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Items: 1 to 20 of 66

1.

A comparison of Landsat 8, RapidEye and Pleiades products for improving empirical predictions of satellite-derived bathymetry.

Cahalane C, Magee A, Monteys X, Casal G, Hanafin J, Harris P.

Remote Sens Environ. 2019 Nov;233:111414. doi: 10.1016/j.rse.2019.111414.

2.

Response to: Commentary on: Bright et al. (2018) Internal validation of STRmix™ - A multi laboratory response to PCAST, Forensic Science International: Genetics, 34: 11-24.

Buckleton JS, Bright JA, Ciecko A, Kruijver M, Mallinder B, Magee A, Malsom S, Moretti T, Weitz S, Bille T, Noël S, Oefelein RH, Peck B, Kalafut T, Taylor DA.

Forensic Sci Int Genet. 2020 Jan;44:102198. doi: 10.1016/j.fsigen.2019.102198. Epub 2019 Nov 4. No abstract available.

PMID:
31710898
3.

XMAP215 promotes microtubule-F-actin interactions to regulate growth cone microtubules during axon guidance in Xenopus laevis.

Slater PG, Cammarata GM, Samuelson AG, Magee A, Hu Y, Lowery LA.

J Cell Sci. 2019 Apr 30;132(9). pii: jcs224311. doi: 10.1242/jcs.224311.

4.

Severe Migraine Associated With Nickel Allergy Requiring Surgical Removal of Atrial Septal Device.

Fernandes P, Sharma SR, Magee A, Michielon G, Fraisse A.

Ann Thorac Surg. 2019 Sep;108(3):e183-e184. doi: 10.1016/j.athoracsur.2019.01.034. Epub 2019 Feb 19.

PMID:
30794784
5.

Correction: Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.

Tatton-Brown K, Hanks S, Ruark E, Zachariou A, Del Vecchio Duarte S, Ramsay E, Snape K, Murray A, Perdeaux ER, Seal S, Loveday C, Banka S, Clericuzio C, Flinter F, Magee A, McConnell V, Patton M, Raith W, Rankin J, Splitt M, Strenger V, Taylor C, Wheeler P, Temple IK, Cole T; Childhood Overgrowth Collaboration, Douglas J, Rahman N.

Oncotarget. 2018 Nov 30;9(94):36719. doi: 10.18632/oncotarget.26429. eCollection 2018 Nov 30.

6.

Noma surgery.

Shaye DA, Winters R, Rabbels J, Adentunji AS, Magee A, Vo D.

Laryngoscope. 2019 Jan;129(1):96-99. doi: 10.1002/lary.27230. Epub 2018 Sep 8.

PMID:
30194753
7.

Evaluation of the Noma Disease Burden Within the Noma Belt.

Shaye DA, Rabbels J, Adetunji AS, Magee A, Vo D, Winters R.

JAMA Facial Plast Surg. 2018 Jul 1;20(4):332-333. doi: 10.1001/jamafacial.2018.0133. No abstract available.

8.

The effect of history of abnormal pap smear or preceding HPV infection on the humoral immune response to Quadrivalent Human Papilloma virus (qHPV) vaccine in women with systemic lupus erythematosus.

Dhar JP, Essenmacher L, Dhar R, Magee A, Ager J, Sokol RJ.

Hum Vaccin Immunother. 2018;14(9):2318-2322. doi: 10.1080/21645515.2018.1469592. Epub 2018 Jun 8.

9.

A Trib2-p38 axis controls myeloid leukaemia cell cycle and stress response signalling.

Salomé M, Magee A, Yalla K, Chaudhury S, Sarrou E, Carmody RJ, Keeshan K.

Cell Death Dis. 2018 May 1;9(5):443. doi: 10.1038/s41419-018-0467-3.

10.

Internal validation of STRmix™ - A multi laboratory response to PCAST.

Bright JA, Richards R, Kruijver M, Kelly H, McGovern C, Magee A, McWhorter A, Ciecko A, Peck B, Baumgartner C, Buettner C, McWilliams S, McKenna C, Gallacher C, Mallinder B, Wright D, Johnson D, Catella D, Lien E, O'Connor C, Duncan G, Bundy J, Echard J, Lowe J, Stewart J, Corrado K, Gentile S, Kaplan M, Hassler M, McDonald N, Hulme P, Oefelein RH, Montpetit S, Strong M, Noël S, Malsom S, Myers S, Welti S, Moretti T, McMahon T, Grill T, Kalafut T, Greer-Ritzheimer M, Beamer V, Taylor DA, Buckleton JS.

Forensic Sci Int Genet. 2018 May;34:11-24. doi: 10.1016/j.fsigen.2018.01.003. Epub 2018 Jan 8.

