Sirpa Arte

2.5k total citations · 1 hit paper
29 papers, 1.8k citations indexed

About

Sirpa Arte is a scholar working on Molecular Biology, Genetics and Oral Surgery. According to data from OpenAlex, Sirpa Arte has authored 29 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 18 papers in Genetics and 15 papers in Oral Surgery. Recurrent topics in Sirpa Arte's work include dental development and anomalies (20 papers), Oral and Maxillofacial Pathology (15 papers) and Cleft Lip and Palate Research (13 papers). Sirpa Arte is often cited by papers focused on dental development and anomalies (20 papers), Oral and Maxillofacial Pathology (15 papers) and Cleft Lip and Palate Research (13 papers). Sirpa Arte collaborates with scholars based in Finland, Spain and United States. Sirpa Arte's co-authors include Sinikka Pirinen, Pekka Nieminen, Irma Thesleff, Satu Apajalahti, Heikki Järvinen, Mirja Somer, Päivi Lahermo, Satu Alaluusua, Pekka Nieminen and Leena Peltonen and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Sirpa Arte

28 papers receiving 1.7k citations

Hit Papers

Mutations in AXIN2 Cause Familial Tooth Agenesis and Pred... 2004 2026 2011 2018 2004 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sirpa Arte Finland 17 1.5k 1.0k 794 241 140 29 1.8k
Piranit Nik Kantaputra Thailand 22 888 0.6× 333 0.3× 517 0.7× 294 1.2× 158 1.1× 105 1.4k
Gorlin Rj United States 14 413 0.3× 309 0.3× 293 0.4× 172 0.7× 87 0.6× 42 924
Adrian K. Jowett United Kingdom 10 1.2k 0.8× 370 0.4× 298 0.4× 334 1.4× 55 0.4× 16 1.5k
Alen Braut Croatia 13 637 0.4× 143 0.1× 287 0.4× 222 0.9× 154 1.1× 22 1.1k
Javier Catón United Kingdom 15 634 0.4× 478 0.5× 73 0.1× 464 1.9× 48 0.3× 23 1.0k
Claire E. L. Smith United Kingdom 14 614 0.4× 79 0.1× 174 0.2× 474 2.0× 33 0.2× 25 835
Alanna F. Bree United States 15 402 0.3× 92 0.1× 229 0.3× 38 0.2× 140 1.0× 23 648
Tamizchelvi Thyagarajan United States 10 710 0.5× 252 0.3× 90 0.1× 820 3.4× 37 0.3× 10 1.1k
Janna Waltimo‐Sirén Finland 15 237 0.2× 131 0.1× 311 0.4× 264 1.1× 72 0.5× 35 644
H Nikai Japan 17 375 0.3× 595 0.6× 27 0.0× 393 1.6× 166 1.2× 32 985

