Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 28

1.

The employment gap: the relationship between medical student career choices and the future needs of the New Zealand medical workforce.

Seleq S, Jo E, Poole P, Wilkinson T, Hyland F, Rudland J, Verstappen A, Bagg W.

N Z Med J. 2019 Nov 8;132(1505):52-59.

PMID:
31778372
2.

Developing New Zealand's medical workforce: realising the potential of longitudinal career tracking.

Poole P, Wilkinson TJ, Bagg W, Freegard J, Hyland F, Jo CE, Kool B, Roberts E, Rudland J, Smith B, Verstappen A.

N Z Med J. 2019 May 17;132(1495):65-73.

PMID:
31095546
3.

A scalable solution for tumor mutational burden from formalin-fixed, paraffin-embedded samples using the Oncomine Tumor Mutation Load Assay.

Chaudhary R, Quagliata L, Martin JP, Alborelli I, Cyanam D, Mittal V, Tom W, Au-Young J, Sadis S, Hyland F.

Transl Lung Cancer Res. 2018 Dec;7(6):616-630. doi: 10.21037/tlcr.2018.08.01.

4.

User involvement in digital health: Working together to design smart home health technology.

Burrows A, Meller B, Craddock I, Hyland F, Gooberman-Hill R.

Health Expect. 2019 Feb;22(1):65-73. doi: 10.1111/hex.12831. Epub 2018 Oct 5.

5.

Analytical Validation of a Next-Generation Sequencing Assay to Monitor Immune Responses in Solid Tumors.

Conroy JM, Pabla S, Glenn ST, Burgher B, Nesline M, Papanicolau-Sengos A, Andreas J, Giamo V, Lenzo FL, Hyland FCL, Omilian A, Bshara W, Qin M, He J, Puzanov I, Ernstoff MS, Gardner M, Galluzzi L, Morrison C.

J Mol Diagn. 2018 Jan;20(1):95-109. doi: 10.1016/j.jmoldx.2017.10.001. Epub 2017 Oct 20.

PMID:
29061374
6.

Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.

Lubin IM, Aziz N, Babb LJ, Ballinger D, Bisht H, Church DM, Cordes S, Eilbeck K, Hyland F, Kalman L, Landrum M, Lockhart ER, Maglott D, Marth G, Pfeifer JD, Rehm HL, Roy S, Tezak Z, Truty R, Ullman-Cullere M, Voelkerding KV, Worthey EA, Zaranek AW, Zook JM.

J Mol Diagn. 2017 May;19(3):417-426. doi: 10.1016/j.jmoldx.2016.12.001. Epub 2017 Mar 18.

7.

Extensive sequencing of seven human genomes to characterize benchmark reference materials.

Zook JM, Catoe D, McDaniel J, Vang L, Spies N, Sidow A, Weng Z, Liu Y, Mason CE, Alexander N, Henaff E, McIntyre AB, Chandramohan D, Chen F, Jaeger E, Moshrefi A, Pham K, Stedman W, Liang T, Saghbini M, Dzakula Z, Hastie A, Cao H, Deikus G, Schadt E, Sebra R, Bashir A, Truty RM, Chang CC, Gulbahce N, Zhao K, Ghosh S, Hyland F, Fu Y, Chaisson M, Xiao C, Trow J, Sherry ST, Zaranek AW, Ball M, Bobe J, Estep P, Church GM, Marks P, Kyriazopoulou-Panagiotopoulou S, Zheng GX, Schnall-Levin M, Ordonez HS, Mudivarti PA, Giorda K, Sheng Y, Rypdal KB, Salit M.

Sci Data. 2016 Jun 7;3:160025. doi: 10.1038/sdata.2016.25.

8.

Good laboratory practice for clinical next-generation sequencing informatics pipelines.

Gargis AS, Kalman L, Bick DP, da Silva C, Dimmock DP, Funke BH, Gowrisankar S, Hegde MR, Kulkarni S, Mason CE, Nagarajan R, Voelkerding KV, Worthey EA, Aziz N, Barnes J, Bennett SF, Bisht H, Church DM, Dimitrova Z, Gargis SR, Hafez N, Hambuch T, Hyland FC, Luna RA, MacCannell D, Mann T, McCluskey MR, McDaniel TK, Ganova-Raeva LM, Rehm HL, Reid J, Campo DS, Resnick RB, Ridge PG, Salit ML, Skums P, Wong LJ, Zehnbauer BA, Zook JM, Lubin IM.

