Popis radova u zadnjih 5 godina
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1. Vitart V, Biloglav Z, Hayward C, Janicijevic B, Smolej-Narancic N, Barac L, Pericic M, Klaric IM, Skaric-Juric T, Barbalic M, Polasek O, Kolcic I, Carothers A, Rudan P, Hastie N, Wright A, Campbell H, Rudan I. 3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia. Eur J Hum Genet, 14:478-487, 2006.
2. Carothers AD, Rudan I, Kolcic I, Polasek O, Hayward C, Wright AF, Campbell H, Teague P, Hastie ND, Weber JL: Estimating human inbreeding coefficients: comparison of genealogical and marker heterozygosity approaches. Ann Hum Genet, 70: 666-676, 2006.
3. Barbalic M, Skaric-Juric T, Cambien F, Barbaux S, Poirier O, Turek S, Vrhovski-Hebrang D, Cubrilo-Turek M, Rudan I, Rudan P, Smolej Narancic N. Gene polymorphisms of the renin-angiotensin system and early development of hypertension. Am J Hyperten, 19:837-842, 2006.
4. Rudan I. The land of 1,000 islands. Croat Med J, 47: 524-526, 2006.
5. Rudan I. Health effects of human population isolation and admixture. Croat Med J, 47: 526-531, 2006.
6. Rudan I, Biloglav Z, Carothers AD, Wright AF, Campbell H. Strategy for mapping quantitative trait loci (QTL) using human metapopulations. Croat Med J, 47: 601-610, 2006.
7. Rudan I, Biloglav Z, Vorko-Jovic A, Kujundzic-Tiljak M, Stevanovic R, Ropac D, Puntaric D, Cucevic B, Salzer B, Campbell H. Effects of inbreeding, endogamy, genetic admixture, and outbreeding on human health: a ‘1001 Dalmatians’ study. Croat Med J, 47: 601-610, 2006.
8. Rudan I, Campbell H, Carothers AD, Hastie ND, Wright AF. Contribution of consanguinity to polygenic and multifactorial diseases. Nature Genet, 38: 1224-1225, 2006.
9. Bilic E, Bilic E, Rudan I, Kusec V, Zurak N, Delimar D, Zagar M. Comparison of the growth hormone, IGF-1 and insulin in cerebrospinal fluid and serum between patients with motor neuron disease and healthy controls. Eur J Neurol, 13: 1340 -1345, 2006.
10. Rudan I, El Arifeen S, Black RE, Campbell H. Childhood pneumonia and diarrhoea: Setting our priorities right. Lancet Inf Dis, 7: 56-61, 2007.
11. Campbell H, Carothers AD, Rudan I, Hayward C, Biloglav Z, Barac L, Pericic M, Janicijevic B, Smolej-Narancic N, Polasek O, Kolcic I, Weber JL, Hastie ND, Rudan P, Wright AF. Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits. Hum Mol Genet, 16: 233-241, 2007.
12. Tomlinson M, Chopra M, Sanders D, Bradshaw D, Hendricks M, Greenfield D, Black RE, El Arifeen S, Rudan I. Setting Priorities in Child Health Research Investments for South Africa. PLoS Med 2007; 4(8):E259.
13. Rudan I, Gibson J, Kapiriri L, Lansang MA, Hyder AA, Lawn J, Darmstadt GL, Cousens S, Bhutta ZA, Brown KH, Hess SY, Black M, Gardner JM, Webster J, Carneiro I, Chandramohan D, Kosek M, Lanata CF, Tomlinson M, Chopra M, Ameratunga S, Campbell H, El Arifeen S, Black RE; Child Health and Nutrition Research Initiative (CHNRI). Setting priorities in global child health research investments: Assessment of principles and practice. Croat Med J. 2007; 48: 595-604.
14. Kapiriri L, Tomlinson M, Gibson J, Chopra M, El Arifeen S, Black RE, Rudan I; Child Health and Nutrition Research Initiative (CHNRI): Setting priorities in global child health research investments: Addressing the values of the stakeholders. Croat Med J. 2007; 48: 618-627.
