Loading...

Edwards, Karen L

TitleProfessor
InstitutionUniversity of California, Irvine
DepartmentEpidemiology
Address1001 Health Sciences Road
CA 92697-3950
Phone(949) 824-9054
vCardDownload vCard

    Collapse Research 
    Collapse Research Activities and Funding
    Identifying genes underlying linkage peaks for clusters of CVD risk factors
    NIH/NHLBI R01HL113189Apr 1, 2012 - Mar 31, 2017
    Role: Principal Investigator
    Identification of Issues and Expectations of Subjects Participating in Genetic St
    NIH/NCI R01CA149051Mar 1, 2011 - Feb 29, 2016
    Role: Principal Investigator
    GENETIC EPIDEMIOLOGY OF THE INSULIN RESISTANCE SYNDROME
    NIH/NIDDK F32DK009645Sep 5, 1997
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
    List All   |   Timeline
    1. Cholerton B, Johnson CO, Fish B, Quinn JF, Chung KA, Peterson-Hiller AL, Rosenthal LS, Dawson TM, Albert MS, Hu SC, Mata IF, Leverenz JB, Poston KL, Montine TJ, Zabetian CP, Edwards K. Sex differences in progression to mild cognitive impairment and dementia in Parkinson's disease. Parkinsonism Relat Disord. 2018 May; 50:29-36. PMID: 29478836.
      View in: PubMed
    2. Goodman D, Johnson CO, Bowen D, Smith M, Wenzel L, Edwards K. A comparison of views regarding the use of de-identified data. Transl Behav Med. 2018 Jan 29; 8(1):113-118. PMID: 29385588.
      View in: PubMed
    3. Goodman D, Bowen D, Wenzel L, Tehrani P, Fernando F, Khacheryan A, Chowdhury F, Johnson CO, Edwards K. The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature. Transl Behav Med. 2018 Jan 29; 8(1):119-129. PMID: 29385589.
      View in: PubMed
    4. Licking N, Murchison C, Cholerton B, Zabetian CP, Hu SC, Montine TJ, Peterson-Hiller AL, Chung KA, Edwards K, Leverenz JB, Quinn JF. Homocysteine and cognitive function in Parkinson's disease. Parkinsonism Relat Disord. 2017 Nov; 44:1-5. PMID: 28807493.
      View in: PubMed
    5. Mata IF, Johnson CO, Leverenz JB, Weintraub D, Trojanowski JQ, Van Deerlin VM, Ritz B, Rausch R, Factor SA, Wood-Siverio C, Quinn JF, Chung KA, Peterson-Hiller AL, Espay AJ, Revilla FJ, Devoto J, Yearout D, Hu SC, Cholerton BA, Montine TJ, Edwards K, Zabetian CP. Large-scale exploratory genetic analysis of cognitive impairment in Parkinson's disease. Neurobiol Aging. 2017 Aug; 56:211.e1-211.e7. PMID: 28526295.
      View in: PubMed
    6. Goodman D, Johnson CO, Bowen D, Smith M, Wenzel L, Edwards K. De-identified genomic data sharing: the research participant perspective. J Community Genet. 2017 Jul; 8(3):173-181. PMID: 28382417.
      View in: PubMed
    7. Mata IF, Davis MY, Lopez AN, Dorschner MO, Martinez E, Yearout D, Cholerton BA, Hu SC, Edwards K, Bird TD, Zabetian CP. The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot. Am J Med Genet B Neuropsychiatr Genet. 2017 01; 174(1):113. PMID: 27943640.
      View in: PubMed
    8. Cooper CA, Jain N, Gallagher MD, Weintraub D, Xie SX, Berlyand Y, Espay AJ, Quinn J, Edwards K, Montine T, Van Deerlin VM, Trojanowski J, Zabetian CP, Chen-Plotkin AS. Common variant rs356182 near SNCA defines a Parkinson's disease endophenotype. Ann Clin Transl Neurol. 2017 Jan; 4(1):15-25. PMID: 28078311.
      View in: PubMed
    9. Davis MY, Johnson CO, Leverenz JB, Weintraub D, Trojanowski JQ, Chen-Plotkin A, Van Deerlin VM, Quinn JF, Chung KA, Peterson-Hiller AL, Rosenthal LS, Dawson TM, Albert MS, Goldman JG, Stebbins GT, Bernard B, Wszolek ZK, Ross OA, Dickson DW, Eidelberg D, Mattis PJ, Niethammer M, Yearout D, Hu SC, Cholerton BA, Smith M, Mata IF, Montine TJ, Edwards K, Zabetian CP. Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease. JAMA Neurol. 2016 Oct 01; 73(10):1217-1224. PMID: 27571329.
      View in: PubMed
    10. Condit CM, Shen L, Edwards K, Bowen DJ, Korngiebel DM, Johnson CO. Participants' Role Expectations in Genetics Research and Re-consent: Revising the Theory and Methods of Mental Models Research Relating to Roles. J Health Commun. 2016; 21(sup2):16-24. PMID: 27653592.
      View in: PubMed
    11. Hyams T, Bowen DJ, Condit C, Grossman J, Fitzmaurice M, Goodman D, Wenzel L, Edwards K. Views of Cohort Study Participants about Returning Research Results in the Context of Precision Medicine. Public Health Genomics. 2016; 19(5):269-75. PMID: 27553645.
      View in: PubMed
    12. Goodman D, Johnson CO, Wenzel L, Bowen D, Condit C, Edwards K. Consent Issues in Genetic Research: Views of Research Participants. Public Health Genomics. 2016; 19(4):220-8. PMID: 27376949.
      View in: PubMed
    13. Mata IF, Davis MY, Lopez AN, Dorschner MO, Martinez E, Yearout D, Cholerton BA, Hu SC, Edwards K, Bird TD, Zabetian CP. The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot. Am J Med Genet B Neuropsychiatr Genet. 2016 10; 171(7):925-30. PMID: 27111571.
      View in: PubMed
    14. Edwards K, Korngiebel DM, Pfeifer L, Goodman D, Renz A, Wenzel L, Bowen DJ, Condit CM. Participant views on consent in cancer genetics research: preparing for the precision medicine era. J Community Genet. 2016 Apr; 7(2):133-43. PMID: 26801345; PMCID: PMC4796049.
    15. LeBlanc K, Baranoski S, Christensen D, Langemo D, Edwards K, Holloway S, Gloeckner M, Williams A, Campbell K, Alam T, Woo KY. The Art of Dressing Selection: A Consensus Statement on Skin Tears and Best Practice. Adv Skin Wound Care. 2016 Jan; 29(1):32-46. PMID: 26650095.
      View in: PubMed
    16. Mata IF, Jang Y, Kim CH, Hanna DS, Dorschner MO, Samii A, Agarwal P, Roberts JW, Klepitskaya O, Shprecher DR, Chung KA, Factor SA, Espay AJ, Revilla FJ, Higgins DS, Litvan I, Leverenz JB, Yearout D, Inca-Martinez M, Martinez E, Thompson TR, Cholerton BA, Hu SC, Edwards K, Kim KS, Zabetian CP. The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease. Mol Neurodegener. 2015 Sep 24; 10:50. PMID: 26399558; PMCID: PMC4581468.
    17. Mata IF, Leverenz JB, Weintraub D, Trojanowski JQ, Chen-Plotkin A, Van Deerlin VM, Ritz B, Rausch R, Factor SA, Wood-Siverio C, Quinn JF, Chung KA, Peterson-Hiller AL, Goldman JG, Stebbins GT, Bernard B, Espay AJ, Revilla FJ, Devoto J, Rosenthal LS, Dawson TM, Albert MS, Tsuang D, Huston H, Yearout D, Hu SC, Cholerton BA, Montine TJ, Edwards K, Zabetian CP. GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson's disease. Mov Disord. 2016 Jan; 31(1):95-102. PMID: 26296077; PMCID: PMC4724255 [Available on 01/01/17].
    18. Condit CM, Korngiebel DM, Pfeifer L, Renz AD, Bowen DJ, Kaufman D, Kollar LM, Edwards K. What Should Be the Character of the Researcher- Participant Relationship? Views of Participants in a Long-standing Cancer Genetic Registry. IRB. 2015 Jul-Aug; 37(4):1-10. PMID: 26331187.
      View in: PubMed
    19. Srivatsal S, Cholerton B, Leverenz JB, Wszolek ZK, Uitti RJ, Dickson DW, Weintraub D, Trojanowski JQ, Van Deerlin VM, Quinn JF, Chung KA, Peterson AL, Factor SA, Wood-Siverio C, Goldman JG, Stebbins GT, Bernard B, Ritz B, Rausch R, Espay AJ, Revilla FJ, Devoto J, Rosenthal LS, Dawson TM, Albert MS, Mata IF, Hu SC, Montine KS, Johnson C, Montine TJ, Edwards K, Zhang J, Zabetian CP. Cognitive profile of LRRK2-related Parkinson's disease. Mov Disord. 2015 Apr 15; 30(5):728-33. PMID: 25650144; PMCID: PMC4397146.
    20. Jelakovic B, Vukovic Lela I, Karanovic S, Dika Ž, Kos J, Dickman K, Šekoranja M, Poljicanin T, Mišic M, Premužic V, Abramovic M, Matijevic V, Miletic Medved M, Cvitkovic A, Edwards K, Fucek M, Leko N, Teskera T, Laganovic M, Cvorišcec D, Grollman AP. Chronic dietary exposure to aristolochic acid and kidney function in native farmers from a Croatian endemic area and Bosnian immigrants. Clin J Am Soc Nephrol. 2015 Feb 06; 10(2):215-23. PMID: 25587102; PMCID: PMC4317733.
    21. Mata IF, Leverenz JB, Weintraub D, Trojanowski JQ, Hurtig HI, Van Deerlin VM, Ritz B, Rausch R, Rhodes SL, Factor SA, Wood-Siverio C, Quinn JF, Chung KA, Peterson AL, Espay AJ, Revilla FJ, Devoto J, Hu SC, Cholerton BA, Wan JY, Montine TJ, Edwards K, Zabetian CP. APOE, MAPT, and SNCA genes and cognitive performance in Parkinson disease. JAMA Neurol. 2014 Nov; 71(11):1405-12. PMID: 25178429; PMCID: PMC4227942.
    22. Santorico SA, Edwards K. Challenges of linkage analysis in the era of whole-genome sequencing. Genet Epidemiol. 2014 Sep; 38 Suppl 1:S92-6. PMID: 25112196.
      View in: PubMed
    23. Burdick DJ, Cholerton B, Watson GS, Siderowf A, Trojanowski JQ, Weintraub D, Ritz B, Rhodes SL, Rausch R, Factor SA, Wood-Siverio C, Quinn JF, Chung KA, Srivatsal S, Edwards K, Montine TJ, Zabetian CP, Leverenz JB. People with Parkinson's disease and normal MMSE score have a broad range of cognitive performance. Mov Disord. 2014 Sep; 29(10):1258-64. PMID: 25073717; PMCID: PMC4162839.
    24. Yorgov D, Edwards K, Santorico SA. Use of admixture and association for detection of quantitative trait loci in the Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Ethnic Samples (T2D-GENES) study. BMC Proc. 2014; 8(Suppl 1):S6. PMID: 25519335; PMCID: PMC4143673.
    25. Cholerton BA, Zabetian CP, Wan JY, Montine TJ, Quinn JF, Mata IF, Chung KA, Peterson A, Espay AJ, Revilla FJ, Devoto J, Watson GS, Hu SC, Leverenz JB, Edwards K. Evaluation of mild cognitive impairment subtypes in Parkinson's disease. Mov Disord. 2014 May; 29(6):756-64. PMID: 24710804; PMCID: PMC4013249.
    26. Hill DA, Horick NK, Isaacs C, Domchek SM, Tomlinson GE, Lowery JT, Kinney AY, Berg JS, Edwards K, Moorman PG, Plon SE, Strong LC, Ziogas A, Griffin CA, Kasten CH, Finkelstein DM. Long-term risk of medical conditions associated with breast cancer treatment. Breast Cancer Res Treat. 2014 May; 145(1):233-43. PMID: 24696430; PMCID: PMC4096572.
    27. Ivkovic V, Karanovic S, Fištrek Prlic M, Mišic M, Kos J, Juric D, Vukovic Lela I, Vitale K, Cvitkovic A, Laganovic M, Fodor L, Edwards K, Grollman AP, Jelakovic B. Is herbal tea consumption a factor in endemic nephropathy? Eur J Epidemiol. 2014 Mar; 29(3):221-4. PMID: 24623403.
      View in: PubMed
    28. Jelakovic B, Nikolic J, Radovanovic Z, Nortier J, Cosyns JP, Grollman AP, Bašic-Jukic N, Belicza M, Bukvic D, Cavaljuga S, Cvorišcec D, Cvitkovic A, Dika Ž, Dimitrov P, Ðukanovic L, Edwards K, Ferluga D, Fuštar-Preradovic L, Gluhovschi G, Imamovic G, Jakovina T, Kes P, Leko N, Medverec Z, Mesic E, Miletic-Medved M, Miller F, Pavlovic N, Pasini J, Pleština S, Polenakovic M, Stefanovic V, Tomic K, Trnacevic S, Vukovic Lela I, Štern-Padovan R. Consensus statement on screening, diagnosis, classification and treatment of endemic (Balkan) nephropathy. Nephrol Dial Transplant. 2014 Nov; 29(11):2020-7. PMID: 24166461; PMCID: PMC4288114.
    29. Wan JY, Edwards K, Hutter CM, Mata IF, Samii A, Roberts JW, Agarwal P, Checkoway H, Farin FM, Yearout D, Zabetian CP. Association mapping of the PARK10 region for Parkinson's disease susceptibility genes. Parkinsonism Relat Disord. 2014 Jan; 20(1):93-8. PMID: 24156912; PMCID: PMC3946853.
    30. LeBlanc K, Baranoski S, Christensen D, Langemo D, Sammon MA, Edwards K, Holloway S, Gloeckner M, Williams A, Sibbald RG, Regan M. International Skin Tear Advisory Panel: a tool kit to aid in the prevention, assessment, and treatment of skin tears using a Simplified Classification System ©. Adv Skin Wound Care. 2013 Oct; 26(10):459-76; quiz 477-8. PMID: 24045566.
      View in: PubMed
    31. Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Trojanowski JQ, Weintraub D, Chen-Plotkin AS, Irwin DJ, Rick J, Schellenberg GD, Watson GS, Kukull W, Nelson PT, Jicha GA, Neltner JH, Galasko D, Masliah E, Quinn JF, Chung KA, Yearout D, Mata IF, Wan JY, Edwards K, Montine TJ, Zabetian CP. APOE e4 increases risk for dementia in pure synucleinopathies. JAMA Neurol. 2013 Feb; 70(2):223-8. PMID: 23407718; PMCID: PMC3580799.
    32. Conte MS, Owens CD, Belkin M, Creager MA, Edwards K, Gasper WJ, Kenagy RD, LeBoeuf RC, Sobel M, Clowes A. A single nucleotide polymorphism in the p27(Kip1) gene is associated with primary patency of lower extremity vein bypass grafts. J Vasc Surg. 2013 May; 57(5):1179-85.e1-2. PMID: 23312942; PMCID: PMC3644510.
    33. Peterson AL, Murchison C, Zabetian C, Leverenz JB, Watson GS, Montine T, Carney N, Bowman GL, Edwards K, Quinn JF. Memory, mood, and vitamin D in persons with Parkinson's disease. J Parkinsons Dis. 2013; 3(4):547-55. PMID: 24081441; PMCID: PMC3966187.
    34. Cholerton BA, Zabetian CP, Quinn JF, Chung KA, Peterson A, Espay AJ, Revilla FJ, Devoto J, Watson GS, Hu SC, Edwards K, Montine TJ, Leverenz JB. Pacific Northwest Udall Center of excellence clinical consortium: study design and baseline cohort characteristics. J Parkinsons Dis. 2013; 3(2):205-14. PMID: 23938350; PMCID: PMC3779428.
    35. Fetherston SM, Boyd P, McCoy CF, McBride MC, Edwards K, Ampofo S, Malcolm RK. A silicone elastomer vaginal ring for HIV prevention containing two microbicides with different mechanisms of action. Eur J Pharm Sci. 2013 Feb 14; 48(3):406-15. PMID: 23266465.
      View in: PubMed
    36. Hall TO, Wan JY, Mata IF, Kerr KF, Snapinn KW, Samii A, Roberts JW, Agarwal P, Zabetian CP, Edwards K. Risk prediction for complex diseases: application to Parkinson disease. Genet Med. 2013 May; 15(5):361-7. PMID: 23222663; PMCID: PMC3687522.
    37. Mata IF, Checkoway H, Hutter CM, Samii A, Roberts JW, Kim HM, Agarwal P, Alvarez V, Ribacoba R, Pastor P, Lorenzo-Betancor O, Infante J, Sierra M, Gómez-Garre P, Mir P, Ritz B, Rhodes SL, Colcher A, Van Deerlin V, Chung KA, Quinn JF, Yearout D, Martinez E, Farin FM, Wan JY, Edwards K, Zabetian CP. Common variation in the LRRK2 gene is a risk factor for Parkinson's disease. Mov Disord. 2012 Dec; 27(14):1822-5. PMID: 23115130; PMCID: PMC3536918.
    38. Dika Ž, Juras J, Kos J, Edwards K, Fištrek M, Premužic V, Laganovic M, Abramovic-Baríc M, Cvitkovic A, Vukovic Lela I, Karanovic S, Juric D, Bitunjac M, Teskera T, Jelakovic B. Prevalence, treatment and control of hypertension in a Croatian endemic nephropathy area. Kidney Blood Press Res. 2012; 35(6):678-86. PMID: 23128352.
