SA Boyadjiev

478 total citations
8 papers, 334 citations indexed

About

SA Boyadjiev is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, SA Boyadjiev has authored 8 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in SA Boyadjiev's work include Craniofacial Disorders and Treatments (5 papers), Cleft Lip and Palate Research (4 papers) and Pharmacological Effects and Toxicity Studies (2 papers). SA Boyadjiev is often cited by papers focused on Craniofacial Disorders and Treatments (5 papers), Cleft Lip and Palate Research (4 papers) and Pharmacological Effects and Toxicity Studies (2 papers). SA Boyadjiev collaborates with scholars based in United States, Australia and United Kingdom. SA Boyadjiev's co-authors include Ethylin Wang Jabs, Michael T. Geraghty, Saul W. Brusilow, Lewis Waber, Akira Hata, Chad Haldeman‐Englert, E H Zackai, S Hamamoto, Jin Oh Kim and Fernando Kok and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Journal of Inherited Metabolic Disease.

In The Last Decade

SA Boyadjiev

8 papers receiving 326 citations

Peers

Countries citing papers authored by SA Boyadjiev

Since Specialization

Citations

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

Fields of papers citing papers by SA Boyadjiev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of SA Boyadjiev

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Cranio‐lenticulo‐sutural dysplasia associated with defects in collagen secretion 2010 ·Clinical Genetics ·SA Boyadjiev, (unknown), Akira Hata, Chad Haldeman‐Englert, E H Zackai, (unknown), S Hamamoto, (unknown), Jin Oh Kim	55
2	Genetic analysis of non‐syndromic craniosynostosis 2007 ·Orthodontics and Craniofacial Research ·SA Boyadjiev	100
3	Molecular screening for microdeletions at 9p22‐p24 and 11q23‐q24 in a large cohort of patients with trigonocephaly 2005 ·Clinical Genetics ·(unknown), David Johnson, Luís Garcia Alonso, (unknown), Eloisa De Sá Moreira, (unknown), Fernando Kok, Chong Ae Kim, (unknown), Ethylin Wang Jabs, SA Boyadjiev, Andrew O.M. Wilkie, (unknown)	37
4	The relationship of plasma glutamine to ammonium and of glycine to acid–base balance in propionic acidaemia 2003 ·Journal of Inherited Metabolic Disease ·Zuhair N. Al‐Hassnan, SA Boyadjiev, Verayuth Praphanphoj, Ada Hamosh, Nancy Braverman, Gilles Thomas, Michael T. Geraghty	18
5	Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonaemia 2000 ·Journal of Inherited Metabolic Disease ·(unknown), SA Boyadjiev, Lewis Waber, Saul W. Brusilow, Michael T. Geraghty	44
6	Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disorders 2000 ·Clinical Genetics ·SA Boyadjiev, Ethylin Wang Jabs	67
7	Paternal origin of FGFR2 mutations in sporadic cases of Crouzon and Pfeiffer syndromes. 1999 ·The American Journal of Human Genetics ·Robert L. Glaser, Wen G. Jiang, SA Boyadjiev, (unknown), (unknown), Michael Oldridge, (unknown), (unknown), Ethylin Wang Jabs	3
8	Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndrome. 1998 ·Journal of Medical Genetics ·Niamh Flanagan, SA Boyadjiev, John Harper, (unknown), Michael Earley, Roger Watson, Ethylin Wang Jabs, Michael T. Geraghty	10

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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