STrengthening the REporting of Genetic Association Studies (STREGA)— An Extension of the STROBE Statement
article has not abstract
Vyšlo v časopise:
STrengthening the REporting of Genetic Association Studies (STREGA)— An Extension of the STROBE Statement. PLoS Med 6(2): e32767. doi:10.1371/journal.pmed.1000022
Kategorie:
Guidelines and Guidance
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pmed.1000022
Souhrn
article has not abstract
Zdroje
1. KhouryMJLittleJBurkeW
2004
Human genome epidemiology: Scope and strategies.
KhouryMJLittleJBurkeW
editors In
Human genome epidemiology: A scientific foundation for using genetic information to improve health and prevent disease
New York
Oxford University Press
3
16
2. Genomics, Health and Society Working Group
2004
Genomics, health and society. Emerging issues for public policy
Ottawa
Government of Canada Policy Research Initiative
3. LinBKClyneMWalshMGomezOYuW
2006
Tracking the epidemiology of human genes in the literature: The HuGE published literature database.
Am J Epidemiol
164
1
4
4. YuWYesupriyaAClyneMWulfAGwinnM
2008
HuGE Literature Finder. HuGE Navigator.
Available: http://www.hugenavigator.net/HuGENavigator/searchSummary.do?firstQuery=Gene-disease+association&publitSearchType=now&whichContinue=firststart&check=n&dbType=publit&Mysubmit=go. Accessed 15 December 2008
5. LawrenceRWEvansDMCardonLR
2005
Prospects and pitfalls in whole genome association studies.
Philos Trans R Soc Lond B Biol Sci
360
1589
1595
6. ThomasDC
2006
Are we ready for genome-wide association studies?
Cancer Epidemiol Biomarkers Prev
15
595
598
7. KhouryMJLittleJGwinnMIoannidisJP
2007
On the synthesis and interpretation of consistent but weak gene-disease associations in the era of genome-wide association studies.
Int J Epidemiol
36
439
445
8. LittleJKhouryMJBradleyLClyneMGwinnM
2003
The human genome project is complete. How do we develop a handle for the pump?
Am J Epidemiol
157
667
673
9. IoannidisJPBernsteinJBoffettaPDaneshJDolanS
2005
A network of investigator networks in human genome epidemiology.
Am J Epidemiol
162
302
304
10. IoannidisJPGwinnMLittleJHigginsJPBernsteinJL
2006
A road map for efficient and reliable human genome epidemiology.
Nat Genet
38
3
5
11. von ElmEEggerM
2004
The scandal of poor epidemiological research.
BMJ
329
868
869
12. [Anonymous]
1999
Freely associating (editorial).
Nat Genet
22
1
2
13. CardonLBellJ
2001
Association study designs for complex diseases.
Nat Rev Genet
2
91
99
14. WeissS
2001
Association studies in asthma genetics.
Am J Respir Crit Care Med
164
2014
2015
15. WeissSTSilvermanEKPalmerLJ
2001
Case-control association studies in pharmacogenetics.
Pharmacogenomics J
1
157
158
16. CooperDNNussbaumRLKrawczakM
2002
Proposed guidelines for papers describing DNA polymorphism-disease associations.
Hum Genet
110
208
17. HegeleR
2002
SNP judgements and freedom of association.
Arterioscler Thromb Vasc Biol
22
1058
1061
18. LittleJBradleyLBrayMSClyneMDormanJ
2002
Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations.
Am J Epidemiol
156
300
310
19. RomeroRKuivaniemiHTrompGOlsonJM
2002
The design, execution, and interpretation of genetic association studies to decipher complex diseases.
Am J Obstet Gynecol
187
1299
1312
20. ColhounHMMcKeiguePMDavey SmithG
2003
Problems of reporting genetic associations with complex outcomes.
Lancet
361
865
872
21. van DuijnCMPortaM
2003
Good prospects for genetic and molecular epidemiologic studies in the European Journal of Epidemiology.
