Milja Kaare

433 total citations
14 papers, 335 citations indexed

About

Milja Kaare is a scholar working on Pediatrics, Perinatology and Child Health, Immunology and Obstetrics and Gynecology. According to data from OpenAlex, Milja Kaare has authored 14 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 5 papers in Immunology and 4 papers in Obstetrics and Gynecology. Recurrent topics in Milja Kaare's work include Prenatal Screening and Diagnostics (6 papers), Pregnancy and preeclampsia studies (4 papers) and Reproductive System and Pregnancy (4 papers). Milja Kaare is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Pregnancy and preeclampsia studies (4 papers) and Reproductive System and Pregnancy (4 papers). Milja Kaare collaborates with scholars based in Finland, Sweden and Estonia. Milja Kaare's co-authors include Kristiina Aittomäki, Veli‐Matti Ulander, Päivi Heikkilä, Heli Nevanlinna, Carl Blomqvist, Jonna Tallila, Johanna Tommiska, Risto Kaaja, Ari Ristimäki and Jodie N. Painter and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Clinical Cancer Research and International Journal of Cancer.

In The Last Decade

Milja Kaare

14 papers receiving 323 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Milja Kaare Finland	9	149	148	87	71	60	14	335
Weizhi Xue China	10	271 1.8×	45 0.3×	92 1.1×	85 1.2×	39 0.7×	12	406
Xuewei Zhuang China	11	201 1.3×	147 1.0×	123 1.4×	15 0.2×	163 2.7×	26	460
Hossein Pashaiefar Iran	11	224 1.5×	47 0.3×	167 1.9×	46 0.6×	41 0.7×	32	344
Eva Glud Denmark	13	196 1.3×	244 1.6×	100 1.1×	68 1.0×	85 1.4×	15	523
Marcin Śniadecki Poland	8	92 0.6×	62 0.4×	50 0.6×	69 1.0×	58 1.0×	30	256
Heather Foster United Kingdom	6	136 0.9×	99 0.7×	39 0.4×	43 0.6×	37 0.6×	11	421
Nathalie L.G. Sieben Netherlands	8	195 1.3×	108 0.7×	131 1.5×	32 0.5×	41 0.7×	8	433
Guangshuai Jia China	6	387 2.6×	108 0.7×	98 1.1×	37 0.5×	113 1.9×	8	520
Jennifer L. Geurts United States	9	245 1.6×	136 0.9×	102 1.2×	290 4.1×	13 0.2×	27	505
W. Kleine Germany	10	73 0.5×	124 0.8×	126 1.4×	91 1.3×	27 0.5×	33	449

Countries citing papers authored by Milja Kaare

Since Specialization

Citations

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

Fields of papers citing papers by Milja Kaare

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Milja Kaare

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

All Works

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14 of 14 papers shown

Brunfeldt, Minna, et al.. (2023). Opt‐in for secondary findings as part of diagnostic whole‐exome sequencing: Real‐life experience from an international diagnostic laboratory. Molecular Genetics & Genomic Medicine. 11(8). e2180–e2180. 5 indexed citations

Kaare, Milja, et al.. (2022). Phenotype expansion and neurological manifestations of neurobehavioural disease caused by a variant in RFX7. European Journal of Medical Genetics. 66(1). 104657–104657. 5 indexed citations

Spagnoli, Carlotta, Grazia Salerno, Daniele Frattini, et al.. (2021). Infantile-Onset Charcot–Marie–Tooth Disease With Pyramidal Features and White Matter Abnormalities Due to a De novo MORC2 Gene Variant: A Case Report and Brief Review of the Literature. Frontiers in Neurology. 12. 718808–718808. 1 indexed citations

Ålgars, Annika, Jari Sundström, Minnamaija Lintunen, et al.. (2016). EGFR gene copy number predicts response to anti‐EGFR treatment in RAS wild type and RAS/BRAF/PIK3CA wild type metastatic colorectal cancer. International Journal of Cancer. 140(4). 922–929. 23 indexed citations

Kaare, Milja, Alexandra Götz, Veli‐Matti Ulander, et al.. (2009). Do mitochondrial mutations cause recurrent miscarriage?. Molecular Human Reproduction. 15(5). 295–300. 12 indexed citations

Kaare, Milja, Ralf Bützow, Veli‐Matti Ulander, et al.. (2009). Study of p53 gene mutations and placental expression in recurrent miscarriage cases. Reproductive BioMedicine Online. 18(3). 430–435. 17 indexed citations

Heino, Sanna, Milja Kaare, Sture Andersson, & Hannele Laivuori. (2008). Non-synonymous sequence variants within the oxygen-dependent degradation domain of the HIF1Agene are not associated with pre-eclampsia in the Finnish population. BMC Medical Genetics. 9(1). 96–96. 7 indexed citations

Kaare, Milja, Sanna Seitsonen, Irma Järvelä, Seppo Meri, & Hannele Laivuori. (2008). Complement Factor H Variant Y402H is Not a Risk Factor for Preeclampsia in the Finnish Population. Hypertension in Pregnancy. 27(4). 328–336. 2 indexed citations

Kaare, Milja, Jodie N. Painter, Veli‐Matti Ulander, Risto Kaaja, & Kristiina Aittomäki. (2008). Sex chromosome characteristics and recurrent miscarriage. Fertility and Sterility. 90(6). 2328–2333. 16 indexed citations

10.

Rull, Kristiina, Liina Nagirnaja, Veli‐Matti Ulander, et al.. (2008). Chorionic Gonadotropin β-Gene Variants Are Associated with Recurrent Miscarriage in Two European Populations. The Journal of Clinical Endocrinology & Metabolism. 93(12). 4697–4706. 28 indexed citations

11.

Kaare, Milja, et al.. (2006). Variations in the thrombomodulin and endothelial protein C receptor genes in couples with recurrent miscarriage. Human Reproduction. 22(3). 864–868. 27 indexed citations

12.

Kaare, Milja, Jodie N. Painter, Veli‐Matti Ulander, Risto Kaaja, & Kristiina Aittomäki. (2006). Variations of the Amnionless gene in recurrent spontaneous abortions. Molecular Human Reproduction. 12(1). 25–29. 8 indexed citations

13.

Tommiska, Johanna, Sheila Seal, Anthony Renwick, et al.. (2005). Evaluation of RAD50 in familial breast cancer predisposition. International Journal of Cancer. 118(11). 2911–2916. 47 indexed citations

14.

Tommiska, Johanna, Hannaleena Eerola, Mira Heinonen, et al.. (2005). Breast Cancer Patients with p53 Pro72 Homozygous Genotype Have a Poorer Survival. Clinical Cancer Research. 11(14). 5098–5103. 137 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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