Sujatha Jagadeesh

1.5k total citations
39 papers, 456 citations indexed

About

Sujatha Jagadeesh is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sujatha Jagadeesh has authored 39 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sujatha Jagadeesh's work include Prenatal Screening and Diagnostics (9 papers), Metabolism and Genetic Disorders (4 papers) and Lysosomal Storage Disorders Research (4 papers). Sujatha Jagadeesh is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Metabolism and Genetic Disorders (4 papers) and Lysosomal Storage Disorders Research (4 papers). Sujatha Jagadeesh collaborates with scholars based in India, United States and United Kingdom. Sujatha Jagadeesh's co-authors include Suresh Seshadri, Sheela Nampoothiri, Katta M. Girisha, Sudha Srinivasan, Osamu Sakamoto, Gandham SriLakshmi Bhavani, Shriraam Mahadevan, Kumarasamy Thangaraj, Priya Moorjani and Mohammed S. Mustak and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Sujatha Jagadeesh

35 papers receiving 439 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sujatha Jagadeesh India 12 178 165 72 61 58 39 456
Emily C. Lisi United States 13 142 0.8× 182 1.1× 123 1.7× 65 1.1× 64 1.1× 22 411
Aria Setoodeh Iran 13 140 0.8× 119 0.7× 64 0.9× 51 0.8× 60 1.0× 44 414
Sunita Bijarnia‐Mahay India 13 257 1.4× 128 0.8× 75 1.0× 133 2.2× 65 1.1× 63 522
Prajnya Ranganath India 11 150 0.8× 115 0.7× 84 1.2× 32 0.5× 56 1.0× 56 367
María Juliana Ballesta‐Martínez Spain 14 308 1.7× 274 1.7× 39 0.5× 82 1.3× 70 1.2× 33 569
Pilar Magoulas United States 15 383 2.2× 290 1.8× 57 0.8× 132 2.2× 71 1.2× 24 727
Michal Inbar‐Feigenberg Canada 10 191 1.1× 113 0.7× 111 1.5× 81 1.3× 63 1.1× 30 419
Ishwar C. Verma India 12 217 1.2× 162 1.0× 79 1.1× 111 1.8× 19 0.3× 47 558
Michael Volodarsky Israel 14 211 1.2× 141 0.9× 26 0.4× 58 1.0× 48 0.8× 30 546
Julie Neidich United States 17 270 1.5× 231 1.4× 31 0.4× 148 2.4× 74 1.3× 42 698

Countries citing papers authored by Sujatha Jagadeesh

Since Specialization
Citations

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

Fields of papers citing papers by Sujatha Jagadeesh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sujatha Jagadeesh

This figure shows the co-authorship network connecting the top 25 collaborators of Sujatha Jagadeesh. A scholar is included among the top collaborators of Sujatha Jagadeesh 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 Sujatha Jagadeesh. Sujatha Jagadeesh 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.
Harms, Frederike L., Christian Müller, Fanny Kortüm, et al.. (2025). Novel biallelic COL25A1 variants broaden the clinical spectrum from congenital cranial dysinnervation disorders to fetal lethal phenotypes. European Journal of Human Genetics. 33(12). 1616–1626.
2.
Bareke, Eric, Sanaa Choufani, Sujatha Jagadeesh, et al.. (2024). A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage. Molecular Genetics & Genomic Medicine. 12(2). e2402–e2402. 1 indexed citations
3.
Guillemyn, Brecht, Jan Willem Bek, Delfien Syx, et al.. (2023). A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract. Human Genetics. 142(3). 457–476. 4 indexed citations
4.
Rezaei, Maryam, Mónica Aguinaga‐Ríos, Jianhua Qian, et al.. (2021). Novel pathogenic variants in NLRP7 , NLRP5 , and PADI6 in patients with recurrent hydatidiform moles and reproductive failure. Clinical Genetics. 99(6). 823–828. 25 indexed citations
5.
Puri, Ratna Dua, Sujatha Jagadeesh, Sheela Nampoothiri, et al.. (2021). Late onset Pompe Disease in India – Beyond the Caucasian phenotype. Neuromuscular Disorders. 31(5). 431–441. 7 indexed citations
6.
Jagadeesh, Sujatha, et al.. (2020). Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family. Journal of Clinical Pathology. 74(10). 620–624. 4 indexed citations
7.
Nampoothiri, Sheela, Ratna Dua Puri, Neerja Gupta, et al.. (2020). Fabry disease in India: A multicenter study of the clinical and mutation spectrum in 54 patients. JIMD Reports. 56(1). 82–94. 16 indexed citations
8.
Girisha, Katta M., Sheela Nampoothiri, Kalpana Gowrishankar, et al.. (2018). Locus and allelic heterogeneity and phenotypic variability in Waardenburg syndrome. Clinical Genetics. 95(3). 398–402. 17 indexed citations
9.
Cho, Tae‐Joon, Shubha R. Phadke, Kalpana Gowrishankar, et al.. (2017). Additional three patients with Smith‐McCort dysplasia due to novel RAB33B mutations. American Journal of Medical Genetics Part A. 173(3). 588–595. 15 indexed citations
10.
Seshadri, Suresh, et al.. (2016). Usefulness of fetal autopsy in the diagnosis of blomstrand chondrodysplasia: a report of three cases. The Journal of Maternal-Fetal & Neonatal Medicine. 30(9). 1041–1044. 3 indexed citations
11.
Jagadeesh, Sujatha, et al.. (2015). Mutations in ARSB in MPS VI patients in India. SHILAP Revista de lepidopterología. 4. 53–61. 14 indexed citations
12.
Mahadevan, Shriraam, et al.. (2015). Congenital Hypothyroidism: Recent Indian data. Indian Journal of Endocrinology and Metabolism. 19(3). 436–436. 17 indexed citations
13.
Mahadevan, Shriraam, et al.. (2014). Normative data for stretched penile length in term neonates born in Tamil Nadu. Indian Journal of Endocrinology and Metabolism. 18(4). 585–586. 8 indexed citations
14.
Jagadeesh, Sujatha, et al.. (2013). Pyridoxine-dependent epilepsy owing to antiquitin deficiency — mutation in theALDH7A1gene. Paediatrics and International Child Health. 33(2). 113–115. 6 indexed citations
15.
Below, Jennifer E., Anita E. Beck, Heidi Gildersleeve, et al.. (2012). Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D. The American Journal of Human Genetics. 92(1). 150–156. 52 indexed citations
16.
Jagadeesh, Sujatha, et al.. (2012). Mucopolysaccharidoses type IV A (Morquio syndrome): A case series of three siblings. Journal of Indian Society of Pedodontics and Preventive Dentistry. 30(1). 66–66. 10 indexed citations
17.
Jagadeesh, Sujatha, et al.. (2010). Prenatal Diagnosis in Pericentric Inversion 6. International Journal of Human Genetics. 10(1-3). 175–178. 2 indexed citations
18.
Seshadri, Suresh, et al.. (2008). Perinatal outcome after multifetal pregnancy reduction. The Indian Journal of Pediatrics. 75(9). 907–909.
19.
Ramprasad, Vedam L., Jagadeesan Madhavan, Sakthivel Murugan, et al.. (2007). Retinoblastoma in India. Molecular Diagnosis & Therapy. 11(1). 63–70. 12 indexed citations
20.
Gopumadhavan, S., et al.. (1993). Protective Effect of Liv.52 on Alcohol‐Induced Fetotoxicity. Alcoholism Clinical and Experimental Research. 17(5). 1089–1092. 9 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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