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There are 3072 results for: content related to: A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q

  1. Genomic evidence that resource-based trade-offs limit host-range expansion in a seed beetle

    Evolution

    Volume 70, Issue 6, June 2016, Pages: 1249–1264, Zachariah Gompert and Frank J. Messina

    Version of Record online : 22 MAY 2016, DOI: 10.1111/evo.12933

  2. You have full text access to this OnlineOpen article
    Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing

    Human Mutation

    Volume 36, Issue 9, September 2015, Pages: 903–914, Eric Samorodnitsky, Benjamin M. Jewell, Raffi Hagopian, Jharna Miya, Michele R. Wing, Ezra Lyon, Senthilkumar Damodaran, Darshna Bhatt, Julie W. Reeser, Jharna Datta and Sameek Roychowdhury

    Version of Record online : 15 JUL 2015, DOI: 10.1002/humu.22825

  3. The evolution of novel host use is unlikely to be constrained by trade-offs or a lack of genetic variation

    Molecular Ecology

    Volume 24, Issue 11, June 2015, Pages: 2777–2793, Zachariah Gompert, Joshua P. Jahner, Cynthia F. Scholl, Joseph S. Wilson, Lauren K. Lucas, Victor Soria-Carrasco, James A. Fordyce, Chris C. Nice, C. Alex Buerkle and Matthew L. Forister

    Version of Record online : 27 MAY 2015, DOI: 10.1111/mec.13199

  4. Variations in the exome of the LNCaP prostate cancer cell line

    The Prostate

    Volume 72, Issue 12, 1 September 2012, Pages: 1317–1327, Lien Spans, Zeynep Kalender Atak, Filip Van Nieuwerburgh, Dieter Deforce, Evelyne Lerut, Stein Aerts and Frank Claessens

    Version of Record online : 27 DEC 2011, DOI: 10.1002/pros.22480

  5. You have full text access to this OnlineOpen article
    Towards a whole-genome sequence for rye (Secale cereale L.)

    The Plant Journal

    Volume 89, Issue 5, March 2017, Pages: 853–869, Eva Bauer, Thomas Schmutzer, Ivan Barilar, Martin Mascher, Heidrun Gundlach, Mihaela M. Martis, Sven O. Twardziok, Bernd Hackauf, Andres Gordillo, Peer Wilde, Malthe Schmidt, Viktor Korzun, Klaus F.X. Mayer, Karl Schmid, Chris-Carolin Schön and Uwe Scholz

    Version of Record online : 8 FEB 2017, DOI: 10.1111/tpj.13436

  6. A small deletion of 16q23.1[RIGHTWARDS ARROW]16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348−, P5432+)] in a boy with iris coloboma and minor anomalies

    American Journal of Medical Genetics

    Volume 70, Issue 4, 27 June 1997, Pages: 371–376, Walter Werner, Sabine Kraft, David F. Callen, Oliver Bartsch and Georg Klaus Hinkel

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19970627)70:4<371::AID-AJMG8>3.0.CO;2-W

  7. The Number of Point Mutations in Induced Pluripotent Stem Cells and Nuclear Transfer Embryonic Stem Cells Depends on the Method and Somatic Cell Type Used for Their Generation

    STEM CELLS

    Volume 35, Issue 5, May 2017, Pages: 1189–1196, Ryoko Araki, Eiji Mizutani, Yuko Hoki, Misato Sunayama, Sayaka Wakayama, Hiroaki Nagatomo, Yasuji Kasama, Miki Nakamura, Teruhiko Wakayama and Masumi Abe

    Version of Record online : 27 MAR 2017, DOI: 10.1002/stem.2601

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    The molecular spectrum and clinical impact of DIS3 mutations in multiple myeloma

    British Journal of Haematology

    Volume 169, Issue 1, April 2015, Pages: 57–70, Susann Weißbach, Christian Langer, Bernhard Puppe, Theodora Nedeva, Elisa Bach, Miriam Kull, Ralf Bargou, Hermann Einsele, Andreas Rosenwald, Stefan Knop and Ellen Leich

    Version of Record online : 17 DEC 2014, DOI: 10.1111/bjh.13256

  9. Reducing False-Positive Incidental Findings with Ensemble Genotyping and Logistic Regression Based Variant Filtering Methods

    Human Mutation

    Volume 35, Issue 8, August 2014, Pages: 936–944, Kyu-Baek Hwang, In-Hee Lee, Jin-Ho Park, Tina Hambuch, Yongjoon Choe, MinHyeok Kim, Kyungjoon Lee, Taemin Song, Matthew B. Neu, Neha Gupta, Isaac S. Kohane, Robert C. Green and Sek Won Kong

    Version of Record online : 24 JUN 2014, DOI: 10.1002/humu.22587

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    Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis

    Journal of Thrombosis and Haemostasis

    Volume 11, Issue 7, July 2013, Pages: 1228–1239, L. A. Lotta, G. Tuana, J. Yu, I. Martinelli, M. Wang, F. Yu, S. M. Passamonti, E. Pappalardo, C. Valsecchi, S. E. Scherer, W. Hale IV, D. M. Muzny, G. Randi, F. R. Rosendaal, R. A. Gibbs and F. Peyvandi

