Pregled po CROSBI profilu: Martina Rinčić (CROSBI Profil: 26561, MBZ: 311472, ORCID: 0000-0003-0390-5967)

1.

Rinčić, Martina; Liehr, Thomas

FISH - in Human Sperm and Infertility // Cytogenetics and Molecular Cytogenetics / Liehr, Thomas (ur.).
Boca Raton (FL): CRC Press, 2022. str. 111-116 doi:10.1201/9781003223658-9

doi www.taylorfrancis.com

2.

Rinčić, Martina; Kopić, Janja; Jakšić, Boris; Krsnik, Željka; Borovečki, Fran; Brečević, Lukrecija

Evolutionary novel genes in neurodevelopmental disorders // MNS Full Proceedings
Dubrovnik, Hrvatska, 2022. str. 159-159 (poster, međunarodna recenzija, sažetak, znanstveni)

3.

Kadioglu, Onat; Saeed, Mohamed E.M.; Mahmoud, Nuha; Hussein Azawi, Shaymaa S.; Rinčić, Martina; Liehr, Thomas; Efferth, Thomas

Identification of metastasis-related genes by genomic and transcriptomic studies in murine melanoma // Life sciences, 267 (2021), 118922, 8 doi:10.1016/j.lfs.2020.118922 (međunarodna recenzija, članak, znanstveni)

doi

4.

Azawi, Shaymaa; Rinčić, Martina; Liehr, Thomas

Cytogenomic characteristics of murine breast cancer cell line JC // Molecular Cytogenetics, 14 (2021), 1; 7, 8 doi:10.1186/s13039-020-00524-z (međunarodna recenzija, članak, znanstveni)

doi

5.

Piaszinski, Katja; Rinčić, Martina; Liehr, Thomas; Azawi, Shaymaa

Molecular cytogenetic characterization of the murine melanoma cell lines S91 clone M3 and B16- F1 with variant B16-4A5 // Cytogenetic and genome research, 161 (2021), 1-2; 82-92 doi:10.1159/000513174 (međunarodna recenzija, članak, znanstveni)

doi

6.

Rinčić, Martina; Radoš, Milan; Kopić, Janja; Krsnik, Željka; Liehr, Thomas

7p21.3 together with a 12p13.32 deletion in a patient with microcephaly - does 12p13.32 locus possibly comprises a candidate gene region for microcephaly? // Frontiers in Molecular Neuroscience, 14 (2021), 613091, 12 doi:10.3389/fnmol.2021.613091 (međunarodna recenzija, članak, znanstveni)

doi

7.

Azawi, Shaymaa; Liehr, Thomas; Rinčić, Martina; Manferrari, Mattia

Molecular cytogenomic characterization of the murine breast cancer cell lines C-127I, EMT6/P and TA3 Hauschka // International journal of molecular sciences, 21 (2020), 13; 4716, 13 doi:10.3390/ijms21134716 (međunarodna recenzija, članak, znanstveni)

doi doi.org

8.

Wahlbuhl, Eva; Liehr, Thomas; Rinčić, Martina; Azawi, Shaymaa

Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines // Molecular Cytogenetics, 13 (2020), 43, 10 doi:10.1186/s13039-020-00511-4 (međunarodna recenzija, članak, znanstveni)

doi doi.org

9.

Liehr, Thomas; Carreira, Isabel M.; Balogh, Zsofia; Garrido, Elena Dominguez; Verdorfer, Irmgard; Coviello, Domenico A.; Florentin, Lina; Scheffer, Hans; Rincic, Martina; Williams, Heather E.

Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems ; results of a survey in over 50 countries // European Journal of Human Genetics, 27 (2019), 8; 1168-1174 doi:10.1038/s41431-019-0379-4 (međunarodna recenzija, članak, stručni)

doi

10.

Vucak, Jerko; Turudic, Daniel; Milosevic, Danko; Bilic, Marko; Salek, Zrinko; Rincic, Martina; Bilic, Ernest

Genotype-phenotype Correlation of β-Thalassemia in Croatian Patients: A Specific HBB Gene Mutations // Journal of Pediatric Hematology/Oncology, 40 (2018), 2; e77-e82 doi:10.1097/mph.0000000000001039 (međunarodna recenzija, članak, znanstveni)

doi

11.

Steinacker, Ralf; Liehr, Thomas; Kosyakova, Nadezda; Rincic, Martina; Azawi, Shaymaa S. Hussein

Molecular cytogenetic characterization of two murine cancer cell lines derived from salivary gland // Biological Communications, 63 (2018), 4; 243-255 doi:10.21638/spbu03.2018.403 (međunarodna recenzija, članak, znanstveni)

doi

12.

