Seema Thakur

864 total citations
42 papers, 452 citations indexed

About

Seema Thakur is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Seema Thakur has authored 42 papers receiving a total of 452 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 16 papers in Pediatrics, Perinatology and Child Health and 16 papers in Genetics. Recurrent topics in Seema Thakur's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Oral and Maxillofacial Pathology (4 papers). Seema Thakur is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Oral and Maxillofacial Pathology (4 papers). Seema Thakur collaborates with scholars based in India, United States and Germany. Seema Thakur's co-authors include Suraksha Agrawal, Manoj K. Pandey, Bhudev C. Das, Rajesh K. Grover, Ajay K. Yadav, Sanjay Gupta, Renu Saxena, Thomas Fothergill, Nicole Hertel and Rita-Eva Varga and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and International Journal of Gynecology & Obstetrics.

In The Last Decade

Seema Thakur

38 papers receiving 431 citations

Peers

Seema Thakur

GENET

IMMUN

PPCH

PHEOH

Jennifer Hebert United States

Kriti Mohan United States

Anita Wischmeijer Italy

Michail Spiliopoulos United States

Thomas A. Maher United States

Koh‐ichiro Yoshiura Japan

Elizabeth Wohler United States

Michael Michalec United States

Manuela Priolo Italy

Hala Taha Egypt

Jennifer Hebert United States

Seema Thakur

640 ×3.6

274 ×3.0

GENET

86 ×1.0

IMMUN

40 ×0.5

PPCH

37 ×0.5

PHEOH

Citations per year, relative to Seema Thakur Seema Thakur (= 1×) peers Jennifer Hebert

Countries citing papers authored by Seema Thakur

Since Specialization

Citations

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

Fields of papers citing papers by Seema Thakur

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seema Thakur

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

All Works

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20 of 20 papers shown

Thakur, Seema, Preeti Paliwal, & Kuldeep K. Saxena. (2023). Regions of homozygosity and a novel variant in Steel syndrome: An added dilemma to diagnosis. Journal of Postgraduate Medicine. 69(2). 99–101.

Thakur, Seema, et al.. (2021). Surgical Management of Impacted Supernumerary Tooth: A Case Series. International Journal of Clinical Pediatric Dentistry. 14(5). 726–729. 4 indexed citations

Thakur, Seema, et al.. (2021). Neu–Laxova's Syndrome: A Case Report of a Fetus with Novel Mutation in PHGDH Gene and a Literature Review. Journal of Pediatric Genetics. 12(3). 233–236.

Thakur, Seema, et al.. (2020). Fetal pulmonary choristoma: report of first case and literature review. Case Reports in Perinatal Medicine. 9(1). 1 indexed citations

Thakur, Seema, et al.. (2020). Prenatal Diagnosis of Bardet-Biedl Syndrome: A Case Study and Review of Literature. Journal of Fetal Medicine. 7(4). 301–306. 1 indexed citations

Thakur, Seema, et al.. (2016). Utility of gene expression signature in treatment decision of breast cancer. Translational Cancer Research. 5(7). 1 indexed citations

Bijarnia‐Mahay, Sunita, Sudha Kohli, Renu Saxena, et al.. (2016). Seventeen Novel Mutations in PCCA and PCCB Genes in Indian Propionic Acidemia Patients, and Their Outcomes. Genetic Testing and Molecular Biomarkers. 20(7). 373–382. 10 indexed citations

Thakur, Seema, Rajesh K. Grover, Sanjay Gupta, Ajay K. Yadav, & Bhudev C. Das. (2016). Identification of Specific miRNA Signature in Paired Sera and Tissue Samples of Indian Women with Triple Negative Breast Cancer. PLoS ONE. 11(7). e0158946–e0158946. 61 indexed citations

Thakur, Seema, et al.. (2016). Comparative evaluation of dexmedetomidine and midazolam-ketamine combination as sedative agents in pediatric dentistry: A double-blinded randomized controlled trial. Contemporary Clinical Dentistry. 7(2). 186–186. 21 indexed citations

10.

Thakur, Seema, et al.. (2016). Novel ATRX gene damaging missense mutation c.6740A>C segregates with profound to severe intellectual deficiency without alpha thalassaemia. The Indian Journal of Medical Research. 143(1). 43–43. 4 indexed citations

11.

Thakur, Seema, et al.. (2014). Dens invagination: A review of literature and report of two cases. Journal of Natural Science Biology and Medicine. 5(1). 218–218. 21 indexed citations

12.

Thakur, Seema, et al.. (2013). Talon cusp: A case report with management guidelines for practicing dentists. Dental Hypotheses. 4(2). 67–67. 9 indexed citations

13.

Athanasakis, Emmanouil, Sophie Dahoun, Ambroise Wonkam, et al.. (2013). Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations. European Journal of Medical Genetics. 56(8). 404–410. 7 indexed citations

14.

Thakur, Seema, et al.. (2013). Facial talon cusp on permanent maxillary canine: A rare dental anomaly. European Journal of General Dentistry. 2(3). 324–327. 8 indexed citations

15.

Kumar, Manisha, et al.. (2012). Prenatal sonographic evaluation and postnatal outcome of renal anomalies. Indian journal of human genetics. 18(1). 75–75. 4 indexed citations

16.

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

17.

Thakur, Seema, et al.. (2011). A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum. Molecular Cytogenetics. 4(1). 19–19. 9 indexed citations

18.

Thakur, Seema, et al.. (2011). ATR-X syndrome in two siblings with a novel mutation (c.6718C>T mutation in exon 31).. PubMed. 134. 483–6. 5 indexed citations

19.

Pandey, Manoj K., Seema Thakur, & Suraksha Agrawal. (2004). Lymphocyte immunotherapy and its probable mechanism in the maintenance of pregnancy in women with recurrent spontaneous abortion. Archives of Gynecology and Obstetrics. 269(3). 161–172. 74 indexed citations

20.

Thakur, Seema, et al.. (1996). A case of tuberculous infection of the placenta.. PubMed. 94(9). 355–6.

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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