Emma Krzesinski

831 total citations
6 papers, 43 citations indexed

About

Emma Krzesinski is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Emma Krzesinski has authored 6 papers receiving a total of 43 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Emma Krzesinski's work include Genomics and Rare Diseases (2 papers), RNA modifications and cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Emma Krzesinski is often cited by papers focused on Genomics and Rare Diseases (2 papers), RNA modifications and cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Emma Krzesinski collaborates with scholars based in Australia, United States and Denmark. Emma Krzesinski's co-authors include Lauren Akesson, L. Geerts, Michael Urban, Zornitza Stark, Sebastian Lunke, David R. Thorburn, Matthew F. Hunter, John Christodoulou, Adam Bournazos and Vamsi K. Mootha and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Human Mutation.

In The Last Decade

Emma Krzesinski

5 papers receiving 43 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emma Krzesinski Australia	4	24	18	12	6	5	6	43
Noah L. Tsao United States	4	19 0.8×	9 0.5×	9 0.8×	3 0.5×	7 1.4×	8	38
Anand Vasudevan Australia	3	14 0.6×	9 0.5×	13 1.1×	2 0.3×	7 1.4×	5	36
Meraj Ahmad India	2	6 0.3×	18 1.0×	3 0.3×	7 1.2×	5 1.0×	2	35
T. Williams United Kingdom	2	27 1.1×	8 0.4×	23 1.9×	1 0.2×	4 0.8×	2	45
Mohammed M. Saleh Saudi Arabia	3	17 0.7×	12 0.7×	11 0.9×	1 0.2×	3 0.6×	4	28
Magdalena Macech Poland	2	20 0.8×	6 0.3×	4 0.3×	3 0.5×		2	30
Emily S Doherty United States	4	38 1.6×	29 1.6×	8 0.7×		2 0.4×	4	56
Vincenzo Raimondo Italy	3	17 0.7×	4 0.2×	14 1.2×		5 1.0×	6	29
Camila Zolini Brazil	4	10 0.4×	19 1.1×	2 0.2×	2 0.3×	9 1.8×	4	41
Inmaculada Rueda Spain	4	23 1.0×	8 0.4×	33 2.8×	1 0.2×	20 4.0×	7	56

Countries citing papers authored by Emma Krzesinski

Since Specialization

Citations

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

Fields of papers citing papers by Emma Krzesinski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Krzesinski

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

All Works

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6 of 6 papers shown

1.

Ashton, Katie A., K.T. Lee, Omkar L. Patkar, et al.. (2024). Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia. SHILAP Revista de lepidopterología. 3. 101958–101958.

2.

Hock, Daniella H., Nicole J. Lake, Sarah E. Calvo, et al.. (2023). Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease. Human Molecular Genetics. 32(15). 2441–2454. 13 indexed citations

3.

Akesson, Lauren, Adam Bournazos, Andrew Fennell, et al.. (2020). Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate. Human Mutation. 41(11). 1884–1891. 8 indexed citations

4.

Akesson, Lauren, Adam Bournazos, Andrew Fennell, et al.. (2020). Rapid exome sequencing and adjunct rna studies confirm pathogenicity of a novel homozygous asns splicing variant in a critically ill neonate. Pathology. 52. S106–S106. 2 indexed citations

5.

Akesson, Lauren, Stefanie Eggers, Belinda Chong, et al.. (2019). Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing. European Journal of Human Genetics. 27(12). 1821–1826. 14 indexed citations

6.

Krzesinski, Emma, L. Geerts, & Michael Urban. (2019). Neural tube defect diagnosis and outcomes at a tertiary South African hospital with intensive case ascertainment. South African Medical Journal. 109(9). 698–698. 6 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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