15. Kljaković-Gašpić M, Petrak J, Rudan I, Biloglav Z. For free or for fee? Dilemma of small scientific journals. Croat Med J. 2007; 48: 292-299.
16. Ivković V, Vitart V, Rudan I, Janićijević B, Smolej Narančić N, Škarić-Jurić T, Barbalić M, Biloglav Z, Polasek O, Kolcic I, Visscher P, Hayward C, Hastie N, Anderson N, Campbell H, Wright A, Rudan P, Deary IJ. The Eysenck personality factors: psychometric structure, reliability, heritability and phenotypic and genetic correlations with psychological distress in an isolated Croatian population. Person Individ Diff 2007; 42: 123-133.
17. Jelušić M, Lukić IK, Tambić-Bukovac L, Dubravčić K, Malčić I, Rudan I, Batinić D. Interleukin-18 as a mediator of systemic juvenile idiopathic arthritis. Clinical Rheumatology 2007; 26: 1332-1334.
18. Rudan I, Carothers AD, Polašek O, Hayward C, Vitart V, Biloglav Z, Kolčić I, Zgaga L, Ivanković D, Vorko-Jović A, Wilson JF, Weber JL, Hastie ND, Wright AF, Campbell H. Quantifying the increase in average human heterozygosity due to urbanisation. Eur J Hum Genet 2008; 16:1097-1102.
19. Rudan I. Preventing inequity in international research. Science 2008; 319:1336-1337.
20. Vitart V, Rudan I, Hayward C, Gray NK, Floyd J, Palmer CNA, Knott SA, Kolcic I, Polašek O, Graessler J, Wilson JF, Marinaki A, Riches PL, Shu X, Janićijević B, Smolej-Narančić N, Gorgoni B, Morgan J, Campbell S, Biloglav Z, Barać-Lauc L, Peričić M, Martinović-Klarić I, Zgaga L, Škarić-Jurić T, Wild SH, Richardson WA, Hohenstein P, Kimber CK, Tenesa A, Donnelly LA, Fairbanks LD, Aringer M, McKeigue PM, Ralston SH, Morris AD, Rudan P, Hastie ND, Campbell H, Wright AF. SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout. Nature Genet 2008; 40: 437-442.
21. Rudan I, Boschi-Pinto C, Biloglav Z, Mulholland K, Campbell H.Epidemiology and aetiology of childhood pneumonia. Bull World Health Organ 2008; 86: 408-416.
22. Campbell H, Biloglav Z, Rudan I. Reducing bias from test misclassification in burden of disease studies: use of test to actual positive ratio - new test parameter. Croat Med J 2008; 48: 402-414.
23. McQuillan R, Leutenegger AL, Abdel-Rahman R, Pericic M, Barac-Lauc L, Smolej-Narancic N, Janicijevic B, Franklin CS, Polasek O, Tenesa A, MacLeod AK, Rudan P, Hayward C, Vitart V, Rudan I, Wild SK, Dunlop MD, Wright AF, Campbell H, Wilson JF. Runs of homozygosity in European populations. Am J Hum Genet 2008; 83:359-372.
24. Rudan I, Chopra M, Kapiriri L, Gibson J, Lansang MA, Carneiro I, Ameratunga S, Tsai AC, Chan KY, Tomlinson M, Hess SY, Campbell H, El Arifeen S, Black RE. Setting priorities in global child health research investments: universal challenges and conceptual framework. Croat Med J 2008; 49: 307-317.
25. Rudan I, Ivaniš A. Scaling-up of training and education for health workers. Croat Med J 2008; 48: 295-297.
26. Rudan I, Campbell H. A new role for health workers in preventing deaths from childhood pneumonia. The Lancet 2008; 372:781-782.
27. Walley J, Lawn JE, Tinker A, De Francisco A, Chopra M, Rudan I, Bhutta ZA, Black RE. Primary Health Care: making Alma Ata a reality. The Lancet 2008; 372:1001-1007.
