Karen L Edwards

Title(s)Professor, Epidemiology and Biostats
SchoolUC Irvine Joe C. Wen School of Population & Public Health
Address856 Health Sciences Quad
University of California, Irvine
Irvine CA 92697-3957
Phone(949) 824-9054
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    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. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Multivariate prediction of dementia in Parkinson's disease. NPJ Parkinsons Dis. 2020; 6:20. Phongpreecha T, Cholerton B, Mata IF, Zabetian CP, Poston KL, Aghaeepour N, Tian L, Quinn JF, Chung KA, Hiller AL, Hu SC, Edwards KL, Montine TJ. PMID: 32885039; PMCID: PMC7447766.
      View in: PubMed   Mentions: 20  
    2. Hallucinations and Development of Dementia in Parkinson's Disease. J Parkinsons Dis. 2020; 10(4):1643-1648. Gryc W, Roberts KA, Zabetian CP, Weintraub D, Trojanowski JQ, Quinn JF, Hiller AL, Chung KA, Poston KL, Yang L, Hu SC, Edwards KL, Montine TJ, Cholerton BA. PMID: 32741842; PMCID: PMC7609584.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    3. Evidence for gene-smoking interactions for hearing loss and deafness in Japanese American families. Hear Res. 2020 03 01; 387:107875. Wan JY, Cataby C, Liem A, Jeffrey E, Norden-Krichmar TM, Goodman D, Santorico SA, Edwards KL, American Diabetes Association GENNID Study Group. PMID: 31896498; PMCID: PMC7046312.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    4. Participant and Study Partner Reported Impact of Cognition on Functional Activities in Parkinson's Disease. Mov Disord Clin Pract. 2020 Jan; 7(1):61-69. Cholerton B, Poston KL, Tian L, Quinn JF, Chung KA, Hiller AL, Hu SC, Specketer K, Montine TJ, Edwards KL, Zabetian CP. PMID: 31970213; PMCID: PMC6962683.
      View in: PubMed   Mentions: 6     Fields:    
    5. Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Genet Epidemiol. 2020 01; 44(1):16-25. Willems EL, Wan JY, Norden-Krichmar TM, Edwards KL, Santorico SA. PMID: 31647587; PMCID: PMC6986323.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    6. Prediction of cognitive progression in Parkinson's disease using three cognitive screening measures. Clin Park Relat Disord. 2019; 1:91-97. Kim HM, Nazor C, Zabetian CP, Quinn JF, Chung KA, Hiller AL, Hu SC, Leverenz JB, Montine TJ, Edwards KL, Cholerton B. PMID: 32368733; PMCID: PMC7197868.
      View in: PubMed   Mentions: 16  
    7. Cognitive associations with comprehensive gait and static balance measures in Parkinson's disease. Parkinsonism Relat Disord. 2019 12; 69:104-110. Morris R, Martini DN, Smulders K, Kelly VE, Zabetian CP, Poston K, Hiller A, Chung KA, Yang L, Hu SC, Edwards KL, Cholerton B, Grabowski TJ, Montine TJ, Quinn JF, Horak F. PMID: 31731260; PMCID: PMC6900452.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    8. Visuospatial functioning is associated with sleep disturbance and hallucinations in nondemented patients with Parkinson's disease. J Clin Exp Neuropsychol. 2019 10; 41(8):803-813. Specketer K, Zabetian CP, Edwards KL, Tian L, Quinn JF, Peterson-Hiller AL, Chung KA, Hu SC, Montine TJ, Cholerton BA. PMID: 31177941; PMCID: PMC6681669.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    9. Race-, Age-, and Anatomic Site-Specific Gender Differences in Cutaneous Melanoma Suggest Differential Mechanisms of Early- and Late-Onset Melanoma. Int J Environ Res Public Health. 2019 03 13; 16(6). Yuan TA, Lu Y, Edwards K, Jakowatz J, Meyskens FL, Liu-Smith F. PMID: 30871230; PMCID: PMC6466415.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    10. Comparative sensitivity of the MoCA and Mattis Dementia Rating Scale-2 in Parkinson's disease. Mov Disord. 2019 02; 34(2):285-291. Hendershott TR, Zhu D, Llanes S, Zabetian CP, Quinn J, Edwards KL, Leverenz JB, Montine T, Cholerton B, Poston KL. PMID: 30776152; PMCID: PMC6532623.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    11. Controversies among Cancer Registry Participants, Genomic Researchers, and Institutional Review Boards about Returning Participants' Genomic Results. Public Health Genomics. 2018; 21(1-2):18-26. Edwards KL, Goodman D, Johnson CO, Wenzel L, Condit C, Bowen D. PMID: 30227419; PMCID: PMC7833045.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    12. Cumulative Antidepressant Use and Risk of Dementia in a Prospective Cohort Study. J Am Geriatr Soc. 2018 10; 66(10):1948-1955. Heath L, Gray SL, Boudreau DM, Thummel K, Edwards KL, Fullerton SM, Crane PK, Larson EB. PMID: 30221747.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    13. Sex differences in progression to mild cognitive impairment and dementia in Parkinson's disease. Parkinsonism Relat Disord. 2018 05; 50:29-36. 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 KL. PMID: 29478836; PMCID: PMC5943177.
