Research/art/teacher profile of a person
Name and surname:
MUDr. Nina Lenhartová, PhD.
Document type:
Research/art/teacher profile of a person
The name of the university:
Comenius University Bratislava
The seat of the university:
Šafárikovo námestie 6, 818 06 Bratislava

I. - Basic information

I.1 - Surname
Lenhartová
I.2 - Name
Nina
I.3 - Degrees
MUDr., PhD.
I.4 - Year of birth
1989
I.5 - Name of the workplace
Deparment of medical genetics, ÚKIaLG, University hospital Martin, Jessenius Medical Faculty in Martin
I.6 - Address of the workplace
Kollárova 2, Martin, 036 59, Slovakia
I.7 - Position
medical geneticist
I.8 - E-mail address
lenhartova5@uniba.sk
I.9 - Hyperlink to the entry of a person in the Register of university staff
https://www.portalvs.sk/regzam/detail/27424
I.10 - Name of the study field in which a person works at the university
medical genetics

II. - Higher education and further qualification growth

II.1 - First degree of higher education
II.a - Name of the university or institution
Jessenius Medical Faculty in Martin, Commenius University in Bratislava
II.b - Year
2015
II.c - Study field and programme
general medicine
II.2 - Second degree of higher education
II.a - Name of the university or institution
Jessenius Medical Faculty in Martin, Commenius University in Bratislava
II.b - Year
2015
II.c - Study field and programme
general medicine
II.3 - Third degree of higher education
II.a - Name of the university or institution
Jessenius Medical Faculty in Martin, Commenius University in Bratislava
II.b - Year
2021
II.c - Study field and programme
pediatrics - neonatology
II.4 - Associate professor
II.5 - Professor
II.6 - Doctor of Science (DrSc.)

III. - Current and previous employment

IV. - Development of pedagogical, professional, language, digital and other skills

IV.a - Activity description, course name, other IV.b - Name of the institution IV.c - Year
DNA laboratory research, Department of pediatrics, Research student program, Japanese government (MEXT) scholarship (MONBUNKAGAKUSHO) Kyushu University 2020
Online kurz, Coursera: UNM - Google AI Google v asociácii s UNM 2025

V. - Overview of activities within the teaching career at the university

V.1 - Overview of the profile courses taught in the current academic year according to study programmes
V.1.a - Name of the profile course V.1.b - Study programme V.1.c - Degree V.1.d - Field of study
Medical Genetics and Dysmorphology general medicine I.+II. General Medicine
V.2 - Overview of the responsibility for the delivery, development and quality assurance of the study programme or its part at the university in the current academic year
V.3 - Overview of the responsibility for the development and quality of the field of habilitation procedure and inaugural procedure in the current academic year
V.4 - Overview of supervised final theses
V.4.1 - Number of currently supervised theses
V.4.b - Diploma (second degree)
The influence of hereditary genetic factors on the development, prevention and treatment of oncological diseases
V.4.2 - Number of defended theses
V.4.b - Diploma (second degree)
Echinococcosis – pathogenesis, clinical presentation, diagnostical possibilities and therapy
V.4.c - Dissertation (third degree)
Genetic predisposition to retinopathy of prematurity
V.5 - Overview of other courses taught in the current academic year according to study programmes

VI. - Overview of the research/artistic/other outputs

VI.1 - Overview of the research/artistic/other outputs and the corresponding citations
VI.1.1 - Number of the research/artistic/other outputs
VI.1.a - Overall
13
VI.1.b - Over the last six years
9
VI.1.2 - Number of the research/artistic/other outputs registered in the Web of Science or Scopus databases
VI.1.a - Overall
6
VI.1.b - Over the last six years
4
VI.1.3 - Number of citations corresponding to the research/artistic/other outputs
VI.1.4 - Number of citations registered in the Web of Science or Scopus databases
VI.1.a - Overall
40
VI.1.5 - Number of invited lectures at the international, national level
VI.1.a - Overall
1
VI.1.b - Over the last six years
1
VI.2 - The most significant research/artistic/other outputs
1

Article - Lenhartova N, Matasova K, Lasabova Z, Javorka K, Calkovska A. Impact of early aggressive nutrition

on retinal development in premature infants. Physiol Res. 2017 Sep 22;66(Suppl 2):S215-S226. doi:

10.33549/physiolres.933677. PMID: 28937236.

