• 193 Citations
  • 6 h-Index
20132019
If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Ashley Crook is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 12 Similar Profiles
Genetic Testing Medicine & Life Sciences
Genetic Counseling Medicine & Life Sciences
Hereditary Nonpolyposis Colorectal Neoplasms Medicine & Life Sciences
Breast Neoplasms Medicine & Life Sciences
Decision Making Medicine & Life Sciences
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Ovarian Neoplasms Medicine & Life Sciences
Fumarate Hydratase Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects 2017 2017

Research Outputs 2013 2019

  • 193 Citations
  • 6 h-Index
  • 11 Article
  • 2 Review article
  • 1 Meeting abstract

Development and validation of a targeted gene sequencing panel for application to disparate cancers

McCabe, M. J., Gauthier, M-E. A., Chan, C-L., Thompson, T. J., De Sousa, S. M. C., Puttick, C., Grady, J. P., Gayevskiy, V., Tao, J., Ying, K., Cipponi, A., Deng, N., Swarbrick, A., Thomas, M. L., kConFab, Lord, R. V., Johns, A. L., Kohonen-Corish, M., O’Toole, S. A., Clark, J. & 5 othersMueller, S. A., Gupta, R., McCormack, A. I., Dinger, M. E. & Cowley, M. J., 1 Dec 2019, In : Scientific Reports. 9, 1, 16 p., 17052.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
File
Genes
Neoplasms
Biopsy
DNA
Neoplasm Genes

Genetic testing for familial amyotrophic lateral sclerosis (ALS): insights and challenges

Crook, A., Hogden, A., Mumford, V., Blair, I. P., Williams, K. L. & Rowe, D. B., 1 Nov 2019, In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 20, Supplement 1, p. 327 1 p., CMS-01.

Research output: Contribution to journalMeeting abstractResearchpeer-review

Genetic Testing
Amyotrophic Lateral Sclerosis
Decision Making
Genetic Counseling
Interviews

Homologous recombination DNA repair defects in PALB2-associated breast cancers

Li, A., Geyer, F. C., Blecua, P., Lee, J. Y., Selenica, P., Brown, D. N., Pareja, F., Lee, S. S. K., Kumar, R., Rivera, B., Bi, R., Piscuoglio, S., Wen, H. Y., Lozada, J. R., Gularte-Mérida, R., Cavallone, L., kConFab Investigators, Rezoug, Z., Nguyen-Dumont, T., Peterlongo, P. & 19 othersTondini, C., Terkelsen, T., Rønlund, K., Boonen, S. E., Mannerma, A., Winqvist, R., Janatova, M., Rajadurai, P., Xia, B., Norton, L., Robson, M. E., Ng, P-S., Looi, L. M., Southey, M. C., Weigelt, B., Soo-Hwang, T., Tischkowitz, M., Foulkes, W. D. & Reis-Filho, J. S., 23 Nov 2019, In : npj Breast Cancer. 5, 1, p. 1-14 14 p., 23.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
File
Recombinational DNA Repair
Breast Neoplasms
Loss of Heterozygosity
Homologous Recombination
Alleles

The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counseling

Crook, A., McEwen, A., Fifita, J. A., Zhang, K., Kwok, J. B., Halliday, G., Blair, I. P. & Rowe, D. B., Jul 2019, In : Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 20, 5-6, p. 310-316 7 p.

Research output: Contribution to journalReview articleResearchpeer-review

Genetic Counseling
Genetic Testing
Genetic Phenomena
Motor Neuron Disease
Amyotrophic Lateral Sclerosis