      View in: PubMed   Mentions: 62     Fields:    Translation:Humans
    14. A comparison of views regarding the use of de-identified data. Transl Behav Med. 2018 01 29; 8(1):113-118. Goodman D, Johnson CO, Bowen D, Smith M, Wenzel L, Edwards KL. PMID: 29385588; PMCID: PMC6065539.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    15. The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature. Transl Behav Med. 2018 01 29; 8(1):119-129. Goodman D, Bowen D, Wenzel L, Tehrani P, Fernando F, Khacheryan A, Chowdhury F, Johnson CO, Edwards K. PMID: 29385589; PMCID: PMC6065547.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    16. Homocysteine and cognitive function in Parkinson's disease. Parkinsonism Relat Disord. 2017 Nov; 44:1-5. Licking N, Murchison C, Cholerton B, Zabetian CP, Hu SC, Montine TJ, Peterson-Hiller AL, Chung KA, Edwards K, Leverenz JB, Quinn JF. PMID: 28807493; PMCID: PMC5858907.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    17. Large-scale exploratory genetic analysis of cognitive impairment in Parkinson's disease. Neurobiol Aging. 2017 08; 56:211.e1-211.e7. 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 KL, Zabetian CP. PMID: 28526295; PMCID: PMC5536182.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    18. De-identified genomic data sharing: the research participant perspective. J Community Genet. 2017 Jul; 8(3):173-181. Goodman D, Johnson CO, Bowen D, Smith M, Wenzel L, Edwards K. PMID: 28382417; PMCID: PMC5496839.
      View in: PubMed   Mentions: 33  
    19. 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. Mata IF, Davis MY, Lopez AN, Dorschner MO, Martinez E, Yearout D, Cholerton BA, Hu SC, Edwards KL, Bird TD, Zabetian CP. PMID: 27943640.
      View in: PubMed   Mentions: 2     Fields:    
    20. Common variant rs356182 near SNCA defines a Parkinson's disease endophenotype. Ann Clin Transl Neurol. 2017 01; 4(1):15-25. Cooper CA, Jain N, Gallagher MD, Weintraub D, Xie SX, Berlyand Y, Espay AJ, Quinn J, Edwards KL, Montine T, Van Deerlin VM, Trojanowski J, Zabetian CP, Chen-Plotkin AS. PMID: 28078311; PMCID: PMC5221454.
      View in: PubMed   Mentions: 24     Fields:    
    21. 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. 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 KL, Zabetian CP. PMID: 27571329; PMCID: PMC5056861.
      View in: PubMed   Mentions: 118     Fields:    Translation:Humans
    22. 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. Condit CM, Shen L, Edwards KL, Bowen DJ, Korngiebel DM, Johnson CO. PMID: 27653592; PMCID: PMC7868084.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    23. Views of Cohort Study Participants about Returning Research Results in the Context of Precision Medicine. Public Health Genomics. 2016; 19(5):269-75. Hyams T, Bowen DJ, Condit C, Grossman J, Fitzmaurice M, Goodman D, Wenzel L, Edwards KL. PMID: 27553645; PMCID: PMC5053808.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    24. Consent Issues in Genetic Research: Views of Research Participants. Public Health Genomics. 2016; 19(4):220-8. Goodman D, Johnson CO, Wenzel L, Bowen D, Condit C, Edwards KL. PMID: 27376949; PMCID: PMC4996754.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    25. 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. Mata IF, Davis MY, Lopez AN, Dorschner MO, Martinez E, Yearout D, Cholerton BA, Hu SC, Edwards KL, Bird TD, Zabetian CP. PMID: 27111571; PMCID: PMC5028305.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    26. Participant views on consent in cancer genetics research: preparing for the precision medicine era. J Community Genet. 2016 Apr; 7(2):133-43. Edwards KL, Korngiebel DM, Pfeifer L, Goodman D, Renz A, Wenzel L, Bowen DJ, Condit CM. PMID: 26801345; PMCID: PMC4796049.
      View in: PubMed   Mentions: 9  
    27. The Art of Dressing Selection: A Consensus Statement on Skin Tears and Best Practice. Adv Skin Wound Care. 2016 Jan; 29(1):32-46. LeBlanc K, Baranoski S, Christensen D, Langemo D, Edwards K, Holloway S, Gloeckner M, Williams A, Campbell K, Alam T, Woo KY. PMID: 26650095.
