Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

Manuela Pigors; John E. A. Common; Xuan Fei Colin C. Wong; Sajid Malik; Claire A. Scott; Niloofar Tabarra; Herty Liany; Jianjun Liu; Vachiranee Limviphuvadh; Sebastian Maurer-Stroh; Mark By Tang; Nicholas Lench; David J. Margolis; David A. van Heel; Charles A. Mein; Natalija Novak; Hansjörg Baurecht; Stephan Weidinger; W. H. Irwin McLean; Alan D. Irvine; Edel A. O'Toole; Michael A. Simpson; David P. Kelsell

doi:10.1016/j.jid.2018.05.013

Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

Manuela Pigors, John E. A. Common, Xuan Fei Colin C. Wong, Sajid Malik, Claire A. Scott, Niloofar Tabarra, Herty Liany, Jianjun Liu, Vachiranee Limviphuvadh, Sebastian Maurer-Stroh, Mark By Tang, Nicholas Lench, David J. Margolis, David A. van Heel, Charles A. Mein, Natalija Novak, Hansjörg Baurecht, Stephan Weidinger, W. H. Irwin McLean, Alan D. IrvineEdel A. O'Toole, Michael A. Simpson, David P. Kelsell

Biological Chemistry and Drug Discovery

Research output: Contribution to journal › Letter

8 Citations (Scopus)

67 Downloads (Pure)

Original language	English
Pages (from-to)	2674-2677
Number of pages	4
Journal	Journal of Investigative Dermatology
Volume	138
Issue number	12
Early online date	30 May 2018
DOIs	https://doi.org/10.1016/j.jid.2018.05.013
Publication status	Published - Dec 2018

Cite this

Pigors, M., Common, J. E. A., Wong, X. F. C. C., Malik, S., Scott, C. A., Tabarra, N., Liany, H., Liu, J., Limviphuvadh, V., Maurer-Stroh, S., Tang, M. B., Lench, N., Margolis, D. J., van Heel, D. A., Mein, C. A., Novak, N., Baurecht, H., Weidinger, S., McLean, W. H. I., ... Kelsell, D. P. (2018). Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes. Journal of Investigative Dermatology, 138(12), 2674-2677. https://doi.org/10.1016/j.jid.2018.05.013

Pigors, Manuela ; Common, John E. A. ; Wong, Xuan Fei Colin C. ; Malik, Sajid ; Scott, Claire A. ; Tabarra, Niloofar ; Liany, Herty ; Liu, Jianjun ; Limviphuvadh, Vachiranee ; Maurer-Stroh, Sebastian ; Tang, Mark By ; Lench, Nicholas ; Margolis, David J. ; van Heel, David A. ; Mein, Charles A. ; Novak, Natalija ; Baurecht, Hansjörg ; Weidinger, Stephan ; McLean, W. H. Irwin ; Irvine, Alan D. ; O'Toole, Edel A. ; Simpson, Michael A. ; Kelsell, David P. / Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes. In: Journal of Investigative Dermatology. 2018 ; Vol. 138, No. 12. pp. 2674-2677.

@article{510931e515464b88804e8c2055ce9dd2,

title = "Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes",

author = "Manuela Pigors and Common, {John E. A.} and Wong, {Xuan Fei Colin C.} and Sajid Malik and Scott, {Claire A.} and Niloofar Tabarra and Herty Liany and Jianjun Liu and Vachiranee Limviphuvadh and Sebastian Maurer-Stroh and Tang, {Mark By} and Nicholas Lench and Margolis, {David J.} and {van Heel}, {David A.} and Mein, {Charles A.} and Natalija Novak and Hansj{\"o}rg Baurecht and Stephan Weidinger and McLean, {W. H. Irwin} and Irvine, {Alan D.} and O'Toole, {Edel A.} and Simpson, {Michael A.} and Kelsell, {David P.}",

year = "2018",

month = dec

doi = "10.1016/j.jid.2018.05.013",

language = "English",

volume = "138",

pages = "2674--2677",

journal = "Journal of Investigative Dermatology",

issn = "0022-202X",

publisher = "Nature Publishing Group",

number = "12",

}

Pigors, M, Common, JEA, Wong, XFCC, Malik, S, Scott, CA, Tabarra, N, Liany, H, Liu, J, Limviphuvadh, V, Maurer-Stroh, S, Tang, MB, Lench, N, Margolis, DJ, van Heel, DA, Mein, CA, Novak, N, Baurecht, H, Weidinger, S, McLean, WHI, Irvine, AD, O'Toole, EA, Simpson, MA & Kelsell, DP 2018, 'Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes', Journal of Investigative Dermatology, vol. 138, no. 12, pp. 2674-2677. https://doi.org/10.1016/j.jid.2018.05.013

Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes. / Pigors, Manuela; Common, John E. A.; Wong, Xuan Fei Colin C.; Malik, Sajid; Scott, Claire A.; Tabarra, Niloofar; Liany, Herty; Liu, Jianjun; Limviphuvadh, Vachiranee; Maurer-Stroh, Sebastian; Tang, Mark By; Lench, Nicholas; Margolis, David J.; van Heel, David A.; Mein, Charles A.; Novak, Natalija; Baurecht, Hansjörg; Weidinger, Stephan; McLean, W. H. Irwin; Irvine, Alan D.; O'Toole, Edel A.; Simpson, Michael A.; Kelsell, David P. (Lead / Corresponding author).

In: Journal of Investigative Dermatology, Vol. 138, No. 12, 12.2018, p. 2674-2677.

Research output: Contribution to journal › Letter

TY - JOUR

T1 - Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

AU - Pigors, Manuela

AU - Common, John E. A.

AU - Wong, Xuan Fei Colin C.

AU - Malik, Sajid

AU - Scott, Claire A.

AU - Tabarra, Niloofar

AU - Liany, Herty

AU - Liu, Jianjun

AU - Limviphuvadh, Vachiranee

AU - Maurer-Stroh, Sebastian

AU - Tang, Mark By

AU - Lench, Nicholas

AU - Margolis, David J.

AU - van Heel, David A.

AU - Mein, Charles A.

AU - Novak, Natalija

AU - Baurecht, Hansjörg

AU - Weidinger, Stephan

AU - McLean, W. H. Irwin

AU - Irvine, Alan D.

AU - O'Toole, Edel A.

AU - Simpson, Michael A.

AU - Kelsell, David P.

PY - 2018/12

Y1 - 2018/12

UR - http://www.scopus.com/inward/record.url?scp=85050405001&partnerID=8YFLogxK

U2 - 10.1016/j.jid.2018.05.013

DO - 10.1016/j.jid.2018.05.013

M3 - Letter

C2 - 29857066

VL - 138

SP - 2674

EP - 2677

JO - Journal of Investigative Dermatology

JF - Journal of Investigative Dermatology

SN - 0022-202X

IS - 12

ER -

Access to Document

10.1016/j.jid.2018.05.013

Author Accepted Manuscript
© 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
Accepted author manuscript, 1.42 MBLicence: CC BY-NC-ND

Link to publication in Scopus