Ewa Goljan

1.2k total citations
9 papers, 218 citations indexed

About

Ewa Goljan is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Ewa Goljan has authored 9 papers receiving a total of 218 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Neurology. Recurrent topics in Ewa Goljan's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Parkinson's Disease Mechanisms and Treatments (2 papers). Ewa Goljan is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Parkinson's Disease Mechanisms and Treatments (2 papers). Ewa Goljan collaborates with scholars based in Saudi Arabia. Ewa Goljan's co-authors include Dorota Monies, Mohamed Abouelhoda, Mohamed El-Kalioby, Nada Al Tassan, Shazia Subhani, Brian F. Meyer, Hindi Al‐Hindi, Tariq Faquih, Bashayer Al‐Mubarak and Jameela Shinwari and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Ewa Goljan

9 papers receiving 215 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ewa Goljan Saudi Arabia	7	90	81	41	30	30	9	218
Sara Bertok Slovenia	10	166 1.8×	122 1.5×	25 0.6×	18 0.6×	27 0.9×	35	354
T. Yamamoto Japan	9	88 1.0×	90 1.1×	12 0.3×	37 1.2×	55 1.8×	18	334
Amarilis Sanchez‐Valle United States	12	289 3.2×	165 2.0×	96 2.3×	10 0.3×	32 1.1×	26	642
Mariateresa Falco Italy	9	94 1.0×	175 2.2×	46 1.1×	11 0.4×	30 1.0×	22	334
Frances Elmslie United Kingdom	10	117 1.3×	99 1.2×	22 0.5×	14 0.5×	50 1.7×	16	291
Emma J. Hodson United Kingdom	9	107 1.2×	126 1.6×	39 1.0×	23 0.8×	14 0.5×	12	361
Sherin Shaaban United States	10	94 1.0×	93 1.1×	30 0.7×	4 0.1×	19 0.6×	17	274
Christine Broissand France	7	138 1.5×	130 1.6×	37 0.9×	20 0.7×	67 2.2×	10	416
Dirk Oliver Wennmann Germany	11	230 2.6×	30 0.4×	33 0.8×	47 1.6×	13 0.4×	14	489

Countries citing papers authored by Ewa Goljan

Since Specialization

Citations

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

Fields of papers citing papers by Ewa Goljan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ewa Goljan

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

All Works

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9 of 9 papers shown

1.

Goljan, Ewa, et al.. (2024). Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population. Human Genomics. 18(1). 30–30. 2 indexed citations

2.

Goljan, Ewa, et al.. (2022). Identification of pharmacogenetic variants from large scale next generation sequencing data in the Saudi population. PLoS ONE. 17(1). e0263137–e0263137. 14 indexed citations

3.

Alzahrani, Ali S., et al.. (2020). Genetic Alterations in Pediatric Thyroid Cancer Using a Comprehensive Childhood Cancer Gene Panel. The Journal of Clinical Endocrinology & Metabolism. 105(10). 3324–3334. 31 indexed citations

4.

Monies, Dorota, Thamer Alkhairallah, Saeed Bohlega, et al.. (2019). Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease. Scientific Reports. 9(1). 3344–3344. 28 indexed citations

5.

Al‐Mubarak, Bashayer, Mohamed Abouelhoda, Hesham Aldhalaan, et al.. (2017). Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families. Scientific Reports. 7(1). 5679–5679. 66 indexed citations

6.

Monies, Dorota, Hussam Abou‐Al‐Shaar, Ewa Goljan, et al.. (2017). Identification of a novel genetic locus underlying tremor and dystonia. Human Genomics. 11(1). 25–25. 5 indexed citations

7.

Alsemari, Abdulaziz, Banan Al‐Younes, Ewa Goljan, et al.. (2017). Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism. Human Genomics. 11(1). 28–28. 13 indexed citations

8.

Burkholder, John A., Dieter C. Bröering, Mohamed Abouelhoda, et al.. (2016). Genetic profiling of children with advanced cholestatic liver disease. Clinical Genetics. 92(1). 52–61. 30 indexed citations

9.

Monies, Dorota, Hindi Al‐Hindi, Mohamed Abouelhoda, et al.. (2016). A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies. Human Genomics. 10(1). 32–32. 29 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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