      View in: PubMed   Mentions: 6     Fields:    
    28. The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease. Mol Neurodegener. 2015 Sep 24; 10:50. 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 KL, Kim KS, Zabetian CP. PMID: 26399558; PMCID: PMC4581468.
      View in: PubMed   Mentions: 48     Fields:    Translation:HumansAnimals
    29. GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson's disease. Mov Disord. 2016 Jan; 31(1):95-102. 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 KL, Zabetian CP. PMID: 26296077; PMCID: PMC4724255.
      View in: PubMed   Mentions: 101     Fields:    Translation:Humans
    30. 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. Condit CM, Korngiebel DM, Pfeifer L, Renz AD, Bowen DJ, Kaufman D, Kollar LM, Edwards KL. PMID: 26331187.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    31. Association of cognitive domains with postural instability/gait disturbance in Parkinson's disease. Parkinsonism Relat Disord. 2015 Jul; 21(7):692-7. Kelly VE, Johnson CO, McGough EL, Shumway-Cook A, Horak FB, Chung KA, Espay AJ, Revilla FJ, Devoto J, Wood-Siverio C, Factor SA, Cholerton B, Edwards KL, Peterson AL, Quinn JF, Montine TJ, Zabetian CP, Leverenz JB. PMID: 25943529; PMCID: PMC4524498.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    32. Cognitive profile of LRRK2-related Parkinson's disease. Mov Disord. 2015 Apr 15; 30(5):728-33. 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 KL, Zhang J, Zabetian CP. PMID: 25650144; PMCID: PMC4397146.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    33. 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. 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. PMID: 25587102; PMCID: PMC4317733.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansPHPublic Health
    34. APOE, MAPT, and SNCA genes and cognitive performance in Parkinson disease. JAMA Neurol. 2014 Nov; 71(11):1405-12. 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 KL, Zabetian CP. PMID: 25178429; PMCID: PMC4227942.
      View in: PubMed   Mentions: 109     Fields:    Translation:Humans
    35. Challenges of linkage analysis in the era of whole-genome sequencing. Genet Epidemiol. 2014 Sep; 38 Suppl 1:S92-6. Santorico SA, Edwards KL. PMID: 25112196.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    36. People with Parkinson's disease and normal MMSE score have a broad range of cognitive performance. Mov Disord. 2014 Sep; 29(10):1258-64. 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 KL, Montine TJ, Zabetian CP, Leverenz JB. PMID: 25073717; PMCID: PMC4162839.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    37. 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. Yorgov D, Edwards KL, Santorico SA. PMID: 25519335; PMCID: PMC4143673.
      View in: PubMed   Mentions: 6  
    38. Evaluation of mild cognitive impairment subtypes in Parkinson's disease. Mov Disord. 2014 May; 29(6):756-64. 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 KL. PMID: 24710804; PMCID: PMC4013249.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    39. Long-term risk of medical conditions associated with breast cancer treatment. Breast Cancer Res Treat. 2014 May; 145(1):233-43. Hill DA, Horick NK, Isaacs C, Domchek SM, Tomlinson GE, Lowery JT, Kinney AY, Berg JS, Edwards KL, Moorman PG, Plon SE, Strong LC, Ziogas A, Griffin CA, Kasten CH, Finkelstein DM. PMID: 24696430; PMCID: PMC4096572.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    40. Metastatic spinal cord compression as a result of the unknown primary tumour. Eur Spine J. 2014 Jul; 23(7):1502-7. Quraishi NA, Ramoutar D, Sureshkumar D, Manoharan SR, Spencer A, Arealis G, Edwards KL, Boszczyk BM. PMID: 24691912.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    41. Is herbal tea consumption a factor in endemic nephropathy? Eur J Epidemiol. 2014 Mar; 29(3):221-4. 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. PMID: 24623403.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimalsPHPublic Health
    42. Consensus statement on screening, diagnosis, classification and treatment of endemic (Balkan) nephropathy. Nephrol Dial Transplant. 2014 Nov; 29(11):2020-7. 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. PMID: 24166461; PMCID: PMC4288114.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansPHPublic Health
    43. Association mapping of the PARK10 region for Parkinson's disease susceptibility genes. Parkinsonism Relat Disord. 2014 Jan; 20(1):93-8. Wan JY, Edwards KL, Hutter CM, Mata IF, Samii A, Roberts JW, Agarwal P, Checkoway H, Farin FM, Yearout D, Zabetian CP. PMID: 24156912; PMCID: PMC3946853.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    44. 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. LeBlanc K, Baranoski S, Christensen D, Langemo D, Sammon MA, Edwards K, Holloway S, Gloeckner M, Williams A, Sibbald RG, Regan M. PMID: 24045566.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    45. APOE ε4 increases risk for dementia in pure synucleinopathies. JAMA Neurol. 2013 Feb; 70(2):223-8. 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 KL, Montine TJ, Zabetian CP. PMID: 23407718; PMCID: PMC3580799.
      View in: PubMed   Mentions: 191     Fields:    Translation:HumansCells
    46. Accuracy of the revised Tokuhashi score in predicting survival in patients with metastatic spinal cord compression (MSCC). Eur Spine J. 2013 Mar; 22 Suppl 1:S21-6. Quraishi NA, Manoharan SR, Arealis G, Khurana A, Elsayed S, Edwards KL, Boszczyk BM. PMID: 23328875; PMCID: PMC3578515.
      View in: PubMed   Mentions: 44     Fields:    Translation:Humans
    47. 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. Conte MS, Owens CD, Belkin M, Creager MA, Edwards KL, Gasper WJ, Kenagy RD, LeBoeuf RC, Sobel M, Clowes A. PMID: 23312942; PMCID: PMC3644510.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    48. Memory, mood, and vitamin D in persons with Parkinson's disease. J Parkinsons Dis. 2013; 3(4):547-55. Peterson AL, Murchison C, Zabetian C, Leverenz JB, Watson GS, Montine T, Carney N, Bowman GL, Edwards K, Quinn JF. PMID: 24081441; PMCID: PMC3966187.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    49. Pacific Northwest Udall Center of excellence clinical consortium: study design and baseline cohort characteristics. J Parkinsons Dis. 2013; 3(2):205-14. Cholerton BA, Zabetian CP, Quinn JF, Chung KA, Peterson A, Espay AJ, Revilla FJ, Devoto J, Watson GS, Hu SC, Edwards KL, Montine TJ, Leverenz JB. PMID: 23938350; PMCID: PMC3779428.
      View in: PubMed   Mentions: 53     Fields:    Translation:Humans
    50. 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. Fetherston SM, Boyd P, McCoy CF, McBride MC, Edwards KL, Ampofo S, Malcolm RK. PMID: 23266465.
      View in: PubMed   Mentions: 33     Fields:    
    51. Risk prediction for complex diseases: application to Parkinson disease. Genet Med. 2013 May; 15(5):361-7. Hall TO, Wan JY, Mata IF, Kerr KF, Snapinn KW, Samii A, Roberts JW, Agarwal P, Zabetian CP, Edwards KL. PMID: 23222663; PMCID: PMC3687522.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    52. Common variation in the LRRK2 gene is a risk factor for Parkinson's disease. Mov Disord. 2012 Dec; 27(14):1822-5. 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 KL, Zabetian CP. PMID: 23115130; PMCID: PMC3536918.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    53. Prevalence, treatment and control of hypertension in a Croatian endemic nephropathy area. Kidney Blood Press Res. 2012; 35(6):678-86. 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. PMID: 23128352.
      View in: PubMed   Mentions:    Fields:    Translation:HumansPHPublic Health
    54. GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology. Neurology. 2012 Nov 06; 79(19):1944-50. 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 KL, Montine TJ, Zabetian CP. PMID: 23035075; PMCID: PMC3484986.
      View in: PubMed   Mentions: 81     Fields:    Translation:Humans
    55. 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. Hall TO, Renz AD, Snapinn KW, Bowen DJ, Edwards KL. PMID: 22731649; PMCID: PMC4077008.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    56. Aristolochic acid-associated urothelial cancer in Taiwan. Proc Natl Acad Sci U S A. 2012 May 22; 109(21):8241-6. Chen CH, Dickman KG, Moriya M, Zavadil J, Sidorenko VS, Edwards KL, Gnatenko DV, Wu L, Turesky RJ, Wu XR, Pu YS, Grollman AP. PMID: 22493262; PMCID: PMC3361449.
      View in: PubMed   Mentions: 158     Fields:    Translation:Humans
    57. Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis. Genet Med. 2012 Feb; 14(2):236-42. Edwards KL, Lemke AA, Trinidad SB, Lewis SM, Starks H, Snapinn KW, Griffin MQ, Wiesner GL, Burke W, GRRIP Consortium. PMID: 22241102; PMCID: PMC3448270.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    58. What are our AIMs? Interdisciplinary Perspectives on the Use of Ancestry Estimation in Disease Research. AJOB Prim Res. 2012; 3(4):87-97. Yu JH, Taylor JS, Edwards KL, Fullerton SM. PMID: 25419472; PMCID: PMC4238888.
