Vidu Garg

8.9k total citations · 3 hit papers
106 papers, 5.8k citations indexed

About

Vidu Garg is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Vidu Garg has authored 106 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 56 papers in Epidemiology and 29 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Vidu Garg's work include Congenital heart defects research (64 papers), Congenital Heart Disease Studies (54 papers) and Cardiac Valve Diseases and Treatments (15 papers). Vidu Garg is often cited by papers focused on Congenital heart defects research (64 papers), Congenital Heart Disease Studies (54 papers) and Cardiac Valve Diseases and Treatments (15 papers). Vidu Garg collaborates with scholars based in United States, Canada and Japan. Vidu Garg's co-authors include Deepak Srivastava, Marie K. Schluterman, Isabelle N. King, R. Bowling Barnes, J. Ransom, Paul Grossfeld, Sara N. Koenig, Irfan S. Kathiriya, Madhumita Basu and Kunitaka Joo and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Circulation.

In The Last Decade

Vidu Garg

100 papers receiving 5.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in NOTCH1 cause aortic valve disease

2005 1.0k citations Vidu Garg et al. profile →
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

2003 878 citations Vidu Garg et al. profile →
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

2018 370 citations Vidu Garg, Seema Mital et al. Circulation profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vidu Garg United States	38	3.8k	2.5k	1.7k	1.6k	1.2k	106	5.8k
Craig T. Basson United States	41	4.4k 1.1×	1.9k 0.8×	2.7k 1.6×	1.4k 0.8×	1.3k 1.1×	87	7.9k
Grégor Andelfinger Canada	32	1.5k 0.4×	880 0.4×	1.4k 0.8×	901 0.6×	405 0.3×	96	3.2k
Atsuyoshi Takao Japan	33	2.0k 0.5×	2.2k 0.9×	1.3k 0.8×	1.8k 1.1×	554 0.5×	152	4.3k
Takayuki Morisaki Japan	34	2.1k 0.6×	399 0.2×	645 0.4×	501 0.3×	747 0.6×	154	3.7k
Akihiro Yasoda Japan	32	1.4k 0.4×	283 0.1×	710 0.4×	526 0.3×	777 0.6×	114	3.6k
Isao Shiraishi Japan	26	857 0.2×	883 0.4×	1.1k 0.6×	618 0.4×	172 0.1×	144	2.8k
Steve Jeffery United Kingdom	37	3.3k 0.9×	274 0.1×	1.4k 0.8×	349 0.2×	782 0.7×	94	6.5k
Sonia Alamowitch France	27	1000 0.3×	848 0.3×	378 0.2×	825 0.5×	362 0.3×	83	4.1k
Toshiaki Sano Japan	45	1.6k 0.4×	1.2k 0.5×	165 0.1×	702 0.4×	497 0.4×	219	6.1k
Leslie Smoot United States	23	1.9k 0.5×	384 0.2×	890 0.5×	243 0.2×	437 0.4×	45	3.0k

Countries citing papers authored by Vidu Garg

Since Specialization

Citations

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

Fields of papers citing papers by Vidu Garg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vidu Garg

This figure shows the co-authorship network connecting the top 25 collaborators of Vidu Garg. A scholar is included among the top collaborators of Vidu Garg 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 Vidu Garg. Vidu Garg 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

Zhang, Bingyu, Deepika Thacker, Ting Zhou, et al.. (2025). Cardiovascular post-acute sequelae of SARS-CoV-2 in children and adolescents: cohort study using electronic health records. Nature Communications. 16(1). 3445–3445. 2 indexed citations

Yasuhara, Jun, et al.. (2025). Genetics of Congenital Heart Disease. Clinics in Perinatology. 52(3). 589–608.

