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Items: 1 to 20 of 189

1.

Separate and Joint Associations of Shift Work and Sleep Quality with Lipids.

Charles LE, Gu JK, Tinney-Zara CA, Fekedulegn D, Ma CC, Baughman P, Hartley TA, Andrew ME, Violanti JM, Burchfiel CM.

Saf Health Work. 2016 Jun;7(2):111-9. doi: 10.1016/j.shaw.2015.11.007. Epub 2015 Dec 8.

2.

Effects of rhythm on memory for spoken sequences: A model and tests of its stimulus-driven mechanism.

Hartley T, Hurlstone MJ, Hitch GJ.

Cogn Psychol. 2016 Jun;87:135-78. doi: 10.1016/j.cogpsych.2016.05.001. Epub 2016 Jun 1.

PMID:
27261540
3.

Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events.

Armour CM, Smith A, Hartley T, Chardon JW, Sawyer S, Schwartzentruber J, Hennekam R, Majewski J, Bulman DE; FORGE Canada Consortium, Suri M, Boycott KM.

Am J Med Genet A. 2016 Jul;170(7):1820-5. doi: 10.1002/ajmg.a.37684. Epub 2016 May 2.

PMID:
27133561
4.

Shiftwork and Diurnal Salivary Cortisol Patterns Among Police Officers.

Charles LE, Fekedulegn D, Burchfiel CM, Hartley TA, Andrew ME, Violanti JM, Miller DB.

J Occup Environ Med. 2016 Jun;58(6):542-9. doi: 10.1097/JOM.0000000000000729.

5.

Shift Work and Sleep Quality Among Urban Police Officers: The BCOPS Study.

Fekedulegn D, Burchfiel CM, Charles LE, Hartley TA, Andrew ME, Violanti JM.

J Occup Environ Med. 2016 Mar;58(3):e66-71. doi: 10.1097/JOM.0000000000000620.

PMID:
26949891
6.

Allelic variation in the vacuolar TPK1 channel affects its calcium dependence and may impact on stomatal conductance.

Hartley TN, Maathuis FJ.

FEBS Lett. 2016 Jan;590(1):110-7. doi: 10.1002/1873-3468.12035. Epub 2015 Dec 29.

PMID:
26765783
7.

Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.

Ejaz R, Qin W, Huang L, Blaser S, Tetreault M, Hartley T, Boycott KM, Carter MT; Care4Rare Canada Consortium.

Am J Med Genet A. 2016 Apr;170(4):1070-5. doi: 10.1002/ajmg.a.37541. Epub 2016 Jan 11.

PMID:
26754023
8.

Correlates of hopelessness in the high suicide risk police occupation.

Violanti JM, Andrew ME, Mnatsakanova A, Hartley TA, Fekedulegn D, Burchfiel CM.

Police Pract Res. 2016;17(5):408-419. Epub 2015 Feb 27.

PMID:
26752981
9.

Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability.

Stray-Pedersen A, Cobben JM, Prescott TE, Lee S, Cang C, Aranda K, Ahmed S, Alders M, Gerstner T, Aslaksen K, Tétreault M, Qin W, Hartley T, Jhangiani SN, Muzny DM, Tarailo-Graovac M, van Karnebeek CD; Care4Rare Canada Consortium; Baylor-Hopkins Center for Mendelian Genomics, Lupski JR, Ren D, Yoon G.

Am J Hum Genet. 2016 Jan 7;98(1):202-9. doi: 10.1016/j.ajhg.2015.11.004. Epub 2015 Dec 17.

10.

A versatile segmental bioimpedance analysis platform for use on people with limb amputation.

Sanders J, Moehring M, Rothlisberger T, Phillips R, Hartley T, Dietrich C, Redd C, Gardner D, Cagle J.

IEEE Trans Biomed Eng. 2015 Nov 19. [Epub ahead of print]

PMID:
26595906
11.

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.

Huang L, Vanstone MR, Hartley T, Osmond M, Barrowman N, Allanson J, Baker L, Dabir TA, Dipple KM, Dobyns WB, Estrella J, Faghfoury H, Favaro FP, Goel H, Gregersen PA, Gripp KW, Grix A, Guion-Almeida ML, Harr MH, Hudson C, Hunter AG, Johnson J, Joss SK, Kimball A, Kini U, Kline AD, Lauzon J, Lildballe DL, López-González V, Martinezmoles J, Meldrum C, Mirzaa GM, Morel CF, Morton JE, Pyle LC, Quintero-Rivera F, Richer J, Scheuerle AE, Schönewolf-Greulich B, Shears DJ, Silver J, Smith AC, Temple IK; UCLA Clinical Genomics Center, van de Kamp JM, van Dijk FS, Vandersteen AM, White SM, Zackai EH, Zou R; Care4Rare Canada Consortium, Bulman DE, Boycott KM, Lines MA.