      View in: PubMed   Mentions: 3  
    59. Cerebrospinal fluid amyloid β and tau in LRRK2 mutation carriers. Neurology. 2012 Jan 03; 78(1):55-61. Aasly JO, Shi M, Sossi V, Stewart T, Johansen KK, Wszolek ZK, Uitti RJ, Hasegawa K, Yokoyama T, Zabetian CP, Kim HM, Leverenz JB, Ginghina C, Armaly J, Edwards KL, Snapinn KW, Stoessl AJ, Zhang J. PMID: 22170881; PMCID: PMC3466497.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    60. Could disappearance of endemic (Balkan) nephropathy be expected in forthcoming decades? Kidney Blood Press Res. 2012; 35(3):147-52. Cvitkovic A, Vukovic-Lela I, Edwards KL, Karanovic S, Juric D, Cvorišcec D, Fucek M, Jelakovic B. PMID: 22116163; PMCID: PMC3696381.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansPHPublic Health
    61. Aristolactam-DNA adducts are a biomarker of environmental exposure to aristolochic acid. Kidney Int. 2012 Mar; 81(6):559-67. Jelakovic B, Karanovic S, Vukovic-Lela I, Miller F, Edwards KL, Nikolic J, Tomic K, Slade N, Brdar B, Turesky RJ, Stipancic Ž, Dittrich D, Grollman AP, Dickman KG. PMID: 22071594; PMCID: PMC3560912.
      View in: PubMed   Mentions: 74     Fields:    Translation:HumansPHPublic Health
    62. Conditions comorbid with chronic fatigue in a population-based sample. Psychosomatics. 2012 Jan-Feb; 53(1):44-50. Dansie EJ, Furberg H, Afari N, Buchwald D, Edwards K, Goldberg J, Schur E, Sullivan PF. PMID: 22221720; PMCID: PMC3254018.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    63. Skin care behaviors among melanoma survivors. Psychooncology. 2012 Dec; 21(12):1285-91. Bowen D, Jabson J, Haddock N, Hay J, Edwards K. PMID: 21780240.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansPHPublic Health
    64. Clinically relevant changes in family history of cancer over time. JAMA. 2011 Jul 13; 306(2):172-8. Ziogas A, Horick NK, Kinney AY, Lowery JT, Domchek SM, Isaacs C, Griffin CA, Moorman PG, Edwards KL, Hill DA, Berg JS, Tomlinson GE, Anton-Culver H, Strong LC, Kasten CH, Finkelstein DM, Plon SE. PMID: 21750294; PMCID: PMC3367662.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    65. Attitudes toward genetic research review: results from a survey of human genetics researchers. Public Health Genomics. 2011; 14(6):337-45. Edwards KL, Lemke AA, Trinidad SB, Lewis SM, Starks H, Quinn Griffin MT, Wiesner GL. PMID: 21487211; PMCID: PMC3221257.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    66. 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. 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 KL, Snapinn KW, Goldstein DS, Shi M, Zhang J. PMID: 21435440; PMCID: PMC3078443.
      View in: PubMed   Mentions: 52     Fields:    Translation:Humans
    67. Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease. Mov Disord. 2011 Apr; 26(5):819-23. 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 KL, Zabetian CP. PMID: 21425343; PMCID: PMC3082603.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    68. The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population. Parkinsonism Relat Disord. 2011 Jul; 17(6):473-5. 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 KL, Zabetian CP. PMID: 21345711; PMCID: PMC3119730.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    69. Multivariate linkage scan for metabolic syndrome traits in families with type 2 diabetes. Obesity (Silver Spring). 2011 Jun; 19(6):1235-43. Edwards KL, Wan JY, Hutter CM, Fong PY, Santorico SA. PMID: 21183932.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    70. Advances in microbicide vaginal rings. Antiviral Res. 2010 Dec; 88 Suppl 1:S30-9. Malcolm RK, Edwards KL, Kiser P, Romano J, Smith TJ. PMID: 21109066.
      View in: PubMed   Mentions: 69     Fields:    Translation:HumansCells
    71. SNCA variant associated with Parkinson disease and plasma alpha-synuclein level. Arch Neurol. 2010 Nov; 67(11):1350-6. Mata IF, Shi M, Agarwal P, Chung KA, Edwards KL, 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. PMID: 21060011; PMCID: PMC3010848.
      View in: PubMed   Mentions: 85     Fields:    Translation:HumansCells
    72. 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. Lemke AA, Trinidad SB, Edwards KL, Starks H, Wiesner GL, GRRIP Consortium. PMID: 20235866; PMCID: PMC2902178.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    73. 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. Heike CL, Starr JR, Rieder MJ, Cunningham ML, Edwards KL, Stanaway IB, Crawford DC. PMID: 19645056; PMCID: PMC4535433.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    74. 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. Ragland M, Hutter C, Zabetian C, Edwards K. PMID: 19864305; PMCID: PMC2778765.
