Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 37

1.

Weakly-Emergent Strain-Dependent Properties of High Field Superconductors.

Branch P, Tsui Y, Osamura K, Hampshire DP.

Sci Rep. 2019 Sep 30;9(1):13998. doi: 10.1038/s41598-019-50266-1.

2.

A Bioinformatics Toolkit: In Silico Tools and Online Resources for Investigating Genetic Variation.

Webster SJ, Aldossary MA, Hampshire DJ.

Semin Thromb Hemost. 2019 Oct;45(7):674-684. doi: 10.1055/s-0039-1692978. Epub 2019 Aug 5.

PMID:
31382308
3.

A derivation of Maxwell's equations using the Heaviside notation.

Hampshire DP.

Philos Trans A Math Phys Eng Sci. 2018 Oct 29;376(2134). pii: 20170447. doi: 10.1098/rsta.2017.0447.

4.

The common VWF single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance.

Mufti AH, Ogiwara K, Swystun LL, Eikenboom JCJ, Budde U, Hopman WM, Halldén C, Goudemand J, Peake IR, Goodeve AC, Lillicrap D, Hampshire DJ; European Group on von Willebrand disease (EU-VWD) and Zimmerman Program for the Molecular and Clinical Biology of von Willebrand disease (ZPMCB-VWD) Study Groups.

Blood Adv. 2018 Jul 10;2(13):1585-1594. doi: 10.1182/bloodadvances.2017011643.

5.

The effects of intrauterine infusion of peanut oil on endometrial health, salivary cortisol and interovulatory period in mares.

Campbell MLH, Hampshire D, Hamstead LE, Rose BV, Smith KC, de Mestre AM.

Theriogenology. 2017 Oct 15;102:116-125. doi: 10.1016/j.theriogenology.2017.07.009. Epub 2017 Jul 13.

PMID:
28759834
6.

In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion.

Cartwright A, Peake IR, Goodeve AC, Hampshire DJ.

Haemophilia. 2016 Sep;22(5):e484-7. doi: 10.1111/hae.13059. Epub 2016 Aug 1. No abstract available.

7.

Congenital macrothrombocytopenia is a heterogeneous disorder in India.

Ali S, Ghosh K, Daly ME, Hampshire DJ, Makris M, Ghosh M, Mukherjee L, Bhattacharya M, Shetty S.

Haemophilia. 2016 Jul;22(4):570-82. doi: 10.1111/hae.12917. Epub 2016 Jun 13.

8.

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.

Simeoni I, Stephens JC, Hu F, Deevi SV, Megy K, Bariana TK, Lentaigne C, Schulman S, Sivapalaratnam S, Vries MJ, Westbury SK, Greene D, Papadia S, Alessi MC, Attwood AP, Ballmaier M, Baynam G, Bermejo E, Bertoli M, Bray PF, Bury L, Cattaneo M, Collins P, Daugherty LC, Favier R, French DL, Furie B, Gattens M, Germeshausen M, Ghevaert C, Goodeve AC, Guerrero JA, Hampshire DJ, Hart DP, Heemskerk JW, Henskens YM, Hill M, Hogg N, Jolley JD, Kahr WH, Kelly AM, Kerr R, Kostadima M, Kunishima S, Lambert MP, Liesner R, López JA, Mapeta RP, Mathias M, Millar CM, Nathwani A, Neerman-Arbez M, Nurden AT, Nurden P, Othman M, Peerlinck K, Perry DJ, Poudel P, Reitsma P, Rondina MT, Smethurst PA, Stevenson W, Szkotak A, Tuna S, van Geet C, Whitehorn D, Wilcox DA, Zhang B, Revel-Vilk S, Gresele P, Bellissimo DB, Penkett CJ, Laffan MA, Mumford AD, Rendon A, Gomez K, Freson K, Ouwehand WH, Turro E.

Blood. 2016 Jun 9;127(23):2791-803. doi: 10.1182/blood-2015-12-688267. Epub 2016 Apr 15.

9.

Transcriptional diversity during lineage commitment of human blood progenitors.

Chen L, Kostadima M, Martens JHA, Canu G, Garcia SP, Turro E, Downes K, Macaulay IC, Bielczyk-Maczynska E, Coe S, Farrow S, Poudel P, Burden F, Jansen SBG, Astle WJ, Attwood A, Bariana T, de Bono B, Breschi A, Chambers JC, Consortium B, Choudry FA, Clarke L, Coupland P, van der Ent M, Erber WN, Jansen JH, Favier R, Fenech ME, Foad N, Freson K, van Geet C, Gomez K, Guigo R, Hampshire D, Kelly AM, Kerstens HHD, Kooner JS, Laffan M, Lentaigne C, Labalette C, Martin T, Meacham S, Mumford A, Nürnberg S, Palumbo E, van der Reijden BA, Richardson D, Sammut SJ, Slodkowicz G, Tamuri AU, Vasquez L, Voss K, Watt S, Westbury S, Flicek P, Loos R, Goldman N, Bertone P, Read RJ, Richardson S, Cvejic A, Soranzo N, Ouwehand WH, Stunnenberg HG, Frontini M, Rendon A.

