Pragna I. Patel

12.9k total citations · 1 hit paper
116 papers, 7.9k citations indexed

About

Pragna I. Patel is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Pragna I. Patel has authored 116 papers receiving a total of 7.9k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 41 papers in Genetics and 40 papers in Cellular and Molecular Neuroscience. Recurrent topics in Pragna I. Patel's work include Hereditary Neurological Disorders (33 papers), Genomic variations and chromosomal abnormalities (19 papers) and Genetic Neurodegenerative Diseases (15 papers). Pragna I. Patel is often cited by papers focused on Hereditary Neurological Disorders (33 papers), Genomic variations and chromosomal abnormalities (19 papers) and Genetic Neurodegenerative Diseases (15 papers). Pragna I. Patel collaborates with scholars based in United States, Italy and France. Pragna I. Patel's co-authors include James R. Lupski, Pentao Liu, A. Craig Chinault, Sanjay I. Bidichandani, Parimal Das, Tetsuo Ashizawa, Carol A. Wise, Carlos A. Garcia, David W. Stockton and Rena N. D’Souza and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Pragna I. Patel

114 papers receiving 7.7k 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.

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1991 1.0k citations James R. Lupski, Pentao Liu et al. profile →

Peers

Countries citing papers authored by Pragna I. Patel

Since Specialization

Citations

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

Fields of papers citing papers by Pragna I. Patel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pragna I. Patel. 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 Pragna I. Patel. The network helps show where Pragna I. Patel may publish in the future.

Co-authorship network of co-authors of Pragna I. Patel

This figure shows the co-authorship network connecting the top 25 collaborators of Pragna I. Patel. A scholar is included among the top collaborators of Pragna I. Patel 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 Pragna I. Patel. Pragna I. Patel 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

#	Work	Indexed citations
1	Hypodontia: genetics and future Hypodontia: genetics and future perspectives 2015 ·SHILAP Revista de lepidopterología ·Trevor J. Pemberton, Parimal Das, Pragna I. Patel	1
2	The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis 2012 ·PLoS Genetics ·Chen Siang Ng, Ping Wu, John Foley, Anne Foley, Merry‐Lynn McDonald, Wen‐Tau Juan, Chih-Jen Huang, Yu-Ting Lai, (unknown), Chih-Feng Chen, Suzanne M. Leal, Huanmin Zhang, Randall B. Widelitz, Pragna I. Patel, Wen‐Hsiung Li, Cheng‐Ming Chuong	75
3	A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia 2010 ·Clinical Genetics ·(unknown), (unknown), Shifra Ben‐Dor, Catalina González‐Quevedo, Kwanghyuk Lee, Yuya Kobayashi, Jaana Hartiala, (unknown), (unknown), Hooman Allayee, Pragna I. Patel	10
4	Tooth dimensions in hypodontia with a known PAX9 mutation 2008 ·Archives of Oral Biology ·A.H. Brook, Claire Elcock, (unknown), (unknown), Jean Russell, Pragna I. Patel, Richard Smith	40
5	Inherited Dental Anomalies: A Review and Prospects for the Future Role of Clinicians 2007 ·Journal of the California Dental Association ·Trevor J. Pemberton, (unknown), (unknown), Pragna I. Patel	9
6	Allele-specific germ cell epimutation in the spacer promoter of the gene after Cr(III) exposure 2004 ·Toxicology and Applied Pharmacology ·Yih‐Horng Shiao, Ellen Crawford, (unknown), Pragna I. Patel, Ko Ko	35
7	Competitive Binding of Triplex-Forming Oligonucleotides in the Two Alternate Promoters of the PMP22 Gene 2001 ·Antisense and Nucleic Acid Drug Development ·(unknown), Sanjay I. Bidichandani, Michael E. Hogan, Pragna I. Patel	13
8	Assignment<footref rid="foot01"><sup>1</sup></footref> of β-centractin (CTRN2) to human chromosome 2 bands q11.1→q11.2 with somatic cell hybrids and in situ hybridization 1999 ·Cytogenetic and Genome Research ·Sarah H. Elsea, (unknown), Ramesh C. Juyal, (unknown), David I. Meyer, Pragna I. Patel	1
9	Reply to Callen 1998 ·The American Journal of Human Genetics ·Sanjay I. Bidichandani, Antonio Baldini, Pragna I. Patel	1
10	Cloning of a human “epidermal-type” 12-lipoxygenase-related gene and chromosomal localization to 17p13 1998 ·Cytogenetic and Genome Research ·Daxi Sun, Sarah H. Elsea, Pragna I. Patel, Colin Funk	23
11	Definition of the critical interval for Smith-Magenis syndrome 1997 ·Cytogenetic and Genome Research ·Sarah H. Elsea, Smita M. Purandare, (unknown), Ramesh C. Juyal, Jessica G. Davis, Brenda Finucane, R.E. Magenis, Pragna I. Patel	25
12	Mosaicism for del(17) (p11.2p11.2) underlying the Smith-Magenis syndrome 1996 ·American Journal of Medical Genetics ·Ramesh C. Juyal, Akira Kuwano, (unknown), Federico Zara, Antonio Baldini, Pragna I. Patel	20
13	Ubiquitous and Neuronal DNA-Binding Proteins Interact with a Negative Regulatory Element of the Human Hypoxanthine Phosphoribosyltransferase Gene 1995 ·Molecular and Cellular Biology ·Diego E. Rincón-Limas, Felipe Amaya‐Manzanares, (unknown), Yongjia Yu, Thomas P. Yang, Pragna I. Patel	9
14	Mapping of genes predisposing to idiopathic generalized epilepsy 1995 ·Human Molecular Genetics ·Federico Zara, (unknown), G. Avanzini, Stefano Di Donato, Barbara Castellotti, Pragna I. Patel, Massimo Pandolfo	93
15	Smith‐Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization 1995 ·American Journal of Medical Genetics ·Ramesh C. Juyal, Frank Greenberg, (unknown), James R. Lupski, Barbara J. Trask, Ger van den Engh, Elizabeth A. Lindsay, (unknown), Ken‐Shiung Chen, Antonio Baldini, Lisa G. Shaffer, Pragna I. Patel	22
16	Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17 1994 ·Human Molecular Genetics ·Phillip F. Chance, Nacer Abbas, M. William Lensch, Pentao Liu, Benjamin B. Roa, Pragna I. Patel, James R. Lupski	253
17	Stable inheritance of the CMT1A DNA duplication in two patients with CMT1 and NF1 1993 ·American Journal of Medical Genetics ·James R. