Find Research Outputs

Search in all content

Filters for Research Outputs

Search concepts
Selected filters

Publication Year

  • 2020
  • 2019
  • 2018
  • 2017
  • 2016
  • 2015
  • 2014
  • 2013
  • 2012
  • 2011

Author

  • Irwin McLean
2011

High-speed imaging of microbubble formation in a novel flow focusing microfluidics chip

Hegde, V., Mason, A., McLean, D., Smith, F. D. J., McLean, W. & Campbell, P., 2011, Bio-Optics: Design and Application. Optical Society of America, JTuA19. (Optics in the Life Sciences).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

2014

Jitter reduction using native fiducials in rotating mirror ultra-fast microphotography

Goh, B. H. T., Khoo, B. C., McLean, W. H. I. & Campbell, P. A., 30 Jun 2014, In : Optics Express. 22, 13, p. 16282-16288 7 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
Open Access
File
2 Citations (Scopus)
46 Downloads (Pure)

Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis

Cole, C., Kroboth, K., Schurch, N. J., Sandilands, A., Sherstnev, A., O'Regan, G. M., Watson, R. M., McLean, W. H. I., Barton, G. J., Irvine, A. D. & Brown, S. J., Jul 2014, In : Journal of Allergy and Clinical Immunology. 134, 1, p. 82-91 10 p.

Research output: Contribution to journalArticle

Open Access
File
75 Citations (Scopus)
186 Downloads (Pure)
2012

Filaggrin mutations: Prognosis and response to therapy overtime

Margolis, D. J., Mitra, N., Sandilands, A., McLean, I. & Rebbeck, T., May 2012, In : Journal of Investigative Dermatology. 132, p. S41-S41 1 p.

Research output: Contribution to journalArticle

2018

Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis

Martinez-Fabregas, J., Prescott, A., van Kasteren, S., Leslie Pedrioli, D., McLean, W., Moles, A., Reinheckel, T., Poli, V. & Watts, C., 17 Dec 2018, In : Nature Communications. 9, 1, p. 1-16 16 p., 5343.

Research output: Contribution to journalArticle

Open Access
File
6 Citations (Scopus)
136 Downloads (Pure)
2013

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

Ellinghaus, D., Baurecht, H., Esparza-Gordillo, J., Rodríguez, E., Matanovic, A., Marenholz, I., Hübner, N., Schaarschmidt, H., Novak, N., Michel, S., Maintz, L., Werfel, T., Meyer-Hoffert, U., Hotze, M., Prokisch, H., Heim, K., Herder, C., Hirota, T., Tamari, M., Kubo, M. & 29 others, Takahashi, A., Nakamura, Y., Tsoi, L. C., Stuart, P., Elder, J. T., Sun, L., Zuo, X., Yang, S., Zhang, X., Hoffmann, P., Nöthen, M. M., Fölster-Holst, R., Winkelmann, J., Illig, T., Boehm, B. O., Duerr, R. H., Büning, C., Brand, S., Glas, J., McAleer, M. A., Fahy, C. M., Kabesch, M., Brown, S., McLean, W. H. I., Irvine, A. D., Schreiber, S., Lee, Y-A., Franke, A. & Weidinger, S., Jul 2013, In : Nature Genetics. 45, 7, p. 808-812 5 p.

Research output: Contribution to journalArticle

106 Citations (Scopus)

Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status

Asai, Y., Greenwood, C., Hull, P. R., Alizadehfar, R., Ben-Shoshan, M., Brown, S. J., Campbell, L., Michel, D. L., Bussières, J., Rousseau, F., Fujiwara, T. M., Morgan, K., Irvine, A. D., McLean, W. H. I. & Clarke, A., Jul 2013, In : Journal of Allergy and Clinical Immunology. 132, 1, p. 239-242.e7 4 p.

Research output: Contribution to journalLetter

35 Citations (Scopus)
2011

Copy number variation within the filaggrin gene contributes to risk of atopic dermatitis

Brown, S. J., Kroboth, K., Sandilands, A., Campbell, L. E., Pohler, E., Irvine, A. D., Cordell, H. J. & McLean, W., Apr 2011, In : Journal of Investigative Dermatology. 131, Supplement 1, p. S63-S63 1 p., 375.

