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Koczok Katalin

Koczok Katalin

Name: Koczok Katalin

Other profiles: MTMT

Profession: laboratory specialist

Publication list

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Uploaded publications:

19

Publications in DEA:

19

OA:

9

Date range:

2008-2022

2022

Deák, A., Koczok, K., Bessenyei, B., Szűcs, Z., Madar, L., Csorba, G., Orosz, O., Laki, I., Halász, A., Marsal, G., Balogh, I.: A magyar Cystás Fibrosis Regiszter genetikai revíziója.
Orv. hetil. 163 (51), 2052-2059, 2022.

Journal metrics:

Q4 Medicine (miscellaneous) (2021)
Szűcs, Z., Pinti, É., Haltrich, I., Pálné, S., Nagy, T., Barta, E., Méhes, G., Bidiga, L., Török, O., Ujfalusi, A., Koczok, K., Balogh, I.: An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: duchenne Muscular Dystrophy in a Female Patient.
Int. J. Mol. Sci. 23 (21), 1-15, 2022.

Journal metrics:

Q2 Catalysis (2021)
Q1 Computer Science Applications (2021)
Q1 Inorganic Chemistry (2021)
Q1 Medicine (miscellaneous) (2021)
Q2 Molecular Biology (2021)
Q1 Organic Chemistry (2021)
Q1 Physical and Theoretical Chemistry (2021)
D1 Spectroscopy (2021)
Andó, S., Koczok, K., Bessenyei, B., Balogh, I., Ujfalusi, A.: Cytogenetic Investigation of Infertile Patients in Hungary: a 10-Year Retrospective Study.
Genes. 13 (11), 1-13, 2022.

Journal metrics:

Q2 Genetics (2021)
Q2 Genetics (clinical) (2021)
Szabó, T., Balogh, I., Ujfalusi, A., Szűcs, Z., Madar, L., Koczok, K., Bessenyei, B., Csürke, I., Szakszon, K.: Helsmoortel-Van der Aa Syndrome: Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies.
Genes. 13 (12), 1-13, 2022.

Journal metrics:

Q2 Genetics (2021)
Q2 Genetics (clinical) (2021)

2021

Koczok, K., Horváth, L., Korade, Z., Mezei, Z., P. Szabó, G., Porter, N., Kovács, E., Mirnics, K., Balogh, I.: Biochemical and Clinical Effects of Vitamin E Supplementation in Hungarian Smith-Lemli-Opitz Syndrome Patients.
Biomolecules. 11 (8), 1-11, 2021.

Journal metrics:

Q2 Biochemistry
Q2 Molecular Biology
Anderson, A., Genaro-Mattos, T., Allen, L., Koczok, K., Korade, Z., Mirnics, K.: Interaction of maternal immune activation and genetic interneuronal inhibition.
Brain Res. 1759 1-10, 2021.

Journal metrics:

Q2 Developmental Biology
Q2 Molecular Biology
Q2 Neurology (clinical)
Q2 Neuroscience (miscellaneous)

2019

Madar, L., Szakszon, K., Pfliegler, G., P. Szabó, G., Brúgós, B., Ronen, N., Papp, J., Zahuczky, K., Szakos, E., Fekete, G., Oláh, É., Koczok, K., Balogh, I.: FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies.
J. Biotechnol. 301 105-111, 2019.

Journal metrics:

Q1 Applied Microbiology and Biotechnology
Q2 Bioengineering
Q1 Biotechnology
Q1 Medicine (miscellaneous)
Koczok, K., Gurumurthy, C., Balogh, I., Korade, Z., Mirnics, K.: Subcellular localization of sterol biosynthesis enzymes.
J. Mol. Histol. 50 (1), 63-73, 2019.

Journal metrics:

Q3 Cell Biology
Q2 Histology
Q2 Medicine (miscellaneous)
Q2 Physiology

2018

Ivády, G., Madar, L., Dzsudzsák, E., Koczok, K., Kappelmayer, J., Krulisova, V., Macek, J., Horváth, A., Balogh, I.: Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system.
BMC Genomics. 19 1-8, 2018.

