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There are 4356 results for: content related to: A Multiclass Likelihood Ratio Approach for Genetic Risk Prediction Allowing for Phenotypic Heterogeneity

  1. A Clustered Multiclass Likelihood-Ratio Ensemble Method for Family-Based Association Analysis Accounting for Phenotypic Heterogeneity

    Genetic Epidemiology

    Volume 40, Issue 6, September 2016, Pages: 512–519, Yalu Wen and Qing Lu

    Version of Record online : 19 JUN 2016, DOI: 10.1002/gepi.21987

  2. Familiality and diagnostic patterns of subphenotypes in the National Institutes of Mental Health Bipolar sample

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 1, 5 January 2008, Pages: 18–26, Erika H. Saunders, Laura J. Scott, Melvin G. McInnis and Margit Burmeister

    Version of Record online : 24 MAY 2007, DOI: 10.1002/ajmg.b.30558

  3. You have free access to this content
    Polychromatic flow cytometry: A rapid method for the reduction and analysis of complex multiparameter data

    Cytometry Part A

    Volume 69A, Issue 12, 1 December 2006, Pages: 1162–1173, Ulf Petrausch, Daniel Haley, William Miller, Kevin Floyd, Walter J. Urba and Edwin Walker

    Version of Record online : 6 NOV 2006, DOI: 10.1002/cyto.a.20342

  4. Using Phenotypic Heterogeneity to Increase the Power of Genome-Wide Association Studies: Application to Age at Onset of Ischaemic Stroke Subphenotypes

    Genetic Epidemiology

    Volume 37, Issue 5, July 2013, Pages: 495–503, Matthew Traylor, Steve Bevan, Peter M. Rothwell, Cathie Sudlow, Wellcome Trust Case Control Consortium 2 (WTCCC2), Martin Dichgans, Hugh S. Markus and Cathryn M. Lewis

    Version of Record online : 14 MAY 2013, DOI: 10.1002/gepi.21729

  5. Identifying Subphenotypes of Antibody-Mediated Rejection in Kidney Transplants

    American Journal of Transplantation

    Volume 16, Issue 3, March 2016, Pages: 908–920, P. F. Halloran, M. Merino Lopez and A. Barreto Pereira

    Version of Record online : 6 JAN 2016, DOI: 10.1111/ajt.13551

  6. You have free access to this content
    Investigation of the HIN200 Locus in UK SLE Families Identifies Novel Copy Number Variants

    Annals of Human Genetics

    Volume 75, Issue 3, May 2011, Pages: 383–397, Michelle M. A. Fernando, Adam J. de Smith, Lachlan Coin, David L. Morris, Philippe Froguel, Jonathan Mangion, Alexandra I. F. Blakemore, Robert R. Graham, Timothy W. Behrens and Timothy J. Vyse

    Version of Record online : 14 MAR 2011, DOI: 10.1111/j.1469-1809.2011.00641.x

  7. Rs4948496 within ARID5B gene is associated with clinical features of systemic lupus erythematosus in the Chinese Han population

    The Journal of Dermatology

    Volume 42, Issue 6, June 2015, Pages: 608–612, Long Jiang, Jianping Wu, Weiran Li, Juan Du, Wenjun Wang, Zhengwei Zhu, Jinping Gao, Yujun Sheng, Xianyong Yin, Xiaodong Zheng, Hui Li, Yang Li, Li Meng, Xing Fan, Shengxiu Liu, Ming Zeng, Zaixing Wang, Yong Cui, Huayang Tang, Liangdan Sun, Sen Yang and Xuejun Zhang

    Version of Record online : 21 MAR 2015, DOI: 10.1111/1346-8138.12841

  8. Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies

    Human Mutation

    Volume 32, Issue 12, December 2011, Pages: 1407–1416, Gareth J. McKay, Chris C. Patterson, Usha Chakravarthy, Shilpa Dasari, Caroline C. Klaver, Johannes R. Vingerling, Lintje Ho, Paulus T.V.M. de Jong, Astrid E. Fletcher, Ian S. Young, Johan H. Seland, Mati Rahu, Gisele Soubrane, Laura Tomazzoli, Fotis Topouzis, Jesus Vioque, Aroon D. Hingorani, Reecha Sofat, Michael Dean, Julie Sawitzke, Johanna M. Seddon, Inga Peter, Andrew R. Webster, Anthony T. Moore, John R.W. Yates, Valentina Cipriani, Lars G. Fritsche, Bernhard H.F. Weber, Claudia N. Keilhauer, Andrew J. Lotery, Sarah Ennis, Michael L. Klein, Peter J. Francis, Dwight Stambolian, Anton Orlin, Michael B. Gorin, Daniel E. Weeks, Chia-Ling Kuo, Anand Swaroop, Mohammad Othman, Atsuhiro Kanda, Wei Chen, Goncalo R. Abecasis, Alan F. Wright, Caroline Hayward, Paul N. Baird, Robyn H. Guymer, John Attia, Ammarin Thakkinstian and Giuliana Silvestri