Hum Mutat. 2016 Feb;37(2):148-54. doi: 10.1002/humu.22924. Epub 2015 Nov 19.

PMID:
26507355
12.

Dementia Knowledge Assessment Scale: Development and Preliminary Psychometric Properties.

Annear MJ, Toye CM, Eccleston CE, McInerney FJ, Elliott KE, Tranter BK, Hartley T, Robinson AL.

J Am Geriatr Soc. 2015 Nov;63(11):2375-81. doi: 10.1111/jgs.13707. Epub 2015 Oct 27.

PMID:
26503020
13.

Merkel cell carcinoma presenting as malignant ascites: A case report and review of literature.

Policarpio-Nicolas ML, Avery DL, Hartley T.

Cytojournal. 2015 Aug 13;12:19. doi: 10.4103/1742-6413.162775. eCollection 2015.

14.

Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations.

Faden M, AlZahrani F, Mendoza-Londono R, Dupuis L, Hartley T, Kannu P, Raiman JA, Howard A, Qin W, Tetreault M, Xi JQ, Al-Thamer I; Care4Rare Canada Consortium, Maas RL, Boycott K, Alkuraya FS.

Am J Hum Genet. 2015 Oct 1;97(4):608-15. doi: 10.1016/j.ajhg.2015.08.007. Epub 2015 Sep 10.

15.

Patterns of neural response in scene-selective regions of the human brain are affected by low-level manipulations of spatial frequency.

Watson DM, Hymers M, Hartley T, Andrews TJ.

Neuroimage. 2016 Jan 1;124(Pt A):107-17. doi: 10.1016/j.neuroimage.2015.08.058. Epub 2015 Sep 2.

PMID:
26341028
16.

Axons to Exons: the Molecular Diagnosis of Rare Neurological Diseases by Next-Generation Sequencing.

Warman Chardon J, Beaulieu C, Hartley T, Boycott KM, Dyment DA.

Curr Neurol Neurosci Rep. 2015 Sep;15(9):64. doi: 10.1007/s11910-015-0584-7. Review.

PMID:
26289954
17.

Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.

Sawyer SL, Hartley T, Dyment DA, Beaulieu CL, Schwartzentruber J, Smith A, Bedford HM, Bernard G, Bernier FP, Brais B, Bulman DE, Warman Chardon J, Chitayat D, Deladoëy J, Fernandez BA, Frosk P, Geraghty MT, Gerull B, Gibson W, Gow RM, Graham GE, Green JS, Heon E, Horvath G, Innes AM, Jabado N, Kim RH, Koenekoop RK, Khan A, Lehmann OJ, Mendoza-Londono R, Michaud JL, Nikkel SM, Penney LS, Polychronakos C, Richer J, Rouleau GA, Samuels ME, Siu VM, Suchowersky O, Tarnopolsky MA, Yoon G, Zahir FR; FORGE Canada Consortium; Care4Rare Canada Consortium, Majewski J, Boycott KM.

Clin Genet. 2016 Mar;89(3):275-84. doi: 10.1111/cge.12654. Epub 2015 Sep 22. Review.

PMID:
26283276
18.

The Matchmaker Exchange API: automating patient matching through the exchange of structured phenotypic and genotypic profiles.

Buske OJ, Schiettecatte F, Hutton B, Dumitriu S, Misyura A, Huang L, Hartley T, Girdea M, Sobreira N, Mungall C, Brudno M.

Hum Mutat. 2015 Oct;36(10):922-7. doi: 10.1002/humu.22850.

PMID:
26255989
19.

PhenomeCentral: a portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases.

Buske OJ, Girdea M, Dumitriu S, Gallinger B, Hartley T, Trang H, Misyura A, Friedman T, Beaulieu C, Bone WP, Links AE, Washington NL, Haendel MA, Robinson PN, Boerkoel CF, Adams D, Gahl WA, Boycott KM, Brudno M.

Hum Mutat. 2015 Oct;36(10):931-40. doi: 10.1002/humu.22851. Epub 2015 Aug 31.

PMID:
26251998
20.

High-protein meal challenge reveals the association between the salivary cortisol response and metabolic syndrome in police officers.

Baughman P, Andrew ME, Burchfiel CM, Fekedulegn D, Hartley TA, Violanti JM, Miller DB.

Am J Hum Biol. 2016 Jan-Feb;28(1):138-44. doi: 10.1002/ajhb.22748. Epub 2015 Jun 19.

PMID:
26088798
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