Nat Biotechnol. 2015 Jul;33(7):689-93. doi: 10.1038/nbt.3237. No abstract available.

9.

Development and validation of a scalable next-generation sequencing system for assessing relevant somatic variants in solid tumors.

Hovelson DH, McDaniel AS, Cani AK, Johnson B, Rhodes K, Williams PD, Bandla S, Bien G, Choppa P, Hyland F, Gottimukkala R, Liu G, Manivannan M, Schageman J, Ballesteros-Villagrana E, Grasso CS, Quist MJ, Yadati V, Amin A, Siddiqui J, Betz BL, Knudsen KE, Cooney KA, Feng FY, Roh MH, Nelson PS, Liu CJ, Beer DG, Wyngaard P, Chinnaiyan AM, Sadis S, Rhodes DR, Tomlins SA.

Neoplasia. 2015 Apr;17(4):385-99. doi: 10.1016/j.neo.2015.03.004.

10.

Characterizing the heterogeneity of triple-negative breast cancers using microdissected normal ductal epithelium and RNA-sequencing.

Radovich M, Clare SE, Atale R, Pardo I, Hancock BA, Solzak JP, Kassem N, Mathieson T, Storniolo AM, Rufenbarger C, Lillemoe HA, Blosser RJ, Choi MR, Sauder CA, Doxey D, Henry JE, Hilligoss EE, Sakarya O, Hyland FC, Hickenbotham M, Zhu J, Glasscock J, Badve S, Ivan M, Liu Y, Sledge GW, Schneider BP.

Breast Cancer Res Treat. 2014 Jan;143(1):57-68. doi: 10.1007/s10549-013-2780-y. Epub 2013 Nov 29.

11.

RNA-Seq mapping and detection of gene fusions with a suffix array algorithm.

Sakarya O, Breu H, Radovich M, Chen Y, Wang YN, Barbacioru C, Utiramerur S, Whitley PP, Brockman JP, Vatta P, Zhang Z, Popescu L, Muller MW, Kudlingar V, Garg N, Li CY, Kong BS, Bodeau JP, Nutter RC, Gu J, Bramlett KS, Ichikawa JK, Hyland FC, Siddiqui AS.

PLoS Comput Biol. 2012;8(4):e1002464. doi: 10.1371/journal.pcbi.1002464. Epub 2012 Apr 5.

12.

Expanding data and resources for forensic use of SNPs in individual identification.

Kidd KK, Kidd JR, Speed WC, Fang R, Furtado MR, Hyland FC, Pakstis AJ.

Forensic Sci Int Genet. 2012 Sep;6(5):646-52. doi: 10.1016/j.fsigen.2012.02.012. Epub 2012 Mar 22.

PMID:
22445421
13.

SNPs for a universal individual identification panel.

Pakstis AJ, Speed WC, Fang R, Hyland FC, Furtado MR, Kidd JR, Kidd KK.

Hum Genet. 2010 Mar;127(3):315-24. doi: 10.1007/s00439-009-0771-1.

PMID:
19937056
14.

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding.

McKernan KJ, Peckham HE, Costa GL, McLaughlin SF, Fu Y, Tsung EF, Clouser CR, Duncan C, Ichikawa JK, Lee CC, Zhang Z, Ranade SS, Dimalanta ET, Hyland FC, Sokolsky TD, Zhang L, Sheridan A, Fu H, Hendrickson CL, Li B, Kotler L, Stuart JR, Malek JA, Manning JM, Antipova AA, Perez DS, Moore MP, Hayashibara KC, Lyons MR, Beaudoin RE, Coleman BE, Laptewicz MW, Sannicandro AE, Rhodes MD, Gottimukkala RK, Yang S, Bafna V, Bashir A, MacBride A, Alkan C, Kidd JM, Eichler EE, Reese MG, De La Vega FM, Blanchard AP.

Genome Res. 2009 Sep;19(9):1527-41. doi: 10.1101/gr.091868.109. Epub 2009 Jun 22.

