GET
json api

Publication List

List publications.

Fields

id (integer)

Primary key.

name (string)

Name of doctoral school.

emails (string[])

Contact emails.

Expansions

To activate relation expansion add the desired fields as a comma separated list to the expand query parameter like this:

?expand=<field>,<field>,<field>,...

The following relational fields can be expanded:

  • persons
  • category
  • document
  • organization_authorship

Filters

To filter for exact value matches:

?<fieldname>=<value>

Possible exact filters:

  • year
  • category
  • document
  • persons

For advanced filtering use lookups:

?<fieldname>__<lookup>=<value>

All fields with advanced lookups can also be used for exact value matches as described above.

Possible advanced lookups:

  • year: gt, gte, lt, lte
  • sci: iexact, contains, icontains, startswith, istartswith
  • pubmed: iexact, contains, icontains, startswith, istartswith
  • doi: iexact, contains, icontains, startswith, istartswith
  • pmc: iexact, contains, icontains, startswith, istartswith
  • organization_authorship: in
  • impact: isnull, gt, gte, lt, lte
  • imported: isnull, gt, gte, lt, lte, date
GET /v1/research/publication/?format=api&offset=1820&ordering=-year
HTTP 200 OK
  Allow: GET, HEAD, OPTIONS
  Content-Type: application/json
  Vary: Accept
  