      View in: PubMed
    39. Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Kukull W, Nelson PT, Jicha GA, Neltner JH, Galasko D, Masliah E, Trojanowski JQ, Schellenberg GD, Yearout D, Huston H, Fritts-Penniman A, Mata IF, Wan JY, Edwards K, Montine TJ, Zabetian CP. GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology. Neurology. 2012 Nov 06; 79(19):1944-50. PMID: 23035075.
      View in: PubMed
    40. Hall TO, Renz AD, Snapinn KW, Bowen DJ, Edwards K. Awareness and uptake of direct-to-consumer genetic testing among cancer cases, their relatives, and controls: the Northwest Cancer Genetics Network. Genet Test Mol Biomarkers. 2012 Jul; 16(7):744-8. PMID: 22731649; PMCID: PMC4077008.
    41. Chen CH, Dickman KG, Moriya M, Zavadil J, Sidorenko VS, Edwards K, Gnatenko DV, Wu L, Turesky RJ, Wu XR, Pu YS, Grollman AP. Aristolochic acid-associated urothelial cancer in Taiwan. Proc Natl Acad Sci U S A. 2012 May 22; 109(21):8241-6. PMID: 22493262; PMCID: PMC3361449.
    42. Edwards K, Lemke AA, Trinidad SB, Lewis SM, Starks H, Snapinn KW, Griffin MQ, Wiesner GL, Burke W. Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis. Genet Med. 2012 Feb; 14(2):236-42. PMID: 22241102; PMCID: PMC3448270.
    43. Yu JH, Taylor JS, Edwards K, Fullerton SM. What are our AIMs? Interdisciplinary Perspectives on the Use of Ancestry Estimation in Disease Research. AJOB Prim Res. 2012; 3(4):87-97. PMID: 25419472.
      View in: PubMed
    44. Cvitkovic A, Vukovic-Lela I, Edwards K, Karanovic S, Juric D, Cvorišcec D, Fucek M, Jelakovic B. Could disappearance of endemic (Balkan) nephropathy be expected in forthcoming decades? Kidney Blood Press Res. 2012; 35(3):147-52. PMID: 22116163; PMCID: PMC3696381.
    45. Jelakovic B, Karanovic S, Vukovic-Lela I, Miller F, Edwards K, Nikolic J, Tomic K, Slade N, Brdar B, Turesky RJ, Stipancic Ž, Dittrich D, Grollman AP, Dickman KG. Aristolactam-DNA adducts are a biomarker of environmental exposure to aristolochic acid. Kidney Int. 2012 Mar; 81(6):559-67. PMID: 22071594; PMCID: PMC3560912.
    46. Dansie EJ, Furberg H, Afari N, Buchwald D, Edwards K, Goldberg J, Schur E, Sullivan PF. Conditions comorbid with chronic fatigue in a population-based sample. Psychosomatics. 2012 Jan-Feb; 53(1):44-50. PMID: 22221720; PMCID: PMC3254018.
    47. Bowen D, Jabson J, Haddock N, Hay J, Edwards K. Skin care behaviors among melanoma survivors. Psychooncology. 2012 Dec; 21(12):1285-91. PMID: 21780240.
      View in: PubMed
    48. Ziogas A, Horick NK, Kinney AY, Lowery JT, Domchek SM, Isaacs C, Griffin CA, Moorman PG, Edwards K, Hill DA, Berg JS, Tomlinson GE, Anton-Culver H, Strong LC, Kasten CH, Finkelstein DM, Plon SE. Clinically relevant changes in family history of cancer over time. JAMA. 2011 Jul 13; 306(2):172-8. PMID: 21750294; PMCID: PMC3367662.
    49. Wang Y, Hancock AM, Bradner J, Chung KA, Quinn JF, Peskind ER, Galasko D, Jankovic J, Zabetian CP, Kim HM, Leverenz JB, Montine TJ, Ginghina C, Edwards K, Snapinn KW, Goldstein DS, Shi M, Zhang J. Complement 3 and factor h in human cerebrospinal fluid in Parkinson's disease, Alzheimer's disease, and multiple-system atrophy. Am J Pathol. 2011 Apr; 178(4):1509-16. PMID: 21435440; PMCID: PMC3078443.
    50. Mata IF, Yearout D, Alvarez V, Coto E, de Mena L, Ribacoba R, Lorenzo-Betancor O, Samaranch L, Pastor P, Cervantes S, Infante J, Garcia-Gorostiaga I, Sierra M, Combarros O, Snapinn KW, Edwards K, Zabetian CP. Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease. Mov Disord. 2011 Apr; 26(5):819-23. PMID: 21425343; PMCID: PMC3082603.
