E H Zackai

618 total citations
12 papers, 434 citations indexed

About

E H Zackai is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, E H Zackai has authored 12 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in E H Zackai's work include Genomic variations and chromosomal abnormalities (5 papers), Connective tissue disorders research (3 papers) and Genomics and Rare Diseases (2 papers). E H Zackai is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Connective tissue disorders research (3 papers) and Genomics and Rare Diseases (2 papers). E H Zackai collaborates with scholars based in United States, United Arab Emirates and Australia. E H Zackai's co-authors include Donna M. McDonald‐McGinn, B S Emanuel, Sulagna C. Saitta, Linda M. Ernst, Helen Kingston, Lindsay Keir, Anne George, Andrew H. Crosby, Jianjun Hao and Victoria Murday and has published in prestigious journals such as Journal of Bone and Joint Surgery, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

E H Zackai

12 papers receiving 428 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E H Zackai United States	7	258	213	87	66	44	12	434
Siham Chafai Elalaoui Morocco	14	262 1.0×	158 0.7×	47 0.5×	56 0.8×	23 0.5×	41	525
A.B. Mukherjee United States	8	193 0.7×	85 0.4×	43 0.5×	41 0.6×	16 0.4×	13	397
Adi Reich Israel	12	176 0.7×	252 1.2×	143 1.6×	26 0.4×	60 1.4×	17	458
Hans J. van der Harten Netherlands	13	235 0.9×	231 1.1×	53 0.6×	57 0.9×	36 0.8×	19	543
Fathiya Al-Murshedi Oman	10	221 0.9×	99 0.5×	154 1.8×	23 0.3×	32 0.7×	20	534
B. G. A. ter Haar Netherlands	15	212 0.8×	160 0.8×	18 0.2×	12 0.2×	30 0.7×	20	423
Ezzat Elsobky Egypt	12	303 1.2×	300 1.4×	83 1.0×	44 0.7×	33 0.8×	21	570
Wolfram Henn Germany	12	190 0.7×	145 0.7×	80 0.9×	21 0.3×	117 2.7×	27	540
Natalie C. Butterfield Australia	12	332 1.3×	162 0.8×	55 0.6×	22 0.3×	9 0.2×	16	482
Mika Kikkawa Japan	13	284 1.1×	102 0.5×	16 0.2×	54 0.8×	45 1.0×	22	620

Countries citing papers authored by E H Zackai

Since Specialization

Citations

This map shows the geographic impact of E H 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 H 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 H Zackai more than expected).

Fields of papers citing papers by E H Zackai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of E H Zackai. A scholar is included among the top collaborators of E H 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 H Zackai. E H 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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12 of 12 papers shown

Boyadjiev, SA, Akira Hata, Chad Haldeman‐Englert, et al.. (2010). Cranio‐lenticulo‐sutural dysplasia associated with defects in collagen secretion. Clinical Genetics. 80(2). 169–176. 55 indexed citations

Theisen, Aaron, et al.. (2008). Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2. Clinical Genetics. 74(5). 469–475. 63 indexed citations

Simpson, Michael A., Ray C. J. Hsu, Lindsay Keir, et al.. (2007). Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development. The American Journal of Human Genetics. 81(5). 906–912. 161 indexed citations

McDonald‐McGinn, Donna M., Ralph J. DeBerardinis, Sean Bartlett, et al.. (2003). Molecular characterization of Pfeiffer syndrome: Implications for prognosis and genetic counseling.. The American Journal of Human Genetics. 73. 212–212. 1 indexed citations

Emanuel, B S, Donna M. McDonald‐McGinn, Sulagna C. Saitta, & E H Zackai. (2001). The 22q11.2 deletion syndrome.. PubMed. 48. 39–73. 86 indexed citations

Wilkie, Andrew O.M., Sharon W. Horsley, Robert E. Kearney, et al.. (1998). Genes in craniosynostosis. European Journal of Human Genetics. 6. 27–27. 1 indexed citations

Zackai, E H, Donna M. McDonald‐McGinn, & N B Spinner. (1994). Classical Wolf-Hirschhorn Syndrome confirmed molecularly despite normal results using commercially available probes: Redefinition of critical region. The American Journal of Human Genetics. 55. 2 indexed citations

Biegel, Jaclyn A., E H Zackai, Charles D. Scher, et al.. (1993). Constitutional Ip36 deletion in a child with neuroblastoma. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 3 indexed citations

Callen, David F., Helen J. Eyre, Sharon Lane, et al.. (1993). High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.. Journal of Medical Genetics. 30(10). 828–832. 33 indexed citations

10.

Boden, Scott D., et al.. (1987). Metatropic dwarfism. Uncoupling of endochondral and perichondral growth.. Journal of Bone and Joint Surgery. 69(2). 174–184. 22 indexed citations

11.

Donnenfeld, Alan E., E H Zackai, Donna M. McDonald‐McGinn, Rosana Aquino, & B S Emanuel. (1987). De novo 2q+ masquerading as Smith-Lemli-Opitz syndrome.. Journal of Medical Genetics. 24(7). 436–439. 6 indexed citations

12.

Zackai, E H, et al.. (1978). A (14;20) translocation, unbalanced, from a subject with severe congenital anomalies. Cytogenetic and Genome Research. 21(3). 173–173. 1 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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