Vučak, Jerko; Turudić, Daniel; Milošević, Danko; Bilić, Marko; Rinčić, Martina; Salek, Zrinko; Bilić, Ernest.

Genotype-phenotype Correlation of β-Thalassemia in Croatian Patients: A Specific HBB Gene Mutations. // Journal of Pediatric Hematology/Oncology, 1 (2018), 1-6 doi:10.1097/MPH.0000000000001039. (međunarodna recenzija, članak, znanstveni)

doi www.ncbi.nlm.nih.gov

13.

Kubicova, Eva; Trifonov, Vladimir; Borovecki, Fran; Liehr, Thomas; Rincic, Martina; Kosyakova, Nadezda; Hussein, Shaymaa

First Molecular Cytogenetic Characterization of Murine Malignant Mesothelioma Cell Line AEl7 and silico Translation to the Human Genome // Current bioinformatics, 12 (2017), 1; 11-18 doi:10.2174/1574893611666160606164459 (međunarodna recenzija, članak, znanstveni)

doi

14.

Liehr, Thomas; on behalf of the Clinical Laboratory Geneticists Professional Branch Board, European Board of Medical Genetics, Vienna, Austria; Carreira, Isabel M; Aktas, Dilek; Bakker, Egbert; Rodríguez de Alba, Marta; Coviello, Domenico A; Florentin, Lina; Scheffer, Hans; Rincic, Martina

European registration process for Clinical Laboratory Geneticists in genetic healthcare // European Journal of Human Genetics, 25 (2017), 5; 515-519 doi:10.1038/ejhg.2017.25 (međunarodna recenzija, članak, stručni)

doi

15.

Guja, Karolina; Liehr, Thomas; Rincic, Martina; Kosyakova, Nadezda; Hussein Azawi, Shaymaa S.

Molecular Cytogenetic Characterization Identified the Murine B-Cell Lymphoma Cell Line A-20 as a Model for Sporadic Burkitt's Lymphoma // Journal of Histochemistry & Cytochemistry, 65 (2017), 11; 669-677 doi:10.1369/0022155417731319 (međunarodna recenzija, članak, znanstveni)

doi

16.

Rinčić, Martina; Iourov, Ivan Y.; Liehr, Thomas

Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting // Molecular Cytogenetics, 9 (2016), 56, 6 doi:10.1186/s13039-016-0271-7 (međunarodna recenzija, članak, stručni)

doi

17.

Rinčić, Martina; Radoš, Milan; Krsnik, Zeljka; Liehr, Thomas; Brecevic, Lukrecija

Microdeletion of 7p21.3 and 12p13.32 in a female patient with severe microcephaly // 6th Belgian Brain Congress : abstracts ; u: Frontiers
Mons, Belgija, 2016. (poster, međunarodna recenzija, sažetak, ostalo)

18.

OTHMAN, MONEEB A.K.; GRYGALEWICZ, BEATA; PIENKOWSKA‑GRELA, BARBARA; RYGIER, JOLANTA; EJDUK, ANNA; RINCIC, MARTINA; MELO, JOANA B.; CARREIRA, ISABEL M.; MEYER, BRITTA; LIEHR, THOMAS

A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia // Oncology Letters, 11 (2016), 3; 2117-2122 (međunarodna recenzija, članak, znanstveni)

19.

Rincic, Martina; Rados, Milan; Krsnik, Zeljka; Gotovac, Kristina; Borovecki, Fran; Liehr, Thomas; Brecevic, Lukrecija

Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex // Molecular Cytogenetics, 9 (2016), 19-- doi:10.1186/s13039-016-0221-4 (međunarodna recenzija, članak, znanstveni)

doi

20.

Alhourani, Eyad; Rincic, Martina; Melo, Joana B; Carreira, Isabel M; Glaser, Anita; Pohle, Beate; Schlie, Cordula; Liehr, Thomas

Isochromosome 17q in Chronic Lymphocytic Leukemia // Leukemia Research and Treatment, 2015:489592 (2015) (međunarodna recenzija, članak, znanstveni)

21.

Othman, Moneeb A.K.; Melo, Joana B.; Carreira, Isabel M.; Rincic, Martina; Alhourani, Eyad; Wilhelm, Kathleen; Gruhn, Bernd; Glaser, Anita; Liehr, Thomas

MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report // Oncology reports, 33 (2015), 2; 625-630 doi:10.3892/or.2014.3624 (podatak o recenziji nije dostupan, prikaz, znanstveni)

doi www.spandidos-publications.com

22.

