Jeanette McCarthy, MPH, PhD

Title(s)Associate Professor, Medicine
SchoolSchool of Medicine
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    As a genome scientist, I spent years doing research on the genetic underpinnings of complex diseases, both infectious and chronic, and working to advance the field of precision medicine. More recently, I've turned my attention to educating stakeholders in this field. I believe informed consumers will play a major role in their health care going forward.In 2014, I helped launch the first consumer-facing magazine in this field, Genome (genomemag.com), where I was founding Editor-in-Chief. Health care providers also require education that is accessible and practical. I have developed courses in precision medicine at UC Berkeley Extension and through UCSF via Coursera (www.coursera.org/course/genomicmedicine). I also design and delivers workshops, symposia and webinars on more general as well as technical topics related to precision medicine through my consulting business, Precision Medicine Advisors (precisionmedicineadvisors.com) and the Precision Medicine Academy (precisionmedicineacademy.org).

    Collapse Research 
    Collapse Research Activities and Funding
    Pharmacogenetics of lipid response to estrogen therapy
    NIH R01HL085191Jul 1, 2006 - Jun 30, 2010
    Role: Principal Investigator

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    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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    1. Welcome to the 18th volume of Personalized Medicine. Per Med. 2021 01; 18(1):1-3. McCarthy J, Patrinos G, Ginsburg G. PMID: 33459576.
      View in: PubMed   Mentions:    Fields:    
    2. P-30 Antigen. . 2020 Jan 1; 1603-1603. Coons CM, Steglitz SJ, Coons CM, McCracken ML, Coons CM, Shaw SW, Pransky PG, Shaw SW, Pransky PG, Coons CM, Steglitz SJ, Coons CM, Coons CM, Iwase IS, Mori MC, Coons CM, Coons CM, Turner TJ, Richter RM, Wright WR, McClintock MS, Chansard CM, Husain HM, Zimmerman ZS, Carroll CL, Rabbi RM, Witthöft WM, Gidron GY, Cunningham CC, Kikuchi KH, Marsac MM, Alderfer AM, Jiang JR, Leung LY, Hall HP, Zehr ZC, Gidron GY, Phillips PA, Chan CS, La Greca LA, Salomon SK, Karlsdóttir KM, Rosenberg RL, Brosschot BJ, Verkuil VB, Thayer TJ, Cribbet CM, Williams WP, Garcia GR, Barrett BC, Turner TJ, Ditzen DB, Nater NU, Heim HC, McCarthy MJ, Bernardine BM, Frierson FG, Stoutenberg SM, Arigo AD, Pasko PK, Brady BS, Veldhuijzen van Zanten VJ, Duda DJ, Kitas KG, Fenton FS, Hammersla HM, Campbell CN, De Jesus DS, Prapavessis PH, Clark CT, Moffat MM, Salomon SK, O’Brien OE, Turner TJ, Heaney HJ, Flaten FM, Al’absi AM, Wakefield WM, Newman NJ, Turner TJ, Kline KC, Hall HP, Zehr ZC, Singh SA, Lieb LR, Tran TV, Fortenberry FK, Jansen JK, Clark CM, Ferguson FS, Aspinwall AL, Pengchit PW, Zimmerman ZC, Herge HW, La Greca LA, Okun OM, Tran TV, Burdzy BD, Pargament PK, Julian JM, Ramos RI, Mahrer MN, Dunkel Schetter DC, Okun OM, Newman NJ, Carroll CL, Baumann BL, Ylinen YA, Idzik IS, Harlapur HM, Shimbo SD, Idzik IS, Gambert GS, Idzik IS, Turner TJ, Turner TJ, Margolis MS, Osborne OP, Gonzalez GJ, Carroll CL, Ramirez RP, Turner TB, Kowalkouski KM, Goltz GH, Hart HS, Latini LD, Kowalkouski KM, Goltz GH, Hart HS, Latini LD, Shaughnessy SM, Turner TJ, Okuyama OT, Holmqvist HM, Suzuki SS, Tanoue TA, Holmqvist HM, Upton UJ, Holmqvist HM, Hall HP, Suzuki SS, Ito ID, Tran TV, Ginty GA, Turner TJ, Wolf WJ, Saucier SE, Wolf WJ, Rene RK, Hamer HM, Hamer HM, Carroll CD, Lovallo LW, Buchanan BT, Chan CF, da Silva Cardoso dE, Chronister CJ, Hiatt HE, LaCaille LR, Marshall ME, Vizzotto VA, de Oliveira dA, Elkis EH, Cordeiro CQ, Buchain BP, Upton UJ, Suzuki SS, Yanai YY, de Oliveira dA, Buchain BP, Vizzotto VA, Elkis EH, Cordeiro CQ, Long LJ, Cumming CJ, Long LJ, Cumming CJ, Jacobs JK, Hellman HM, Markowitz MJ, Wuest WE, Ito IM, Ando AT, Carroll CD, Carrillo CA, Gomez-Meade GC, Gellman GM, Mitani MA, Sabol SV. .