28. Zgaga L, Hayward C, Vatavuk Z, Bencic G, Zemunik T, Valkovic A, Valkovic-Antic I, Bucan K, Rudan I. High prevalence of glaucoma in Veli Brgud, Croatia, is caused by dominantly inherited T377M mutation in MYOC gene. Br J Ophthalmol 2008; 92:1567-1568.
29. Lawn JE, Rudan I, Rubens C: Four million newborn deaths: Is the global health research agenda evidence-based? Early Hum Develop 2008; 84:809-814.
30. Rudan I, Gibson JL, Ameratunga S, El Arifeen S, Bhutta ZA, Black M, Black RE, Brown KH, Campbell H, Carneiro I, Chan KY, Chandramohan D, Chopra M, Cousens S, Darmstadt GL, Meeks Gardner J, Hess SY, Hyder AA, Kapiriri L, Kosek M, Lanata CF, Lansang MA, Lawn J, Tomlinson M, Tsai AC, Webster J, on behalf of Child Health and Nutrition Research Initiative (CHNRI): Setting Priorities in Global Child Health Research Investments: Guidelines for implementation of the CHNRI Method. Croat Med J 2008; 49:720-733.
31. Pulanić D, Polašek O, Hayward C, Vitart V, Petrovečki M, Vorko-Jović A, Peričić M, Barać Lauc L, Martinović Klarić I, Biloglav Z, Kolčić I, Zgaga L, Carothers AD, Janićijević B, Smolej Narančić N, Bućan K, Rudan D, Lowe G, Rumley A, Wright AF, Rudan P, Hastie ND, Campbell H, Rudan I. Effects of human genome-wide heterozygosity on biochemical markers of hemostasis and inflammation. Hum Biol. 2008; 80:513-533.
32. Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Brenda W J H Penninx, A Cecile J W Janssens, James F Wilson, Tim Spector, Nicholas G Martin, Nancy L Pedersen, Kirsten Ohm Kyvik, Jaakko Kaprio, Albert Hofman, Nelson B Freimer, Marjo-Riitta Jarvelin, Ulf Gyllensten, Harry Campbell, Rudan I, Åsa Johansson, Fabio Marroni, Caroline Hayward, Veronique Vitart, Inger Jonasson, Cristian Pattaro, Alan Wright, Nick Hastie, Irene Pichler, Andrew A Hicks, Mario Falchi, Gonneke Willemsen, Jouke-Jan Hottenga, Eco J C de Geus, Grant W Montgomery, John Whitfield, Patrik Magnusson, Juha Saharinen, Markus Perola, Kaisa Silander, Aaron Isaacs, Eric J G Sijbrands, Andre G Uitterlinden, Jacqueline C M Witteman, Ben A Oostra, Paul Elliott, Aimo Ruokonen, Chiara Sabatti, Christian Gieger, Thomas Meitinger, Florian Kronenberg, Angela Döring, H-Erich Wichmann, Johannes H Smit, Mark I McCarthy, Cornelia M van Duijn & Leena Peltonen for the ENGAGE Consortium. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genet 2009; 41:47-55.
33. Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Floyd J, Hastie N, Knott S, Kolcic I, Pichler I, Polasek O, Wild SH, Zorkoltseva IV, Meitinger T, Wilson JF, Rudan I, Campbell H, Pattaro C, Pramstaller P, Oostra BA, Wright AF, van Duijn CM, Aulchenko YS, Gyllensten U, the EUROSPAN Consortium. Common variants of the JAZF1 gene associated with height identified by linkage and whole genome association analysis. Hum Mol Genet 2009; 18: 373-380.
34. Bahl R, Martines J, Ali N, Bhan MK, Carlo W, Chan KY, Darmstadt GL, Hamer DH, Lawn JE, McMillan DD, Mohan P, Paul V, Tsai AC, Victora C, Weber M, Zaidi A, Rudan I. Research Priorities to reduce Global Mortality from Newborn Infections by 2015. Pediatr Inf Dis J 2009; 28 (Suppl 1): S43-S48.