Othman, Moneeb A. K.; Grygalewicz, Beata; Pienkowska-Grela, Barbara; Rincic, Martina; Rittscher, Katharina; Melo, Joana B.; Carreira, Isabel M.; Meyer, Meyer, Britta; Marzena, Watek; Liehr, Thomas

Novel Cryptic Rearrangements in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Involving the MLL Gene // The journal of histochemistry and cytochemistry, 63 (2015), 5; 384-390 doi:10.1369/0022155415576201 (međunarodna recenzija, članak, znanstveni)

doi journals.sagepub.com

23.

Othman, Moneeb A. K.; Melo, Joana B.; Carreira, Isabel M.; Rincic, Martina; Glaser, Anita; Grygalewicz, Beata; Gruhn, Bernd; Wilhelm, Kathleen; Rittscher, Katharina; Meyer, Britta et al.

High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia // Molecular Cytogenetics, 8 (2015) (međunarodna recenzija, članak, znanstveni)

24.

Rincic, Martina; Rados, Milan; Krsnik, Zeljka; Gotovac, Kristina; Nelle H; Liehr, Thomas; Borovecki, Fran; Brecevic, Lukrecija

Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex // 5th Croatian Neuroscience Congress
Split, Hrvatska, 2015. (poster, domaća recenzija, sažetak, znanstveni)

25.

Rinčić Martina; Krsnik Željka; Gotovac Kristina; Liehr Thomas; Borovecki Fran; Brecevic Lukrecija

Customized high resolution arrayCGH for neurodevelopmental disorders: our experience // 5th Croatian Neuroscience Congress
Split, Hrvatska, 2015. (poster, domaća recenzija, sažetak, znanstveni)

26.

Rinčić Martina; Krsnik Željka; Sedmak Goran; Ahmed B. Hamid; Galić Ivan; Borovečki Fran; Liehr Thomas; Brečević Lukerecija

Neurodevelopmental genes in new microdeletion/microduplication region in chromosome 1p21 // 5th Croatian Neuroscience Congress
Split, Hrvatska, 2015. (poster, domaća recenzija, sažetak, znanstveni)

27.

Brečević, Lukrecija; Rinčić, Martina; Krsnik, Željka; Sedmak, Goran; Hamid, Ahmed B.; Kosyakova, Nadezda; Galić, Ivan; Liehr, Thomas; Borovečki, Fran

Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma // Translational Neuroscience, 6 (2015), 1; 59-86 doi:10.1515/tnsci-2015-0007 (međunarodna recenzija, članak, znanstveni)

doi www.degruyter.com

28.

Othman, Moneeb A K; Rincic, Martina; Melo, Joana B; Carreira, Isabel M; Alhourani, Eyad; Hunstig, Friederike; Glaser, Anita; Liehr, Thomas

A Novel Cryptic Three-Way Translocation t(2 ; 9 ; 18)(p23.2 ; p21.3 ; q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia. // Leukemia Research and Treatment, 2014 (2014) (podatak o recenziji nije dostupan, prikaz, znanstveni)

29.

Alhourani, Eyad; Rincic, Martina; Othman, Moneeb AK; Pohle, Beate; Schlie, Cordula; Glaser, Anita; Liehr, Thomas

Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH) // MOLECULAR CYTOGENETICS, 7 (2014) (međunarodna recenzija, članak, znanstveni)

30.

Merkaš, Martina; Gotovac, Kristina; Brečević, Lukrecija; Borovečki, Fran; Liehr, Thomas

Evaluation of chromosomal mosaicism by aCGH and MLPA:molecular characterization of mosaic ring chromosome 22. // XII Russian Federation Congress “Modern technologies in pediatrics and pediatric surgery”, Moscow, Russia, 2013
Moskva, Ruska Federacija, 2013. (poster, međunarodna recenzija, sažetak, znanstveni)

31.

Kosyakova, N.; ...; Merkaš, Martina; Brečević, Lukrecija; ...; Ergul, E.

Heteromorphic variants of chromosome 9 // Molecular cytogenetics, 6 (2013), 14-1 doi:10.1186/1755-8166-6-14 (međunarodna recenzija, članak, znanstveni)

doi link.springer.com

32.

