Evidence map›Paper›PMID 38136956›Full record

ArticleGenes2023

Work-Up and Treatment Strategies for Individuals with

Andrea Gazzin, Chiara Leoni, Germana Viscogliosi, Federica Borgini, Lucrezia Perri, Matteo Iacoviello, Marilidia Piglionica, Maurizio De Pellegrin, Giovanni Battista Ferrero, Andrea Bartuli and 5 more

Open access · goldAbstract readConsensus Statement
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. [Effectiveness analysis of tibial nerve transection with epineurial suture and division of common plantar digital nerve branches in treatment of congenital macrodactyly in children].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Uncovering somatic mosaic variants ofFrontiers in genetics · 2024
    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

15 authors at 6 institutions in 1 country.

Andrea GazzinClinical Pediatric Genetics Unit, Department of Public Health and Pediatrics, University of Torino, Regina Margherita Children's Hospital, 10126 Torino, Italy.ORCID 0000-0002-5230-2831
Chiara LeoniCenter for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168 Rome, Italy.ORCID 0000-0002-4089-637X
Germana ViscogliosiCenter for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168 Rome, Italy.ORCID 0000-0002-1697-6337
Federica BorginiItalian Macrodactyly and PROS Association, 27010 San Genesio ed Uniti (PV), Italy.
Lucrezia PerriCenter for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168 Rome, Italy.
Matteo IacovielloMedical Genetics Unit, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0003-4253-4361
Marilidia PiglionicaMedical Genetics Unit, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", 70124 Bari, Italy.
Maurizio De PellegrinPediatric Orthopedic Unit, Piccole Figlie Hospital, 43125 Parma, Italy.
Giovanni Battista FerreroDepartment of Clinical and Biological Sciences, University of Torino, 10126 Torino, Italy.
Andrea BartuliRare Disease and Medical Genetics Unit, Bambino Gesù Children's Hospital, IRCCS, 00168 Rome, Italy.ORCID 0000-0001-9765-7460
Giuseppe ZampinoCenter for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168 Rome, Italy.
Paola Sabrina BuonuomoRare Disease and Medical Genetics Unit, Bambino Gesù Children's Hospital, IRCCS, 00168 Rome, Italy.
Nicoletta RestaMedical Genetics Unit, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0001-8640-5532
Alessandro MussaClinical Pediatric Genetics Unit, Department of Public Health and Pediatrics, University of Torino, Regina Margherita Children's Hospital, 10126 Torino, Italy.ORCID 0000-0003-2795-6013
Italian Macrodactyly and PROS Association
Agostino Gemelli University Polyclinic · ITUniversity of Bari Aldo Moro · ITBambino Gesù Children's Hospital · ITUniversity of Turin · ITOspedale Papa Giovanni XXIII · ITUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Phosphatidylinositol 3-KinasesClass I Phosphatidylinositol 3-KinasesFingersHumansItalyLimb Deformities, CongenitalMutationClass I Phosphatidylinositol 3-KinasesPhosphatidylinositol 3-KinasesPIK3CA protein, humanovergrowthpersonalized medicinePI3K/AKT/mTORPIK3CAPIK3CA-related overgrowth spectrumrepurposed drugstarget therapy

Identifiers

PMID38136956
PMCPMC10742781
OpenAlexW4389056200

What OpenQuestion 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 OpenQuestion graph.