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Items: 1 to 50 of 70

1.

Work of breathing during HHHFNC and synchronised NIPPV following extubation.

Charles E, Hunt KA, Rafferty GF, Peacock JL, Greenough A.

Eur J Pediatr. 2018 Oct 30. doi: 10.1007/s00431-018-3254-3. [Epub ahead of print]

PMID:
30374754
2.

Small for gestational age and extremely low birth weight infant outcomes.

Charles E, Hunt KA, Harris C, Hickey A, Greenough A.

J Perinat Med. 2018 Oct 18. pii: /j/jpme.ahead-of-print/jpm-2018-0295/jpm-2018-0295.xml. doi: 10.1515/jpm-2018-0295. [Epub ahead of print]

PMID:
30335614
3.

Multiscale analysis of autotroph-heterotroph interactions in a high-temperature microbial community.

Hunt KA, Jennings RM, Inskeep WP, Carlson RP.

PLoS Comput Biol. 2018 Sep 27;14(9):e1006431. doi: 10.1371/journal.pcbi.1006431. eCollection 2018 Sep.

4.

Prediction of bronchopulmonary dysplasia development.

Hunt KA, Dassios T, Ali K, Greenough A.

Arch Dis Child Fetal Neonatal Ed. 2018 Nov;103(6):F598-F599. doi: 10.1136/archdischild-2018-315343. Epub 2018 Jun 12. No abstract available.

PMID:
29895571
5.

Detection of exhaled carbon dioxide following intubation during resuscitation at delivery.

Hunt KA, Yamada Y, Murthy V, Srihari Bhat P, Campbell M, Fox GF, Milner AD, Greenough A.

Arch Dis Child Fetal Neonatal Ed. 2018 Mar 17. pii: fetalneonatal-2017-313982. doi: 10.1136/archdischild-2017-313982. [Epub ahead of print]

PMID:
29550769
6.
7.

Neurally adjusted ventilatory assist compared to other forms of triggered ventilation for neonatal respiratory support.

Rossor TE, Hunt KA, Shetty S, Greenough A.

Cochrane Database Syst Rev. 2017 Oct 27;10:CD012251. doi: 10.1002/14651858.CD012251.pub2. Review.

PMID:
29077984
8.

A multi-zoo investigation of nutrient provision for captive red-crested turacos.

Hulbert AJ, Hunt KA, Rose PE.

Zoo Biol. 2017 Mar;36(2):152-160. doi: 10.1002/zoo.21354. Epub 2017 Feb 16.

PMID:
28206675
9.

Stoichiometric modelling of assimilatory and dissimilatory biomass utilisation in a microbial community.

Hunt KA, Jennings RD, Inskeep WP, Carlson RP.

Environ Microbiol. 2016 Dec;18(12):4946-4960. doi: 10.1111/1462-2920.13444. Epub 2016 Aug 11.

10.

Health and population effects of rare gene knockouts in adult humans with related parents.

Narasimhan VM, Hunt KA, Mason D, Baker CL, Karczewski KJ, Barnes MR, Barnett AH, Bates C, Bellary S, Bockett NA, Giorda K, Griffiths CJ, Hemingway H, Jia Z, Kelly MA, Khawaja HA, Lek M, McCarthy S, McEachan R, O'Donnell-Luria A, Paigen K, Parisinos CA, Sheridan E, Southgate L, Tee L, Thomas M, Xue Y, Schnall-Levin M, Petkov PM, Tyler-Smith C, Maher ER, Trembath RC, MacArthur DG, Wright J, Durbin R, van Heel DA.

Science. 2016 Apr 22;352(6284):474-7. doi: 10.1126/science.aac8624. Epub 2016 Mar 3.

11.

Potential Role of Acetyl-CoA Synthetase (acs) and Malate Dehydrogenase (mae) in the Evolution of the Acetate Switch in Bacteria and Archaea.

Barnhart EP, McClure MA, Johnson K, Cleveland S, Hunt KA, Fields MW.

Sci Rep. 2015 Aug 3;5:12498. doi: 10.1038/srep12498.

12.

The solute specificity profiles of nucleobase cation symporter 1 (NCS1) from Zea mays and Setaria viridis illustrate functional flexibility.

Rapp M, Schein J, Hunt KA, Nalam V, Mourad GS, Schultes NP.

Protoplasma. 2016 Mar;253(2):611-23. doi: 10.1007/s00709-015-0838-x. Epub 2015 May 29.