35. Knezević A, Polasek O, Gornik O, Rudan I, Campbell H, Hayward C, Wright A, Kolcic I, O'Donoghue N, Bones J, Rudd PM, Lauc G. Variability, Heritability and Environmental Determinants of Human Plasma N-Glycome. J Proteome Res. 2009; 8:694-701.
36. Brown KH, Hess SY; Boy E, Gibson RS, Horton S, Osendarp SJ, Sempertegui F, Shrimpton R, Rudan I. Setting priorities for zinc-related health research to reduce children's disease burden worldwide: An application of the Child Health and Nutrition Research Initiative's research priority-setting method. Public Health Nutr. 2009; 12:389-396.
37. Kolcic I, Polasek O, Rudan I. Gender differences in spousal household material status estimation. J Epidemiol Commun Health 2009; 63:175-176.
38. Tomlinson M, Rudan I, Saxena S, Swartz L, Tsai AC, Patel V. Setting investment priorities for research in global mental health. Bull World Health Organ 2009; 87: 438-446.
39. Fontaine O, Kosek M, Bhatnagar S, Boschi-Pinto C, Chan KY, Duggan C, Martinez H, Ribeiro H, Rollins NC, Salam MA, Shantosham M, Snyder JD, Tsai AC, Vargas B, Rudan I. Setting Research Priorities to reduce Global Mortality from Childhood Diarrhoea by 2015. PLoS Med 2009; 6:e41.
40. Rudd PM, Rudan I, Wright AF. High-throughput glycome analysis is set to join high-throughput genomics. J Proteome Res. 2009; 8:1105.
41. Rudan I, Marusić A, Janković S, Rotim K, Boban M, Lauc G, Grković I, Dogas Z, Zemunik T, Vatavuk Z, Bencić G, Rudan D, Mulić R, Krzelj V, Terzić J, Stojanović D, Puntarić D, Bilić E, Ropac D, Vorko-Jović A, Znaor A, Stevanović R, Biloglav Z, Polasek O. "10001 Dalmatians:" Croatia launches its national biobank. Croat Med J. 2009; 50:4-6.
42. Polasek O, Marusić A, Rotim K, Hayward C, Vitart V, Huffman J, Campbell S, Janković S, Boban M, Biloglav Z, Kolcić I, Krzelj V, Terzić J, Matec L, Tometić G, Nonković D, Nincević J, Pehlić M, Zedelj J, Velagić V, Juricić D, Kirac I, Belak Kovacević S, Wright AF, Campbell H, Rudan I. Genome-wide association study of anthropometric traits in Korcula Island, Croatia. Croat Med J. 2009; 50:7-16.
43. Zemunik T, Boban M, Lauc G, Janković S, Rotim K, Vatavuk Z, Bencić G, Dogas Z, Boraska V, Torlak V, Susac J, Zobić I, Rudan D, Pulanić D, Modun D, Mudnić I, Gunjaca G, Budimir D, Hayward C, Vitart V, Wright AF, Campbell H, Rudan I. Genome-wide association study of biochemical traits in Korcula Island, Croatia. Croat Med J. 2009; 50:23-33.
44. Biloglav Z, Zgaga L, Smoljanović M, Hayward C, Polasek O, Kolcić I, Vitart V, Zemunik T, Boraska V, Torlak V, Mulić R, Ropac D, Grković I, Rudan D, Ristić S, Barbalić M, Campbell H, Wright AF, Rudan I. Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemics. Croat Med J. 2009;50(1):34-42.
45. Barbalić M, Narancić NS, Skarić-Jurić T, Salihović MP, Klarić IM, Lauc LB, Janićijević B, Farrall M, Rudan I, Campbell H, Wright AF, Hastie ND, Rudan P. A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolate. Am J Hypertens. 2009; 22:663-8.