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Figlioli, G., Bogliolo, M., Catucci, I., Caleca, L., Lasheras, S. V., Pujol, R., Kiiski, J. I., Muranen, T. A., Barnes, D. R., Dennis, J., Michailidou, K., Bolla, M. K., Leslie, G., Aalfs, C. M., ABCTB Investigators, Adank, M. A., Adlard, J., Agata, S., Cadoo, K., Agnarsson, B. A. & 261 othersAhearn, T., Aittomäki, K., Ambrosone, C. B., Andrews, L., Anton-Culver, H., Antonenkova, N. N., Arndt, V., Arnold, N., Aronson, K. J., Arun, B. K., Asseryanis, E., Auber, B., Auvinen, P., Azzollini, J., Balmaña, J., Barkardottir, R. B., Barrowdale, D., Barwell, J., Beane Freeman, L. E., Beauparlant, C. J., Beckmann, M. W., Behrens, S., Benitez, J., Berger, R., Bermisheva, M., Blanco, A. M., Blomqvist, C., Bogdanova, N. V., Bojesen, A., Bojesen, S. E., Bonanni, B., Borg, A., Brady, A. F., Brauch, H., Brenner, H., Brüning, T., Burwinkel, B., Buys, S. S., Caldés, T., Caliebe, A., Caligo, M. A., Campa, D., Campbell, I. G., Canzian, F., Castelao, J. E., Chang-Claude, J., Chanock, S. J., Claes, K. B. M., Clarke, C. L., Collavoli, A., Conner, T. A., Cox, D. G., Cybulski, C., Czene, K., Daly, M. B., de la Hoya, M., Devilee, P., Diez, O., Ding, Y. C., Dite, G. S., Ditsch, N., Domchek, S. M., Dorfling, C. M., dos-Santos-Silva, I., Durda, K., Dwek, M., Eccles, D. M., Ekici, A. B., Eliassen, A. H., Ellberg, C., Eriksson, M., Evans, D. G., Fasching, P. A., Figueroa, J., Flyger, H., Foulkes, W. D., Friebel, T. M., Friedman, E., Gabrielson, M., Gaddam, P., Gago-Dominguez, M., Gao, C., Gapstur, S. M., Garber, J., García-Closas, M., García-Sáenz, J. A., Gaudet, M. M., Gayther, S. A., GEMO Study Collaborators, Giles, G. G., Glendon, G., Godwin, A. K., Goldberg, M. S., Goldgar, D. E., Guénel, P., Gutierrez-Barrera, A. M., Haeberle, L., Haiman, C. A., Håkansson, N., Hall, P., Hamann, U., Harrington, P. A., Hein, A., Heyworth, J., Hillemanns, P., Hollestelle, A., Hopper, J. L., Hosgood, H. D., Howell, A., Hu, C., Hulick, P. J., Hunter, D. J., Imyanitov, E. N., kConFab, Heiniger, L., Fenton, G., Issacs, C., Jakimovska, M., Jakubowska, A., James, P., Janavicius, R., Janni, W., John, E. M., Jones, M. E., Jung, A., Kaaks, R., Karlan, B. Y., Khusnutdinova, E., Kitahara, C. M., Konstantopoulou, I., Koutros, S., Kraft, P., Lambrects, D., Lazaro, C., Marchand, L. L., Lester, J., Lesueur, F., Lilyquist, J., Loud, J. T., Lu, K. H., Luben, R. N., Lubiński, J., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Martens, J. W. M., Maurer, T., Mavroudis, D., Mebirouk, N., Meindl, A., Menon, U., Miller, A., Montagna, M., Nathanson, K. L., Neuhausen, S. L., Newman, W. G., Nguyen-Dumont, T., Nielsen, F. C., Nielsen, S., Nikitina-Zake, L., Offit, K., Olah, E., Olopade, O. I., Olshan, A. F., Olson, J. E., Olsson, H., Osorio, A., Ottini, L., Peissel, B., Peixoto, A., Peto, J., Plaseska-Karanfilska, D., Pocza, T., Presneau, N., Pujana, M. A., Punie, K., Rack, B., Rantala, J., Rashid, M. U., Rau-Murthy, R., Rennert, G., Lejbkowicz, F., Rhenius, V., Romero, A., Rookus, M. A., Ross, E. A., Rossing, M., Rudaitis, V., Ruebner, M., Saloustros, E., Sanden, K., Santamarina, M., Scheuner, M. T., Schmutzler, R. K., Schneider, M., Scott, C., Senter, L., Shah, M., Sharma, P., Shu, X-O., Simard, J., Singer, C. F., Sohn, C., Soucy, P., Southey, M. C., Spinelli, J. J., Steele, L., Stoppa-Lyonnet, D., Tapper, W. J., Teixeira, M. R., Terry, M. B., Thomassen, M., Thompson, J., Thull, D. L., Tischkowitz, M., Tollenaar, R. A. E. M., Torres, D., Troester, M. A., Truong, T., Tung, N., Untch, M., Vachon, C. M., van Rensburg, E. J., van Veen, E. M., Vega, A., Viel, A., Wappenschmidt, B., Weitzel, J. N., Wendt, C., Wieme, G., Wolk, A., Yang, X. R., Zheng, W., Ziogas, A., Zorn, K. K., Dunning, A. M., Lush, M., Wang, Q., McGuffog, L., Parsons, M. T., Pharoah, P. D. P., Fostira, F., Toland, A. E., Andrulis, I. L., Ramus, S. J., Swerdlow, A. J., Greene, M. H., Chung, W. K., Milne, R. L., Chenevix-Trench, G., Dörk, T., Schmidt, M. K., Easton, D. F., Radice, P., Hahnen, E., Antoniou, A. C., Couch, F. J., Nevanlinna, H., Surralles, J. & Peterlongo, P., 1 Dec 2019, In : npj Breast Cancer. 5, 1, p. 1-14 14 p., 38.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
File
Triple Negative Breast Neoplasms
Breast Neoplasms
Chromosome Fragility
BRCA2 Gene
BRCA1 Gene