    51. Snapinn KW, Larson EB, Kawakami H, Ujike H, Borenstein AR, Izumi Y, Kaji R, Maruyama H, Mata IF, Morino H, Oda M, Tsuang DW, Yearout D, Edwards K, Zabetian CP. The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population. Parkinsonism Relat Disord. 2011 Jul; 17(6):473-5. PMID: 21345711; PMCID: PMC3119730.
    52. Edwards K, Wan JY, Hutter CM, Fong PY, Santorico SA. Multivariate linkage scan for metabolic syndrome traits in families with type 2 diabetes. Obesity (Silver Spring). 2011 Jun; 19(6):1235-43. PMID: 21183932.
      View in: PubMed
    53. Malcolm RK, Edwards K, Kiser P, Romano J, Smith TJ. Advances in microbicide vaginal rings. Antiviral Res. 2010 Dec; 88 Suppl 1:S30-9. PMID: 21109066.
      View in: PubMed
    54. Mata IF, Shi M, Agarwal P, Chung KA, Edwards K, Factor SA, Galasko DR, Ginghina C, Griffith A, Higgins DS, Kay DM, Kim H, Leverenz JB, Quinn JF, Roberts JW, Samii A, Snapinn KW, Tsuang DW, Yearout D, Zhang J, Payami H, Zabetian CP. SNCA variant associated with Parkinson disease and plasma alpha-synuclein level. Arch Neurol. 2010 Nov; 67(11):1350-6. PMID: 21060011; PMCID: PMC3010848.
    55. Lemke AA, Trinidad SB, Edwards K, Starks H, Wiesner GL. Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protection. J Empir Res Hum Res Ethics. 2010 Mar; 5(1):83-91. PMID: 20235866; PMCID: PMC2902178.
    56. Heike CL, Starr JR, Rieder MJ, Cunningham ML, Edwards K, Stanaway IB, Crawford DC. Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome. Birth Defects Res A Clin Mol Teratol. 2010 Jan; 88(1):54-63. PMID: 19645056; PMCID: PMC4535433.
    57. Ragland M, Hutter C, Zabetian C, Edwards K. Association between the ubiquitin carboxyl-terminal esterase L1 gene (UCHL1) S18Y variant and Parkinson's Disease: a HuGE review and meta-analysis. Am J Epidemiol. 2009 Dec 01; 170(11):1344-57. PMID: 19864305; PMCID: PMC2778765.
    58. Khoury MJ, Feero WG, Reyes M, Citrin T, Freedman A, Leonard D, Burke W, Coates R, Croyle RT, Edwards K, Kardia S, McBride C, Manolio T, Randhawa G, Rasooly R, St Pierre J, Terry S. The genomic applications in practice and prevention network. Genet Med. 2009 Jul; 11(7):488-94. PMID: 19471162; PMCID: PMC2743616.
    59. McGrath BB, Edwards K. When family means more (or less) than genetics: the intersection of culture, family and genomics. J Transcult Nurs. 2009 Jul; 20(3):270-7. PMID: 19398610; PMCID: PMC2773542.
    60. Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards K, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H. LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Mov Disord. 2009 May 15; 24(7):1034-41. PMID: 19343804; PMCID: PMC2827255.
    61. Mata IF, Hutter CM, González-Fernández MC, de Pancorbo MM, Lezcano E, Huerta C, Blazquez M, Ribacoba R, Guisasola LM, Salvador C, Gómez-Esteban JC, Zarranz JJ, Infante J, Jankovic J, Deng H, Edwards K, Alvarez V, Zabetian CP. Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain. Neurogenetics. 2009 Oct; 10(4):347-53. PMID: 19308469; PMCID: PMC2821036.
    62. Sonicki Z, Cvitkovic A, Edwards K, Miletic-Medved M, Cvoriscec D, Babus V, Jelakovic B. Visual assessment of endemic nephropathy markers relationship. Stud Health Technol Inform. 2009; 150:836-40. PMID: 19745430.
      View in: PubMed
    63. Goddard KA, Duquette D, Zlot A, Johnson J, Annis-Emeott A, Lee PW, Bland MP, Edwards K, Oehlke K, Giles RT, Rafferty A, Cook ML, Khoury MJ. Public awareness and use of direct-to-consumer genetic tests: results from 3 state population-based surveys, 2006. Am J Public Health. 2009 Mar; 99(3):442-5. PMID: 19106425; PMCID: PMC2661444.
    64. Edwards K, Hutter CM, Wan JY, Kim H, Monks SA. Genome-wide linkage scan for the metabolic syndrome: the GENNID study. Obesity (Silver Spring). 2008 Jul; 16(7):1596-601. PMID: 18421265.
