HCEMM-SU Molecular Oncohematology Research Group

Lili Kotmayer

Lili Kotmayer

EDUCATION

  • 2020- Doctoral School of Pathology, Semmelweis University
  • 2016- Faculty of Medicine, Semmelweis UniversityGPA (9 semesters): 4,73
  • 2012-2016 ELTE Apáczai Csere János High School, BudapestGPA: 5,0
  • 2008-2012 Prohászka Ottokár Catholic High School,
 

LANGUAGE EXAMS

  • 2013 English, Level B2 complex language exam
  • 2016 Latin, Level B2 complex language exam

SCIENTIFIC ACTIVITY

  • 2018-Member of Korányi Frigyes College for Advanced Studies
  • Member of the Scientific Committee(2019-)
  • II. Semmelweis Talent Conference, member of the organizing committee(2020)
  • 2019- Kerpel-Fronius Ödön Talent Program membership Mentor: Dr. Gergely Kriván
  • 2019-Hungarian Medical Association of America (HMAA) junior membership
 

ACHIEVEMENTS

  • 2016-1stDepartment of Pathology and Experimental Cancer Research, Semmelweis UniversityMTA-SEMomentum Molecular Oncohematology Research GroupSupervisors: Dr. Csaba Bödör,Dr. Richárd Kiss, Dr.DonátAlpár

     
  •  2019-1st Department of Pathology and Experimental Cancer Research, Semmelweis University, student secretaryfor Scientific Student Research(TDK)
  • 2019-Semmelweis University, Scientific Student Committee (TDT) membership
  • 2019Screening for genomic copy number alterations in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification
    Semmelweis University TDK Conference –1stPrizeNational TDKConference, Debrecen, participant
  • 2020 Screening for DNA copy number alterations in the oncohaematologic diagnostics using multiplex ligation-dependent probe amplification Semmelweis University Rectorial Competition –1stPrize
  • 2020 Next-generation sequencing methods in oncohematological diagnostics and therapySemmelweis University ScientificCompetition –1stPrize
  • 2020 Kerpel-Fronius Talent PrizeKerpel-Fronius Ödön Talent Program
  • 2020 Mutational profilingof 50 Hungarianpediatric AML patients with next-generationsequencingSemmelweis University TDK Conference –2ndPrize
  • 2021 Screening and monitoring of BTKC481S mutation in patients with relapsed/refractory chronic lymphocytic leukemia during ibrutinib therapySemmelweis University TDK Conference –2nd Prize
  • 2021Screening and monitoring of BTKC481S mutation in patients with relapsed/refractory chronic lymphocytic leukemia during ibrutinib therapyNational TDKConference–1stPrize
  • 2021 Screening and monitoring of BTKC481S mutation in patients with relapsed/refractory chronic lymphocytic leukemia during ibrutinib therapyXVII. Burdenko International Scientific Conference–1stPrize

Publications

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6. Screening and monitoring of BTKC481S mutation in patients with relapsed/refractory chronic lymphocytic leukemia during ibrutinib therapy

Csaba Bödör, Lili Kotmayer,  ESH 1stTranslational Research Conference on Chronic Lymphocytic Leukemia, 17 Nov 2020, Online conference, oral poster presentation

Pub

5. Quantitative Analysis and Monitoring of EZH2 Mutations Using Liquid Biopsy in Follicular Lymphoma

Ákos Nagy, Bence Bátai, Alexandra Balogh, Sarolta Illés, Gábor Mikala, Noémi Nagy, Laura Kiss, Lili Kotmayer, András Matolcsy, Donát Alpár, Tamás Masszi, András Masszi, Csaba Bödör, 2020, Genes, 11(7):785

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4. Hereditary haematological malignancies

Lili Kotmayer, Krisztián Kállay, Csaba Bödör,  2020, Magyar Onkológia, 64(1), pp. 43-55

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3. Screening for genomic copy number alterations in a family suffering from myelodysplastic syndrome using multiplex ligation-dependent probe amplification

Lili Kotmayer, Richárd Kiss, Attila Péter Király, Judit Csomor, Krisztián Kállay, Donát Alpár, Csaba Bödör,  2018, Hematológia–Transzfuziológia, 51(4), 214-220

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2.  Screening for genomic copy number alterations in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification

Richárd Kiss, Gergő Papp, Szilvia Krizsán, Lili Kotmayer, Ambrus Gángó, Noémi Nagy, Bence Bátai, Zoltán Mátrai, Csaba Bödör, Donár Alpár, 2018, Hematológia–Transzfuziológia, 51(1), pp. 31-40

Pub

1. Screening for genomic copy number alterations in a family suffering from myelodysplastic syndrome using multiplex ligation-dependent probe amplification

LiliKotmayer, 27thCongress of the Hungarian Society of Haematology and Transfusion, 23 May 2019, Pécs, poster

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