Verena Klämbt

The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.

Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.

How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.

Assessed papers (1)

• Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.
  2023 L1 85/100

1 assessed by us (1 reproduced) · 37 not yet assessed — every PubMed paper on record, linked below.

• Cytosine base editing achieves robust lipoprotein(a) reduction while preserving genomic integrity ↗

  Molecular Therapy · 2026 · PMID 42140191
  not yet assessed
• Kidney-specific Wdr72 deletion leads to incomplete distal renal tubular acidosis through impaired V-ATPase B1 subunit localization ↗

  Genes & Diseases · 2026
  not yet assessed
• Pediatric Hemolytic Uremic Syndrome in North-Eastern Germany during the STEC O45:H2 Outbreak in 2025: Clinical Features and Short-Term Outcomes ↗

  Open Forum Infectious Diseases · 2026
  not yet assessed
• In vivo base editing reduces liver cysts in autosomal dominant polycystic kidney disease ↗

  Molecular Therapy · 2025 · PMID 40842155
  not yet assessed
• Outcomes and prognostic factors in childhood-onset steroid-resistant nephrotic syndrome: a retrospective single-center study ↗

  Pediatric Nephrology · 2025 · PMID 40021511
  not yet assessed
• <i>In vivo</i> base editing reduces liver cysts in autosomal dominant polycystic kidney disease ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2025 · PMID 39975003
  not yet assessed
• Outcomes and prognostic factors in childhood-onset steroid-resistant nephrotic syndrome ↗

  Pediatric Nephrology · 2025 · PMID 41042368
  not yet assessed
• Kidney-specific <i>Wdr72</i> deletion leads to incomplete distal renal tubular acidosis through impaired V-ATPase B1 subunit localization ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2025
  not yet assessed
• Biallelic TMEM72 Variants in Patients with a Nephronophthisis-Like Phenotype ↗

  ˜The œNephron journals/Nephron journals · 2025 · PMID 41308066
  not yet assessed
• Biallelic TMEM72 Variants in Patients with a Nephronophthisis-Like Phenotype

  Utrecht University Repository (Utrecht University) · 2025
  not yet assessed
• Ciliopathy organoid models: a comprehensive review ↗

  American Journal of Physiology-Cell Physiology · 2024 · PMID 39495251
  not yet assessed
• Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome ↗

  Genes & Diseases · 2024 · PMID 39584075
  not yet assessed
• Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions ↗

  Genes & Diseases · 2023 · PMID 38868576
  not yet assessed
• Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs

  Journal of the American Society of Nephrology · 2022 · PMID 36414417
  L1 85/100
• Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency ↗

  Journal of Allergy and Clinical Immunology · 2021 · PMID 33872655
  not yet assessed
• Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT ↗

  Genetics in Medicine · 2021 · PMID 34906515
  not yet assessed
• Recessive <i>NOS1AP</i> variants impair actin remodeling and cause glomerulopathy in humans and mice ↗

  Science Advances · 2021 · PMID 33523862
  not yet assessed
• Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome ↗

  Journal of the American Society of Nephrology · 2021 · PMID 33593823
  not yet assessed
• De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis ↗

  The American Journal of Human Genetics · 2021 · PMID 33508234
  not yet assessed
• Correction to: Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis ↗

  Pediatric Nephrology · 2021 · PMID 34553238
  not yet assessed
• A CRISPR-based assay for the detection of opportunistic infections post-transplantation and for the monitoring of transplant rejection ↗

  Nature Biomedical Engineering · 2020 · PMID 32284553
  not yet assessed
• Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations ↗

  The American Journal of Human Genetics · 2020 · PMID 32891193
  not yet assessed
• DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation ↗

  The American Journal of Human Genetics · 2020 · PMID 33232676
  not yet assessed
• Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches ↗

  Kidney International Reports · 2020 · PMID 33615071
  not yet assessed
• Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT) ↗

  Genetics in Medicine · 2020 · PMID 32475988
  not yet assessed
• Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis ↗

  Pediatric Nephrology · 2020 · PMID 32715379
  not yet assessed
• Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans ↗

  Nephrology Dialysis Transplantation · 2020 · PMID 33097957
  not yet assessed
• Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome ↗

  Kidney International Reports · 2020 · PMID 33615072
  not yet assessed
• A CRISPR-based assay for the detection of opportunistic infections post-transplantation and for the monitoring of transplant rejection

  DSpace@MIT (Massachusetts Institute of Technology) · 2020
  not yet assessed
• Generation of Monogenic Candidate Genes of Human Nephrotic Syndrome via Three Independent Approaches ↗

  Journal of the American Society of Nephrology · 2020
  not yet assessed
• Recessive Mutations in SEMA3G as a Potential Novel Cause of Nephrotic Syndrome ↗

  Journal of the American Society of Nephrology · 2020
  not yet assessed
• Whole-Exome Sequencing Reveals a Monogenic Cause of Disease in 23.1% of 276 Families with Steroid-Resistant Nephrotic Syndrome ↗

  Journal of the American Society of Nephrology · 2020
  not yet assessed
• RhoA-Rac1-CDC42 Regulators as Candidates for Monogenic Nephrotic Syndrome ↗

  Journal of the American Society of Nephrology · 2020
  not yet assessed
• Whole-Exome Sequencing in 97 Families with Renal Ciliopathies Reveals a Causative Mutation in a Known Kidney Disease Gene in 62% and Identifies Potential Novel Causative Genes ↗

  Journal of the American Society of Nephrology · 2020
  not yet assessed
• Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis ↗

  Kidney International · 2019 · PMID 31959358
  not yet assessed
• CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations ↗

  The American Journal of Human Genetics · 2019 · PMID 31708116
  not yet assessed
• Ribavirin therapy of hepatitis E infection may cause hyporegenerative anemia in pediatric renal transplant patients ↗

  Pediatric Transplantation · 2018 · PMID 29665156
  not yet assessed
• A Novel Function for P2Y2 in Myeloid Recipient–Derived Cells during Graft-versus-Host Disease ↗

  The Journal of Immunology · 2015 · PMID 26538394
  not yet assessed