Niru Chennagiri

2.5k total citations
6 papers, 271 citations indexed

About

Niru Chennagiri is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Niru Chennagiri has authored 6 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Niru Chennagiri's work include Genomics and Rare Diseases (3 papers), Cystic Fibrosis Research Advances (2 papers) and Prenatal Screening and Diagnostics (2 papers). Niru Chennagiri is often cited by papers focused on Genomics and Rare Diseases (3 papers), Cystic Fibrosis Research Advances (2 papers) and Prenatal Screening and Diagnostics (2 papers). Niru Chennagiri collaborates with scholars based in United States and Brazil. Niru Chennagiri's co-authors include Pontus Skoglund, David Reich, Swapan Mallick, Nick Patterson, María Cátira Bortolini, Tábita Hünemeier, Maria Luiza Petzl‐Erler, Francisco M. Salzano, Gregory J. Porreca and Stephanie Hallam and has published in prestigious journals such as Nature, Cancer Research and Scientific Reports.

In The Last Decade

Niru Chennagiri

6 papers receiving 260 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Niru Chennagiri United States	4	154	62	59	47	46	6	271
Avinash Arvind Rasalkar India	6	216 1.4×	89 1.4×	30 0.5×	143 3.0×	33 0.7×	11	373
Matthew C. Dulik United States	15	421 2.7×	103 1.7×	49 0.8×	163 3.5×	34 0.7×	28	647
Sameer Soi United States	6	324 2.1×	45 0.7×	23 0.4×	100 2.1×	44 1.0×	7	451
Ryan J. Bohlender United States	6	126 0.8×	35 0.6×	29 0.5×	49 1.0×	49 1.1×	7	220
Rodrigo Nores Argentina	9	104 0.7×	70 1.1×	33 0.6×	103 2.2×	25 0.5×	29	248
Karen Davis United States	5	247 1.6×	68 1.1×	28 0.5×	241 5.1×	23 0.5×	5	443
Stéphanie Plaza France	8	285 1.9×	145 2.3×	22 0.4×	55 1.2×	13 0.3×	13	393
Antonio González‐Martín Spain	14	420 2.7×	181 2.9×	82 1.4×	148 3.1×	99 2.2×	46	725
Natalia Volodko Russia	13	367 2.4×	151 2.4×	49 0.8×	284 6.0×	20 0.4×	28	685

Countries citing papers authored by Niru Chennagiri

Since Specialization

Citations

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

Fields of papers citing papers by Niru Chennagiri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Niru Chennagiri

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

All Works

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6 of 6 papers shown

1.

Basu, Gargi D., Niru Chennagiri, Turgut Dogruluk, et al.. (2024). Abstract PO5-13-06: Classifying HER2-low breast cancer using a combination of ERBB2 mRNA expression and altered genes. Cancer Research. 84(9_Supplement). PO5–13. 1 indexed citations

2.

Chennagiri, Niru, Eric J. White, Daniel S. Lieber, et al.. (2016). Orthogonal NGS for High Throughput Clinical Diagnostics. Scientific Reports. 6(1). 24650–24650. 11 indexed citations

3.

Skoglund, Pontus, Swapan Mallick, María Cátira Bortolini, et al.. (2015). Genetic evidence for two founding populations of the Americas. Nature. 525(7567). 104–108. 197 indexed citations

4.

Hallam, Stephanie, Heather H. Nelson, Valerie Greger, et al.. (2014). Validation for Clinical Use of, and Initial Clinical Experience with, a Novel Approach to Population-Based Carrier Screening using High-Throughput, Next-Generation DNA Sequencing. Journal of Molecular Diagnostics. 16(2). 180–189. 31 indexed citations

5.

Hallam, Stephanie, et al.. (2013). Carrier screening of 8,500 IVF patients utilizing next generation DNA sequencing detects common, rare and otherwise undetectable mutations across society-recommended diseases. Fertility and Sterility. 100(3). S479–S480. 1 indexed citations

6.

Umbarger, Mark A., Caleb J. Kennedy, Niru Chennagiri, et al.. (2013). Next-generation carrier screening. Genetics in Medicine. 16(2). 132–140. 30 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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