Science. 2014 Sep 26;345(6204):1251033. doi: 10.1126/science.1251033.

11.

p.P2063S: a neutral VWF variant masquerading as a mutation.

Hampshire DJ, Goodeve AC.

Ann Hematol. 2014 Mar;93(3):505-6. doi: 10.1007/s00277-013-1817-y. Epub 2013 Jun 18. No abstract available.

12.

Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort.

Hampshire DJ, Abuzenadah AM, Cartwright A, Al-Shammari NS, Coyle RE, Eckert M, Al-Buhairan AM, Messenger SL, Budde U, Gürsel T, Ingerslev J, Peake IR, Goodeve AC.

Thromb Haemost. 2013 Aug;110(2):264-74. doi: 10.1160/TH13-02-0135. Epub 2013 May 23.

13.

The international society on thrombosis and haematosis von Willebrand disease database: an update.

Hampshire DJ, Goodeve AC.

Semin Thromb Hemost. 2011 Jul;37(5):470-9. doi: 10.1055/s-0031-1281031. Epub 2011 Nov 18. Review.

PMID:
22102189
14.

The molecular basis of von Willebrand disease: the under investigated, the unexpected and the overlooked.

Hampshire DJ, Goodeve AC.

Haematologica. 2011 Jun;96(6):798-800. doi: 10.3324/haematol.2011.046623. No abstract available.

15.

Effect of the VWF promoter (GT)n repeat and single-nucleotide polymorphism c.-2527G>A on circulating von Willebrand factor levels under normal conditions.

Hickson N, Hampshire D, Castaman G, Eikenboom J, Rodeghiero F, Peake I, Goodeve A; MCMDM-1VWD and ZPMCB-VWD Study Groups.

J Thromb Haemost. 2011 Mar;9(3):603-5. doi: 10.1111/j.1538-7836.2010.04161.x. No abstract available.

16.

Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort.

Hampshire DJ, Burghel GJ, Goudemand J, Bouvet LC, Eikenboom JC, Schneppenheim R, Budde U, Peake IR, Goodeve AC; EU-VWD and ZPMCB-VWD study groups.

Haematologica. 2010 Dec;95(12):2163-5. doi: 10.3324/haematol.2010.027177. Epub 2010 Sep 17. No abstract available.

17.

Functional characterization of a 13-bp deletion (c.-1522_-1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease.

Othman M, Chirinian Y, Brown C, Notley C, Hickson N, Hampshire D, Buckley S, Waddington S, Parker AL, Baker A, James P, Lillicrap D.

Blood. 2010 Nov 4;116(18):3645-52. doi: 10.1182/blood-2009-12-261131. Epub 2010 Aug 9.

18.

von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels.

Hickson N, Hampshire D, Winship P, Goudemand J, Schneppenheim R, Budde U, Castaman G, Rodeghiero F, Federici AB, James P, Peake I, Eikenboom J, Goodeve A; MCMDM-1VWD and ZPMCB-VWD study groups.

J Thromb Haemost. 2010 Sep;8(9):1986-93. doi: 10.1111/j.1538-7836.2010.03927.x.

19.

INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse.

Jacoby M, Cox JJ, Gayral S, Hampshire DJ, Ayub M, Blockmans M, Pernot E, Kisseleva MV, Compère P, Schiffmann SN, Gergely F, Riley JH, Pérez-Morga D, Woods CG, Schurmans S.

Nat Genet. 2009 Sep;41(9):1027-31. doi: 10.1038/ng.427. Epub 2009 Aug 9.

PMID:
19668215
20.

The molecular landscape of ASPM mutations in primary microcephaly.

Nicholas AK, Swanson EA, Cox JJ, Karbani G, Malik S, Springell K, Hampshire D, Ahmed M, Bond J, Di Benedetto D, Fichera M, Romano C, Dobyns WB, Woods CG.

J Med Genet. 2009 Apr;46(4):249-53. doi: 10.1136/jmg.2008.062380. Epub 2008 Nov 21.

21.

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.

Ramirez A, Heimbach A, Gründemann J, Stiller B, Hampshire D, Cid LP, Goebel I, Mubaidin AF, Wriekat AL, Roeper J, Al-Din A, Hillmer AM, Karsak M, Liss B, Woods CG, Behrens MI, Kubisch C.

Nat Genet. 2006 Oct;38(10):1184-91. Epub 2006 Sep 10.

PMID:
16964263
22.

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.

Woods CG, Cox J, Springell K, Hampshire DJ, Mohamed MD, McKibbin M, Stern R, Raymond FL, Sandford R, Malik Sharif S, Karbani G, Ahmed M, Bond J, Clayton D, Inglehearn CF.

Am J Hum Genet. 2006 May;78(5):889-896. doi: 10.1086/503875. Epub 2006 Mar 21.

23.

MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34.

