Perturbation Analysis: A Simple Method for Filtering SNPs with Erroneous Genotyping in Genome-Wide Association Studies (English)
- New search for: Teo, Y. Y.
- New search for: Small, K. S.
- New search for: Clark, T. G.
- New search for: Kwiatkowski, D. P.
- New search for: Teo, Y. Y.
- New search for: Small, K. S.
- New search for: Clark, T. G.
- New search for: Kwiatkowski, D. P.
In:
ANNALS OF HUMAN GENETICS
;
72
, 3
;
368-374
;
2008
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ISSN:
- Article (Journal) / Print
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Title:Perturbation Analysis: A Simple Method for Filtering SNPs with Erroneous Genotyping in Genome-Wide Association Studies
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Contributors:Teo, Y. Y. ( author ) / Small, K. S. ( author ) / Clark, T. G. ( author ) / Kwiatkowski, D. P. ( author )
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Published in:ANNALS OF HUMAN GENETICS ; 72, 3 ; 368-374
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Publisher:
- New search for: Blackwell Publishing Ltd
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Publication date:2008-01-01
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Size:7 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 599.935
- Further information on Dewey Decimal Classification
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Classification:
DDC: 599.935 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 72, Issue 3
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 297
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The MTHFD1 Gene is not Involved in Cleft Lip with or Without Palate Onset Among the Italian PopulationPalmieri, A. / Masiero, E. / Martinelli, M. / Scapoli, L. / Pezzetti, F. / Caramelli, E. / Guidotti, L. / Carinci, F. et al. | 2008
- 300
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Age of SERPINA1 Gene PI Z Mutation: Swedish and Latvian Population AnalysisLace, B. / Sveger, T. / Krams, A. / Cernevska, G. / Krumina, A. et al. | 2008
- 305
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A Mutation Analysis of the Phenylalanine Hydroxylase (PAH) Gene in the Israeli PopulationBercovich, D. / Elimelech, A. / Yardeni, T. / Korem, S. / Zlotogora, J. / Gal, N. / Goldstein, N. / Vilensky, B. / Segev, R. / Avraham, S. et al. | 2008
- 310
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Reconstructing the Genealogy of a BRCA1 Founder Mutation by Phylogenetic AnalysisMarroni, F. / Cipollini, G. / Peissel, B. / D'Andrea, E. / Pensabene, M. / Radice, P. / Caligo, M. A. / Presciuttini, S. / Bevilacqua, G. et al. | 2008
- 319
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Genomewide Linkage Scan for Combined Obesity Phenotypes using Principal Component AnalysisHe, L.‐N. / Liu, Y.‐J. / Xiao, P. / Zhang, L. / Guo, Y. / Yang, T.‐L. / Zhao, L.‐J. / Drees, B. / Hamilton, J. / Deng, H.‐Y. et al. | 2008
- 327
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Significant Association Between TIM1 Promoter Polymorphisms and Protection Against Cerebral Malaria in ThailandNuchnoi, P. / Ohashi, J. / Kimura, R. / Hananantachai, H. / Naka, I. / Krudsood, S. / Looareesuwan, S. / Tokunaga, K. / Patarapotikul, J. et al. | 2008
- 337
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Migration Waves to the Baltic Sea RegionLappalainen, T. / Laitinen, V. / Salmela, E. / Andersen, P. / Huoponen, K. / Savontaus, M.‐L. / Lahermo, P. et al. | 2008
- 349
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Mitochondrial DNA Variation in Karkar IslandersRicaut, F. X. / Thomas, T. / Arganini, C. / Staughton, J. / Leavesley, M. / Bellatti, M. / Foley, R. / Mirazon Lahr, M. et al. | 2008
- 368
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Perturbation Analysis: A Simple Method for Filtering SNPs with Erroneous Genotyping in Genome‐Wide Association StudiesTeo, Y. Y. / Small, K. S. / Clark, T. G. / Kwiatkowski, D. P. et al. | 2008
- 375
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Optimal Two‐Stage Design for Case‐Control Association Analysis Incorporating Genotyping ErrorsZuo, Y. / Zou, G. / Wang, J. / Zhao, H. / Liang, H. et al. | 2008
- 388
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EMK: A Novel Program for Family‐Based Allelic and Genotypic Association Tests on Quantitative TraitsLi, Y. W. / Martin, E. R. / Li, Y. J. et al. | 2008
- 397
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Efficient Approximation of P‐value of the Maximum of Correlated Tests, with Applications to Genome‐Wide Association StudiesLi, Qizhai / Zheng, Gang / Li, Zhaohai / Yu, Kai et al. | 2008
- 407
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A Note on Allelic Tests in Case‐Control Association StudiesGuedj, M. / Nuel, G. / Prum, B. et al. | 2008
- 410
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Exon Deletion in the Non‐catalytic Domain of eIF2Bɛ Due to a Splice Site Mutation Leads to Infantile Forms of CACH/VWM with Severe Decrease of eIF2B GEF ActivityHorzinski, L. / Gonthier, C. / Rodriguez, D. / Scherer, C. / Boespflug‐Tanguy, O. / Fogli, A. et al. | 2008
- 416
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Charcot‐Marie‐Tooth Disease: A Clinico‐genetic ConfrontationBarisic, N. / Claeys, K. G. / Sirotković‐Skerlev, M. / Löfgren, A. / Nelis, E. / De Jonghe, P. / Timmerman, V. et al. | 2008