Eur J Epidemiol
18
285
286
22. CrossmanDWatkinsH
2004
Jesting Pilate, genetic case-control association studies, and Heart.
Heart
90
831
832
23. HuizingaTWPisetskyDSKimberlyRP
2004
Associations, populations, and the truth: Recommendations for genetic association studies in arthritis & rheumatism.
Arthritis Rheum
50
2066
2071
24. LittleJ
2004
Reporting and review of human genome epidemiology studies.
KhouryMJLittleJBurkeW
editors In
Human genome epidemiology: A scientific foundation for using genetic information to improve health and prevent disease
New York
Oxford University Press
168
192
25. RebbeckTRMartinezMESellersTAShieldsPGWildCP
2004
Genetic variation and cancer: Improving the environment for publication of association studies.
Cancer Epidemiol Biomarkers Prev
13
1985
1986
26. TanNMulleyJBerkovicS
2004
Association studies in epilepsy: “The truth is out there”.
Epilepsia
45
1429
1442
27. [Anonymous]
2005
Framework for a fully powered risk engine.
Nat Genet
37
1153
28. EhmMGNelsonMRSpurrNK
2005
Guidelines for conducting and reporting whole genome/large-scale association studies.
Hum Mol Genet
14
2485
2488
29. FreimerNBSabattiC
2005
Guidelines for association studies in human molecular genetics.
Hum Mol Genet
14
2481
2483
30. HattersleyATMcCarthyMI
2005
What makes a good genetic association study?
Lancet
366
1315
1323
31. ManlyK
2005
Reliability of statistical associations between genes and disease.
Immunogenetics
57
549
558
32. ShenHLiuYLiuPReckerRDengH
2005
Nonreplication in genetic studies of complex diseases—Lessons learned from studies of osteoporosis and tentative remedies.
J Bone Miner Res
20
365
376
33. VitaliSRandolphA
2005
Assessing the quality of case-control association studies on the genetic basis of sepsis.
Pediatr Crit Care Med
6
S74
S77
34. WedzichaJAHallIP
2005
Publishing genetic association studies in Thorax.
Thorax
60
357
35. HallIPBlakeyJD
2005
Genetic association studies in Thorax.
Thorax
60
357
359
36. DeLisiLEFaraoneSV
2006
When is a “positive” association truly a “positive” in psychiatric genetics? A commentary based on issues debated at the world congress of psychiatric genetics, Boston, October 12–18, 2005.
Am J Med Genet B Neuropsychiatr Genet
141
319
322
37. SaitoYATalleyNJde AndradeMPetersenGM
2006
Case-control genetic association studies in gastrointestinal disease: Review and recommendations.
Am J Gastroenterol
101
1379
1389
38. UhligKMenonVSchmidCH
2007
Recommendations for reporting of clinical research studies.
Am J Kidney Dis
49
3
7
39. NCI-NHGRI Working Group on Replication in Association Studies
ChanockSJManolioTBoehnkeMBoerwinkleE
2007
Replicating genotype-phenotype associations.
Nature
447
655
660
40. BeggCB
2005
Reflections on publication criteria for genetic association studies.
Cancer Epidemiol Biomarkers Prev
14
1364
1365
41. ByrnesGGurrinLDowtyJHopperJL
2005
Publication policy or publication bias?
Cancer Epidemiol Biomarkers Prev
14
1363
42. PharoahPDDunningAMPonderBAEastonDF
2005
The reliable identification of disease-gene associations.
Cancer Epidemiol Biomarkers Prev
14
1362
43. WacholderS
2005
Publication environment and broad investigation of the genome.
Cancer Epidemiol Biomarkers Prev
14
1361
44. WhittemoreAS
2005
Genetic association studies: Time for a new paradigm?
Cancer Epidemiol Biomarkers Prev
14
1359
1360
45. BogardusSTJrConcatoJFeinsteinAR
1999
Clinical epidemiological quality in molecular genetic research. The need for methodological standards.