      View in: PubMed   Mentions: 31     Fields:    Translation:Humans
    75. When family means more (or less) than genetics: the intersection of culture, family and genomics. J Transcult Nurs. 2009 Jul; 20(3):270-7. McGrath BB, Edwards KL. PMID: 19398610; PMCID: PMC2773542.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    76. The genomic applications in practice and prevention network. Genet Med. 2009 Jul; 11(7):488-94. 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, GAPPNet Planning Group. PMID: 19471162; PMCID: PMC2743616.
      View in: PubMed   Mentions: 21     Fields:    
    77. LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Mov Disord. 2009 May 15; 24(7):1034-41. Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards KL, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H. PMID: 19343804; PMCID: PMC2827255.
      View in: PubMed   Mentions: 31     Fields:    Translation:Humans
    78. 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. 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 KL, Alvarez V, Zabetian CP. PMID: 19308469; PMCID: PMC2821036.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    79. Visual assessment of endemic nephropathy markers relationship. Stud Health Technol Inform. 2009; 150:836-40. Sonicki Z, Cvitkovic A, Edwards KL, Miletic-Medved M, Cvoriscec D, Babus V, Jelakovic B. PMID: 19745430.
      View in: PubMed   Mentions:    Fields:    Translation:HumansPHPublic Health
    80. 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. Goddard KA, Duquette D, Zlot A, Johnson J, Annis-Emeott A, Lee PW, Bland MP, Edwards KL, Oehlke K, Giles RT, Rafferty A, Cook ML, Khoury MJ. PMID: 19106425; PMCID: PMC2661444.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansPHPublic Health
    81. Genome-wide linkage scan for the metabolic syndrome: the GENNID study. Obesity (Silver Spring). 2008 Jul; 16(7):1596-601. Edwards KL, Hutter CM, Wan JY, Kim H, Monks SA. PMID: 18421265.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    82. Cytochrome p450 enzyme polymorphism frequency in indigenous and native american populations: a systematic review. Community Genet. 2008; 11(3):141-9. Jaja C, Burke W, Thummel K, Edwards K, Veenstra DL. PMID: 18376110.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    83. Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease. Eur J Neurol. 2008 Feb; 15(2):134-9. Hutter CM, Samii A, Factor SA, Nutt JG, Higgins DS, Bird TD, Griffith A, Roberts JW, Leis BC, Montimurro JS, Kay DM, Edwards KL, Payami H, Zabetian CP. PMID: 18093156; PMCID: PMC2823263.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    84. Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease. Ann Neurol. 2007 Aug; 62(2):137-44. Zabetian CP, Hutter CM, Factor SA, Nutt JG, Higgins DS, Griffith A, Roberts JW, Leis BC, Kay DM, Yearout D, Montimurro JS, Edwards KL, Samii A, Payami H. PMID: 17514749; PMCID: PMC2836920.
      View in: PubMed   Mentions: 77     Fields:    Translation:Humans
    85. DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease. Ann Neurol. 2007 Jul; 62(1):99-101. Chun LS, Samii A, Hutter CM, Griffith A, Roberts JW, Leis BC, Mosley AD, Wander PL, Edwards KL, Payami H, Zabetian CP. PMID: 17503507; PMCID: PMC2823266.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    86. 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. 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 KL, Samii A, Payami H. PMID: 16960813; PMCID: PMC1592578.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    87. 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. Ramos EM, Lin MT, Larson EB, Maezawa I, Tseng LH, Edwards KL, Schellenberg GD, Hansen JA, Kukull WA, Jin LW. PMID: 16908746.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansCells
    88. LDL composition in E2/2 subjects and LDL distribution by Apo E genotype in type 1 diabetes. Atherosclerosis. 2007 May; 192(1):138-47. Murdoch SJ, Boright AP, Paterson AD, Zinman B, Steffes M, Cleary P, Edwards K, Marcovina SS, Purnell JQ, Brunzell JD, DCCT/EDIC Research Group. PMID: 16740268; PMCID: PMC2628303.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    89. 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. Sieh W, Edwards KL, Fitzpatrick AL, Srinouanprachanh SL, Farin FM, Monks SA, Kronmal RA, Eaton DL. PMID: 16425097.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    90. Functional variants of the lipoprotein lipase gene and the risk of preeclampsia among non-Hispanic Caucasian women. Clin Genet. 2006 Jan; 69(1):33-9. Zhang C, Austin MA, Edwards KL, Farin FM, Li N, Hsu L, Srinouanprachanh SL, Williams MA. PMID: 16451134.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    91. 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. Kim H, Hutter CM, Monks SA, Edwards KL. PMID: 16451661; PMCID: PMC1866734.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    92. 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. Hutter CM, Austin MA, Farin FM, Viernes HM, Edwards KL, Leonetti DL, McNeely MJ, Fujimoto WY. PMID: 16023652.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    93. Developing academic-practice partnerships to enhance the integration of genomics into public health. Prev Chronic Dis. 2005 Apr; 2(2):A02. Raup SF, Oehlke KP, Edwards KL. PMID: 15888213; PMCID: PMC1327696.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansPHPublic Health
