Concepedia

Author

Daniel Kotlarz

Ludwig-Maximilians-Universität MünchenORCID

Also Known As

D KOTLARZ, D Kotlarz, Daniel Kotlarz, Kotlarz, Daniel

111

Publications

7K

Citations

31

H-Index

51

Concepts

All Affiliations

Ludwig-Maximilians-Universität MünchenBrigham and Women's HospitalBoston Children's HospitalHarvard UniversityUniversity of Toronto
DK

About

Daniel Kotlarz is an author at Ludwig-Maximilians-Universität München specializing in medicine, immunology, and autoimmunity.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

14

15

1.9K

2

Cell Biology

6

6

916

3

Health Sciences

2

2

669

4

Allergy

1

1

62

5

Biomedical Engineering

1

1

38

Daniel Kotlarz

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40

Publications

5.9K

Citations

28

H-Index

YearCitations

Inflammatory Bowel Disease and Mutations Affecting the Interleukin-10 Receptor

Erik‐Oliver Glocker, Daniel Kotlarz, Kaan Boztuǧ,

New England Journal of Medicine

2009

1.4K

The Transforming Growth Factor-β Superfamily Member Growth-Differentiation Factor-15 Protects the Heart From Ischemia/Reperfusion Injury

Tibor Kempf, Matthias Eden, Jens Strelau,

Circulation Research

2006

631

Loss of Interleukin-10 Signaling and Infantile Inflammatory Bowel Disease: Implications for Diagnosis and Therapy

Daniel Kotlarz, Rita Beier, Dhaarini Murugan,

Gastroenterology

2012

462

Statin-Induced Improvement of Endothelial Progenitor Cell Mobilization, Myocardial Neovascularization, Left Ventricular Function, and Survival After Experimental Myocardial Infarction Requires Endothelial Nitric Oxide Synthase

Ulf Landmesser, Niels Engberding, Ferdinand H. Bahlmann,

Circulation

2004

420

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

Alexandra Y. Kreins, Michael J. Ciancanelli, Satoshi Okada,

The Journal of Experimental Medicine

2015

349

The phenotype of human STK4 deficiency

Hengameh Abdollahpour, Giridharan Appaswamy, Daniel Kotlarz,

Blood

2012

321

Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome

Daniel Kotlarz, Natalia Ziętara, Gülbû Uzel,

The Journal of Experimental Medicine

2013

214

Mutations in Tetratricopeptide Repeat Domain 7A Result in a Severe Form of Very Early Onset Inflammatory Bowel Disease

Yaron Avitzur, Conghui Guo, Lucas A. Mastropaolo,

Gastroenterology

2014

206

Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases

Yue Li, Marita Führer, Ehsan Bahrami,

Proceedings of the National Academy of Sciences

2018

186

Optimized human intestinal organoid model reveals interleukin-22-dependency of paneth cell formation

Gui-Wei He, Lin Lin, Jeff DeMartino,

Cell stem cell

2022

148

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