Bassem A. Bejjani

7.5k total citations
83 papers, 4.1k citations indexed

About

Bassem A. Bejjani is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Bassem A. Bejjani has authored 83 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 40 papers in Molecular Biology and 24 papers in Plant Science. Recurrent topics in Bassem A. Bejjani's work include Genomic variations and chromosomal abnormalities (43 papers), Chromosomal and Genetic Variations (24 papers) and Prenatal Screening and Diagnostics (18 papers). Bassem A. Bejjani is often cited by papers focused on Genomic variations and chromosomal abnormalities (43 papers), Chromosomal and Genetic Variations (24 papers) and Prenatal Screening and Diagnostics (18 papers). Bassem A. Bejjani collaborates with scholars based in United States, Poland and Canada. Bassem A. Bejjani's co-authors include Lisa G. Shaffer, Blake C. Ballif, Justine Coppinger, Aaron Theisen, Emily A. Rorem, Beth S. Torchia, Catherine D. Kashork, Kyle Sundin, Jill A. Rosenfeld and Allen N. Lamb and has published in prestigious journals such as Nature Genetics, Annals of the New York Academy of Sciences and The American Journal of Human Genetics.

In The Last Decade

Bassem A. Bejjani

83 papers receiving 3.9k citations

Peers

Bassem A. Bejjani
Arnold Munnich France
Alessandra Baumer Switzerland
Yoshinori Tsurusaki Japan
Nicole de Leeuw Netherlands
Willy M. Nillesen Netherlands
Sabrina Giglio Italy
Mordechai Shohat Israel
Melissa A. Parisi United States
Christophe Philippe France
F. Lucy Raymond United Kingdom
Arnold Munnich France
Bassem A. Bejjani
Citations per year, relative to Bassem A. Bejjani Bassem A. Bejjani (= 1×) peers Arnold Munnich

Countries citing papers authored by Bassem A. Bejjani

Since Specialization
Citations

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

Fields of papers citing papers by Bassem A. Bejjani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bassem A. Bejjani. 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 Bassem A. Bejjani. The network helps show where Bassem A. Bejjani may publish in the future.

Co-authorship network of co-authors of Bassem A. Bejjani

This figure shows the co-authorship network connecting the top 25 collaborators of Bassem A. Bejjani. A scholar is included among the top collaborators of Bassem A. Bejjani 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 Bassem A. Bejjani. Bassem A. Bejjani 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.
Sahoo, Trilochan, Aaron Theisen, Jill A. Rosenfeld, et al.. (2011). Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems. Genetics in Medicine. 13(10). 868–880. 75 indexed citations
2.
Sahoo, Trilochan, Aaron Theisen, Pedro A. Sanchez‐Lara, et al.. (2011). Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate. American Journal of Medical Genetics Part A. 155(7). 1646–1653. 53 indexed citations
3.
Neill, Nicholas J., Beth S. Torchia, Bassem A. Bejjani, Lisa G. Shaffer, & Blake C. Ballif. (2010). Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH. Molecular Cytogenetics. 3(1). 11–11. 48 indexed citations
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Rosenfeld, Jill A., Kathleen A. Leppig, Blake C. Ballif, et al.. (2009). Genotype–phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations. Genetics in Medicine. 11(11). 797–805. 55 indexed citations
7.
Li, Xin, et al.. (2008). Human anterior chamber angle development without cell death or macrophage involvement.. PubMed. 14. 2492–8. 4 indexed citations
8.
Shevell, Michael, Bassem A. Bejjani, Myriam Srour, et al.. (2008). Array comparative genomic hybridization in global developmental delay. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1101–1108. 36 indexed citations
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Ballif, Blake C., et al.. (2007). The clinical utility of enhanced subtelomeric coverage in array CGH. American Journal of Medical Genetics Part A. 143A(16). 1850–1857. 60 indexed citations
11.
Lalani, Seema R., et al.. (2006). Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2). BMC Medical Genetics. 7(1). 8–8. 18 indexed citations
12.
Shaffer, Lisa G., Catherine D. Kashork, Reza Saleki, et al.. (2006). Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases. The Journal of Pediatrics. 149(1). 98–102.e5. 165 indexed citations
13.
Bejjani, Bassem A., Reza Saleki, Blake C. Ballif, et al.. (2005). Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?. American Journal of Medical Genetics Part A. 134A(3). 259–267. 155 indexed citations
14.
Curry, Stacey, et al.. (2004). Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in Ecuador. Ophthalmic Genetics. 25(1). 3–9. 25 indexed citations
15.
Mammen, Jennifer S., Gary S. Pittman, Yulong Li, et al.. (2003). Single amino acid mutations, but not common polymorphisms, decrease the activity of CYP1B1 against (-)benzo[a]pyrene-7R-trans-7,8-dihydrodiol. Carcinogenesis. 24(7). 1247–1255. 30 indexed citations
16.
Berend, Sue Ann, Bassem A. Bejjani, Christopher McCaskill, & Lisa G. Shaffer. (2002). Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocations. American Journal of Medical Genetics. 111(4). 362–365. 28 indexed citations
17.
Bejjani, Bassem A., Frank A.E. Kruyt, Reet Kurg, et al.. (1999). Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two Patients with Seckel syndrome. American Journal of Medical Genetics. 83(5). 388–391. 10 indexed citations
18.
Berend, Sue Ann, Lisa G. Shaffer, & Bassem A. Bejjani. (1999). Pure trisomy 10p involving an isochromosome 10p. Clinical Genetics. 55(5). 367–371. 27 indexed citations
19.
Bejjani, Bassem A., Richard A. Lewis, Karim F. Tomey, et al.. (1998). Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia. The American Journal of Human Genetics. 62(2). 325–333. 255 indexed citations
20.
Zhao, Qi, et al.. (1998). Cloning, Genomic Structure, and Expression of Mouse Ring Finger Protein GeneZnf179. Genomics. 49(3). 394–400. 15 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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