Helena Valta

1.4k total citations
41 papers, 919 citations indexed

About

Helena Valta is a scholar working on Genetics, Oncology and Molecular Biology. According to data from OpenAlex, Helena Valta has authored 41 papers receiving a total of 919 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 11 papers in Oncology and 10 papers in Molecular Biology. Recurrent topics in Helena Valta's work include Connective tissue disorders research (11 papers), Bone health and treatments (11 papers) and Bone and Joint Diseases (6 papers). Helena Valta is often cited by papers focused on Connective tissue disorders research (11 papers), Bone health and treatments (11 papers) and Bone and Joint Diseases (6 papers). Helena Valta collaborates with scholars based in Finland, Sweden and United States. Helena Valta's co-authors include Outi Mäkitie, Hannu Jalanko, Sanna Toiviainen‐Salo, Ilkka Helenius, Heli Viljakainen, Saila Laakso, Matti Verkasalo, Minna Pekkinen, Christer Holmberg and Mervi K Mäyränpää and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Journal of Bone and Mineral Research.

In The Last Decade

Helena Valta

39 papers receiving 893 citations

Peers

Helena Valta

GENET

SURGE

OSM

EPIDE

Moira Cheung United Kingdom

Rita Herskovitz United States

Mervi K Mäyränpää Finland

Catherine Glastre France

Fergus E. McKiernan United States

Athanasios Christoforidis Greece

Eino Marttinen Finland

JE Compston United Kingdom

Javier del Pino‐Montes Spain

J. Teichmann Germany

Moira Cheung United Kingdom

Helena Valta

752 ×2.1

GENET

174 ×0.8

SURGE

245 ×1.1

OSM

188 ×0.9

264 ×1.5

EPIDE

Citations per year, relative to Helena Valta Helena Valta (= 1×) peers Moira Cheung

Countries citing papers authored by Helena Valta

Since Specialization

Citations

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

Fields of papers citing papers by Helena Valta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helena Valta

This figure shows the co-authorship network connecting the top 25 collaborators of Helena Valta. A scholar is included among the top collaborators of Helena Valta 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 Helena Valta. Helena Valta 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

Valta, Helena, et al.. (2025). Dental and craniofacial manifestations in sponastrime dysplasia - An observational study. Bone. 195. 117469–117469.

Bachour, Adel, Leif Bäck, Helena Valta, et al.. (2021). Positive airway pressure therapy for obstructive sleep apnea in patients with Osteogenesis imperfecta: a prospective pilot study. BMC Musculoskeletal Disorders. 22(1). 61–61. 3 indexed citations

Costantini, Alice, Helena Valta, Anne‐Maarit Suomi, Outi Mäkitie, & Fulya Taylan. (2021). Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia. Frontiers in Genetics. 12. 680838–680838. 7 indexed citations

Ain, Noor Ul, et al.. (2018). Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux. European Journal of Medical Genetics. 62(9). 103554–103554. 12 indexed citations

Costantini, Alice, Helena Valta, Nissan Baratang, et al.. (2018). Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with “corner fractures”. Bone. 121. 163–171. 12 indexed citations

Vakkilainen, Svetlana, Riikka E. Mäkitie, Paula Klemetti, et al.. (2018). A Wide Spectrum of Autoimmune Manifestations and Other Symptoms Suggesting Immune Dysregulation in Patients With Cartilage-Hair Hypoplasia. Frontiers in Immunology. 9. 2468–2468. 14 indexed citations

Kämpe, Anders, Alice Costantini, Riikka E. Mäkitie, et al.. (2017). PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants. Osteoporosis International. 28(10). 3023–3032. 34 indexed citations

Valta, Helena, Marja Ekholm, Helena Ranta, et al.. (2016). Timing of dental development in osteogenesis imperfecta patients with and without bisphosphonate treatment. Bone. 94. 29–33. 27 indexed citations

Valta, Helena, Minna Pekkinen, S Andersson, et al.. (2016). Body composition and adipokines in patients with juvenile idiopathic arthritis and systemic glucocorticoids.. PubMed. 33(6). 924–30. 6 indexed citations

10.

Pereira, Renata C., Helena Valta, Isidro B. Salusky, et al.. (2015). Altered Osteocyte-Specific Protein Expression in Bone after Childhood Solid Organ Transplantation. PLoS ONE. 10(9). e0138156–e0138156. 15 indexed citations

11.

Tenhola, Sirpa, Geoffrey N. Hendy, Helena Valta, et al.. (2015). Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused byAP2S1Mutation. The Journal of Clinical Endocrinology & Metabolism. 100(7). 2515–2518. 19 indexed citations

12.

Viljakainen, Heli, Johanna C. Andersson‐Assarsson, Minna Pekkinen, et al.. (2015). Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland. PLoS ONE. 10(7). e0131883–e0131883. 61 indexed citations

13.

Tamminen, Inari S, Helena Valta, Hannu Jalanko, et al.. (2014). Pediatric solid organ transplantation and osteoporosis: a descriptive study on bone histomorphometric findings. Pediatric Nephrology. 29(8). 1431–1440. 13 indexed citations

14.

Laakso, Saila, Helena Valta, Matti Verkasalo, Sanna Toiviainen‐Salo, & Outi Mäkitie. (2014). Compromised Peak Bone Mass in Patients with Inflammatory Bowel Disease–A Prospective Study. The Journal of Pediatrics. 164(6). 1436–1443.e1. 53 indexed citations

15.

Laakso, Saila, Helena Valta, Matti Verkasalo, et al.. (2012). Impaired Bone Health in Inflammatory Bowel Disease: A Case–Control Study in 80 Pediatric Patients. Calcified Tissue International. 91(2). 121–130. 63 indexed citations

16.

Qvist, Erik, Kirsi Jahnukainen, Tuula Hölttä, et al.. (2011). Pubertal Development is Normal in Adolescents After Renal Transplantation in Childhood. Transplantation. 92(4). 404–409. 22 indexed citations

17.

Valta, Helena, Liisa Kerttula, Irma Soini, et al.. (2011). Prevalence of Vertebral Compression Fractures and Associated Factors in Children and Adolescents with Severe Juvenile Idiopathic Arthritis. The Journal of Rheumatology. 39(2). 365–373. 24 indexed citations

18.

Toiviainen‐Salo, Sanna, et al.. (2011). The Thoracic and Lumbar Spine in Severe Juvenile Idiopathic Arthritis: Magnetic Resonance Imaging Analysis in 50 Children. The Journal of Pediatrics. 160(1). 140–146. 9 indexed citations

19.

Mäyränpää, Mervi K, Ilkka Helenius, Helena Valta, et al.. (2007). Bone densitometry in the diagnosis of vertebral fractures in children: Accuracy of vertebral fracture assessment. Bone. 41(3). 353–359. 40 indexed citations

20.

Valta, Helena, Hannu Jalanko, Christer Holmberg, Ilkka Helenius, & Outi Mäkitie. (2007). Impaired Bone Health in Adolescents After Liver Transplantation. American Journal of Transplantation. 8(1). 150–157. 46 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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