ANTIMICROB AGENTS CHEMOTHER 2012;56:5296-302.
PubMed ID: 22869564

McCarty CA, Berg R, Patchett R, Wilke RA, Burmester JK. Lack of association between polymorphisms in the prostaglandin F2a receptor and solute carrier organic anion transporter family 2A1 genes and intraocular pressure response to prostaglandin analogs. OPHTHALMIC GENET 2012;33(2):74-6.
PubMed ID: 22060278

Crosslin DR, McDavid A, Weston N, Nelson SC, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Pretel S, Saip A, Ritchie MD, Crawford DC, Crane PK, Newton K, Li R, Mirel DB, Crenshaw A, Larson EB, Carlson CS, Jarvik GP; Electronic Medical Records and Genomics (eMERGE) Network. Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. HUM GENET 2012;131(4):639-52.
PubMed ID: 22037903

Anderson ER, Burmester JK, Caldwell MD. Evaluation of a mitochondrial DNA mutation in maternally inherited and sporadic cases of Dupuytren disease. CLIN MED RES 2012; 10(3)3:122-6.
PubMed ID: 22634541

Peissig PL, Rasmussen LV, Berg RL, Linneman JG, McCarty CA, Waudby CJ, Chen L, Denny JC, Wilke R, Pathak J, Carrell D, Kho A, Starren JB. Importance of multi-modal approaches to effectively identify cataract cases from electronic health records. J AM MED INFORM ASSN 2012;19:225-34.
PubMed ID: 22319176

Pichereau S, Pantrangi M, Couet W, Badiou C, Lina G, Shukla SK, Rose WE. Simulated antibiotic exposures in an in vitro hollow-fiber infection model influence toxin gene expression and production in community-associated methicillin-resistant Staphylococcus aureus strain MW2. ANTIMICROB AGENTS CHEMOTHER 2012;56:140-7.
PubMed ID: 22064533

McCarty CA, Berg RL, Welter JD, Kitchner TE, Kemnitz JW. A novel gene-environment interaction involved in endometriosis. INT J GYNAECOL OBSTET 2012;116:61-3.
PubMed ID: 22024213

Schrodi SJ. Oral health in the age of genome-wide studies. In: Integration of Medical and Dental Care and Patient Data: Progress in Health Care Informatics. Eds. Powell VJH, Din FM, Acharya A, Torres-Urquidy MH. Springer London, UK (2012).

Pichereau S, Moran JJ, Hayney MS, Shukla SK, Sakoulas G, Rose WE. Concentration-dependent effects of antimicrobials on Staphylococcus aureus toxin-mediated cytokine production from peripheral blood mononuclear cells. J ANTIMICROB CHEMOTHER 2012;67:123-9.
PubMed ID: 21980070

Rosenfeld JA, Traylor RN, Schaefer GB, McPherson EW, Ballif BC, Klopocki E, Mundlos S, Shaffer LG, Aylsworth AS. Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes. Eur J Hum Genet Feb 8, 2012.
PubMed ID: 22317977



2011 Publications

Kullo IJ, Ding K, Shameer K, McCarty CA, Jarvik GP, Denny JC, Ritchie MD, Ye Z, Crosslin DR, Chisholm RL, Manolio TA, Chute CG. Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. AM J HUM GENET 2011;89(1):131-8.
PubMed ID: 21700265

McGuire AL, Basford M, Dressler LG, Fullerton SM, Koenig BA, Li R, McCarty CA, Ramos E, Smith ME, Somkin CP, Waudby C, Wolf WA, Clayton EW. Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience. GENOME RES 2011;21(7):1001-7.
PubMed ID: 21632745

McCarty CA, Chisholm RL, Chute CG, Kullo IJ, Jarvik GP, Larson EB, Li R, Masys DR, Ritchie MD, Roden DM, Struewing JP, Wolf WA; eMERGE Team. The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies. BMC MED GENOMICS 2011;4:13.
PubMed ID: 21269473

Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G, Jarvik G, Jiang L, Kullo IJ, Li R, Ling H, Manolio TA, Matsumoto M, McCarty CA, McDavid AN, Mirel DB, Paschall JE, Pugh EW, Rasmussen LV, Wilke RA, Zuvich RL, Ritchie MD. Quality control procedures for genome-wide association studies. CURR PROTOC HUM GENET 2011;Chapter 1:Unit 1.19.
PubMed ID: 21234875

Burmester JK, Berg RL, Glurich IE, Yale SH, Schmelzer JR, Caldwell MD. Absence of novel CYP4F2 and VKORC1 coding region DNA variants in patients requiring high warfarin doses. CLIN MED RES 2011;9:119-24.
PubMed ID: 21562135

Waudby CJ, Berg RL, Linneman JG, Rasmussen LV, Peissig PL, Chen L, McCarty CA. Cataract research using electronic health records. BMC OPHTHALMOLOGY 2011;11
PubMed ID: 22078460

Kopp JB, Nelson GW, Sampath K, Johnson RC, Genovese G, An P, Friedman D, Briggs W, Dart RA, Korbet S, Mokrzycki M, Kimmel PL, Limou S, Ahuja TS, Berns JS, Fryc J, Simon EE, Smith M, Trachtman H, Michel DM, Schelling JR, Vlahov D, Pollak M, Winkler CA. APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy. J AM SOC NEPHROL 2011;22:2129-37.
PubMed ID: 21997394

Piller LB, Baranjuk S, Simpson LM, Cushman WC, Massie BM, Einhorn PT, Oparil S, Ford CE, Graumlich J, Dart RA, Parish DC, Retta TM, Cuyjet AB, Jafri SZ, Furberg CD, Saklayen MG, Thadani U, Probstfield JL, Davis BR, ALLHAT Collaborative Research Group . Long-term follow-up of participants with heart failure in the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). CIRCULATION 2011;124:1811-8.
PubMed ID: 21969009

Aswani V, Tremblay DM, Moineau S, Shukla SK. Staphylococcus epidermidis bacteriophages from the anterior nares of humans. APPL ENVIRON MICROBIOL 2011;77:7853-5.
PubMed ID: 21926216

