Concepedia

Author

Paul Tuijnenburg

University of AmsterdamORCID

Also Known As

Christopher J. Penkett, P Tuijnenburg, Paul Tuijnenburg, Tuijnenburg, Paul

18

Publications

1K

Citations

9

H-Index

19

Concepts

All Affiliations

University of AmsterdamEmma KinderziekenhuisGreat Ormond Street HospitalUniversity of CambridgeUniversity College London
PT

About

Paul Tuijnenburg is an author at University of Amsterdam specializing in genetics, medicine, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

447

2

Immunology

2

2

347

3

Pathology

2

2

327

4

Molecular Genetics

1

1

120

5

Autoimmune Disease

1

1

120

Paul Tuijnenburg

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7

Publications

637

Citations

7

H-Index

YearCitations

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

Paul Tuijnenburg, Hana Lango Allen, Siobhan O. Burns,

Journal of Allergy and Clinical Immunology

2018

227

The TNF Receptor Superfamily-NF-κB Axis Is Critical to Maintain Effector Regulatory T Cells in Lymphoid and Non-lymphoid Tissues

Ajithkumar Vasanthakumar, Yang Liao, Peggy P. Teh,

Cell Reports

2017

134

Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer,

Journal of Allergy and Clinical Immunology

2020

120

Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome

Machteld M. Oud, Paul Tuijnenburg, Maja Hempel,

The American Journal of Human Genetics

2017

100

High‐throughput compound screen reveals mTOR inhibitors as potential therapeutics to reduce (auto)antibody production by human plasma cells

Paul Tuijnenburg, Daan J. aan de Kerk, Machiel H. Jansen,

European Journal of Immunology

2019

23

Whole genome sequencing of a sporadic primary immunodeficiency cohort

James Thaventhiran, Hana Lango Allen, Oliver S. Burren,

2018

22

Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency

Paul Tuijnenburg, Hana Lango Allen, Godelieve J. de Bree,

Clinical Immunology

2019

11

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