E. Zackai

436 total citations
7 papers, 243 citations indexed

About

E. Zackai is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, E. Zackai has authored 7 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Plant Science. Recurrent topics in E. Zackai's work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Chromosomal and Genetic Variations (2 papers). E. Zackai is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Chromosomal and Genetic Variations (2 papers). E. Zackai collaborates with scholars based in United States, Finland and Canada. E. Zackai's co-authors include Donna M. McDonald‐McGinn, Markku Keinänen, Darrell Ricke, Teresa L. Yang‐Feng, Tracy J. Wright, Philip D. Cotter, Kurt Hirschhorn, Michael R. Altherr, N B Spinner and Mirja Somer and has published in prestigious journals such as Human Molecular Genetics, Schizophrenia Research and Cytogenetic and Genome Research.

In The Last Decade

E. Zackai

7 papers receiving 237 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. Zackai United States	5	179	146	65	60	20	7	243
Anna Jauch Germany	10	137 0.8×	200 1.4×	91 1.4×	33 0.6×	32 1.6×	11	319
Robert A. Conte United States	11	257 1.4×	167 1.1×	163 2.5×	89 1.5×	19 0.9×	41	361
M. Murer‐Orlando United Kingdom	11	118 0.7×	200 1.4×	68 1.0×	43 0.7×	32 1.6×	19	294
Rosetta Lecce Italy	9	243 1.4×	175 1.2×	99 1.5×	87 1.4×	18 0.9×	11	318
Patrick L. Wilmot United States	10	148 0.8×	95 0.7×	29 0.4×	49 0.8×	10 0.5×	26	238
Jill K. Northup United States	8	155 0.9×	115 0.8×	39 0.6×	26 0.4×	21 1.1×	13	224
T. M. Schroeder-Kurth Germany	7	143 0.8×	227 1.6×	135 2.1×	47 0.8×	54 2.7×	10	330
Lie‐Jiau Hsieh Taiwan	9	159 0.9×	82 0.6×	85 1.3×	61 1.0×	15 0.8×	15	257
Caron D. Glotzbach United States	11	244 1.4×	137 0.9×	102 1.6×	52 0.9×	20 1.0×	11	312
Carmelo Laganà Italy	9	148 0.8×	137 0.9×	33 0.5×	62 1.0×	18 0.9×	21	266

Countries citing papers authored by E. Zackai

Since Specialization

Citations

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

Fields of papers citing papers by E. Zackai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Zackai

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

All Works

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7 of 7 papers shown

1.

Takarae, Yukari, et al.. (2007). Overlapping numerical cognition impairments in Chromosome 22q11.2 Deletion and Turner Syndromes.. Digital Repository at the University of Maryland (University of Maryland College Park). 4 indexed citations

2.

Zackai, E., et al.. (2004). Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects. Clinical Genetics. 66(1). 46–52. 16 indexed citations

3.

Bearden, Carrie E., David R. Lynch, Abbas F. Jawad, et al.. (2003). Effects of a functional COMT polymorphism on neurocognitive function in the 22Q deletion syndrome. Schizophrenia Research. 60(1). 78–79. 1 indexed citations

4.

Wright, Tracy J., Darrell Ricke, Philip D. Cotter, et al.. (1997). A Transcript Map of the Newly Defined 165 kb Wolf-Hirschhorn Syndrome Critical Region. Human Molecular Genetics. 6(2). 317–324. 169 indexed citations

5.

Holmes, Susan E., Wànkuí Gǒng, Heather E. McDermid, et al.. (1997). Disruption of the Clathrin Heavy Chain-Like Gene (CLTCL) Associated with Features of DGS/VCFS: A Balanced (21;22)(p12;q11) Translocation. Human Molecular Genetics. 6(3). 357–367. 39 indexed citations

6.

Aronson, M.M., E. Zackai, William J. Mellman, et al.. (1975). A (13) terminal deletion, 46 chromosomes. Cytogenetic and Genome Research. 15(1). 57–58. 7 indexed citations

7.

Zackai, E., William J. Mellman, M.M. Aronson, et al.. (1975). A (10;17) translocation, unbalanced, 46 chromosomes. Cytogenetic and Genome Research. 14(1). 90–91. 7 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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