PMID:
26022088
13.

Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease.

Gutierrez-Achury J, Zhernakova A, Pulit SL, Trynka G, Hunt KA, Romanos J, Raychaudhuri S, van Heel DA, Wijmenga C, de Bakker PI.

Nat Genet. 2015 Jun;47(6):577-8. doi: 10.1038/ng.3268. Epub 2015 Apr 20.

14.

Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up.

Mistry V, Bockett NA, Levine AP, Mirza MM, Hunt KA, Ciclitira PJ, Hummerich H, Neuhausen SL, Simpson MA, Plagnol V, van Heel DA.

PLoS One. 2015 Jan 30;10(1):e0116845. doi: 10.1371/journal.pone.0116845. eCollection 2015.

15.

Complete enumeration of elementary flux modes through scalable demand-based subnetwork definition.

Hunt KA, Folsom JP, Taffs RL, Carlson RP.

Bioinformatics. 2014 Jun 1;30(11):1569-78. doi: 10.1093/bioinformatics/btu021. Epub 2014 Feb 3.

16.

New York State Health Foundation: integrating mental health and substance abuse care.

Isaacs S, Jellinek P, Martinez Garcel J, Hunt KA, Bunch W.

Health Aff (Millwood). 2013 Oct;32(10):1846-50. doi: 10.1377/hlthaff.2013.0479.

PMID:
24101075
17.

The nucleobase cation symporter 1 of Chlamydomonas reinhardtii and that of the evolutionarily distant Arabidopsis thaliana display parallel function and establish a plant-specific solute transport profile.

Schein JR, Hunt KA, Minton JA, Schultes NP, Mourad GS.

Plant Physiol Biochem. 2013 Sep;70:52-60. doi: 10.1016/j.plaphy.2013.05.015. Epub 2013 May 25.

PMID:
23770594
18.

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.

Hunt KA, Mistry V, Bockett NA, Ahmad T, Ban M, Barker JN, Barrett JC, Blackburn H, Brand O, Burren O, Capon F, Compston A, Gough SC, Jostins L, Kong Y, Lee JC, Lek M, MacArthur DG, Mansfield JC, Mathew CG, Mein CA, Mirza M, Nutland S, Onengut-Gumuscu S, Papouli E, Parkes M, Rich SS, Sawcer S, Satsangi J, Simmonds MJ, Trembath RC, Walker NM, Wozniak E, Todd JA, Simpson MA, Plagnol V, van Heel DA.

Nature. 2013 Jun 13;498(7453):232-5. doi: 10.1038/nature12170. Epub 2013 May 22.

19.

Genetic and molecular characterization reveals a unique nucleobase cation symporter 1 in Arabidopsis.

Mourad GS, Tippmann-Crosby J, Hunt KA, Gicheru Y, Bade K, Mansfield TA, Schultes NP.

FEBS Lett. 2012 May 7;586(9):1370-8. doi: 10.1016/j.febslet.2012.03.058. Epub 2012 Apr 3.

20.

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.

Hunt KA, Smyth DJ, Balschun T, Ban M, Mistry V, Ahmad T, Anand V, Barrett JC, Bhaw-Rosun L, Bockett NA, Brand OJ, Brouwer E, Concannon P, Cooper JD, Dias KR, van Diemen CC, Dubois PC, Edkins S, Fölster-Holst R, Fransen K, Glass DN, Heap GA, Hofmann S, Huizinga TW, Hunt S, Langford C, Lee J, Mansfield J, Marrosu MG, Mathew CG, Mein CA, Müller-Quernheim J, Nutland S, Onengut-Gumuscu S, Ouwehand W, Pearce K, Prescott NJ, Posthumus MD, Potter S, Rosati G, Sambrook J, Satsangi J, Schreiber S, Shtir C, Simmonds MJ, Sudman M, Thompson SD, Toes R, Trynka G, Vyse TJ, Walker NM, Weidinger S, Zhernakova A, Zoledziewska M; Type 1 Diabetes Genetics Consortium; UK Inflammatory Bowel Disease (IBD) Genetics Consortium; Wellcome Trust Case Control Consortium, Weersma RK, Gough SC, Sawcer S, Wijmenga C, Parkes M, Cucca F, Franke A, Deloukas P, Rich SS, Todd JA, van Heel DA.

