Vanessa Hertlein

Austrian Academy of Sciences AT

0000-0003-4476-6748

Publications

478

Citations

H-Index

i10-Index

2yr Mean Cite

Cite/Paper

Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar

Verify on Google Scholar

Publication & Citation Trends

Publications

0 total

Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis. OA

Sevgi Kostel Bal, S. Giuliani, J. Block, Peter Repiscak, Christoph Hafemeister - Blood, 2023

Cited by 8 Semantic Scholar

Research Topics

Cell death mechanisms and regulation (3) RNA Interference and Gene Delivery (2) Advanced biosensing and bioanalysis techniques (1) Mitochondrial Function and Pathology (1) Photosynthetic Processes and Mechanisms (1)

Affiliations

Austrian Academy of Sciences

AT 2023 - 2023

St Anna Children's Hospital

AT 2023 - 2023

CeMM Research Center for Molecular Medicine

AT 2023 - 2023

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases

AT 2023 - 2023

St. Anna Children's Cancer Research Institute

2023 - 2023

External Profiles

OpenAlex Profile Semantic Scholar Profile ORCID Profile Google Scholar

Share Profile

Back to Researchers

Vanessa Hertlein

Publication & Citation Trends

Publications

Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis. OA

Research Topics

Affiliations

External Profiles

Share Profile

Journal Details

Join JournalsHub

Welcome Back