Sanna Puusepp

541 total citations
8 papers, 149 citations indexed

About

Sanna Puusepp is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Sanna Puusepp has authored 8 papers receiving a total of 149 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 3 papers in Genetics. Recurrent topics in Sanna Puusepp's work include Genetic Neurodegenerative Diseases (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Sanna Puusepp is often cited by papers focused on Genetic Neurodegenerative Diseases (3 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Sanna Puusepp collaborates with scholars based in Estonia, Germany and Netherlands. Sanna Puusepp's co-authors include Katrin Õunap, Inga Talvik, Sander Pajusalu, Eve Õiglane‐Shlik, Karit Reinson, Tiia Reimand, Tiiu Tomberg, Rita Teek, Ulvi Vaher and Reet Rein and has published in prestigious journals such as Neuromuscular Disorders, American Journal of Medical Genetics Part A and European Journal of Paediatric Neurology.

In The Last Decade

Sanna Puusepp

7 papers receiving 126 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sanna Puusepp Estonia	6	84	77	36	30	18	8	149
Stephanie Karch Germany	8	101 1.2×	50 0.6×	23 0.6×	14 0.5×	11 0.6×	8	146
A. T. Pagnamenta United Kingdom	3	142 1.7×	81 1.1×	33 0.9×	50 1.7×	16 0.9×	3	215
Karit Reinson Estonia	8	122 1.5×	67 0.9×	36 1.0×	80 2.7×	28 1.6×	14	198
Patrícia B. S. Celestino-Soper United States	5	97 1.2×	76 1.0×	26 0.7×	12 0.4×	8 0.4×	8	166
Dana Marafi United States	8	88 1.0×	70 0.9×	22 0.6×	6 0.2×	6 0.3×	24	171
Nicoletta Zanotta Italy	8	70 0.8×	53 0.7×	59 1.6×	8 0.3×	32 1.8×	16	169
Anaïs Begemann Switzerland	3	51 0.6×	47 0.6×	10 0.3×	36 1.2×	9 0.5×	4	108
Sohnee Ahmed Canada	5	75 0.9×	62 0.8×	23 0.6×	9 0.3×	11 0.6×	9	132
Amy Crunk United States	6	58 0.7×	59 0.8×	16 0.4×	5 0.2×	15 0.8×	10	131
Raffaella Minardi Italy	7	45 0.5×	80 1.0×	25 0.7×	19 0.6×	12 0.7×	21	134

Countries citing papers authored by Sanna Puusepp

Since Specialization

Citations

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

Fields of papers citing papers by Sanna Puusepp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sanna Puusepp

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

All Works

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8 of 8 papers shown

Õunap, Katrin, Tiia Reimand, Eve Õiglane‐Shlik, et al.. (2024). TTN -Related Muscular Dystrophies, LGMD, and TMD, in an Estonian Family Caused by the Finnish Founder Variant. Neurology Genetics. 10(6). e200199–e200199.

Puusepp, Sanna, et al.. (2023). Autosomal recessive Leber's hereditary optic neuropathy caused by a homozygous variant in DNAJC30 gene. European Journal of Medical Genetics. 66(9). 104821–104821. 1 indexed citations

Puusepp, Sanna, Karit Reinson, Sander Pajusalu, et al.. (2020). Atypical presentation of Arts syndrome due to a novel hemizygous loss-of-function variant in the PRPS1 gene. Molecular Genetics and Metabolism Reports. 25. 100677–100677. 10 indexed citations

Puusepp, Sanna, Karit Reinson, Sander Pajusalu, et al.. (2018). Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia. Molecular Genetics and Metabolism Reports. 15. 80–89. 30 indexed citations

Reinson, Karit, Eve Õiglane‐Shlik, Inga Talvik, et al.. (2016). Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy. American Journal of Medical Genetics Part A. 170(8). 2173–2176. 62 indexed citations

Leffler, Melanie, Sanna Puusepp, Olga Žilina, et al.. (2015). Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1R. European Journal of Medical Genetics. 59(4). 257–262. 20 indexed citations

Pajusalu, Sander, Inga Talvik, Tiina Talvik, et al.. (2015). De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportion. Neuromuscular Disorders. 26(3). 236–239. 8 indexed citations

Õiglane‐Shlik, Eve, Sanna Puusepp, Inga Talvik, et al.. (2014). Monosomy 1p36 – A multifaceted and still enigmatic syndrome: Four clinically diverse cases with shared white matter abnormalities. European Journal of Paediatric Neurology. 18(3). 338–346. 18 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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