Nat Genet. 2011 Dec 27;44(1):3-5. doi: 10.1038/ng.1037. No abstract available.

21.

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

Trynka G, Hunt KA, Bockett NA, Romanos J, Mistry V, Szperl A, Bakker SF, Bardella MT, Bhaw-Rosun L, Castillejo G, de la Concha EG, de Almeida RC, Dias KR, van Diemen CC, Dubois PC, Duerr RH, Edkins S, Franke L, Fransen K, Gutierrez J, Heap GA, Hrdlickova B, Hunt S, Plaza Izurieta L, Izzo V, Joosten LA, Langford C, Mazzilli MC, Mein CA, Midah V, Mitrovic M, Mora B, Morelli M, Nutland S, Núñez C, Onengut-Gumuscu S, Pearce K, Platteel M, Polanco I, Potter S, Ribes-Koninckx C, Ricaño-Ponce I, Rich SS, Rybak A, Santiago JL, Senapati S, Sood A, Szajewska H, Troncone R, Varadé J, Wallace C, Wolters VM, Zhernakova A; Spanish Consortium on the Genetics of Coeliac Disease (CEGEC); PreventCD Study Group; Wellcome Trust Case Control Consortium (WTCCC), Thelma BK, Cukrowska B, Urcelay E, Bilbao JR, Mearin ML, Barisani D, Barrett JC, Plagnol V, Deloukas P, Wijmenga C, van Heel DA.

Nat Genet. 2011 Nov 6;43(12):1193-201. doi: 10.1038/ng.998.

22.

Construction and elementary mode analysis of a metabolic model for Shewanella oneidensis MR-1.

Flynn CM, Hunt KA, Gralnick JA, Srienc F.

Biosystems. 2012 Feb;107(2):120-8. doi: 10.1016/j.biosystems.2011.10.003. Epub 2011 Oct 17.

PMID:
22024451
23.
24.

Enabling unbalanced fermentations by using engineered electrode-interfaced bacteria.

Flynn JM, Ross DE, Hunt KA, Bond DR, Gralnick JA.

MBio. 2010 Nov 2;1(5). pii: e00190-10. doi: 10.1128/mBio.00190-10.

25.

Structure, function, and insights into the biosynthesis of a head-to-head hydrocarbon in Shewanella oneidensis strain MR-1.

Sukovich DJ, Seffernick JL, Richman JE, Hunt KA, Gralnick JA, Wackett LP.

Appl Environ Microbiol. 2010 Jun;76(12):3842-9. doi: 10.1128/AEM.00433-10. Epub 2010 Apr 23.

26.

Substrate-level phosphorylation is the primary source of energy conservation during anaerobic respiration of Shewanella oneidensis strain MR-1.

Hunt KA, Flynn JM, Naranjo B, Shikhare ID, Gralnick JA.

J Bacteriol. 2010 Jul;192(13):3345-51. doi: 10.1128/JB.00090-10. Epub 2010 Apr 16.

27.

Multiple common variants for celiac disease influencing immune gene expression.

Dubois PC, Trynka G, Franke L, Hunt KA, Romanos J, Curtotti A, Zhernakova A, Heap GA, Adány R, Aromaa A, Bardella MT, van den Berg LH, Bockett NA, de la Concha EG, Dema B, Fehrmann RS, Fernández-Arquero M, Fiatal S, Grandone E, Green PM, Groen HJ, Gwilliam R, Houwen RH, Hunt SE, Kaukinen K, Kelleher D, Korponay-Szabo I, Kurppa K, MacMathuna P, Mäki M, Mazzilli MC, McCann OT, Mearin ML, Mein CA, Mirza MM, Mistry V, Mora B, Morley KI, Mulder CJ, Murray JA, Núñez C, Oosterom E, Ophoff RA, Polanco I, Peltonen L, Platteel M, Rybak A, Salomaa V, Schweizer JJ, Sperandeo MP, Tack GJ, Turner G, Veldink JH, Verbeek WH, Weersma RK, Wolters VM, Urcelay E, Cukrowska B, Greco L, Neuhausen SL, McManus R, Barisani D, Deloukas P, Barrett JC, Saavalainen P, Wijmenga C, van Heel DA.

Nat Genet. 2010 Apr;42(4):295-302. doi: 10.1038/ng.543. Epub 2010 Feb 28. Erratum in: Nat Genet.2010 May;42(5):465.

28.

Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.

