Jyotsna Sudi

2.1k total citations
14 papers, 1.5k citations indexed

About

Jyotsna Sudi is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Jyotsna Sudi has authored 14 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Cognitive Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Jyotsna Sudi's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Autism Spectrum Disorder Research (5 papers). Jyotsna Sudi is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Autism Spectrum Disorder Research (5 papers). Jyotsna Sudi collaborates with scholars based in United States, Italy and Netherlands. Jyotsna Sudi's co-authors include Susan L. Christian, William B. Dobyns, Camille W. Brune, Edwin H. Cook, Norma J. Nowak, Samer Karamohamed, Judith A. Badner, T. Conrad Gilliam, Revati Kumar and Donald F. Conrad and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Jyotsna Sudi

14 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jyotsna Sudi United States	13	1.0k	705	451	189	148	14	1.5k
Anne Moncla France	24	1.3k 1.3×	1.1k 1.5×	343 0.8×	185 1.0×	89 0.6×	38	1.9k
Laia Rodríguez‐Revenga Spain	23	1.4k 1.4×	873 1.2×	455 1.0×	356 1.9×	128 0.9×	87	1.9k
Britt‐Marie Anderlid Sweden	22	813 0.8×	607 0.9×	200 0.4×	209 1.1×	51 0.3×	56	1.3k
Susan Walker Canada	20	572 0.6×	466 0.7×	210 0.5×	153 0.8×	176 1.2×	48	1.1k
Zohreh Talebizadeh United States	17	1.0k 1.0×	973 1.4×	422 0.9×	123 0.7×	75 0.5×	31	1.7k
Bai-Lin Wu United States	21	1.4k 1.4×	1.0k 1.5×	646 1.4×	209 1.1×	67 0.5×	43	2.2k
Siddharth Srivastava United States	21	1000 1.0×	700 1.0×	392 0.9×	100 0.5×	143 1.0×	80	1.7k
Erwin Petek Austria	21	469 0.5×	669 0.9×	229 0.5×	155 0.8×	242 1.6×	60	1.5k
Tychele N. Turner United States	20	1.1k 1.1×	915 1.3×	530 1.2×	61 0.3×	82 0.6×	47	1.7k
Keiko Shimojima Japan	25	1.2k 1.2×	1.0k 1.5×	99 0.2×	218 1.2×	190 1.3×	125	1.9k

Countries citing papers authored by Jyotsna Sudi

Since Specialization

Citations

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

Fields of papers citing papers by Jyotsna Sudi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jyotsna Sudi

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

All Works

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14 of 14 papers shown

Nicodemus‐Johnson, Jessie, Katherine A. Naughton, Jyotsna Sudi, et al.. (2015). Genome-Wide Methylation Study Identifies an IL-13–induced Epigenetic Signature in Asthmatic Airways. American Journal of Respiratory and Critical Care Medicine. 193(4). 376–385. 82 indexed citations

Nicodemus‐Johnson, Jessie, Bharathi Laxman, Randi Stern, et al.. (2013). Maternal asthma and microRNA regulation of soluble HLA-G in the airway. Journal of Allergy and Clinical Immunology. 131(6). 1496–1503.e4. 40 indexed citations

Sajan, Samin A., Liliana Fernández, Sahar Esmaeeli Nieh, et al.. (2013). Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria. PLoS Genetics. 9(10). e1003823–e1003823. 62 indexed citations

Conti, Valerio, Carla Marini, Simone Gana, et al.. (2011). Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARX. American Journal of Medical Genetics Part A. 155(4). 892–897. 13 indexed citations

Bedoyan, Jirair K., Ravinesh A. Kumar, Jyotsna Sudi, et al.. (2010). Duplication 16p11.2 in a child with infantile seizure disorder. American Journal of Medical Genetics Part A. 152A(6). 1567–1574. 37 indexed citations

Kumar, Revati, Jyotsna Sudi, Camille W. Brune, et al.. (2009). A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. Journal of Medical Genetics. 47(2). 81–90. 39 indexed citations

Kumar, Ravinesh A., Christian R. Marshall, Judith A. Badner, et al.. (2009). Association and Mutation Analyses of 16p11.2 Autism Candidate Genes. PLoS ONE. 4(2). e4582–e4582. 73 indexed citations

Pavone, Piero, Martino Ruggieri, Jyotsna Sudi, et al.. (2009). Microcephaly, sensorineural deafness and Currarino triad with duplication–deletion of distal 7q. European Journal of Pediatrics. 169(4). 475–481. 19 indexed citations

Marsh, Eric D., Carl T. Fulp, Ernest Gomez, et al.. (2009). Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females. Brain. 132(6). 1563–1576. 157 indexed citations

10.

Babatz, Timothy D., Ravinesh A. Kumar, Jyotsna Sudi, William B. Dobyns, & Susan L. Christian. (2009). Copy number and sequence variants implicate APBA2 as an autism candidate gene. Autism Research. 2(6). 359–364. 31 indexed citations

11.

Najm, Juliane, Denise Horn, Isabella Wimplinger, et al.. (2008). Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics. 40(9). 1065–1067. 202 indexed citations

12.

Christian, Susan L., Camille W. Brune, Jyotsna Sudi, et al.. (2008). Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder. Biological Psychiatry. 63(12). 1111–1117. 216 indexed citations

13.

Sudi, Jyotsna, et al.. (2008). Coincidence of P-Insertion Sites and Breakpoints of Deletions Induced by Activating P Elements in Drosophila. Genetics. 179(1). 227–235. 4 indexed citations

14.

Kumar, Revati, Samer Karamohamed, Jyotsna Sudi, et al.. (2007). Recurrent 16p11.2 microdeletions in autism. Human Molecular Genetics. 17(4). 628–638. 487 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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