      View in: Publisher Site   Mentions:
    3. Genomics. . 2020 Jan 1; 939-939. McCarthy MJ, Turner TJ. .
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    4. Phenotype. . 2020 Jan 1; 1664-1664. McCarthy MJ. .
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    5. Educating healthcare providers in the delivery of genomic medicine. Per Med. 2019 05; 16(3):187-188. McCarthy J, Patrinos GP. PMID: 31189426.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    6. A note from the editors. Per Med. 2018 07 01; 15(4):237-238. Ginsburg GS, McCarthy JJ, Patrinos GP. PMID: 29927353.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    7. Toward clinical genomics in everyday medicine: perspectives and recommendations. Expert Rev Mol Diagn. 2016; 16(5):521-32. Delaney SK, Hultner ML, Jacob HJ, Ledbetter DH, McCarthy JJ, Ball M, Beckman KB, Belmont JW, Bloss CS, Christman MF, Cosgrove A, Damiani SA, Danis T, Delledonne M, Dougherty MJ, Dudley JT, Faucett WA, Friedman JR, Haase DH, Hays TS, Heilsberg S, Huber J, Kaminsky L, Ledbetter N, Lee WH, Levin E, Libiger O, Linderman M, Love RL, Magnus DC, Martland A, McClure SL, Megill SE, Messier H, Nussbaum RL, Palaniappan L, Patay BA, Popovich BW, Quackenbush J, Savant MJ, Su MM, Terry SF, Tucker S, Wong WT, Green RC. PMID: 26810587; PMCID: PMC4841021.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    8. Clinical application of pharmacogenetics: focusing on practical issues. Pharmacogenomics. 2015; 16(15):1733-41. Chang MT, McCarthy JJ, Shin J. PMID: 26411302.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    9. Driving personalized medicine forward: the who, what, when, and how of educating the health-care workforce. Mol Genet Genomic Med. 2014 Nov; 2(6):455-7. McCarthy JJ. PMID: 25614866; PMCID: PMC4303214.
      View in: PubMed   Mentions: 1     Fields:    
    10. Genomic medicine: a decade of successes, challenges, and opportunities. Sci Transl Med. 2013 Jun 12; 5(189):189sr4. McCarthy JJ, McLeod HL, Ginsburg GS. PMID: 23761042.
      View in: PubMed   Mentions: 101     Fields:    Translation:Humans
    11. Development and evaluation of a genetic risk score for obesity. Biodemography Soc Biol. 2013; 59(1):85-100. Belsky DW, Moffitt TE, Sugden K, Williams B, Houts R, McCarthy J, Caspi A. PMID: 23701538; PMCID: PMC3671353.
