Crook A - Search Results

1

Systematic review of outcomes in studies of reproductive genetic carrier screening: Towards development of a core outcome set.

Richardson E, McEwen A, Newton-John T, Crook A, Jacobs C. Richardson E, et al. Among authors: crook a. Genet Med. 2022 Jan;24(1):1-14. doi: 10.1016/j.gim.2021.08.005. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906455 Free article. Review.

2

Identification of six new susceptibility loci for invasive epithelial ovarian cancer.

Kuchenbaecker KB, Ramus SJ, Tyrer J, Lee A, Shen HC, Beesley J, Lawrenson K, McGuffog L, Healey S, Lee JM, Spindler TJ, Lin YG, Pejovic T, Bean Y, Li Q, Coetzee S, Hazelett D, Miron A, Southey M, Terry MB, Goldgar DE, Buys SS, Janavicius R, Dorfling CM, van Rensburg EJ, Neuhausen SL, Ding YC, Hansen TV, Jønson L, Gerdes AM, Ejlertsen B, Barrowdale D, Dennis J, Benitez J, Osorio A, Garcia MJ, Komenaka I, Weitzel JN, Ganschow P, Peterlongo P, Bernard L, Viel A, Bonanni B, Peissel B, Manoukian S, Radice P, Papi L, Ottini L, Fostira F, Konstantopoulou I, Garber J, Frost D, Perkins J, Platte R, Ellis S; EMBRACE; Godwin AK, Schmutzler RK, Meindl A, Engel C, Sutter C, Sinilnikova OM; GEMO Study Collaborators; Damiola F, Mazoyer S, Stoppa-Lyonnet D, Claes K, De Leeneer K, Kirk J, Rodriguez GC, Piedmonte M, O'Malley DM, de la Hoya M, Caldes T, Aittomäki K, Nevanlinna H, Collée JM, Rookus MA, Oosterwijk JC; Breast Cancer Family Registry; Tihomirova L, Tung N, Hamann U, Isaccs C, Tischkowitz M, Imyanitov EN, Caligo MA, Campbell IG, Hogervorst FB; HEBON; Olah E, Diez O, Blanco I, Brunet J, Lazaro C, Pujana MA, Jakubowska A, Gronwald J, Lubinski J, Sukiennicki G, Barkardottir RB, Plante M, Sim… See abstract for full author list ➔ Kuchenbaecker KB, et al. Nat Genet. 2015 Feb;47(2):164-71. doi: 10.1038/ng.3185. Epub 2015 Jan 12. Nat Genet. 2015. PMID: 25581431 Free PMC article.

3

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

Crook A, McEwen A, Fifita JA, Zhang K, Kwok JB, Halliday G, Blair IP, Rowe DB. Crook A, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Aug;20(5-6):310-316. doi: 10.1080/21678421.2019.1588904. Epub 2019 Mar 23. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 30907153 Review.

4

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. Crook A, et al. J Neurol. 2022 Feb;269(2):676-692. doi: 10.1007/s00415-021-10461-5. Epub 2021 Mar 1. J Neurol. 2022. PMID: 33649871 Free PMC article. Review.

5

Health system interventions to integrate genetic testing in routine oncology services: A systematic review.

O'Shea R, Taylor N, Crook A, Jacobs C, Jung Kang Y, Lewis S, Rankin NM. O'Shea R, et al. Among authors: crook a. PLoS One. 2021 May 19;16(5):e0250379. doi: 10.1371/journal.pone.0250379. eCollection 2021. PLoS One. 2021. PMID: 34010335 Free PMC article.

6

Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD: A Systematic Scoping Review.

Crook A, Jacobs C, Newton-John T, Richardson E, McEwen A. Crook A, et al. Alzheimer Dis Assoc Disord. 2021 Oct-Dec 01;35(4):374-385. doi: 10.1097/WAD.0000000000000458. Alzheimer Dis Assoc Disord. 2021. PMID: 34054018

7

Genetic counselling and testing for neurodegenerative disorders using a proposed standard of practice for ALS/MND: diagnostic testing comes first.

Crook A, McEwen A. Crook A, et al. Eur J Hum Genet. 2022 Apr;30(4):394-395. doi: 10.1038/s41431-021-01036-z. Epub 2022 Jan 5. Eur J Hum Genet. 2022. PMID: 34983943 Free PMC article. No abstract available.

8

Toward genetic counseling practice standards for diagnostic testing in amyotrophic lateral sclerosis and frontotemporal dementia.

Crook A, Jacobs C, Newton-John T, McEwen A. Crook A, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Nov;23(7-8):562-574. doi: 10.1080/21678421.2022.2051553. Epub 2022 Mar 27. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 35343344 Free article.

9

Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review.

Richardson E, McEwen A, Newton-John T, Crook A, Jacobs C. Richardson E, et al. Among authors: crook a. Eur J Hum Genet. 2022 Jul;30(7):756-765. doi: 10.1038/s41431-022-01090-1. Epub 2022 Mar 28. Eur J Hum Genet. 2022. PMID: 35347269 Free PMC article. Review.

10

Predictive genetic testing for Motor neuron disease: time for a guideline?

McNeill A, Amador MD, Bekker H, Clarke A, Crook A, Cummings C, McEwen A, McDermott C, Quarrell O, Renieri A, Roggenbuck J, Salmon K, Volk A, Weishaupt J; International Alliance of ALS/MND Associations. McNeill A, et al. Among authors: crook a. Eur J Hum Genet. 2022 Jun;30(6):635-636. doi: 10.1038/s41431-022-01093-y. Epub 2022 Apr 5. Eur J Hum Genet. 2022. PMID: 35379930 Free PMC article. No abstract available.

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