Eeva‐Maria Laitinen

759 total citations
17 papers, 516 citations indexed

About

Eeva‐Maria Laitinen is a scholar working on Reproductive Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Eeva‐Maria Laitinen has authored 17 papers receiving a total of 516 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Reproductive Medicine, 6 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Eeva‐Maria Laitinen's work include Hypothalamic control of reproductive hormones (13 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Growth Hormone and Insulin-like Growth Factors (3 papers). Eeva‐Maria Laitinen is often cited by papers focused on Hypothalamic control of reproductive hormones (13 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Growth Hormone and Insulin-like Growth Factors (3 papers). Eeva‐Maria Laitinen collaborates with scholars based in Finland, United Kingdom and Italy. Eeva‐Maria Laitinen's co-authors include Taneli Raivio, Johanna Tommiska, Kirsi Vaaralahti, Leena Valanne, Leo Dunkel, Matti Hero, Mari Tervaniemi, Johanna Känsäkoski, Karoliina Wehkalampi and Jorma Toppari and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Fertility and Sterility.

In The Last Decade

Eeva‐Maria Laitinen

16 papers receiving 506 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eeva‐Maria Laitinen Finland 11 353 234 211 139 64 17 516
Kirsi Vaaralahti Finland 16 438 1.2× 332 1.4× 283 1.3× 198 1.4× 69 1.1× 35 719
Maria Tereza Matias Baptista Brazil 16 267 0.8× 413 1.8× 366 1.7× 187 1.3× 38 0.6× 46 687
Luciana Mattos Barros Oliveira Brazil 7 474 1.3× 296 1.3× 260 1.2× 74 0.5× 32 0.5× 12 584
Johanna Känsäkoski Finland 12 227 0.6× 233 1.0× 189 0.9× 92 0.7× 27 0.4× 21 405
Alexandre Moerman France 5 247 0.7× 186 0.8× 152 0.7× 55 0.4× 60 0.9× 11 378
Milena Beranova United States 7 523 1.5× 325 1.4× 271 1.3× 80 0.6× 25 0.4× 10 643
Julie Sarfati France 11 215 0.6× 131 0.6× 100 0.5× 138 1.0× 22 0.3× 23 384
Samuel D. Quaynor United States 6 275 0.8× 160 0.7× 169 0.8× 58 0.4× 23 0.4× 8 406
Cecilia Martin United States 9 353 1.0× 171 0.7× 120 0.6× 82 0.6× 14 0.2× 10 517
Beatriz R. Versiani Brazil 10 178 0.5× 126 0.5× 149 0.7× 26 0.2× 34 0.5× 16 335

Countries citing papers authored by Eeva‐Maria Laitinen

Since Specialization
Citations

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

Fields of papers citing papers by Eeva‐Maria Laitinen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eeva‐Maria Laitinen. 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 Eeva‐Maria Laitinen. The network helps show where Eeva‐Maria Laitinen may publish in the future.

Co-authorship network of co-authors of Eeva‐Maria Laitinen

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

All Works

17 of 17 papers shown
1.
Varimo, Tero, Matti Hero, Eeva‐Maria Laitinen, et al.. (2015). Childhood growth in boys with congenital hypogonadotropic hypogonadism. Pediatric Research. 79(5). 705–709. 18 indexed citations
2.
Känsäkoski, Johanna, Rainer Fagerholm, Eeva‐Maria Laitinen, et al.. (2014). Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism. Pediatric Research. 75(5). 641–644. 57 indexed citations
3.
Vaaralahti, Kirsi, Johanna Tommiska, Vallo Tillmann, et al.. (2014). De novo SOX10 nonsense mutation in a patient with Kallmann syndrome and hearing loss. Pediatric Research. 76(1). 115–116. 26 indexed citations
4.
Hero, Matti, Eeva‐Maria Laitinen, Tero Varimo, et al.. (2014). Childhood growth of females with Kallmann syndrome and FGFR1 mutations. Clinical Endocrinology. 82(1). 122–126. 8 indexed citations
5.
Tommiska, Johanna, Jorma Toppari, Kirsi Vaaralahti, et al.. (2012). PROKR2 mutations in autosomal recessive Kallmann syndrome. Fertility and Sterility. 99(3). 815–818. 18 indexed citations
6.
Hero, Matti, Johanna Tommiska, Kirsi Vaaralahti, et al.. (2012). Circulating antimüllerian hormone levels in boys decline during early puberty and correlate with inhibin B. Fertility and Sterility. 97(5). 1242–1247. 37 indexed citations
7.
Vaaralahti, Kirsi, et al.. (2012). Genetic Overlap between Holoprosencephaly and Kallmann Syndrome. Molecular Syndromology. 3(1). 1–5. 24 indexed citations
8.
Laitinen, Eeva‐Maria, Matti Hero, Kirsi Vaaralahti, Johanna Tommiska, & Taneli Raivio. (2012). Bone mineral density, body composition and bone turnover in patients with congenital hypogonadotropic hypogonadism. International Journal of Andrology. 35(4). 534–540. 50 indexed citations
9.
Laitinen, Eeva‐Maria, Johanna Tommiska, Timo Sane, et al.. (2012). Reversible Congenital Hypogonadotropic Hypogonadism in Patients with CHD7, FGFR1 or GNRHR Mutations. PLoS ONE. 7(6). e39450–e39450. 52 indexed citations
10.
Laitinen, Eeva‐Maria. (2012). Kallmann Syndrome : Clinical and molecular genetic features in Finland. Työväentutkimus Vuosikirja. 1 indexed citations
11.
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
12.
Laitinen, Eeva‐Maria, Johanna Tommiska, Helena E. Virtanen, et al.. (2011). Isolated cryptorchidism: No evidence for involvement of genes underlying isolated hypogonadotropic hypogonadism. Molecular and Cellular Endocrinology. 341(1-2). 35–38. 10 indexed citations
13.
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. Fertility and Sterility. 95(8). 2756–2758. 34 indexed citations
14.
Laitinen, Eeva‐Maria, Kirsi Vaaralahti, Johanna Tommiska, et al.. (2011). Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland. Orphanet Journal of Rare Diseases. 6(1). 41–41. 129 indexed citations
15.
Laitinen, Eeva‐Maria, Johanna Tommiska, Leo Dunkel, et al.. (2010). Idiopathic hypogonadotropic hypogonadism in a mother and her monozygotic twins born after a single embryo transfer. Fertility and Sterility. 93(6). 2074.e13–2074.e16. 7 indexed citations
16.
Tommiska, Johanna, Karoliina Wehkalampi, Kirsi Vaaralahti, et al.. (2010). LIN28B in Constitutional Delay of Growth and Puberty. The Journal of Clinical Endocrinology & Metabolism. 95(6). 3063–3066. 39 indexed citations
17.
Laitinen, Eeva‐Maria. (1963). CHANGES IN THE ELEMENTAL STRUCTURES OF THE AORTA IN HUMAN AND EXPERIMENTAL ATHEROSCLEROSIS. LIGHT AND ELECTRON MICROSCOPE STUDIES.. PubMed. SUPPL167:1–92. 2 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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