PMID:
29367014
11.

Bioimpedance spectroscopy measurements of phase angle and height for age are predictive of outcome in children following surgery for congenital heart disease.

Marino LV, Meyer R, Johnson M, Newell C, Johnstone C, Magee A, Sykes K, Wootton SA, Pappachan JV.

Clin Nutr. 2018 Aug;37(4):1430-1436. doi: 10.1016/j.clnu.2017.06.020. Epub 2017 Jun 28.

PMID:
28684015
12.

The safety and immunogenicity of Quadrivalent HPV (qHPV) vaccine in systemic lupus erythematosus.

Dhar JP, Essenmacher L, Dhar R, Magee A, Ager J, Sokol RJ.

Vaccine. 2017 May 9;35(20):2642-2646. doi: 10.1016/j.vaccine.2017.04.001. Epub 2017 Apr 9.

PMID:
28404357
13.

CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis.

Hengel H, Magee A, Mahanjah M, Vallat JM, Ouvrier R, Abu-Rashid M, Mahamid J, Schüle R, Schulze M, Krägeloh-Mann I, Bauer P, Züchner S, Sharkia R, Schöls L.

Neurol Genet. 2017 Mar 22;3(2):e144. doi: 10.1212/NXG.0000000000000144. eCollection 2017 Apr.

14.

A Plant-Based Nutrition Program.

Evans J, Magee A, Dickman K, Sutter R, Sutter C.

Am J Nurs. 2017 Mar;117(3):56-61. doi: 10.1097/01.NAJ.0000513289.14377.0f.

PMID:
28230693
15.

De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome.

Sleven H, Welsh SJ, Yu J, Churchill MEA, Wright CF, Henderson A, Horvath R, Rankin J, Vogt J, Magee A, McConnell V, Green A, King MD, Cox H, Armstrong L, Lehman A, Nelson TN; Deciphering Developmental Disorders study; CAUSES study, Williams J, Clouston P, Hagman J, Németh AH.

Am J Hum Genet. 2017 Jan 5;100(1):138-150. doi: 10.1016/j.ajhg.2016.11.020. Epub 2016 Dec 23.

16.

Mutations in Histone Acetylase Modifier BRPF1 Cause an Autosomal-Dominant Form of Intellectual Disability with Associated Ptosis.

Mattioli F, Schaefer E, Magee A, Mark P, Mancini GM, Dieterich K, Von Allmen G, Alders M, Coutton C, van Slegtenhorst M, Vieville G, Engelen M, Cobben JM, Juusola J, Pujol A, Mandel JL, Piton A.

Am J Hum Genet. 2017 Jan 5;100(1):105-116. doi: 10.1016/j.ajhg.2016.11.010. Epub 2016 Dec 8.

17.

Techniques for transcatheter retrieval of the occlutech ASD device United Kingdom-European multicenter report.

Shebani SO, Rehman R, Taliotis D, Magee A, Hayes NJ, Baspinar O, Martínez Z, Haas N, Duke C.

Catheter Cardiovasc Interv. 2017 Mar 1;89(4):690-698. doi: 10.1002/ccd.26838. Epub 2016 Nov 10.

PMID:
27860188
18.

Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region.

Vallat JM, Nizon M, Magee A, Isidor B, Magy L, Péréon Y, Richard L, Ouvrier R, Cogné B, Devaux J, Zuchner S, Mathis S.

J Neuropathol Exp Neurol. 2016 Dec 1;75(12):1155-1159. doi: 10.1093/jnen/nlw093.

19.

Clinical and genetic aspects of KBG syndrome.

Low K, Ashraf T, Canham N, Clayton-Smith J, Deshpande C, Donaldson A, Fisher R, Flinter F, Foulds N, Fryer A, Gibson K, Hayes I, Hills A, Holder S, Irving M, Joss S, Kivuva E, Lachlan K, Magee A, McConnell V, McEntagart M, Metcalfe K, Montgomery T, Newbury-Ecob R, Stewart F, Turnpenny P, Vogt J, Fitzpatrick D, Williams M; DDD Study, Smithson S.

Am J Med Genet A. 2016 Nov;170(11):2835-2846. doi: 10.1002/ajmg.a.37842. Epub 2016 Sep 26.

20.

Beaulieu-Boycott-Innes syndrome: an intellectual disability syndrome with characteristic facies.

Casey J, Jenkinson A, Magee A, Ennis S, Monavari A, Green A, Lynch SA, Crushell E, Hughes J.

Clin Dysmorphol. 2016 Oct;25(4):146-51. doi: 10.1097/MCD.0000000000000134.

PMID:
27295358

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