Publications by authors named "Dylan Lawless"

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A Practical Guide to Diagnosing Immunodeficiency.
Maarja Soomann, Austen Worth, Dylan Lawless, Johannes Trück

Pediatr Infect Dis J· October 2025

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Genome-to-genome analysis reveals associations between human and mycobacterial genetic variation in tuberculosis patients from Tanzania.
Zhi Ming Xu, Michaela Zwyer, Hellen Hiza, Sarah Schmidiger, Mohamed Sasamalo, Dylan Lawless

BMC Med Genomics· June 2025

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Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variation.
Zhi Ming Xu, Gnimah Eva Gnouamozi, Sina Rüeger, Patrick R Shea, Maria Buti, Dylan Lawless

Am J Hum Genet· June 2024

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Reply to Dages et al: You AIn't using it right-artificial intelligence progress in allergy.
Dylan Lawless

J Allergy Clin Immunol· January 2024

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Prevalence of CFTR variants in primary immunodeficiency patients with bronchiectasis is an important modifying cofactor.
Dylan Lawless, Hana Lango Allen, James E D Thaventhiran, Sarah Goddard, Oliver S Burren

J Allergy Clin Immunol· July 2023

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Viral Genetic Determinants of Prolonged Respiratory Syncytial Virus Infection Among Infants in a Healthy Term Birth Cohort.
Dylan Lawless, Christopher G McKennan, Suman R Das, Thomas Junier, Zhi Ming Xu

J Infect Dis· May 2023

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Incomplete Recovery of Zebrafish Retina Following Cryoinjury.
Denisa Džulová, Dylan Lawless, Gaëtan G Pinton, Nicole A Renner, Daniel F Schorderet

Cells· April 2022

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Biallelic mutations in ) cause a primary immunodeficiency disorder.
Beibei Wu, Laura Rice, Jennifer Shrimpton, Dylan Lawless, Kieran Walker

Elife· December 2021

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Author Correction: The influence of human genetic variation on Epstein-Barr virus sequence diversity.
Sina Rüeger, Christian Hammer, Alexis Loetscher, Paul J McLaren, Dylan Lawless

Sci Rep· April 2021

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A Novel RELA Truncating Mutation in a Familial Behçet's Disease-like Mucocutaneous Ulcerative Condition.
Fahd Adeeb, Emma R Dorris, Niamh E Morgan, Dylan Lawless, Aqeel Maqsood

Arthritis Rheumatol· March 2021

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The influence of human genetic variation on Epstein-Barr virus sequence diversity.
Sina Rüeger, Christian Hammer, Alexis Loetscher, Paul J McLaren, Dylan Lawless

Sci Rep· February 2021

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Germline TET2 loss of function causes childhood immunodeficiency and lymphoma.
Jarmila Stremenova Spegarova, Dylan Lawless, Siti Mardhiana Binti Mohamad, Karin R Engelhardt, Gina Doody

Blood· August 2020

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Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency.
Hassan Abolhassani, Yasser M El-Sherbiny, Gururaj Arumugakani, Clive Carter, Stephen Richards, Dylan Lawless

J Clin Immunol· February 2020

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Predicting the Occurrence of Variants in RAG1 and RAG2.
Dylan Lawless, Hana Lango Allen, James Thaventhiran, , Flavia Hodel

J Clin Immunol· October 2019

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A novel mutation reveals a critical in vivo role for HMGB1/2 during V(D)J recombination.
Daniel T Thwaites, Clive Carter, Dylan Lawless, Sinisa Savic, Joan M Boyes

Blood· February 2019

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A Case of Adult-Onset Still's Disease Caused by a Novel Splicing Mutation in Successfully Treated With Tocilizumab.
Dylan Lawless, Shelly Pathak, Thomas Edward Scambler, Lylia Ouboussad, Rashida Anwar

Front Immunol· July 2018

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Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency.
Dylan Lawless, Christoph B Geier, Jocelyn R Farmer, Hana Lango Allen, Daniel Thwaites

J Allergy Clin Immunol· June 2018

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Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy.
Dylan Lawless, Anoop Mistry, Philip M Wood, Jens Stahlschmidt, Gururaj Arumugakani

J Clin Immunol· October 2017

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Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation.
Seth L Masters, Vasiliki Lagou, Isabelle Jéru, Paul J Baker, Lien Van Eyck, Dylan Lawless

Sci Transl Med· March 2016

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