Sondhya Ghedia

757 total citations
5 papers, 123 citations indexed

About

Sondhya Ghedia is a scholar working on Genetics, Neurology and Molecular Biology. According to data from OpenAlex, Sondhya Ghedia has authored 5 papers receiving a total of 123 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Neurology and 1 paper in Molecular Biology. Recurrent topics in Sondhya Ghedia's work include Genomics and Rare Diseases (2 papers), Vascular Malformations Diagnosis and Treatment (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Sondhya Ghedia is often cited by papers focused on Genomics and Rare Diseases (2 papers), Vascular Malformations Diagnosis and Treatment (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Sondhya Ghedia collaborates with scholars based in Australia, United Kingdom and United States. Sondhya Ghedia's co-authors include Rong Zhang, Weizhi Liu, Oriana S. Fisher, Titus J. Boggon, Amy L. Stiegler, James L. Weber, Bernard Ng, Marianne Vonau, Veronica Wiley and Maximilian Muenke and has published in prestigious journals such as Journal of Biological Chemistry, European Journal of Human Genetics and Molecular Syndromology.

In The Last Decade

Sondhya Ghedia

5 papers receiving 112 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sondhya Ghedia Australia	5	59	36	25	25	11	5	123
Meghan Candee United States	6	71 1.2×	10 0.3×	31 1.2×	17 0.7×	9 0.8×	10	123
Timo Roser Germany	7	18 0.3×	33 0.9×	30 1.2×	19 0.8×	11 1.0×	11	113
Agnès Guët France	6	39 0.7×	6 0.2×	53 2.1×	11 0.4×	15 1.4×	12	102
August Allocco United States	6	22 0.4×	10 0.3×	23 0.9×	24 1.0×	2 0.2×	6	72
Hanène Benrhouma Tunisia	8	21 0.4×	57 1.6×	62 2.5×	5 0.2×	35 3.2×	37	150
Ilya Kanivets Russia	7	61 1.0×	10 0.3×	91 3.6×	26 1.0×	29 2.6×	39	162
Federica Rachele Danti Italy	5	49 0.8×	17 0.5×	32 1.3×	10 0.4×	14 1.3×	12	95
Mona Grimmel Germany	5	26 0.4×	9 0.3×	38 1.5×	6 0.2×	9 0.8×	11	93
Heba Y. El Khashab Saudi Arabia	7	40 0.7×	17 0.5×	39 1.6×	11 0.4×	1 0.1×	11	86
Lynette Rives United States	4	52 0.9×	4 0.1×	33 1.3×	10 0.4×	5 0.5×	7	97

Countries citing papers authored by Sondhya Ghedia

Since Specialization

Citations

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

Fields of papers citing papers by Sondhya Ghedia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sondhya Ghedia

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

All Works

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5 of 5 papers shown

1.

Fleming, Jane, Kristine Barlow‐Stewart, Sondhya Ghedia, et al.. (2023). Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?. European Journal of Human Genetics. 31(6). 703–711. 19 indexed citations

2.

Weiss, Karin, Kristen Wigby, Madeleine Fannemel, et al.. (2017). Haploinsufficiency of ZNF462 is associated with craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay. European Journal of Human Genetics. 25(8). 946–951. 27 indexed citations

3.

Fisher, Oriana S., Weizhi Liu, Rong Zhang, et al.. (2014). Structural Basis for the Disruption of the Cerebral Cavernous Malformations 2 (CCM2) Interaction with Krev Interaction Trapped 1 (KRIT1) by Disease-associated Mutations. Journal of Biological Chemistry. 290(5). 2842–2853. 32 indexed citations

4.

Kogelenberg, Margriet van, Sondhya Ghedia, George McGillivray, et al.. (2010). Periventricular Heterotopia in Common Microdeletion Syndromes. Molecular Syndromology. 1(1). 35–41. 32 indexed citations

5.

Ng, Bernard, Ellie Mulyadi, J K Pereira, et al.. (2006). Familial cerebral cavernous haemangioma diagnosed in an infant with a rapidly growing cerebral lesion. Australasian Radiology. 50(6). 583–590. 13 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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