Heap GA, Yang JH, Downes K, Healy BC, Hunt KA, Bockett N, Franke L, Dubois PC, Mein CA, Dobson RJ, Albert TJ, Rodesch MJ, Clayton DG, Todd JA, van Heel DA, Plagnol V.

Hum Mol Genet. 2010 Jan 1;19(1):122-34. doi: 10.1093/hmg/ddp473.

29.

Recent advances in coeliac disease genetics.

Hunt KA, van Heel DA.

Gut. 2009 Apr;58(4):473-6. doi: 10.1136/gut.2008.155879. Review. No abstract available.

PMID:
19299378
30.

Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling.

Trynka G, Zhernakova A, Romanos J, Franke L, Hunt KA, Turner G, Bruinenberg M, Heap GA, Platteel M, Ryan AW, de Kovel C, Holmes GK, Howdle PD, Walters JR, Sanders DS, Mulder CJ, Mearin ML, Verbeek WH, Trimble V, Stevens FM, Kelleher D, Barisani D, Bardella MT, McManus R, van Heel DA, Wijmenga C.

Gut. 2009 Aug;58(8):1078-83. doi: 10.1136/gut.2008.169052. Epub 2009 Feb 24.

PMID:
19240061
31.

Complex nature of SNP genotype effects on gene expression in primary human leucocytes.

Heap GA, Trynka G, Jansen RC, Bruinenberg M, Swertz MA, Dinesen LC, Hunt KA, Wijmenga C, Vanheel DA, Franke L.

BMC Med Genomics. 2009 Jan 7;2:1. doi: 10.1186/1755-8794-2-1.

32.

Shared and distinct genetic variants in type 1 diabetes and celiac disease.

Smyth DJ, Plagnol V, Walker NM, Cooper JD, Downes K, Yang JH, Howson JM, Stevens H, McManus R, Wijmenga C, Heap GA, Dubois PC, Clayton DG, Hunt KA, van Heel DA, Todd JA.

N Engl J Med. 2008 Dec 25;359(26):2767-77. doi: 10.1056/NEJMoa0807917. Epub 2008 Dec 10.

33.

Suspicious breast lesions: assessment of 3D Doppler US indexes for classification in a test population and fourfold cross-validation scheme.

LeCarpentier GL, Roubidoux MA, Fowlkes JB, Krücker JF, Hunt KA, Paramagul C, Johnson TD, Thorson NJ, Engle KD, Carson PL.

Radiology. 2008 Nov;249(2):463-70. doi: 10.1148/radiol.2492060888.

34.

Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.

Franke L, de Kovel CG, Aulchenko YS, Trynka G, Zhernakova A, Hunt KA, Blauw HM, van den Berg LH, Ophoff R, Deloukas P, van Heel DA, Wijmenga C.

Am J Hum Genet. 2008 Jun;82(6):1316-33. doi: 10.1016/j.ajhg.2008.05.008.

35.

No evidence in a large UK collection for celiac disease risk variants reported by a Spanish study.

Hunt KA, Franke L, Deloukas P, Wijmenga C, van Heel DA.

Gastroenterology. 2008 May;134(5):1629-30; author reply 1630-1. doi: 10.1053/j.gastro.2008.03.068. No abstract available.

36.

Are the uninsured responsible for the increase in emergency department visits in the United States?

Weber EJ, Showstack JA, Hunt KA, Colby DC, Grimes B, Bacchetti P, Callaham ML.

Ann Emerg Med. 2008 Aug;52(2):108-15. doi: 10.1016/j.annemergmed.2008.01.327. Epub 2008 Apr 14.

PMID:
18407374
37.

Newly identified genetic risk variants for celiac disease related to the immune response.

Hunt KA, Zhernakova A, Turner G, Heap GA, Franke L, Bruinenberg M, Romanos J, Dinesen LC, Ryan AW, Panesar D, Gwilliam R, Takeuchi F, McLaren WM, Holmes GK, Howdle PD, Walters JR, Sanders DS, Playford RJ, Trynka G, Mulder CJ, Mearin ML, Verbeek WH, Trimble V, Stevens FM, O'Morain C, Kennedy NP, Kelleher D, Pennington DJ, Strachan DP, McArdle WL, Mein CA, Wapenaar MC, Deloukas P, McGinnis R, McManus R, Wijmenga C, van Heel DA.

Nat Genet. 2008 Apr;40(4):395-402. doi: 10.1038/ng.102. Epub 2008 Mar 2.