Research output: Contribution to journalBook/Film/Article review

2017

Calpain 12 function revealed through the study of an atypical case of autosomal recessive congenital ichthyosis

Bochner, R., Samuelov, L., Sarig, O., Li, Q., Adase, C. A., Isakov, O., Malchin, N., Vodo, D., Shayevitch, R., Peled, A., Yu, B. D., Fainberg, G., Warshauer, E., Adir, N., Erez, N., Gat, A., Gottlieb, Y., Rogers, T., Pavlovsky, M., Goldberg, I. & 9 others, Shomron, N., Sandilands, A., Campbell, L. E., MacCallum, S., McLean, W. H. I., Ast, G., Gallo, R. L., Uitto, J. & Sprecher, E., Feb 2017, In : Journal of Investigative Dermatology. 137, 2, p. 385-393 9 p.

Research output: Contribution to journalArticle

Open Access
File
6 Citations (Scopus)
162 Downloads (Pure)
2019

Longitudinal analysis of the effect of water hardness on atopic eczema: evidence for gene-environment interaction

Jabbar-Lopez, Z. K., Craven, J., Logan, K., Greenblatt, D., Marrs, T., Radulovic, S., McLean, W. H. I., Lack, G., Strachan, D. P., Perkin, M. R., Peacock, J. L. & Flohr, C., 10 Oct 2019, In : British Journal of Dermatology. 9 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)
2017

Keratin 6b variant p.Gly499Ser reported in delayed-onset pachyonychia congenita is a non-pathogenic polymorphism

Smith, F. J. D. & McLean, W. H. I., 3 Dec 2017, In : Journal of Dermatology. 44, 12, p. e312 1 p.

Research output: Contribution to journalLetter

Open Access
File
1 Citation (Scopus)
149 Downloads (Pure)
2014

SiRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy

Courtney, D. G., Atkinson, S. D., Allen, E. H. A., Moore, J. E., Walsh, C. P., Leslie Pedrioli, D. M., MacEwen, C. J., Pellegrini, G., Maurizi, E., Serafini, C., Fantacci, M., Liao, H., Irvine, A. D., McLean, W. H. I. & Moore, C. B. T., 29 May 2014, In : Investigative Ophthalmology & Visual Science. 55, 5, p. 3352-3360 9 p.

Research output: Contribution to journalArticle

8 Citations (Scopus)
2019

Systemic and stratum corneum biomarkers of severity in infant atopic dermatitis include markers of innate and T helper cell-related immunity and angiogenesis

McAleer, M. A., Jakasa, I., Hurault, G., Sarvari, P., McLean, W., Tanaka, R. J., Kezic, S. & Irvine, A. D., Mar 2019, In : British Journal of Dermatology. 180, 3, p. 586-596 11 p.

Research output: Contribution to journalArticle

Open Access
File
15 Citations (Scopus)
135 Downloads (Pure)
2013

Possibilities for human skin characterization based on strongly reduced Raman spectroscopic information

Baclig, A. C., Bakker Schut, T. C., O'Regan, G. M., Irvine, A. D., McLean, W. H. I., Puppels, G. J. & Caspers, P. J., 2013, In : Journal of Raman Spectroscopy. 44, 3, p. 340-345 6 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)
2011

Identification of a novel C16orf57 mutation in Athabaskan patients wth poikiloderma with neutropenia

Clericuzio, C., Harutyunyan, K., Jin, W., Erickson, R. P., Irvine, A. D., McLean, W. H. I., Wen, Y., Bagatell, R., Griffin, T. A., Shwayder, T. A., Plon, S. E. & Wang, L. L., Feb 2011, In : American Journal of Medical Genetics Part A. 155A, 2, p. 337-342 6 p.

Research output: Contribution to journalArticle

25 Citations (Scopus)

Keratin disorders: from gene to therapy

McLean, W. H. I. & Moore, C. B. T., 15 Oct 2011, In : Human Molecular Genetics. 20, p. R189-R197 9 p.

