Evidence map›Paper›PMID 31087283›Full record

ArticleHormones (Athens, Greece)2019

A novel FGF8 mutation in a female patient with isolated congenital anosmia.

M I Stamou, L Plummer, V Koika, A Galli-Tsinopoulou, N A Georgopoulos

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

Article in Hormones (Athens, Greece), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 55% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 2 countries.

M I StamouHarvard Reproductive Science Center, Harvard Medical School, Mount Auburn Hospital, Harvard Medical School Teaching Hospital, Massachusetts General Hospital, Boston, MA, USA. mstamou@mah.harvard.edu.
L PlummerHarvard Reproductive Science Center, Harvard Medical School, Mount Auburn Hospital, Harvard Medical School Teaching Hospital, Massachusetts General Hospital, Boston, MA, USA.
V KoikaDepartment of Obstetrics and Gynecology, Division of Reproductive Endocrinology, University Regional Hospital of Patras, Rio, Greece.
A Galli-Tsinopoulou4th Department of Pediatrics, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.
N A GeorgopoulosDepartment of Obstetrics and Gynecology, Division of Reproductive Endocrinology, University Regional Hospital of Patras, Rio, Greece.
General University Hospital of Patras · GRMount Auburn Hospital · USAristotle University of Thessaloniki · GR

Funding

The Genetic Determinants of Human GNRH DeficiencyP50HD028138 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI CROWLEY, WILLIAM FRANCIS · 2014 to 2020
$12.9M
Alexander S. Onassis Public Benefit Foundation ScholarshipNICHD NIH HHS P50 HD028138
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Predisposition to DiseaseMutationChildFemaleFibroblast Growth Factor 8Gene Expression Regulation, DevelopmentalHumansMagnetic Resonance AngiographyOlfaction DisordersOlfactory BulbFGF8 protein, humanFibroblast Growth Factor 8

Identifiers

PMID31087283
PMCPMC8832634
OpenAlexW2946119545

What OpenQuestion holds

Textmetadata
LicenceTDM
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.