Evidence map›Paper›PMID 36999056›Full record

ArticleFrontiers in genetics2023

Hereditary orotic aciduria identified by newborn screening.

Orna Staretz-Chacham, Nadirah S Damseh, Suha Daas, Nasser Abu Salah, Yair Anikster, Ortal Barel, Elena Dumin, Aviva Fattal-Valevski, Tzipora C Falik-Zaccai, Eli Hershkovitz and 14 more

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

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

24 authors at 16 institutions in 2 countries.

Orna Staretz-ChachamMetabolic Clinic, Pediatric Division, Soroka University Medical Center, Ben Gurion University, Beer- Sheva, Israel.
Nadirah S DamsehFaculty of Medicine, Al-Quds University, Palestinian National Authority, Abu Deis, Palestine.
Suha DaasNational Newborn Screening Program, Public Health Services, Ministry of Health, Ramat-Gan, Israel.
Nasser Abu SalahDepartment of Neonatology, Red Crescent Society Hospital, Jerusalem, Israel.
Yair AniksterSackler School of Medicine, Tel Aviv University, Tel-Aviv, Israel.
Ortal BarelGenomics Unit, The Center for Cancer Research, Sheba Medical Center, Ramat Gan, Israel.
Elena DuminMetabolic Laboratory, Sheba Medical Center, Ramat Gan, Israel.
Aviva Fattal-ValevskiTel Aviv Sourasky Medical Center, Dana Children Hospital, Pediatric Neurology Institute, Tel Aviv, Israel.
Tzipora C Falik-ZaccaiGalilee Medical Center, Institute of Human Genetics, Naharia, Israel.
Eli HershkovitzMetabolic Clinic, Pediatric Division, Soroka University Medical Center, Ben Gurion University, Beer- Sheva, Israel.
Sagi JosefsbergKaplan Medical Center, Genetics Institute, Rehovot, Israel.
Yuval LandauMetabolic Disease Unit, Schneider Children's Medical Center, Petah Tikva, Israel.
Tally Lerman-SagieMagen Center for Rare Diseases-Metabolic, Neurogenetic, Wolfson Medical Center, Holon, Israel.
Hanna MandelMetabolic Unit, Department of Genetics, Rebecca Sieff Hospital, Safed, Israel.
Rachel RockNational Newborn Screening Program, Public Health Services, Ministry of Health, Ramat-Gan, Israel.
Nira RostamiNational Newborn Screening Program, Public Health Services, Ministry of Health, Ramat-Gan, Israel.
Talya Saraf-LevyNational Newborn Screening Program, Public Health Services, Ministry of Health, Ramat-Gan, Israel.
Nava Shaul LotanDepartment of Genetics, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Ronen SpiegelDepartment of Pediatrics B, Metabolic Service, Emek Medical Center, Afula, Israel.
Galit TalRambam Medical Center, Metabolic Clinic, Ruth Rappaport Children's Hospital, Haifa, Israel.
Igor UlanovskyNational Newborn Screening Program, Public Health Services, Ministry of Health, Ramat-Gan, Israel.
Yael WilnaiTel Aviv Sourasky Medical Center, Genetic Institute, Tel Aviv, Israel.
Stanley H KormanRambam Medical Center, Metabolic Clinic, Ruth Rappaport Children's Hospital, Haifa, Israel.
Shlomo AlmashanuNational Newborn Screening Program, Public Health Services, Ministry of Health, Ramat-Gan, Israel.
Israel Ministry of Health · ILTechnion – Israel Institute of Technology · ILTel Aviv Sourasky Medical Center · ILAl-Quds University · PSBen-Gurion University of the Negev · ILHadassah Medical Center · ILHebrew University of Jerusalem · ILKaplan Medical Center · ILRappaport Family Institute for Research in the Medical Sciences · ILRebecca Sieff Hospital · ILSchneider Children's Medical Center · ILSheba Medical Center · ILSoroka Medical Center · ILTel Aviv University · ILWestern Galilee Hospital · ILWolfson Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

hereditary orotic aciduriamegaloblastic anemianeurodevelopmental disabilitynewborn screening (NBS)orotic aciduridine monophosphate synthase

Identifiers

PMID36999056
PMCPMC10043439
OpenAlexW4324145892

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read2
measurements read13
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.