Inder Gadi

3.9k total citations · 1 hit paper
39 papers, 3.0k citations indexed

About

Inder Gadi is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Inder Gadi has authored 39 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 22 papers in Molecular Biology and 9 papers in Plant Science. Recurrent topics in Inder Gadi's work include Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (9 papers) and Genetic Syndromes and Imprinting (7 papers). Inder Gadi is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (9 papers) and Genetic Syndromes and Imprinting (7 papers). Inder Gadi collaborates with scholars based in United States, India and Switzerland. Inder Gadi's co-authors include Colin L. Stewart, Susan J. Abbondanzo, Harshida Bhatt, Petr Kašpar, Frank Köntgen, Lisa J. Brunet, Ruth Sager, Margaret L. Harbison, Jeff Mann and Stuart Schwartz and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Inder Gadi

36 papers receiving 2.8k 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.

Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor

1992 1.6k citations Colin L. Stewart, Petr Kašpar et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Inder Gadi United States	19	1.3k	1.3k	977	744	491	39	3.0k
Harshida Bhatt United States	8	2.2k 1.7×	1.7k 1.3×	711 0.7×	957 1.3×	639 1.3×	9	4.2k
Masami Kanai‐Azuma Japan	33	2.7k 2.0×	320 0.2×	1.1k 1.1×	486 0.7×	396 0.8×	82	3.7k
Diana L. Carlone United States	24	1.1k 0.8×	269 0.2×	736 0.8×	161 0.2×	218 0.4×	39	2.1k
Kazuyuki Ohbo Japan	26	2.2k 1.7×	799 0.6×	971 1.0×	936 1.3×	919 1.9×	49	3.7k
Chikashi Tachi Japan	18	568 0.4×	420 0.3×	349 0.4×	184 0.2×	232 0.5×	85	1.2k
Anne Camus France	20	1.6k 1.2×	309 0.2×	387 0.4×	110 0.1×	201 0.4×	32	2.4k
K. John McLaughlin United States	29	2.8k 2.1×	165 0.1×	937 1.0×	359 0.5×	804 1.6×	58	3.6k
Tomonori Nakamura Japan	27	2.6k 2.0×	128 0.1×	677 0.7×	241 0.3×	686 1.4×	62	3.2k
David Karr United States	6	1.6k 1.2×	156 0.1×	358 0.4×	182 0.2×	227 0.5×	6	2.2k
Tomoyuki Tokunaga Japan	22	1.8k 1.3×	231 0.2×	582 0.6×	87 0.1×	363 0.7×	50	2.4k

Countries citing papers authored by Inder Gadi

Since Specialization

Citations

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

Fields of papers citing papers by Inder Gadi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inder Gadi

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

Arreola, Alexandra, Gloria Haskell, Inder Gadi, Andrea Penton, & Stuart Schwartz. (2024). Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomes. Genetics in Medicine. 26(12). 101275–101275.

Haskell, Gloria, Alexandra Arreola, Christine M. Riordan, et al.. (2024). Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes. Prenatal Diagnosis. 44(5). 586–594.

Haskell, Gloria, et al.. (2023). P479: Mosaicism for genome wide homozygosity identified as an incidental finding in two healthy pregnant women*. SHILAP Revista de lepidopterología. 1(1). 100526–100526. 1 indexed citations

Xu, Qiong, Jennifer Goldstein, Ping Wang, et al.. (2016). Chromosomal microarray analysis in clinical evaluation of neurodevelopmental disorders-reporting a novel deletion of SETDB1 and illustration of counseling challenge. Pediatric Research. 80(3). 371–381. 16 indexed citations

Atwal, Paldeep S., et al.. (2015). Mosaic paternal genome‐wide uniparental isodisomy with down syndrome. American Journal of Medical Genetics Part A. 167(10). 2463–2469. 26 indexed citations

Burnside, Rachel D., John Pappas, Stephanie Sacharow, et al.. (2013). Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype. American Journal of Medical Genetics Part A. 161(4). 822–828. 30 indexed citations

Weisfeld‐Adams, James D., Lisa Edelmann, Inder Gadi, & Lakshmi Mehta. (2012). Phenotypic heterogeneity in a family with a small atypical microduplication of chromosome 22q11.2 involving TBX1. European Journal of Medical Genetics. 55(12). 732–736. 21 indexed citations

Burnside, Rachel D., Romela Pasion, Fady M. Mikhail, et al.. (2011). Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Human Genetics. 130(4). 517–528. 182 indexed citations

Puvabanditsin, Surasak, et al.. (2009). Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review. American Journal of Medical Genetics Part A. 149A(8). 1782–1785. 4 indexed citations

10.

Mehta, Lakshmi, et al.. (2008). Ovotesticular Disorder of Sexual Development (True Hermaphroditism). Urology. 73(2). 293–296. 17 indexed citations

11.

Blanco, Enrique, J. Athene Lane, Patricia Galvin‐Parton, et al.. (2007). Glucose metabolism and insulin secretion in a patient with ABCC8 mutation and Fanconi–Bickel syndrome caused by maternal isodisomy of chromosome 3. Clinical Genetics. 71(6). 551–557. 25 indexed citations

12.

Stewart, Colin L., Inder Gadi, & Harshida Bhatt. (1994). Stem Cells from Primordial Germ Cells Can Reenter the Germ Line. Developmental Biology. 161(2). 626–628. 174 indexed citations

13.

Abbondanzo, Susan J., Inder Gadi, & Colin L. Stewart. (1993). [49] Derivation of embryonic stem cell lines. Methods in enzymology on CD-ROM/Methods in enzymology. 225. 803–823. 183 indexed citations

14.

Stewart, Colin L., Petr Kašpar, Lisa J. Brunet, et al.. (1992). Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor. Nature. 359(6390). 76–79. 1647 indexed citations breakdown →

15.

Mann, Jeff, Inder Gadi, Margaret L. Harbison, Susan J. Abbondanzo, & Colin L. Stewart. (1990). Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: Implications for genetic imprinting. Cell. 62(2). 251–260. 129 indexed citations

16.

González-Lavin, Lorenzo, Alan J. Spotnitz, James W. Mackenzie, et al.. (1990). Homograft valve durability: Host or donor influence?. Heart and Vessels. 5(2). 102–106. 8 indexed citations

17.

Segelman, Alvin B., et al.. (1988). Highly Purified Pheophorbide A As A Photosensitizer In Human Bladder Carcinoma In Vitro. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 847. 205–205. 9 indexed citations

18.

Lau, Ching C., et al.. (1985). Plasmid-induced "hit-and-run" tumorigenesis in Chinese hamster embryo fibroblast (CHEF) cells.. Proceedings of the National Academy of Sciences. 82(9). 2839–2843. 29 indexed citations

19.

Gadi, Inder, T. Sharma, & Rajiva Raman. (1982). Supernumerary chromosomes in Bandicota indica nemorivaga and a female individual with XX/XO mosaicism. Genetica. 58(2). 103–108. 5 indexed citations

20.

Sharma, T. & Inder Gadi. (1977). Constitutive heterochromatin variation in two species of rattus with apparently similar karyotypes. Genetica. 47(1). 77–80. 6 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