Journal metrics:

D1 Biotechnology
Q1 Genetics
Koczok, K., Merő, G., P. Szabó, G., Madar, L., Gombos, É., Ajzner, É., Mótyán, J., Hortobágyi, T., Balogh, I.: A novel point mutation affecting Asn76 of dystrophin protein leads to dystrophinopathy.
Neuromusc. Disord. 28 (2), 129-136, 2018.

Journal metrics:

Q2 Genetics (clinical)
Q2 Neurology
Q1 Neurology (clinical)
Q1 Pediatrics, Perinatology and Child Health
Koczok, K., Gombos, É., Madar, L., Török, O., Balogh, I.: Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing.
Prenat. Diagn. 38 (9), 713-719, 2018.

Journal metrics:

Q2 Genetics (clinical)
D1 Obstetrics and Gynecology

2017

Korade, Z., Genaro-Mattos, T., Tallman, K., Liu, W., Garbett, K., Koczok, K., Balogh, I., Mirnics, K., Porter, N.: Vulnerability of DHCR7+/- mutation carriers to aripiprazole and trazodone exposure.
J. Lipid Res. 58 (11), 2139-2146, 2017.

Journal metrics:

D1 Biochemistry
Q1 Cell Biology
D1 Endocrinology

2016

Korade, Z., Kim, H., Tallman, K., Liu, W., Koczok, K., Balogh, I., Xu, L., Mirnics, K., Porter, N.: The Effect of Small Molecules on Sterol Homeostasis: Measuring 7-Dehydrocholesterol in Dhcr7-Deficient Neuro2a Cells and Human Fibroblasts.
J. Med. Chem. 59 (3), 1102-1115, 2016.

Journal metrics:

D1 Drug Discovery
Q1 Molecular Medicine

2015

Koczok, K., Oláh, A., P. Szabó, G., Oláh, É., Török, O., Balogh, I.: A koleszterin-bioszintézis veleszületett zavara: a Smith-Lemli-Opitz-szindróma.
Orv. hetil. 156 (42), 1695-1702, 2015.

Journal metrics:

Q3 Medicine (miscellaneous)
Oláh, A., Koczok, K., P. Szabó, G., Varga, J., Balogh, I., Harangi, J.: A veleszületett koleszterinhiány jellemző biomarkerei Smith-Lemli-Opitz-szindrómás betegekben és hordozókban.
Metabolizmus. 13 (3), 196-201, 2015.
Ivády, G., Koczok, K., Madar, L., Gombos, É., Tóth, I., Győri, K., Balogh, I.: Molecular Analysis of Cystic Fibrosis Patients in Hungary - an Update to the Mutational Spectrum.
J. Med. Biochem. 34 1-6, 2015.

Journal metrics:

Q3 Biochemistry (medical)
Q4 Clinical Biochemistry

2012

Balogh, I., Koczok, K., P. Szabó, G., Török, O., Hadzsiev, K., Csábi, G., Balogh, L., Dzsudzsák, E., Ajzner, É., Szabó, L., Csákváry, V., Oláh, A.: Mutational spectrum of Smith-Lemli-Opitz syndrome patients in Hungary.
Mol Syndromol. 3 (5), 215-222, 2012.

Journal metrics:

Q2 Genetics
Q3 Genetics (clinical)

2011

Bubán, T., Koczok, K., Földesi, R., Szabó Gabriella, Sümegi, A., Tanyi, M., Szerafin, L., Udvardy, M., Kappelmayer, J., Antal-Szalmás, P.: Detection of internal tandem duplications in the FLT3 gene by different electrophoretic methods.
Clin. Chem. Lab. Med. 50 (2), 301-310, 2011.

Journal metrics:

Q2 Biochemistry (medical)
Q2 Clinical Biochemistry
Q2 Medicine (miscellaneous)

2008

Szodoray, P., Koczok, K., Szántó, A., Horváth, I., Nakken, B., Molnár, I., Zeher, M.: Autoantibodies to novel membrane and cytosolic antigens of the lachrymal gland in primary Sjögren's syndrome.
Clin. Rheumatol. 27 (2), 195-199, 2008.

Journal metrics:

Q2 Medicine (miscellaneous)
Q2 Rheumatology

updated: 2023-03-23, 01:58