Muhsin Elmas

416 total citations
25 papers, 89 citations indexed

About

Muhsin Elmas is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Muhsin Elmas has authored 25 papers receiving a total of 89 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Epidemiology. Recurrent topics in Muhsin Elmas's work include Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Congenital heart defects research (3 papers). Muhsin Elmas is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Congenital heart defects research (3 papers). Muhsin Elmas collaborates with scholars based in Türkiye, United States and Colombia. Muhsin Elmas's co-authors include Mustafa Solak, Müjgan Özdemir Erdoğan, Ayşegül Bükülmez, Murat Yeşil, Alper Gezdirici, Mustafa Doğan, Reşat Duman, Mehmet Yaman, Nuray Varol and Mustafa Solak and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Molecular Neuroscience and Brain and Development.

In The Last Decade

Muhsin Elmas

20 papers receiving 85 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Muhsin Elmas Türkiye	6	47	32	12	11	10	25	89
Newell Belnap United States	7	84 1.8×	49 1.5×	8 0.7×	12 1.1×	4 0.4×	12	126
Charu Kaiwar United States	6	56 1.2×	61 1.9×	11 0.9×	10 0.9×	5 0.5×	10	103
Mary Koziura United States	4	51 1.1×	70 2.2×	6 0.5×	8 0.7×	12 1.2×	5	114
Nurit Assia Batzir Israel	5	58 1.2×	43 1.3×	6 0.5×	6 0.5×	11 1.1×	9	92
Jessica Sebastian United States	6	64 1.4×	92 2.9×	11 0.9×	9 0.8×	21 2.1×	11	146
James J. O’Byrne Ireland	8	95 2.0×	81 2.5×	11 0.9×	7 0.6×	9 0.9×	24	174
Fathiya Al Murshedi Oman	6	45 1.0×	56 1.8×	14 1.2×	10 0.9×	8 0.8×	14	114
Rena A. Godfrey United States	4	30 0.6×	54 1.7×	7 0.6×	4 0.4×	5 0.5×	8	96
Mona Grimmel Germany	5	38 0.8×	26 0.8×	10 0.8×	12 1.1×	6 0.6×	11	93
Girolamo Aurelio Vitello Italy	6	43 0.9×	25 0.8×	5 0.4×	4 0.4×	6 0.6×	17	96

Countries citing papers authored by Muhsin Elmas

Since Specialization

Citations

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

Fields of papers citing papers by Muhsin Elmas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muhsin Elmas

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

All Works

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20 of 20 papers shown

Ulusoy, Mahmut Oğuz, et al.. (2025). H syndrome with bilateral choroidal osteoma: Coincidence or association?. European Journal of Ophthalmology. 35(2). NP55–NP60.

Varol, Nuray, et al.. (2023). Relationship between expression levels of TDRD7 and CRYBB3 and development of age-related cortico-nuclear cataracts. SHILAP Revista de lepidopterología. 24(1). 1 indexed citations

Doğan, Mustafa, et al.. (2022). Genetic and Clinical Evaluation of Retinitis Pigmentosa. SHILAP Revista de lepidopterología.

Köse, Melis, et al.. (2022). A female case of 5,10-methenyltetrahydrofolate synthetase deficiency with novel neuro-imaging abnormalities. Brain and Development. 44(9). 640–644. 2 indexed citations

Elmas, Muhsin, et al.. (2022). The road from mutation to next generation phenotyping: contribution of deep learning technology (Face2Gene) to diagnosis neurofibromatosis type 1. The European Research Journal. 8(2). 145–154. 1 indexed citations

Elmas, Muhsin, et al.. (2021). Neurodevelopment and Genetic Evaluation of Sotos Syndrome Cases with a Novel Mutation: a Single-Center Experience. Journal of Molecular Neuroscience. 72(1). 149–157. 4 indexed citations

Elmas, Muhsin, et al.. (2020). Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience. Molecular Syndromology. 11(1). 4–14. 20 indexed citations

Elmas, Muhsin, et al.. (2020). Two different homozygous mutations in two Turkish siblings: DGUOK and HPS5. SHILAP Revista de lepidopterología. 3(1). 41–44. 1 indexed citations

Elmas, Muhsin, et al.. (2020). Genetic and Clinical Approach To Microcephaly: A 5-Year Single Center Experience. Journal of Pediatric Genetics. 11(2). 110–116.

10.

Elmas, Muhsin, et al.. (2020). Association of vitamin D level and CYP27B1 gene polymorphism with multiple sclerosis in Turkish population. SHILAP Revista de lepidopterología. 3(1). 3–6. 1 indexed citations

11.

Elmas, Muhsin, et al.. (2020). Understanding What You Have Found: A Family With a Mutation in the LAMA1 Gene With Literature Review. SHILAP Revista de lepidopterología. 13. 3572579002–3572579002. 6 indexed citations

12.

Elmas, Muhsin, et al.. (2020). Genetic and clinical approach to macrocephaly: a 5-year single-center study. SHILAP Revista de lepidopterología. 3(2). 54–59. 2 indexed citations

13.

Elmas, Muhsin, et al.. (2018). A case of Bethlem Myopathy with autosomal recessive inheritance with a novel mutation in the COL6A2 gene. SHILAP Revista de lepidopterología. 1(2). 81–83. 2 indexed citations

14.

Elmas, Muhsin, et al.. (2018). Comparison of clinical parameters with whole exome sequencing analysis results of autosomal recessive patients; a center experience. Molecular Biology Reports. 46(1). 287–299. 22 indexed citations

15.

Solak, Mustafa, et al.. (2018). Evaluation of cytogenetic and y chromosome microdeletion analyzes in infertile cases. Meta Gene. 19. 78–81.

16.

Elmas, Muhsin, et al.. (2016). Coexisting urogenital anomaly and duodenal atresia in two atypical Holt-Oram syndrome. Journal of Indian Association of Pediatric Surgeons. 21(4). 193–193. 1 indexed citations

17.

Elmas, Muhsin, et al.. (2016). Infantile Type Sandhoff Disease with Striking Brain MRI Findings and a Novel Mutation. Polish Journal of Radiology. 81. 86–89. 10 indexed citations

18.

Duman, Reşat, et al.. (2015). First case of neurofibromatosis type 1 associated with chorioretinal coloboma, optic disc pseudodoubling, and vitiligo. Clinical Dysmorphology. 25(1). 31–34. 1 indexed citations

19.

Elmas, Muhsin, et al.. (2014). A rare case of 3C disease: Ritscher–Schinzel syndrome presenting with recurrent talipes equinovarus. International Journal of Surgery Case Reports. 7. 130–133. 5 indexed citations

20.

Elmas, Muhsin, et al.. (2012). 46,XX, der(15),t(Y;15)(q12;p11) karyotype in an azoospermic male. Indian journal of human genetics. 18(2). 241–241. 5 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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