      View in: PubMed
    65. Jaja C, Burke W, Thummel K, Edwards K, Veenstra DL. Cytochrome p450 enzyme polymorphism frequency in indigenous and native american populations: a systematic review. Community Genet. 2008; 11(3):141-9. PMID: 18376110.
      View in: PubMed
    66. Hutter CM, Samii A, Factor SA, Nutt JG, Higgins DS, Bird TD, Griffith A, Roberts JW, Leis BC, Montimurro JS, Kay DM, Edwards K, Payami H, Zabetian CP. Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease. Eur J Neurol. 2008 Feb; 15(2):134-9. PMID: 18093156; PMCID: PMC2823263.
    67. Zabetian CP, Hutter CM, Factor SA, Nutt JG, Higgins DS, Griffith A, Roberts JW, Leis BC, Kay DM, Yearout D, Montimurro JS, Edwards K, Samii A, Payami H. Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease. Ann Neurol. 2007 Aug; 62(2):137-44. PMID: 17514749; PMCID: PMC2836920.
    68. Chun LS, Samii A, Hutter CM, Griffith A, Roberts JW, Leis BC, Mosley AD, Wander PL, Edwards K, Payami H, Zabetian CP. DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease. Ann Neurol. 2007 Jul; 62(1):99-101. PMID: 17503507; PMCID: PMC2823266.
    69. Zabetian CP, Hutter CM, Yearout D, Lopez AN, Factor SA, Griffith A, Leis BC, Bird TD, Nutt JG, Higgins DS, Roberts JW, Kay DM, Edwards K, Samii A, Payami H. LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. Am J Hum Genet. 2006 Oct; 79(4):752-8. PMID: 16960813; PMCID: PMC1592578.
    70. Ramos EM, Lin MT, Larson EB, Maezawa I, Tseng LH, Edwards K, Schellenberg GD, Hansen JA, Kukull WA, Jin LW. Tumor necrosis factor alpha and interleukin 10 promoter region polymorphisms and risk of late-onset Alzheimer disease. Arch Neurol. 2006 Aug; 63(8):1165-9. PMID: 16908746.
      View in: PubMed
    71. Murdoch SJ, Boright AP, Paterson AD, Zinman B, Steffes M, Cleary P, Edwards K, Marcovina SS, Purnell JQ, Brunzell JD. LDL composition in E2/2 subjects and LDL distribution by Apo E genotype in type 1 diabetes. Atherosclerosis. 2007 May; 192(1):138-47. PMID: 16740268.
      View in: PubMed
    72. Sieh W, Edwards K, Fitzpatrick AL, Srinouanprachanh SL, Farin FM, Monks SA, Kronmal RA, Eaton DL. Genetic Susceptibility to Prostate Cancer: Prostate-specific Antigen and its Interaction with the Androgen Receptor (United States). Cancer Causes Control. 2006 Mar; 17(2):187-97. PMID: 16425097.
      View in: PubMed
    73. Kim H, Hutter CM, Monks SA, Edwards K. Comparison of single-nucleotide polymorphisms and microsatellites in detecting quantitative trait loci for alcoholism: the Collaborative Study on the Genetics of Alcoholism. BMC Genet. 2005 Dec 30; 6 Suppl 1:S5. PMID: 16451661; PMCID: PMC1866734.
    74. Hutter CM, Austin MA, Farin FM, Viernes HM, Edwards K, Leonetti DL, McNeely MJ, Fujimoto WY. Association of endothelial lipase gene (LIPG) haplotypes with high-density lipoprotein cholesterol subfractions and apolipoprotein AI plasma levels in Japanese Americans. Atherosclerosis. 2006 Mar; 185(1):78-86. PMID: 16023652.
      View in: PubMed
    75. Raup SF, Oehlke KP, Edwards K. Developing academic-practice partnerships to enhance the integration of genomics into public health. Prev Chronic Dis. 2005 Apr; 2(2):A02. PMID: 15888213; PMCID: PMC1327696.
    76. Harrison TA, Burke W, Edwards K. The asthma consultative process: a collaborative approach to integrating genomics into public health practice. Prev Chronic Dis. 2005 Apr; 2(2):A27. PMID: 15888238; PMCID: PMC1327721.
    77. Hindorff LA, Heckbert SR, Psaty BM, Lumley T, Siscovick DS, Herrington DM, Edwards K, Tracy RP. beta(2)-Adrenergic receptor polymorphisms and determinants of cardiovascular risk: the Cardiovascular Health Study. Am J Hypertens. 2005 Mar; 18(3):392-7. PMID: 15797659.
