Maya Chopra

1.5k total citations
25 papers, 406 citations indexed

About

Maya Chopra is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Maya Chopra has authored 25 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Maya Chopra's work include Genomics and Rare Diseases (7 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maya Chopra is often cited by papers focused on Genomics and Rare Diseases (7 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maya Chopra collaborates with scholars based in United States, Australia and China. Maya Chopra's co-authors include David Mowat, John A. Lawson, Seán Kennedy, Danny Flanagan, Michael Cardamone, Anthony Vandersteen, Uluç Yiş, Cecilia Giunta, Matthias R. Baumgartner and Marius Kraenzlin and has published in prestigious journals such as Journal of Clinical Investigation, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Maya Chopra

23 papers receiving 400 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maya Chopra United States 11 174 151 110 57 51 25 406
Eugênia Ribeiro Valadares Brazil 12 148 0.9× 149 1.0× 159 1.4× 21 0.4× 18 0.4× 38 433
Geetha Anand United Kingdom 13 105 0.6× 303 2.0× 34 0.3× 47 0.8× 36 0.7× 34 565
Cristina da Silva United States 12 218 1.3× 225 1.5× 43 0.4× 21 0.4× 22 0.4× 19 528
Mislen Bauer United States 10 84 0.5× 143 0.9× 269 2.4× 37 0.6× 17 0.3× 19 561
Susanne Gerit Kircher Austria 12 73 0.4× 81 0.5× 214 1.9× 15 0.3× 29 0.6× 48 420
G. Bartalini Italy 12 129 0.7× 111 0.7× 106 1.0× 43 0.8× 36 0.7× 16 332
Luigina Spaccini Italy 13 159 0.9× 208 1.4× 43 0.4× 11 0.2× 104 2.0× 47 455
Alina Kurolap Israel 12 118 0.7× 150 1.0× 89 0.8× 24 0.4× 61 1.2× 42 399
Kei Shioda Japan 14 82 0.5× 274 1.8× 125 1.1× 26 0.5× 40 0.8× 25 517
Karin Weiss Israel 13 190 1.1× 188 1.2× 86 0.8× 14 0.2× 26 0.5× 36 433

Countries citing papers authored by Maya Chopra

Since Specialization
Citations

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

Fields of papers citing papers by Maya Chopra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maya Chopra

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

All Works

20 of 20 papers shown
1.
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.
2.
Srivastava, Siddharth, Julie S. Cohen, Maya Chopra, et al.. (2024). Survey of the Landscape of Society Practice Guidelines for Genetic Testing of Neurodevelopmental Disorders. Annals of Neurology. 96(5). 900–913. 1 indexed citations
3.
Gable, Dustin L., Abigail Sveden, Maya Chopra, et al.. (2024). Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders. Annals of Clinical and Translational Neurology. 11(2). 251–262. 2 indexed citations
4.
Lewis, Sara A., Maya Chopra, Julie S. Cohen, et al.. (2024). Clinical Actionability of Genetic Findings in Cerebral Palsy. JAMA Pediatrics. 179(2). 3 indexed citations
5.
Planas‐Serra, Laura, Abigail Sveden, Amy Tam, et al.. (2024). Biallelic variants in RINT1 present as early-onset pure hereditary spastic paraplegia. Journal of Clinical Investigation. 134(17).
6.
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
7.
Rockowitz, Shira, Ted Lee, Bo Zhang, et al.. (2023). Toward representative genomic research: the children’s rare disease cohorts experience. PubMed. 4. 921091166–921091166. 3 indexed citations
8.
Chopra, Maya, Meera E. Modi, Kira A. Dies, et al.. (2022). GENE TARGET: A framework for evaluating Mendelian neurodevelopmental disorders for gene therapy. Molecular Therapy — Methods & Clinical Development. 27. 32–46. 5 indexed citations
9.
Chopra, Maya, Richard Caswell, Giulia Barcia, et al.. (2022). Mild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1. European Journal of Human Genetics. 30(8). 960–966. 1 indexed citations
10.
Chan, Nicholas, et al.. (2021). Sex Differences in Coronary Arterial Calcification in Symptomatic Patients. The American Journal of Cardiology. 149. 16–20. 12 indexed citations
11.
Bayat, Allan, Sumaiya Iqbal, Jeanne Amiel, et al.. (2021). PRICKLE2 revisited—further evidence implicating PRICKLE2 in neurodevelopmental disorders. European Journal of Human Genetics. 29(8). 1235–1244. 7 indexed citations
12.
Xiong, Shiyi, et al.. (2018). A novel TSC2 missense variant associated with a variable phenotype of tuberous sclerosis complex: case report of a Chinese family. BMC Medical Genetics. 19(1). 90–90. 9 indexed citations
13.
Sun, Jun, Jason Pinner, Zhihui Yan, et al.. (2016). Diaphragmatic Eventration in Sisters with Asparagine Synthetase Deficiency: A Novel Homozygous ASNS Mutation and Expanded Phenotype. JIMD Reports. 34. 1–9. 23 indexed citations
14.
Chong, Jessica X., Viviana Caputo, Ian G. Phelps, et al.. (2016). Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy. The American Journal of Human Genetics. 98(4). 772–781. 39 indexed citations
15.
Xiong, Shiyi, David Chitayat, Wei Xing, et al.. (2016). A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome. Clinical Dysmorphology. 25(4). 186–189. 1 indexed citations
16.
Chopra, Maya, et al.. (2015). Unusual cause of hyperbilirubinaemia in a preterm baby. Journal of Paediatrics and Child Health. 51(12). 1226–1227. 3 indexed citations
17.
Cardamone, Michael, Danny Flanagan, David Mowat, et al.. (2014). Mammalian Target of Rapamycin Inhibitors for Intractable Epilepsy and Subependymal Giant Cell Astrocytomas in Tuberous Sclerosis Complex. The Journal of Pediatrics. 164(5). 1195–1200. 101 indexed citations
18.
Suri, Mohnish, Susan M. White, Nicole de Leeuw, et al.. (2011). Pierpont syndrome: A collaborative study. American Journal of Medical Genetics Part A. 155(9). 2203–2211. 13 indexed citations
19.
Rohrbach, Marianne, Anthony Vandersteen, Uluç Yiş, et al.. (2011). Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation. Orphanet Journal of Rare Diseases. 6(1). 46–46. 67 indexed citations
20.
Chopra, Maya, David J. Amor, L. E. Sutton, Elizabeth M. Algar, & David Mowat. (2010). Russell–Silver syndrome due to paternal H19/IGF2 hypomethylation in a patient conceived using intracytoplasmic sperm injection. Reproductive BioMedicine Online. 20(6). 843–847. 20 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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