personal data approved: 2023. VII. 05.
| Personal data | |
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| name | Irén Haltrich |
| name of institution | |
| doctoral school | SE Károly Rácz Doctoral School of Clinical Medicine (Announcer of research topic) SE Doctoral School of University Semmelweis (Supervisor) |
| the share of work in the different doctoral schools. | SE Doctoral School of University Semmelweis 100% |
| accreditation statement submitted to: | Semmelweis University, Budapest |
| Contact details | |
| E-mail address | haltrich.iren med.semmelweis-univ.hu |
| phone number | +36 1 215-1380/52840 |
| Academic title | |
| scientific degree, title | Ph.D. |
| year degree was obtained | 2006 |
| discipline to which degree belongs | clinical medicine |
| institution granting the degree | SEmmelweis University |
| scientific degree, title | Ph.D. |
| year degree was obtained | 2006 |
| discipline to which degree belongs | clinical medicine |
| institution granting the degree | Semmelweis University |
| scientific degree, title | Ph.D. |
| year degree was obtained | 2006 |
| discipline to which degree belongs | clinical medicine |
| institution granting the degree | Semmelweis University |
| Employment | |
| 1997 - | Semmelweis University, Budapest egyetemi kutató |
| Thesis topic supervisor | |||||||||||
| number of doctoral students supervised until now | 3 | ||||||||||
| number of students who fulfilled course requirements | 3 | ||||||||||
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| Research | |
| research area | Cytogenetic and molecular genetic characterization of chromosomal rearrangements in developmental disorders and hematological malignancies |
| research field in which current research is conducted | clinical medicine general health sciences |
| Publications | |||
2023 |
Hammer Anne Sofie Borg, Juul-Dam Kristian Løvvik, Sandahl Julie Damgaard, Abrahamsson Jonas, Czogala Malgorzata, Delabesse Emmanuelle, Haltrich Iren, Jahnukainen Kirsi, Kolb E. Anders, Kovács Gábor T, Leverger Guy, Locatelli Franco, Masetti Riccardo, Noren-Nystrom Ulrika, Raimondi Susana, Rasche Mareike, Reinhardt Dirk, Taki Tomohiko, Tomizawa Daisuke, Zeller Bernward, Hasle Henrik, Kjeldsen Eigil: Hypodiploidy has Unfavorable Impact on Survival in Pediatric Acute Myeloid Leukemia:An I-BFM Study Group collaboration, BLOOD ADVANCES 7: (6) pp. 1045-1055. type of document: number of independent citations: 2 language: English URL |
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| 2023 |
Péterffy Borbála, Krizsán Szilvia, Egyed Bálint, Bedics Gábor, Bekő Anna, Erdélyi Dániel János, Müller Judit, Nagy Tibor, Hegyi Lajos László, Jakab Zsuzsanna, Péter György, Zombori Marianna, Csanádi Krisztina, Ottóffy Gábor, Csernus Katalin, Vojcek Ágnes, Tiszlavicz Lilla Györgyi, Gábor Krisztina Míta, Kelemen Ágnes, Hauser Péter, Kállay Krisztián, Kertész Gabriella, Gaál Zsuzsanna, Szegedi István, Márk Ágnes, Haltrich Irén, Hevessy Zsuzsanna, Ujfalusi Anikó, Kajtár Béla, Kiss Csongor, Kriván Gergely, Matolcsy András, Kovács Gábor, Bödör Csaba, Alpár Donát: PB1699: GENOMIC AND TRANSCRIPTOMIC PROFILING REVEALS NOVEL GENE FUSIONS AND MARKERS OF CLINICAL RESPONSE IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA, HEMASPHERE 7: (S3) e5932101 type of document: language: English URL |
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| 2022 |
Szűcs Zsuzsanna, Pinti Éva, Haltrich Irén, Szén Orsolya Pálné, Nagy Tibor, Barta Endre, Méhes Gábor, Bidiga László, Török Olga, Ujfalusi Anikó, Koczok Katalin, Balogh István: An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 23: (21) 13076 type of document: Journal paper/Article number of independent citations: 2 language: English URL |
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| 2022 |
Lengyel Anna, Pinti Éva, Pikó Henriett, Kristóf Árvai, Abonyi Tünde, Némethi Zaránd, Fekete György, Haltrich Irén: Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort, MOLECULAR CYTOGENETICS 15: (1) 47 type of document: Journal paper/Article number of independent citations: 3 language: English URL |
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| 2021 |
Pinti Eva, Nemeth Krisztina, Staub Krisztina, Lengyel Anna, Fekete Gyorgy, Haltrich Iren: Diagnostic difficulties and possibilities of NF1-like syndromes in childhood, BMC PEDIATRICS 21: (1) 331 type of document: Journal paper/Article number of independent citations: 9 language: English URL |
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| 2020 |
Eva Pinti, Anna Lengyel, Gyorgy Fekete, Iren Haltrich: What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature, BMC PEDIATRICS 20: 17 type of document: Journal paper/Review paper number of independent citations: 7 language: English URL |
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| 2020 |
Lengyel Anna, Pinti Éva, Pikó Henriett, Jávorszky Eszter, David Dezső, Tihanyi Mariann, Gönczi Éva, Kiss Eszter, Tóth Zsuzsa, Tory Kálmán, Fekete György, Haltrich Irén: Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature, EUROPEAN JOURNAL OF MEDICAL GENETICS 63: (10) 104027 type of document: Journal paper/Article number of independent citations: 4 language: English URL |
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| 2019 |
Eva Pinti, Henriett Piko, Anna Lengyel, Andrea Luczay, Veronika Karcagi, Gyorgy Fekete, Iren Haltrich: Similar cause, different phenotype: SOX9 enhancer duplication in a family, HORMONE RESEARCH IN PAEDIATRICS 92: (5) pp. 335-339. type of document: Journal paper/Article number of independent citations: 3 language: English URL |
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| 2018 |
Mohacsik P, Erdelyi F, Baranyi M, Botz B, Szabo G, Toth M, Haltrich I, Helyes Z, Sperlagh B, Toth Z, Sinko R, Lechan RM, Bianco AC, Fekete C, Gereben B: A transgenic mouse model for detection of tissue-specific thyroid hormone action, ENDOCRINOLOGY 159: (2) pp. 1159-1171. type of document: Journal paper/Article number of independent citations: 8 language: English URL |
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| 2014 |
Harrison CJ, Moorman AV, Schwab C, Carroll AJ, Raetz EA, Devidas M, Strehl S, Nebral K, Harbott J, Teigler-Schlegel A, Zimmerman M, Dastuge N, Baruchel A, Soulier J, Auclerc MF, Attarbaschi A, Mann G, Stark B, Cazzaniga G, Chilton L, Vandenberghe P, Forestier E, Haltrich I, Raimondi SC, Parihar M, Bourquin JP, Tchinda J, Haferlach C, Vora A, Hunger SP, Heerema NA, Ponte di Legno International Workshop in Childhood Acute Lymphoblastic Leukemia, Haas OA: An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome, LEUKEMIA 28: (5) pp. 1015-1021. type of document: number of independent citations: 180 language: English URL |
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