      View in: PubMed
    78. Zhang C, Williams MA, Edwards K, Austin MA. Trp64Arg polymorphism of the beta3-adrenergic receptor gene, pre-pregnancy obesity and risk of pre-eclampsia. J Matern Fetal Neonatal Med. 2005 Jan; 17(1):19-28. PMID: 15804782.
      View in: PubMed
    79. Kim H, Friedlander Y, Longstreth WT, Edwards K, Schwartz SM, Siscovick DS. Family history as a risk factor for stroke in young women. Am J Prev Med. 2004 Dec; 27(5):391-6. PMID: 15556739.
      View in: PubMed
    80. Austin MA, Edwards K, McNeely MJ, Chandler WL, Leonetti DL, Talmud PJ, Humphries SE, Fujimoto WY. Heritability of multivariate factors of the metabolic syndrome in nondiabetic Japanese americans. Diabetes. 2004 Apr; 53(4):1166-9. PMID: 15047637.
      View in: PubMed
    81. Austin MA, Talmud PJ, Farin FM, Nickerson DA, Edwards K, Leonetti D, McNeely MJ, Viernes HM, Humphries SE, Fujimoto WY. Association of apolipoprotein A5 variants with LDL particle size and triglyceride in Japanese Americans. Biochim Biophys Acta. 2004 Jan 20; 1688(1):1-9. PMID: 14732475.
      View in: PubMed
    82. Goode EL, Badzioch MD, Kim H, Gagnon F, Rozek LS, Edwards K, Jarvik GP. Multiple genome-wide analyses of smoking behavior in the Framingham Heart Study. BMC Genet. 2003 Dec 31; 4 Suppl 1:S102. PMID: 14975170; PMCID: PMC1866440.
    83. Bis JC, Smith NL, Psaty BM, Heckbert SR, Edwards K, Lemaitre RN, Lumley T, Rosendaal FR. Angiotensinogen Met235Thr polymorphism, angiotensin-converting enzyme inhibitor therapy, and the risk of nonfatal stroke or myocardial infarction in hypertensive patients. Am J Hypertens. 2003 Dec; 16(12):1011-7. PMID: 14643574.
      View in: PubMed
    84. Hebert MF, Dowling AL, Gierwatowski C, Lin YS, Edwards K, Davis CL, Marsh CL, Schuetz EG, Thummel KE. Association between ABCB1 (multidrug resistance transporter) genotype and post-liver transplantation renal dysfunction in patients receiving calcineurin inhibitors. Pharmacogenetics. 2003 Nov; 13(11):661-74. PMID: 14583679.
      View in: PubMed
    85. Doria-Rose VP, Kim HS, Augustine ET, Edwards K. Parity and the risk of Down's syndrome. Am J Epidemiol. 2003 Sep 15; 158(6):503-8. PMID: 12965874.
      View in: PubMed
    86. Austin MA, Edwards K, Monks SA, Koprowicz KM, Brunzell JD, Motulsky AG, Mahaney MC, Hixson JE. Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia. J Lipid Res. 2003 Nov; 44(11):2161-8. PMID: 12923221.
      View in: PubMed
    87. McKone EF, Emerson SS, Edwards K, Aitken ML. Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study. Lancet. 2003 May 17; 361(9370):1671-6. PMID: 12767731.
      View in: PubMed
    88. Heckbert SR, Hindorff LA, Edwards K, Psaty BM, Lumley T, Siscovick DS, Tang Z, Durda JP, Kronmal RA, Tracy RP. Beta2-adrenergic receptor polymorphisms and risk of incident cardiovascular events in the elderly. Circulation. 2003 Apr 22; 107(15):2021-4. PMID: 12682000.
      View in: PubMed
    89. Harrison TA, Hindorff LA, Kim H, Wines RC, Bowen DJ, McGrath BB, Edwards K. Family history of diabetes as a potential public health tool. Am J Prev Med. 2003 Feb; 24(2):152-9. PMID: 12568821.
      View in: PubMed
    90. Hindorff LA, Heckbert SR, Tracy R, Tang Z, Psaty BM, Edwards K, Siscovick DS, Kronmal RA, Nazar-Stewart V. Angiotensin II type 1 receptor polymorphisms in the cardiovascular health study: relation to blood pressure, ethnicity, and cardiovascular events. Am J Hypertens. 2002 Dec; 15(12):1050-6. PMID: 12460700.
      View in: PubMed
    Karen's Networks
    Concepts
    Derived automatically from this person's publications.
    _
    Co-Authors
    People in Profiles who have published with this person.
    _
    Related Authors
    People who share related concepts with this person.
    _