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There are 4142 results for: content related to: GENETIC VARIATION AND THE EVOLUTION OF EPIGENETIC REGULATION

  1. Epimutations and Cancer Susceptibility

    Standard Article


    Mathew Aidan Sloane, Luke Benjamin Hesson and Robyn Lynne Ward

    Published Online : 17 MAR 2014, DOI: 10.1002/9780470015902.a0024615

  2. Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility

    Human Mutation

    Volume 33, Issue 1, January 2012, Pages: 180–188, Michel Crépin, Marie-Claire Dieu, Sophie Lejeune, Fabienne Escande, Denis Boidin, Nicole Porchet, Gilles Morin, Sylvie Manouvrier, Michèle Mathieu and Marie-Pierre Buisine

    Version of Record online : 31 OCT 2011, DOI: 10.1002/humu.21617

  3. Germline Epimutation: A Basis for Epigenetic Disease in Humans

    Annals of the New York Academy of Sciences

    Volume 1054, Issue 1, November 2005, Pages: 68–77, DAVID I.K. MARTIN, ROBYN WARD and CATHERINE M. SUTER

    Version of Record online : 6 JAN 2006, DOI: 10.1196/annals.1345.009

  4. Epigenetic mechanisms in the pathogenesis of Lynch syndrome

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 403–412, P. Peltomäki

    Version of Record online : 17 FEB 2014, DOI: 10.1111/cge.12349

  5. Frequency and mitotic heritability of epimutations in Schistosoma mansoni

    Molecular Ecology

    Volume 25, Issue 8, April 2016, Pages: 1741–1758, David Roquis, Anne Rognon, Cristian Chaparro, Jerome Boissier, Nathalie Arancibia, Celine Cosseau, Hugues Parrinello and Christoph Grunau

    Version of Record online : 20 APR 2016, DOI: 10.1111/mec.13555

  6. MLH1 germline epimutations in selected patients with early-onset non-polyposis colorectal cancer

    Clinical Genetics

    Volume 71, Issue 3, March 2007, Pages: 232–237, L Valle, P Carbonell, V Fernandez, AM Dotor, M Sanz, J Benitez and M Urioste

    Version of Record online : 12 JAN 2007, DOI: 10.1111/j.1399-0004.2007.00751.x

  7. Identification of new cases of early-onset colorectal cancer with an MLH1 epimutation in an ethnically diverse South African cohort

    Clinical Genetics

    Volume 80, Issue 5, November 2011, Pages: 428–434, MP Hitchins, SE Owens, C-T Kwok, G Godsmark, UF Algar and RS Ramesar

    Version of Record online : 4 MAY 2011, DOI: 10.1111/j.1399-0004.2011.01660.x

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    De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one

    International Journal of Cancer

    Volume 128, Issue 4, 15 February 2011, Pages: 869–878, Ajay Goel, Thuy-Phuong Nguyen, Hon-Chiu E. Leung, Takeshi Nagasaka, Jennifer Rhees, Erin Hotchkiss, Mildred Arnold, Pia Banerji, Minoru Koi, Chau-To Kwok, Deborah Packham, Lara Lipton, C. Richard Boland, Robyn L. Ward and Megan P. Hitchins

    Version of Record online : 27 APR 2010, DOI: 10.1002/ijc.25422

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    Large genomic rearrangements and germline epimutations in Lynch syndrome

    International Journal of Cancer

    Volume 124, Issue 10, 15 May 2009, Pages: 2333–2340, Annette Gylling, Maaret Ridanpää, Outi Vierimaa, Kristiina Aittomäki, Kristiina Avela, Helena Kääriäinen, Hannele Laivuori, Minna Pöyhönen, Satu-Leena Sallinen, Carina Wallgren-Pettersson, Heikki J. Järvinen, Jukka-Pekka Mecklin and Paivi Peltomäki

    Version of Record online : 18 DEC 2008, DOI: 10.1002/ijc.24230



    Volume 68, Issue 3, March 2014, Pages: 644–655, Koen J.F. Verhoeven and Veronica Preite

