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There are 44745 results for: content related to: Reconstructing the Genealogy of a BRCA1 Founder Mutation by Phylogenetic Analysis

  1. Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation

    Clinical Genetics

    Volume 76, Issue 2, August 2009, Pages: 152–160, M-W Seong, SI Cho, D-Y Noh, W Han, S-W Kim, C-M Park, H-W Park, SY Kim, JY Kim and SS Park

    Version of Record online : 28 JUL 2009, DOI: 10.1111/j.1399-0004.2009.01202.x

  2. Haplotype analysis of two recurrent genomic rearrangements in the BRCA1 gene suggests they are founder mutations for the Greek population

    Clinical Genetics

    Volume 80, Issue 4, October 2011, Pages: 375–382, M Pertesi, I Konstantopoulou and D Yannoukakos

    Version of Record online : 15 SEP 2010, DOI: 10.1111/j.1399-0004.2010.01532.x

  3. You have free access to this content
    The Impact of BRCA1 on Spina Bifida Meningomyelocele Lesions

    Annals of Human Genetics

    Volume 71, Issue 6, November 2007, Pages: 719–728, Terri M. King, Kit-Sing Au, Timothy J. Kirkpatrick, Christina Davidson, Jack M. Fletcher, Irene Townsend, Gayle H. Tyerman, Lawrence C. Shimmin and Hope Northrup

    Version of Record online : 19 JUL 2007, DOI: 10.1111/j.1469-1809.2007.00377.x

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    Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non BRCA1/2 French Canadian breast and ovarian cancer families

    International Journal of Cancer

    Volume 122, Issue 1, 1 January 2008, Pages: 108–116, Sylvie Desjardins, Pascal Belleau, Yvan Labrie, Geneviève Ouellette, Paul Bessette, Jocelyne Chiquette, Rachel Laframboise, Jean Lépine, Bernard Lespérance, Roxane Pichette, Marie Plante and Francine Durocher

    Version of Record online : 31 AUG 2007, DOI: 10.1002/ijc.23058

  5. Genetic polymorphisms in AURKA and BRCA1 are associated with breast cancer susceptibility in a Chinese Han population

    The Journal of Pathology

    Volume 225, Issue 4, December 2011, Pages: 535–543, Yuan Ruan, Ai-Ping Song, Hui Wang, Yun-Tao Xie, Ji-Yuan Han, Constantin Sajdik, Xin-Xia Tian and Wei-Gang Fang

    Version of Record online : 19 MAY 2011, DOI: 10.1002/path.2902

  6. Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families

    Clinical Genetics

    Volume 72, Issue 4, October 2007, Pages: 311–320, JM Hartikainen, V Kataja, M Pirskanen, A Arffman, U Ristonmaa, P Vahteristo, M Ryynänen, S Heinonen, V-M Kosma and A Mannermaa

    Version of Record online : 28 AUG 2007, DOI: 10.1111/j.1399-0004.2007.00866.x

  7. Haplotype analysis of a BRCA1: 185delAG mutation in a Chilean family supports its Ashkenazi origins

    Clinical Genetics

    Volume 62, Issue 2, August 2002, Pages: 151–156, N Ah Mew, N Hamel, M Galvez, M Al-Saffar and WD Foulkes

    Version of Record online : 6 SEP 2002, DOI: 10.1034/j.1399-0004.2002.620208.x

  8. Identification of a founder BRCA1 mutation in the Moroccan population

    Clinical Genetics

    F. Quiles, À. Teulé, N. Martinussen Tandstad, L. Feliubadaló, E. Tornero, J. del Valle, M. Menéndez, M. Salinas, V. Wethe Rognlien, A. Velasco, A. Izquierdo, G. Capellá, J. Brunet and C. Lázaro

    Version of Record online : 4 MAR 2016, DOI: 10.1111/cge.12747

  9. BRCA1 Polymorphisms and Breast Cancer Epidemiology in the Western New York Exposures and Breast Cancer (WEB) Study

    Genetic Epidemiology

    Volume 37, Issue 5, July 2013, Pages: 504–511, Luisel J. Ricks-Santi, Jing Nie, Catalin Marian, Heather M. Ochs-Balcom, Maurizio Trevisan, Stephen B. Edge, Jo L. Freudenheim and Peter G. Shields

    Version of Record online : 14 MAY 2013, DOI: 10.1002/gepi.21730

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    Erratum: BRCA1 polymorphisms and breast cancer epidemiology in the Western New York Exposures and Breast Cancer (WEB) study

    Vol. 37, Issue 7, 758, Version of Record online: 15 OCT 2013

  10. BRCA1 5272-1G>A and BRCA2 5374delTATG are founder mutations of high relevance for genetic counselling in breast/ovarian cancer families of Spanish origin

