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There are 19006 results for: content related to: Variants of uncertain significance in BRCA testing: evaluation of surgical decisions, risk perception, and cancer distress

  1. Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing

    Clinical Genetics

    Volume 88, Issue 6, December 2015, Pages: 523–529, C.L. Scherr, N.M. Lindor, T.L. Malo, F.J. Couch and S.T. Vadaparampil

    Version of Record online : 26 FEB 2015, DOI: 10.1111/cge.12563

  2. You have full text access to this OnlineOpen article
    A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes

    Clinical Genetics

    Volume 86, Issue 3, September 2014, Pages: 229–237, J.M. Eggington, K.R. Bowles, K. Moyes, S. Manley, L. Esterling, S. Sizemore, E. Rosenthal, A. Theisen, J. Saam, C. Arnell, D. Pruss, J. Bennett, L.A. Burbidge, B. Roa and R.J. Wenstrup

    Version of Record online : 20 DEC 2013, DOI: 10.1111/cge.12315

  3. You have full text access to this OnlineOpen article
    Use of panel tests in place of single gene tests in the cancer genetics clinic

    Clinical Genetics

    Volume 88, Issue 3, September 2015, Pages: 278–282, A. Yorczyk, L.S. Robinson and T.S. Ross

    Version of Record online : 16 OCT 2014, DOI: 10.1111/cge.12488

  4. Preferences for results from genomic microarrays: comparing parents and health care providers

    Clinical Genetics

    Volume 87, Issue 1, January 2015, Pages: 21–29, E. Turbitt, J.L. Halliday, D.J. Amor and S.A. Metcalfe

    Version of Record online : 29 APR 2014, DOI: 10.1111/cge.12398

  5. A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants

    Human Mutation

    Volume 33, Issue 3, March 2012, Pages: 488–494, Mark Drost, José B.M. Zonneveld, Sandrine van Hees, Lene Juel Rasmussen, Robert M.W. Hofstra and Niels de Wind

    Version of Record online : 29 DEC 2011, DOI: 10.1002/humu.22000

  6. Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families

    Clinical Genetics

    Volume 83, Issue 1, January 2013, Pages: 23–30, M Reiff, K Ross, S Mulchandani, KJ Propert, RE Pyeritz, NB Spinner and BA Bernhardt

    Version of Record online : 18 SEP 2012, DOI: 10.1111/cge.12004

  7. End-Recovery QTc: A Useful Metric for Assessing Genetic Variants of Unknown Significance in Long-QT syndrome

    Journal of Cardiovascular Electrophysiology

    Volume 23, Issue 6, June 2012, Pages: 637–642, MANOJ N. OBEYESEKERE, RAYMOND W. SY, GEORGE J. KLEIN, LORNE J. GULA, SIMON MODI, SUSAN CONACHER, PETER LEONG-SIT, ALLAN C. SKANES, RAYMOND YEE and ANDREW D. KRAHN

    Version of Record online : 19 MAR 2012, DOI: 10.1111/j.1540-8167.2011.02265.x

  8. You have full text access to this OnlineOpen article
    Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory

    Clinical Genetics

    Volume 86, Issue 6, December 2014, Pages: 510–520, D. Cragun, C. Radford, J.S. Dolinsky, M. Caldwell, E. Chao and T. Pal

    Version of Record online : 20 MAR 2014, DOI: 10.1111/cge.12359

  9. A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS)

    Human Mutation

    Volume 33, Issue 1, January 2012, Pages: 8–21, Noralane M. Lindor, Lucia Guidugli, Xianshu Wang, Maxime P. Vallée, Alvaro N. A. Monteiro, Sean Tavtigian, David E. Goldgar and Fergus J. Couch

    Version of Record online : 3 NOV 2011, DOI: 10.1002/humu.21627

  10. Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients

    Human Mutation

    Volume 33, Issue 8, August 2012, Pages: 1294–1301, Jukka Kantelinen, Minttu Kansikas, Satu Candelin, Heather Hampel, Betsy Smith, Liisa Holm, Reetta Kariola and Minna Nyström

    Version of Record online : 11 JUN 2012, DOI: 10.1002/humu.22119

  11. CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment

    Human Mutation

    Volume 35, Issue 7, July 2014, Pages: 828–840, Maria Chiara Scaini, Giovanni Minervini, Lisa Elefanti, Paola Ghiorzo, Lorenza Pastorino, Silvia Tognazzo, Simona Agata, Monica Quaggio, Daniela Zullato, Giovanna Bianchi-Scarrà, Marco Montagna, Emma D'Andrea, Chiara Menin and Silvio C.E. Tosatto

    Version of Record online : 21 MAY 2014, DOI: 10.1002/humu.22550

  12. Clinical utility of a next generation sequencing panel assay for Marfan and Marfan-like syndromes featuring aortopathy