    Version of Record online : 13 DEC 2013, DOI: 10.1111/evo.12320

  11. Prenatal findings and epimutations for paternal uniparental disomy for chromosome 14 syndrome

    Journal of Obstetrics and Gynaecology Research

    Volume 41, Issue 7, July 2015, Pages: 1133–1136, Takafumi Watanabe, Hayato Go, Masayo Kagami, Shun Yasuda, Yasuhisa Nomura and Keiya Fujimori

    Version of Record online : 6 FEB 2015, DOI: 10.1111/jog.12665

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    Brief Report: Attention Deficit and Hyperactivity Disorder Scores Are Elevated and Respond to N-Acetylcysteine Treatment in Patients With Systemic Lupus Erythematosus

    Arthritis & Rheumatism

    Volume 65, Issue 5, May 2013, Pages: 1313–1318, Ricardo J. Garcia, Lisa Francis, Maha Dawood, Zhi-Wei Lai, Stephen V. Faraone and Andras Perl

    Version of Record online : 23 APR 2013, DOI: 10.1002/art.37893

  13. Epigenetic Mechanisms in Lynch Syndrome

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    Taina T Nieminen, Anni Niskakoski and Päivi Peltomäki

    Published Online : 15 APR 2016, DOI: 10.1002/9780470015902.a0026560

  14. Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype

    Clinical Genetics

    Volume 75, Issue 3, March 2009, Pages: 251–258, U Zechner, N Kohlschmidt, G Rittner, N Damatova, V Beyer, T Haaf and O Bartsch

    Version of Record online : 31 DEC 2008, DOI: 10.1111/j.1399-0004.2008.01116.x

  15. Dawning of the epigenetic era in hereditary cancer

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 413–416, M.P. Hitchins and H.T. Lynch

    Version of Record online : 1 APR 2014, DOI: 10.1111/cge.12369

  16. The Causes and Consequences of Accelerated Stock Repurchases

    International Review of Finance

    Volume 14, Issue 3, September 2014, Pages: 319–343, Ali Akyol, Jin S. Kim and Chander Shekhar

    Version of Record online : 26 MAY 2014, DOI: 10.1111/irfi.12035

  17. Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell–Silver syndrome

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 11, November 2009, Pages: 2415–2423, Shin-Ichi Horike, Jose Carlos P. Ferreira, Makiko Meguro-Horike, Sanaa Choufani, Adam C. Smith, Cheryl Shuman, Wendy Meschino, David Chitayat, Elaine Zackai, Stephen W. Scherer and Rosanna Weksberg

    Version of Record online : 28 OCT 2009, DOI: 10.1002/ajmg.a.33065

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    Attention-deficit/hyperactivity disorder symptoms in adults with self-reported epilepsy: Results from a national epidemiologic survey of epilepsy


    Volume 56, Issue 2, February 2015, Pages: 218–224, Alan B. Ettinger, Ruth Ottman, Richard B. Lipton, Joyce A. Cramer, Kristina M. Fanning and Michael L. Reed

    Version of Record online : 15 JAN 2015, DOI: 10.1111/epi.12897

  19. Genome-Wide Allelic Methylation Analysis Reveals Disease-Specific Susceptibility to Multiple Methylation Defects in Imprinting Syndromes

    Human Mutation

    Volume 34, Issue 4, April 2013, Pages: 595–602, Franck Court, Alex Martin-Trujillo, Valeria Romanelli, Intza Garin, Isabel Iglesias-Platas, Ira Salafsky, Miriam Guitart, Guiomar Perez de Nanclares, Pablo Lapunzina and David Monk

    Version of Record online : 19 FEB 2013, DOI: 10.1002/humu.22276

  20. Do age-associated DNA methylation changes increase the risk of malignant transformation?


    Volume 37, Issue 1, January 2015, Pages: 20–24, Wolfgang Wagner, Carola I. Weidner and Qiong Lin

    Version of Record online : 9 OCT 2014, DOI: 10.1002/bies.201400063