Laura M. Tanner

977 total citations
34 papers, 602 citations indexed

About

Laura M. Tanner is a scholar working on Biochemistry, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Laura M. Tanner has authored 34 papers receiving a total of 602 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Biochemistry, 13 papers in Clinical Biochemistry and 9 papers in Rheumatology. Recurrent topics in Laura M. Tanner's work include Amino Acid Enzymes and Metabolism (14 papers), Metabolism and Genetic Disorders (13 papers) and Folate and B Vitamins Research (8 papers). Laura M. Tanner is often cited by papers focused on Amino Acid Enzymes and Metabolism (14 papers), Metabolism and Genetic Disorders (13 papers) and Folate and B Vitamins Research (8 papers). Laura M. Tanner collaborates with scholars based in Finland, United States and United Kingdom. Laura M. Tanner's co-authors include Olli Simell, Harri Niinikoski, Kirsti Näntö‐Salonen, Jean Adams, Susanna Mills, Kirsi Huoponen, Juha Mykkänen, Mikael Knip, Jorma Ilonen and Lawrence C. Fritz and has published in prestigious journals such as PLoS ONE, Clinical Infectious Diseases and Journal of Nutrition.

In The Last Decade

Laura M. Tanner

34 papers receiving 588 citations

Peers

Laura M. Tanner

BIOCH

EPIDE

GENET

Peter Smit Netherlands

Charlotte Dawson United Kingdom

Gilles J. Lauzon Canada

Michael Kaiser United States

David G. Ritchie United States

Ke Qiao China

J Hamburger France

E. Koumantakis Greece

O Thalhammer Austria

F Pearce United Kingdom

Peter Smit Netherlands

Laura M. Tanner

169 ×1.3

110 ×0.9

BIOCH

174 ×1.5

EPIDE

98 ×0.9

245 ×2.2

GENET

Citations per year, relative to Laura M. Tanner Laura M. Tanner (= 1×) peers Peter Smit

Countries citing papers authored by Laura M. Tanner

Since Specialization

Citations

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

Fields of papers citing papers by Laura M. Tanner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura M. Tanner

This figure shows the co-authorship network connecting the top 25 collaborators of Laura M. Tanner. A scholar is included among the top collaborators of Laura M. Tanner 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 Laura M. Tanner. Laura M. Tanner 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

Sáenz, Joseph & Laura M. Tanner. (2025). Associations between low food security and subjective memory complaints among Latino adults. BMC Public Health. 25(1). 1200–1200. 1 indexed citations

Toiviainen‐Salo, Sanna, et al.. (2024). The Role of Prenatal Ultrasound and Added Value of Post‐Mortem Radiographic Imaging With X‐Ray and CT in Suspected Fetal Skeletal Dysplasia. Prenatal Diagnosis. 45(1). 77–88. 1 indexed citations

Tanner, Laura M., et al.. (2023). X‐linked pyruvate dehydrogenase complex deficiency due to a novel PDHA1 variant associated with structural brain abnormalities in a fetus. Prenatal Diagnosis. 43(6). 730–733. 4 indexed citations

Tanner, Laura M., et al.. (2023). Plasma calprotectin is extremely high in patients with lysinuric protein intolerance. JIMD Reports. 64(4). 293–299. 1 indexed citations

Toiviainen‐Salo, Sanna, et al.. (2022). Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort. Prenatal Diagnosis. 42(12). 1525–1537. 3 indexed citations

Leskinen, Heidi, Heli Karjalainen, Terhi Iso‐Touru, et al.. (2020). APOE Genotype Disclosure and Lifestyle Advice in a Randomized Intervention Study with Finnish Participants. Journal of Nutrition. 151(1). 85–97. 2 indexed citations

Karjalainen, Heli, Laura M. Tanner, Kirsi Vähäkangas, et al.. (2018). A Long-Term Follow-Up Study on Disclosing Genetic Risk Information (<b><i>APOE</i></b>) to Promote Healthy Lifestyles in Finland. Lifestyle Genomics. 11(3-6). 147–154. 6 indexed citations

Fouquet, Baptiste, Patrycja Pawlikowska, Sandrine Caburet, et al.. (2017). A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency. eLife. 6. 51 indexed citations

Tanner, Laura M., Kirsti Näntö‐Salonen, Mari Vähä-Mäkilä, et al.. (2016). Imbalance of plasma amino acids, metabolites and lipids in patients with lysinuric protein intolerance (LPI). Metabolism. 65(9). 1361–1375. 12 indexed citations

10.

Tanner, Laura M., Heikki Aho, Juha Mykkänen, et al.. (2016). Inhaled Sargramostim Induces Resolution of Pulmonary Alveolar Proteinosis in Lysinuric Protein Intolerance. JIMD Reports. 34. 97–104. 11 indexed citations

11.

Kantola, Kalle, Lea Hedman, Laura M. Tanner, et al.. (2015). B-Cell Responses to Human Bocaviruses 1–4: New Insights from a Childhood Follow-Up Study. PLoS ONE. 10(9). e0139096–e0139096. 36 indexed citations

12.

Näntö‐Salonen, Kirsti, et al.. (2015). Urine Beta2-Microglobulin Is an Early Marker of Renal Involvement in LPI. JIMD Reports. 25. 47–55. 11 indexed citations

13.

Vähä-Mäkilä, Mari, Laura M. Tanner, Sari Paavanen‐Huhtala, et al.. (2015). Dysfunction in macrophage toll-like receptor signaling caused by an inborn error of cationic amino acid transport. Molecular Immunology. 67(2). 416–425. 18 indexed citations

14.

Siljander, Heli, Róbert Hermann, Anne Hekkala, et al.. (2013). Insulin secretion and sensitivity in the prediction of type 1 diabetes in children with advanced β-cell autoimmunity. European Journal of Endocrinology. 169(4). 479–485. 20 indexed citations

15.

Hedman, Lea, Laura M. Tanner, Ville Simell, et al.. (2012). Association of Human Bocavirus 1 Infection with Respiratory Disease in Childhood Follow-up Study, Finland. Emerging infectious diseases. 18(2). 264–271. 87 indexed citations

16.

Tanner, Laura M., Olli Nevalainen, Harri Niinikoski, et al.. (2011). Exploring the transcriptomic variation caused by the Finnish founder mutation of lysinuric protein intolerance (LPI). Molecular Genetics and Metabolism. 105(3). 408–415. 13 indexed citations

17.

Niinikoski, Harri, Risto Lapatto, Matti Nuutinen, et al.. (2011). Growth Hormone Therapy Is Safe and Effective in Patients with Lysinuric Protein Intolerance. JIMD Reports. 1. 43–47. 8 indexed citations

18.

Tanner, Laura M., Kirsti Näntö‐Salonen, Mohamed S. Rashed, et al.. (2008). Carnitine deficiency and l-carnitine supplementation in lysinuric protein intolerance. Metabolism. 57(4). 549–554. 15 indexed citations

19.

Tanner, Laura M., Kirsti Näntö‐Salonen, Harri Niinikoski, Kirsi Huoponen, & Olli Simell. (2007). Long-term oral lysine supplementation in lysinuric protein intolerance. Metabolism. 56(2). 185–189. 17 indexed citations

20.

Lin, Tao, George Perides, Laura M. Tanner, & Mark S. Klempner. (1997). Detection of a 130-kD Matrix Metalloproteinase in Cerebrospinal Fluid from a Patient with Lyme Neuroborreliosis. Clinical Infectious Diseases. 24(6). 1276–1277. 4 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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