M H Polymeropoulos

904 total citations
9 papers, 756 citations indexed

About

M H Polymeropoulos is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, M H Polymeropoulos has authored 9 papers receiving a total of 756 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Oncology. Recurrent topics in M H Polymeropoulos's work include Endoplasmic Reticulum Stress and Disease (2 papers), Adenosine and Purinergic Signaling (1 paper) and Genetic Syndromes and Imprinting (1 paper). M H Polymeropoulos is often cited by papers focused on Endoplasmic Reticulum Stress and Disease (2 papers), Adenosine and Purinergic Signaling (1 paper) and Genetic Syndromes and Imprinting (1 paper). M H Polymeropoulos collaborates with scholars based in United States, Greece and Hungary. M H Polymeropoulos's co-authors include Rosarelis Torres, M Swift, Ronnie Gorman Swift, Éva Mezey, M Papp, M. Brownstein, Anindya Dehejia, G Harta, Rosa Isela Ortiz De Luna and Clair A. Francomano and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

M H Polymeropoulos

9 papers receiving 737 citations

Peers

M H Polymeropoulos

MB

CB

PHYSI

GENET

NEURO

Sebahattin Çırak Germany

Ezequiel Surace Argentina

Keiko Nakanishi Japan

Luc Régal Belgium

Valérie Race Belgium

Barry A. Chioza United Kingdom

Franco Ajmar Italy

Pierre Mazot France

Márcia A. Liz Portugal

Joanne Wuu United States

Sebahattin Çırak Germany

M H Polymeropoulos

538 ×1.3

MB

142 ×0.8

CB

157 ×0.9

PHYSI

170 ×1.2

GENET

119 ×0.9

NEURO

Citations per year, relative to M H Polymeropoulos M H Polymeropoulos (= 1×) peers Sebahattin Çırak

Countries citing papers authored by M H Polymeropoulos

Since Specialization

Citations

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

Fields of papers citing papers by M H Polymeropoulos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M H Polymeropoulos. 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 M H Polymeropoulos. The network helps show where M H Polymeropoulos may publish in the future.

Co-authorship network of co-authors of M H Polymeropoulos

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

All Works

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9 of 9 papers shown

1.

Torres, Rosarelis, Elizabeth C. LeRoy, Xun Hu, et al.. (2000). Mutation screening of the Wolfram syndrome gene in psychiatric patients. Molecular Psychiatry. 6(1). 39–43. 37 indexed citations

2.

Mezey, Éva, Anindya Dehejia, G Harta, et al.. (1998). Alpha synuclein in neurodegenerative disorders: Murderer or accomplice?. Nature Medicine. 4(7). 755–757. 161 indexed citations

3.

Swift, Ronnie Gorman, M H Polymeropoulos, Rosarelis Torres, & M Swift. (1998). Predisposition of Wolfram syndrome heterozygotes to psychiatric illness. Molecular Psychiatry. 3(1). 86–91. 116 indexed citations

4.

Johnson, M R, M H Polymeropoulos, Hans L. Vos, Rosa Isela Ortiz De Luna, & Clair A. Francomano. (1996). A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis.. Genome Research. 6(11). 1050–1055. 106 indexed citations

5.

Brinkmann, Ulrich, Maria Gallo, M H Polymeropoulos, & Ira Pastan. (1996). The human CAS (cellular apoptosis susceptibility) gene mapping on chromosome 20q13 is amplified in BT474 breast cancer cells and part of aberrant chromosomes in breast and colon cancer cell lines.. Genome Research. 6(3). 187–194. 89 indexed citations

6.

Ide, Susan, Rosa Isela Ortiz De Luna, Clair A. Francomano, & M H Polymeropoulos. (1996). Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish. Human Genetics. 98(5). 572–575. 10 indexed citations

7.

Lee, Hoi Young, Jun Murata, Timothy Clair, et al.. (1996). Cloning, Chromosomal Localization, and Tissue Expression of Autotaxin from Human Teratocarcinoma Cells. Biochemical and Biophysical Research Communications. 218(3). 714–719. 93 indexed citations

8.

Yano, Koichi, Akinari Hidaka, Motoyasu Saji, et al.. (1994). A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases.. The Journal of Clinical Endocrinology & Metabolism. 79(6). 1818–1823. 53 indexed citations

9.

Carstea, Eugene D., M H Polymeropoulos, Clarissa C. Parker, et al.. (1993). Linkage of Niemann-Pick disease type C to human chromosome 18.. Proceedings of the National Academy of Sciences. 90(5). 2002–2004. 91 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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