  {
    "count": 157148,
    "next": "https://api-test.medunigraz.at/v1/research/publication/?format=api&limit=20&offset=1840&ordering=-year",
    "previous": "https://api-test.medunigraz.at/v1/research/publication/?format=api&limit=20&offset=1800&ordering=-year",
    "results": [
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            "id": 217605,
            "title": "Endothelial dysfunction in Fabry disease",
            "abstract": "Introduction: Fabry disease (FD) is a rare lysosomal storage disorder caused by pathogenic variants in the GLA-gene, which encodes the enzyme alpha-Galactosidase (AGAL), required for degradation of globotriaosylceramid (Gb3). Deficiency of AGAL results in Gb3 accumulation in various cells and tissues. Endothelial cells are commonly affected, and their impairment leads to endothelial dysfunction (ED). Although men usually present with more severe symptoms sue to, X-linked inheritance, women can also present with serious manifestations, despite showing less Gb3 accumulation. Patients under enzyme replacement therapy (ERT) may still develop ED-related symptoms. Therefore, ED in FD might not solely be related to Gb3 storage, and other influences need to be elucidated.",
            "authors": [
                "Regenstein, G"
            ],
            "year": 2025,
            "source": "Humanmedizin; [ Diplomarbeit ] Medizinische Universität Graz; 2025. pp. 81",
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            "document_type": 15,
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            "university": "Medizinische Universität Graz",
            "country": "40",
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        },
        {
            "id": 219574,
            "title": "Neues aus der Forschung: Psychosomatik? Der Zusammenhang zwischen Körper und Psyche",
            "abstract": null,
            "authors": [
                "Wagner-Skacel, J"
            ],
            "year": 2025,
            "source": "MeinMed; 07.10.2025; Knittelfeld. 2025. ",
            "category": 20,
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            "id": 219617,
            "title": "Characterization of Growth Differentiation Factor 15 (GDF-15) as a \r\nTherapeutic Target in Urothelial Carcinoma",
            "abstract": null,
            "authors": [
                "Koll, FJ"
            ],
            "year": 2025,
            "source": "https://www.ibcnweb.com/wp-content/uploads/2025/10/IBCN.2025.Progam.pdf. 2025; -IBCN Annual Meeting - 2025; Oct 9-11, 2025; Munich, Germany. ",
            "category": 2,
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        {
            "id": 215411,
            "title": "Prospective study \"Quality analysis and risk assessment of microlaryngoscopy in outpatient setting\".",
            "abstract": "Microlaryngoscopic surgery under general anesthesia is generally considered generally to be a procedure of short duration and low degree of invasiveness. Complication rates reported in the international literature are ranging from 1% to 79%. Because microlaryngoscopic surgeries are considered to be sufficiently safe they are usually performed on outpatient basis in Northern Europe, Western Europe, Canada and the United States.\nAs microlaryngoscopic surgery is considered sufficiently safe, it is generally performed on an outpatient basis in Northern Europe, Western Europe, Canada and the United States. In view of these facts, it is relevant to investigate the complication rates of microlaryngoscopic procedures and the advantages and disadvantages of outpatient procedures, both for quality control and for international comparison with the aim of risk assessment for outpatient procedures.",
            "authors": [
                "Frank, L"
            ],
            "year": 2025,
            "source": "Humanmedizin; [ Diplomarbeit ] Medizinische Universität Graz; 2025. pp. 55",
            "category": 5,
            "document_type": 15,
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        {
            "id": 219604,
            "title": "MICU proteins facilitate Ca2+-dependent mitochondrial metabolon formation to regulate cellular energetics - independent of MCU.",
            "abstract": null,
            "authors": [
                "Cohen, HM",
                "Gottschalk, B",
                "Choya-Foces, C",
                "Chathoff, A",
                "Wilkinson, A",
                "Garbincius, JF",
                "Johnson, A",
                "Stevens, TL",
                "Howe, JE",
                "Megill, E",
                "Ngo, J",
                "Tomar, D",
                "Snyder, NW",
                "Graier, WF",
                "Elrod, JW"
            ],
            "year": 2025,
            "source": "Res Sq. 2025; ",
            "category": 1,
            "document_type": 26,
            "sci": null,
            "pubmed": "40678212",
            "doi": "10.21203/rs.3.rs-6346822/v1",
            "pmc": "PMC12270237",
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            ],
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                "219604-51860",
                "219604-90394"
            ],
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            "journal": "Res Sq",
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        },
        {
            "id": 219554,
            "title": "Der „Delir-Leitfaden“: Verbesserung der Aufklärung von Patienten und Angehörigen über Delir",
            "abstract": null,
            "authors": [
                "Wagner-Skacel, J"
            ],
            "year": 2025,
            "source": "25. Jahrestagung der ÖGPP; 2.04. - 05.04.2025; Wien. 2025. ",
            "category": 20,
            "document_type": null,
            "sci": null,
            "pubmed": null,
            "doi": null,
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                "219554-29447"
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        },
        {
            "id": 219627,
            "title": "HerzMobil",
            "abstract": null,
            "authors": [
                "Wagner-Skacel, J"
            ],
            "year": 2025,
            "source": "LKH Graz; 20.10.2025; Graz. 2025. ",
            "category": 20,
            "document_type": null,
            "sci": null,
            "pubmed": null,
            "doi": null,
            "pmc": null,
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                "219627-29447"
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        },
        {
            "id": 217197,