    Version of Record online : 15 JUL 2013, DOI: 10.1111/jth.12291

  11. Systematic analysis and functional annotation of variations in the genome of an Indian individual

    Human Mutation

    Volume 33, Issue 7, July 2012, Pages: 1133–1140, Ashok Patowary, Ramya Purkanti, Meghna Singh, Rajendra Kumar Chauhan, Deeksha Bhartiya, Om Prakash Dwivedi, Ganesh Chauhan, Dwaipayan Bharadwaj, Sridhar Sivasubbu and Vinod Scaria

    Version of Record online : 16 APR 2012, DOI: 10.1002/humu.22091

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    The potential of the riboSNitch in personalized medicine

    Wiley Interdisciplinary Reviews: RNA

    Volume 6, Issue 5, September/October 2015, Pages: 517–532, Amanda C. Solem, Matthew Halvorsen, Silvia B. V. Ramos and Alain Laederach

    Version of Record online : 26 JUN 2015, DOI: 10.1002/wrna.1291

  13. Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations

    Human Mutation

    Volume 36, Issue 8, August 2015, Pages: 797–807, Jonathan H. Chung, Jinlu Cai, Barrie G. Suskin, Zhengdong Zhang, Karlene Coleman and Bernice E. Morrow

    Version of Record online : 2 JUL 2015, DOI: 10.1002/humu.22814

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    The Mutational Landscape in Pediatric Acute Lymphoblastic Leukemia Deciphered by Whole Genome Sequencing

    Human Mutation

    Volume 36, Issue 1, January 2015, Pages: 118–128, Carl Mårten Lindqvist, Jessica Nordlund, Diana Ekman, Anna Johansson, Behrooz Torabi Moghadam, Amanda Raine, Elin Övernäs, Johan Dahlberg, Per Wahlberg, Niklas Henriksson, Jonas Abrahamsson, Britt-Marie Frost, Dan Grandér, Mats Heyman, Rolf Larsson, Josefine Palle, Stefan Söderhäll, Erik Forestier, Gudmar Lönnerholm, Ann-Christine Syvänen and Eva C. Berglund

    Version of Record online : 30 DEC 2014, DOI: 10.1002/humu.22719

  15. Genome sequencing of mucosal melanomas reveals that they are driven by distinct mechanisms from cutaneous melanoma

    The Journal of Pathology

    Volume 230, Issue 3, July 2013, Pages: 261–269, Simon J Furney, Samra Turajlic, Gordon Stamp, Mahrokh Nohadani, Anna Carlisle, J Meirion Thomas, Andrew Hayes, Dirk Strauss, Martin Gore, Joost van den Oord, James Larkin and Richard Marais

    Version of Record online : 7 JUN 2013, DOI: 10.1002/path.4204

  16. Construction and assessment of individualized proteogenomic databases for large-scale analysis of nonsynonymous single nucleotide variants

    PROTEOMICS

    Volume 14, Issue 23-24, December 2014, Pages: 2699–2708, Karsten Krug, Sasa Popic, Alejandro Carpy, Christoph Taumer and Boris Macek

    Version of Record online : 17 NOV 2014, DOI: 10.1002/pmic.201400219

  17. Sequencing of Charcot–Marie–Tooth disease genes in a toxic polyneuropathy

    Annals of Neurology

    Volume 76, Issue 5, November 2014, Pages: 727–737, Andreas S. Beutler, Amit A. Kulkarni, Rahul Kanwar, Christopher J. Klein, Terry M. Therneau, Rui Qin, Michaela S. Banck, Ganesh K. Boora, Kathryn J. Ruddy, Yanhong Wu, Regenia L. Smalley, Julie M. Cunningham, Nguyet Anh Le-Lindqwister, Peter Beyerlein, Gary P. Schroth, Anthony J. Windebank, Stephan Züchner and Charles L. Loprinzi

    Version of Record online : 17 SEP 2014, DOI: 10.1002/ana.24265

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    Rapid genetic diagnosis of heritable platelet function disorders with next-generation sequencing: proof-of-principle with Hermansky–Pudlak syndrome

    Journal of Thrombosis and Haemostasis

    Volume 10, Issue 2, February 2012, Pages: 306–309, M. L. JONES, S. L. MURDEN, D. BEM, S. J. MUNDELL, P. GISSEN, M. E. DALY, S. P. WATSON, A. D. MUMFORD and on behalf of the UK GAPP study group

    Version of Record online : 2 FEB 2012, DOI: 10.1111/j.1538-7836.2011.04569.x

  19. You have full text access to this OnlineOpen article
    Genome-wide association studies and prediction of 17 traits related to phenology, biomass and cell wall composition in the energy grass Miscanthus sinensis

    New Phytologist

    Volume 201, Issue 4, March 2014, Pages: 1227–1239, Gancho T. Slavov, Rick Nipper, Paul Robson, Kerrie Farrar, Gordon G. Allison, Maurice Bosch, John C. Clifton-Brown, Iain S. Donnison and Elaine Jensen

    Version of Record online : 6 DEC 2013, DOI: 10.1111/nph.12621

  20. MicroRNA Genetic Variation: From Population Analysis to Functional Implications of Three Allele Variants Associated with Cancer

    Human Mutation

    Volume 37, Issue 10, October 2016, Pages: 1060–1073, Ignasi Torruella-Loran, Hafid Laayouni, Begoña Dobon, Alicia Gallego, Ingrid Balcells, Eva Garcia-Ramallo and Yolanda Espinosa-Parrilla

    Version of Record online : 29 AUG 2016, DOI: 10.1002/humu.23045