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All papers authored by McLean Wh

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2019 Youssef Elhaji, Denis Sasseville

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, Melanie Pratt, Yuka Asai

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, Kara Matheson, William H. I. McLean

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, Peter R. Hull

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Filaggrin gene loss‐of‐function mutations constitute a factor in patients with multiple contact allergies

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2018 Manuela Pigors, John E. A. Common, Xuan Fei Colin C. Wong, Sajid Malik

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, Claire A. Scott, Niloofar Tabarra, Herty Liany, Jianjun Liu, Vachiranee Limviphuvadh, Sebastian Maurer-Stroh, Mark B. Y. Tang, Nicholas Lench, David J. Margolis, David A. van Heel, Charles A. Mein and 8 other authors

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

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2017 Frances J. D. Smith, W. H. Irwin McLean

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

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Ron Bochner, Liat Samuelov, Ofer Sarig, Qiaoli Li

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, Christopher A. Adase, Ofer Isakov, Natalia Malchin, Dan Vodo, Ronna Shayevitch, Alon Peled, Benjamin D. Yu, Gilad Fainberg, Emily Warshauer, Noam Adir, Noam Erez and 14 other authors

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis

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