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

Journal of allergy and clinical immunology, 2024-01, Vol.153 (1), p.355-356

Lawless, Dylan

2024

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A Case of Adult-Onset Still's Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab

Frontiers in immunology, 2018-07, Vol.9, p.1527-1527

2018

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Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A ) cause a primary immunodeficiency disorder

eLife, 2021-12, Vol.10

2021

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Incomplete Recovery of Zebrafish Retina Following Cryoinjury

Cells (Basel, Switzerland), 2022-04, Vol.11 (8), p.1373

2022

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A novel RAG1 mutation reveals a critical in vivo role for HMGB1/2 during V(D)J recombination

Blood, 2019-02, Vol.133 (8), p.820-829

2019

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Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation

Science translational medicine, 2016-03, Vol.8 (332), p.332ra45

2016

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Prevalence of CFTR variants in primary immunodeficiency patients with bronchiectasis is an important modifying cofactor

Journal of allergy and clinical immunology, 2023-07, Vol.152 (1), p.257-265

2023

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Viral Genetic Determinants of Prolonged Respiratory Syncytial Virus Infection Among Infants in a Healthy Term Birth Cohort

The Journal of infectious diseases, 2023-05, Vol.227 (10), p.1194-1202

2023

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Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variation

American journal of human genetics, 2024-06, Vol.111 (6), p.1018-1034

2024

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A Novel RELA Truncating Mutation in a Familial Behçet’s Disease–like Mucocutaneous Ulcerative Condition

Arthritis & rheumatology (Hoboken, N.J.), 2021-03, Vol.73 (3), p.490-497

2021

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Novel Genetic Discoveries in Rare Primary Immunodeficiencies

Lawless, Dylan

2019

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Predicting the Occurrence of Variants in RAG1 and RAG2

Journal of clinical immunology, 2019-10, Vol.39 (7), p.688-701

2019

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Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency

Journal of clinical immunology, 2020-02, Vol.40 (2), p.277-288

2020

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Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency

Journal of allergy and clinical immunology, 2018-06, Vol.141 (6), p.2303-2306

2018

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Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

Journal of clinical immunology, 2017-10, Vol.37 (7), p.617-622

2017

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Prevalence and clinical challenges among adult primary immunodeficiency patients with RAG deficiency

Journal of allergy and clinical immunology, 2018-03, Vol.141 (6), p.2303-2306

2018

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Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

Journal of clinical immunology, 2017, Vol.37 (7), p.617-622

2017

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Predictors of successful natural sleep MRI for sensorineural hearing loss in infants

International journal of pediatric otorhinolaryngology, 2023-02, Vol.165, p.111430-111430, Article 111430

2023

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Explanatory Modeling in Science Through Text-Based Investigation: Testing the Efficacy of the Project READI Intervention Approach

American educational research journal, 2019-08, Vol.56 (4), p.1148-1216

2019

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Reports of the AAAI 2019 Spring Symposium Series

The AI magazine, 2019-09, Vol.40 (3), p.59-66

2019

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

A Case of Adult-Onset Still's Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab

Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A ) cause a primary immunodeficiency disorder

Incomplete Recovery of Zebrafish Retina Following Cryoinjury

A novel RAG1 mutation reveals a critical in vivo role for HMGB1/2 during V(D)J recombination

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation

Prevalence of CFTR variants in primary immunodeficiency patients with bronchiectasis is an important modifying cofactor

Germline TET2 loss of function causes childhood immunodeficiency and lymphoma

Viral Genetic Determinants of Prolonged Respiratory Syncytial Virus Infection Among Infants in a Healthy Term Birth Cohort

Joint host-pathogen genomic analysis identifies hepatitis B virus mutations associated with human NTCP and HLA class I variation

A Novel RELA Truncating Mutation in a Familial Behçet’s Disease–like Mucocutaneous Ulcerative Condition

Novel Genetic Discoveries in Rare Primary Immunodeficiencies

Predicting the Occurrence of Variants in RAG1 and RAG2

Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency

Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

Prevalence and clinical challenges among adult primary immunodeficiency patients with RAG deficiency

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

Predictors of successful natural sleep MRI for sensorineural hearing loss in infants

Explanatory Modeling in Science Through Text-Based Investigation: Testing the Efficacy of the Project READI Intervention Approach

Reports of the AAAI 2019 Spring Symposium Series

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