    94. The asthma consultative process: a collaborative approach to integrating genomics into public health practice. Prev Chronic Dis. 2005 Apr; 2(2):A27. Harrison TA, Burke W, Edwards KL. PMID: 15888238; PMCID: PMC1327721.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansPHPublic Health
    95. beta(2)-Adrenergic receptor polymorphisms and determinants of cardiovascular risk: the Cardiovascular Health Study. Am J Hypertens. 2005 Mar; 18(3):392-7. Hindorff LA, Heckbert SR, Psaty BM, Lumley T, Siscovick DS, Herrington DM, Edwards KL, Tracy RP. PMID: 15797659.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    96. 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. Zhang C, Williams MA, Edwards KL, Austin MA. PMID: 15804782.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    97. Family history as a risk factor for stroke in young women. Am J Prev Med. 2004 Dec; 27(5):391-6. Kim H, Friedlander Y, Longstreth WT, Edwards KL, Schwartz SM, Siscovick DS. PMID: 15556739.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    98. Heritability of C-reactive protein and association with apolipoprotein E genotypes in Japanese Americans. Ann Hum Genet. 2004 May; 68(Pt 3):179-88. Austin MA, Zhang C, Humphries SE, Chandler WL, Talmud PJ, Edwards KL, Leonetti DL, McNeely MJ, Fujimoto WY. PMID: 15180698.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    99. Heritability of multivariate factors of the metabolic syndrome in nondiabetic Japanese americans. Diabetes. 2004 Apr; 53(4):1166-9. Austin MA, Edwards KL, McNeely MJ, Chandler WL, Leonetti DL, Talmud PJ, Humphries SE, Fujimoto WY. PMID: 15047637.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    100. Association of apolipoprotein A5 variants with LDL particle size and triglyceride in Japanese Americans. Biochim Biophys Acta. 2004 Jan 20; 1688(1):1-9. Austin MA, Talmud PJ, Farin FM, Nickerson DA, Edwards KL, Leonetti D, McNeely MJ, Viernes HM, Humphries SE, Fujimoto WY. PMID: 14732475.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    101. Multiple genome-wide analyses of smoking behavior in the Framingham Heart Study. BMC Genet. 2003 Dec 31; 4 Suppl 1:S102. Goode EL, Badzioch MD, Kim H, Gagnon F, Rozek LS, Edwards KL, Jarvik GP, Framingham Heart Study. PMID: 14975170; PMCID: PMC1866440.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansCells
    102. 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. Bis JC, Smith NL, Psaty BM, Heckbert SR, Edwards KL, Lemaitre RN, Lumley T, Rosendaal FR. PMID: 14643574.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    103. 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. Hebert MF, Dowling AL, Gierwatowski C, Lin YS, Edwards KL, Davis CL, Marsh CL, Schuetz EG, Thummel KE. PMID: 14583679.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    104. Parity and the risk of Down's syndrome. Am J Epidemiol. 2003 Sep 15; 158(6):503-8. Doria-Rose VP, Kim HS, Augustine ET, Edwards KL. PMID: 12965874.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    105. 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. Austin MA, Edwards KL, Monks SA, Koprowicz KM, Brunzell JD, Motulsky AG, Mahaney MC, Hixson JE. PMID: 12923221.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    106. Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study. Lancet. 2003 May 17; 361(9370):1671-6. McKone EF, Emerson SS, Edwards KL, Aitken ML. PMID: 12767731.
      View in: PubMed   Mentions: 114     Fields:    Translation:Humans
    107. Beta2-adrenergic receptor polymorphisms and risk of incident cardiovascular events in the elderly. Circulation. 2003 Apr 22; 107(15):2021-4. Heckbert SR, Hindorff LA, Edwards KL, Psaty BM, Lumley T, Siscovick DS, Tang Z, Durda JP, Kronmal RA, Tracy RP. PMID: 12682000.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    108. Family history of diabetes as a potential public health tool. Am J Prev Med. 2003 Feb; 24(2):152-9. Harrison TA, Hindorff LA, Kim H, Wines RC, Bowen DJ, McGrath BB, Edwards KL. PMID: 12568821.
