Hanns-georg T. Klein

Martinsried, BY, Germany

Last Updated: 09/26/2026

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Found 19 publications

Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results.

Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results.

Journal: European journal of human genetics : EJHG

Published: June 19, 2025

Development and clinical validation of a novel algorithmic score (GAAD) for detecting HCC in prospective cohort studies.

Development and clinical validation of a novel algorithmic score (GAAD) for detecting HCC in prospective cohort studies.

Journal: Hepatology communications

Published: July 17, 2023

Performance evaluation of the Elecsys PIVKA-II and Elecsys AFP assays for hepatocellular carcinoma diagnosis.

Performance evaluation of the Elecsys PIVKA-II and Elecsys AFP assays for hepatocellular carcinoma diagnosis.

Journal: JGH open : an open access journal of gastroenterology and hepatology

Published: February 01, 2022

Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases.

Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases.

Journal: Genes

Published: December 22, 2020

Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.

Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.

Journal: Neuropediatrics

Published: October 21, 2020

Variant panorama in 1,385 index patients and sensitivity of expanded next-generation sequencing panels in arrhythmogenic disorders.

Variant panorama in 1,385 index patients and sensitivity of expanded next-generation sequencing panels in arrhythmogenic disorders.

Journal: Cardiovascular diagnosis and therapy

Published: November 19, 2019

Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providers.

Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providers.

Journal: European journal of medical genetics

Published: September 13, 2018

Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis.

Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis.

Journal: Frontiers in pediatrics

Published: March 25, 2018

Genetic heterogeneity of cytogenetically normal AML with mutations of CEBPA.

Genetic heterogeneity of cytogenetically normal AML with mutations of CEBPA.

Journal: Blood advances

Published: January 31, 2018

Severe bleeding complications and multiple kidney transplants in a patient with tuberous sclerosis complex caused by a novel TSC2 missense variant.

Severe bleeding complications and multiple kidney transplants in a patient with tuberous sclerosis complex caused by a novel TSC2 missense variant.

Journal: Croatian medical journal

Published: January 09, 2018

Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.

Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 07, 2017

Lessons From the EThIGII Trial: Proper Putative Benefit Assessment of Low-Molecular-Weight Heparin Treatment in M2/ANXA5 Haplotype Carriers.

Lessons From the EThIGII Trial: Proper Putative Benefit Assessment of Low-Molecular-Weight Heparin Treatment in M2/ANXA5 Haplotype Carriers.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: July 16, 2016

Showing 1-12 of 19

Last Updated: 09/26/2026