Research output: Contribution to journalReview article

77 Citations (Scopus)
2014

The molecular genetic analysis of the expanding pachyonychia congenita case collection

Wilson, N. J., O'Toole, E., Milstone, L. M., Hansen, C. D., Shepherd, A. A., Al-Asadi, E., Schwartz, M. E., McLean, W. H. I., Sprecher, E. & Smith, F. J. D., Aug 2014, In : British Journal of Dermatology. 171, 2, p. 343-355 13 p., 12958.

Research output: Contribution to journalArticle

Open Access
File
36 Citations (Scopus)
152 Downloads (Pure)
2012

Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility

McGrath, J. A., Stone, K. L., Begum, R., Simpson, M. A., Dopping-Hepenstal, P. J., Liu, L., McMillan, J. R., South, A. P., Pourreyron, C., McLean, W. H. I., Martinez, A. E., Mellerio, J. E. & Parsons, M., 7 Dec 2012, In : American Journal of Human Genetics. 91, 6, p. 1115-1121 7 p.

Research output: Contribution to journalArticle

39 Citations (Scopus)
2011

Development of allele-specific therapeutic siRNA for keratin 5 mutations in epidermolysis bullosa simplex

Atkinson, S. D., McGilligan, V. E., Liao, H., Szeverenyi, I., Smith, F. J. D., Moore, C. B. T. & McLean, W. H. I., Oct 2011, In : Journal of Investigative Dermatology. 131, 10, p. 2079-2086 8 p.

Research output: Contribution to journalArticle

49 Citations (Scopus)
2013

Frontal fibrosing alopecia

Becher, G. L., Holmes, S. & McLean, I., 2013, In : Journal of Investigative Dermatology. 133, 5, p. 1401 1 p., PO64.

Research output: Contribution to journalMeeting abstract

2015

Novel TGM5 mutations in acral peeling skin syndrome

van der Velden, J. . J. A. J., van Geel, M., Nellen, R. G. L., Jonkman, M. F., McGrath, J. A., Nanda, A., Sprecher, E., van Steensel, M. A. M., Mclean, W. H. I. & Cassidy, A. J., Apr 2015, In : Experimental Dermatology. 24, 4, p. 285-289 5 p.

Research output: Contribution to journalArticle

8 Citations (Scopus)
2013

Novel mutation in keratin 10 causing autosomal dominant epidermolytic ichthyosis

Lamb, R. C., Terron-Kwiatkowski, A., Lang, J., McLean, W. H. I. & Zamiri, M., 2013, In : British Journal of Dermatology. 169, Suppl. 1, p. 29-30 2 p., P23.

Research output: Contribution to journalMeeting abstract

2012

Homozygous dominant missense mutation in keratin 17 leads to alopecia in addition to severe pachyonychia congenita

Wilson, N. J., Pérez, M. L. C., Vahlquist, A., Schwartz, M. E., Hansen, C. D., McLean, W. H. I. & Smith, F. J. D., 2012, In : Journal of Investigative Dermatology.

Research output: Contribution to journalLetter

11 Citations (Scopus)
2019

A minimally invasive tool to study immune response and skin barrier in children with atopic dermatitis

Hulshof, L., Hack, D. P., Hasnoe, Q. C. J., Dontje, B., Jakasa, I., Riethmüller, C., McLean, W. H. I., van Aalderen, W. M. C., Van't Land, B., Kezic, S., Sprikkelman, A. B. & Middelkamp-Hup, M. A., Mar 2019, In : British Journal of Dermatology. 180, 3, p. 621-630 10 p.

Research output: Contribution to journalArticle

Open Access
File
11 Citations (Scopus)
99 Downloads (Pure)
2013

Recessive mutations in the gene encoding frizzled 6 cause twenty nail dystrophy: Expanding the differential diagnosis for pachyonychia congenita

Wilson, N. J., Hansen, C. D., Azkur, D., Kocabas, C. N., Metin, A., Coskun, Z., Schwartz, M. E., Hull, P. R., McLean, W. H. I. & Smith, F. J. D., Apr 2013, In : Journal of Dermatological Science. 70, 1, p. 58-60 3 p.