      View in: PubMed   Mentions: 76     Fields:    Translation:Humans
    12. Pleiotropy and allelic heterogeneity in the TOMM40-APOE genomic region related to clinical and metabolic features of hepatitis C infection. Hum Genet. 2012 Dec; 131(12):1911-20. Chiba-Falek O, Linnertz C, Guyton J, Gardner SD, Roses AD, McCarthy JJ, Patel K. PMID: 22898894.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    13. Metaprotein expression modeling for label-free quantitative proteomics. BMC Bioinformatics. 2012 May 04; 13:74. Lucas JE, Thompson JW, Dubois LG, McCarthy J, Tillmann H, Thompson A, Shire N, Hendrickson R, Dieguez F, Goldman P, Schwarz K, Patel K, McHutchison J, Moseley MA. PMID: 22559859; PMCID: PMC3436780.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    14. Reply to: “Interaction between IL28B and PNPLA3 genotypes in the pathogenesis of steatosis in chronic hepatitis C non genotype-3 patients”. Journal of Hepatology. 2012 May 1; 56(5):1210-1212. Trépo TE, Pradat PP, McCarthy MJ, Tillmann TH. .
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    15. Reply to: “Favorable association between genetic polymorphisms near the IL28B gene and hepatic steatosis: Direct or indirect?”. Journal of Hepatology. 2012 Mar 1; 56(3):739. Tillmann TH, McCarthy MJ. .
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    16. Characterization of the poly-T variant in the TOMM40 gene in diverse populations. PLoS One. 2012; 7(2):e30994. Linnertz C, Saunders AM, Lutz MW, Crenshaw DM, Grossman I, Burns DK, Whitfield KE, Hauser MA, McCarthy JJ, Ulmer M, Allingham R, Welsh-Bohmer KA, Roses AD, Chiba-Falek O. PMID: 22359560; PMCID: PMC3281049.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    17. A more rapid approach to systematically assessing published associations of genetic polymorphisms and disease risk: type 2 diabetes as a test case. Comparative Effectiveness Research. 2012 Jan 26; 2(0):1-20. Cho CA, Jiang JX, Mann MD, Kawamoto KK, Robinson RT, Wang WN, McCarthy MJ, Woodward WM, Ginsburg GG. .
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    18. Thrombospondin-4 polymorphism (A387P) predicts cardiovascular risk in postinfarction patients with high HDL cholesterol and C-reactive protein levels. Thromb Haemost. 2011 Dec; 106(6):1170-8. Corsetti JP, Ryan D, Moss AJ, McCarthy J, Goldenberg I, Zareba W, Sparks CE. PMID: 22011848.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    19. Characterization of serum proteins associated with IL28B genotype among patients with chronic hepatitis C. PLoS One. 2011; 6(7):e21854. Cyr DD, Lucas JE, Thompson JW, Patel K, Clark PJ, Thompson A, Tillmann HL, McHutchison JG, Moseley MA, McCarthy JJ. PMID: 21750736; PMCID: PMC3130042.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    20. High predictive accuracy of an unbiased proteomic profile for sustained virologic response in chronic hepatitis C patients. Hepatology. 2011 Jun; 53(6):1809-18. Patel K, Lucas JE, Thompson JW, Dubois LG, Tillmann HL, Thompson AJ, Uzarski D, Califf RM, Moseley MA, Ginsburg GS, McHutchison JG, McCarthy JJ, MURDOCK Horizon 1 Study Team. PMID: 21381069.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    21. Beneficial IL28B genotype associated with lower frequency of hepatic steatosis in patients with chronic hepatitis C. J Hepatol. 2011 Dec; 55(6):1195-200. Tillmann HL, Patel K, Muir AJ, Guy CD, Li JH, Lao XQ, Thompson A, Clark PJ, Gardner SD, McHutchison JG, McCarthy JJ. PMID: 21703198; PMCID: PMC3763913.
      View in: PubMed   Mentions: 42     Fields:    Translation:HumansCTClinical Trials
    22. 1345 INTERACTION BETWEEN IL28B CCR5?32, AND HCV PERSISTENCE WITH GBV-C VIREMIA AND SYMPTOMS DURING ACUTE INFECTION. Journal of Hepatology. 2011 Mar 1; 54:s531. Tenckhoff TS, Wiegand WJ, Patel PK, Wiese WM, Tenckhoff TH, Nischalke NH, Kullig KU, Gobel GU, Capka CE, Schiefte SI, Güthoff GW, Grüngreiff GK, König KI, Spengler SU, McCarthy MJ, Thompson TA, McHutchison MJ, Timm TJ, Viazov VS, Nattermann NJ, Tillmann TH, Group GG. .
