Publication:
Gestaltmatcher database - a global reference for facial phenotypic variability in rare human diseases

dc.contributor.coauthorLesmann, Hellen
dc.contributor.coauthorHustinx, Alexander
dc.contributor.coauthorShahida, Moosa
dc.contributor.coauthorKlinkhammer, Hannah
dc.contributor.coauthorMarchi, Elaine
dc.contributor.coauthorCaro, Pilar
dc.contributor.coauthorAbdelrazek, Ibrahim M.
dc.contributor.coauthorPantel, Jean Tori
dc.contributor.coauthorHagen, Merle Ten
dc.contributor.coauthorThong
dc.contributor.coauthorMeow-Keong
dc.contributor.coauthorBinti Mazlan, Rifhan Azwani
dc.contributor.coauthorTae, Sok Kun
dc.contributor.coauthorKamphans, Tom
dc.contributor.coauthorMeiswinkel, Wolfgang
dc.contributor.coauthorLi, Jing-Mei
dc.contributor.coauthorJavanmardi, Behnam
dc.contributor.coauthorKnaus, Alexej
dc.contributor.coauthorUwineza, Annette
dc.contributor.coauthorKnopp, Cordula
dc.contributor.coauthorTkemaladze, Tinatin
dc.contributor.coauthorElbracht, Miriam
dc.contributor.coauthorMattern, Larissa
dc.contributor.coauthorJamra, Rami Abou
dc.contributor.coauthorVelmans, Clara
dc.contributor.coauthorStrehlow, Vincent
dc.contributor.coauthorJacob, Maureen
dc.contributor.coauthorPeron, Angela
dc.contributor.coauthorDias, Cristina
dc.contributor.coauthorNunes, Beatriz Carvalho
dc.contributor.coauthorVilella, Thainá
dc.contributor.coauthorPinheiro, Isabel Furquim
dc.contributor.coauthorKim, Chong Ae
dc.contributor.coauthorMelaragno, Maria Isabel
dc.contributor.coauthorWeiland,Hannah
dc.contributor.coauthorKaptain, Sophia
dc.contributor.coauthorChwiałkowska, Karolina
dc.contributor.coauthorKwasniewski, Miroslaw
dc.contributor.coauthorSaad, Ramy
dc.contributor.coauthorWiethoff, Sarah
dc.contributor.coauthorGoel, Himanshu
dc.contributor.coauthorTang, Clara
dc.contributor.coauthorHau, Anna
dc.contributor.coauthorBarakat, Tahsin Stefan
dc.contributor.coauthorPanek, Przemysław
dc.contributor.coauthorNabil, Amira
dc.contributor.coauthorSuh, Julia
dc.contributor.coauthorBraun, Frederik
dc.contributor.coauthorGomy, Israel
dc.contributor.coauthorAverdunk, Luisa
dc.contributor.coauthorEkure, Ekanem
dc.contributor.coauthorBergant, Gaber
dc.contributor.coauthorPeterlin, Borut
dc.contributor.coauthorGraziano, Claudio
dc.contributor.coauthorGaboon, Nagwa
dc.contributor.coauthorFiesco-Roa, Moisés
dc.contributor.coauthorSpinelli, Alessandro Mauro
dc.contributor.coauthorWilpert, Nina-Maria
dc.contributor.coauthorPhowthongkum, Prasit
dc.contributor.coauthorGüzel, Nergis
dc.contributor.coauthorHaack, Tobias B.
dc.contributor.coauthorBitar, Rana
dc.contributor.coauthorTzschach, Andreas
dc.contributor.coauthorRodriguez-Palmero, Agust
dc.contributor.coauthorBrunet, Theresa
dc.contributor.coauthorRudnik-Schöneborn, Sabine
dc.contributor.coauthorContreras-Capetillo, Silvina Noemi
dc.contributor.coauthorOberlack, Ava
dc.contributor.coauthorSamango-Sprouse, Carole
dc.contributor.coauthorSadeghin, Teresa
dc.contributor.coauthorOlaya Margaret
dc.contributor.coauthorPlatzer, Konrad
dc.contributor.coauthorBorovikov, Artem
dc.contributor.coauthorSchnabel, Franziska
dc.contributor.coauthorHeuft, Lara
dc.contributor.coauthorHerrmann, Vera
dc.contributor.coauthorOegema, Renske
dc.contributor.coauthorElkhateeb, Nour
dc.contributor.coauthorKumar, Sheetal
dc.contributor.coauthorKomlosi, Katalin
dc.contributor.coauthorMohamed, Khoushoua
dc.contributor.coauthorKalantari, Silvia
dc.contributor.coauthorSirchia, Fabio
dc.contributor.coauthorMartinez-Monseny, Antonio F.
dc.contributor.coauthorHöller, Matthias
dc.contributor.coauthorToutouna
dc.contributor.coauthorLouiza
dc.contributor.coauthorMohamed, Amal
dc.contributor.coauthorLasa-Aranzasti, Amaia
dc.contributor.coauthorSayer, John A.
dc.contributor.coauthorEhmke, Nadja
dc.contributor.coauthorDanyel, Magdalena
dc.contributor.coauthorSczakiel, Henrike
dc.contributor.coauthorSchwartzmann, Sarina
dc.contributor.coauthorBoschann, Felix
dc.contributor.coauthorZhao, Max
dc.contributor.coauthorAdam, Ronja
dc.contributor.coauthorEinicke, Lara
dc.contributor.coauthorHorn, Denise
dc.contributor.coauthorChew, Kee Seang
dc.contributor.coauthorKam, Choy Chen
dc.contributor.coauthorKarakoyun, Miray
dc.contributor.coauthorPode-Shakked, Ben
dc.contributor.coauthorEliyahu, Aviva
dc.contributor.coauthorRock, Rachel
dc.contributor.coauthorCarrion, Teresa
dc.contributor.coauthorChorin, Odelia
dc.contributor.coauthorZarate, Yuri A.
