Søgeresultater - Spurdle, A

Y chromosome probe p49a detects complex PvuII haplotypes and many new TaqI haplotypes in southern African populations. af Spurdle, A, Jenkins, T

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The origins of the Lemba "Black Jews" of southern Africa: evidence from p12F2 and other Y-chromosome markers. af Spurdle, A. B., Jenkins, T.

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pDP1007, detects an X polymorphism with HindIII in negroids at the ZFX locus af Spurdle, A.B., Jenkins, T.

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The Y-associated XY275 low allele is not restricted to indigenous African peoples. af Spurdle, A, Ramsay, M, Jenkins, T

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The Y Alu polymorphism in southern African populations and its relationship to other Y-specific polymorphisms. af Spurdle, A. B., Hammer, M. F., Jenkins, T.

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New TaqI allele detected by X-chromosome probe S21 (DXS17) af Stevens, G., Spurdle, A.B., Jenkins, Trefor

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Referral of Queensland women with endometrial cancer to genetic services af Tan, YY, McGaughran, J, Obermair, A, Spurdle, A

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Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance af Parsons, M, Thompson, B, Goldgar, D, Hopper, J, Jenkins, M, Buchanan, D, Young, J, Spurdle, A

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Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group af Kerkhofs, C. H. H., Spurdle, A. B., Lindsey, P. J., Goldgar, D. E., Gómez-García, E. B.

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Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers. af Starfield, M, Hennies, H C, Jung, M, Jenkins, T, Wienker, T, Hull, P, Spurdle, A, Küster, W, Ramsay, M, Reis, A

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Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals af Jekimovs, C R, Chen, X, Arnold, J, Gatei, M, Richard, D J, Spurdle, A B, Khanna, K K, Chenevix-Trench, G

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BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance af Eccles, D. M., Mitchell, G., Monteiro, A. N. A., Schmutzler, R., Couch, F. J., Spurdle, A. B., Gómez-García, E. B.

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The Geographic Distribution of Human Y Chromosome Variation af Hammer, M. F., Spurdle, A. B., Karafet, T., Bonner, M. R., Wood, E. T., Novelletto, A., Malaspina, P., Mitchell, R. J., Horai, S., Jenkins, T., Zegura, S. L.

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Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants af Thompson, B, Goldgar, D, Paterson, C, Clendenning, M, Walters, R, Arnold, S, Parsons, M, Walsh, M, Hopper, J, Jenkins, M, Greenblatt, M, Buchanan, D, Young, J, Tavtigian, S, Spurdle, A

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Genetic, functional, and histopathological evaluation of two C‐terminal BRCA1 missense variants af Lovelock, P K, Healey, S, Au, W, Sum, E Y M, Tesoriero, A, Wong, E M, Hinson, S, Brinkworth, R, Bekessy, A, Diez, O, Izatt, L, Solomon, E, Jenkins, M, Renard, H, Hopper, J, Waring, P, Investigators, kConFab, Tavtigian, S V, Goldgar, D, Lindeman, G J, Visvader, J E, Couch, F J, Henderson, B R, Southey, M, Chenevix‐Trench, G, Spurdle, A B, Brown, M A

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Use of aspirin, other nonsteroidal anti-inflammatory drugs and acetaminophen and risk of endometrial cancer: the Epidemiology of Endometrial Cancer Consortium af Webb, P M, Na, R, Weiderpass, E, Adami, H O, Anderson, K E, Bertrand, K A, Botteri, E, Brasky, T M, Brinton, L A, Chen, C, Doherty, J A, Lu, L, McCann, S E, Moysich, K B, Olson, S, Petruzella, S, Palmer, J R, Prizment, A E, Schairer, C, Setiawan, V W, Spurdle, A B, Trabert, B, Wentzensen, N, Wilkens, L, Yang, H P, Yu, H, Risch, H A, Jordan, S J

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Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript af Kote-Jarai, Z., Amin Al Olama, A., Leongamornlert, D., Tymrakiewicz, M., Saunders, E., Guy, M., Giles, G. G., Severi, G., Southey, M., Hopper, J. L., Sit, K. C., Harris, J. M., Batra, J., Spurdle, A. B., Clements, J. A., Hamdy, F., Neal, D., Donovan, J., Muir, K., Pharoah, P. D. P., Chanock, S. J., Brown, N., Benlloch, S., Castro, E., Mahmud, N., O’Brien, L., Hall, A., Sawyer, E., Wilkinson, R., Easton, D. F., Eeles, R. A.

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Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers af Nones, K, Johnson, J, Newell, F, Patch, A M, Thorne, H, Kazakoff, S H, de Luca, X M, Parsons, M T, Ferguson, K, Reid, L E, McCart Reed, A E, Srihari, S, Lakis, V, Davidson, A L, Mukhopadhyay, P, Holmes, O, Xu, Q, Wood, S, Leonard, C, Beesley, J, Harris, J M, Barnes, D, Degasperi, A, Ragan, M A, Spurdle, A B, Khanna, K K, Lakhani, S R, Pearson, J V, Nik-Zainal, S, Chenevix-Trench, G, Waddell, N, Simpson, P T

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Infertility and incident endometrial cancer risk: a pooled analysis from the epidemiology of endometrial cancer consortium (E2C2) af Yang, H P, Cook, L S, Weiderpass, E, Adami, H-O, Anderson, K E, Cai, H, Cerhan, J R, Clendenen, T V, Felix, A S, Friedenreich, C M, Garcia-Closas, M, Goodman, M T, Liang, X, Lissowska, J, Lu, L, Magliocco, A M, McCann, S E, Moysich, K B, Olson, S H, Petruzella, S, Pike, M C, Polidoro, S, Ricceri, F, Risch, H A, Sacerdote, C, Setiawan, V W, Shu, X O, Spurdle, A B, Trabert, B, Webb, P M, Wentzensen, N, Xiang, Y-B, Xu, Y, Yu, H, Zeleniuch-Jacquotte, A, Brinton, L A

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Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium af Pearce, C L, Near, A M, Van Den Berg, D J, Ramus, S J, Gentry-Maharaj, A, Menon, U, Gayther, S A, Anderson, A R, Edlund, C K, Wu, A H, Chen, X, Beesley, J, Webb, P M, Holt, S K, Chen, C, Doherty, J A, Rossing, M A, Whittemore, A S, McGuire, V, DiCioccio, R A, Goodman, M T, Lurie, G, Carney, M E, Wilkens, L R, Ness, R B, Moysich, K B, Edwards, R, Jennison, E, Kjaer, S K, Hogdall, E, Hogdall, C K, Goode, E L, Sellers, T A, Vierkant, R A, Cunningham, J C, Schildkraut, J M, Berchuck, A, Moorman, P G, Iversen, E S, Cramer, D W, Terry, K L, Vitonis, A F, Titus-Ernstoff, L, Song, H, Pharoah, P D P, Spurdle, A B, Anton-Culver, H, Ziogas, A, Brewster, W, Galitovskiy, V, Chenevix-Trench, G

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