            "title": "Neurogene Dysphagie in der Frührehabilitation nach Schlaganfall und der Einsatz von PEG-Sonden: Häufigkeit, Komplikationen und klinische Auswirkungen",
            "abstract": "Einleitung: Die neurogene Dysphagie ist eine häufige Komplikation des ischämischen Schlaganfalls. Sollte die Schluckstörung voraussichtlich länger als 28 Tage bestehen, ist die Anlage einer Sonde via perkutaner endoskopischer Gastrostomie (PEG-Sonde) empfohlen. In der Literatur finden sich Lücken bezüglich des optimalen Zeitpunktes einer PEG-Anlage sowie prognostischer Faktoren, welche für ein Wiedererlangen der Schluckfunktion und eine Entfernung der PEG-Sonde sprechen. Das Ziel dieser Arbeit war es, den Einfluss des Zeitpunktes der PEG-Platzierung sowie Prädiktoren für eine PEG-Entfernung zu identifizieren.",
            "authors": [
                "Krainer, A"
            ],
            "year": 2025,
            "source": "Humanmedizin; [ Diplomarbeit ] Medizinische Universität Graz; 2025. pp. 68",
            "category": 5,
            "document_type": 15,
            "sci": null,
            "pubmed": null,
            "doi": null,
            "pmc": null,
            "organizations": [],
            "persons": [],
            "imported": "2025-07-29T15:51:02+02:00",
            "journal": null,
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            "university": "Medizinische Universität Graz",
            "country": "40",
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        },
        {
            "id": 219589,
            "title": "Non-linear association of coagulation factor XI with mortality.",
            "abstract": null,
            "authors": [
                "Prystupa, K",
                "Heni, M",
                "Hörber, S",
                "Peter, A",
                "Delgado, G",
                "Kleber, M",
                "Hellstern, P",
                "Kelm, M",
                "Yamazaki, H",
                "Roden, M",
                "März, W",
                "Wagner, R"
            ],
            "year": 2025,
            "source": "Med. 2025; 100934",
            "category": 1,
            "document_type": 1,
            "sci": null,
            "pubmed": "41455467",
            "doi": "10.1016/j.medj.2025.100934",
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            "imported": "2026-01-05T01:00:00+01:00",
            "journal": "Med",
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        },
        {
            "id": 217693,
            "title": "Left ventricular hypertrophy and myocardial fibrosis in heart failure with preserved ejection fraction: mechanisms and treatment.",
            "abstract": null,
            "authors": [
                "Peikert, A",
                "Fontana, M",
                "Solomon, SD",
                "Thum, T"
            ],
            "year": 2025,
            "source": "Eur Heart J. 2025; ",
            "category": 1,
            "document_type": 1,
            "sci": "ISI:001561835500001",
            "pubmed": "40892534",
            "doi": "10.1093/eurheartj/ehaf524",
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                "217693-124914-1"
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            "imported": "2025-09-08T02:00:00+02:00",
            "journal": "Eur Heart J",
            "issn": "0195-668X",
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            "impactfactor": 35.7,
            "impactfactor_year": 2025,
            "impactfactor_norm": 0.986,
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            "impactfactor_norm_super_year": 2023,
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        },
        {
            "id": 219622,
            "title": "Burnout in Europa: Warum unsere Gesellschaft immer erschöpfter wird",
            "abstract": null,
            "authors": [
                "Wagner-Skacel, J"
            ],
            "year": 2025,
            "source": "Grazer Fortbildungstage 2025; 10.10.2025; Graz. 2025. ",
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                "219622-29447"
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            "imported": "2026-01-05T10:06:05+01:00",
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        },
        {
            "id": 219620,
            "title": "Wie können wir Gespräche im klinischen Alltag zum Heilmittel machen?",
            "abstract": null,
            "authors": [
                "Wagner-Skacel, J"
            ],
            "year": 2025,
            "source": "7. Jahreskongress des Netzwerks Altersmedizin Steiermark; 16.10.2025; Graz. 2025. ",
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        },
        {
            "id": 217214,
            "title": "Retrospektive Evaluierung von schwer verletzten Kindern und Jugendlichen nach Versorgung im Schockraum von 2017 bis 2022",
            "abstract": "Unfälle im Kindes- und Jugendalter sind keine Seltenheit. Verletzungen können sich hierbei in jeglichen Lebensbereichen wie im Straßenverkehr oder bei Freizeitaktivitäten ereignen. Bei besonders schwerwiegenden Traumata ist eine Versorgung im Schockraum erforderlich. Diese Diplomarbeit analysiert die häufigsten Unfallursachen und die daraus resultierenden Verletzungsmuster von Kindern und Jugendlichen, die im Schockraum behandelt wurden.",
            "authors": [
                "Wildbacher, V"
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            "id": 219480,
            "title": "Intrapulmonary intra-arterial malposition of a port catheter-an exceptionally rare complication",
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                "Ahmic, E",
                "Swatek, P",
                "Mykoliuk, I",
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                "Maier, A",
                "Lindenmann, J"
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            "source": "WIEN KLIN WOCHENSCHR. 2025; 137(SUPPL9):",
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        {
            "id": 218478,
            "title": "Ticept: Wideband Electrical Properties Tomography by Tissue Composition Assessment With Quantitative http://www.w3.org/1998/Math/MathML\">   1   $$ {}^1 $$  H http://www.w3.org/1998/Math/MathML\">   23   $$ {}^{23} $$  Na http://www.w3.org/1998/Math/MathML\">   39   $$ {}^{39} $$  K Multinuclear MRI.",
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            "authors": [
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                "Sumser, K",
                "Gerhalter, T",
                "Mestrom, RMC",
                "Nagel, AM",
                "Paulides, MM"
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        {
            "id": 217600,