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    23. Gene by sex interaction for measures of obesity in the framingham heart study. J Obes. 2011; 2011:329038. Benjamin AM, Suchindran S, Pearce K, Rowell J, Lien LF, Guyton JR, McCarthy JJ. PMID: 21253498; PMCID: PMC3021872.
      View in: PubMed   Mentions: 11     Fields:    
    24. The Alzheimer's associated 5' region of the SORL1 gene cis regulates SORL1 transcripts expression. Neurobiol Aging. 2012 Jul; 33(7):1485.e1-8. McCarthy JJ, Saith S, Linnertz C, Burke JR, Hulette CM, Welsh-Bohmer KA, Chiba-Falek O. PMID: 21185108; PMCID: PMC3117021.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    25. The effect of SNCA 3' region on the levels of SNCA-112 splicing variant. Neurogenetics. 2011 Feb; 12(1):59-64. McCarthy JJ, Linnertz C, Saucier L, Burke JR, Hulette CM, Welsh-Bohmer KA, Chiba-Falek O. PMID: 21046180; PMCID: PMC3030669.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansCells
    26. A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundice. Gastroenterology. 2010 Nov; 139(5):1586-92, 1592.e1. Tillmann HL, Thompson AJ, Patel K, Wiese M, Tenckhoff H, Nischalke HD, Lokhnygina Y, Kullig U, Göbel U, Capka E, Wiegand J, Schiefke I, Güthoff W, Grüngreiff K, König I, Spengler U, McCarthy J, Shianna KV, Goldstein DB, McHutchison JG, Timm J, Nattermann J, German Anti-D Study Group. PMID: 20637200.
      View in: PubMed   Mentions: 117     Fields:    Translation:Humans
    27. Hepatitis C trials that combine investigational agents with pegylated interferon should be stratified by interleukin-28B genotype. Hepatology. 2010 Dec; 52(6):2243-4. Thompson AJ, Muir AJ, Sulkowski MS, Patel K, Tillmann HL, Clark PJ, Naggie S, Fellay J, Ge D, McCarthy JJ, Goldstein DB, McHutchison JG. PMID: 20890887.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    28. Interferon-lambda genotype and low serum low-density lipoprotein cholesterol levels in patients with chronic hepatitis C infection. Hepatology. 2010 Jun; 51(6):1904-11. Li JH, Lao XQ, Tillmann HL, Rowell J, Patel K, Thompson A, Suchindran S, Muir AJ, Guyton JR, Gardner SD, McHutchison JG, McCarthy JJ. PMID: 20235331; PMCID: PMC2921623.
      View in: PubMed   Mentions: 50     Fields:    Translation:Humans
    29. Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. PLoS Genet. 2010 Apr 29; 6(4):e1000928. Suchindran S, Rivedal D, Guyton JR, Milledge T, Gao X, Benjamin A, Rowell J, Ginsburg GS, McCarthy JJ. PMID: 20442857; PMCID: PMC2861686.
      View in: PubMed   Mentions: 39     Fields:    Translation:Humans
    30. 125 IL28B POLYMORPHISM IS ASSOCIATED WITH JAUNDICE DURING ACUTE HCV INFECTION AND IS A STRONG PREDICTOR FOR SPONTANEOUS CLEARANCE IN THE PROSPECTIVE GERMAN ANTI-D COHORT. Journal of Hepatology. 2010 Apr 1; 52:s56. Tillmann TH, Thompson TA, Patel PK, Wiese WM, Tenckhoff TH, Nischalke NH, Kullig KU, Goebel GU, Capka CE, Wiegand WJ, Schiefke SI, Spengler SU, McCarthy MJ, Shianna SK, Goldstein GD, McHutchison MJ, Timm TJ, Nattermann NJ, Group Ga. .
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    31. 1179 INTERFERON LAMBDA GENOTYPE AND LOW SERUM LDL CHOLESTEROL LEVELS IN PATIENTS WITH CHRONIC HEPATITIS C INFECTION. Journal of Hepatology. 2010 Apr 1; 52:s456. Li LJ, Lao LX, Tillmann TH, Rowell RJ, Patel PK, Thompson TA, Suchindran SS, Muir MA, Guyton GJ, Gardner GS, McHutchison MJ, McCarthy MJ. .