Denny JC, Crawford D, Ritchie MD, Bielinski S, Basford MA, Bradford Y, Chai H, Bastarache L, Zuvich R, Peissig PL, Carrell D, Ramirez A, Pathak J, Wilke R, Rasmussen LV, Wang X, Pacheco J, Kho A, Hayes M, Weston N, Matsumoto M, Kopp P, Newton KM, Jarvik G, Li R, Manolio T, Kullo IJ, Chute CG, Chisholm R, Larson EB, McCarty CA, Masys DR, Roden DM, De Andrade M. Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. AM J HUM GENET 2011;89:529-42.
PubMed ID: 21981779

Bajaj A, Dyke II PC, Zaleski CA, Cava J, McPherson EW. Mild Tessier No. 7 cleft with PHACE syndrome: the case for pulmonary vascular steal. AM J MED GENET A 2011;155A:2298-301.
PubMed ID: 21834042

McPherson EW, Thomas GD, Manlick C, Zaleski CA, Reynolds KK, Rasmussen K, Giampietro PF, Wiley CL, Mascola MA. Extreme values of maternal serum analytes in second trimester screening: looking beyond trisomy and NTD's. J GENET COUNS 2011;20:396-403.
PubMed ID: 21505920

Talsness SR, Shukla SK, Mazza JJ, Yale SH. Rhabdomyolysis-induced acute kidney injury secondary to Anaplasma phagocytophilum and concomitant statin use. WMJ 2011;110:82-4.
PubMed ID: 21560563

Ito S, Nakanishi Y, Valenzuela RK, Brilliant MH, Kolbe L, Wakamatsu K. Usefulness of alkaline hydrogen peroxide oxidation to analyze eumelanin and pheomelanin in various tissue samples: application to chemical analysis of human hair melanins. PIGMENT CELL MELANOMA RES 2011;24:605-13.
PubMed ID: 21535429

Okon TR, Vats HS, Dart RA. Palliative medicine referral in patients undergoing continuous renal replacement therapy for acute kidney injury. REN FAIL 2011;33:707-17.
PubMed ID: 21787162

Vats HS, Dart RA, Okon TR, Liang H, Paganini EP. Does early initiation of continuous renal replacement therapy affect outcome: experience in a tertiary care center. REN FAIL 2011;33:698-706.
PubMed ID: 21787161

Aswani V, Shukla SK. Two unusual pediatric cases of fungal infections in farming families. J AGROMEDICINE 2011;16:153-7. Erratum in: J AGROMEDICINE 2011;16:240.
PubMed ID: 21462027

Burmester JK, Berg RL, Yale SH, Rottscheit CM, Glurich IE, Schmelzer JR, Caldwell MD. A randomized controlled trial of genotype-based Coumadin initiation. GENET MED 2011;13:509-18.
PubMed ID: 21423021

Vanderwielen B, Zaleski CA, Cold CJ, McPherson EW. Wisconsin stillbirth services program: A multifocal approach to stillbirth analysis. AM J MED GENET A 2011;155:1073-80.
PubMed ID: 21480484

Turner SD, Berg RL, Linneman JG, Peissig PL, Crawford DC, Denny JC, Roden DM, McCarty CA, Ritchie MD, Wilke RA. Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks. PLoS ONE 2011;6:e19586.
PubMed ID: 21589926

Aswani VH, Shukla SK. Prevalence of Staphylococcus aureus and lack of its lytic bacteriophages in the anterior nares of patients and healthcare workers at a rural clinic. CLIN MED RES 2011;9:75-81.
PubMed ID: 20974887

Baumgardner DJ, Temte JL, Gutowski E, Agger WA, Bailey H, Burmester JK, Banerjee I. The differential diagnosis of pulmonary blastomycosis using case vignettes: A Wisconsin Network for Health Research (WiNHR) study. WMJ 2011;110:68-73.
PubMed ID: 21560560

McCarty CA, Garber A, Reeser JC, Fost NC, for the Personalized Medicine Research Project Community Advisory Group and Ethics and Security Advisory Board. Study newsletters, community and ethics advisory boards, and focus group discussions provide ongoing feedback for a large biobank. AM J MED GENET A 2011;155:737-41.
PubMed ID: 21572889

Ghebranious N, Mukesh BN, Giampietro PF, Glurich IE, Mickel SF, Waring SC, McCarty CA. A pilot study of gene/gene and gene/environment interactions in Alzheimer disease. CLIN MED RES 2011;9:17-25.
PubMed ID: 20682755

Lin Y, Barker E, Kislow J, Kaldhone P, Stemper ME, Pantrangi M, Moore FM, Hall M, Fritsche TR, Novicki T, Foley SL, Shukla SK. Evidence of multiple virulence subtypes in nosocomial and community-associated MRSA genotypes in companion animals from the upper Midwestern and northeastern United States. CLIN MED RES 2011;9:7-16.
PubMed ID: 20739580

Reeser JC, Payne E, Kitchner TE, McCarty CA. Apolipoprotein e4 genotype increases the risk of being diagnosed with posttraumatic fibromyalgia. PMR 2011;3:193-7.
PubMed ID: 21402364

Strobush L, Berg RL, Cross DS, Foth WS, Kitchner TE, Coleman LA, McCarty CA. Dietary intake in the Personalized Medicine Research Project: a resource for studies of gene-diet interaction. NUTR J 2011;10:13-25.
PubMed ID: 21276236



2010 Publications

Cross DS, McCarty CA, Reding DJ. PS1-13: Using the PMRP cohort to develop a model for incorporating genetic and environmental factors into prostate cancer screening decisions. CLIN MED RES 2010;8:192.

Cross DS, Craven M, Yale SH. C-B4-02: Determining genetic risk factors for post-hospitalization development of deep-vein thrombosis. CLIN MED RES 2010;8:202.

