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Items: 28

1.

Noninvasive Prenatal Detection of Trisomy 21 by Targeted Semiconductor Sequencing: A Technical Feasibility Study.

Xi Y, Arbabi A, McNaughton AJM, Hamilton A, Hull D, Perras H, Chiu T, Morrison S, Goldsmith C, Creede E, Anger GJ, Honeywell C, Cloutier M, Macchio N, Kiss C, Liu X, Crocker S, Davies GA, Brudno M, Armour CM.

Fetal Diagn Ther. 2017;42(4):302-310. doi: 10.1159/000460248. Epub 2017 May 17.

PMID:
28511174
2.

A novel NaV1.5 voltage sensor mutation associated with severe atrial and ventricular arrhythmias.

Wang HG, Zhu W, Kanter RJ, Silva JR, Honeywell C, Gow RM, Pitt GS.

J Mol Cell Cardiol. 2016 Mar;92:52-62. doi: 10.1016/j.yjmcc.2016.01.014. Epub 2016 Jan 19.

3.

Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia.

Xi Y, Honeywell C, Zhang D, Schwartzentruber J, Beaulieu CL, Tetreault M, Hartley T, Marton J, Vidal SM, Majewski J, Aravind L; Care4Rare Canada Consortium, Gollob M, Boycott KM, Gow RM.

Int J Cardiol. 2015 Apr 15;185:114-6. doi: 10.1016/j.ijcard.2015.03.130. Epub 2015 Mar 11. No abstract available.

4.

Activity intensity during free-living activities in children and adolescents with inherited arrhythmia syndromes: assessment by combined accelerometer and heart rate monitor.

Gow RM, Borghese MM, Honeywell CR, Colley RC.

Circ Arrhythm Electrophysiol. 2013 Oct;6(5):939-45. doi: 10.1161/CIRCEP.113.000514. Epub 2013 Aug 30.

PMID:
23994883
5.

A family genetic risk communication framework: guiding tool development in genetics health services.

Wiens ME, Wilson BJ, Honeywell C, Etchegary H.

J Community Genet. 2013 Apr;4(2):233-42. doi: 10.1007/s12687-012-0134-9. Epub 2013 Jan 15.

6.

Factors associated with knowledge of and satisfaction with newborn screening education: a survey of mothers.

Araia MH, Wilson BJ, Chakraborty P, Gall K, Honeywell C, Milburn J, Ramsay T, Potter BK.

Genet Med. 2012 Dec;14(12):963-70. doi: 10.1038/gim.2012.87. Epub 2012 Aug 16.

7.

Apparent transmission distortion of a pericentric chromosome one inversion in a large multi-generation pedigree.

Honeywell C, Argiropoulos B, Douglas S, Blumenthal AL, Allanson J, McGowan-Jordan J, McCready ME.

Am J Med Genet A. 2012 Jun;158A(6):1262-8. doi: 10.1002/ajmg.a.35286. Epub 2012 May 11.

PMID:
22581752
8.

Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper.

Gollob MH, Blier L, Brugada R, Champagne J, Chauhan V, Connors S, Gardner M, Green MS, Gow R, Hamilton R, Harris L, Healey JS, Hodgkinson K, Honeywell C, Kantoch M, Kirsh J, Krahn A, Mullen M, Parkash R, Redfearn D, Rutberg J, Sanatani S, Woo A.

Can J Cardiol. 2011 Mar-Apr;27(2):232-45. doi: 10.1016/j.cjca.2010.12.078. Review.

PMID:
21459272
9.

Peer Observed Interaction and Structured Evaluation (POISE): a Canadian experience with peer supervision for genetic counselors.

Goldsmith C, Honeywell C, Mettler G.

J Genet Couns. 2011 Apr;20(2):204-14. doi: 10.1007/s10897-010-9341-x. Epub 2011 Jan 4.

PMID:
21203807
10.

Genetics: factor V Leiden.

Cremin C, Carroll JC, Allanson J, Blaine SM, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Wilson BJ.

Can Fam Physician. 2010 Apr;56(4):353. No abstract available.

11.

Genetics: Preimplantation genetic diagnosis.

Gibbons CA, Allanson J, Blaine SM, Cremin C, Dorman H, Honeywell C, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2010 Mar;56(3):247. No abstract available.

12.

Genetics: familial melanoma.

Cremin C, Blaine SM, Allanson J, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2010 Jan;56(1):31. No abstract available.

13.

Genetics: schizophrenia.