38.

Disparities in health: perspectives of a multi-ethnic, multi-racial America.

Blendon RJ, Buhr T, Cassidy EF, Perez DJ, Hunt KA, Fleischfresser C, Benson JM, Herrmann MJ.

Health Aff (Millwood). 2007 Sep-Oct;26(5):1437-47.

PMID:
17848456
39.

Recurrent cancer after breast-conserving surgery with radiation therapy for ductal carcinoma in situ: mammographic features, method of detection, and stage of recurrence.

Pinsky RW, Rebner M, Pierce LJ, Ben-David MA, Vicini F, Hunt KA, Helvie MA.

AJR Am J Roentgenol. 2007 Jul;189(1):140-4.

PMID:
17579163
40.

A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.

van Heel DA, Franke L, Hunt KA, Gwilliam R, Zhernakova A, Inouye M, Wapenaar MC, Barnardo MC, Bethel G, Holmes GK, Feighery C, Jewell D, Kelleher D, Kumar P, Travis S, Walters JR, Sanders DS, Howdle P, Swift J, Playford RJ, McLaren WM, Mearin ML, Mulder CJ, McManus R, McGinnis R, Cardon LR, Deloukas P, Wijmenga C.

Nat Genet. 2007 Jul;39(7):827-9. Epub 2007 Jun 10.

41.

Genetic variation in myosin IXB is associated with ulcerative colitis.

van Bodegraven AA, Curley CR, Hunt KA, Monsuur AJ, Linskens RK, Onnie CM, Crusius JB, Annese V, Latiano A, Silverberg MS, Bitton A, Fisher SA, Steinhart AH, Forbes A, Sanderson J, Prescott NJ, Strachan DP, Playford RJ, Mathew CG, Wijmenga C, Daly MJ, Rioux JD, van Heel DA.

Gastroenterology. 2006 Dec;131(6):1768-74. Epub 2006 Sep 8.

PMID:
17087940
42.

Health care organizations' use of data on race/ethnicity to address disparities in health care.

Nerenz DR, Hunt KA, Escarce JJ.

Health Serv Res. 2006 Aug;41(4 Pt 1):1444-50. No abstract available.

43.

Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's disease.

van Heel DA, Hunt KA, King K, Ghosh S, Gabe SM, Mathew CG, Forbes A, Playford RJ.

Inflamm Bowel Dis. 2006 Jul;12(7):598-605.

PMID:
16804397
44.

Characteristics of frequent users of emergency departments.

Hunt KA, Weber EJ, Showstack JA, Colby DC, Callaham ML.

Ann Emerg Med. 2006 Jul;48(1):1-8. Epub 2006 Mar 30.

PMID:
16781914
45.
46.

Lack of association of MYO9B genetic variants with coeliac disease in a British cohort.

Hunt KA, Monsuur AJ, McArdle WL, Kumar PJ, Travis SP, Walters JR, Jewell DP, Strachan DP, Playford RJ, Wijmenga C, van Heel DA.

Gut. 2006 Jul;55(7):969-72. Epub 2006 Jan 19.

47.

Clinical and radiologic assessments to predict breast cancer pathologic complete response to neoadjuvant chemotherapy.

Schott AF, Roubidoux MA, Helvie MA, Hayes DF, Kleer CG, Newman LA, Pierce LJ, Griffith KA, Murray S, Hunt KA, Paramagul C, Baker LH.

Breast Cancer Res Treat. 2005 Aug;92(3):231-8.

48.

Synergy between TLR9 and NOD2 innate immune responses is lost in genetic Crohn's disease.

van Heel DA, Ghosh S, Hunt KA, Mathew CG, Forbes A, Jewell DP, Playford RJ.

Gut. 2005 Nov;54(11):1553-7. Epub 2005 May 31.

49.

Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease.

van Heel DA, Ghosh S, Butler M, Hunt KA, Lundberg AM, Ahmad T, McGovern DP, Onnie C, Negoro K, Goldthorpe S, Foxwell BM, Mathew CG, Forbes A, Jewell DP, Playford RJ.

Lancet. 2005 May 21-27;365(9473):1794-6.

PMID:
15910952
50.

Racial and ethnic disparities and perceptions of health care: does health plan type matter?

Hunt KA, Gaba A, Lavizzo-Mourey R.

Health Serv Res. 2005 Apr;40(2):551-76.

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