Feng Q, Jiang L, Berg RL, Antonik M, MacKinney E, Gunnell-Santoro J, McCarty CA, Wilke RA. A common CNR1 (Cannabinoid Receptor 1) haplotype attenuates the decrease in HDL cholesterol that typically accompanies weight gain. PLoS ONE 2010;5:e15779.
PubMed ID: 21209828

Shukla SK, Karow ME, Brady JM, Stemper ME, Kislow J, Moore N, Wroblewski K, Chyou PH, Warshauer DM, Reed KD, Lynfield R, Schwan WR. Virulence genes and genotypic associations in nasal carriage, community-associated methicillin-susceptible and methicillin-resistant USA400 Staphylococcus aureus isolates. J CLIN MICROBIOL 2010;48:3582-92.
PubMed ID: 20668125

Bales A, Zaleski CA, McPherson EW. Patient and family experiences and opinions on adding 22q11 deletion syndrome to the newborn screen. J GENET COUNS 2010;19:526-34.
PubMed ID: 20496046

Clayton EW, Smith M, Fullerton SM, Burke W, McCarty CA, Koenig BA, McGuire AL, Beskow LM, Dressler L, Lemke AA, Ramos EM, Rodriguez LL, for the Consent and Community Consultation Working Group of the eMERGE Consortium. Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium. GENET MED 2010;12:616-20.
PubMed ID: 20733502

Hoppman-Chaney NL, Dawson DB, Nguyen LM, Sengupta S, Reynolds KK, McPherson EW, Velagaleti G. Partial hexasomy for the Prader-Willi-Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome. AM J MED GENET A 2010;152A:2034-8.
PubMed ID: 20602489

Endogenous Hormones and Breast Cancer Collaborative Group , Key TJ, Appleby PN, Reeves GK, Roddam AW, McCarty CA. Insulin-like growth factor 1 (IGF1), IGF binding protein 3 (IGFBP3), and breast cancer risk: pooled individual data analysis of 17 prospective studies. LANCET ONCOL 2010;11:530-42.
PubMed ID: 20472501

Cross DS, Ivacic LC, Stefanski EL, McCarty CA. Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project. BMC GENET 2010;11:51.
PubMed ID: 20565774

Gopalakrishnan PP, Shukla SK, Tak T. Antibiotic prophylaxis and anaphylaxis. CLIN MED RES 2010;8:80-1.
PubMed ID: 20660929

Glurich IE, Burmester JK, Caldwell MD. Understanding the pharmacogenetic approach to warfarin dosing. HEART FAIL REV 2010;13:239-48.
PubMed ID: 18998206

Lenzini P, Wadelius M, Kimmel S, Anderson JL, Jorgensen AL, Pirmohamed M, Caldwell MD, Limdi NA, Burmester JK, Dowd MB, Angchaisuksiri P, Bass AR, Chen J, Eriksson N, Rane A, Carlquist JF, Horne BD, Grice G, Milligan PE, Eby C, Shin J, Kim HH, Kurnik D, Stein CM, McMillin G, Pendleton RC, Berg RL, Deloukas P, Gage BF. Integration of genetic, clinical, and INR data to refine warfarin dosing. CLIN PHARMACOL THER 2010;87:572-8.
PubMed ID: 20375999

McCarty CA, Wilke RA. Biobanking and pharmacogenomics. PHARMACOGENOMICS 2010;11:637-41.
PubMed ID: 20415552

Pantrangi M, Singh VK, Wolz C, Shukla SK. Staphylococcal superantigen-like genes, ssI5 and ssI8, are positively regulated by Sae and negatively by Agr in the Newman strain. FEMS MICROBIOL LETT 2010;308:175-84.
PubMed ID: 20528938

Wilke RA, Berg RL, Linneman JG, Peissig P, Starren J, Ritchie MD, McCarty CA. Quantification of the clinical modifiers impacting high-density lipoprotein cholesterol in the community: Personalized Medicine Research Project. Prev Cardio, 2010;13:63-8.
PubMed ID: 20377807

Giampietro PF, McCarty CA, Mukesh BN, McKiernan FE, Wilson DA, Shuldiner A, Liu J, Levasseur JA, Ivacic LC, Kitchner TE, Ghebranious N. The role of cigarette smoking and statins in the development of postmenopausal osteoporosis: a pilot study utilizing the Marshfield Clinic Personalized Medicine Cohort. OSTEOPOROS INT 2010;21:467-77.
PubMed ID: 19506792

Nubel U, Dordel J, Kurt K, Strommenger B, Westh H, Shukla SK, Zemlickova H, Leblois R, Wirth T, Jombart T, Balloux F, Witte W. A timescale for evolution, population expansion, and spatial spread of an emerging clone of methicillin-resistant Staphylococcus aureus. PLoS PATHOG 2010;6:e1000855.
PubMed ID: 20386717

Wiley CL, Switzer SP, Berg RL, Glurich IE, Dart RA, Association of B-type natriuretic peptide (BNP) levels with estimated glomerular filtration rate (eGFR) and congestive heart failure (CHF). CLIN MED RES 2010;8:7-11.
PubMed ID: 19920165

Bales A, Zaleski CA, McPherson EW. Newborn screening programs: Should 22q11 deletion syndrome be added? GENET MED 2010;12:135-44.
PubMed ID: 20071995

Barber MJ, Mangravite LM, Hyde CL, Chasman DI, Smith JD, McCarty CA, Li X, Wilke RA, Rieder MJ, Williams PT, Ridker PM, Chatterjee A, Rotter JI, Nickerson DA, Stephens M, Krauss RM. Genome-wide association of lipid-lowering response to statins in combined study populations. PLoS ONE 2010;5:e9763.
PubMed ID: 20339536

Trost E, Gotker S, Schneider J, Schneiker-Bekel S, Szczepanowski R, Tilker A, Viehoever P, Arnold W, Bekel T, Blom J, Gartemann KH, Linke B, Goesmann A, Puhler A, Shukla SK, Tauch A. Complete genome sequence and lifestyle of black-pigmented Corynebacterium aurimucosum ATCC 700975 (formerly C. nigricans CN-1) isolated from a vaginal swab of a woman with a spontaneous abortion. BMC GENOMICS 2010;11:91.
PubMed ID: 20137072

Cross DS, Ivacic LC, Stefanski EL, McCarty CA. Development and implementation of a genetic fingerprinting assay for the Personalized Medicine Research Project. CLIN MED RES 2010;8:50.