            "title": "X-chromosomale Hypophosphatämie (XLH) - ein Fallbericht",
            "abstract": "Erhöhte Konzentrationen von FGF23, einem Hormon, das vermehrt in den Osteozyten produziert wird, prägen das Bild der X-chromosomalen Hypophosphatämie (XLH), welche genetisch bedingt ist und eine Vielzahl von klinischen Erscheinungen hervorrufen kann. Erste Symptome können sowohl im Kindes- als auch im Erwachsenalter auftreten und beeinflussen die Bewältigung des alltäglichen Lebens in unterschiedlicher Art und Weise. Während bei Kinder Deformitäten vor allem an den unteren Extremitäten, Kraniosynostosen oder Chiari Malformationen auffallend sind, berichten Erwachsene von vermehrten Schmerzen in den Gelenken und Knochen sowie Enthesiopathien und Frakturen. Mit einer Prävalenz von 1 zu 20 000 bis 1 zu 60 000 Personen stellt die Erkrankung nach wie vor eine Herausforderung in der Diagnostik und Therapie dar. Neben weiteren genetischen hypophosphatämischen Rachitisformen wie beispielsweise der autosomal dominanten hypophosphatämischen Rachitis (ADHR) und der autosomal rezessiven hypophosphatämischen Rachitis (ARHR) müssen auch tumorinduzierte Osteomalazien (TIO) oder mögliche Fanconi-Syndrome als relevante Differentialdiagnosen berücksichtigt werden. Um diese Differentialdiagnosen ausschließen zu können, bieten insbesondere bildgebende Verfahren, bestimmte Laborparameter und spezifische klinische Ausprägungen eine große Hilfestellung für eine sichere Diagnosefindung. Ein frühzeitiges Erkennen der Erkrankung und ein rechtzeitiges zielgerichtetes Eingreifen verhindern den Verlauf mit schwerwiegenden Komplikationen. Nach wie vor wird eine konventionelle Therapie mit Phosphat- und Vitamin D-Substitution angestrebt, abhängig vom Alter und Ausprägungsgrad der Erkrankung in unterschiedlichen Dosierungen. Hemiepiphysiodesen, Methoden zur chirurgischen Versorgung bei Beeinträchtigungen des Knochenwachstums, haben sich mittlerweile gut etabliert, um Fehlstellungen an den Extremitäten bei jungen PatientInnen auszugleichen. Die mit der Erkrankung assoziierten Störungen im Phosphat- und Kalziumhaushalt bedingen auch die Funktionsstörung der Nebenschilddrüsen und dessen erhöhte Parathormon (PTH)-Sekretion. Bei Ausprägung eines tertiären Hyperparathyreoidismus wird eine chirurgische Resektion der Glandulae parathyreoideae empfohlen. Vielversprechend ist eine neuere monoklonale Antikörpertherapie mit Burosumab, welche darauf abzielt, die ursächlich bedingte erhöhte FGF23-Konzentration zu reduzieren. Unter bestimmten Voraussetzungen kann die kausale Therapie mit Burosumab in Erwägung gezogen werden, um eine Verbesserung der Symptome und der Lebensqualität zu erzielen. Ein Fallbericht von einer 20-jährigen Patientin schildert die Besonderheiten der XLH und ebenso die Herausforderungen in Bezug auf die Behandlung der Erkrankung. Laufende Kontrollen der Laborparameter und die Beobachtung der klinischen Beschwerden sind entscheidend für eine adäquate Therapie. Die neue Therapiemöglichkeit mit Burosumab präsentiert im Fallbericht äußerst positive Ergebnisse und scheint eine wirksame Möglichkeit für XLH-Erkrankte zu sein.",
            "authors": [
                "Melbinger, N"
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        {
            "id": 217604,
            "title": "Influence of high-grade trochlear dysplasia on the extent of patellar tilt in children and adolescents - A retrospective analysis based on MR images of the knee",
            "abstract": "Background: The aim of this diploma thesis was to find out whether and to what extent high-grade trochlear dysplasia influences patellar tilt in children and adolescents. Both anatomical features are known risk factors for patellofemoral instability, which is a common pathology, especially in children and adolescents. Trochlear dysplasia has been well studied, can be classified using imaging methods and plays an important role in treatment decisions. The patellar tilt is also considered an easy to determine and reliable parameter for diagnosing patellofemoral instability. It indicates the inclination of the patella in the horizontal plane in relation to the femur and is measured in an axial image of the knee joint. An increased lateral tilt of the patella in the horizontal plane - resulting in an increased patellar tilt - is considered a risk factor for patellofemoral instability. Little is currently known about the extent of the correlation between trochlear dysplasia and patellar tilt.",
            "authors": [
                "Schmid, F"
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            "year": 2025,
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        {
            "id": 216602,
            "title": "Pattern and Prognostic Impact of radiographic and pathological lymph node metastases in patients with kidney cancer",
            "abstract": "Lymph node invasion (LNI) is a known adverse prognostic factor in metastatic renal cell carcinoma (mRCC), yet its relevance in the era of modern systemic therapies remains unclear. This dissertation investigates the prognostic significance of both pathological and radiographic LNI in contemporary mRCC patients. The work is based on three population-based studies conducted during a research fellowship at the Cancer Prognostics and Health Outcomes Unit in Montreal, Canada, utilizing the SEER database.",
            "authors": [
                "Scheipner, L"
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            "source": "Doktoratsstudium der Medizinischen Wissenschaft; Humanmedizin; [ Dissertation ] Medizinische Universität Graz; 2025. pp. 69",
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            "id": 219463,
            "title": "Brain Changes in Alcohol Induced Liver Cirrhosis Patients: Insights from Quantitative Susceptibility Mapping",
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                "Vovk, A",
                "Ropele, S",
                "Stefanovic, S",
                "Stabuc, B",
                "Suput, D",
                "Jerovsek, MT",
                "Zupan, G"
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        {
            "id": 219526,
            "title": "Spatial Epidemiology of Pediatric Cancer in Romania: A Decade of Persistence, Continuity, and Localized Hotspots (Temporal Trend 2008-2017)",
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            "authors": [
                "Nedelcu, ID",
                "Andronache, I",
                "Liritzis, I",
                "Ahammer, H",
                "Jelinek, HF",
                "Gruia, AK",
                "Peptenatu, D",
                "Radulovic, M"
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