Alaa K. Kamel

473 total citations
34 papers, 227 citations indexed

About

Alaa K. Kamel is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Alaa K. Kamel has authored 34 papers receiving a total of 227 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 20 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Alaa K. Kamel's work include Sexual Differentiation and Disorders (13 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers). Alaa K. Kamel is often cited by papers focused on Sexual Differentiation and Disorders (13 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers). Alaa K. Kamel collaborates with scholars based in Egypt, France and United States. Alaa K. Kamel's co-authors include Inas Mazen, Mona K. Mekkawy, Mona Aglan, Ken McElreavey, Maha S. Zaki, Mona El Gammal, Samira Ismail, Mona L. Essawi, Samia A. Temtamy and Mohamed S. Abdel‐Hamid and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Sexual Medicine and Cytogenetic and Genome Research.

In The Last Decade

Alaa K. Kamel

31 papers receiving 212 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alaa K. Kamel Egypt 9 180 138 61 33 25 34 227
Capucine Hyon France 12 262 1.5× 210 1.5× 98 1.6× 43 1.3× 47 1.9× 21 376
Linda Ramsdell United States 6 145 0.8× 182 1.3× 60 1.0× 63 1.9× 5 0.2× 12 244
M. Crocker United Kingdom 9 183 1.0× 88 0.6× 68 1.1× 8 0.2× 52 2.1× 16 245
Ariella Weinberg‐Shukron Israel 9 173 1.0× 229 1.7× 55 0.9× 14 0.4× 15 0.6× 15 377
Tossaporn Seeherunvong United States 7 113 0.6× 131 0.9× 15 0.2× 29 0.9× 12 0.5× 14 201
Ellen Markljung Sweden 11 123 0.7× 146 1.1× 29 0.5× 122 3.7× 12 0.5× 15 312
John Hutson Australia 4 119 0.7× 149 1.1× 8 0.1× 37 1.1× 7 0.3× 6 201
Gianna Carvalheira Brazil 14 144 0.8× 182 1.3× 21 0.3× 8 0.2× 99 4.0× 25 381
M. Barr United States 6 144 0.8× 199 1.4× 93 1.5× 14 0.4× 24 1.0× 6 346
Nadja Kokalj Vokač Slovenia 8 62 0.3× 79 0.6× 49 0.8× 8 0.2× 11 0.4× 27 179

Countries citing papers authored by Alaa K. Kamel

Since Specialization
Citations

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

Fields of papers citing papers by Alaa K. Kamel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alaa K. Kamel. 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 Alaa K. Kamel. The network helps show where Alaa K. Kamel may publish in the future.

Co-authorship network of co-authors of Alaa K. Kamel

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

All Works

20 of 20 papers shown
1.
2.
Mazen, Inas, et al.. (2022). A Homozygous Missense Variant in Hedgehog Acyltransferase (HHAT) Gene Associated with 46,XY Gonadal Dysgenesis. Sexual Development. 16(4). 261–265. 6 indexed citations
3.
Kamel, Alaa K., et al.. (2021). Interstitial Deletion of 2q22.2q22.3 Involving the Entire <b><i>ZEB2</i></b> Gene in a Case of Mowat-Wilson Syndrome. Molecular Syndromology. 12(2). 87–95. 3 indexed citations
4.
Kamel, Alaa K., et al.. (2020). Phenotypic and Molecular Cytogenetic Analysis of a Case of Monosomy 1p36 Syndrome due to Unbalanced Translocation. Molecular Syndromology. 11(5-6). 284–295. 1 indexed citations
5.
Mekkawy, Mona K., et al.. (2019). Cytogenetic Spectrum of Ovotesticular Difference of Sex Development (OT DSD) among a Large Cohort of DSD Patients and Literature Review. Sexual Development. 13(5-6). 221–227. 4 indexed citations
6.
Mazen, Inas, et al.. (2018). Clinical and Cytogenetic Study of Egyptian Patients with Sex Chromosome Disorders of Sex Development. Sexual Development. 12(5). 211–217. 3 indexed citations
7.
Zaki, Maha S., et al.. (2018). Unbalanced 14;X Translocation and Pattern of X Inactivation in a Female Patient with Multiple Congenital Anomalies. Cytogenetic and Genome Research. 156(2). 71–79. 2 indexed citations
8.
El‐Bassyouni, Hala T., et al.. (2018). Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation. Molecular Cytogenetics. 11(1). 57–57. 8 indexed citations
9.
Mekkawy, Mona K., et al.. (2018). An infertile azoospermic male with 45,X karyotype and a unique complex (Y;14); (Y;22) translocation: cytogenetic and molecular characterization. Journal of Assisted Reproduction and Genetics. 35(8). 1503–1508. 2 indexed citations
10.
Mazen, Inas, et al.. (2017). <b><i>WT1</i></b> Gene Mutation, p.R462W, in a 46,XY DSD Patient from Egypt with Gonadoblastoma and Review of the Literature. Sexual Development. 11(5-6). 280–283. 5 indexed citations
11.
Mazen, Inas, et al.. (2017). Aromatase Deficiency due to a Homozygous <b><i>CYP19A1</i></b> Mutation in a 46,XX Egyptian Patient with Ambiguous Genitalia. Sexual Development. 11(5-6). 275–279. 16 indexed citations
12.
Mazen, Inas, et al.. (2016). Homozygous Mutation of the <b><i>FGFR1</i></b> Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex Development. Sexual Development. 10(1). 16–22. 11 indexed citations
13.
Kamel, Alaa K., et al.. (2015). Sex Chromosome Mosaicism in the Gonads of DSD Patients: A Karyotype/Phenotype Correlation. Sexual Development. 9(5). 279–288. 3 indexed citations
14.
Ellaithi, Mona, Ralf Werner, Felix G. Riepe, et al.. (2014). 46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the <b><i>HSD17B3</i></b> Gene. Sexual Development. 8(4). 151–155. 8 indexed citations
15.
16.
Zaki, Maha S., et al.. (2012). Bartsocas-Papas syndrome with variable expressivity in an Egyptian family.. PubMed. 23(2). 269–79. 3 indexed citations
17.
Mekkawy, Mona K., et al.. (2012). Isodicentric Y chromosomes in Egyptian patients with disorders of sex development (DSD). American Journal of Medical Genetics Part A. 158A(7). 1594–1603. 24 indexed citations
18.
19.
Kamel, Alaa K., et al.. (2009). Constitutional retinoblastoma gene deletion in Egyptian patients. World Journal of Pediatrics. 5(3). 222–225. 7 indexed citations
20.
Temtamy, Samia A., et al.. (2007). Phenotypic and cytogenetic spectrum of 9p trisomy. PubMed. 18(1). 29–48. 39 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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