Vimla S. Aggarwal

5.2k total citations
34 papers, 1.0k citations indexed

About

Vimla S. Aggarwal is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Vimla S. Aggarwal has authored 34 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Vimla S. Aggarwal's work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital heart defects research (7 papers). Vimla S. Aggarwal is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital heart defects research (7 papers). Vimla S. Aggarwal collaborates with scholars based in United States, United Kingdom and Canada. Vimla S. Aggarwal's co-authors include Bernice E. Morrow, Laina Freyer, Brynn Levy, Jun Liao, David B. Goldstein, Slavé Petrovski, Gundula Povysil, Joseph Hostyk, Andrew S. Allen and Shari R. Lipner and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Internal Medicine and Nature Reviews Genetics.

In The Last Decade

Vimla S. Aggarwal

34 papers receiving 1.0k citations

Peers

Vimla S. Aggarwal

GENET

PPCH

EPIDE

SURGE

Kerry K. Brown United States

Tamar Tenne Israel

Duangrurdee Wattanasirichaigoon Thailand

Almuth Caliebe Germany

Thierry Vilboux United States

Khushnooda Ramzan Saudi Arabia

Rannar Airik United States

Christopher R. Futtner United States

Peter Gustavsson Sweden

Erawati V. Bawle United States

Kerry K. Brown United States

Vimla S. Aggarwal

532 ×1.0

914 ×2.5

GENET

322 ×1.4

PPCH

55 ×0.5

EPIDE

104 ×0.9

SURGE

Citations per year, relative to Vimla S. Aggarwal Vimla S. Aggarwal (= 1×) peers Kerry K. Brown

Countries citing papers authored by Vimla S. Aggarwal

Since Specialization

Citations

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

Fields of papers citing papers by Vimla S. Aggarwal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vimla S. Aggarwal. 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 Vimla S. Aggarwal. The network helps show where Vimla S. Aggarwal may publish in the future.

Co-authorship network of co-authors of Vimla S. Aggarwal

This figure shows the co-authorship network connecting the top 25 collaborators of Vimla S. Aggarwal. A scholar is included among the top collaborators of Vimla S. Aggarwal 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 Vimla S. Aggarwal. Vimla S. Aggarwal 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

Goldstein, Jennifer, Amanda Thomas‐Wilson, Emily Groopman, et al.. (2024). ClinGen variant curation expert panel recommendations for classification of variants in GAMT, GATM and SLC6A8 for cerebral creatine deficiency syndromes. Molecular Genetics and Metabolism. 142(1). 108362–108362. 4 indexed citations

Alkelai, Anna, Jessica L. Giordano, Chia‐Ling Nhan‐Chang, et al.. (2023). Investigation into the genetics of fetal congenital lymphatic anomalies. Prenatal Diagnosis. 43(6). 703–716. 14 indexed citations

Jain, Namrata G., Dina Ahram, Maddalena Marasà, et al.. (2022). Clinical Real-Time Genome Sequencing to Solve the Complex and Confounded Presentation of a Child With Focal Segmental Glomerulosclerosis and Multiple Malignancies. Kidney International Reports. 7(10). 2312–2316. 2 indexed citations

Sharma, Rahul K., Joseph Hostyk, Evan H. Baugh, et al.. (2022). Myosin Mutations and Sudden Sensorineural Hearing Loss: Results of Whole Exome Sequencing. Otology & Neurotology. 44(1). 16–20. 1 indexed citations

Rasouly, Hila Milo, Vimla S. Aggarwal, Louise Bier, David B. Goldstein, & Ali G. Gharavi. (2021). Cases in Precision Medicine: Genetic Testing to Predict Future Risk for Disease in a Healthy Patient. Annals of Internal Medicine. 174(4). 540–547. 4 indexed citations

Mellis, Rhiannon, Mark D. Kilby, ER Maher, et al.. (2021). Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?. BJOG An International Journal of Obstetrics & Gynaecology. 129(1). 52–61. 43 indexed citations

Cohen, Adi, Joseph Hostyk, Evan H. Baugh, et al.. (2021). Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosis. Bone. 154. 116253–116253. 16 indexed citations

Lippa, Natalie, et al.. (2021). A novel de novo KDM5C variant in a female with global developmental delay and ataxia: a case report. BMC Neurology. 21(1). 358–358. 5 indexed citations

Povysil, Gundula, Slavé Petrovski, Joseph Hostyk, et al.. (2019). Rare-variant collapsing analyses for complex traits: guidelines and applications. Nature Reviews Genetics. 20(12). 747–759. 109 indexed citations

10.

Wattacheril, Julia, Patrick R. Shea, Saeed Mohammad, et al.. (2018). Exome sequencing of an adolescent with nonalcoholic fatty liver disease identifies a clinically actionable case of Wilson disease. Molecular Case Studies. 4(5). a003087–a003087. 3 indexed citations

11.

Rotemberg, Veronica, Maria C. Garzón, Christine T. Lauren, et al.. (2017). A Novel Mutation in Junctional Plakoglobin Causing Lethal Congenital Epidermolysis Bullosa. The Journal of Pediatrics. 191. 266–269.e1. 6 indexed citations

12.

Sireci, Anthony, Vimla S. Aggarwal, Andrew T. Turk, et al.. (2016). Clinical Genomic Profiling of a Diverse Array of Oncology Specimens at a Large Academic Cancer Center. Journal of Molecular Diagnostics. 19(2). 277–287. 21 indexed citations

13.

Levy, Brynn, Styrmir Sigurjonsson, B. Pettersen, et al.. (2014). Genomic Imbalance in Products of Conception. Obstetrics and Gynecology. 124(2). 202–209. 158 indexed citations

14.

Northrop, Lesley E., et al.. (2014). Tetratricopeptide Repeat Domain 7A (TTC7A) Mutation in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency. Journal of Clinical Immunology. 34(6). 607–610. 24 indexed citations

15.

Kotsinas, Athanassios, Vimla S. Aggarwal, E‐Jean Tan, Brynn Levy, & Vassilis G. Gorgoulis. (2011). PIG3: A novel link between oxidative stress and DNA damage response in cancer. Cancer Letters. 327(1-2). 97–102. 51 indexed citations

16.

Aggarwal, Vimla S., et al.. (2010). Mesodermal Tbx1 is required for patterning the proximal mandible in mice. Developmental Biology. 344(2). 669–681. 36 indexed citations

17.

Braunstein, Evan M., et al.. (2009). Tbx1 and Brn4regulate retinoic acid metabolic genes during cochlear morphogenesis. BMC Developmental Biology. 9(1). 31–31. 31 indexed citations

18.

Liao, Jun, et al.. (2008). Identification of downstream genetic pathways of Tbx1 in the second heart field. Developmental Biology. 316(2). 524–537. 102 indexed citations

19.

Aggarwal, Vimla S. & Bernice E. Morrow. (2008). Genetic modifiers of the physical malformations in velo‐cardio‐facial syndrome/DiGeorge syndrome. PubMed. 14(1). 19–25. 42 indexed citations

20.

Aggarwal, Vimla S., Jun Liao, Thomas Schimmang, et al.. (2006). Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy. Human Molecular Genetics. 15(21). 3219–3228. 42 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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