Efthymia Melista

1.3k total citations
14 papers, 626 citations indexed

About

Efthymia Melista is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Efthymia Melista has authored 14 papers receiving a total of 626 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Hematology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Efthymia Melista's work include Hemoglobinopathies and Related Disorders (9 papers), Iron Metabolism and Disorders (5 papers) and Blood groups and transfusion (3 papers). Efthymia Melista is often cited by papers focused on Hemoglobinopathies and Related Disorders (9 papers), Iron Metabolism and Disorders (5 papers) and Blood groups and transfusion (3 papers). Efthymia Melista collaborates with scholars based in United States, Saudi Arabia and Italy. Efthymia Melista's co-authors include Clinton T. Baldwin, Martin H. Steinberg, Paola Sebastiani, Nadia Solovieff, Stephen W. Hartley, Daniel A. Dworkis, Thomas T. Perls, Monty Montano, Jemma B. Wilk and Annibale Alessandro Puca and has published in prestigious journals such as Blood, PLoS ONE and Hypertension.

In The Last Decade

Efthymia Melista

14 papers receiving 607 citations

Peers

Countries citing papers authored by Efthymia Melista

Since Specialization

Citations

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

Fields of papers citing papers by Efthymia Melista

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Efthymia Melista

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype 2013 ·Blood Cells Molecules and Diseases ·Duyen Ngo, Harold Bae, Martin H. Steinberg, Paola Sebastiani, Nadia Solovieff, Clinton T. Baldwin, Efthymia Melista, Surinder Safaya, Lindsay A. Farrer, Ahmed Alsuliman, Waleed H. Albuali, (unknown), Zaki A. Naserullah, Idowu Akinsheye, Patrick G. Gallagher, Hongyuan Luo, David H.K. Chui, John Farrell, Amein K. Al‐Ali, Abdulrahman Alsultan	42
2	The ankyrin-3 gene is associated with posttraumatic stress disorder and externalizing comorbidity 2013 ·Psychoneuroendocrinology ·Mark W. Logue, Nadia Solovieff, Melanie P. Leussis, Erika J. Wolf, Efthymia Melista, Clinton T. Baldwin, Karestan C. Koenen, Tracey L. Petryshen, Mark W. Miller	28
3	Genetic Signatures of Exceptional Longevity in Humans 2012 ·PLoS ONE ·Paola Sebastiani, Nadia Solovieff, Andrew T. DeWan, Kyle M. Walsh, Annibale Alessandro Puca, Stephen W. Hartley, Efthymia Melista, Stacy L. Andersen, Daniel A. Dworkis, Jemma B. Wilk, Richard H. Myers, Martin H. Steinberg, Monty Montano, Clinton T. Baldwin, Josephine Hoh, Thomas T. Perls	295
4	A functional promoter polymorphism of the δ‐globin gene is a specific marker of the Arab‐Indian haplotype 2012 ·American Journal of Hematology ·Abdulrahman Alsultan, Duyen Ngo, John J. Farrell, Idowu Akinsheye, Nadia Solovieff, Hazem A. Ghabbour, Amein K. Al‐Ali, Ahmed Alsuliman, (unknown), Waleed H. Albuali, (unknown), Clinton T. Baldwin, Lindsay A. Farrer, Hong Luo, Efthymia Melista, Surinder Safaya, (unknown), David H.K. Chui, Martin H. Steinberg	11
5	Severe sickle cell anemia is associated with increased plasma levels of TNF‐R1 and VCAM‐1 2010 ·American Journal of Hematology ·Daniel A. Dworkis, Elizabeth S. Klings, Nadia Solovieff, Guihua Li, Jacqueline N. Milton, Stephen W. Hartley, Efthymia Melista, (unknown), Paola Sebastiani, Martin H. Steinberg, Clinton T. Baldwin	30
6	Genetic modifiers of the severity of sickle cell anemia identified through a genome‐wide association study 2009 ·American Journal of Hematology ·Paola Sebastiani, Nadia Solovieff, Stephen W. Hartley, Jacqueline N. Milton, Alberto Riva, Daniel A. Dworkis, Efthymia Melista, Elizabeth S. Klings, Melanie E. Garrett, Marilyn J. Telen, Allison E. Ashley‐Koch, Clinton T. Baldwin, Martin H. Steinberg	72
7	Genome-Wide Association Study of Stroke in Sickle Cell Anemia. 2009 ·Blood ·Paola Sebastiani, Jacqueline N. Milton, (unknown), Stephen W. Hartley, Daniel A. Dworkis, Efthymia Melista, Clinton T. Baldwin, Martin H. Steinberg	3
8	A Genome-Wide Association Study of the Alloimmunization Responder Phenotype in Sickle Cell Disease. 2009 ·Blood ·Daniel A. Dworkis, (unknown), Jacqueline N. Milton, Stephen W. Hartley, Mayetri Gupta, Paola Sebastiani, Clinton T. Baldwin, Efthymia Melista, (unknown), Karen Quillen, Martin H. Steinberg	1
9	A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples 2008 ·BMC Genetics ·Paola Sebastiani, Zhenming Zhao, María M. Abad‐Grau, Alberto Riva, Stephen W. Hartley, (unknown), Alessandro Doria, Monty Montano, Efthymia Melista, Dellara F. Terry, Thomas T. Perls, Martin H. Steinberg, Clinton T. Baldwin	23
10	Fetal Hemoglobin in Sickle Cell Anemia: A Novel Method for High-Resolution Discovery of Associated Genomic Copy Number Variations 2008 ·Blood ·Daniel A. Dworkis, Paola Sebastiani, Efthymia Melista, (unknown), (unknown), (unknown), David H.K. Chui, Martin H. Steinberg, Clinton T. Baldwin	1
11	Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations 2007 ·American Journal of Hematology ·Paola Sebastiani, Ling Wang, Val Nolan, Efthymia Melista, Qianli Ma, Clinton T. Baldwin, Martin H. Steinberg	27
12	Sequence variation of bradykinin receptors B1 and B2 and association with hypertension 2005 ·Journal of Hypertension ·Jing Cui, Efthymia Melista, Irmarie Chazaro, (unknown), Xiaofeng Zhou, Athanasios Manolis, Clinton T. Baldwin, Anita L. DeStefano, Haralambos Gavras	26
13	Association of NEDD4L Ubiquitin Ligase With Essential Hypertension 2005 ·Hypertension ·Christopher J. Russo, Efthymia Melista, Jing Cui, Anita L. DeStefano, George L. Bakris, Athanasios Manolis, Haralambos Gavras, Clinton T. Baldwin	65
14	SEQUENCE VARIATION OF BRADYKININ RECEPTORS B1 AND B2 AND ASSOCIATION WITH HYPERTENSION 2004 ·Journal of Hypertension ·Haralambos Gavras, J Cui, Efthymia Melista, Irmarie Chazaro, Tracy Zhang, (unknown), (unknown), Christopher L. Baldwin, Anita L. DeStefano	2

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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