    American Journal of Medical Genetics Part A

    Volume 167, Issue 8, August 2015, Pages: 1747–1757, Whitney Wooderchak-Donahue, Chad VanSant-Webb, Tatiana Tvrdik, Parker Plant, Tracey Lewis, Jennifer Stocks, Joshua A. Raney, Lindsay Meyers, Alizabeth Berg, Alan F. Rope, Anji T. Yetman, Steven B. Bleyl, Rebecca Mesley, David A. Bull, R. Thomas Collins, Mayra Martinez Ojeda, Amy Roberts, Ronald Lacro, Audrey Woerner, Joan Stoler and Pinar Bayrak-Toydemir

    Version of Record online : 5 MAY 2015, DOI: 10.1002/ajmg.a.37085

  13. Comparison of three-dimensional ROC surfaces for clustered and correlated markers, with a proteomics application

    Statistica Neerlandica

    Volume 69, Issue 4, November 2015, Pages: 399–418, Mst. Papia Sultana and Jialiang Li and Jianhua Hu

    Version of Record online : 7 APR 2015, DOI: 10.1111/stan.12065

  14. Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future

    Human Mutation

    Volume 33, Issue 12, December 2012, Pages: 1617–1625, Lene Juel Rasmussen, Christopher D. Heinen, Brigitte Royer-Pokora, Mark Drost, Sean Tavtigian, Robert M.W. Hofstra and Niels de Wind

    Version of Record online : 13 AUG 2012, DOI: 10.1002/humu.22168

  15. Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants

    Human Mutation

    Volume 33, Issue 8, August 2012, Pages: 1228–1238, Claude Houdayer, Virginie Caux-Moncoutier, Sophie Krieger, Michel Barrois, Françoise Bonnet, Violaine Bourdon, Myriam Bronner, Monique Buisson, Florence Coulet, Pascaline Gaildrat, Cédrick Lefol, Mélanie Léone, Sylvie Mazoyer, Danielle Muller, Audrey Remenieras, Françoise Révillion, Etienne Rouleau, Joanna Sokolowska, Jean-Philippe Vert, Rosette Lidereau, Florent Soubrier, Hagay Sobol, Nicolas Sevenet, Brigitte Bressac-de Paillerets, Agnès Hardouin, Mario Tosi, Olga M. Sinilnikova and Dominique Stoppa-Lyonnet

    Version of Record online : 11 MAY 2012, DOI: 10.1002/humu.22101

  16. Contrast-enhanced gray-scale and color doppler voiding urosonography versus voiding cystourethrography in the diagnosis and grading of vesicoureteral reflux

    Journal of Clinical Ultrasound

    Volume 29, Issue 2, February 2001, Pages: 65–71, Anna Lia Valentini, Elio Salvaggio, Carlo Manzoni, Claudia Rendeli, Carmelo Destito, Vincenzo Summaria, Paolo Campioni and Pasquale Marano

    Version of Record online : 31 JAN 2001, DOI: 10.1002/1097-0096(200102)29:2<65::AID-JCU1000>3.0.CO;2-I

  17. Practical considerations in the clinical application of whole-exome sequencing

    Clinical Genetics

    Volume 89, Issue 2, February 2016, Pages: 173–181, V. Shashi, A. McConkie-Rosell, K. Schoch, V. Kasturi, C. Rehder, Y.H. Jiang, D.B. Goldstein and M.T. McDonald

    Version of Record online : 15 MAR 2015, DOI: 10.1111/cge.12569

  18. Deregulation of epidermal stem cell niche contributes to pathogenesis of nonhealing venous ulcers

    Wound Repair and Regeneration

    Volume 22, Issue 2, March-April 2014, Pages: 220–227, Olivera Stojadinovic, Irena Pastar, Aron G. Nusbaum, Sasa Vukelic, Agata Krzyzanowska and Marjana Tomic-Canic

    Version of Record online : 17 MAR 2014, DOI: 10.1111/wrr.12142

  19. You have free access to this content
    A systematic approach to assessing the clinical significance of genetic variants

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 453–463, H Duzkale, J Shen, H McLaughlin, A Alfares, MA Kelly, TJ Pugh, BH Funke, HL Rehm and MS Lebo

    Version of Record online : 17 OCT 2013, DOI: 10.1111/cge.12257

  20. Simultaneous voiding cystourethrography and voiding urosonography reveals utility of sonographic diagnosis of vesicoureteral reflux in children

    Acta Paediatrica

    Volume 92, Issue 12, December 2003, Pages: 1422–1426, M Nakamura, T Shinozaki, N Taniguchi, H Koibuchi, M Momoi and K Itoh

    Version of Record online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.2003.tb00826.x