Evidence map›Paper›PMID 30388780›Full record

ArticleNutrients2018

Low Salivary Amylase Gene (

Paola León-Mimila, Hugo Villamil-Ramírez, Blanca E López-Contreras, Sofía Morán-Ramos, Luis R Macias-Kauffer, Víctor Acuña-Alonzo, Blanca E Del Río-Navarro, Jorge Salmerón, Rafael Velazquez-Cruz, Teresa Villarreal-Molina and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

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  9. [From genotype to phenotype: amylase gene in childhood obesity].Revista medica del Instituto Mexicano del Seguro Social · 2023
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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 4 institutions in 1 country.

Paola León-MimilaFacultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico. paov_lemi@yahoo.com.mx.
Hugo Villamil-RamírezFacultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico. hugo_villamil@hotmail.com.
Blanca E López-ContrerasFacultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico. blopez@inmegen.gob.mx.
Sofía Morán-RamosFacultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico. smoran@inmegen.gob.mx.ORCID 0000-0003-0421-1166
Luis R Macias-KaufferFacultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico. luisrmacias@gmail.com.ORCID 0000-0002-3080-2835
Víctor Acuña-AlonzoEscuela Nacional de Antropología e Historia, Laboratorio de genética molecular, Mexico City 14030, Mexico. victor_acuna@inah.gob.mx.
Blanca E Del Río-NavarroDepartamento de Alergia e Inmunología Clínica, Hospital Infantil de México Federico Gómez, Mexico City 06720, Mexico. blancadelrionavarro@gmail.com.
Jorge SalmerónUnidad Académica de Investigación Epidemiológica del Centro de Investigación en Políticas, Población y Salud, Facultad de Medicina-UNAM, Mexico City 04510, Mexico. jorge.salmec@gmail.com.
Rafael Velazquez-CruzLaboratorio de Genómica del Metabolismo Óseo, INMEGEN, Mexico City 14610, Mexico. rvelazquez@inmegen.gob.mx.
Teresa Villarreal-MolinaLaboratorio de Enfermedades Cardiovasculares, INMEGEN, Mexico City 14610, Mexico. mvillareal@inmegen.gob.mx.ORCID 0000-0003-4450-7690
Carlos A Aguilar-SalinasUnidad de Investigación en Enfermedades Metabólicas and Departamento de Endocrinología y Metabolismo, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City 14000, Mexico. caguilarsalinas@yahoo.com.
Samuel Canizales-QuinterosFacultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City 14610, Mexico. cani@unam.mx.
National Institute of Genomic Medicine · MXHospital Infantil de México Federico Gómez · MXInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXNational Institute of Anthropology and History · MX

Funding

Universidad Nacional Autónoma de México (UNAM) PAPIIT/UNAM IA202413
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have identified copy number variants (CNVs) associated with obesity in chromosomal regions 1p31.1, 10q11.22, 11q11, 16p12.3, and recently 1p21.1, which contains the salivary amylase gene (

Indexed as

DNA Copy Number VariationsGenetic Predisposition to DiseasePrevotellaAdolescentAdultAgedCase-Control StudiesChildFemaleGastrointestinal MicrobiomeGenetic VariationGenome-Wide Association StudyHumansMaleMexicoMiddle AgedSalivary alpha-AmylasesAMY1CNVsMexicanobesityPrevotella

Identifiers

PMID30388780
PMCPMC6266693
OpenAlexW2899484787

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.