Evidence map›Paper›PMID 35506546›Full record

ArticlePrenatal diagnosis2022

Discordant cfDNA-NIPT result unraveling a trisomy 12 chronic lymphocytic leukemia in a 37 years old pregnant woman.

Niccolò Di Giosaffatte, Irene Bottillo, Luigi Laino, Giovanni Iaquinta, Alessandro Ferraris, Mariagrazia Garzia, Simone Bargiacchi, Claudia Mulargia, Maria Rosaria Angelitti, Fabiana Palumbo and 5 more

Open access · greenAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Prenatal diagnosis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 23% 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, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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 2 institutions in 2 countries.

Niccolò Di GiosaffatteDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Irene BottilloDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.ORCID 0000-0003-0396-7981
Luigi LainoDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Giovanni IaquintaDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Alessandro FerrarisDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Mariagrazia GarziaHaematology and Stem Cell Transplantation Unit, San Camillo-Forlanini Hospital, Rome, Italy.
Simone BargiacchiDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Claudia MulargiaDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Maria Rosaria AngelittiDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Fabiana PalumboHaematology and Stem Cell Transplantation Unit, San Camillo-Forlanini Hospital, Rome, Italy.
Barbara GrammaticoDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
Cinzia BartolelliObstetrics and Gynecology Unit, San Camillo-Forlanini Hospital, Rome, Italy.
Maria Giovanna SalernoObstetrics and Gynecology Unit, San Camillo-Forlanini Hospital, Rome, Italy.
Luigi RigacciHaematology and Stem Cell Transplantation Unit, San Camillo-Forlanini Hospital, Rome, Italy.
Paola GrammaticoDepartment of Molecular Medicine, Laboratory of Medical Genetics, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.
IRCCS San Camillo Hospital · ITCarlo Forlanini Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cell-Free Nucleic AcidsLeukemia, Lymphocytic, Chronic, B-CellAdultFemaleHumansPregnancyPregnant PeoplePrenatal DiagnosisTrisomyTrisomy 13 SyndromeTrisomy 18 SyndromeCell-Free Nucleic Acids

Identifiers

PMID35506546
PMCPMC9546086
OpenAlexW4225374313

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.