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  1. Respighi, Ottorino [Author] ; Gardelli, Lamberto [Other]; Kincses, Veronika [Performer]; Nagy, János B. [Performer]; Miller, Lajos [Performer]; Zempléni, Mária [Performer]; Komlósi, Ildikó [Performer]; Kálmándi, Mihály [Performer]; Farkas, Katalin [Performer] Magyar Rádió és Televízió Budapest Énekkar, Magyar Állami Hangversenyzenekar Budapest

    Maria Egiziaca : [triptych for concert in three episodes] (1 CD)

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    [Budapest]: Hungaroton, P 1989

  2. Liszt, Franz [Author] ; Pál, Tamás [Performer]; Kállay, Gábor [Performer]; Zádori, Mária [Performer]; Farkas, Katalin [Performer]; Hamari, Julia [Performer]; Komlósi, Ildikó [Performer]; Garino, Gérard [Performer]; Gáti, István [Performer] Magyar Rádió és Televízió Budapest Énekkar, Magyar Állami Operaház Zenekar

    Don Sanche : opera 1 felvonásban, két részben (2 Schallpl)

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    [S.l.]: Hungaroton, P 1986

    Published in: Artisjus

  3. Respighi, Ottorino [Author] ; Guastalla, Claudio [Other]; Gardelli, Lamberto [Performer]; Sapszon, Ferenc [Performer]; Kincses, Veronika [Performer]; Nagy, János B. [Performer]; Miller, Lajos [Performer]; Zempléni, Mária [Performer]; Komlósi, Ildikó [Performer]; Kalmandi, Michele [Performer]; Farkas, Katalin [Performer] Magyar Rádió és Televízió Budapest Énekkar, Magyar Állami Hangversenyzenekar Budapest

    Maria Egiziaca = Mary of Egypt : triptych for Concert in three episodes = Egyiptomi Maria : koncert-triptichon három epizódban (2 Schallpl)

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    [S.l.]: Hungarton, P 1989

  4. Hotz, Alrun Göntje [Author]; Kopp, Julia [Author]; Komlosi, Katalin [Author]; Has, Cristina [Author]; Yang, Zhou [Author]; Zimmer, Andreas D. [Author]; Alter, Svenja [Author]; Fischer, Judith [Author]

    Meta-analysis of mutations in ALOX12B or ALOXE3 identified in a large cohort of 224 patients

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    Basel: MDPI, 2021

    Published in: Genes ; 12, 1 (2021), 80

  5. Resch, Luise D. [Author]; Hotz, Alrun Göntje [Author]; Zimmer, Andreas D. [Author]; Komlosi, Katalin [Author]; Singh, Nina [Author]; Tzschach, Andreas [Author]; Windfuhr-Blum, Marisa [Author]; Juhasz-Böss, Ingolf [Author]; Erbes, Thalia [Author]; Fischer, Judith [Author]; Alter, Svenja [Author]

    The importance of extended analysis using current molecular genetic methods based on the example of a cohort of 228 patients with hereditary breast and ovarian cancer syndrome

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    Basel: MDPI, 2021

    Published in: Genes ; 12, 10 (2021), 1483

  6. Komlosi, Katalin [Author]; Gläser, Selina [Author]; Kopp, Julia [Author]; Hotz, Alrun Göntje [Author]; Alter, Svenja [Author]; Zimmer, Andreas D. [Author]; Beger, Carmela [Author]; Heinzel, Stefan [Author]; Schmidt, Christoph [Author]; Fischer, Judith [Author]

    Neonatal presentation of COG6‐CDG with prominent skin phenotype

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    Hoboken, NJ: Wiley, 2020

    Published in: JIMD reports ; 55, 1 (2020), 51-58

  7. Endres, Dominique [Author]; Decher, Niels [Author]; Röhr, Isabell [Author]; Vowinkel, Kirsty Sophia [Author]; Domschke, Katharina [Author]; Komlosi, Katalin [Author]; Tzschach, Andreas [Author]; Gläser, Birgitta [Author]; Schiele, Miriam A. [Author]; Runge, Kimon [Author]; Süß, Patrick [Author]; Schuchardt, Florian [Author]; Nickel, Kathrin Alexandra [Author]; Stallmeyer, Birgit [Author]; Rinné, Susanne [Author]; Schulze-Bahr, Eric [Author]; Tebartz van Elst, Ludger [Author]

    New Cav1.2 channelopathy with high-functioning autism, affective disorder, severe dental enamel defects, a short QT interval, and a novel CACNA1C loss-of-function mutation

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    Basel: MDPI, 2020

    Published in: International journal of molecular sciences ; 21, 22 (2020), 8611

  8. Endres, Dominique [Author]; Süß, Patrick [Author]; Maier, Simon [Author]; Friedel, Evelyn [Author]; Nickel, Kathrin Alexandra [Author]; Ziegler, Christiane [Author]; Fiebich, Bernd L. [Author]; Glocker, Franz Xaver [Author]; Stock, Friedrich [Author]; Egger, Karl [Author]; Lange, Thomas [Author]; Dacko, Michael [Author]; Venhoff, Nils [Author]; Erny, Daniel [Author]; Doostkam, Soroush [Author]; Komlosi, Katalin [Author]; Domschke, Katharina [Author]; Tebartz van Elst, Ludger [Author]

    New variant of MELAS syndrome with executive dysfunction, heteroplasmic point mutation in the MT-ND4 gene (m.12015T>C; p.Leu419Pro) and comorbid polyglandular autoimmune syndrome type 2

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    Lausanne: Frontiers Media, 2019

    Published in: Frontiers in immunology ; 10 (2019), 412$z1664-3224

  13. Hadzsiev, Kinga; Polgar, Noemi; Bene, Judit; Komlosi, Katalin; Karteszi, Judit; Hollody, Katalin; Kosztolanyi, Gyorgy; Renieri, Alessandra; Melegh, Bela

    Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations

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    Springer Science and Business Media LLC, 2011

    Published in: Journal of Human Genetics, 56 (2011) 3, Seite 183-187

  14. Komlósi, Katalin; Kellermayer, Richárd; Maász, Anita; Havasi, Viktória; Hollódy, Katalin; Vincze, Olga; Merkli, Hajnalka; Pál, Endre; Melegh, Béla

    Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation

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    Springer Science and Business Media LLC, 2005

    Published in: Pathology & Oncology Research, 11 (2005) 2, Seite 82-86

  15. Koutra, Eleni; Lusmöller, Elke; Fischer, Judith; Komlosi, Katalin; Stadler, Rudolf; Gutzmer, Ralf

    Focal dermal hypoplasia associated with pathogenic PORCN gene variant in postzygotic, unilateral mosaic form Fokale dermale Hypoplasie durch pathogene Variante im PORCN-Gen in postzygotischer, unilateraler Mosaik-Konstellation

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    Springer Science and Business Media LLC, 2024

    Published in: Die Dermatologie, 75 (2024) 6, Seite 486-491

  16. Emmert, Steffen; Iben, Sebastian; Fischer, Judith; Komlosi, Katalin; Betz, Regina C.; Frank J, Jorge; Has, Christina

    Ein neues Forum für seltene Hauterkrankungen

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    Wiley, 2019

    Published in: JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 17 (2019) 6, Seite 672-673