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    32. Replicated association between an IL28B gene variant and a sustained response to pegylated interferon and ribavirin. Gastroenterology. 2010 Jun; 138(7):2307-14. McCarthy JJ, Li JH, Thompson A, Suchindran S, Lao XQ, Patel K, Tillmann HL, Muir AJ, McHutchison JG. PMID: 20176026; PMCID: PMC2883666.
      View in: PubMed   Mentions: 99     Fields:    Translation:HumansCells
    33. Impact of gene variants on sex-specific regulation of human Scavenger receptor class B type 1 (SR-BI) expression in liver and association with lipid levels in a population-based study. BMC Med Genet. 2010 Jan 19; 11:9. Chiba-Falek O, Nichols M, Suchindran S, Guyton J, Ginsburg GS, Barrett-Connor E, McCarthy JJ. PMID: 20085651; PMCID: PMC2822818.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    34. Racial differences in the interaction between family history and risk factors associated with diabetes in the National Health and Nutritional Examination Survey, 1999-2004. Genet Med. 2009 Jul; 11(7):542-7. Suchindran S, Vana AM, Shaffer RA, Alcaraz JE, McCarthy JJ. PMID: 19606541.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    35. Polymorphisms of the scavenger receptor class B member 1 are associated with insulin resistance with evidence of gene by sex interaction. J Clin Endocrinol Metab. 2009 May; 94(5):1789-96. McCarthy JJ, Somji A, Weiss LA, Steffy B, Vega R, Barrett-Connor E, Talavera G, Glynne R. PMID: 19276229; PMCID: PMC2684479.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    36. Transforming the practice of medicine using genomics. Clin Cases Miner Bone Metab. 2009 Jan; 6(1):25-8. Ginsburg GS, Ginsburg GS, J McCarthy J. . PMID: 22461094; PMCID: PMC2781216.
      View in: PubMed   Mentions: 1  
    37. Validity of reported genetic risk factors for acute coronary syndrome. JAMA. 2007 Oct 17; 298(15):1758; author reply 1759. McCarthy JJ, Topol EJ. PMID: 17940228.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    38. Family History of Diabetes, Acculturation, and the Metabolic Syndrome among Mexican Americans: Proyecto SALSA. Metab Syndr Relat Disord. 2007 Sep; 5(3):262-9. Nelson T, Perez A, Alcaraz J, Talavera G, McCarthy JJ. PMID: 18370780.
      View in: PubMed   Mentions: 8     Fields:    
    39. Taking cardiovascular genetic association studies to the next level. J Am Coll Cardiol. 2007 Sep 04; 50(10):930-2. Ginsburg GS, Shah SH, McCarthy JJ. PMID: 17765118.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    40. Gene by sex interaction in the etiology of coronary heart disease and the preceding metabolic syndrome. Nutr Metab Cardiovasc Dis. 2007 Feb; 17(2):153-61. McCarthy JJ. PMID: 17306735.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimals
    41. Life, diversity and the pursuit of haplotypes. Nat Biotechnol. 2005 Nov; 23(11):1376-7. McCarthy J. PMID: 16273067.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    42. Atherosclerotic risk genotypes and recurrent coronary events after myocardial infarction. Am J Cardiol. 2005 Jul 15; 96(2):177-82. Moss AJ, Ryan D, Oakes D, Goldstein RE, Greenberg H, Bodenheimer MM, Brown MW, Case RB, Dwyer EM, Eberly SW, Francis CW, Gillespie JA, Krone RJ, Lichstein E, MacCluer JW, Marcus FI, McCarthy J, Sparks CE, Zareba W. PMID: 16018837.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    43. Aspirin resistance and a single gene. Am J Cardiol. 2005 Mar 15; 95(6):805-8. Jefferson BK, Foster JH, McCarthy JJ, Ginsburg G, Parker A, Kottke-Marchant K, Topol EJ. PMID: 15757620.