dc.contributor.coauthorConti, Marcelo Martinez
dc.contributor.coauthorKarakaya, Mert
dc.contributor.coauthorTung, Moon Ley
dc.contributor.coauthorChandra, Bharatendu
dc.contributor.coauthorBouman, Arjan
dc.contributor.coauthorLumaka, Aime
dc.contributor.coauthorWasif, Naveed
dc.contributor.coauthorShinawi, Marwan
dc.contributor.coauthorBlackburn, Patrick R.
dc.contributor.coauthorWang, Tianyun
dc.contributor.coauthorNiehues, Tim
dc.contributor.coauthorSchmidt, Axel
dc.contributor.coauthorRoth, Regina Rita
dc.contributor.coauthorWieczorek, Dagmar
dc.contributor.coauthorHu, Ping
dc.contributor.coauthorWaikel, Rebekah L.
dc.contributor.coauthorLedgister Hanchard, Suzanna E.
dc.contributor.coauthorElmakkawy, Gehad
dc.contributor.coauthorSafwat, Sylvia
dc.contributor.coauthorEbstein, Frédéric
dc.contributor.coauthorKrüger, Elke
dc.contributor.coauthorKüry, Sébastien
dc.contributor.coauthorBézieau, Stéphane
dc.contributor.coauthorArlt, Annabelle
dc.contributor.coauthorOlinger, Eric
dc.contributor.coauthorMarbach, Felix
dc.contributor.coauthorLi, Dong
dc.contributor.coauthorDupuis, Lucie
dc.contributor.coauthorMendoza-Londono, Roberto
dc.contributor.coauthorHouge, Sofia Douzgou
dc.contributor.coauthorWeis, Denisa
dc.contributor.coauthorChung, Brian Hon-Yin
dc.contributor.coauthorMak, Christopher C. Y.
dc.contributor.coauthorElçioğlu, Nursel
dc.contributor.coauthorAykut, Ayça
dc.contributor.coauthorŞimşek-Kiper, Peli Özlem
dc.contributor.coauthorBögershausen, Nina
dc.contributor.coauthorWollnik, Bernd
dc.contributor.coauthorBentzen, Heidi Beate
dc.contributor.coauthorKurth, Ingo
dc.contributor.coauthorNetzer, Christian
dc.contributor.coauthorJezela-Stanek, Aleksandra
dc.contributor.coauthorDevriendt, Koen
dc.contributor.coauthorGripp, Karen W.
dc.contributor.coauthorMücke, Martin
dc.contributor.coauthorVerloes, Alain
dc.contributor.coauthorSchaaf, Christian P.
dc.contributor.coauthorNellåker, Christoffer
dc.contributor.coauthorSolomon, Benjamin D.
dc.contributor.coauthorNöthen, Markus M.
dc.contributor.coauthorAbdalla, Ebtesam
dc.contributor.coauthorLyon, Gholson J.
dc.contributor.coauthorKrawitz, Peter M.
dc.contributor.coauthorHsieh, Tzung-Chien
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-12-29T09:39:35Z
dc.date.issued2024
dc.description.abstractThe most important factor that complicates the work of dysmorphologists is the significant phenotypic variability of the human face. Next-Generation Phenotyping (NGP) tools that assist clinicians with recognizing characteristic syndromic patterns are particularly challenged when confronted with patients from populations different from their training data. To that end, we systematically analyzed the impact of genetic ancestry on facial dysmorphism. For that purpose, we established the GestaltMatcher Database (GMDB) as a reference dataset for medical images of patients with rare genetic disorders from around the world. We collected 10,980 frontal facial images - more than a quarter previously unpublished - from 8,346 patients, representing 581 rare disorders. Although the predominant ancestry is still European (67%), data from underrepresented populations have been increased considerably via global collaborations (19% Asian and 7% African). This includes previously unpublished reports for more than 40% of the African patients. The NGP analysis on this diverse dataset revealed characteristic performance differences depending on the composition of training and test sets corresponding to genetic relatedness. For clinical use of NGP, incorporating non-European patients resulted in a profound enhancement of GestaltMatcher performance. The top-5 accuracy rate increased by +11.29%. Importantly, this improvement in delineating the correct disorder from a facial portrait was achieved without decreasing the performance on European patients. By design, GMDB complies with the FAIR principles by rendering the curated medical data findable, accessible, interoperable, and reusable. This means GMDB can also serve as data for training and benchmarking. In summary, our study on facial dysmorphism on a global sample revealed a considerable cross ancestral phenotypic variability confounding NGP that should be counteracted by international efforts for increasing data diversity. GMDB will serve as a vital reference database for clinicians and a transparent training set for advancing NGP technology.
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume1
dc.identifier.doi10.21203/rs.3.rs-4438861/v1
dc.identifier.quartileN/A
dc.identifier.urihttps://doi.org/10.21203/rs.3.rs-4438861/v1
dc.identifier.urihttps://hdl.handle.net/20.500.14288/23058
dc.keywordsGenetics research
dc.keywordsMedical research
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofResearch Square
dc.subjectHealth sciences
dc.titleGestaltmatcher database - a global reference for facial phenotypic variability in rare human diseases
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKayserili, Hülya
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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