Research output: Contribution to journalLetter

14 Citations (Scopus)
2016

CRISPR/Cas9 DNA cleavage at SNP-derived PAM enables both in vitro and in vivo KRT12 mutation-specific targeting

Courtney, D. G., Moore, J. E., Atkinson, S. D., Maurizi, E., Allen, E. H. A., Leslie Pedrioli, D. M. L., Mclean, W. H. I., Nesbit, M. A. & Moore, C. B. T., 2016, In : Gene Therapy. 23, 1, p. 108-112

Research output: Contribution to journalArticle

Open Access
File
59 Citations (Scopus)
143 Downloads (Pure)
2014

Report of the 10th annual international pachyonychia congenita consortium meeting

van Steensel, M., Coulombe, P. A., Kaspar, R. L., Milstone, L. M., McLean, I. W. H., Roop, D. R., Smith, F. J. D., Sprecher, E. & Schwartz, M. E., Mar 2014, In : Journal of Investigative Dermatology. 134, 3, p. 588-91 4 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
2019
Open Access
File
2 Citations (Scopus)
124 Downloads (Pure)
2011

The phenotypic and molecular genetic features of pachyonychia congenita

McLean, W. H. I., Hansen, C. D., Eliason, M. J. & Smith, F. J. D., May 2011, In : Journal of Investigative Dermatology. 131, 5, p. 1015-1017 3 p.

Research output: Contribution to journalReview article

77 Citations (Scopus)
2013

Keratin 9 Is Required for the Structural Integrity and Terminal Differentiation of the Palmoplantar Epidermis

Fu, D. J., Thomson, C., Lunny, D. P., Dopping-Hepenstal, P. J., McGrath, J. A., Smith, F. J. D., McLean, W. H. I. & Leslie Pedrioli, D. M., 2013, In : Journal of Investigative Dermatology. n/a, n/a.

Research output: Contribution to journalArticle

45 Citations (Scopus)
2012

One remarkable molecule: filaggrin

Brown, S. J. & McLean, W. H. I., Mar 2012, In : Journal of Investigative Dermatology. 132, 3, p. 751-762 12 p.

Research output: Contribution to journalArticle

271 Citations (Scopus)
2018

Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

Kürklü, E., Öztürk, Ş., Cassidy, A. J., Ak, G., Koray, M., Çefle, K., Palandüz, Ş., Güllüoğlu, M. G., Tanyeri, H. & McLean, W. H. I., 1 Mar 2018, In : Medicina Oral Patologia Oral y Cirugia Bucal. 23, 2, p. e144-e150 7 p., 21437.

Research output: Contribution to journalArticle

Open Access
File
2 Citations (Scopus)
130 Downloads (Pure)
2015

Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis

Pohler, E., Cunningham, F., Sandilands, A., Cole, C., Digby, S., McMillan, J. R., Aristodemou, S., McGrath, J. A., Smith, F. J. D., Mclean, W. H. I., Munro, C. S. & Zamiri, M., 26 Nov 2015, In : British Journal of Dermatology. 173, 5, p. 1292-1294 4 p.

Research output: Contribution to journalLetter

Open Access
File
3 Citations (Scopus)
140 Downloads (Pure)
2014

Mutations in GRHL2 result in an autosomal-recessive ectodermal dysplasia syndrome

Petrof, G., Nanda, A., Howden, J., Takeichi, T., McMillan, J. R., Aristodemou, S., Ozoemena, L., Liu, L., South, A. P., Pourreyron, C., Dafou, D., Proudfoot, L. E., Al-Ajmi, H., Akiyama, M., McLean, W. H. I., Simpson, M. A., Parsons, M. & McGrath, J. A., 4 Sep 2014, In : American Journal of Human Genetics. 95, 3, p. 308-314 7 p.