      View in: PubMed   Mentions: 119     Fields:    Translation:HumansPHPublic Health
    109. Lipoprotein and apolipoprotein abnormalities in familial combined hyperlipidemia: a 20-year prospective study. Atherosclerosis. 2001 Dec; 159(2):471-81. McNeely MJ, Edwards KL, Marcovina SM, Brunzell JD, Motulsky AG, Austin MA. PMID: 11730829.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    110. Lipoprotein(a) as a risk factor for maternal cardiovascular disease mortality in kindreds with familial combined hyperlipidemia or familial hypertriglyceridemia. Clin Genet. 2001 Sep; 60(3):188-97. Kim H, Marcovina SM, Edwards KL, McKnight B, Bradley CM, McNeely MJ, Psaty BM, Motulsky AG, Austin MA. PMID: 11595020.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    111. Low-density lipoprotein particle size, triglycerides, and high-density lipoprotein cholesterol as risk factors for coronary heart disease in older Japanese-American men. Am J Cardiol. 2000 Aug 15; 86(4):412-6. Austin MA, Rodriguez BL, McKnight B, McNeely MJ, Edwards KL, Curb JD, Sharp DS. PMID: 10946034.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    112. Sib-pair linkage analysis of longitudinal changes in lipoprotein risk factors and lipase genes in women twins. J Lipid Res. 2000 Aug; 41(8):1302-9. Friedlander Y, Talmud PJ, Edwards KL, Humphries SE, Austin MA. PMID: 10946018.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    113. Cardiovascular disease mortality in familial forms of hypertriglyceridemia: A 20-year prospective study. Circulation. 2000 Jun 20; 101(24):2777-82. Austin MA, McKnight B, Edwards KL, Bradley CM, McNeely MJ, Psaty BM, Brunzell JD, Motulsky AG. PMID: 10859281.
      View in: PubMed   Mentions: 51     Fields:    Translation:Humans
    114. Linkage of the cholesteryl ester transfer protein (CETP) gene to LDL particle size: use of a novel tetranucleotide repeat within the CETP promoter. Circulation. 2000 May 30; 101(21):2461-6. Talmud PJ, Edwards KL, Turner CM, Newman B, Palmen JM, Humphries SE, Austin MA. PMID: 10831518.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    115. Pleiotropic genetic effects on LDL size, plasma triglyceride, and HDL cholesterol in families. Arterioscler Thromb Vasc Biol. 1999 Oct; 19(10):2456-64. Edwards KL, Mahaney MC, Motulsky AG, Austin MA. PMID: 10521376.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    116. Inheritance of LDL peak particle diameter: results from a segregation analysis in Israeli families. Genet Epidemiol. 1999; 16(4):382-96. Friedlander Y, Kark JD, Sinnreich R, Edwards KL, Austin MA. PMID: 10207719.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    117. Factors of the insulin resistance syndrome in nondiabetic and diabetic elderly Japanese-American men. Am J Epidemiol. 1998 Mar 01; 147(5):441-7. Edwards KL, Burchfiel CM, Sharp DS, Curb JD, Rodriguez BL, Fujimoto WY, LaCroix AZ, Vitiello MV, Austin MA. PMID: 9525530.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    118. Hypertriglyceridemia as a cardiovascular risk factor. Am J Cardiol. 1998 Feb 26; 81(4A):7B-12B. Austin MA, Hokanson JE, Edwards KL. PMID: 9526807.
      View in: PubMed   Mentions: 189     Fields:    Translation:Humans
    119. Candidate-gene studies of the atherogenic lipoprotein phenotype: a sib-pair linkage analysis of DZ women twins. Am J Hum Genet. 1998 Feb; 62(2):406-19. Austin MA, Talmud PJ, Luong LA, Haddad L, Day IN, Newman B, Edwards KL, Krauss RM, Humphries SE. PMID: 9463319; PMCID: PMC1376888.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    120. Heritability of factors of the insulin resistance syndrome in women twins. Genet Epidemiol. 1997; 14(3):241-53. Edwards KL, Newman B, Mayer E, Selby JV, Krauss RM, Austin MA. PMID: 9181354.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    121. Small, dense low density lipoproteins, the insulin resistance syndrome and noninsulin-dependent diabetes. Curr Opin Lipidol. 1996 Jun; 7(3):167-71. Austin MA, Edwards KL. PMID: 8818515.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    122. Prospective study of small LDLs as a risk factor for non-insulin dependent diabetes mellitus in elderly men and women. Circulation. 1995 Oct 01; 92(7):1770-8. Austin MA, Mykkänen L, Kuusisto J, Edwards KL, Nelson C, Haffner SM, Pyörälä K, Laakso M. PMID: 7671360.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    123. Evidence for genetic influences on smoking in adult women twins. Clin Genet. 1995 May; 47(5):236-44. Edwards KL, Austin MA, Jarvik GP. PMID: 7554348.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    124. Multivariate analysis of the insulin resistance syndrome in women. Arterioscler Thromb. 1994 Dec; 14(12):1940-5. Edwards KL, Austin MA, Newman B, Mayer E, Krauss RM, Selby JV. PMID: 7981183.
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