Methods to impute missing genotypes for population data (English)
- New search for: Yu, Zhaoxia
- New search for: Schaid, Daniel J.
- New search for: Yu, Zhaoxia
- New search for: Schaid, Daniel J.
In:
Human Genetics
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122
, 5
; 495-504
;
2007
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ISSN:
- Article (Journal) / Electronic Resource
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Title:Methods to impute missing genotypes for population data
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Contributors:Yu, Zhaoxia ( author ) / Schaid, Daniel J. ( author )
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Published in:Human Genetics ; 122, 5 ; 495-504
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Publisher:
- New search for: Springer-Verlag
- New search for: Springer
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Place of publication:Berlin
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Publication date:2007
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ISSN:
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ZDBID:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
- New search for: 44.48
- Further information on Basic classification
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Keywords:
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Classification:
BKL: 44.48 Medizinische Genetik -
Source:
Table of contents – Volume 122, Issue 5
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.
- 423
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Wolf–Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16Zollino, Marcella / Lecce, Rosetta / Murdolo, Marina / Orteschi, Daniela / Marangi, Giuseppe / Selicorni, Angelo / Midro, Alina / Sorge, Giovanni / Zampino, Giuseppe / Memo, Luigi et al. | 2007
- 445
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The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Ain, Quratul / Nazli, Sabiha / Riazuddin, Saima / Jaleel, Ateeq-ul / Riazuddin, S. Amer / Zafar, Ahmad U. / Khan, Shaheen N. / Husnain, Tayyab / Griffith, Andrew J. / Ahmed, Zubair M. et al. | 2007
- 451
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Genotype–phenotype correlations for SLC26A4-related deafnessAzaiez, Hela / Yang, Tao / Prasad, Sai / Sorensen, Jessica L. / Nishimura, Carla J. / Kimberling, William J. / Smith, Richard J. H. et al. | 2007
- 459
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High-density oligonucleotide array with sub-kilobase resolution reveals breakpoint information of submicroscopic deletions in nevoid basal cell carcinoma syndromeFujii, Katsunori / Ishikawa, Shumpei / Uchikawa, Hideki / Komura, Daisuke / Shapero, Michael H. / Shen, Fan / Hung, Jing / Arai, Hiroshi / Tanaka, Yoko / Sasaki, Kimio et al. | 2007
- 467
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Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesisCarré, Aurore / Castanet, Mireille / Sura-Trueba, Sylvia / Szinnai, Gabor / Van Vliet, Guy / Trochet, Delphine / Amiel, Jeanne / Léger, Juliane / Czernichow, Paul / Scotet, Virginie et al. | 2007
- 477
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A most distant intergeneric hybrid offspring (Larcon) of lesser apes, Nomascus leucogenys and Hylobates larHirai, Hirohisa / Hirai, Yuriko / Domae, Hiroshi / Kirihara, Yoko et al. | 2007
- 485
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IL-6 gene variation is associated with IL-6 and C-reactive protein levels but not cardiovascular outcomes in the Cardiovascular Health StudyWalston, Jeremy D. / Fallin, M. Daniele / Cushman, Mary / Lange, Leslie / Psaty, Bruce / Jenny, Nancy / Browner, Warren / Tracy, Russell / Durda, Peter / Reiner, Alex et al. | 2007
- 495
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Methods to impute missing genotypes for population dataYu, Zhaoxia / Schaid, Daniel J. et al. | 2007
- 505
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Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in malesEl-Maarri, Osman / Becker, Tim / Junen, Judith / Manzoor, Syed Saadi / Diaz-Lacava, Amalia / Schwaab, Rainer / Wienker, Thomas / Oldenburg, Johannes et al. | 2007
- 515
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RAAS gene polymorphisms influence progression of pediatric hypertrophic cardiomyopathyKaufman, Beth D. / Auerbach, Scott / Reddy, Sushma / Manlhiot, Cedric / Deng, Liyong / Prakash, Ashwin / Printz, Beth F. / Gruber, Dorota / Papavassiliou, Dimitrios P. / Hsu, Daphne T. et al. | 2007
- 525
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One-carbon metabolism gene polymorphisms and risk of non-Hodgkin lymphoma in AustraliaLee, Kyoung-Mu / Lan, Qing / Kricker, Anne / Purdue, Mark P. / Grulich, Andrew E. / Vajdic, Claire M. / Turner, Jennifer / Whitby, Denise / Kang, Daehee / Chanock, Stephen et al. | 2007
- 535
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Interaction between the UCP2–866G/A, mtDNA 10398G/A and PGC1α p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian populationRai, E. / Sharma, S. / Koul, A. / Bhat, A. K. / Bhanwer, A. J. S. / Bamezai, R. N. K. et al. | 2007
- 541
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The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patientMarques Pereira, Patricia / Heron, Delphine / Hanauer, André et al. | 2007
- 545
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Novel human pathological mutations| 2007
- 561
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Barbara Migeon: Females are mosaics: X inactivation and sex differences in diseaseReardon, William et al. | 2007
- 563
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Imprinting detection by extending a regression-based QTL analysis methodGorlova, Olga Y. / Lei, Lei / Zhu, Dakai / Weng, Shih-Feng / Shete, Sanjay / Zhang, Yiqun / Li, Wei-Dong / Price, R. Arlen / Amos, Christopher I. et al. | 2007
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Tracing genetic history of modern humans using X-chromosome lineagesYotova, Vania / Lefebvre, Jean-François / Kohany, Oleksiy / Jurka, Jerzy / Michalski, Roman / Modiano, David / Utermann, Gerd / Williams, Scott M. / Labuda, Damian et al. | 2007