JAMA
281
1919
1926
46. PetersDLBarberRCFloodEMGarnerHRO'KeefeGE
2003
Methodologic quality and genotyping reproducibility in studies of tumor necrosis factor –308 G–>A single nucleotide polymorphism and bacterial sepsis: Implications for studies of complex traits.
Crit Care Med
31
1691
1696
47. ClarkMFBaudouinSV
2006
A systematic review of the quality of genetic association studies in human sepsis.
Intensive Care Med
32
1706
1712
48. LeeWBindmanJFordTGlozierNMoranP
2007
Bias in psychiatric case-control studies: Literature survey.
Br J Psychiatry
190
204
209
49. YesupriyaAEvangelouEKavvouraFKPatsopoulosNAClyneM
2008
Reporting of human genome epidemiology (HuGE) association studies: An empirical assessment.
BMC Med Res Methodol
8
31
50. ReidMCLachsMSFeinsteinAR
1995
Use of methodological standards in diagnostic test research. Getting better but still not good.
JAMA
274
645
651
51. BrazmaAHingampPQuackenbushJSherlockGSpellmanP
2001
Minimum information about a microarray experiment (MIAME)—Toward standards for microarray data.
Nat Genet
29
356
371
52. PocockSJCollierTJDandreoKJde StavolaBLGoldmanMB
2004
Issues in the reporting of epidemiological studies: A survey of recent practice.
BMJ
329
883
53. AltmanDMoherD
2005
Developing guidelines for reporting healthcare research: Scientific rationale and procedures.
Med Clin (Barc)
125
8
13
54. GluudLL
2006
Bias in clinical intervention research.
Am J Epidemiol
163
493
501
55. von ElmEAltmanDGEggerMPocockSJGotzschePC
2007
The strengthening the reporting of observational studies in epidemiology (STROBE) statement: Guidelines for reporting observational studies.
PLoS Med
4
e296
doi:10.1371/journal.pmed.0040296
56. VandenbrouckeJPvon ElmEAltmanDGGotzschePCMulrowCD
2007
Strengthening the reporting of observational studies in epidemiology (STROBE): Explanation and elaboration.
Ann Intern Med
147
W163
W194
57. LittleJHigginsJPT
editors
2006
The HuGENet™ HuGE Review Handbook, version 1.0.
Available: http://www.hugenet.ca. Accessed 28 February 2006
58. HigginsJPLittleJIoannidisJPBrayMSManolioTA
2007
Turning the pump handle: Evolving methods for integrating the evidence on gene-disease association.
Am J Epidemiol
166
863
866
59. AltmanDGSchulzKFMoherDEggerMDavidoffF
2001
The revised CONSORT statement for reporting randomized trials: Explanation and elaboration.
Ann Intern Med
134
663
694
60. MoherDSchultzKFAltmanD
2001
The CONSORT statement: Revised recommendations for improving the quality of reports of parallel-group randomized trials.
JAMA
285
1987
1991
61. PompanonFBoninABellemainETaberletP
2005
Genotyping errors: Causes, consequences and solutions.
Nat Rev Genet
6
847
859
62. AkeyJMZhangKXiongMDorisPJinL
2001
The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures.
Am J Hum Genet
68
1447
1456
63. DequekerERamsdenSGrodyWWStenzelTTBartonDE
2001
Quality control in molecular genetic testing.
Nat Rev Genet
2
717
723
64. MitchellAACutlerDJChakravartiA
2003
Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test.
Am J Hum Genet
72
598
610
65. RothmanNStewartWFCaporasoNEHayesRB
1993
Misclassification of genetic susceptibility biomarkers: Implications for case-control studies and cross-population comparisons.
Cancer Epidemiol Biomarkers Prev
2
299
303
66. Garcia-ClosasMWacholderSCaporasoNRothmanN
2004
Inference issues in cohort and case-control studies of genetic effects and gene-environment interactions.
