Taneli Raivio

8.9k total citations · 1 hit paper
135 papers, 5.0k citations indexed

About

Taneli Raivio is a scholar working on Molecular Biology, Reproductive Medicine and Genetics. According to data from OpenAlex, Taneli Raivio has authored 135 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 61 papers in Reproductive Medicine and 47 papers in Genetics. Recurrent topics in Taneli Raivio's work include Hypothalamic control of reproductive hormones (43 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (27 papers) and Sexual Differentiation and Disorders (26 papers). Taneli Raivio is often cited by papers focused on Hypothalamic control of reproductive hormones (43 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (27 papers) and Sexual Differentiation and Disorders (26 papers). Taneli Raivio collaborates with scholars based in Finland, United Kingdom and United States. Taneli Raivio's co-authors include Leo Dunkel, Nelly Pitteloud, Johanna Tommiska, Andrew Dwyer, Kirsi Vaaralahti, Anne M. Wikström, Eeva‐Maria Laitinen, Matti Hero, Olli A. Jänne and Päivi J. Miettinen and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Blood.

In The Last Decade

Taneli Raivio

134 papers receiving 4.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment

2015 528 citations Mehul Dattani, Leo Dunkel et al. profile →

Peers

Taneli Raivio

GENET

EDM

PHEOH

Richard Quinton United Kingdom

Philippe Touraine France

Geri Méduri France

Tomonobu Hasegawa Japan

John C. Achermann United Kingdom

Ana Cláudia Latronico Brazil

Ora Hirsch Pescovitz United States

Najiba Lahlou France

Zhenmin Lei United States

Maki Fukami Japan

Richard Quinton United Kingdom

Taneli Raivio

2.1k ×0.8

2.8k ×1.2

1.9k ×1.0

GENET

1.7k ×1.5

EDM

365 ×0.7

PHEOH

Citations per year, relative to Taneli Raivio Taneli Raivio (= 1×) peers Richard Quinton

Countries citing papers authored by Taneli Raivio

Since Specialization

Citations

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

Fields of papers citing papers by Taneli Raivio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taneli Raivio

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Li, Shiqian, Yafei Wang, Miesje M. van der Stoel, et al.. (2024). HiHo-AID2: boosting homozygous knock-in efficiency enables robust generation of human auxin-inducible degron cells. Genome biology. 25(1). 58–58. 5 indexed citations

Varimo, Tero, et al.. (2024). Central precocious puberty in boys: secular trend and clinical features. European Journal of Endocrinology. 190(3). 211–219. 4 indexed citations

Vermeesch, Joris, et al.. (2024). Polygenic embryo screening: quo vadis?. Journal of Assisted Reproduction and Genetics. 41(7). 1719–1726. 4 indexed citations

Vaaralahti, Kirsi, et al.. (2023). Congenital hypogonadotropic hypogonadism in a patient with a de novoPOGZmutation. European Journal of Endocrinology. 189(2). 271–280. 1 indexed citations

Vermeesch, Joris, et al.. (2023). Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores. European Journal of Human Genetics. 31(10). 1133–1138. 17 indexed citations

Wang, Yafei, et al.. (2022). FGF8–FGFR1 signaling regulates human GnRH neuron differentiation in a time- and dose-dependent manner. Disease Models & Mechanisms. 15(8). 8 indexed citations

Kvist, Jouni, et al.. (2022). Deciphering the Transcriptional Landscape of Human Pluripotent Stem Cell-Derived GnRH Neurons: The Role of Wnt Signaling in Patterning the Neural Fate. Stem Cells. 40(12). 1107–1121. 6 indexed citations

Lundin, Karolina, Bishwa Ghimire, Johanna Känsäkoski, et al.. (2022). Human pluripotent stem cell-derived cells endogenously expressing follicle-stimulating hormone receptors: modeling the function of an inactivating receptor mutation. Molecular Human Reproduction. 28(5). 1 indexed citations

Varimo, Tero, Päivi J. Miettinen, Kirsi Vaaralahti, et al.. (2022). Circulating Liver-enriched Antimicrobial Peptide-2 Decreases During Male Puberty. Journal of the Endocrine Society. 6(3). bvac013–bvac013. 5 indexed citations

10.

Kosola, Silja, Hayley Loftus, Michelle Telfer, et al.. (2021). Bridge study protocol: an international, observational cohort study on the transition of healthcare for adolescents with chronic conditions. BMJ Open. 11(6). e048340–e048340. 5 indexed citations

11.

Hero, Matti, Tero Varimo, & Taneli Raivio. (2020). Aromatase inhibitors in puberty. Current Opinion in Endocrine and Metabolic Research. 14. 37–41. 6 indexed citations

12.

Vuoristo, Sanna, Diego Balboa, Sara Trova, et al.. (2020). Characterization of the human GnRH neuron developmental transcriptome using a GNRH1 -TdTomato reporter line in human pluripotent stem cells. Disease Models & Mechanisms. 13(3). 19 indexed citations

13.

Hietamäki, Johanna, Louise Gregory, Kirsi Vaaralahti, et al.. (2020). Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism. The Journal of Clinical Endocrinology & Metabolism. 105(6). 1748–1758. 18 indexed citations

14.

Korpela, Katri, Matti Hero, Päivi J. Miettinen, et al.. (2019). Intestinal Microbiota Development Differs Between Pubertal Boys and Girls. 92. 1 indexed citations

15.

Huopio, Hanna, Matti Hero, Päivi J. Miettinen, et al.. (2018). Recombinant Human FSH Treatment Outcomes in Five Boys With Severe Congenital Hypogonadotropic Hypogonadism. Journal of the Endocrine Society. 2(12). 1345–1356. 17 indexed citations

16.

Osborn, Daniel P. S., Ji‐Young Lee, Masatake Araki, et al.. (2017). WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome. EMBO Reports. 19(2). 269–289. 40 indexed citations

17.

Sulonen, Anna-Maija, Pekka Ellonen, Henrikki Almusa, et al.. (2011). Comparison of solution-based exome capture methods for next generation sequencing. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 1 indexed citations

18.

Vaaralahti, Kirsi, Karoliina Wehkalampi, Johanna Tommiska, et al.. (2011). The role of gene defects underlying isolated hypogonadotropic hypogonadism in patients with constitutional delay of growth and puberty. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 4 indexed citations

19.

Pitteloud, Nelly, et al.. (2010). Complex Genetics in Idiopathic Hypogonadotropic Hypogonadism. Frontiers of hormone research. 39. 142–153. 45 indexed citations

20.

Kolho, Kaija‐Leena, et al.. (2009). Circulating Adiponectin as a Marker for Glucocorticoid‐related Side Effects in Children and Adolescents With Inflammatory Bowel Disease. Journal of Pediatric Gastroenterology and Nutrition. 48(4). 504–506. 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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