Hasmik Mkrtchyan

542 total citations
29 papers, 320 citations indexed

About

Hasmik Mkrtchyan is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Hasmik Mkrtchyan has authored 29 papers receiving a total of 320 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 10 papers in Molecular Biology and 10 papers in Plant Science. Recurrent topics in Hasmik Mkrtchyan's work include Genomic variations and chromosomal abnormalities (15 papers), Chromosomal and Genetic Variations (10 papers) and Prenatal Screening and Diagnostics (7 papers). Hasmik Mkrtchyan is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Chromosomal and Genetic Variations (10 papers) and Prenatal Screening and Diagnostics (7 papers). Hasmik Mkrtchyan collaborates with scholars based in Germany, Brazil and Armenia. Hasmik Mkrtchyan's co-authors include Thomas Liehr, Nadezda Kosyakova, Anja Weise, Vladimir A. Trifonov, Sophie Hinreiner, Kristin Mrasek, Elisabeth Ewers, Michael Glei, Marianne Volleth and Marina Manvelyan and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Journal of Histochemistry & Cytochemistry.

In The Last Decade

Hasmik Mkrtchyan

28 papers receiving 316 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Hasmik Mkrtchyan Germany 11 194 146 111 70 42 29 320
Peter Papenhausen United States 9 194 1.0× 154 1.1× 105 0.9× 49 0.7× 27 0.6× 15 341
Judith Dagan Israel 12 223 1.1× 231 1.6× 88 0.8× 96 1.4× 85 2.0× 27 457
Chiara Perfumo Italy 11 211 1.1× 173 1.2× 75 0.7× 95 1.4× 66 1.6× 17 357
Anna Jauch Germany 10 137 0.7× 200 1.4× 91 0.8× 33 0.5× 32 0.8× 11 319
Michael J. Macera United States 13 193 1.0× 165 1.1× 130 1.2× 76 1.1× 19 0.5× 43 400
V. D. Marković Canada 8 183 0.9× 258 1.8× 80 0.7× 76 1.1× 18 0.4× 10 419
Iskra Petković Croatia 11 164 0.8× 179 1.2× 56 0.5× 24 0.3× 38 0.9× 31 305
T. M. Schroeder-Kurth Germany 7 143 0.7× 227 1.6× 135 1.2× 47 0.7× 54 1.3× 10 330
M. F. Croquette France 11 293 1.5× 274 1.9× 100 0.9× 49 0.7× 56 1.3× 17 444
Jesper Eisfeldt Sweden 12 166 0.9× 191 1.3× 55 0.5× 33 0.5× 60 1.4× 50 349

Countries citing papers authored by Hasmik Mkrtchyan

Since Specialization
Citations

This map shows the geographic impact of Hasmik Mkrtchyan's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hasmik Mkrtchyan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hasmik Mkrtchyan more than expected).

Fields of papers citing papers by Hasmik Mkrtchyan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hasmik Mkrtchyan. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hasmik Mkrtchyan. The network helps show where Hasmik Mkrtchyan may publish in the future.

Co-authorship network of co-authors of Hasmik Mkrtchyan

This figure shows the co-authorship network connecting the top 25 collaborators of Hasmik Mkrtchyan. A scholar is included among the top collaborators of Hasmik Mkrtchyan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hasmik Mkrtchyan. Hasmik Mkrtchyan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Pinthong, Krit, Hasmik Mkrtchyan, Nadezda Kosyakova, et al.. (2013). First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae). Molecular Cytogenetics. 6(1). 58–58. 12 indexed citations
2.
3.
Mkrtchyan, Hasmik, et al.. (2012). Extra Copies of der(21)t(12;21) plus Deletion ofETV6Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome. SHILAP Revista de lepidopterología. 2012. 1–4. 1 indexed citations
4.
Mkrtchyan, Hasmik, Sophie Hinreiner, Marina Manvelyan, et al.. (2010). The Human Genome Puzzle — the Role of Copy Number Variation in Somatic Mosaicism. Current Genomics. 11(6). 426–431. 30 indexed citations
5.
Achkar, Walid Al, et al.. (2010). A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17). Oncology Letters. 1(5). 793–795. 2 indexed citations
6.
7.
Weise, Anja, et al.. (2010). POD-FISH: A New Technique for Parental Origin Determination Based on Copy Number Variation Polymorphism. Methods in molecular biology. 659. 291–298. 10 indexed citations
8.
Mkrtchyan, Hasmik, Sophie Hinreiner, Marina Manvelyan, et al.. (2010). Early Embryonic Chromosome Instability Results in Stable Mosaic Pattern in Human Tissues. PLoS ONE. 5(3). e9591–e9591. 41 indexed citations
9.
Mkrtchyan, Hasmik, et al.. (2010). Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 197(1). 71–74. 3 indexed citations
10.
Liehr, Thomas, Anja Weise, Sophie Hinreiner, et al.. (2010). Characterization of Chromosomal Rearrangements Using Multicolor-Banding (MCB/m-band). Methods in molecular biology. 659. 231–238. 2 indexed citations
11.
Mkrtchyan, Hasmik, et al.. (2010). Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosis. Cancer Genetics and Cytogenetics. 200(2). 167–169. 2 indexed citations
12.
Achkar, Walid Al, et al.. (2009). Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report. Molecular Cytogenetics. 2(1). 21–21. 11 indexed citations
13.
Polityko, A., et al.. (2009). Paternally derived der(7)t(Y;7)(p11.1∼11.2;p22.3)dn in a mosaic case with Turner syndrome. European Journal of Medical Genetics. 52(4). 207–210. 5 indexed citations
14.
15.
Mkrtchyan, Hasmik, Stefan Scheler, Isaac A. Klein, et al.. (2009). Molecular Cytogenetic Characterization of the Human Cerebral Microvessel Endothelial Cell Line hCMEC/D3. Cytogenetic and Genome Research. 126(4). 313–317. 12 indexed citations
16.
Liehr, Thomas, et al.. (2009). A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia. Cancer Genetics and Cytogenetics. 189(1). 59–62. 3 indexed citations
17.
Raimondi, Susana C., Eliana Abdelhay, Hasmik Mkrtchyan, et al.. (2008). Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo. Cancer Genetics and Cytogenetics. 182(1). 56–60. 5 indexed citations
18.
Trifonov, Vladimir A., Franz Binkert, Laura Rodríguez, et al.. (2008). Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?. Molecular Cytogenetics. 1(1). 6–6. 24 indexed citations
19.
Starke, Heike, Günther Ernst, Nadezda Kosyakova, et al.. (2007). A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1—evidence for high variability in mosaicism in different tissues of sSMC carriers. Prenatal Diagnosis. 27(8). 783–785. 29 indexed citations
20.
Mkrtchyan, Hasmik, et al.. (2006). Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2). Cytogenetic and Genome Research. 114(3-4). 270–273. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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