• Source: Scopus
  • Calculated based on no. of publications stored in Pure and citations from Scopus
20132021

Research activity per year

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Search results

  • 2021

    Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review

    Crook, A., Jacobs, C., Newton-John, T., O’Shea, R. & McEwen, A., 1 Mar 2021, In: Journal of Neurology. 17 p.

    Research output: Contribution to journalReview articlepeer-review

  • Helping young children understand inherited cancer predisposition syndromes using bibliotherapy

    Schlub, G. M., Crook, A., Barlow-Stewart, K., Fleming, J., Kirk, J., Tucker, K. & Greening, S., 31 Mar 2021, In: Journal of Genetic Counseling. 14 p.

    Research output: Contribution to journalArticlepeer-review

  • 2019

    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 others, Mueller, 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 journalArticlepeer-review

    Open Access
    File
    1 Citation (Scopus)
    17 Downloads (Pure)
  • 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 abstractpeer-review

  • 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 others, Tondini, 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 journalArticlepeer-review

    Open Access
    File
    14 Citations (Scopus)
    6 Downloads (Pure)
  • 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 articlepeer-review

    8 Citations (Scopus)
  • 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 others, Ahearn, 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 journalArticlepeer-review

    Open Access
    File
    8 Citations (Scopus)
    6 Downloads (Pure)
  • 2018

    Bayesian approach to determining penetrance of pathogenic SDH variants

    Benn, D. E., Zhu, Y., Andrews, K. A., Wilding, M., Duncan, E. L., Dwight, T., Tothill, R. W., Burgess, J., Crook, A., Gill, A. J., Hicks, R. J., Kim, E., Luxford, C., Marfan, H., Richardson, A. L., Robinson, B., Schlosberg, A., Susman, R., Tacon, L., Trainer, A. & 4 others, Tucker, K., Maher, E. R., Field, M. & Clifton-Bligh, R. J., Nov 2018, In: Journal of Medical Genetics. 55, 11, p. 729-734 6 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    18 Citations (Scopus)
    26 Downloads (Pure)
  • Heritable DNA methylation marks associated with susceptibility to breast cancer

    Joo, J. E., Dowty, J. G., Milne, R. L., Wong, E. M., Dugué, P. A., kConFab, English, D., Hopper, J. L., Goldgar, D. E., Giles, G. G. & Southey, M. C., 1 Dec 2018, In: Nature Communications. 9, 1, p. 1-12 12 p., 867.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    38 Citations (Scopus)
    19 Downloads (Pure)
  • 2017

    Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy

    Najdawi, F., Crook, A., Maidens, J., McEvoy, C., Fellowes, A., Pickett, J., Ho, M., Nevell, D., McIlroy, K., Sheen, A., Sioson, L., Ahadi, M., Turchini, J., Clarkson, A., Hogg, R., Valmadre, S., Gard, G., Dooley, S. J., Scott, R. J., Fox, S. B. & 2 others, Field, M. & Gill, A. J., Aug 2017, In: Pathology. 49, 5, p. 457-464 8 p.

    Research output: Contribution to journalArticlepeer-review

    20 Citations (Scopus)
  • Patient-centered decision-making in amyotrophic lateral sclerosis: where are we?

    Hogden, A. & Crook, A., 22 Nov 2017, In: Neurodegenerative Disease Management. 7, 6, p. 377-386 10 p.

    Research output: Contribution to journalReview articlepeer-review

    Open Access
    File
    2 Citations (Scopus)
    11 Downloads (Pure)
    10 Citations (Scopus)
  • 2016

    Fumarate hydratase-deficient uterine leiomyomas occur in both the syndromic and sporadic settings

    Harrison, W. J., Andrici, J., Maclean, F., Madadi-Ghahan, R., Farzin, M., Sioson, L., Toon, C. W., Clarkson, A., Watson, N., Pickett, J., Field, M., Crook, A., Tucker, K., Goodwin, A., Anderson, L., Srinivasan, B., Grossmann, P., Martinek, P., Ondič, O., Hes, O. & 4 others, Trpkov, K., Clifton-Bligh, R. J., Dwight, T. & Gill, A. J., May 2016, In: American Journal of Surgical Pathology. 40, 5, p. 599-607 9 p.

    Research output: Contribution to journalArticlepeer-review

    47 Citations (Scopus)
  • 2015

    Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS)

    Crook, A., Plunkett, L., Forrest, L. E., Hallowell, N., Wake, S., Alsop, K., Gleeson, M., Bowtell, D., Mitchell, G., Young, M-A. & Australian Ovarian Cancer Study Group, Feb 2015, In: European Journal of Human Genetics. 23, 2, p. 152-158 7 p.

    Research output: Contribution to journalArticlepeer-review

    8 Citations (Scopus)
  • 2013

    BRAFV600E immunohistochemistry facilitates universal screening of colorectal cancers for Lynch syndrome

    Toon, C. W., Walsh, M. D., Chou, A., Capper, D., Clarkson, A., Sioson, L., Clarke, S., Mead, S., Walters, R. J., Clendenning, M., Rosty, C., Young, J. P., Win, A. K., Hopper, J. L., Crook, A., Von Deimling, A., Jenkins, M. A., Buchanan, D. D. & Gill, A. J., Oct 2013, In: American Journal of Surgical Pathology. 37, 10, p. 1592-1602 11 p.

    Research output: Contribution to journalArticlepeer-review

    99 Citations (Scopus)
  • The responses of research participants and their next of kin to receiving feedback of genetic test results following participation in the Australian Ovarian Cancer Study

    Hallowell, N., Alsop, K., Gleeson, M., Crook, A., Plunkett, L., Bowtell, D., Mitchell, G., Australian Ovarian Cancer Study Group & Young, M-A., 1 Jun 2013, In: Genetics in Medicine. 15, 6, p. 458-465 8 p.

    Research output: Contribution to journalArticlepeer-review

    17 Citations (Scopus)