46. Pattaro C, Aulchenko YS, Isaacs A, Vitart V, Hayward C, Franklin CS, Polasek O, Kolcic I, Biloglav Z, Campbell S, Hastie N, Lauc G, Meitinger T, Oostra BA, Gyllensten U, Wilson JF, Pichler I, Hicks AA, Campbell H, Wright AF, Rudan I, van Duijn CM, Riegler P, Marroni F, Pramstaller PP. Genome-wide linkage analysis of serum creatinine in three isolated European populations. Kidney Int. 2009; (in press)
47. Black RE, Bhan MK, Chopra M, Rudan I, Victora CG. Accelerating the health impact of the Gates Foundation. Lancet. 2009; 373:1584-5.
48. Kolz M, Johnson T, Sanna S, Teumer A, Vitart V, Perola M, Mangino M, Albrecht E, Wallace C, Farrall M, Johansson A, Nyholt DR, Aulchenko Y, Beckmann JS, Bergmann S, Bochud M, Brown M, Campbell H; EUROSPAN Consortium, Connell J, Dominiczak A, Homuth G, Lamina C, McCarthy MI; ENGAGE Consortium, Meitinger T, Mooser V, Munroe P, Nauck M, Peden J, Prokisch H, Salo P, Salomaa V, Samani NJ, Schlessinger D, Uda M, Völker U, Waeber G, Waterworth D, Wang-Sattler R, Wright AF, Adamski J, Whitfield JB, Gyllensten U, Wilson JF, Rudan I, Pramstaller P, Watkins H; PROCARDIS Consortium, Doering A, Wichmann HE; KORA Study, Spector TD, Peltonen L, Völzke H, Nagaraja R, Vollenweider P, Caulfield M; WTCCC, Illig T, Gieger C. Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet. 2009; 5(6):e1000504
49. Kosek M, Lanata CF, Black RE, Walker DG, Snyder JD, Salam MA, Mahalanabis D, Fontaine O, Bhutta ZA, Bhatnagar S, Rudan I. Directing diarrhoeal disease research towards disease-burden reduction. J Health Popul Nutr. 2009; 27:319-31.
50. Rudan I. The complex challenge of setting priorities in health research investments. Indian J Med Res. 2009;129(4):351-3.
51. Heard-Costa NL, Zillikens MC, Monda KL, Johansson A, Harris TB, Fu M, Haritunians T, Feitosa MF, Aspelund T, Eiriksdottir G, Garcia M, Launer LJ, Smith AV, Mitchell BD, McArdle PF, Shuldiner AR, Bielinski SJ, Boerwinkle E, Brancati F, Demerath EW, Pankow JS, Arnold AM, Chen YD, Glazer NL, McKnight B, Psaty BM, Rotter JI, Amin N, Campbell H, Gyllensten U, Pattaro C, Pramstaller PP, Rudan I, Struchalin M, Vitart V, Gao X, Kraja A, Province MA, Zhang Q, Atwood LD, Dupuis J, Hirschhorn JN, Jaquish CE, O'Donnell CJ, Vasan RS, White CC, Aulchenko YS, Estrada K, Hofman A, Rivadeneira F, Uitterlinden AG, Witteman JC, Oostra BA, Kaplan RC, Gudnason V, O'Connell JR, Borecki IB, van Duijn CM, Cupples LA, Fox CS, North KE. NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. PLoS Genet. 2009; 5(6):e1000539.
52. Rudan I, Campbell H. The deadly toll of S pneumoniae and H influenzae type b. Lancet. 2009; 374(9693):854-6.
53. Navarro P, Vitart V, Hayward C, Tenesa A, Zgaga L, Juricic D, Polasek O, Hastie ND, Rudan I, Campbell H, Wright AF, Haley CS, Knott SA. Genetic comparison of a Croatian isolate and CEPH European founders. Genet Epidemiol. 2009; (in press)
54. Hicks AA, Pramstaller PP, Johansson A, Vitart V, Rudan I, Ugocsai P, Aulchenko Y, Franklin CS, Liebisch G, Erdmann J, Jonasson I, Zorkoltseva IV, Pattaro C, Hayward C, Isaacs A, Hengstenberg C, Campbell S, Gnewuch C, Janssens AC, Kirichenko AV, König IR, Marroni F, Polasek O, Demirkan A, Kolcic I, Schwienbacher C, Igl W, Biloglav Z, Witteman JC, Pichler I, Zaboli G, Axenovich TI, Peters A, Schreiber S, Wichmann HE, Schunkert H, Hastie N, Oostra BA, Wild SH, Meitinger T, Gyllensten U, van Duijn CM, Wilson JF, Wright A, Schmitz G, Campbell H. Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet. 2009;5(10):e1000672.