Research output: Contribution to journalArticle

File
33 Citations (Scopus)
146 Downloads (Pure)
2012

A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome

Van der Velden, J. J. A. J., Steijlen, P. M., van Steensel, M. A. M., Van Geel, M., Jonkman, M. F., McLean, W. H. I. & Hamm, H., 1 Jan 2012, In : Journal of Dermatological Science. 65, 1, p. 74-76 3 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)
2018

Gentamicin-induced readthrough and nonsense-mediated mRNA decay of SERPINB7 nonsense mutant transcripts

Ohguchi, Y., Nomura, T., Suzuki, S., Takeda, M., Miyauchi, T., Mizuno, O., Shinkuma, S., Fujita, Y., Nemoto, O., Ono, K., McLean, W. H. I. & Shimizu, H., 1 Apr 2018, In : Journal of Investigative Dermatology. 138, 4, p. 836-843 8 p.

Research output: Contribution to journalArticle

Open Access
File
9 Citations (Scopus)
170 Downloads (Pure)
2017

Biallelic mutations in KDSR disrupt ceramide synthesis and result in a spectrum of keratinization disorders associated with thrombocytopenia

Takeichi, T., Torrelo, A., Lee, J. Y. W., Ohno, Y., Lozano, M. L., Kihara, A., Liu, L., Yasuda, Y., Ishikawa, J., Murase, T., Rodrigo, A. B., Fernández-Crehuet, P., Toi, Y., Mellerio, J. E., Rivera, J., Vicente, V., Kelsell, D. P., Nishimura, Y., Okuno, Y., Kojima, D. & 6 others, Ogawa, Y., Sugiura, K., Simpson, M. A., McLean, W. H. I., Akiyama, M. & McGrath, J. A., Nov 2017, In : Journal of Investigative Dermatology. 137, 11, p. 2344-2353 10 p.

Research output: Contribution to journalArticle

Open Access
File
21 Citations (Scopus)
181 Downloads (Pure)
2016

Association between domestic water hardness, chlorine, and atopic dermatitis risk in early life: A population-based cross-sectional study

Perkin, M. R., Craven, J., Logan, K., Strachan, D., Marrs, T., Radulovic, S., Campbell, L. E., MacCallum, S. F., McLean, W. H. I., Lack, G. & Flohr, C., Aug 2016, In : Journal of Allergy and Clinical Immunology. 138, 2, p. 509-516 8 p.

Research output: Contribution to journalArticle

29 Citations (Scopus)
2012

The persistence of atopic dermatitis and filaggrin (FLG) mutations in a US longitudinal cohort

Margolis, D. J., Apter, A. J., Gupta, J., Hoffstad, O., Papadopoulos, M., Campbell, L. E., Sandilands, A., McLean, W. H. I., Rebbeck, T. R. & Mitra, N., 2012, In : Journal of Allergy and Clinical Immunology. 130, 4, p. 912-917 6 p.

Research output: Contribution to journalArticle

105 Citations (Scopus)
2015

Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms

Baurecht, H., Hotze, M., Brand, S., Büning, C., Cormican, P., Corvin, A., Ellinghaus, D., Ellinghaus, E., Esparza-Gordillo, J., Fölster-Holst, R., Franke, A., Gieger, C., Hubner, N., Illig, T., Irvine, A. D., Kabesch, M., Lee, Y. A. E., Lieb, W., Marenholz, I., McLean, W. H. I. & 19 others, Morris, D. W., Mrowietz, U., Nair, R., Nöthen, M. M., Novak, N., O'Regan, G. M., PAGE Consortium, Schreiber, S., Smith, C., Strauch, K., Stuart, P. E., Trembath, R., Tsoi, L. C., Weichenthal, M., Barker, J., Elder, J. T., Weidinger, S., Cordell, H. J. & Brown, S. J., 8 Jan 2015, In : American Journal of Human Genetics. 96, 1, p. 104-120 17 p.

Research output: Contribution to journalArticle

67 Citations (Scopus)

Loss-of-function mutations in CAST cause peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads

Lin, Z., Zhao, J., Nitoiu, D., Scott, C. A., Plagnol, V., Smith, F. J. D., Wilson, N. J., Cole, C., Schwartz, M. E., McLean, W. H. I., Wang, H., Feng, C., Duo, L., Zhou, E. Y., Ren, Y., Dai, L., Chen, Y., Zhang, J., Xu, X., O'Toole, E. A. & 2 others, Kelsell, D. P. & Yang, Y., 5 Mar 2015, In : American Journal of Human Genetics. 96, 3, p. 440-447 8 p.

