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Germline CBM-opathies: From immunodeficiency to atopy

Journal of allergy and clinical immunology, 2019-05, Vol.143 (5), p.1661-1673

2019

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Inborn errors of immunity manifesting as atopic disorders

Journal of allergy and clinical immunology, 2021-11, Vol.148 (5), p.1130-1139

2021

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MALT1-Dependent Cleavage of HOIL1 Modulates Canonical NF-κB Signaling and Inflammatory Responsiveness

Frontiers in immunology, 2021-10, Vol.12, p.749794-749794

2021

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Rare diseases of epigenetic origin: Challenges and opportunities

Frontiers in genetics, 2023-02, Vol.14, p.1113086-1113086

2023

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Prognostic role of diuretic failure in determining mortality for patients hospitalized with acute decompensated heart failure

Heart and vessels, 2022-08, Vol.37 (8), p.1373-1379

2022

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Transcription factor defects in inborn errors of immunity with atopy

Frontiers in allergy, 2023-09, Vol.4, p.1237852-1237852

2023

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A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations

Mitochondrion, 2019-05, Vol.46, p.298-301

2019

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Gain-of-function MARK4 variant associates with pediatric neurodevelopmental disorder and dysmorphism

HGG advances, 2024-01, Vol.5 (1), p.100259-100259, Article 100259

2024

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Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report

BMC pediatrics, 2021-01, Vol.21 (1), p.45-45, Article 45

2021

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Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy

Allergy, asthma, and clinical immunology, 2021-01, Vol.17 (1), p.9-9, Article 9

2021

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Advancing Security in the Industrial Internet of Things Using Deep Progressive Neural Networks

Mobile networks and applications, 2023-04, Vol.28 (2), p.782-794

2023

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Efficacy of Dupilumab in STAT6 GOF disease: 30 months follow-up of a single patient

Clinical immunology (Orlando, Fla.), 2023-05, Vol.250, p.109513, Article 109513

2023

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Human Germline Heterozygous Gain-of-Function STAT6 Variants Cause Severe Allergic Disease

Clinical immunology (Orlando, Fla.), 2023-05, Vol.250, p.109364, Article 109364

2023

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Enabling security for the Industrial Internet of Things using deep learning, blockchain, and coalitions

Transactions on emerging telecommunications technologies, 2021-07, Vol.32 (7), p.n/a

2021

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Homozygous RMRP Promoter Duplications Cause Severely Reduced Transcript Abundance and SCID Associated with Cartilage Hair Hypoplasia

Journal of clinical immunology, 2023-08, Vol.43 (6), p.1139-1142

2023

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Dominant Negative Variants in IKZF2 Cause ICHAD Syndrome, a New Disorder Characterized by Immunodysregulation, Craniofacial Anomalies, Hearing Impairment, Athelia, and Developmental Delay

Clinical immunology (Orlando, Fla.), 2023-05, Vol.250, p.109546, Article 109546

2023

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Apt-RAN: A Flexible Split-Based 5G RAN to Minimize Energy Consumption and Handovers

IEEE eTransactions on network and service management, 2020-03, Vol.17 (1), p.473-487

2020

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Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiency

Journal of allergy and clinical immunology, 2021-12, Vol.148 (6), p.1559-1574.e13

2021

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A novel autosomal recessive primary atopic disorder associated with loss-of-function variants in OSMR

Journal of allergy and clinical immunology, 2022-02, Vol.149 (2), p.AB137-AB137

2022

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Extracellular granzyme K mediates endothelial activation through the cleavage of protease‐activated receptor‐1

The FEBS journal, 2016-05, Vol.283 (9), p.1734-1747

2016

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Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond

Trends in immunology, 2024-02, Vol.45 (2), p.138-153

2024

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Expanding the molecular and phenotypic spectrum of CTLA‐4 insufficiency

Pediatric allergy and immunology, 2024-02, Vol.35 (2), p.e14077-n/a

2024

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Enforcing Intelligent Learning-Based Security in Internet of Everything

IEEE internet of things journal, 2023-02, Vol.10 (4), p.3071-3078

2023

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Ant Router: An efficient routing protocol for social opportunistic networks using ant routing

IET networks, 2020-03, Vol.9 (2), p.83-93

2020

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Germline CBM-opathies: From immunodeficiency to atopy

Inborn errors of immunity manifesting as atopic disorders

MALT1-Dependent Cleavage of HOIL1 Modulates Canonical NF-κB Signaling and Inflammatory Responsiveness

Rare diseases of epigenetic origin: Challenges and opportunities

Prognostic role of diuretic failure in determining mortality for patients hospitalized with acute decompensated heart failure

Transcription factor defects in inborn errors of immunity with atopy

A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations

Gain-of-function MARK4 variant associates with pediatric neurodevelopmental disorder and dysmorphism

Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report

Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy

Advancing Security in the Industrial Internet of Things Using Deep Progressive Neural Networks

Efficacy of Dupilumab in STAT6 GOF disease: 30 months follow-up of a single patient

Human Germline Heterozygous Gain-of-Function STAT6 Variants Cause Severe Allergic Disease

Enabling security for the Industrial Internet of Things using deep learning, blockchain, and coalitions

Homozygous RMRP Promoter Duplications Cause Severely Reduced Transcript Abundance and SCID Associated with Cartilage Hair Hypoplasia

Dominant Negative Variants in IKZF2 Cause ICHAD Syndrome, a New Disorder Characterized by Immunodysregulation, Craniofacial Anomalies, Hearing Impairment, Athelia, and Developmental Delay

Apt-RAN: A Flexible Split-Based 5G RAN to Minimize Energy Consumption and Handovers

Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiency

A novel autosomal recessive primary atopic disorder associated with loss-of-function variants in OSMR

Extracellular granzyme K mediates endothelial activation through the cleavage of protease‐activated receptor‐1

Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond

Expanding the molecular and phenotypic spectrum of CTLA‐4 insufficiency

Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancy

Enforcing Intelligent Learning-Based Security in Internet of Everything

Ant Router: An efficient routing protocol for social opportunistic networks using ant routing

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