55. Campbell H, Rudan I, Bittles AH, Wright AF. Human population structure, genome autozygosity and human health Genome Med. 2009;1(9):91.
56. Tomlinson M, Swartz L, Officer A, Chan KY, Rudan I, Saxena S. Research priorities for health of people with disabilities: an expert opinion exercise. Lancet 2009; 374: 1857–62.
57. Marroni F, Pfeufer A, Aulchenko YS, Franklin CS, Isaacs A, Pichler I, Wild SH, Oostra BA, Wright AF, Campbell H, Witteman JC, Kääb S, Hicks AA, Gyllensten U, Rudan I, Meitinger T, Pattaro C, van Duijn CM, Wilson JF, Pramstaller PP; EUROSPAN Consortium. A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. Circ Cardiovasc Genet. 2009; 2(4):322-8.
58. Kong A et al. (ncluding Rudan I). Parental origin of sequence variants associated with complex diseases. Nature. 2009; 462:868-74.
59. Soranzo N et al.(including Rudan I). Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways. Diabetes. 2010 Sep 21. [Epub ahead of print]
60. Franklin CS, Aulchenko YS, Huffman JE, Vitart V, Hayward C, Polašek O, Knott S, Zgaga L, Zemunik T, Rudan I, Campbell H, Wright AF, Wild SH, Wilson JF. The TCF7L2 Diabetes Risk Variant is Associated with HbA(1C) Levels: a Genome-Wide Association Meta-Analysis. Ann Hum Genet. 2010 Sep 16. doi: 10.1111/j.1469-1809.2010.00607.x. [Epub ahead of print]
61. Vitart V, Bencic G, Hayward C, Skunca Herman J, Huffman J, Campbell S, Bucan K, Navarro P, Gunjaca G, Marin J, Zgaga L, Kolcic I, Polasek O, Kirin M, Hastie ND, Wilson JF, Rudan I, Campbell H, Vatavuk Z, Fleck B, Wright A. New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8. Hum Mol Genet. 2010 Sep 2. [Epub ahead of print]
62. Teslovich TM et al. (including Rudan I). Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 2010; 466:707-13.
63. Rudan I, Kapiriri L, Tomlinson M, Balliet M, Cohen B, Chopra M. Evidence-based priority setting for health care and research: tools to support policy in maternal, neonatal, and child health in Africa. PLoS Med. 2010; 7:e1000308.
64. Wright AF, Rudan I, Hastie ND, Campbell H. A 'complexity' of urate transporters. Kidney Int. 2010; 78:446-52.
65. Voight BF et al. (including Rudan I). Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature Genetics. 2010; 42:579-89.
66. O'Dushlaine C, McQuillan R, Weale ME, Crouch DJ, Johansson A, Aulchenko Y, Franklin CS, Polašek O, Fuchsberger C, Corvin A, Hicks AA, Vitart V, Hayward C, Wild SH, Meitinger T, van Duijn CM, Gyllensten U, Wright AF, Campbell H, Pramstaller PP, Rudan I, Wilson JF. Genes predict village of origin in rural Europe. Eur J Hum Genet. 2010; [Epub ahead of print]
67. Rudan I. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity. Psychiatr Danub. 2010; 22:190-2.
68. Kestenbaum B, Glazer NL, Köttgen A, Felix JF, Hwang SJ, Liu Y, Lohman K, Kritchevsky SB, Hausman DB, Petersen AK, Gieger C, Ried JS, Meitinger T, Strom TM, Wichmann HE, Campbell H, Hayward C, Rudan I, de Boer IH, Psaty BM, Rice KM, Chen YD, Li M, Arking DE, Boerwinkle E, Coresh J, Yang Q, Levy D, van Rooij FJ, Dehghan A, Rivadeneira F, Uitterlinden AG, Hofman A, van Duijn CM, Shlipak MG, Kao WH, Witteman JC, Siscovick DS, Fox CS. Common genetic variants associate with serum phosphorus concentration. J Am Soc Nephrol. 2010; 21:1223-32.