Research output: Contribution to journalArticle

15 Citations (Scopus)
2012

Scanning Ion Conductance Microscopy of Live Keratinocytes

Hegde, V., Mason, A., Saliev, T., Smith, F., McLean, W. H. I. & Campbell, P. A., 2012, Electron Microscopy and Analysis Group Conference 2011 (EMAG 2011). Bristol: IOP Publishing Ltd., p. - 4 p.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

1 Citation (Scopus)
2011

Filaggrin Genotype in Ichthyosis Vulgaris Predicts Abnormalities in Epidermal Structure and Function

Gruber, R., Elias, P. M., Crumrine, D., Lin, T-K., Brandner, J. M., Hachem, J-P., Presland, R. B., Fleckman, P., Janecke, A. R., Sandilands, A., McLean, W. H. I., Fritsch, P. O., Mildner, M., Tschachler, E. & Schmuth, M., May 2011, In : American Journal of Pathology. 178, 5, p. 2252-2263 12 p.

Research output: Contribution to journalArticle

152 Citations (Scopus)
2013

Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma

Blaydon, D. C., Lind, L. K., Plagnol, V., Linton, K. J., Smith, F. J. D., Wilson, N. J., McLean, W. H. I., Munro, C. S., South, A. P., Leigh, I. M., O'Toole, E. A., Lundström, A. & Kelsell, D. P., 8 Aug 2013, In : American Journal of Human Genetics. 93, 2, p. 330-335 6 p.

Research output: Contribution to journalArticle

48 Citations (Scopus)
2014
Open Access
File
30 Citations (Scopus)
152 Downloads (Pure)
2011

Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis

Winge, M. C. G., Bilcha, K. D., Lieden, A., Shibeshi, D., Sandilands, A., Wahlgren, C-F., McLean, W. H. I., Nordenskjold, M. & Bradley, M., Nov 2011, In : British Journal of Dermatology. 165, 5, p. 1074-1080 7 p.

Research output: Contribution to journalArticle

67 Citations (Scopus)
2015

Loss-of-function mutations in the gene encoding filaggrin are not strongly associated with chronic actinic dermatitis

Harkins, C. P., Waters, A., Kerr, A., Campbell, L., McLean, W. H. I., Brown, S. J. & Ibbotson, S. H., Jul 2015, In : Journal of Investigative Dermatology. 135, 7, p. 1919-1921 3 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)
2013

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

Saunders, S. P., Goh, C. S. M., Brown, S. J., Palmer, C. N. A., Porter, R. M., Cole, C., Campbell, L. E., Gierlinski, M., Barton, G. J., Schneider, G., Balmain, A., Prescott, A. R., Weidinger, S., Baurecht, H., Kabesch, M., Gieger, C., Lee, Y-A., Tavendale, R., Mukhopadhyay, S., Turner, S. W. & 14 others, Madhok, V. B., Sullivan, F. M., Relton, C., Burn, J., Meggitt, S., Smith, C. H., Allen, M. A., Barker, J. N. W. N., Reynolds, N. J., Cordell, H. J., Irvine, A. D., McLean, W. H. I., Sandilands, A. & Fallon, P. G., Nov 2013, In : Journal of Allergy and Clinical Immunology. 132, 5, p. 1121-1129 9 p.

Research output: Contribution to journalArticle

78 Citations (Scopus)
2015

Atopic dermatitis increases the effect of exposure to peanut antigen in dust on peanut sensitization and likely peanut allergy

Brough, H. A., Liu, A. H., Sicherer, S., Makinson, K., Douiri, A., Brown, S. J., Stephens, A. C., McLean, W. H. I., Turcanu, V., Wood, R. A., Jones, S. M., Burks, W., Dawson, P., Stablein, D., Sampson, H. & Lack, G., Jan 2015, In : Journal of Allergy and Clinical Immunology. 135, 1, p. 164-170.e4 11 p.

Research output: Contribution to journalArticle

Open Access
File
161 Citations (Scopus)
322 Downloads (Pure)