Burmester JK, Sedova M, Shapero MH, Mansfield E. DMET microarray technology for pharmacogenomics-based personalized medicine. METHODS MOL BIOL 2010;632:99-124.
PubMed ID: 20217574



2009 Publications

Mareedu RK, Modhia FM, Kanin EI, Linneman JG, Kitchner TE, McCarty CA, Krauss RM, Wilke RA. Use of an electronic medical record to characterize cases of intermediate statin-induced muscle toxicity. PREV CARDIOL 2009;12:88-94.
PubMed ID: 19476582

Bailey H, Agger WA, Baumgardner D, Burmester JK, Cisler R, Everten J, Glurich IE, Hartman D, Yale SH, DeMets D. The Wisconsin Network for Health Research (WiNHR): A statewide, collaborative, multi-disciplinary, research group. WIS MED J 2009;108:453-458.
PubMed ID: 20131687

Dart RA. Professionalism: A 'critical care' component in health care reform. WMJ 2009;108:435-6.
PubMed ID: 20131683

Sue LY, Schairer C, Ma X, Williams C, Chang SC, Miller AB, McCarty CA, Willcox BJ, Ziegler RG. Energy intake and risk of postmenopausal breast cancer: An expanded analysis in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO) cohort. CANCER EPIDEMIOL BIOMARKERS PREV 2009;18:2842-50.
PubMed ID: 19843674

Wilke RA, Simpson RU, Mukesh BN, Bhupathi S, Dart RA, Ghebranious N, McCarty CA. Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension. PHARMACOGENOMICS 2009;10:1789-97.
PubMed ID: 19891555

Grimm R, Davis B, Piller L, Cutler J, Margolis K, Barzilay J, Dart RA, Graumlich J, Murden R, Randall O, ALLHAT Collaborative Research Group . Heart Failure in ALLHAT: Did blood pressure medication at study entrance influence outcome? J CLIN HYPERTENS (Greenwich) 2009;11:466-74.
PubMed ID: 19751458

Gopalakrishnan PP, Shukla SK, Tak T. Infective endocarditis: rationale for revised guidelines for antibiotic prophylaxis. CLIN MED RES 2009;7:63-8.
PubMed ID: 19608722

Hogan KJ, Burmester JK, Caldwell MD, Hogan QH, Coursin DB, Green DN, Selzer RM, Broderick TP, Rusy DA, Poroli M, Lutz AL, Sanders AM, Oldenburg MC, Koelbl JA, de Arruda-Indig M, Halsey JL, Day SP, Domanico MJ. Perioperative genomic profiles using structure-specific oligonucleotide probes. CLIN MED RES 2009;7:69-84.
PubMed ID: 19474452

Ferrucci LM, Cross AJ, Graubard B, Brinton LA, McCarty CA, Ziegler RG, Ma X, Mayne ST, Sinha R. Intake of meat, meat mutagens, and iron and the risk of breast cancer in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial. BR J CANCER 2009;101:178-84.
PubMed ID: 19513076

Onitilo AA, McCarty CA, Wilke RA, Glurich IE, Engel JM, Flockhart DA, Nguyen A, Li L, Mi D, Skaar TC, Gin Y. Estrogen receptor genotype is associated with risk of venous thromboembolism during tamoxifen therapy. BREAST CANCER RES TR 2009;115:643-50.
PubMed ID: 19082882

Thomas G, Jacobs KB, Kraft P, Yeager M, Wacholder S, Cox DG, Hankinson SE, Hutchinson A, Wang Z, Yu K, Chatterjee N, Garcia-Closas M, Gonzalez-Bosquet J, Prokunina-Olsson L, Orr N, Willett WC, Colditz GA, Ziegler RG, Berg CD, Buys SS, McCarty CA, Spenser Feigelson H, Calle EE, Thun MJ, Diver R, Prentice R, Jackson R, Kooperberg C, Chlebowski R, Lissowska J, Peplonska B, Brinton LA, Sigurdson A, Doody M, Bhatti P, Alexander B, Buring J, Lee I, Vatten LJ, Hveem K, Kumle M, Hayes RB, Tucker M, Gerhard DS, Fraumeni JF, Hoover RN, Chanock SJ, Hunter DJ. A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NAT GENET 2009;41:579-84.
PubMed ID: 19330030

Shukla SK, Kislow J, Briska A, Henkhaus J, Dykes C. Optical mapping reveals a large genetic inversion between two methicillin-resistant Staphylococcus aureus strains. J BACTERIOL 2009;191:5717-23.
PubMed ID: 19542272

Ahmed S, Thomas G, Ghoussaini M, Healey CS, Humphreys MK, Platte R, Morrison J, Maranian M, Pooley KA, Luben R, Eccles D, Evans DG, Fletcher O, Johnson N, dos Santos Silva I, Peto J, Stratton MR, Rahman N, Jacobs K, Prentice R, Anderson GL, Rajkovic A, Curb JD, Ziegler RG, Berg CD, Buys SS, McCarty CA, Feigelson HS, Calle EE, Thun MJ, Diver WR, Bojesen S, Nordestgaard BG, Flyger H, Dork T, Schurmann P, Hillemanns P, Karstens JH, Bogdanova NV, Antonenkova NN, Zalutsky IV, Bermisheva M, Fedorova S, Khusnutdinova E, SEARCH , Kang D, Yoo KY, Noh DY, Ahn SH, Devilee P, van Asperen DJ, Tollenaar RA, Sevnaeve D, Garcia-Closas M, Lissowska J, Brinton LA, Peplonska B, Nevanlinna H, Heikkinen T, Aittomaki K, Blomqvist C, Hopper JL, Southey MC, Smith L, Spurdle AB, Schmidt MK, Broeks A, van Hien RR, Cornelissen S, Milne RL, Ribas G, Gonzalez-Neira A, Benitez J, Schmutzler RK, Burwinkel B, Bartram CR, Meindl A, Brauch H, Justenhoven A, Hamann U, GENICA Consortium , Chang-Claude J, Hein R, Wang-Gohrke S, Lindblom A, Margolin S, Mannermaa A, Kosma VM, Olson JE, Wang X, Fredericksen Z, Giles GG, Severi G, Baglietto L, English DR, Hankinson SE, Cox DG, Kraft P, Vatten LJ, Hveem K, Kumle M, Sigurdson A, Doody M, Bhatti P, Alexander B, Hooning MJ, van den Ouweland AM, Oldenburg RA, Schutte M, Hall PM, Czene K, Liu J, Li Y, Cox A, Elliott G, Brock I, Reed MW, Shen CY, Yu JC, Hsu GC, Chen ST, Anton-Culver H, Ziogas A, Andrulis IL, Knight JA, KConFab , Australian Ovarian Cacner Study Group , Beesley J, Goode EL, Couch F, Chenevix-Trench G, Hoover RN, Ponder BA, Hunter DJ, Pharoah PD, Dunning AM, Chanock SJ, Easton DF. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. NAT GENET 2009;41:585-90.
PubMed ID: 19330027