69. Black RE, Cousens S, Johnson HL, Lawn JE, Rudan I, Bassani DG, Jha P, Campbell H, Walker CF, Cibulskis R, Eisele T, Liu L, Mathers C; Child Health Epidemiology Reference Group of WHO and UNICEF. Global, regional, and national causes of child mortality in 2008: a systematic analysis. Lancet. 2010; 375:1969-87.
70. Liu JZ et al. (including Rudan I). Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nature Genetics. 2010; 42:436-40.
71. Edmond K, Clark A, Korczak VS, Sanderson C, Griffiths UK, Rudan I. Global and regional risk of disabling sequelae from bacterial meningitis: a systematic review and meta-analysis. Lancet Infect Dis. 2010; 10:317-28.
72. Nair H, Nokes DJ, Gessner BD, Dherani M, Madhi SA, Singleton RJ, O'Brien KL, Roca A, Wright PF, Bruce N, Chandran A, Theodoratou E, Sutanto A, Sedyaningsih ER, Ngama M, Munywoki PK, Kartasasmita C, Simões EA, Rudan I, Weber MW, Campbell H. Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. Lancet. 2010; 375:1545-55.
73. Köttgen A et al. (including Rudan I). New loci associated with kidney function and chronic kidney disease. Nature Genetics 2010; 42:376-84.
74. Pucic M, Pinto S, Novokmet M, Knezevic A, Gornik O, Polasek O, Vlahovicek K, Wang W, Rudd PM, Wright AF, Campbell H, Rudan I, Lauc G. Common aberrations from the normal human plasma N-glycan profile. Glycobiology. 2010; 20:970-5.
75. Knezevic A, Gornik O, Polasek O, Pucic M, Redzic I, Novokmet M, Rudd PM, Wright AF, Campbell H, Rudan I, Lauc G. Effects of aging, body mass index, plasma lipid profiles, and smoking on human plasma N-glycans. Glycobiology. 2010; 20:959-69.
76. Theodoratou E, Johnson S, Jhass A, Madhi SA, Clark A, Boschi-Pinto C, Bhopal S, Rudan I, Campbell H. The effect of Haemophilus influenzae type b and pneumococcal conjugate vaccines on childhood pneumonia incidence, severe morbidity and mortality. Int J Epidemiol. 2010; 39 Suppl 1:i172-85.
77. Theodoratou E, Al-Jilaihawi S, Woodward F, Ferguson J, Jhass A, Balliet M, Kolcic I, Sadruddin S, Duke T, Rudan I, Campbell H. The effect of case management on childhood pneumonia mortality in developing countries. Int J Epidemiol. 2010; 39 Suppl 1:i155-71.
78. McKeigue PM, Campbell H, Wild S, Vitart V, Hayward C, Rudan I, Wright AF, Wilson JF. Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndrome. Int J Epidemiol. 2010; 39:907-18.
79. Rudan I, Chan KY, Zhang JS, Theodoratou E, Feng XL, Salomon JA, Lawn JE, Cousens S, Black RE, Guo Y, Campbell H; WHO/UNICEF's Child Health Epidemiology Reference Group (CHERG). Causes of deaths in children younger than 5 years in China in 2008. Lancet. 2010; 375:1083-9.