Hampshire DJ, Ayub M, Springell K, Roberts E, Jafri H, Rashid Y, Bond J, Riley JH, Woods CG.

Eur J Hum Genet. 2006 May;14(5):543-8.

24.

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size.

Bond J, Roberts E, Springell K, Lizarraga SB, Scott S, Higgins J, Hampshire DJ, Morrison EE, Leal GF, Silva EO, Costa SM, Baralle D, Raponi M, Karbani G, Rashid Y, Jafri H, Bennett C, Corry P, Walsh CA, Woods CG.

Nat Genet. 2005 Apr;37(4):353-5. Epub 2005 Mar 27. Erratum in: Nat Genet. 2005 May;37(5):555. Lizarraga, Sophia [corrected to Lizarraga, Sofia B].

PMID:
15793586
25.

Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome.

Aligianis IA, Johnson CA, Gissen P, Chen D, Hampshire D, Hoffmann K, Maina EN, Morgan NV, Tee L, Morton J, Ainsworth JR, Horn D, Rosser E, Cole TR, Stolte-Dijkstra I, Fieggen K, Clayton-Smith J, Mégarbané A, Shield JP, Newbury-Ecob R, Dobyns WB, Graham JM Jr, Kjaer KW, Warburg M, Bond J, Trembath RC, Harris LW, Takai Y, Mundlos S, Tannahill D, Woods CG, Maher ER.

Nat Genet. 2005 Mar;37(3):221-3.

PMID:
15696165
26.

Protein-truncating mutations in ASPM cause variable reduction in brain size.

Bond J, Scott S, Hampshire DJ, Springell K, Corry P, Abramowicz MJ, Mochida GH, Hennekam RC, Maher ER, Fryns JP, Alswaid A, Jafri H, Rashid Y, Mubaidin A, Walsh CA, Roberts E, Woods CG.

Am J Hum Genet. 2003 Nov;73(5):1170-7. Epub 2003 Oct 21.

27.

Disordered nanocrystalline superconducting PbMo6S8 with a very large upper critical field.

Niu HJ, Hampshire DP.

Phys Rev Lett. 2003 Jul 11;91(2):027002. Epub 2003 Jul 11.

PMID:
12906503
28.

Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum.

Mubaidin A, Roberts E, Hampshire D, Dehyyat M, Shurbaji A, Mubaidien M, Jamil A, Al-Din A, Kurdi A, Woods CG.

J Med Genet. 2003 Jul;40(7):543-6. No abstract available.

29.

A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2.

Leal GF, Roberts E, Silva EO, Costa SM, Hampshire DJ, Woods CG.

J Med Genet. 2003 Jul;40(7):540-2. No abstract available.

30.

Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation.

Roberts E, Hampshire DJ, Pattison L, Springell K, Jafri H, Corry P, Mannon J, Rashid Y, Crow Y, Bond J, Woods CG.

J Med Genet. 2002 Oct;39(10):718-21.

31.

ASPM is a major determinant of cerebral cortical size.

Bond J, Roberts E, Mochida GH, Hampshire DJ, Scott S, Askham JM, Springell K, Mahadevan M, Crow YJ, Markham AF, Walsh CA, Woods CG.

Nat Genet. 2002 Oct;32(2):316-20. Epub 2002 Sep 23.

PMID:
12355089
32.

Identification of microcephalin, a protein implicated in determining the size of the human brain.

Jackson AP, Eastwood H, Bell SM, Adu J, Toomes C, Carr IM, Roberts E, Hampshire DJ, Crow YJ, Mighell AJ, Karbani G, Jafri H, Rashid Y, Mueller RF, Markham AF, Woods CG.

Am J Hum Genet. 2002 Jul;71(1):136-42. Epub 2002 Jun 3.

33.

Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36.

Hampshire DJ, Roberts E, Crow Y, Bond J, Mubaidin A, Wriekat AL, Al-Din A, Woods CG.

J Med Genet. 2001 Oct;38(10):680-2.

34.

Managing survivor symptoms during and after layoffs, mergers, re-engineering initiatives.

Hampshire D, Strasen L.

Strateg Healthc Excell. 1996 Feb;9(2):8-12. No abstract available.

PMID:
10154517
35.

Reversible and irreversible magnetization of the Chevrel-phase superconductor PbMo6S8.

Zheng DN, Ramsbottom HD, Hampshire DP.

Phys Rev B Condens Matter. 1995 Nov 1;52(17):12931-12938. No abstract available.

PMID:
9980464
36.

The evolution of decision support in a managed care organization.

Hampshire DA, Rosborough BJ.

Top Health Care Financ. 1993 Winter;20(2):26-37.

PMID:
8310431
37.

Scaling law and flux pinning in polycrystalline La1.85Sr0.15CuO4.

Hampshire DP, Ikeda JA, Chiang Y.

Phys Rev B Condens Matter. 1989 Nov 1;40(13):8818-8827. No abstract available.

PMID:
9991363

Supplemental Content

Loading ...
Support Center