<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-08-05T16:13:20Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/15893" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/15893</identifier><datestamp>2025-05-12T07:18:48Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19618</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Salvador, Raymond</subfield>
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      <subfield code="a">García-León, María Ángeles</subfield>
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      <subfield code="a">Feria-Raposo, Isabel</subfield>
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      <subfield code="a">Larrubia-Romero, Jesús</subfield>
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      <subfield code="a">Larraz-Romeo, José Antonio</subfield>
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      <subfield code="a">Guardiola-Ripoll, Maria</subfield>
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      <subfield code="a">Almodóvar-Payá, Carmen</subfield>
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      <subfield code="a">Fatjó-Vilas Mestre, Mar</subfield>
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      <subfield code="a">Sarró, Salvador</subfield>
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      <subfield code="a">McKenna, Peter J</subfield>
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      <subfield code="a">HHFingerprints Group</subfield>
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      <subfield code="a">Pomarol-Clotet, Edith</subfield>
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      <subfield code="c">2023-05-03</subfield>
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      <subfield code="a">Background and hypothesis: The existing developmental bond between fingerprint generation and growth of the central nervous system points to a potential use of fingerprints as risk markers in schizophrenia. However, the high complexity of fingerprints geometrical patterns may require flexible algorithms capable of characterizing such complexity. Study design: Based on an initial sample of scanned fingerprints from 612 patients with a diagnosis of non-affective psychosis and 844 healthy subjects, we have built deep learning classification algorithms based on convolutional neural networks. Previously, the general architecture of the network was chosen from exploratory fittings carried out with an independent fingerprint dataset from the National Institute of Standards and Technology. The network architecture was then applied for building classification algorithms (patients vs controls) based on single fingers and multi-input models. Unbiased estimates of classification accuracy were obtained by applying a 5-fold cross-validation scheme. Study results: The highest level of accuracy from networks based on single fingers was achieved by the right thumb network (weighted validation accuracy = 68%), while the highest accuracy from the multi-input models was attained by the model that simultaneously used images from the left thumb, index and middle fingers (weighted validation accuracy = 70%). Conclusion: Although fitted models were based on data from patients with a well established diagnosis, since fingerprints remain lifelong stable after birth, our results imply that fingerprints may be applied as early predictors of psychosis. Specially, if they are used in high prevalence subpopulations such as those of individuals at high risk for psychosis.</subfield>
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      <subfield code="a">Schizophr Bull. 2023 May 3;49(3):738-745.</subfield>
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      <subfield code="a">10.1093/schbul/sbac173</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/15893</subfield>
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      <subfield code="a">Artificial intelligence</subfield>
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      <subfield code="a">Dermatoglyphics</subfield>
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      <subfield code="a">Fingerprints as Predictors of Schizophrenia: A Deep Learning Study</subfield>
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