Evidence map›Paper›PMID 29892954›Full record

ArticleGenes & genomics2018

Analyses of karyotype by G-banding and high-resolution microarrays in a gender dysphoria population.

Rosa Fernández, Antonio Guillamón, Esther Gómez-Gil, Isabel Esteva, Mari Cruz Almaraz, Joselyn Cortés-Cortés, Beatriz Lamas, Estefanía Lema, Eduardo Pásaro

Abstract read
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In one paragraph

Article in Genes & genomics, 2018. 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
1.4field-weighted citation impact, top 17% 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, 18 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Rosa FernándezDepartment of Psychology, Universidade da Coruña, A Coruña, Spain. rosa.fernandez@udc.es.
Antonio GuillamónDepartment of Psychobiology, UNED, Madrid, Spain.
Esther Gómez-GilUnit of Gender Identity, Clinic Hospital, Barcelona, Spain.
Isabel EstevaUnit of Transsexualism and Gender Identity, Carlos Haya Hospital, Malaga, Spain.
Mari Cruz AlmarazUnit of Transsexualism and Gender Identity, Carlos Haya Hospital, Malaga, Spain.
Joselyn Cortés-CortésDepartment of Psychology, Universidade da Coruña, A Coruña, Spain.
Beatriz LamasDepartment of Psychology, Universidade da Coruña, A Coruña, Spain.
Estefanía LemaDepartment of Family, School and Society, Universidad Internacional de la Rioja, Logroño, Spain.
Eduardo PásaroDepartment of Psychology, Universidade da Coruña, A Coruña, Spain.
Universidade da Coruña · ESHospital Clínic de Barcelona · ESNational University of Distance Education · ESUniversidad Internacional De La Rioja · ES

Funding

Ministerio de Educación, Cultura y Deporte FPU-MECD 15/02558Secretaría de Estado de Investigación, Desarrollo e Innovación PSI2010-15115Secretaría de Estado de Investigación, Desarrollo e Innovación PSI2014-58004-P
6 · The paper itself

Abstract

Gender Dysphoria is characterized by a marked incongruence between the cerebral sex and biological sex. To investigate the possible influence of karyotype on the etiology of Gender Dysphoria we carried out the cytogenetic analysis of karyotypes in 444 male-to-females (MtFs) and 273 female-to-males (FtMs) that attended the Gender Identity Units of Barcelona and Málaga (Spain) between 2000 and 2016. The karyotypes from 23 subjects (18 MtFs and 5 FtMs) were also analysed by Affymetrix CytoScan™ high-density (HD) arrays. Our data showed a higher incidence of cytogenetic alterations in Gender Dysphoria (2.65%) than in the general population (0.53%) (p < 0.0001). When G-banding was performed, 11 MtFs (2.48%) and 8 FtMs (2.93%) showed a cytogenetic alteration. Specifically, Klinefelter syndrome frequency was significantly higher (1.13%) (p < 0.0001), however Turner syndrome was not represented in our sample (p < 0.61). At molecular level, HD microarray analysis revealed a 17q21.31 microduplication which encompasses the gene KANSL1 (MIM612452) in 5 out of 18 MtFs and 2 out of 5 FtMs that corresponds to a copy-number variation region in chromosome 17q21.31. In conclusion, we confirm a significantly high frequency of aneuploidy, specifically Klinefelter syndrome and we identified in 7 out of 23 GD individuals the same microduplication of 572 Kb which encompasses the KANSL1 gene.

Indexed as

AdultChromosome BandingChromosomes, Human, Pair 17FemaleGender DysphoriaGender IdentityGene DuplicationHumansKaryotypeKaryotypingKlinefelter SyndromeMaleMiddle AgedNuclear ProteinsTranssexualismTurner SyndromeNSL1 protein, humanNuclear Proteins17q21.31 microduplicationAneuploidyGender DysphoriaKANSL1Klinefelter syndrome

Identifiers

PMID29892954
OpenAlexW2785155596

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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.