Maria Proytcheva

2.8k total citations · 1 hit paper
36 papers, 2.1k citations indexed

About

Maria Proytcheva is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Maria Proytcheva has authored 36 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 10 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Maria Proytcheva's work include DNA Repair Mechanisms (6 papers), Acute Myeloid Leukemia Research (6 papers) and Genomics and Chromatin Dynamics (5 papers). Maria Proytcheva is often cited by papers focused on DNA Repair Mechanisms (6 papers), Acute Myeloid Leukemia Research (6 papers) and Genomics and Chromatin Dynamics (5 papers). Maria Proytcheva collaborates with scholars based in United States, Canada and Australia. Maria Proytcheva's co-authors include Nathan A. Ellis, David Lennon, James German, Joanna Groden, Joel E. Straughen, J German, Maureen M. Sanz, Becky Alhadeff, Carol Briggs and Earl E. Henderson and has published in prestigious journals such as Cell, Blood and The American Journal of Human Genetics.

In The Last Decade

Maria Proytcheva

33 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Bloom's syndrome gene product is homologous to RecQ helicases

1995 1.1k citations Nathan A. Ellis, Joanna Groden et al. Cell profile →

Peers

Countries citing papers authored by Maria Proytcheva

Since Specialization

Citations

This map shows the geographic impact of Maria Proytcheva'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 Maria Proytcheva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Proytcheva more than expected).

Fields of papers citing papers by Maria Proytcheva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Proytcheva. 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 Maria Proytcheva. The network helps show where Maria Proytcheva may publish in the future.

Co-authorship network of co-authors of Maria Proytcheva

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Proytcheva. A scholar is included among the top collaborators of Maria Proytcheva 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 Maria Proytcheva. Maria Proytcheva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical, Phenotypic and Molecular Characterization of NUP214-ABL1 Fusion Positive Myeloid Malignancies 2024 ·Journal of Medical Cases ·(unknown), (unknown), (unknown), Maria Proytcheva, (unknown)	0
2	Rare monosomy 7 and deletion 7p at diagnosis of chronic myeloid leukemia in accelerated phase 2021 ·Cancer Genetics ·(unknown), (unknown), Li‐Wen Lai, (unknown), Muhammad Sardar, Maria Proytcheva	2
3	Alder-Reilly Anomaly in the Cerebrospinal Fluid of a Child With Hurler Syndrome 2017 ·Journal of Pediatric Hematology/Oncology ·(unknown), Maria Proytcheva	2
4	Noncanonical Regulation of the Hedgehog Mediator GLI1 by c-MYC in Burkitt Lymphoma 2013 ·Molecular Cancer Research ·Joon Won Yoon, Marisa Gallant, Marilyn Lamm, (unknown), (unknown), Maria Proytcheva, Elizabeth Hyjek, Philip M. Iannaccone, David Walterhouse	44
5	Bone marrow evaluation for pediatric patients 2013 ·International Journal of Laboratory Hematology ·Maria Proytcheva	11
6	Shwachman-Diamond Syndrome 2013 ·Journal of Pediatric Hematology/Oncology ·Jeffrey R. Andolina, (unknown), Alexis A. Thompson, Sonali Chaudhury, A. Kyle Mack, Maria Proytcheva, Seth J. Corey	10
7	Serum Neopterin Levels as a Diagnostic Marker of Hemophagocytic Lymphohistiocytosis Syndrome 2011 ·Clinical and Vaccine Immunology ·Maria Ibarra, Marisa Klein‐Gitelman, Elaine Morgan, Maria Proytcheva, Christine Sullivan, Gabrielle Morgan, Lauren M. Pachman, Maurice R.G. O’Gorman	37
8	Juvenile myelomonocytic leukemia 2011 ·Seminars in Diagnostic Pathology ·Maria Proytcheva	8
9	Serum Neopterin Levels as a Diagnostic Marker of Hemophagocytic Lymphohistiocytosis Syndrome 2010 ·Clinical Immunology ·Maria Ibarra, Marisa Klein‐Gitelman, Elaine Morgan, Maria Proytcheva, Christine Sullivan, Gabrielle Morgan, Lauren M. Pachman, Maurice R.G. O’Gorman	3
10	Issues in Neonatal Cellular Analysis 2009 ·American Journal of Clinical Pathology ·Maria Proytcheva	55
11	Case–control study of risk factors for the development of post‐transplant lymphoproliferative disease in a pediatric heart transplant cohort* 2006 ·Pediatric Transplantation ·Ben Z. Katz, Elfriede Pahl, Susan E. Crawford, (unknown), Sherrie Rodgers, R. Seshadri, Maria Proytcheva, Stephen Pophal	42
12	Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT) 2004 ·Bone Marrow Transplantation ·Angela D. Trobaugh‐Lotrario, Morris Kletzel, Ralph Quinones, Loris McGavran, Maria Proytcheva, Stephen P. Hunger, J. Malcolm, Daniel J. Schissel, E. Hild, Roger Giller	22
13	Eosinophilic angiocentric fibrosis 2003 ·The Journal of Laryngology & Otology ·Abtin Tabaee, (unknown), Maria Proytcheva, (unknown)	23
14	BLM, the Bloom’s syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins 2000 ·Cytogenetic and Genome Research ·(unknown), Maria Proytcheva, Nathan A. Ellis, William K. Holloman, J German	47
15	Transfection of BLM into Cultured Bloom Syndrome Cells Reduces the Sister-Chromatid Exchange Rate toward Normal 1999 ·The American Journal of Human Genetics ·Nathan A. Ellis, Maria Proytcheva, Maureen M. Sanz, (unknown), James German	41
16	The Ashkenazic Jewish Bloom Syndrome Mutation blmAsh Is Present in Non-Jewish Americans of Spanish Ancestry 1998 ·The American Journal of Human Genetics ·Nathan A. Ellis, (unknown), Maria Proytcheva, David Lennon, Joanna Groden, James German	47
17	A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene 1998 ·Human Mutation ·Joel E. Straughen, (unknown), (unknown), Maria Proytcheva, Nathan A. Ellis, James German, Joanna Groden	11
18	Physical Mapping of the Bloom Syndrome Region by the Identification of YAC and P1 Clones from Human Chromosome 15 Band q26.1 1996 ·Genomics ·Joel E. Straughen, (unknown), (unknown), (unknown), Maria Proytcheva, Becky Alhadeff, Peter N. Goodfellow, James German, Nathan A. Ellis, Joanna Groden	12
19	Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity 1996 ·Clinical Genetics ·James German, Nathan A. Ellis, Maria Proytcheva	15
20	The Bloom's syndrome gene product is homologous to RecQ helicases breakdown → 1995 ·Cell ·Nathan A. Ellis, Joanna Groden, (unknown), Joel E. Straughen, David Lennon, (unknown), Maria Proytcheva, James German	1136

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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