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    44. Modification of the effects of estrogen therapy on HDL cholesterol levels by polymorphisms of the HDL-C receptor, SR-BI: the Rancho Bernardo Study. Atherosclerosis. 2005 Jun; 180(2):255-62. Richard E, von Muhlen D, Barrett-Connor E, Alcaraz J, Davis R, McCarthy JJ. PMID: 15910850.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    45. Coronary artery disease and the thrombospondin single nucleotide polymorphisms. Int J Biochem Cell Biol. 2004 Jun; 36(6):1013-30. Stenina OI, Byzova TV, Adams JC, McCarthy JJ, Topol EJ, Plow EF. PMID: 15094117.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    46. Replication of the association between the thrombospondin-4 A387P polymorphism and myocardial infarction. Am Heart J. 2004 May; 147(5):905-9. Wessel J, Topol EJ, Ji M, Meyer J, McCarthy JJ. PMID: 15131549.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    47. Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes. J Med Genet. 2004 May; 41(5):334-41. McCarthy JJ, Parker A, Salem R, Moliterno DJ, Wang Q, Plow EF, Rao S, Shen G, Rogers WJ, Newby LK, Cannata R, Glatt K, Topol EJ, GeneQuest Investigators. PMID: 15121769; PMCID: PMC1579684.
      View in: PubMed   Mentions: 46     Fields:    Translation:Humans
    48. 847-3 Aspirin resistance is associated with a single nucleotide polymorphism in the P2Y1 ADP receptor gene. Journal of the American College of Cardiology. 2004 Mar 1; 43(5):a515. Jefferson JB, Foster FJ, McCarthy MJ, Kottke-Marchant KK, Topol TE. .
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    49. Amino acid residue at position 13 in HLA-DR beta chain plays a critical role in the development of Kaposi's sarcoma in AIDS patients. AIDS. 2004 Jan 23; 18(2):199-204. Gayà A, Esteve A, Casabona J, McCarthy JJ, Martorell J, Schulz TF, Whitby D, EURO-SHAKS working group. PMID: 15075536.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    50. Advances in pharmacogenomic research and development. Mol Biotechnol. 2003 Nov; 25(3):275-82. McCarthy JJ. PMID: 14668540.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    51. Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients. Hum Genet. 2003 Dec; 114(1):87-98. McCarthy JJ, Meyer J, Moliterno DJ, Newby LK, Rogers WJ, Topol EJ, GenQuest multicenter study. PMID: 14557872.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    52. Association of genetic variants in the HDL receptor, SR-B1, with abnormal lipids in women with coronary artery disease. J Med Genet. 2003 Jun; 40(6):453-8. McCarthy JJ, Lehner T, Reeves C, Moliterno DJ, Newby LK, Rogers WJ, Topol EJ, Genequest investigators. PMID: 12807968; PMCID: PMC1735488.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    53. Polymorphisms of the HDL receptor gene associated with HDL cholesterol levels in diabetic kindred from three populations. Hum Hered. 2003; 55(4):163-70. McCarthy JJ, Lewitzky S, Reeves C, Permutt A, Glaser B, Groop LC, Lehner T, Meyer JM. PMID: 14566094.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    54. Turning SNPs into Useful Markers of Drug Response. Pharmacogenomics. 2002 Mar 26; 35-55. McCarthy MJ. .
      View in: Publisher Site   Mentions:
    55. Personalized medicine: revolutionizing drug discovery and patient care. Trends Biotechnol. 2001 Dec; 19(12):491-6. Ginsburg GS, McCarthy JJ. PMID: 11711191.
      View in: PubMed   Mentions: 76     Fields:    Translation:Humans
    56. Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction. Circulation. 2001 Nov 27; 104(22):2641-4. Topol EJ, McCarthy J, Gabriel S, Moliterno DJ, Rogers WJ, Newby LK, Freedman M, Metivier J, Cannata R, O'Donnell CJ, Kottke-Marchant K, Murugesan G, Plow EF, Stenina O, Daley GQ. PMID: 11723011.
