Anne Saarinen

999 total citations
17 papers, 698 citations indexed

About

Anne Saarinen is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Anne Saarinen has authored 17 papers receiving a total of 698 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Anne Saarinen's work include Growth Hormone and Insulin-like Growth Factors (4 papers), Connective tissue disorders research (3 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Anne Saarinen is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (4 papers), Connective tissue disorders research (3 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Anne Saarinen collaborates with scholars based in Finland, Hungary and United Kingdom. Anne Saarinen's co-authors include Anna‐Elina Lehesjoki, Albert de la Chapelle, Outi Mäkitie, Mette Warburg, Reijo Norio, Satu Kivitie‐Kallio, Graeme C. Black, Juha Kolehmainen, Kate Chandler and Jill Clayton‐Smith and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

Anne Saarinen

17 papers receiving 679 citations

Peers

Countries citing papers authored by Anne Saarinen

Since Specialization

Citations

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

Fields of papers citing papers by Anne Saarinen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Saarinen

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Mechanisms behind bottom-up effects: eutrophication increases fecundity by shortening the interspawning interval in stickleback 2020 ·PeerJ ·Anne Saarinen, Ulrika Candolin	9
2	Impact of rheumatic diseases on oral health and quality of life 2014 ·Oral Diseases ·Kirsi Ahola, Anne Saarinen, Antti Kuuliala, Marjatta Leirisalo‐Repo, Heikki Murtomaa, Jukka H. Meurman	35
3	Cerebroretinal microangiopathy with calcifications and cysts: Characterization of the skeletal phenotype 2011 ·American Journal of Medical Genetics Part A ·Sanna Toiviainen‐Salo, Tarja Linnankivi, Anne Saarinen, Mervi K Mäyränpää, Riitta Karikoski, Outi Mäkitie	6
4	Decreased variation of inflammatory markers in gestational diabetes 2011 ·Diabetes/Metabolism Research and Reviews ·Maritta Pöyhönen‐Alho, Peter R. Ebeling, Anne Saarinen, Risto Kaaja	16
5	Low-density lipoprotein receptor-related protein 5 (LRP5) variation in fracture prone children 2010 ·Bone ·Anne Saarinen, Mervi K Mäyränpää, Anna‐Elina Lehesjoki, Outi Mäkitie	14
6	Low density lipoprotein receptor‐related protein 5 (LRP5) mutations and osteoporosis, impaired glucose metabolism and hypercholesterolaemia 2009 ·Clinical Endocrinology ·Anne Saarinen, Tero Saukkonen, Tero Kivelä, Ulla Lahtinen, Christine Lainé, Mirja Somer, Sanna Toiviainen‐Salo, William G. Cole, Anna‐Elina Lehesjoki, Outi Mäkitie	78
7	Body Composition and Bone Mineral Density in Children with Premature Adrenarche and the Association of LRP5 Gene Polymorphisms with Bone Mineral Density 2009 ·The Journal of Clinical Endocrinology & Metabolism ·Pauliina Utriainen, Jarmo Jääskeläinen, Anne Saarinen, Esko Vanninen, Outi Mäkitie, Raimo Voutilainen	21
8	LRP5 in premature adrenarche and in metabolic characteristics of prepubertal children 2008 ·Clinical Endocrinology ·(unknown), Anne Saarinen, Pauliina Utriainen, Raimo Voutilainen, Jarmo Jääskeläinen, Outi Mäkitie	11
9	The A1330V polymorphism of the low-density lipoprotein receptor-related protein 5 gene (LRP5) associates with low peak bone mass in young healthy men 2007 ·Bone ·Anne Saarinen, Ville‐Valtteri Välimäki, Matti Välimäki, Eliisa Löyttyniemi, Kirsi Auro, (unknown), (unknown), Anna‐Elina Lehesjoki, Outi Mäkitie	60
10	Children with recurrent fractures and low bone mass or idiopathic juvenile osteoporosis may have abnormalities in the canonical Wnt-signalling pathway through LRP5 2007 ·Bone ·(unknown), R. J. Pollitt, A. Dalton, Anne Saarinen, Nick Bishop	2
11	Heterozygous LRP5 mutations in children with fractures 2007 ·Bone ·Anne Saarinen, Mervi K Mäyränpää, A.-E. Lehesjoki, Outi Mäkitie	1
12	[Muscle-eye-brain disease. Presentation of one case with genetic study]. 2005 ·PubMed ·I Pascual-Castroviejo, Samuel Ignacio Pascual Pascual, (unknown), Anne Saarinen, Tarja Joensuu, Mónica Bayés, Bru Cormand	3
13	Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen 2004 ·The American Journal of Human Genetics ·Juha Kolehmainen, Robert N. Wilkinson, Anna-Elina Lehesjoki, Kate Chandler, Satu Kivitie‐Kallio, Jill Clayton‐Smith, (unknown), (unknown), Anne Saarinen, Jabbar Khan, Varda Gross‐Tsur, Elias I. Traboulsi, Mette Warburg, Jean‐Pierre Fryns, Reijo Norio, Graeme C. Black, Forbes Manson	69
14	Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport 2003 ·The American Journal of Human Genetics ·Juha Kolehmainen, Graeme C. Black, Anne Saarinen, Kate Chandler, Jill Clayton‐Smith, (unknown), Rahat Perveen, Satu Kivitie‐Kallio, Reijo Norio, Mette Warburg, Jean‐Pierre Fryns, Albert de la Chapelle, Anna‐Elina Lehesjoki	249
15	Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia 2003 ·Nature Genetics ·Stephan M. Tanner, Maria Aminoff, Fred A. Wright, Sandya Liyanarachchi, Mervi Kuronen, Anne Saarinen, (unknown), Hanna Mandel, Harald Broch, Albert de la Chapelle	99
16	A distinct phenotype of distal myopathy in a large Finnish family 2003 ·Neurology ·I. Mahjneh, Henna Haravuori, Anders Paetau, Louise V.B. Anderson, Anne Saarinen, Bjarne Udd, Hannu Somer	22
17	Piezoelectric film transducer for recording of oculography in electro-encephalogram-polygraphy 2002 ·Medical & Biological Engineering & Computing ·(unknown), Anne Saarinen	3

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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