Cross DS, Ivacic LC, McCarty CA. Development of a fingerprinting panel using medically relevant polymorphisms. BMC MED GENOMICS 2009;2
PubMed ID: 19379518

International Warfarin Pharmacogenetics Consortium, Klein TE, Altman RB, Eriksson N, Gage BF, Kimmel SE, Lee M, Limdi NA, Page D, Roden DM, Wagner MJ, Caldwell MD, Johnson JA. Berg RL, Burmester JK. Estimation of the warfarin dose with clinical and pharmacogenetic data. NEW ENGL J MED 2009;360:753-64.
PubMed ID: 19228618

Zaleski CA, Bassett AS, Tam K, Shugar AL, Chow EW, McPherson EW. The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome. AM J MED GENET A 2009;149A:525-8.
PubMed ID: 19208384

McPherson EW, Turner L, Zador I, Reynolds KK, Macgregor D, Giampietro PF. Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation. AM J MED GENET A 2009;149A:567-72.
PubMed ID: 19283854

Giampietro PF, Dunwoodie S, Kusumi K, Pourquie O, Tassy O, Offiah A, Cornier AS, Alman B, Blank RD, Raggio CL, Glurich IE, Turnpenny PD. Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans. ANN N Y ACAD SCI 2009;1151:38-67.
PubMed ID: 19154516



2008 Publications

Cross DS, Burmester JK. Functional characterization of the HOXB13 promoter region. MED ONCOL 2008;25:287-93.
PubMed ID: 18163187

McCarty CA, Chapman-Stone DJ, Derfus TL, Giampietro PF, Fost N, Marshfield Clinic PMRP Community Advisory Group . Community consultation and communication for a population-based DNA biobank: The Marshfield clinic personalized medicine research project. AM J MED GENET A 2008;146A:3026-3033.
PubMed ID: 19006210

Giampietro PF, Dunwoodie S, Kusumi K, Pourquie O, Tassy O, Offiah A, Cornier AS, Alman B, Blank RD, Raggio CL, Glurich IE, Turnpenny PD. Molecular diagnosis of vertebral segmentation disorders in humans. EXPERT OPIN MED DIAGN 2008;2:1107-21.

McCarty CA, Dowrick A, Cameron J, McGrath B, Robman L, Dimitrov P, Tikellis G, Nicolas C, McNeill JJ, Guymer RH. Novel measures of cardiovascular health and its association with prevalence and progression of age-related macular degeneration: the CHARM Study. BMC OPHTHALMOLOGY 2008;22:25.
PubMed ID: 19102747

Wesbrook SD, Giampietro PF, Glurich IE, McCarty CA, Peissig PL, Starren JB, Uphoff TS, Zaleski CA, Vidaillet HJ. Marshfield Clinic, Marshfield Wisconsin/ Community based approaches to personalized health care: Marshfield Clinic Personalized Health Care: Pioneers, Partnerships, Progress 2008.

Ghebranious N, Blank RD, Raggio CL, Staubli JC, McPherson EW, Ivacic LC, Rasmussen K, Jacobsen FS, Faciszewski T, Burmester JK, Pauli RM, Boachie-Adjei O, Glurich IE, Giampietro PF. A missense T(Brachyury) mutation contributes to vertebral malformations. J BONE MINER RES 2008;23:1576-83.
PubMed ID: 18466071

Wilke RA, Berg RL, Linneman JG, Zhao C, McCarty CA, Krauss RM. Characterization of low-density lipoprotein cholesterol-lowering efficacy for atorvastatin in a population-based DNA biorepository. BASIC CLIN PHARMACOL TOXICOL 2008;103:354-9.
PubMed ID: 18834356

Kopp JB, Smith JW, Nelson GW, Johnson RC, Freedman BI, Bowden DW, Oleksyk T, McKenzie LM, Kajiyama H, Ahuja TS, Berns JS, Briggs JA, Cho ME, Dart RA, Kimmel PL, Korbet SM, Michel DM, Mokryzcki M, Schelling JR, Simon EE, Trachtman H, Vlahov D, Winkler CA. MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis. NAT GENET 2008;40:1175-84.
PubMed ID: 18794856

McPherson EW, Zaleski CA, Benishek K, McCarty CA, Giampietro PF, Reynolds KK, Rasmussen K. Clinical genetics provider real-time workflow study. GENET MED 2008;10:699-706.
PubMed ID: 18978682

McCarty CA, Peissig PL, Caldwell MD, Wilke RA. The Marshfield Clinic Personalized Medicine Research Project: 2008. Scientific update and lessons learned in the first 6 years. PER MED 2008;5:529-42.

McCarty CA, Mukesh BN, Kitchner TE, Hubbard WC, Wilke RA, Burmester JK, Patchett RB. Intraocular pressure response to medication in a clinical setting: the Marshfield Clinic Personalized Medicine Research Project. J GLAUCOMA 2008;17:372-7.
PubMed ID: 18703947

Patel A, Cheng I, Canzian F, Le Marchand L, Thun MJ, Berg CD, Buring J, Calle EE, Chanock S, Clavel-Chapelon F, Cox DG, Dorronsoro M, Dossus L, Haiman C, Hankinson SE, Henderson BE, Hoover RN, Hunter DJ, Kaaks R, Kolonel L, Kraft P, Linseisen J, Lund E, Manjer J, McCarty CA, Peeters P, Pike M, Pollak M, Riboli E, Stram D, Tjonneland A, Travis R, Trichopoulos D, Tumino R, Yeager M, Ziegler RG, Fiegelson H, Breast and Prostate Cancer Cohort Consortium . IGF-1, IGFBP-1, and IGFBP-3 polymorphisms predict circulating IGF levels but not breast cancer risk: findings from the Breast and Prostate Cancer Cohort Consortium (BPC3). PLoS ONE 2008;3:e2578.
PubMed ID: 18596909

McCarty CA, Burmester JK, Mukesh BN, Patchett RB, Wilke RA. Intraocular pressure response to topical beta-blockers associated with an ADRB2 single-nucleotide polymorphism. ARCH OPHTHALMOL-CHIC 2008;126:959-63.
PubMed ID: 18625943

Giampietro PF, Peterson MG, Raggio CL. Alterations in bone mineral density in Marfan Syndrome and homocystinuria. CLINIC REV BONE MINER METAB 2008;6:46-52.