      View in: PubMed   Mentions: 94     Fields:    Translation:Humans
    57. The use of single-nucleotide polymorphism maps in pharmacogenomics. Nat Biotechnol. 2000 May; 18(5):505-8. McCarthy JJ, Hilfiker R. PMID: 10802616.
      View in: PubMed   Mentions: 64     Fields:    Translation:Humans
    58. Hardy-Weinberg testing for HLA class II (DRB1, DQA1, DQB1, and DPB1) loci in 26 human ethnic groups. Tissue Antigens. 1999 Dec; 54(6):533-42. Chen JJ, Hollenbach JA, Trachtenberg EA, Just JJ, Carrington M, Rønningen KS, Begovich A, King MC, McWeeney S, Mack SJ, Erlich HA, Thomson G. PMID: 10674966.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    59. CCR5del32 in perinatal HIV-1 infection. J Acquir Immune Defic Syndr Hum Retrovirol. 1997 Dec 01; 16(4):239-42. Rousseau CM, Just JJ, Abrams EJ, Casabona J, Stein Z, King MC. PMID: 9402069.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCellsCTClinical Trials
    60. Intercellular adhesion molecule-1 deficiency prolongs survival and protects against the development of pulmonary inflammation during murine lupus. J Clin Invest. 1997 Sep 01; 100(5):963-71. Lloyd CM, Gonzalo JA, Salant DJ, Just J, Gutierrez-Ramos JC. PMID: 9276713; PMCID: PMC508271.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsCells
    61. African-American HLA class II allele and haplotype diversity. Tissue Antigens. 1997 May; 49(5):547-55. Just JJ, King MC, Thomson G, Klitz W. PMID: 9174158.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    62. Polymorphic repeats in the androgen receptor gene: molecular markers of prostate cancer risk. Cancer Res. 1997 Mar 15; 57(6):1194-8. Stanford JL, Just JJ, Gibbs M, Wicklund KG, Neal CL, Blumenstein BA, Ostrander EA. PMID: 9067292.
      View in: PubMed   Mentions: 69     Fields:    Translation:HumansCells
    63. African-American HLA class II allele and haplotype diversity. Tissue Antigens. 1996 Dec; 48(6):636-44. Just JJ, King MC, Thomson G, Klitz W. PMID: 9008305.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    64. MHC class II alleles associated with clinical and immunological manifestations of HIV-1 infection among children in Catalonia, Spain. Tissue Antigens. 1996 Apr; 47(4):313-8. Just JJ, Casabona J, Bertrán J, Montané C, Fortuny C, Rodrigo C, Mur A, Bosque M, Jovane L, King MC. PMID: 8773321.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    65. The role of host genetics in the natural history of HIV-1 infection: the needles in the haystack. AIDS. 1996; 10 Suppl A:S59-67. Keet IP, Klein MR, Just JJ, Kaslow RA. PMID: 8883611.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    66. Genetic predisposition to HIV-1 infection and acquired immune deficiency virus syndrome: a review of the literature examining associations with HLA [corrected]. Hum Immunol. 1995 Nov; 44(3):156-69. Just JJ. PMID: 8666552.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    67. Influence of host genotype on progression to acquired immunodeficiency syndrome among children infected with human immunodeficiency virus type 1. J Pediatr. 1995 Oct; 127(4):544-9. Just JJ, Abrams E, Louie LG, Urbano R, Wara D, Nicholas SW, Stein Z, King MC. PMID: 7562274.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    68. Genetic variation among the Mapuche Indians from the Patagonian region of Argentina: mitochondrial DNA sequence variation and allele frequencies of several nuclear genes. EXS. 1993; 67:211-9. Ginther C, Corach D, Penacino GA, Rey JA, Carnese FR, Hutz MH, Anderson A, Just J, Salzano FM, King MC. PMID: 8400690.
      View in: PubMed   Mentions: 38  Translation:HumansCells
    69. Genetic risk factors for perinatally acquired HIV-1 infection. Paediatr Perinat Epidemiol. 1992 Apr; 6(2):215-24. Just J, Louie L, Abrams E, Nicholas SW, Wara D, Stein Z, King MC. PMID: 1584723.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
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