KhouryMJLittleJBurkeW
editors. In
Human genome epidemiology: A scientific foundation for using genetic information to improve health and prevent disease
New York
Oxford University Press
127
144
67. WongMYDayNELuanJAWarehamNJ
2004
Estimation of magnitude in gene-environment interactions in the presence of measurement error.
Stat Med
23
987
998
68. ClaytonDGWalkerNMSmythDJPaskRCooperJD
2005
Population structure, differential bias and genomic control in a large-scale, case-control association study.
Nat Genet
37
1243
1246
69. KnowlerWCWilliamsRCPettittDJSteinbergAG
1988
Gm3;5,13,14 and type 2 diabetes mellitus: An association in American Indians with genetic admixture.
Am J Human Genet
43
520
526
70. GelernterJGoldmanDRischN
1993
The A1 allele at the D2 dopamine receptor gene and alcoholism: A reappraisal.
JAMA
269
1673
1677
71. KittlesRAChenWPanguluriRKAhaghotuCJacksonA
2002
CYP3A4-V and prostate cancer in African Americans: Causal or confounding association because of population stratification?
Hum Genet
110
553
560
72. ThomasDCWitteJS
2002
Point: Population stratification: A problem for case control studies of candidate-gene associations?
Cancer Epidemiol Biomarkers Prev
11
505
512
73. WacholderSChatterjeeNHartgeP
2002
Joint effects of genes and environment distorted by selection biases: Implications for hospital-based case-control studies.
Cancer Epidemiol Biomarkers Prev
11
885
889
74. CardonLRPalmerLJ
2003
Population stratification and spurious allelic association.
Lancet
361
598
604
75. WacholderSRothmanNCaporasoN
2000
Population stratification in epidemiologic studies of common genetic variants and cancer: Quantification of bias.
J Natl Cancer Inst
92
1151
1158
76. ArdlieKGLunettaKLSeielstadM
2002
Testing for population subdivision and association in four case-control studies.
Am J Human Genet
71
304
311
77. EdlandSDSlagerSFarrerM
2004
Genetic association studies in Alzheimer's disease research: Challenges and opportunities.
Stat Med
23
169
178
78. MillikanRC
2001
Re: Population stratification in epidemiologic studies of common genetic variants and cancer: Quantification of bias.
J Natl Cancer Inst
93
156
157
79. WangYLocalioRRebbeckTR
2004
Evaluating bias due to population stratification in case-control association studies of admixed populations.
Genet Epidemiol
27
14
20
80. IoannidisJPNtzaniEETrikalinosTA
2004
‘Racial’ differences in genetic effects for complex diseases.
Nat Genet
36
1312
1318
81. MarchiniJCardonLRPhillipsMSDonnellyP
2004
The effects of human population structure on large genetic association studies.
Nat Genet
36
512
517
82. FreedmanMLReichDPenneyKLMcDonaldGJMignaultAA
2004
Assessing the impact of population stratification on genetic association studies.
Nat Genet
36
388
393
83. KhlatMCazesMHGeninEGuiguetM
2004
Robustness of case-control studies of genetic factors to population stratification: Magnitude of bias and type I error.
Cancer Epidemiol Biomarkers Prev
13
1660
1664
84. BaldingDJ
2006
A tutorial on statistical methods for population association studies.
Nat Rev Genet
7
781
791
85. Wellcome Trust Case Control Consortium
2007
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Nature
447
661
678
86. IoannidisJP
2007
Non-replication and inconsistency in the genome-wide association setting.