Lin AE, Basson CT, Goldmuntz E, Magoulas PL, McDermott DA, McDonald - McGinn DM, McPherson EW, Morris CA, Noonan J, Nowak C, Pierpont ME, Pyeritz RE, Rope AF, Zackai EH, Pober BR. Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management. GENET MED 2008;10:469-94.

PubMed ID: 18580689

Baird PN, Robman L, Richardson AJ, Dimitrov P, Tikellis G, McCarty CA, Guymer RH. Gene-environment interaction in progression of AMD: the CFH gene, smoking and exposure to chronic infection. HUM MOL GENET 2008;17:1299-305.
PubMed ID: 18203751

Sidjanin DJ, McCarty CA, Patchett RB, Smith E, Wilke RA. Pharmacogenetics of ophthalmic topical beta-blockers. . PER MED 2008;5:377-85.
PubMed ID: 19266054

Vijaya L, George R, Baskaran M, Arvind H, Ramesh SV, Kumaramanickavel G, McCarty CA. Prevalence of primary open-angle glaucoma in an urban South Indian population and comparison with a rural population; the Chennai Glaucoma Study. OPHTHALMOLOGY 2008;115:648-54.e1.
PubMed ID: 17664010

Vijaya L, George R, Arvind H, Baskaran M, Ramesh SV, Raju P, Kumaramanickavel G, McCarty CA. Prevalence of primary angle-closure disease in an urban South Indian population and comparison with a rural population; the Chennai Glaucoma Study. OPHTHALMOLOGY 2008;114:655-60.e1.
PubMed ID: 17869343

Caldwell MD, Awad T, Johnson JA, Gage BF, Falkowski M, Gardina P, Hubbard J, Turpaz Y, Langaee TY, Eby C, King C, Brower A, Schmelzer JR, Glurich IE, Vidaillet HJ, Yale SH, Zhang KQ, Berg RL, Burmester JK. CYP4F2 genetic variant alters required warfarin dose. BLOOD 2008;111:4106-12.
PubMed ID: 18250228

Freedman D, Chang SC, Falk R, Purdue M, Huang WY, McCarty CA, Hollis B, Graubard B, Berg CD, Ziegler RG. Serum levels of vitamin D metabolites and breast cancer risk in the prostate, lung, colorectal, and ovarian cancer screening trial. CANCER EPIDEMIOL BIOMARKERS PREV 2008;17:889-94.
PubMed ID: 18381472

McCarty CA. Sunlight exposure assessment: can we accurately assess vitamin D exposure from sunlight questionnaires? AM J CLIN NUTR 2008;87:1097S-101S.
PubMed ID: 18400741

Reeser JC, Austin DM, Jaros LM, Mukesh BN, McCarty CA. Investigating perceived Institutional Review Board quality and function using the IRB researcher assessment tool. J EMPIR RES HUM RES ETHICS 2008;3:25-34.
PubMed ID: 19385780

Uthra S, Raman R, Mukesh BN, Rajkumar V, Padmaja KR, Paul PG, Lakshmipathy P, Gnanamoorthy P, Sharma T, McCarty CA, Kumaramanickavel G. Association of VEGF gene polymorphisms with diabetic retinopathy in a south Indian cohort. OPHTHALMIC GENET 2008;29:11-5.
PubMed ID: 18363167

Chiong JR, Aronow WS, Khan IA, Nair CK, Vijayaraghavan K, Dart RA, Behrenbeck TR, Geraci SA. Secondary hypertension: current diagnosis and treatment. INT J CARDIOL 2008;124:6-21.
PubMed ID: 17462751

Black HR, Dave BJ, Barzilay J, Nwachuku CE, Baimbridge C, Marginean H, Wright JT, Basile JN, Wong C, Whelton P, Dart RA, Thadani U, Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial. Metabolic and clinical outcomes in nondiabetic individuals with the metabolic syndrome assigned to chlorthalidone, amlodipine, or lisinopril as initial treatment for hypertension: a report from the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). DIABETES CARE 2008;31:353-60.
PubMed ID: 18000186

Cross DS, Burmester JK. Functional characterization of the GDEP promoter and three enhancer elements in retinoblastoma and prostate cell lines. MED ONCOL 2008;25:40-9.
PubMed ID: 18188713

Rasmussen K, Zador I, Zabel C, Krantz ID, Giampietro PF. Bile duct anomalies in a male child with Noonan syndrome: a case for ras and notch pathway synergism. AM J MED GENET A 2008;146:261-3.
PubMed ID: 18080325

Wright JT, Harris-Haywood S, Pressel S, Barzilay J, Baimbridge C, Bareis CJ, Basile JN, Black HR, Dart RA, Gupta AK, Hamilton BP, Einhorn PT, Haywood LJ, Jafri SZ, Louis GT, Whelton PK, Scott CL, Simmons DL, Stanford C, Davis BR. Clinical outcomes by race in hypertensive patients with and without the metabolic syndrome. ARCH INTERN MED 2008;168:207-17.
PubMed ID: 18227370



2007 Publications

McCarty CA, McCarty DJ, Wetter AC. Calories from newspaper dessert recipes are associated with community obesity rates. WMJ 2007;106:68-70.
PubMed ID: 17479822

