Lea M. Merz

Leipzig, SN, Germany

Last Updated: 09/26/2026

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Found 21 publications

Pediatric Hemolytic Uremic Syndrome in North-Eastern Germany During the STEC O45:H2 Outbreak in 2025: Clinical Features and Short-Term Outcomes.

Pediatric Hemolytic Uremic Syndrome in North-Eastern Germany During the STEC O45:H2 Outbreak in 2025: Clinical Features and Short-Term Outcomes.

Journal: Open forum infectious diseases

Published: April 02, 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

CAKUT variants in PRPF8, DYRK2, and CEP78: implications for splicing and ciliogenesis.

CAKUT variants in PRPF8, DYRK2, and CEP78: implications for splicing and ciliogenesis.

Journal: bioRxiv : the preprint server for biology

Published: August 08, 2025

Acute kidney injury due to diarrhoeal diseases in children: a systematic review.

Acute kidney injury due to diarrhoeal diseases in children: a systematic review.

Journal: BMJ paediatrics open

Published: April 17, 2025

Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.

Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.

Journal: Pediatric nephrology (Berlin, Germany)

Published: April 02, 2025

Effects of alpelisib treatment on murine Pten-deficient lipomas.

Effects of alpelisib treatment on murine Pten-deficient lipomas.

Journal: Adipocyte

Published: February 18, 2025

Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center Cohort.

Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center Cohort.

Journal: Kidney international reports

Published: February 17, 2025

Urinary Dickkopf-Related Protein 3-A Potential Long-Term Biomarker for Progressive CKD in Children.

Urinary Dickkopf-Related Protein 3-A Potential Long-Term Biomarker for Progressive CKD in Children.

Journal: Kidney international reports

Published: September 25, 2024

Correction to: Phenotypic quantification of Nphs1‑deficient mice.

Correction to: Phenotypic quantification of Nphs1‑deficient mice.

Journal: Journal of nephrology

Published: August 08, 2024

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 08, 2024

Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.

Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.

Journal: medRxiv : the preprint server for health sciences

Published: April 02, 2024

Quantitative phenotyping of Nphs1 knockout mice as a prerequisite for gene replacement studies.

Quantitative phenotyping of Nphs1 knockout mice as a prerequisite for gene replacement studies.

Journal: American journal of physiology. Renal physiology

Published: March 14, 2024

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Last Updated: 09/26/2026