Deepali N. Shinde

2.6k total citations
22 papers, 889 citations indexed

About

Deepali N. Shinde is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Deepali N. Shinde has authored 22 papers receiving a total of 889 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Deepali N. Shinde's work include Genomics and Rare Diseases (11 papers), Genetic factors in colorectal cancer (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Deepali N. Shinde is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genetic factors in colorectal cancer (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Deepali N. Shinde collaborates with scholars based in United States, Germany and Austria. Deepali N. Shinde's co-authors include Sha Tang, Zöe Powis, Kelly D. Farwell Hagman, Katherine L. Helbig, Cameron Mroske, Shuwei Li, Ingo Helbig, Angelika Niemz, Tanya M. Ferguson and Norman Arnheim and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Analytical Chemistry.

In The Last Decade

Deepali N. Shinde

22 papers receiving 873 citations

Peers

Deepali N. Shinde

GENET

PMH

Tomonari Awaya Japan

Allison M. Keeler United States

John Wiseman Sweden

Rui Jorge Nobre Portugal

Ning Zhu China

Ninette Cohen United States

Sigrid Eckardt United States

Kimberly Goodspeed United States

Karen Woodward United States

Anna Sahakyan United States

Tomonari Awaya Japan

Deepali N. Shinde

691 ×1.3

180 ×0.4

GENET

70 ×0.5

50 ×0.6

PMH

48 ×0.6

Citations per year, relative to Deepali N. Shinde Deepali N. Shinde (= 1×) peers Tomonari Awaya

Countries citing papers authored by Deepali N. Shinde

Since Specialization

Citations

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

Fields of papers citing papers by Deepali N. Shinde

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deepali N. Shinde. 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 Deepali N. Shinde. The network helps show where Deepali N. Shinde may publish in the future.

Co-authorship network of co-authors of Deepali N. Shinde

This figure shows the co-authorship network connecting the top 25 collaborators of Deepali N. Shinde. A scholar is included among the top collaborators of Deepali N. Shinde 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 Deepali N. Shinde. Deepali N. Shinde 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

Towne, Meghan C., Mari Rossi, Jennifer M. Huang, et al.. (2022). Diagnostic testing laboratories are valuable partners for disease gene discovery: 5‐year experience with GeneMatcher. Human Mutation. 43(6). 772–781. 4 indexed citations

Shinde, Deepali N., et al.. (2021). Failure Analysis of a Wheel Hub of Formula Student Racing Car. Journal of The Institution of Engineers (India) Series D. 102(1). 73–78. 3 indexed citations

Powis, Zöe, Kelly D. Farwell Hagman, Kirsten Blanco, et al.. (2019). When moments matter: Finding answers with rapid exome sequencing. Molecular Genetics & Genomic Medicine. 8(2). e1027–e1027. 9 indexed citations

Smith, Erica D., Kirsten Blanco, Samin A. Sajan, et al.. (2019). A retrospective review of multiple findings in diagnostic exome sequencing: halF.A.re distinct and halF.A.re overlapping diagnoses. Genetics in Medicine. 21(10). 2199–2207. 61 indexed citations

Ng, Bobby G., Gege Xu, Deepali N. Shinde, et al.. (2018). Biallelic Mutations in FUT8 Cause a Congenital Disorder of Glycosylation with Defective Fucosylation. The American Journal of Human Genetics. 102(1). 188–195. 53 indexed citations

Sajan, Samin A., Jaya Ganesh, Deepali N. Shinde, et al.. (2018). Biallelic disruption of PKDCC is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic features. Journal of Medical Genetics. 56(12). 850–854. 14 indexed citations

Scheuerle, Angela E., et al.. (2018). An additional case of Hennekam lymphangiectasia–lymphedema syndrome caused by loss‐of‐function mutation in ADAMTS3. American Journal of Medical Genetics Part A. 176(12). 2858–2861. 9 indexed citations

Cohen, Julie S., Wendy Alcaraz, Deepali N. Shinde, et al.. (2017). Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy. American Journal of Medical Genetics Part A. 173(9). 2505–2510. 29 indexed citations

Chamberlin, Adam, Deepali N. Shinde, Maja Hempel, et al.. (2017). De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities. The American Journal of Human Genetics. 101(6). 1013–1020. 43 indexed citations

10.

Powis, Zöe, Igor D. Petrik, Julie S. Cohen, et al.. (2017). De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms. Clinical Genetics. 93(5). 1030–1038. 12 indexed citations

11.

Smith, Erica D., Kelly Radtke, Mari Rossi, et al.. (2017). Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Human Mutation. 38(5). 600–608. 68 indexed citations

12.

Helbig, Katherine L., Kelly D. Farwell Hagman, Deepali N. Shinde, et al.. (2016). Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy. Genetics in Medicine. 18(9). 898–905. 217 indexed citations

13.

Hagman, Kelly D. Farwell, Deepali N. Shinde, Cameron Mroske, et al.. (2016). Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine. 19(2). 224–235. 34 indexed citations

14.

Mroske, Cameron, Kristen Rasmussen, Deepali N. Shinde, et al.. (2015). Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalities. BMC Medical Genetics. 16(1). 102–102. 21 indexed citations

15.

Shinde, Deepali N., et al.. (2013). New evidence for positive selection helps explain the paternal age effect observed in achondroplasia. Human Molecular Genetics. 22(20). 4117–4126. 39 indexed citations

16.

Hickerson, Anna I., et al.. (2013). Simple System for Isothermal DNA Amplification Coupled to Lateral Flow Detection. PLoS ONE. 8(7). e69355–e69355. 67 indexed citations

17.

Qian, Jifeng, Tanya M. Ferguson, Deepali N. Shinde, et al.. (2012). Sequence dependence of isothermal DNA amplification via EXPAR. Nucleic Acids Research. 40(11). e87–e87. 104 indexed citations

18.

Tiemann‐Boege, Irene, Christina Curtis, Deepali N. Shinde, et al.. (2009). Product Length, Dye Choice, and Detection Chemistry in the Bead-Emulsion Amplification of Millions of Single DNA Molecules in Parallel. Analytical Chemistry. 81(14). 5770–5776. 14 indexed citations

19.

Qin, Jian, Peter Calabrese, Irene Tiemann‐Boege, et al.. (2007). The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes. PLoS Biology. 5(9). e224–e224. 52 indexed citations

20.

Lai, Yinglei, Deepali N. Shinde, Norman Arnheim, & Fengzhu Sun. (2003). The Mutation Process of Microsatellites During the Polymerase Chain Reaction. Journal of Computational Biology. 10(2). 143–155. 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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