Omer Shlomovitz

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) · 16 not yet assessed — every PubMed paper on record, linked below.

• Intronic and Coding Genetic Variants in Autosomal Recessive Polycystic Kidney Disease Among Israeli Bedouins of Arabian Peninsula Ancestry ↗

  American Journal of Kidney Diseases · 2025 · PMID 40816622
  not yet assessed
• Genetic Terminal Complement Deficiency in Israeli Bedouins With Kidney Failure ↗

  Kidney International Reports · 2025 · PMID 40303201
  not yet assessed
• Elucidating Mechanisms of Hypomorphic WDR19-Related Kidney Failure ↗

  Kidney International Reports · 2025 · PMID 41141533
  not yet assessed
• A Retrospective Cross‐Sectional Study of 142 Patients in a Multidisciplinary Tuberous Sclerosis Clinic ↗

  Clinical Genetics · 2025 · PMID 41139920
  not yet assessed
• Multiethnic prevalence of the <i>APOL1</i> G1 and G2 variants among the Israeli dialysis population ↗

  Clinical Kidney Journal · 2024 · PMID 39927257
  not yet assessed
• Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure ↗

  Kidney International Reports · 2023 · PMID 37850020
  not yet assessed
• Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders ↗

  Frontiers in Genetics · 2023 · PMID 36699461
  not yet assessed
• Genetic Markers Among the Israeli Druze Minority Population With End-Stage Kidney Disease ↗

  American Journal of Kidney Diseases · 2023 · PMID 37717846
  not yet assessed
• A multidisciplinary nephrogenetic referral clinic for children and adults—diagnostic achievements and insights ↗

  Pediatric Nephrology · 2022 · PMID 34993602
  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
• Mammalian target of rapamycin inhibitors for the treatment of astrocytic hamartoma in tuberous sclerosis complex (TSC) ↗

  Graefe s Archive for Clinical and Experimental Ophthalmology · 2022 · PMID 35230473
  not yet assessed
• Poststreptococcal Myalgia and Protracted Febrile Myalgia Syndrome: Similar Yet Different ↗

  The Journal of Pediatrics · 2022 · PMID 35588798
  not yet assessed
• MO046: Exome sequencing of Israeli Druze individuals on dialysis reveals common as well as population- specific monogenic etiologies in ∼30% ↗

  Nephrology Dialysis Transplantation · 2022
  not yet assessed
• FC035: Exome Sequencing of the Israeli Dialysis-Treated Pediatric Population Reveals Monogenic Etiology in ∼44% of Cases ↗

  Nephrology Dialysis Transplantation · 2022
  not yet assessed
• Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects ↗

  Journal of Medical Genetics · 2021 · PMID 34215651
  not yet assessed
• Prediction of tuberous sclerosis-associated neurocognitive disorders and seizures via machine learning of structural magnetic resonance imaging ↗

  Neuroradiology · 2021 · PMID 34532765
  not yet assessed
• An Israeli tuberous sclerosis cohort: the efficacy of different anti-epileptic strategies ↗

  Child s Nervous System · 2021 · PMID 34491422
  not yet assessed