Hum Hered
64
203
213
87. ParkesMBarrettJCPrescottNJTremellingMAndersonCA
2007
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
Nat Genet
39
830
832
88. ToddJAWalkerNMCooperJDSmythDJDownesK
2007
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
Nat Genet
39
857
864
89. ZegginiEWeedonMNLindgrenCMFraylingTMElliottKS
2007
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
Science
316
1336
1341
90. Diabetes Genetics Initiative of Broad Institute of Harvard and MIT Lund University, and Novartis Institutes of BioMedical Research
SaxenaRVoightBFLyssenkoVBurttNP
2007
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Science
316
1331
1336
91. ScottLJMohlkeKLBonnycastleLLWillerCJLiY
2007
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Science
316
1341
1345
92. HelgadottirAThorleifssonGManolescuAGretarsdottirSBlondalT
2007
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
Science
316
1491
1493
93. McPhersonRPertsemlidisAKavaslarNStewartARobertsR
2007
A common allele on chromosome 9 associated with coronary heart disease.
Science
316
1488
1491
94. EastonDFPooleyKADunningAMPharoahPDThompsonD
2007
Genome-wide association study identifies novel breast cancer susceptibility loci.
Nature
447
1087
1093
95. HunterDJKraftPJacobsKBCoxDGYeagerM
2007
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.
Nat Genet
39
870
874
96. StaceySNManolescuASulemPRafnarTGudmundssonJ
2007
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.
Nat Genet
39
865
869
97. GudmundssonJSulemPSteinthorsdottirVBergthorssonJTThorleifssonG
2007
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.
Nat Genet
39
977
983
98. HaimanCAPattersonNFreedmanMLMyersSRPikeMC
2007
Multiple regions within 8q24 independently affect risk for prostate cancer.
Nat Genet
39
638
644
99. YeagerMOrrNHayesRBJacobsKBKraftP
2007
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
Nat Genet
39
645
649
100. ZankeBWGreenwoodCMRangrejJKustraRTenesaA
2007
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.
Nat Genet
39
989
994
101. TomlinsonIWebbECarvajal-CarmonaLBroderickPKempZ
2007
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
Nat Genet
39
984
988
102. HaimanCALe MarchandLYamamotoJStramDOShengX
2007
A common genetic risk factor for colorectal and prostate cancer.
Nature Genetics
39
954
956
103. RiouxJDXavierRJTaylorKDSilverbergMSGoyetteP
2007
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
Nat Genet
39
596
604
104. LibioulleCLouisEHansoulSSandorCFarnirF
2007
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
PLoS Genet
3
e58
doi:10.1371/journal.pgen.0030058
105. DuerrRHTaylorKDBrantSRRiouxJDSilverbergMS
2006
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
Science
314
1461
1463
106. ZhaoLPLiSSKhalidN
2003
A method for the assessment of disease associations with single-nucleotide polymorphism haplotypes and environmental variables in case-control studies.
Am J Hum Genet
72
1231
1250
107. International HapMap Consortium
FrazerKABallingerDGCoxDRHindsDA
2007
A second generation human haplotype map of over 3.1 million SNPs.
Nature
449
851
861
108. StephensMSmithNJDonnellyP
2001
A new statistical method for haplotype reconstruction from population data.
Am J Hum Genet
68
978
989
109. QinZSNiuTLiuJS
2002
Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms.
Am J Hum Genet
71
1242
1247
110. ScheetPStephensM
2006
A fast and flexible statistical model for large-scale population genotype data: Applications to inferring missing genotypes and haplotypic phase.
Am J Hum Genet
78
629
644
111. BrowningSR
2008
Missing data imputation and haplotype phase inference for genome-wide association studies.
Hum Genet
124
439
450
112. HuangQFuYXBoerwinkleE
2003
Comparison of strategies for selecting single nucleotide polymorphisms for case/control association studies.
Hum Genet
113
253
257
113. KamataniNSekineAKitamotoTIidaASaitoS
2004
Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP maps, of 199 drug-related genes in 752 subjects: The analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed with haplotype-tagging SNPs.
Am J Hum Genet
75
190
203
114. ZhangWCollinsAMortonNE
2004
Does haplotype diversity predict power for association mapping of disease susceptibility?