Rideout AL, Carroll JC, Blaine SM, Cremin C, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Allanson J.

Can Fam Physician. 2009 Dec;55(12):1207. No abstract available.

14.

Genetics: Hypertrophic cardiomyopathy.

Honeywell C, Meschino WS, Allanson J, Blaine SM, Cremin C, Dorman H, Gibbons CA, Permaul J, Carroll JC.

Can Fam Physician. 2009 Nov;55(11):1095. No abstract available.

15.

Genetics: Newborn screening for sickle cell anemia.

Meschino WS, Gibbons CA, Allanson J, Blaine SM, Cremin C, Dorman H, Honeywell C, Permaul J, Wilson BJ, Carroll JC.

Can Fam Physician. 2009 Oct;55(10):1001. No abstract available.

16.

Genetics: type 2 diabetes.

Dorman H, Meschino WS, Allanson J, Blaine SM, Cremin C, Gibbons CA, Honeywell C, Permaul J, Carroll JC.

Can Fam Physician. 2009 Sep;55(9):893. No abstract available.

17.

Genetics: prostate cancer.

Blaine SM, Honeywell C, Allanson J, Cremin C, Dorman H, Gibbons CA, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2009 Jul;55(7):710. No abstract available.

18.

Genetics: Alzheimer disease.

Dorman H, Meschino WS, Allanson J, Blaine SM, Cremin C, Gibbons CA, Honeywell C, Permaul J, Carroll JC.

Can Fam Physician. 2009 Jun;55(6):603. No abstract available.

19.

Genetics: newborn screening for MCAD deficiency.

Carroll JC, Gibbons CA, Blaine SM, Cremin C, Dorman H, Honeywell C, Meschino WS, Permaul J, Allanson J.

Can Fam Physician. 2009 May;55(5):487. Review. No abstract available.

20.

Array CGH ends diagnostic odyssey for infant with features of Williams and Alagille syndrome.

Honeywell C, Gardin L, Jimenez-Rivera C, Allanson J.

Am J Med Genet A. 2009 May;149A(5):1102-3. doi: 10.1002/ajmg.a.32819. No abstract available.

PMID:
19396828
21.

Genetics: Codeine metabolism.

Gibbons CA, Blaine SM, Allanson J, Cremin C, Dorman H, Honeywell C, Meschino WS, Permaul J, Carroll JC.

Can Fam Physician. 2009 Feb;55(2):164. No abstract available.

22.

Genetics: hereditary hemochromatosis.

Allanson J, Honeywell C, Blaine SM, Cremin C, Dorman H, Gibbons CA, Grimshaw J, Meschino WS, Permaul J, Wilson BJ, Carroll JC.

Can Fam Physician. 2009 Jan;55(1):53. No abstract available.

23.

Hereditary breast and ovarian cancers.

Carroll JC, Cremin C, Allanson J, Blaine SM, Dorman H, Gibbons CA, Grimshaw J, Honeywell C, Meschino WS, Permaul J, Wilson BJ.

Can Fam Physician. 2008 Dec;54(12):1691-2. Review. No abstract available.

24.

Discrepant DNA analysis in three patients with inherited arrhythmia: molecular genetic test results deserve a second glance.

Honeywell CR, Gollob MH, Rutberg J, Gow RM, Geraghty MT.

Am J Med Genet A. 2008 Jun 1;146A(11):1466-9. doi: 10.1002/ajmg.a.32336.

PMID:
18449933
25.

Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.

Rutberg J, Green MS, Gow RM, Geraghty MT, Honeywell C, Ewen J, Birnie DH, Tang A, Lemery R, Gollob MH.

Can J Cardiol. 2007 Sep;23(11):904-6.

26.

Clinical considerations for allied professionals: ethical issues in cardiogenetics.

Mullen MA, Honeywell CR, Gow RM.

Heart Rhythm. 2007 Aug;4(8):1110-1. Epub 2007 May 3. No abstract available.

PMID:
17675093
27.

A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14.

Steiner C, Ehtesham N, Taylor KD, Sebald E, Cantor R, King LM, Guo X, Hang T, Hu MS, Cui JR, Friedman B, Norato D, Allanson J, Honeywell C, Mettler G, Field F, Lachman R, Cohn DH, Krakow D.

J Med Genet. 2004 Apr;41(4):266-9.

28.

Spondylocarpotarsal synostosis with epiphyseal dysplasia.

Honeywell C, Langer L, Allanson J.

Am J Med Genet. 2002 May 15;109(4):318-22.

PMID:
11992487

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