Sonal Mahida

1.2k total citations
13 papers, 210 citations indexed

About

Sonal Mahida is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Sonal Mahida has authored 13 papers receiving a total of 210 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Sonal Mahida's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Sonal Mahida is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Sonal Mahida collaborates with scholars based in United States, United Arab Emirates and Canada. Sonal Mahida's co-authors include Annapurna Poduri, Heather E. Olson, McKenna Kelly, Alan Taylor, Anne T. Berg, Shira Rockowitz, Anne Rochtus, Lacey Smith, Beth Rosen Sheidley and Catherine Shain and has published in prestigious journals such as Neurology, Epilepsia and Human Mutation.

In The Last Decade

Sonal Mahida

12 papers receiving 207 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sonal Mahida United States	8	124	93	63	19	18	13	210
Ilona Krey Germany	8	116 0.9×	77 0.8×	83 1.3×	27 1.4×	53 2.9×	21	203
Raffaella Minardi Italy	7	80 0.6×	45 0.5×	55 0.9×	12 0.6×	25 1.4×	21	134
McKenna Kelly United States	6	136 1.1×	75 0.8×	102 1.6×	39 2.1×	39 2.2×	6	226
Anita Shanmugham United States	4	275 2.2×	82 0.9×	94 1.5×	63 3.3×	20 1.1×	4	357
Cheuk Wing Fung China	9	54 0.4×	67 0.7×	31 0.5×	42 2.2×	21 1.2×	18	177
Philip Holmgren Belgium	5	88 0.7×	66 0.7×	48 0.8×	20 1.1×	23 1.3×	5	174
Lisa‐Marie Niestroj United States	6	136 1.1×	83 0.9×	54 0.9×	12 0.6×	20 1.1×	7	190
Line H.G. Larsen Denmark	9	161 1.3×	94 1.0×	103 1.6×	20 1.1×	22 1.2×	11	247
Guo‐Wang Lin China	5	92 0.7×	111 1.2×	113 1.8×	27 1.4×	44 2.4×	10	225
Danielle Nolan United States	6	75 0.6×	46 0.5×	33 0.5×	23 1.2×	17 0.9×	10	129

Countries citing papers authored by Sonal Mahida

Since Specialization

Citations

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

Fields of papers citing papers by Sonal Mahida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonal Mahida

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

All Works

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13 of 13 papers shown

Callahan, Nicholas, Sonal Mahida, Abigail Sveden, et al.. (2025). Expansion of the Genotypic and Phenotypic Spectrum of SETD5 Disorder Using Data From the National Brain Gene Registry. Clinical Genetics. 108(3). 279–291.

Stredny, Coral M., et al.. (2024). CIC-Related Neurodevelopmental Disorder: A Review of the Literature and an Expansion of Genotype and Phenotype. Genes. 15(11). 1425–1425. 1 indexed citations

Blesson, Alyssa, Juliann M. Savatt, Abigail Sveden, et al.. (2024). Expansion of the Genotypic and Phenotypic Spectrum of ASH1L-Related Syndromic Neurodevelopmental Disorder. Genes. 15(4). 423–423. 3 indexed citations

Mahida, Sonal, et al.. (2023). Ezogabine impacts seizures and development in patients with KCNQ2 developmental and epileptic encephalopathy. Epilepsia. 64(7). e143–e147. 13 indexed citations

Mahida, Sonal, et al.. (2022). Racial differences in the dermatological manifestations of tuberous sclerosis complex and the potential effects on diagnosis and care. PubMed. 3. 911049885–911049885. 2 indexed citations

Dohrn, Maike F., Adriana Rebelo, Siddharth Srivastava, et al.. (2022). De Novo ATP1A1 Variants in an Early-Onset Complex Neurodevelopmental Syndrome. Neurology. 98(11). 440–445. 5 indexed citations

Ni, Min, Bushra Afroze, Chao Xing, et al.. (2021). A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy. Genetics in Medicine. 23(5). 900–908. 15 indexed citations

Berg, Anne T., Sonal Mahida, & Annapurna Poduri. (2021). KCNQ2‐DEE: developmental or epileptic encephalopathy?. Annals of Clinical and Translational Neurology. 8(3). 666–676. 25 indexed citations

McGraw, Christopher M., Sonal Mahida, Parul Jayakar, et al.. (2021). Uridine‐responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings. Annals of Clinical and Translational Neurology. 8(3). 716–722. 11 indexed citations

10.

Rochtus, Anne, Heather E. Olson, Lacey Smith, et al.. (2020). Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort. Epilepsia. 61(2). 249–258. 88 indexed citations

11.

Nusbaum, Rachel, et al.. (2019). Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions. Journal of Genetic Counseling. 28(2). 304–312. 14 indexed citations

12.

Srivastava, Siddharth, Ankur Butala, Sonal Mahida, et al.. (2019). Expansion of the clinical spectrum associated with AARS2‐related disorders. American Journal of Medical Genetics Part A. 179(8). 1556–1564. 21 indexed citations

13.

Nguyen, Thi Tuyet Mai, Sonal Mahida, Constance Smith‐Hicks, & Philippe M. Campeau. (2018). APIGHmutation leading to GPI deficiency is associated with developmental delay and autism. Human Mutation. 39(6). 827–829. 12 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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