Seema Kapoor

851 total citations
40 papers, 283 citations indexed

About

Seema Kapoor is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Seema Kapoor has authored 40 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Seema Kapoor's work include Ubiquitin and proteasome pathways (4 papers), Porphyrin Metabolism and Disorders (3 papers) and Neonatal Health and Biochemistry (3 papers). Seema Kapoor is often cited by papers focused on Ubiquitin and proteasome pathways (4 papers), Porphyrin Metabolism and Disorders (3 papers) and Neonatal Health and Biochemistry (3 papers). Seema Kapoor collaborates with scholars based in India, Japan and Germany. Seema Kapoor's co-authors include Manisha Goyal, Kuldeep K. Saxena, Shrish C. Gupta, Ankur Singh, Rajesh Pandey, Monika Yadav, Nar Singh Chauhan, Gyanendra Kumar, Aashima Dabas and Sangeeta Yadav and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Medical Genetics.

In The Last Decade

Seema Kapoor

39 papers receiving 279 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Seema Kapoor India	11	157	62	38	37	34	40	283
Jane Fleming Australia	9	184 1.2×	111 1.8×	57 1.5×	29 0.8×	22 0.6×	30	348
Bret L. Bostwick United States	9	225 1.4×	215 3.5×	35 0.9×	29 0.8×	43 1.3×	17	414
Daniel R. Carvalho Brazil	11	164 1.0×	84 1.4×	57 1.5×	43 1.2×	30 0.9×	31	343
Altuğ Koç Türkiye	11	107 0.7×	157 2.5×	25 0.7×	80 2.2×	18 0.5×	53	356
Qi‐Lun Lai China	11	62 0.4×	41 0.7×	21 0.6×	31 0.8×	24 0.7×	37	295
Ichraf Kraoua Tunisia	9	112 0.7×	54 0.9×	50 1.3×	15 0.4×	17 0.5×	64	270
Enrico Alfei Italy	11	140 0.9×	160 2.6×	22 0.6×	58 1.6×	64 1.9×	25	333
Dalia Ghoneim United States	10	277 1.8×	125 2.0×	31 0.8×	19 0.5×	18 0.5×	15	409
Coralie Rummel Switzerland	8	196 1.2×	42 0.7×	34 0.9×	42 1.1×	27 0.8×	8	398

Countries citing papers authored by Seema Kapoor

Since Specialization

Citations

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

Fields of papers citing papers by Seema Kapoor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seema Kapoor

This figure shows the co-authorship network connecting the top 25 collaborators of Seema Kapoor. A scholar is included among the top collaborators of Seema Kapoor 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 Seema Kapoor. Seema Kapoor 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:

20 of 20 papers shown

Mishra, Devendra, et al.. (2025). Profile of Musculoskeletal Anomalies in Indian Children with Down Syndrome. Indian Pediatrics. 62(8). 599–604.

Kumar, Manish, Istaq Ahmad, Shakti Sagar, et al.. (2021). Generation of induced pluripotent stem cell line (IGIBi007-A) from a patient with a novel acromesomelic dysplasia, PRKG2 type (AMDP). Stem Cell Research. 53. 102340–102340. 2 indexed citations

Yadav, Monika, et al.. (2021). Mapping of the benzoate metabolism by human gut microbiome indicates food-derived metagenome evolution. Scientific Reports. 11(1). 5561–5561. 25 indexed citations

Díaz, Francisca, Miriam Aza‐Carmona, Lucia Sentchordi, et al.. (2020). Biallelic cGMP-dependent type II protein kinase gene (PRKG2) variants cause a novel acromesomelic dysplasia. Journal of Medical Genetics. 59(1). 28–38. 10 indexed citations

Gupta, Sunita, Anju Garg, Shyam Kishor Sah, et al.. (2019). Clinicoradiologic follow up of cherubism with aggressive characteristics: a series of 3 cases. Oral Surgery Oral Medicine Oral Pathology and Oral Radiology. 128(5). e191–e201. 3 indexed citations

Kantaputra, Piranit Nik, et al.. (2018). Split hand-foot malformation and a novel WNT10B mutation. European Journal of Medical Genetics. 61(7). 372–375. 10 indexed citations

Singh, Ankur, et al.. (2016). Early Recognition of Fibrodysplasia Ossificans Progressiva-Important For the Clinician. SHILAP Revista de lepidopterología. 1 indexed citations

Goyal, Manisha, et al.. (2015). Hypohidrotic ectodermal dysplasia with ankylosis of temporomandibular joint and cleft palate: A rare presentation. Contemporary Clinical Dentistry. 6(1). 110–110. 4 indexed citations

Kapoor, Seema, Manisha Goyal, Ankur Singh, & Uwe Kornak. (2015). The diagnostic dilemma of cutis laxa: A report of two cases with genotypic dissimilarity. Indian Journal of Dermatology. 60(5). 521–521. 4 indexed citations

10.

Kapoor, Seema, Nita Khurana, Miriam Entesarian, et al.. (2014). An Indian boy with griscelli syndrome type 2: Case report and review of literature. Indian Journal of Dermatology. 59(4). 394–394. 10 indexed citations

11.

Kapoor, Seema, et al.. (2012). Iptakalim: A novel multi-utility potassium channel opener. Journal of Pharmacology and Pharmacotherapeutics. 3(1). 12–14. 11 indexed citations

12.

Kapoor, Seema, et al.. (2011). Normative Data for Anthropometric Parameters Used in Delineation of Dysmorphic Features in North Indian Children. The Indian Journal of Pediatrics. 79(5). 619–631. 4 indexed citations

13.

Kapoor, Seema, Sharmila B. Mukherjee, Daraius Shroff, et al.. (2011). Case Reports. Indian Pediatrics. 48(9). 727–736. 10 indexed citations

14.

Abu‐Amero, Khaled K., et al.. (2011). Horizontal gaze palsy and progressive scoliosis due to a deleterious mutation inROBO3. Ophthalmic Genetics. 32(4). 231–236. 12 indexed citations

15.

Kumar, Gyanendra, et al.. (2011). Study of antinociceptive activity of SSRI (fluoxetine and escitalopram) and atypical antidepressants (venlafaxine and mirtazepine) and their interaction with morphine and naloxone in mice. Journal of Pharmacy And Bioallied Sciences. 3(3). 412–412. 29 indexed citations

16.

Goyal, Nidhi, et al.. (2010). Unsuspected Sacrococcygeal Teratoma in a Child Presenting with Autoimmune Hemolytic Anemia: A Case Report. European Journal of Pediatric Surgery. 20(5). 353–355. 3 indexed citations

17.

Shroff, Daraius, et al.. (2007). Familial calcific band-shaped keratopathy: Report of two new cases with early recurrence. Indian Journal of Ophthalmology. 55(1). 55–55. 10 indexed citations

18.

Kapoor, Seema, Medha Tatke, Sandeep Aggarwal, & Ashish Gupta. (2005). Beta-sarcoglycanopathy. The Indian Journal of Pediatrics. 72(1). 71–74. 5 indexed citations

19.

Kapoor, Seema, et al.. (2005). Pantothenate kinase associated neurodegeneration (Hallervorden — Spatz syndrome). The Indian Journal of Pediatrics. 72(3). 261–263. 6 indexed citations

20.

Kapoor, Seema, et al.. (2004). Malignant hypertension in a child with solitary functioning hydronephrotic kidney.. PubMed. 41(7). 728–30. 2 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.

Explore authors with similar magnitude of impact