McKenzie LM, Hendrickson SL, Briggs WA, Dart RA, Korbet SM, Mokryzcki M, Kimmel PL, Ahuja TS, Berns JS, Simon EE, Smith M, Trachtman H, Michel DM, Schelling JR, Cho ME, Zhou YC, Binns-Roemer E, Kirk GD, Kopp JB, Winkler CA. NPHS2 variation in sporadic focal segmental glomerulosclerosis. J AM SOC NEPHROL 2007;18:2987-95.
PubMed ID: 17942957

Robman L, Vu H, Hodge A, Tikellis G, Dimitrov P, McCarty CA, Guymer RH. Dietary lutein, zeaxanthin, and fats and the progression of age-related macular degeneration. CAN J OPHTHALMOL 2007;42:720-6.
PubMed ID: 17724493

Ghebranious N, Raggio CL, Blank RD, McPherson EW, Burmester JK, Ivacic LC, Rasmussen K, Kislow JL, Glurich IE, Jacobsen FS, Faciszewski T, Pauli RM, Boachie-Adjei O, Giampietro PF. Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations. SCOLIOSIS 2007;2:13.
PubMed ID: 17888180

Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, Hankinson SE, Wacholder S, Wang Z, Welch R, Hutchinson A, Wang J, Yu K, Chatterjee N, Orr N, Willett WC, Colditz GA, Ziegler RG, Berg CD, Buys SS, McCarty CA, Feigelson HS, Calle EE, Thun MJ, Hayes RB, Tucker M, Gerhard DS, Fraumeni JF, Hoover RN, Thomas G, Chanock SJ. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NAT GENET 2007;39:870-4.
PubMed ID: 17529973

Turnpenny PD, Alman B, Cornier AS, Giampietro PF, Offiah A, Tassy O, Pourquie O, Kusumi K, Dunwoodie S. Abnormal vertebral segmentation and the notch signaling pathway in man. DEV DYN 2007;236:1456-74.
PubMed ID: 17497699

Ghebranious N, Giampietro PF, Wesbrook FP, Rezkalla SH. A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation. AM J MED GENET A 2007;143A:1462-71.
PubMed ID: 17568417

Ghebranious N, McCarty CA, Wilke RA. Clinical phenome scanning. PER MED 2007;4:175-82.

McCarty CA, Mukesh BN, Giampietro PF, Wilke RA. Healthy People 2010 disease prevalence in the Marshfield Clinic Personalized Medicine Research Project cohort: opportunities for public health genomic research. PER MED 2007;4:183-90.

McPherson EW. Renal anomalies in families of individuals with congenital solitary kidney. GENET MED 2007;9:298-302.
PubMed ID: 17505207

Uthra S, Raman R, Mukesh BN, Padmaja KR, Paul PG, Lakshmipathy P, Gnanamoorthy P, Sharma T, McCarty CA, Kumaramanickavel G. Intron 4 VNTR of endothelial nitric oxide synthase (eNOS) gene and diabetic retinopathy in type 2 patients in southern India. OPHTHALMIC GENET 2007;28:77-81.
PubMed ID: 17558849

Peissig PL, Sirohi E, Berg RL, Brown-Switzer C, Ghebranious N, McCarty CA, Wilke RA. Construction of atorvastatin dose-response relationships using data from a large population-based DNA biobank. BASIC CLIN PHARMACOL TOXICOL 2007;100:286-8.
PubMed ID: 17371534

Wilke RA, Berg RL, Peissig PL, Kitchner TE, Sijercic B, McCarty CA, McCarty DJ. Use of an electronic medical record for the identification of research subjects with diabetes mellitus. CLIN MED RES 2007;5:1-7.
PubMed ID: 17456828

Caldwell MD, Berg RL, Zhang KQ, Glurich IE, Schmelzer JR, Yale SH, Vidaillet HJ, Burmester JK. Evaluation of genetic factors for warfarin dose prediction. CLIN MED RES 2007;5:8-16.
PubMed ID: 17456829

Giampietro PF, Peterson MG, Schneider R, Davis JG, Burke SW, Boachie-Adjei O, Mueller CM, Raggio CL. Bone mineral density determinations by dual-energy x-ray absorptiometry in the management of patients with Marfan syndrome--some factors which affect the measurement. HSS J 2007;3:89-92.
PubMed ID: 18751776

Ivacic LC, Reed KD, Mitchell P, Ghebranious N. A LightCycler TaqMan assay for detection of Borrelia burgdorferi sensu lato in clinical samples. DIAGN MICROBIOL INFECT DIS 2007;57:137-43.
PubMed ID: 16989975

Tikellis G, Robman LD, Dimitrov P, Nicolas C, McCarty CA, Guymer RH. Characteristics of progression of early age-related macular degeneration: the Cardiovascular Health and Age-Related Maculopathy Study. EYE 2007;21:169-76.
PubMed ID: 16732219

McCarty CA, Nair AK, Austin DM, Giampietro PF. Informed consent and subject motivation to participate in a large, population-based genomics study: the Marshfield Clinic Personalized Medicine Research Project. COMMUNITY GENET 2007;10:2-9.
PubMed ID: 17167244


2006 Publications

Pan N, Luo J, Kaiser SJ, Frome WL, Dart RA, Tewksbury DA. Specific receptor for angiotensinogen on human renal cells. CLIN CHIM ACTA 2006;373:32-6.
PubMed ID: 16764846

Burmester JK, Salzman SA, Zhang KQ, Dart RA. Small molecule antagonists of the TGF-beta1/TGF-beta receptor binding interaction. MED ONCOL 2006;23:553-62.
PubMed ID: 17303915

Wilke RA. Translational pharmacogenetics and risk management in the cardiovascular arena - using the CYP 3A5*3 allele as a model for gene-based drug selection. PER MED 2006;3:385-90.