Hum Genet
115
157
164
115. CarlsonCSEberleMARiederMJYiQKruglyakL
2004
Selecting a maximally informative set of single-nucleotide polymorphisms for association analysis using linkage disequilibrium.
Am J Hum Genet
74
106
120
116. van Hylckama VliegASandkuijlLARosendaalFRBertinaRMVosHL
2004
Candidate gene approach in association studies: Would the factor V leiden mutation have been found by this approach?
Eur J Hum Genet
12
478
482
117. GreenspanGGeigerD
2004
Model-based inference of haplotype block variation.
J Comput Biol
11
493
504
118. KimmelGShamirR
2005
GERBIL: Genotype resolution and block identification using likelihood.
Proc Natl Acad Sci U S A
102
158
162
119. CardonLRAbecasisGR
2003
Using haplotype blocks to map human complex triat loci.
Trends Genet
19
135
140
120. KeXHuntSTapperWLawrenceRStavridesG
2004
The impact of SNP density on fine-scale patterns of linkage disequilibrium.
Hum Mol Genet
13
577
588
121. ServinBStephensM
2007
Imputation-based analysis of association studies: Candidate regions and quantitative traits.
PLoS Genet
3
e114
doi:10.1371/journal.pgen.0030114
122. MarchiniJHowieBMyersSMcVeanGDonnellyP
2007
A new multipoint method for genome-wide association studies by imputation of genotypes.
Nat Genet
39
906
913
123. HardyGH
1908
Mendelian proportions in a mixed population.
Science
28
49
50
124. WeinbergW
1908
Über den nachweis der vererbung beim menschen.
Jahrhefte Des Vereines Für Vaterländische Naturkunde in Württemberg
64
368
382
125. MinelliCThompsonJRAbramsKRThakkinstianAAttiaJ
2008
How should we use information about HWE in the meta-analyses of genetic association studies?
Int J Epidemiol
37
136
146
126. XuJTurnerALittleJBleeckerERMeyersDA
2002
Positive results in association studies are associated with departure from Hardy-Weinberg equilibrium: Hint for genotyping error?
Hum Genet
111
573
574
127. HoskingLLumsdenSLewisKYeoAMcCarthyL
2004
Detection of genotyping errors by Hardy-Weinberg equilibrium testing.
Eur J Hum Genet
12
395
399
128. SalantiGAmountzaGNtzaniEEIoannidisJP
2005
Hardy-Weinberg equilibrium in genetic association studies: An empirical evaluation of reporting, deviations, and power.
Eur J Hum Genet
13
840
848
129. PearsonTAManolioTA
2008
How to interpret a genome-wide association study.
JAMA
299
1335
1344
130. McCarthyMIAbecasisGRCardonLRGoldsteinDBLittleJ
2008
Genome-wide association studies for complex traits: Consensus, uncertainty and challenges.
Nat Rev Genet
9
356
369
131. ZouGYDonnerA
2006
The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control data: A cautionary note.
Ann Hum Genet
70
923
933
132. ShoemakerJPainterIWeirBS
1998
A Bayesian characterization of Hardy-Weinberg disequilibrium.
Genetics
149
2079
2088
133. AyresKLBaldingDJ
1998
Measuring departures from Hardy-Weinberg: A Markov chain Monte Carlo method for estimating the inbreeding coefficient.
Heredity
80
769
777
134. TrikalinosTASalantiGKhouryMJIoannidisJP
2006
Impact of violations and deviations in Hardy-Weinberg equilibrium on postulated gene-disease associations.
Am J Epidemiol
163
300
309
135. DavidoffFBataldenPStevensDOgrincGMooneyS
2008
Publication guidelines for improvement studies in health care: Evolution of the SQUIRE project.
Ann Intern Med
149
670
676
136. SteinbergKGallagherM
2004
Assessing genotypes in human genome epidemiology studies.