Yu, Yang, Cankun Wang, Shiqiao Ye, et al.. (2024). Abnormal Progenitor Cell Differentiation and Cardiomyocyte Proliferation in Hypoplastic Right Heart Syndrome. Circulation. 149(11). 888–891. 3 indexed citations

Yatsenko, Svetlana A., Cecilia Lo, Xinxiu Xu, et al.. (2024). Case Report: An association of left ventricular outflow tract obstruction with 5p deletions. Frontiers in Genetics. 15. 1451746–1451746. 1 indexed citations

Li, Ming, William L. Border, Sara Fitzgerald‐Butt, et al.. (2023). A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices. SHILAP Revista de lepidopterología. 1(1). 100814–100814. 9 indexed citations

Yasuhara, Jun, et al.. (2023). Congenital aortic valve stenosis: from pathophysiology to molecular genetics and the need for novel therapeutics. Frontiers in Cardiovascular Medicine. 10. 1142707–1142707. 4 indexed citations

Ye, Shiqiao, Cankun Wang, Zhaohui Xu, et al.. (2022). Impaired Human Cardiac Cell Development due to NOTCH1 Deficiency. Circulation Research. 132(2). 187–204. 31 indexed citations

Manivannan, Sathiyanarayanan, Xinmin Zhang, Karthik M. Kodigepalli, et al.. (2022). Single-cell transcriptomic profiling unveils dysregulation of cardiac progenitor cells and cardiomyocytes in a mouse model of maternal hyperglycemia. Communications Biology. 5(1). 820–820. 11 indexed citations

Backes, Carl H., Kevin D. Hill, Elaine L. Shelton, et al.. (2022). Patent Ductus Arteriosus: A Contemporary Perspective for the Pediatric and Adult Cardiac Care Provider. Journal of the American Heart Association. 11(17). e025784–e025784. 38 indexed citations

10.

Gordon, David, David Cunningham, Gloria Zender, et al.. (2022). Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery. PLoS Genetics. 18(6). e1010236–e1010236. 15 indexed citations

11.

Manivannan, Sathiyanarayanan, et al.. (2022). Single-Cell RNA Sequencing Reveals Novel Genes Regulated by Hypoxia in the Lung Vasculature. Journal of Vascular Research. 59(3). 163–175. 6 indexed citations

12.

Trask, Aaron J., et al.. (2021). Human Stem Cell Models of SARS-CoV-2 Infection in the Cardiovascular System. Stem Cell Reviews and Reports. 17(6). 2107–2119. 1 indexed citations

13.

Manivannan, Sathiyanarayanan, David Gordon, Gloria Zender, et al.. (2020). Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy. PLoS Genetics. 16(5). e1008639–e1008639. 19 indexed citations

14.

Basu, Madhumita, Jun‐yi Zhu, Stephanie LaHaye, et al.. (2017). Epigenetic mechanisms underlying maternal diabetes-associated risk of congenital heart disease. JCI Insight. 2(20). 66 indexed citations

15.

Mital, Seema, Kiran Musunuru, Vidu Garg, et al.. (2016). Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association. Circulation Cardiovascular Genetics. 9(5). 448–467. 57 indexed citations

16.

LaHaye, Stephanie, Jessica Bowman, Sara Fitzgerald‐Butt, et al.. (2015). Abstract 12295: Utilization of Whole-Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. Circulation. 132(suppl_3). 1 indexed citations

17.

Hinton, Robert B., Kim L. McBride, Steven B. Bleyl, et al.. (2015). Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach. PMC. 2 indexed citations

18.

Bonachea, Elizabeth, Gloria Zender, Peter White, et al.. (2014). Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve. BMC Medical Genomics. 7(1). 56–56. 43 indexed citations

19.

Acharya, Asha, Chetan P. Hans, Sara N. Koenig, et al.. (2011). Inhibitory Role of Notch1 in Calcific Aortic Valve Disease. PLoS ONE. 6(11). e27743–e27743. 95 indexed citations

20.

McBride, Kim L. & Vidu Garg. (2010). Impact of Mendelian inheritance in cardiovascular disease. Annals of the New York Academy of Sciences. 1214(1). 122–137. 12 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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