    Version of Record online : 12 SEP 2011, DOI: 10.1002/humu.21577

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    Genetic modifiers of sickle cell disease

    American Journal of Hematology

    Volume 87, Issue 8, August 2012, Pages: 795–803, Martin H. Steinberg and Paola Sebastiani

    Version of Record online : 28 MAY 2012, DOI: 10.1002/ajh.23232

  10. Autism spectrum disorders: The quest for genetic syndromes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 327–366, Dimitrios I. Zafeiriou, Athina Ververi, Vaios Dafoulis, Efrosini Kalyva and Euthymia Vargiami

    Version of Record online : 3 MAY 2013, DOI: 10.1002/ajmg.b.32152

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    Multivariate permutation analysis associates multiple polymorphisms with subphenotypes of major depression

    Genes, Brain and Behavior

    Volume 7, Issue 4, June 2008, Pages: 487–495, M. K. Hahn, , J. U. Blackford, K. Haman, M. Mazei-Robison, B. A. English, H. C. Prasad, A. Steele, L. Hazelwood, H. M. Fentress, R. Myers, R. D. Blakely, ,, E. Sanders-Bush and ,, R. Shelton ,

    Version of Record online : 7 DEC 2007, DOI: 10.1111/j.1601-183X.2007.00384.x

  12. A genetic coding variant rs72474224 in GJB2 is associated with clinical features of psoriasis vulgaris in a Chinese Han population

    Tissue Antigens

    Volume 86, Issue 2, August 2015, Pages: 134–138, F. Yao, M. Yue, C. Zhang, X. Zuo, X. Zheng, A. Zhang, Z. Wang, S. Liu, H. Li, L. Meng, M. Zeng, X. Fan, L. Sun and X. Zhang

    Version of Record online : 24 JUN 2015, DOI: 10.1111/tan.12595

  13. Peripheral blood leucocyte subclasses as potential biomarkers of adipose tissue inflammation and obesity subphenotypes in humans

    Obesity Reviews

    Volume 15, Issue 4, April 2014, Pages: 322–337, T. Pecht, A. Gutman-Tirosh, N. Bashan and A. Rudich

    Version of Record online : 20 NOV 2013, DOI: 10.1111/obr.12133

  14. The TNFAIP3 polymorphism rs610604 both associates with the risk of psoriasis vulgaris and affects the clinical severity

    Clinical and Experimental Dermatology

    Volume 40, Issue 4, June 2015, Pages: 426–430, C. Zhang, K.-J. Zhu, H. Liu, C. Quan, Z. Liu, S.-J. Li, C.-Y. Zhu, K.-S. Li and Y.-M. Fan

    Version of Record online : 12 DEC 2014, DOI: 10.1111/ced.12536

  15. Considering the vascular hypothesis for the pathogenesis of small intestinal atresia: A case control study of genetic factors

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 702–710, Tanya Gupta, Wei Yang, David M. Iovannisci, Suzan L. Carmichael, David K. Stevenson, Gary M. Shaw and Edward J. Lammer

    Version of Record online : 26 FEB 2013, DOI: 10.1002/ajmg.a.35775

  16. Summary of contributions to GAW Group 5: Linkage mapping methods, Problem 2

    Genetic Epidemiology

    Volume 29, Issue S1, 2005, Pages: S35–S40, Heather J. Cordell

    Version of Record online : 8 DEC 2005, DOI: 10.1002/gepi.20108

  17. Dual system approach to computer-aided detection of breast masses on mammograms

    Medical Physics

    Volume 33, Issue 11, November 2006, Pages: 4157–4168, Jun Wei, Heang-Ping Chan, Berkman Sahiner, Lubomir M. Hadjiiski, Mark A. Helvie, Marilyn A. Roubidoux, Chuan Zhou and Jun Ge

    Version of Record online : 30 NOV 2016, DOI: 10.1118/1.2357838

  18. Poster session 1, Abstracts 1–90

    Movement Disorders

    Volume 19, Issue S9, 2004, Pages: S19–S47,

    Version of Record online : 10 MAY 2004, DOI: 10.1002/mds.20168

  19. Computer aided detection of clusters of microcalcifications on full field digital mammograms

    Medical Physics

    Volume 33, Issue 8, August 2006, Pages: 2975–2988, Jun Ge, Berkman Sahiner, Lubomir M. Hadjiiski, Heang-Ping Chan, Jun Wei, Mark A. Helvie and Chuan Zhou

    Version of Record online : 30 NOV 2016, DOI: 10.1118/1.2211710

  20. Operating characteristics predicted by models for diagnostic tasks involving lesion localization

    Medical Physics

    Volume 35, Issue 2, February 2008, Pages: 435–445, D. P. Chakraborty and Hong-Jun Yoon

    Version of Record online : 30 NOV 2016, DOI: 10.1118/1.2820902