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

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

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

#	Work	Indexed citations
1	Expansion of the Genotypic and Phenotypic Spectrum of SETD5 Disorder Using Data From the National Brain Gene Registry 2025 ·Clinical Genetics ·Nicholas Callahan, Sonal Mahida, Abigail Sveden, Maryanne Quinn, Maya Chopra, Siddharth Srivastava	0
2	CIC-Related Neurodevelopmental Disorder: A Review of the Literature and an Expansion of Genotype and Phenotype 2024 ·Genes ·(unknown), (unknown), Coral M. Stredny, Sonal Mahida	1
3	Expansion of the Genotypic and Phenotypic Spectrum of ASH1L-Related Syndromic Neurodevelopmental Disorder 2024 ·Genes ·(unknown), Alyssa Blesson, Juliann M. Savatt, Abigail Sveden, Sonal Mahida, Heather C. Hazlett, Erin Rooney Riggs, Maya Chopra	3
4	Ezogabine impacts seizures and development in patients with KCNQ2 developmental and epileptic encephalopathy 2023 ·Epilepsia ·(unknown), Sonal Mahida, McKenna Kelly, Annapurna Poduri, Heather E. Olson	13
5	Racial differences in the dermatological manifestations of tuberous sclerosis complex and the potential effects on diagnosis and care 2022 ·PubMed ·(unknown), (unknown), Sonal Mahida, Bareng A. S. Nonyane, (unknown), (unknown), Tanjala Gipson	2
6	De Novo ATP1A1 Variants in an Early-Onset Complex Neurodevelopmental Syndrome 2022 ·Neurology ·Maike F. Dohrn, Adriana Rebelo, Siddharth Srivastava, Gerarda Cappuccio, Robert Śmigiel, Alka Malhotra, Donald Basel, Ingrid M.B.H. van de Laar, Rinze F. Neuteboom, (unknown), Sonal Mahida, Nicola Brunetti‐Pierri, Ryan J. Taft, Stephan Züchner	5
7	A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy 2021 ·Genetics in Medicine ·Min Ni, Bushra Afroze, Chao Xing, Chunxiao Pan, Yanqiu Shao, Ling Cai, Brandi L. Cantarel, Jimin Pei, Nick V. Grishin, Stacy Hewson, (unknown), Sonal Mahida, (unknown), Mark A. Tarnopolsky, Annapurna Poduri, Alexander Rotenberg, Neal Sondheimer, Ralph J. DeBerardinis	15
8	KCNQ2‐DEE: developmental or epileptic encephalopathy? 2021 ·Annals of Clinical and Translational Neurology ·Anne T. Berg, Sonal Mahida, Annapurna Poduri	25
9	Uridine‐responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings 2021 ·Annals of Clinical and Translational Neurology ·Christopher M. McGraw, Sonal Mahida, Parul Jayakar, Hyun Yong Koh, Alan Taylor, Trevor Resnick, Lance H. Rodan, Marc A. Schwartz, (unknown), Vijay G. Sankaran, Gerard T. Berry, Annapurna Poduri	11
10	Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort 2020 ·Epilepsia ·Anne Rochtus, Heather E. Olson, Lacey Smith, (unknown), Christelle Moufawad El Achkar, Alan Taylor, Sonal Mahida, (unknown), McKenna Kelly, Catherine Shain, Shira Rockowitz, Beth Rosen Sheidley, Annapurna Poduri	88
11	Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions 2019 ·Journal of Genetic Counseling ·(unknown), Rachel Nusbaum, Constance Smith‐Hicks, Leila Jamal, (unknown), Sonal Mahida	14
12	Expansion of the clinical spectrum associated with AARS2‐related disorders 2019 ·American Journal of Medical Genetics Part A ·Siddharth Srivastava, Ankur Butala, Sonal Mahida, (unknown), Weiyi Mu, Andrea Poretti, Hilary J. Vernon, (unknown), Paldeep S. Atwal, Erik H. Middlebrooks, David S. Zee, SakkuBai Naidu	21
13	APIGHmutation leading to GPI deficiency is associated with developmental delay and autism 2018 ·Human Mutation ·Thi Tuyet Mai Nguyen, Sonal Mahida, Constance Smith‐Hicks, Philippe M. Campeau	12

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.

Explore authors with similar magnitude of impact