Countries citing papers authored by Sirpa Arte

Since Specialization
Citations

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

Fields of papers citing papers by Sirpa Arte

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sirpa Arte

This figure shows the co-authorship network connecting the top 25 collaborators of Sirpa Arte. A scholar is included among the top collaborators of Sirpa Arte 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 Sirpa Arte. Sirpa Arte 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.
Arte, Sirpa, et al.. (2023). Craniofacial and dental features of Axenfeld‐Rieger syndrome patients with PITX2 mutations. Orthodontics and Craniofacial Research. 26(3). 320–330. 4 indexed citations
2.
Nieminen, Pekka, et al.. (2017). Blepharocheilodontic (BCD) syndrome: New insights on craniofacial and dental features. American Journal of Medical Genetics Part A. 173(4). 905–913. 7 indexed citations
3.
Palotie, Tuula, et al.. (2016). The Effect of mandible advancement splints in mild, moderate, and severe obstructive sleep apnea—the need for sleep registrations during follow up. European Journal of Orthodontics. 39(5). cjw068–cjw068. 5 indexed citations
5.
Hero, Matti, Anni Suomalainen, Jaana Hagström, et al.. (2012). Anti-tumor necrosis factor treatment in cherubism — Clinical, radiological and histological findings in two children. Bone. 52(1). 347–353. 38 indexed citations
6.
Ingman, Tuula, Sirpa Arte, Adel Bachour, Leif Bäck, & Antti Mäkitie. (2012). Predicting compliance for mandible advancement splint therapy in 96 obstructive sleep apnea patients. European Journal of Orthodontics. 35(6). 752–757. 15 indexed citations
7.
Nieminen, Pekka, Neil V. Morgan, Aimée L Fenwick, et al.. (2011). Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth. The American Journal of Human Genetics. 89(1). 67–81. 135 indexed citations
8.
Heliövaara, Arja, et al.. (2011). Dental development and tooth agenesis in children with velocardiofacial syndrome. International Journal of Paediatric Dentistry. 21(6). 446–450. 10 indexed citations
9.
Nieminen, Pekka, et al.. (2010). An epidemiological study of dental agenesis in a primary health area in Spain: Estimated prevalence and associated factors. Medicina oral, patología oral y cirugía bucal. 15(4). e569–e574. 37 indexed citations
10.
Nieminen, Pekka, et al.. (2010). Oral findings in Midline Syndrome: A case report and literature review. Medicina oral, patología oral y cirugía bucal. 15(4). e579–e582. 3 indexed citations
11.
Pirinen, Sinikka, et al.. (2009). Premolar hypodontia is a common feature in Sotos syndrome with a mutation in the NSD1 gene. American Journal of Medical Genetics Part A. 149A(11). 2409–2414. 8 indexed citations
12.
Manzanares‐Céspedes, María Cristina, et al.. (2007). Identification of a novel mutation in thePAX9gene in a family affected by oligodontia and other dental anomalies. European Journal Of Oral Sciences. 115(6). 427–432. 33 indexed citations
13.
Nieminen, Pekka, Wael M. Abdel‐Rahman, Anu‐Liisa Moisio, et al.. (2005). Adenomatous Polyposis Families That Screen APC Mutation–Negative by Conventional Methods Are Genetically Heterogeneous. Journal of Clinical Oncology. 23(24). 5651–5659. 52 indexed citations
14.
Pirinen, Sinikka, et al.. (2003). A missense mutation in PAX9 in a family with distinct phenotype of oligodontia. European Journal of Human Genetics. 11(11). 866–871. 95 indexed citations
15.
Nieminen, Pekka, Sirpa Arte, Dennis D. Tanner, et al.. (2001). Identification of a nonsense mutation in the PAX9 gene in molar oligodontia. European Journal of Human Genetics. 9(10). 743–746. 146 indexed citations
16.
Arte, Sirpa, Pekka Nieminen, Satu Apajalahti, et al.. (2001). Characteristics of Incisor-Premolar Hypodontia in Families. Journal of Dental Research. 80(5). 1445–1450. 134 indexed citations
17.
Apajalahti, Satu, Sirpa Arte, & Sinikka Pirinen. (1999). Short root anomaly in families and its association with other dental anomalies. European Journal Of Oral Sciences. 107(2). 97–101. 52 indexed citations
18.
Pirinen, Sinikka, Sirpa Arte, & Satu Apajalahti. (1996). Palatal Displacement of Canine is Genetic and Related to Congenital Absence of Teeth. Journal of Dental Research. 75(10). 1742–1746. 135 indexed citations
19.
Nieminen, Pekka, Sirpa Arte, Sinikka Pirinen, Leena Peltonen, & Irma Thesleff. (1995). Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes. Human Genetics. 96(3). 305–8. 79 indexed citations
20.
Hölttä, Päivi, et al.. (1995). Craniofacial and dental characteristics of Silver‐Russell syndrome. American Journal of Medical Genetics. 56(2). 229–236. 27 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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