M Atasu

582 total citations
40 papers, 414 citations indexed

About

M Atasu is a scholar working on Genetics, Molecular Biology and Developmental Biology. According to data from OpenAlex, M Atasu has authored 40 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 23 papers in Molecular Biology and 8 papers in Developmental Biology. Recurrent topics in M Atasu's work include Dermatoglyphics and Human Traits (21 papers), dental development and anomalies (18 papers) and Congenital limb and hand anomalies (8 papers). M Atasu is often cited by papers focused on Dermatoglyphics and Human Traits (21 papers), dental development and anomalies (18 papers) and Congenital limb and hand anomalies (8 papers). M Atasu collaborates with scholars based in Türkiye and United Kingdom. M Atasu's co-authors include Burhan Say, Betül Kargül, Ergül Tunçbılek, Bahar Kuru, Erhan Fıratlı, Martin Bobrow, Kutay Taysi, Sevim Balcı, K. Madan and Gonca Mumcu and has published in prestigious journals such as The Lancet, The Journal of Pediatrics and Journal of Medical Genetics.

In The Last Decade

M Atasu

39 papers receiving 358 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M Atasu Türkiye 13 244 186 89 47 46 40 414
Francisco Cammarata‐Scalisi Venezuela 9 80 0.3× 136 0.7× 38 0.4× 4 0.1× 27 0.6× 55 268
Ross Rb Canada 10 840 3.4× 215 1.2× 24 0.3× 3 0.1× 11 0.2× 12 885
Mary Calvert United Kingdom 7 235 1.0× 79 0.4× 24 0.3× 4 0.1× 14 0.3× 10 290
Dolores Martı́nez-Pérez Spain 7 167 0.7× 61 0.3× 68 0.8× 3 0.1× 34 0.7× 10 360
H Parkash India 9 67 0.3× 160 0.9× 197 2.2× 3 0.1× 115 2.5× 21 341
Howard Aduss United States 16 595 2.4× 184 1.0× 30 0.3× 8 0.2× 22 653
Agneta Karsten Sweden 14 458 1.9× 203 1.1× 66 0.7× 1 0.0× 35 0.8× 42 558
Renuka J Bathi India 8 72 0.3× 158 0.8× 126 1.4× 52 1.1× 13 319
Sara Rizell Sweden 11 316 1.3× 142 0.8× 31 0.3× 4 0.1× 10 0.2× 35 356
Manika Govil United States 11 211 0.9× 100 0.5× 19 0.2× 2 0.0× 18 0.4× 17 379

Countries citing papers authored by M Atasu

Since Specialization
Citations

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

Fields of papers citing papers by M Atasu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Atasu

This figure shows the co-authorship network connecting the top 25 collaborators of M Atasu. A scholar is included among the top collaborators of M Atasu 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 M Atasu. M Atasu 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.
Atasu, M, et al.. (2000). Ellis-van Creveld syndrome: dental, clinical, genetic and dermatoglyphic findings of a case.. PubMed. 24(2). 141–5. 22 indexed citations
3.
Atasu, M, et al.. (1999). Hypocalcification type amelogenesis imperfecta in permanent dentition in association with heavily worn primary teeth, gingival hyperplasia, hypodontia and impacted teeth.. PubMed. 23(2). 117–21. 16 indexed citations
4.
Göker, Kamil, et al.. (1999). Taurodontism in association with supernumerary teeth.. PubMed. 23(2). 151–4. 11 indexed citations
5.
Atasu, M. (1998). Dermatoglyphic findings in dental caries: a preliminary report.. PubMed. 22(2). 147–9. 31 indexed citations
6.
Atasu, M, et al.. (1998). Enamel hypoplasia and essential staining of teeth from erythroblastosis fetalis.. PubMed. 22(3). 249–52. 2 indexed citations
7.
Elçioğlu, Nursel, M Atasu, & Asım Cenani. (1997). Dermatoglyphics in patients with Cenani-Lenz type syndactyly: Studies in a new case. American Journal of Medical Genetics. 70(4). 341–345. 15 indexed citations
8.
Atasu, M, et al.. (1997). Transposition of maxillary permanent left cuspid tooth: a case report.. PubMed. 22(1). 35–6. 2 indexed citations
9.
Atasu, M, et al.. (1997). Congenital hypodontia of maxillary lateral incisors in association with coloboma of the iris and hypomaturation type of amelogenesis imperfecta in a large kindred.. PubMed. 21(4). 341–55. 5 indexed citations
10.
Atasu, M, et al.. (1996). Local, hypoplastic type of amelogenesis imperfecta: a clinical, genetic, radiological and dermatoglyphic study.. PubMed. 20(4). 337–42. 2 indexed citations
11.
Atasu, M, et al.. (1996). Generalized microdontia and associated anomalies: a clinical, genetic, radiologic and dermatoglyphic study.. PubMed. 20(2). 161–72. 2 indexed citations
12.
Atasu, M, et al.. (1989). Dermatoglyphic study in children with phenylketonuria. Journal of Inherited Metabolic Disease. 12(3). 323–326. 1 indexed citations
13.
Tunçbılek, Ergül, et al.. (1977). Aglossia‐adactylia syndrome (special emphasis on the inheritance pattern). Clinical Genetics. 11(5). 421–423. 20 indexed citations
14.
Atasu, M. (1976). Hereditary index finger polydactyly: phenotypic, radiological, dermatoglyphic, and genetic findings in a large family.. Journal of Medical Genetics. 13(6). 469–476. 5 indexed citations
15.
Atasu, M, et al.. (1974). A case of omphalocele with absence of the thumb and syndactily.. PubMed. 16(1). 37–41. 1 indexed citations
16.
Atasu, M, et al.. (1974). Dermatoglyphic findings in familial coxa vara with dominant inheritance.. PubMed. 16(1). 15–20.
17.
Taysi, Kutay, et al.. (1973). Duplication/deficiency product of a pericentric inversion in man: A cause of D1 trisomy syndrome. The Journal of Pediatrics. 82(2). 263–268. 34 indexed citations
18.
Atasu, M, Sevim Balcı, Ergül Tunçbılek, & Burhan Say. (1973). DERMATOGLYPHIC FINDINGS IN LAURENCE-MOON-BIEDL SYNDROME. The Lancet. 302(7820). 98–99. 1 indexed citations
19.
Taysi, Kutay, M Atasu, Burhan Say, & N Bilginturan. (1973). Dermatoglyphics in patients with a syndrome of brachydactyly, short stature and hypertension.. PubMed. 15(2). 67–81. 1 indexed citations
20.
Tunçbılek, Ergül, M Atasu, & Burhan Say. (1972). DERMATOGLYPHICS IN TRISOMY 8. The Lancet. 300(7781). 821–821. 8 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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