Evidence map›Paper›PMID 38674137›Full record

ArticleInternational journal of molecular sciences2024

The Phenotypic Variability Associated with Hepatocyte Nuclear Factor 1B Genetic Defects Poses Challenges in Both Diagnosis and Therapy.

Ioannis Petrakis, Maria Sfakiotaki, Maria Bitsori, Eleni Drosataki, Kleio Dermitzaki, Christos Pleros, Ariadni Androvitsanea, Dimitrios Samonakis, Amalia Sertedaki, Paraskevi Xekouki and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Treatment Options for Patients with Maturity-Onset Diabetes of the Young (MODY): A Systematic Review of Literature: 2026 Update.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2026
    Pooled it
  2. Article
  3. Review
  4. Atypical presentation ofSAGE open medical case reports · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Ioannis PetrakisDepartment of Nephrology, University of Crete, 71500 Heraklion, Greece.ORCID 0000-0002-0095-9823
Maria SfakiotakiDepartment of Endocrinology, University of Crete, 71500 Heraklion, Greece.
Maria BitsoriDepartment of Pediatrics, University of Crete, 71500 Heraklion, Greece.
Eleni DrosatakiDepartment of Nephrology, University of Crete, 71500 Heraklion, Greece.
Kleio DermitzakiDepartment of Nephrology, University of Crete, 71500 Heraklion, Greece.
Christos PlerosDepartment of Nephrology, University of Crete, 71500 Heraklion, Greece.ORCID 0000-0001-8123-771X
Ariadni AndrovitsaneaDepartment of Nephrology, University of Crete, 71500 Heraklion, Greece.
Dimitrios SamonakisDepartment of Gastroenterology, University of Crete, 71500 Heraklion, Greece.
Amalia SertedakiFirst Department of Pediatrics, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.ORCID 0000-0002-3648-3812
Paraskevi XekoukiDepartment of Endocrinology, University of Crete, 71500 Heraklion, Greece.
Emmanouil GalanakisDepartment of Pediatrics, University of Crete, 71500 Heraklion, Greece.
Kostas StylianouDepartment of Nephrology, University of Crete, 71500 Heraklion, Greece.ORCID 0000-0003-3678-9421
University of Crete · GRNational and Kapodistrian University of Athens · GR

Funding

KIDS-CRETE 4/2022
6 · The paper itself

Abstract

The evolving landscape of clinical genetics is becoming increasingly relevant in the field of nephrology. HNF1B-associated renal disease presents with a diverse array of renal and extrarenal manifestations, prominently featuring cystic kidney disease and diabetes mellitus. For the genetic analyses, whole exome sequencing (WES) and multiplex ligation-dependent probe amplification (MLPA) were performed. Bioinformatics analysis was performed with Ingenuity Clinical Insights software (Qiagen). The patient's electronic record was utilized after receiving informed consent. In this report, we present seven cases of HNF1B-associated kidney disease, each featuring distinct genetic abnormalities and displaying diverse extrarenal manifestations. Over 12 years, the mean decline in eGFR averaged -2.22 ± 0.7 mL/min/1.73 m

Indexed as

Hepatocyte Nuclear Factor 1-betaPhenotypeAdolescentAdultChildDiabetes MellitusExome SequencingFemaleHumansKidney Diseases, CysticMaleMiddle AgedMutationYoung AdultHepatocyte Nuclear Factor 1-betaHNF1B protein, humancystic kidney diseasegenetic variabilityhepatic nuclear factor 1B (HNF1B)multiplex ligation-dependent probe amplification (MPLA)whole exome sequencing (WES)

Identifiers

PMID38674137
PMCPMC11050681
OpenAlexW4395000591

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.