Cohen J - Search Results

1

Clinical audit of genetic testing and referral patterns for fragile X and associated conditions.

Cotter M, Archibald AD, McClaren BJ, Burgess T, Francis D, Hills L, Martyn M, Oertel R, Slater H, Cohen J, Metcalfe SA. Cotter M, et al. Among authors: cohen j. Am J Med Genet A. 2016 Jun;170(6):1439-49. doi: 10.1002/ajmg.a.37603. Epub 2016 Feb 18. Am J Med Genet A. 2016. PMID: 26892444

2

The fragile X syndrome.

Lennox N, Cohen J, Slater H, Cook A. Lennox N, et al. Among authors: cohen j. Aust Fam Physician. 1998 Mar;27(3):163-6. Aust Fam Physician. 1998. PMID: 9529704

3

A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study.

Metcalfe S, Jacques A, Archibald A, Burgess T, Collins V, Henry A, McNamee K, Sheffield L, Slater H, Wake S, Cohen J. Metcalfe S, et al. Among authors: cohen j. Genet Med. 2008 Jul;10(7):525-35. doi: 10.1097/gim.0b013e31817c036e. Genet Med. 2008. PMID: 18580686

4

"It's something I need to consider": decisions about carrier screening for fragile X syndrome in a population of non-pregnant women.

Archibald AD, Jaques AM, Wake S, Collins VR, Cohen J, Metcalfe SA. Archibald AD, et al. Among authors: cohen j. Am J Med Genet A. 2009 Dec;149A(12):2731-8. doi: 10.1002/ajmg.a.33122. Am J Med Genet A. 2009. PMID: 19938084

5

A systematic review of population screening for fragile X syndrome.

Hill MK, Archibald AD, Cohen J, Metcalfe SA. Hill MK, et al. Among authors: cohen j. Genet Med. 2010 Jul;12(7):396-410. doi: 10.1097/GIM.0b013e3181e38fb6. Genet Med. 2010. PMID: 20548240 Free article. Review.

6

Inaba Y, Herlihy AS, Schwartz CE, Skinner C, Bui QM, Cobb J, Shi EZ, Francis D, Arvaj A, Amor DJ, Pope K, Wotton T, Cohen J, Hewitt JK, Hagerman RJ, Metcalfe SA, Hopper JL, Loesch DZ, Slater HR, Godler DE. Inaba Y, et al. Among authors: cohen j. Genet Med. 2013 Apr;15(4):290-8. doi: 10.1038/gim.2012.134. Epub 2012 Oct 11. Genet Med. 2013. PMID: 23060046 Free article.

7

"It's about having the choice": stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome.

Archibald AD, Hickerton CL, Jaques AM, Wake S, Cohen J, Metcalfe SA. Archibald AD, et al. Among authors: cohen j. Am J Med Genet A. 2013 Jan;161A(1):48-58. doi: 10.1002/ajmg.a.35674. Epub 2012 Dec 13. Am J Med Genet A. 2013. PMID: 23239566

8

Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome.

Kraan CM, Hocking DR, Bradshaw JL, Fielding J, Cohen J, Georgiou-Karistianis N, Cornish KM. Kraan CM, et al. Among authors: cohen j. Neurosci Biobehav Rev. 2013 Mar;37(3):522-47. doi: 10.1016/j.neubiorev.2013.01.010. Epub 2013 Jan 23. Neurosci Biobehav Rev. 2013. PMID: 23352653 Review.

9

Cognitive-motor interference during postural control indicates at-risk cerebellar profiles in females with the FMR1 premutation.

Kraan CM, Hocking DR, Georgiou-Karistianis N, Metcalfe SA, Archibald AD, Fielding J, Trollor J, Bradshaw JL, Cohen J, Cornish KM. Kraan CM, et al. Among authors: cohen j. Behav Brain Res. 2013 Sep 15;253:329-36. doi: 10.1016/j.bbr.2013.07.033. Epub 2013 Jul 27. Behav Brain Res. 2013. PMID: 23896050

10

Offering fragile X syndrome carrier screening: a prospective mixed-methods observational study comparing carrier screening of pregnant and non-pregnant women in the general population.

Martyn M, Anderson V, Archibald A, Carter R, Cohen J, Delatycki M, Donath S, Emery J, Halliday J, Hill M, Sheffield L, Slater H, Tassone F, Younie S, Metcalfe S. Martyn M, et al. Among authors: cohen j. BMJ Open. 2013 Sep 10;3(9):e003660. doi: 10.1136/bmjopen-2013-003660. BMJ Open. 2013. PMID: 24022395 Free PMC article.

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