Friez MJ, Jones JR, Clarkson K, Lubs H, Abuelo D, Bier JA, Pai S, Simensen R, Williams C, Giampietro PF, Schwartz CE, Stevenson RE. Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28. PEDIATRICS 2006;118:1687-95.
PubMed ID: 17088400

McPherson EW, Zaleski CA, Mascola MA. Prenatal diagnosis of episodic tachypnea in an infant with OFD VI. AM J MED GENET A 2006;140:2146-9.
PubMed ID: 16906567

Giampietro PF, Raggio CL, Reynolds CE, Ghebranious N, Burmester JK, Glurich IE, Rasmussen K, McPherson EW, Pauli RM, Shukla SK, Merchant S, Jacobsen FS, Faciszewski T, Blank RD. DLL3 as a candidate gene for vertebral malformations. AM J MED GENET A 2006;140A:2447-53.
PubMed ID: 17041936

Vu HT, Robman L, Hodge A, McCarty CA, Taylor H. Lutein and zeaxanthin and the risk of cataract: the Melbourne visual impairment project. INVEST OPHTHALMOL VIS SCI 2006;47:3783-6.
PubMed ID: 16936087

Cross DS, Burmester JK. Gene therapy for cancer treatment: past, present and future. CLIN MED RES 2006;4:218-27.
PubMed ID: 16988102

Dart RA, Salzman-Scott SA. Expression of concern - Sudbo J. Novel management of oral cancer: a paradigm of predictive oncology. CLIN MED RES 2006;4:160.
PubMed ID: 16988092

McCarty CA. Timely translation of ophthalmic research into clinical practice. BR J OPHTHALMOL 2006;90:1073-4.
PubMed ID: 16929051

Robman L, Vu H, Hodge A, McCarty CA, Taylor HR. Dietary lutein and zeaxanthin: authors' response. BR J OPHTHALMOL 2006;90:1211-2.
PubMed ID: 16929074

Giampietro PF, Greenlee RT, McPherson EW, Benetti LL, Berg RL, Wagner SF. Acute health events in adult patients with genetic disorders: the Marshfield Epidemiologic Study Area. GENET MED 2006;8:474-90.
PubMed ID: 16912579

Leenen FH, Nwachuku CE, Black HR, Cushman WC, Davis BR, Simpson LM, Alderman MH, Atlas SA, Basile JN, Cuyjet AB, Dart RA, Felicetta JV, Grimm RH, Haywood LJ, Jafri SZ, Proschan MA, Thandani U, Whelton PK, Wright JT, ALLHAT Collaborative Research Group . Clinical events in high-risk hypertensive patients randomly assigned to calcium channel blocker versus angiotensin-converting enzyme inhibitor in the antihypertensive and lipid-lowering treatment to prevent heart attack trial. HYPERTENSION 2006;48:374-84.
PubMed ID: 16864749

McPherson EW. Genetic diagnosis and testing in clinical practice. CLIN MED RES 2006;4:123-9.
PubMed ID: 16809405

Ghebranious N, Burmester JK, Glurich IE, McPherson EW, Ivacic LC, Kislow JL, Rasmussen K, Kumar VR, Raggio CL, Blank RD, Jacobsen FS, Faciszewski T, Womack J, Giampietro PF. Evaluation of SLC35A3 as a candidate gene for human vertebral malformations. AM J MED GENET A 2006;140:1346-8.
PubMed ID: 16691598

McCarty CA. Uncorrected refractive error. BR J OPHTHALMOL 2006;90:521-2.
PubMed ID: 16622075

Neiswanger K, Hohler PM, Hively-Thomas LB, McPherson EW, Hogge WA, Surti U. Variable outcomes in mosaic trisomy 16: Five case reports and literature analysis. PRENAT DIAGN 2006;26:454-61.
PubMed ID: 16557642

Vijaya L, George R, Arvind H, Baskaran M, Raju P, Ramesh SV, Paul PG, Kumaramanickavel G, McCarty CA. Prevalence and cases of blindness in the rural population of the Chennai Glaucoma Study. BR J OPHTHALMOL 2006;90:407-10.
PubMed ID: 16547314

Baird PN, Richardson AJ, Robman L, Dimitrov PN, Tikellis G, McCarty CA, Guymer RH. Apolipoprotein (APOE) gene is associated with progression of age-related macular degeneration (AMD). HUM MUTAT 2006;27:337-42.
PubMed ID: 16453339

Giampietro PF, Schowalter DB, Merchant S, Campbell LR, Swink TD, Roa BB. Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndrome. CHILDS NERV SYST 2006;22:320-324.
PubMed ID: 15875198

Strauss KA, Puffenberger EG, Huentelman M, Gottlieb S, Dobrin SE, Parod JM, Stephan DA, Morton DH. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. NEW ENGL J MED 2006;354:1370-7.
PubMed ID: 16571880

Vijaya L, George R, Arvind H, Baskaran M, Paul PG, Ramesh SV, Raju P, Kumaramanickavel G, McCarty CA. Prevalence of angle-closure disease in a rural southern Indian population. ARCH OPHTHALMOL 2006;124:403-9.
PubMed ID: 16534061

Vu HT, Robman L, McCarty CA, Taylor HR, Hodge A. Does dietary lutein and zeaxanthin increase the risk of age related macular degeneration? The Melbourne Visual Impairment Project. BR J OPHTHALMOL 2006;90:389-90.
PubMed ID: 16488968

Strauss KA, Puffenberger EG, Huentelman MJ, Gottlieb S, Dobrin SE, Parod JM, Stephan DA, Morton DH. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. N ENGL J MED 2006;354:1370-7.
PubMed ID: 16571880

Giampietro PF, Babu D, Zabel C, Silberman TL, Zador I, DeBauche D, Ravnan JB, Dave BJ. Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity. AM J MED GENET 2006;140A:385-7.
PubMed ID: 16411193

McPherson EW, Zaleski CA, Giampietro PF. Robinow syndrome with variable neurologic features. GENET MED 2006;8:59-60.
PubMed ID: 16418601

Mukesh BN, Le A, Dimitrov PN, Ahmed S, Taylor H, McCarty CA. Development of cataract and associated risk factors: the Visual Impairment Project. ARCH OPHTHALMOL 2006;124:79-85.
PubMed ID: 16401788

McPherson EW, Zabel C. Mitochondrial mutation in a child with distal arthrogryposis. AM J MED GENET A 2006;140:184-5.
PubMed ID: 16353243

Zahari M, Mukesh BN, Rait JL, Taylor HR, McCarty CA. Progression of visual field loss in open angle glaucoma in the Melbourne Visual Impairment Project. CLIN EXP OPHTHALMOL 2006;34:20-6.
PubMed ID: 16451254