Kairit Joost

413 total citations
17 papers, 184 citations indexed

About

Kairit Joost is a scholar working on Molecular Biology, Clinical Biochemistry and Sensory Systems. According to data from OpenAlex, Kairit Joost has authored 17 papers receiving a total of 184 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 3 papers in Sensory Systems. Recurrent topics in Kairit Joost's work include Metabolism and Genetic Disorders (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Mitochondrial Function and Pathology (3 papers). Kairit Joost is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Mitochondrial Function and Pathology (3 papers). Kairit Joost collaborates with scholars based in Estonia, Netherlands and United States. Kairit Joost's co-authors include Katrin Õunap, Riina Žordania, Andres Piirsoo, Tiina Kahre, Richard J. Rodenburg, Rita Teek, Bert van den Heuvel, Inga Talvik, Tiia Reimand and Neeme Tõnisson and has published in prestigious journals such as Journal of Neuro-Oncology, Molecular Genetics and Metabolism and Neuromuscular Disorders.

In The Last Decade

Kairit Joost

16 papers receiving 180 citations

Peers

Countries citing papers authored by Kairit Joost

Since Specialization

Citations

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

Fields of papers citing papers by Kairit Joost

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kairit Joost

This figure shows the co-authorship network connecting the top 25 collaborators of Kairit Joost. A scholar is included among the top collaborators of Kairit Joost 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 Kairit Joost. Kairit Joost 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:

17 of 17 papers shown

#	Work	Indexed citations
1	A very early diagnosis of Alstrӧm syndrome by next generation sequencing 2020 ·BMC Medical Genetics ·Leonardo Gatticchi, Ján Miertuš, Paolo Enrico Maltese, (unknown), (unknown), Ľudmila Podracká, (unknown), (unknown), (unknown), (unknown), Kairit Joost, (unknown), Matteo Bertelli	4
2	Treatment outcome of creatine transporter deficiency: international retrospective cohort study 2018 ·Metabolic Brain Disease ·Theodora U. J. Bruun, (unknown), Anabela Bandeira, (unknown), Can Fıçıcıoğlu, Jennifer Goldstein, Kairit Joost, Dwight D. Koeberl, Luísa Diogo, Marie‐Cécile Nassogne, Siobhán O’Sullivan, Katrin Õunap, Andreas Schulze, Lionel Van Maldergem, Gajja S. Salomons, Saadet Mercimek‐Andrews	32
3	The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver–Russell Syndrome and Beckwith–Wiedemann Syndrome 2015 ·Genetic Testing and Molecular Biomarkers ·Mari‐Anne Vals, (unknown), Tiina Kahre, (unknown), Kai Muru, Kairit Joost, Rita Teek, Lukas Soellner, Thomas Eggermann, Katrin Õunap	7
4	De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion 2015 ·Neuromuscular Disorders ·Sander Pajusalu, Inga Talvik, (unknown), Tiina Talvik, (unknown), Kairit Joost, Sanna Puusepp, Andres Piirsoo, Werner Stenzel, Hans H. Goebel, Tiit Nikopensius, Tarmo Annilo, Margit Nõukas, Andres Metspalu, Katrin Õunap, Tiia Reimand	8
5	Üle-eestiline vastsündinute laiendatud sõeltestimine tandemmass-spektromeetria meetodil ravitavate kaasasündinud ainevahetushaiguste suhtes 2014 ·Ajakirjad. Journals by UT ·Karit Reinson, Kairit Joost, (unknown), Riina Žordania, (unknown), Katrin Õunap	1
6	Fenüülketonuuria Eesti ravijuhend 2014 ·Ajakirjad. Journals by UT ·(unknown), Kairit Joost, Riina Žordania, Katrin Õunap	1
7	Hearing impairment in Estonia: An algorithm to investigate genetic causes in pediatric patients 2013 ·Advances in Medical Sciences ·Rita Teek, (unknown), Riina Žordania, Kairit Joost, Tiina Kahre, Neeme Tõnisson, Mari Nelis, Olga Žilina, Lisbeth Tranebjærg, Tiia Reimand, Katrin Õunap	11
8	The Live-Birth Prevalence of Mucopolysaccharidoses in Estonia 2012 ·Genetic Testing and Molecular Biomarkers ·(unknown), Kairit Joost, Riina Žordania, Inga Talvik, Reet Rein, J. G. M. Huijmans, (unknown), Katrin Õunap	19
9	A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children 2012 ·Molecular Syndromology ·Kairit Joost, Richard J. Rodenburg, Andres Piirsoo, Lambert van den Heuvel, Riina Žordania, (unknown), Inga Talvik, (unknown), Ursel Soomets, Katrin Õunap	4
10	Analysis of NADP+-dependent isocitrate dehydrogenase-1/2 gene mutations in pediatric brain tumors: report of a secondary anaplastic astrocytoma carrying the IDH1 mutation 2012 ·Journal of Neuro-Oncology ·Samantha Mascelli, Alessandro Raso, Roberto Biassoni, Mariasavina Severino, Katrin Sak, Kairit Joost, Claudia Milanaccio, Salvina Barra, Grillo Ruggieri F, Irene Vanni, Alessandro Consales, Armando Cama, Valeria Capra, Paolo Nozza, Maria Luisa Garrè	11
11	Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in Estonia 2011 ·JIMD Reports ·Kairit Joost, Katrin Õunap, Riina Žordania, (unknown), Rikke Katrine Jentoft Olsen, (unknown), Kalle Kilk, Ursel Soomets, Tiina Kahre	14
12	Long-term complications in Estonian galactosemia patients with a less strict lactose-free diet and metabolic control 2011 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Kairit Joost, Riina Žordania, Katrin Õunap	20
13	Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia 2010 ·International Journal of Pediatric Otorhinolaryngology ·Rita Teek, (unknown), Riina Žordania, Kairit Joost, Tiia Reimand, Tõnu Möls, Eneli Oitmaa, Tiina Kahre, Neeme Tõnisson, Katrin Õunap	15
14	A Novel Mutation in the SCO2 Gene in a Neonate With Early-Onset Cardioencephalomyopathy 2010 ·Pediatric Neurology ·Kairit Joost, Richard J. Rodenburg, Andres Piirsoo, Bert van den Heuvel, Riina Žordania, Katrin Õunap	26
15	Whole Xp Deletion in a Girl with Mental Retardation, Epilepsy, and Biochemical Features of OTC Deficiency 2010 ·Molecular Syndromology ·Kairit Joost, (unknown), Rita Teek, (unknown), Maire Peters, (unknown), Baiba Lāce, Riina Žordania, Inga Talvik, Katrin Õunap	2
16	Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss 2008 ·International Journal of Pediatric Otorhinolaryngology ·Rita Teek, Eneli Oitmaa, (unknown), Riina Žordania, Kairit Joost, (unknown), Neeme Tõnisson, Phyllis Gardner, Iris Schrijver, Mart Kull, Katrin Õunap	8
17	Differences in resistance against kala-azar (Kenya strain) between males and females. 1969 ·PubMed ·D. J. B. Wijers, Kairit Joost, (unknown), (unknown)	1

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.

Explore authors with similar magnitude of impact