Johannes R. Lemke

Philipp Rosenthal Street 55
Leipzig, SN 04103, Germany

Last Updated: 09/26/2026

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Found 180 publications

Silent refractoriness in epilepsy care: cross-sectoral analysis of prescribing patterns, referrals and workforce capacity in Saxony.

Silent refractoriness in epilepsy care: cross-sectoral analysis of prescribing patterns, referrals and workforce capacity in Saxony.

Journal: Frontiers in neurology

Published: April 14, 2026

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Journal: medRxiv : the preprint server for health sciences

Published: March 13, 2026

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Journal: medRxiv : the preprint server for health sciences

Published: March 13, 2026

Case report: a rare BRCA1 de novo variant in a female with breast cancer.

Case report: a rare BRCA1 de novo variant in a female with breast cancer.

Journal: Hereditary cancer in clinical practice

Published: January 13, 2026

Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.

Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy.

Journal: Molecular psychiatry

Published: January 07, 2026

Clinical impact of genetic testing in inherited kidney diseases.

Clinical impact of genetic testing in inherited kidney diseases.

Journal: Clinical kidney journal

Published: November 19, 2025

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Journal: Brain : a journal of neurology

Published: October 17, 2025

Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Journal: Epilepsia

Published: October 02, 2025

PRS-BC313 integration for tailored breast cancer prevention in female patients and their healthy relatives.

PRS-BC313 integration for tailored breast cancer prevention in female patients and their healthy relatives.

Journal: Journal of medical genetics

Published: September 15, 2025

Memantine treatment in individuals with GRIN gain-of-function variants is associated with improvements in behavior, development, and seizure frequency.

Memantine treatment in individuals with GRIN gain-of-function variants is associated with improvements in behavior, development, and seizure frequency.

Journal: Epilepsia

Published: September 11, 2025

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Journal: Nature genetics

Published: June 24, 2025

Assessment of 1863 GRIN2A Variants Contradicts a Role in Tumorigenesis.

Assessment of 1863 GRIN2A Variants Contradicts a Role in Tumorigenesis.

Journal: International journal of molecular sciences

Published: April 30, 2025

Showing 1-12 of 180

Last Updated: 09/26/2026