2

Article - Lenhartová N, Ochiai M, Sawano T, Yasuoka K, Fujiyoshi J, Inoue H, Ohga S. Serum erythroferrone

levels during the first month of life in premature infants. J Perinatol. 2022 Jan;42(1):97-102. doi:

10.1038/s41372-021-01184-6. Epub 2021 Aug 10. PMID: 34376791.

3

Article - Lenhartová N, Kršiaková J, Maťašová K, Zibolen M. The clinical phenotype and genetic diagnosis of a rare cutis laxa syndrome in a newborn with multiple anomalies. Ces-slov Pediat. 2022;77(4):226-231.

doi: 10.55095/CSPediatrie2022/037.

4

Article (contribution - laboratory/experimental analyses) - Sonoda M, Ishimura M, Eguchi K, Yada Y, Lenhartová N, Shiraishi A, Tanaka T, Sakai Y, Ohga S.

Progressive B cell depletion in human MALT1 deficiency. Clin Exp Immunol. 2021 Dec;206(3):237-

247. doi: 10.1111/cei.13662. Epub 2021 Oct 7. PMID: 34559885; PMCID: PMC8561700.

5

Lecture - Current Trends in Neonatal Screening in Slovakia and Central Europe. 127th Annual Meeting of the

Japan Pediatric Society, April 20024, Fukuoka, Japonsko

VI.3 - The most significant research/artistic/other outputs over the last six years
1

Article - Lenhartová N, Ochiai M, Sawano T, Yasuoka K, Fujiyoshi J, Inoue H, Ohga S. Serum erythroferrone

levels during the first month of life in premature infants. J Perinatol. 2022 Jan;42(1):97-102. doi:

10.1038/s41372-021-01184-6. Epub 2021 Aug 10. PMID: 34376791.

2

Article (contribution - laboratory/experimental analyses) - Sonoda M, Ishimura M, Eguchi K, Yada Y, Lenhartová N, Shiraishi A, Tanaka T, Sakai Y, Ohga S.

Progressive B cell depletion in human MALT1 deficiency. Clin Exp Immunol. 2021 Dec;206(3):237-

247. doi: 10.1111/cei.13662. Epub 2021 Oct 7. PMID: 34559885; PMCID: PMC8561700.

3

Article - Lenhartová N, Kršiaková J, Maťašová K, Zibolen M. The clinical phenotype and genetic diagnosis of a rare cutis laxa syndrome in a newborn with multiple anomalies. Ces-slov Pediat. 2022;77(4):226-231.

doi: 10.55095/CSPediatrie2022/037.

4

Lecture - Current Trends in Neonatal Screening in Slovakia and Central Europe. 127th Annual Meeting of the

Japan Pediatric Society, April 2024, Fukuoka, Japonsko

5

Lecture - Wieacker-Wolff syndrome as a rare cause of congenital arthrogryposis (case report).

Martinská genetická konferencia, 16.-17. marec 2023, Martin

VI.4 - The most significant citations corresponding to the research/artistic/other outputs
VI.5 - Participation in conducting (leading) the most important research projects or art projects over the last six years

VII. - Overview of organizational experience related to higher education and research/artistic/other activities

VIII. - Overview of international mobilities and visits oriented on education and research/artistic/other activities in the given field of study

VIII.a - Name of the institution VIII.b - Address of the institution VIII.c - Duration (indicate the duration of stay) VIII.d - Mobility scheme, employment contract, other (describe)
Kyushu University Fukuoka, Japan OCtober 2018 - July 2020 Research student program - Japanese government (MEXT) scholarship (MONBUNKAGAKUSHO)

IX. - Other relevant facts

Date of last update
2026-02-16