Merkaš, Martina; Gotovac, Kristina; Liehr, Thomas; Borovečki Fran

Evaluation of chromosomal mosaicism by aCGH and MLPA: molecular characterization of mosaic ring chromosome 22 // Book of abstracts of 12th European Symposium on Congenital Anomalies /
Zagreb: European Surveillance of Congenital Anomalies Association, 2013. str. 71-71 (poster, međunarodna recenzija, sažetak, znanstveni)

33.

Liehr, Thomas; Bartels, I.; Zoll, B.; Ewers, Elisabeth; Mrasek, Kristin; Kosyakova, Nadezda; Merkas, Martina; Hamid, Ahmed Basheer; von Eggeling, Ferdinand; Posorski, Nicol; Weise, Anja

Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p? // Cytogenetic and genome research, 132 (2011), 1/2; 121-123 doi:10.1159/000316393 (međunarodna recenzija, kratko priopcenje, znanstveni)

doi content.karger.com

34.

Šrut, Maja; Štambuk, Anamaria; Husnjak, Ivana; Merkaš, Martina; Traven, Luka; Cvetković, Želimira; Klobučar, Göran I.V.

Genotoxicity assessment of soils near heavy traffic roads using native populations of earthworm Aporrectodea caliginosa // 2nd Young Environmental Scientists Meeting Environmental chalenges in the changing world
Aachen, 2011. str. 78-79 (predavanje, sažetak, znanstveni)

Pristup cjelovitom tekstu rada yes2011.sac-online.eu

35.

Klobučar, Göran Igor Vinko; Štambuk, Anamaria; Šrut, Maja; Husnjak, Ivana; Merkaš, Martina; Traven, Luka; Cvetković, Želimira

Aporrectodea caliginosa, a suitable earthworm species for field based genotoxicity assessment? // Environmental pollution, 159 (2011), 4; 841-849 doi:10.1016/j.envpol.2011.01.009 (međunarodna recenzija, članak, znanstveni)

doi www.sciencedirect.com www.sciencedirect.com

36.

Liehr, Thomas; Karamysheva, Tatyana; Merkas, Martina; Brecevic, Lukrecija; . Hamid, Ahmed; Ewers, Elisabeth; Mrasek, Kristin; Nadezda, Kosyakova; Weise, Anja

Somatic mosaicism in cases with small supernumerary marker chromosomes // Current genomics, 11 (2010), 6; 432-439 doi:10.2174/138920210793176029 (međunarodna recenzija, članak, znanstveni)

doi www.ncbi.nlm.nih.gov

37.

Niksic, S.B.; Deretic, V.I.; Pilic, G.R.; Ewers, Elisabeth; Merkas, Martina; Ziegler, Monika; Liehr, Thomas

Trisomy 21 with a Small Supernumerary Marker Chromosome Derived from Chromosomes 13/21 and 18 // Balkan journal of medical genetics, 13 (2010), 1; 55-58 doi:10.2478/v10034-010-0020-x (međunarodna recenzija, kratko priopcenje, znanstveni)

doi

38.

Nelle, H.; Schreyer, I.; Ewers, E.; Mrasek, K.; Kosyakova, N.; Merkas, M.; Hamid, A. B.; Fahsold, R.; Ujfalusi, A.; Anderson, J. et al.

Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report // Molecular Medicine Reports, 3 (2010), 571-574 doi:10.3892/mmr_00000299 (međunarodna recenzija, članak, znanstveni)

doi

39.

Weise, A; Kosyakova, N; Mrasek, K; Ewers, E; Bacino, C; Patel, A; Cheung, SW; Cai, WW; Senger, G; Melo, JB et al.

Detailed characterization of small supernumerary marker chromosomes reveals breakpoint hot spots and narrows down the critical regions of clinical impact. // Medizinische Genetik / T. Grimm ; K. Zerres ; B. Horsthemke ; M. Speicher (ur.).
Heidelberg: Springer, 2010. str. 141-141 (poster, međunarodna recenzija, sažetak, znanstveni)

40.

Šrut, Maja; Štambuk, Anamaria; Merkaš, Martina; Klobučar, I.V. Göran

DNA damage in earthworm coelomocytes after in vivo exposure to heavy metals and pentachlorophenol // EEMS 38th Annual Meeting / Franekić-Čolić, Jasna ; Garaj-Vrhovac, Vera (ur.).
Zagreb: Hrvatsko genetičko društvo, 2008. str. 240-240 (poster, domaća recenzija, sažetak, znanstveni)

41.

Borovecki, Fran; Brecevic, Lukrecija; Gotovac Jerčić, Kristina; Rincic, Martina

Genetic diagnostics of intellectual disability disorder, autism spectrum disorder and epilepsy