KhouryMJLittleJBurkeW
editors. In
Human genome epidemiology: A scientific foundation for using genetic information to improve health and prevent disease
New York
Oxford University Press
79
91
137. PlagnolVCooperJDToddJAClaytonDG
2007
A method to address differential bias in genotyping in large-scale association studies.
PLoS Genet
3
e74
doi:10.1371/journal.pgen.0030074
138. WinkerMA
2006
Race and ethnicity in medical research: Requirements meet reality.
J Law Med Ethics
34
520
525
139. ScuteriASannaSChenWMUdaMAlbaiG
2007
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.
PLoS Genet
3
e115
doi:10.1371/journal.pgen.0030115
140. ChanAWHrobjartssonAHaahrMTGotzschePCAltmanDG
2004
Empirical evidence for selective reporting of outcomes in randomized trials: Comparison of protocols to published articles.
JAMA
291
2457
2465
141. ChanAWKrleza-JericKSchmidIAltmanDG
2004
Outcome reporting bias in randomized trials funded by the Canadian Institutes of Health Research.
CMAJ
171
735
740
142. ChanAWAltmanDG
2005
Identifying outcome reporting bias in randomised trials on PubMed: Review of publications and survey of authors.
BMJ
330
753
143. Contopoulos-IoannidisDGAlexiouGAGouviasTCIoannidisJP
2006
An empirical evaluation of multifarious outcomes in pharmacogenetics: Beta-2 adrenoceptor gene polymorphisms in asthma treatment.
Pharmacogenet Genomics
16
705
711
144. WainHMBrufordEALoveringRCLushMJWrightMW
2002
Guidelines for human gene nomenclature.
Genomics
79
464
470
145. WainHMLushMDucluzeauFPoveyS
2002
Genew: The human gene nomenclature database.
Nucleic Acids Res
30
169
171
146. SherrySTWardMHKholodovMBakerJPhanL
2001
dbSNP: The NCBI database of genetic variation.
Nucleic Acids Res
29
308
311
147. AntonarakisSE
1998
Recommendations for a nomenclature system for human gene mutations. nomenclature working group.
Hum Mutat
11
1
3
148. den DunnenJTAntonarakisSE
2000
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion.
Hum Mutat
15
7
12
149. TobinMDSheehanNAScurrahKJBurtonPR
2005
Adjusting for treatment effects in studies of quantitative traits: Antihypertensive therapy and systolic blood pressure.
Stat Med
24
2911
2935
150. LynchMRitlandK
1999
Estimation of pairwise relatedness with molecular markers.
Genetics
152
1753
1766
151. SlagerSLSchaidDJ
2001
Evaluation of candidate genes in case-control studies: A statistical method to account for related subjects.
Am J Hum Genet
68
1457
1462
152. VoightBFPritchardJK
2005
Confounding from cryptic relatedness in case-control association studies.
PLoS Genet
1
e32
doi:10.1371/journal.pgen.0010032
153. HomerNSzelingerSRedmanMDugganDTembeW
2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.
PLoS Genet
4
e1000167
doi:10.1371/journal.pgen.1000167
154. ZerhouniEANabelEG
2008
Protecting aggregate genomic data.
Science
322
44
Štítky
Interné lekárstvoČlánok vyšiel v časopise
PLOS Medicine
2009 Číslo 2
- Statinová intolerance
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Co dělat při intoleranci statinů?
- Pleiotropní účinky statinů na kardiovaskulární systém
- DESATORO PRE PRAX: Aktuálne odporúčanie ESPEN pre nutričný manažment u pacientov s COVID-19
Najčítanejšie v tomto čísle
- STrengthening the REporting of Genetic Association Studies (STREGA)— An Extension of the STROBE Statement
- How Do Courts Set Health Policy? The Case of the Colombian Constitutional Court
- A 21-Year-Old Pregnant Woman with Hypertension and Proteinuria
- Ovarian Cancer: A Clinical Challenge That Needs Some Basic Answers