15.

Facility-based equipment and capital expenditures. 2008 a roundtable. Decision-makers discuss their purchasing strategies.

Brasser BA, Hyland F, Bennett A, Liston J.

Rehab Manag. 2008 Jan-Feb;21(1):24, 26-8. No abstract available.

PMID:
18335788
16.

Validation of the performance of a comprehensive genotyping assay panel of single nucleotide polymorphisms in drug metabolism enzyme genes.

Welch RA, Lazaruk K, Haque KA, Hyland F, Xiao N, Wronka L, Burdett L, Chanock SJ, Ingber D, De La Vega FM, Yeager M.

Hum Mutat. 2008 May;29(5):750-6. doi: 10.1002/humu.20703.

PMID:
18327779
17.

A second-generation combined linkage physical map of the human genome.

Matise TC, Chen F, Chen W, De La Vega FM, Hansen M, He C, Hyland FC, Kennedy GC, Kong X, Murray SS, Ziegle JS, Stewart WC, Buyske S.

Genome Res. 2007 Dec;17(12):1783-6. Epub 2007 Nov 7.

18.

Patterns of linkage disequilibrium between SNPs in a Sardinian population isolate and the selection of markers for association studies.

Angius A, Hyland FC, Persico I, Pirastu N, Woodage T, Pirastu M, De la Vega FM.

Hum Hered. 2008;65(1):9-22. Epub 2007 Jul 25.

PMID:
17652959
19.

Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel.

Phillips C, Fang R, Ballard D, Fondevila M, Harrison C, Hyland F, Musgrave-Brown E, Proff C, Ramos-Luis E, Sobrino B, Carracedo A, Furtado MR, Syndercombe Court D, Schneider PM; SNPforID Consortium.

Forensic Sci Int Genet. 2007 Jun;1(2):180-5. doi: 10.1016/j.fsigen.2007.02.007. Epub 2007 Mar 23.

PMID:
19083752
20.

Large scale real-time PCR validation on gene expression measurements from two commercial long-oligonucleotide microarrays.

Wang Y, Barbacioru C, Hyland F, Xiao W, Hunkapiller KL, Blake J, Chan F, Gonzalez C, Zhang L, Samaha RR.

BMC Genomics. 2006 Mar 21;7:59.

21.

Perceived stress and coronary heart disease risk factors: the contribution of socio-economic position.

Heslop P, Smith GD, Carroll D, Macleod J, Hyland F, Hart C.

Br J Health Psychol. 2001 May;6(Pt 2):167-78.

PMID:
14596732
22.

Women's views of consultations about familial risk of breast cancer in primary care.

Grande GE, Hyland F, Walter FM, Kinmonth AL.

Patient Educ Couns. 2002 Dec;48(3):275-82.

PMID:
12477612
23.

Experiences and expectations of the new genetics in relation to familial risk of breast cancer: a comparison of the views of GPs and practice nurses.

Walter FM, Kinmonth AL, Hyland F, Murrell P, Marteau TM, Todd C.

Fam Pract. 2001 Oct;18(5):491-4.

PMID:
11604369
24.

Raising concerns about family history of breast cancer in primary care consultations: prospective, population based study. Women's Concerns Study Group.

Hyland F, Kinmonth AL, Marteau TM, Griffin S, Murrell P, Spiegelhalter D, Todd C, Walter F, Berrington B, Bobrow M, Mackay J.

BMJ. 2001 Jan 6;322(7277):27-8. No abstract available.

25.

The history of breast v. bottle.

Hyland F.

Community Outlook. 1990 Mar 14:25-8. No abstract available.

PMID:
2180630
26.

Breastfeeding: for those who won't.

Hyland F.

Community Outlook. 1988 Nov 9:11-2. No abstract available.

PMID:
3203506
27.

Raynaud's disease.

Hyland F.

Nurs Times. 1985 Apr 24-30;81(17):36. No abstract available.

PMID:
3846936
28.

The albumin autoagglutination phenomenon.

CROWLEY LV, HYLAND FR.

Am J Clin Pathol. 1962 Mar;37:244-7. No abstract available.

PMID:
13882439

Supplemental Content

Loading ...
Support Center