    Clinical Genetics

    Volume 77, Issue 1, January 2010, Pages: 60–69, M Infante, M Durán, A Acedo, L Pérez-Cabornero, DJ Sanz, M García-González, E Beristain, E Esteban-Cardeñosa, M De La Hoya, A Teulé, A Vega, M-I Tejada, E Lastra, C Miner and EA Velasco

    Version of Record online : 11 NOV 2009, DOI: 10.1111/j.1399-0004.2009.01272.x

  11. Haplotype Sharing Methods

    Standard Article

    eLS

    Lars Beckmann

    Published Online : 15 SEP 2010, DOI: 10.1002/9780470015902.a0022496

  12. The rare silver gum, Eucalyptus cordata, is leaving its trace in the organellar gene pool of Eucalyptus globulus

    Molecular Ecology

    Volume 13, Issue 12, December 2004, Pages: 3751–3762, GAY E. MCKINNON, RENÉ E. VAILLANCOURT, DOROTHY A. STEANE and BRAD M. POTTS

    Version of Record online : 21 OCT 2004, DOI: 10.1111/j.1365-294X.2004.02364.x

  13. Widespread decoupling of mtDNA variation and species integrity in Grammia tiger moths (Lepidoptera: Noctuidae)

    Systematic Entomology

    Volume 33, Issue 4, October 2008, Pages: 613–634, B. CHRISTIAN SCHMIDT and FELIX A. H. SPERLING

    Version of Record online : 1 OCT 2008, DOI: 10.1111/j.1365-3113.2008.00433.x

  14. Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 507–516, G. Ponti, E. Castellsagué, C. Ruini, A. Percesepe and A. Tomasi

    Version of Record online : 9 DEC 2014, DOI: 10.1111/cge.12529

  15. The founder mutation BRCA1c.2845insA identified in a fallopian tube cancer patient: a case report

    International Journal of Gynecological Cancer

    Volume 16, Issue S1, February 2006, Pages: 362–365, Z DAMAYANTI, A.B. ALI, P.T.C. IAU, A ILANCHERAN and J.H. SNG

    Version of Record online : 24 FEB 2006, DOI: 10.1111/j.1525-1438.2006.00221.x

  16. Haplotype sharing test maps genes for familial cardiomyopathies

    Clinical Genetics

    Volume 79, Issue 5, May 2011, Pages: 459–467, PA van der Zwaag, JP van Tintelen, F Gerbens, JDH Jongbloed, LG Boven, JJ van der Smagt, WP van der Roest, IM van Langen, H Bikker, RNW Hauer, MP van den Berg, RMW Hofstra and GJ te Meerman

    Version of Record online : 22 MAY 2010, DOI: 10.1111/j.1399-0004.2010.01472.x

  17. Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families

    Genes, Chromosomes and Cancer

    Volume 31, Issue 2, June 2001, Pages: 107–116, Jamileh Hashemi, Pär-Ola Bendahl, Therese Sandberg, Anton Platz, Stig Linder, Ulrika Stierner, Håkan Olsson, Christian Ingvar, Johan Hansson and Åke Borg

    Version of Record online : 30 MAR 2001, DOI: 10.1002/gcc.1124

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    Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families

    International Journal of Cancer

    Volume 91, Issue 1, 1 January 2001, Pages: 83–88, Noriko Ikeda, Yasuo Miyoshi, Kohri Yoneda, Eiichi Shiba, Yoshizo Sekihara, Moritoshi Kinoshita and Shinzaburo Noguchi

    Version of Record online : 8 DEC 2000, DOI: 10.1002/1097-0215(20010101)91:1<83::AID-IJC1013>3.0.CO;2-5

  19. The role of targeted BRCA1/BRCA2 mutation analysis in hereditary breast/ovarian cancer families of Portuguese ancestry

    Clinical Genetics

    Volume 88, Issue 1, July 2015, Pages: 41–48, A. Peixoto, C. Santos, P. Pinto, M. Pinheiro, P. Rocha, C. Pinto, S. Bizarro, I. Veiga, A.S. Principe, S. Maia, F. Castro, R. Couto, A. Gouveia and M.R. Teixeira

    Version of Record online : 26 JUL 2014, DOI: 10.1111/cge.12441

  20. A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South Africa

    Clinical Genetics

    Volume 81, Issue 2, February 2012, Pages: 179–184, NC van der Merwe, N Hamel, S-R Schneider, JP Apffelstaedt, JT Wijnen and WD Foulkes

    Version of Record online : 10 JAN 2011, DOI: 10.1111/j.1399-0004.2010.01617.x