80. Smith NL, Chen MH, Dehghan A, Strachan DP, Basu S, Soranzo N, Hayward C, Rudan I, Sabater-Lleal M, Bis JC, de Maat MP, Rumley A, Kong X, Yang Q, Williams FM, Vitart V, Campbell H, Mälarstig A, Wiggins KL, Van Duijn CM, McArdle WL, Pankow JS, Johnson AD, Silveira A, McKnight B, Uitterlinden AG; Wellcome Trust Case Control Consortium;, Aleksic N, Meigs JB, Peters A, Koenig W, Cushman M, Kathiresan S, Rotter JI, Bovill EG, Hofman A, Boerwinkle E, Tofler GH, Peden JF, Psaty BM, Leebeek F, Folsom AR, Larson MG, Spector TD, Wright AF, Wilson JF, Hamsten A, Lumley T, Witteman JC, Tang W, O'Donnell CJ. Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Circulation. 2010; 121:1382-92.
81. Pattaro C, De Grandi A, Vitart V, Hayward C, Franke A, Aulchenko YS, Johansson A, Wild SH, Melville SA, Isaacs A, Polasek O, Ellinghaus D, Kolcic I, Nöthlings U, Zgaga L, Zemunik T, Gnewuch C, Schreiber S, Campbell S, Hastie N, Boban M, Meitinger T, Oostra BA, Riegler P, Minelli C, Wright AF, Campbell H, van Duijn CM, Gyllensten U, Wilson JF, Krawczak M, Rudan I, Pramstaller PP; EUROSPAN consortium. A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. BMC Med Genet. 2010; 11:41.
82. Polasek O, Hayward C, Bellenguez C, Vitart V, Kolcić I, McQuillan R, Saftić V, Gyllensten U, Wilson JF, Rudan I, Wright AF, Campbell H, Leutenegger AL. Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data. BMC Genomics. 2010; 11:139.
83. Polasek O, Gunjaca G, Kolcić I, Zgaga L, Dzijan S, Smolić R, Smolić M, Milas-Ahić J, Serić V, Galić J, Tucak-Zorić S, Tucak A, Rudan I, Lauc G. Association of nephrolithiasis and gene for glucose transporter type 9 (SLC2A9): study of 145 patients. Croat Med J. 2010; 51:48-53.
84. Gunjaca G, Boban M, Pehlić M, Zemunik T, Budimir D, Kolcić I, Lauc G, Rudan I, Polasek O. Predictive value of 8 genetic loci for serum uric acid concentration. Croat Med J. 2010; 51:23-31.
85. Rudan D, Polasek O, Kolcić I, Rudan I. Uric acid: the past decade. Croat Med J. 2010; 51:1-6.
86. Carrasquillo MM, Belbin O, Zou F, Allen M, Ertekin-Taner N, Ansari M, Wilcox SL, Kashino MR, Ma L, Younkin LH, Younkin SG, Younkin CS, Dincman TA, Howard ME, Howell CC, Stanton CM, Watson CM, Crump M, Vitart V, Hayward C, Hastie ND, Rudan I, Campbell H, Polasek O, Brown K, Passmore P, Craig D, McGuinness B, Todd S, Kehoe PG, Mann DM, Smith AD, Beaumont H, Warden D, Holmes C, Heun R, Kölsch H, Kalsheker N, Pankratz VS, Dickson DW, Graff-Radford NR, Petersen RC, Wright AF, Younkin SG, Morgan K. Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease. PLoS One. 2010; 5:e8764.
87. Lauc G, Rudan I, Campbell H, Rudd PM. Complex genetic regulation of protein glycosylation. Mol Biosyst. 2010; 6:329-35.
88. Dupuis J et al. (including Rudan I). New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics. 2010; 42:105-16.
89. Igl W, Johansson A, Wilson JF, Wild SH, Polasek O, Hayward C, Vitart V, Hastie N, Rudan P, Gnewuch C, Schmitz G, Meitinger T, Pramstaller PP, Hicks AA, Oostra BA, van Duijn CM, Rudan I, Wright A, Campbell H, Gyllensten U; EUROSPAN Consortium. Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. PLoS Genet. 2010; 6(1):e1000798.
90. Repapi E et al. (including Rudan I). Genome-wide association study identifies five loci associated with lung function. Nature Genetics. 2010; 42:36-44.
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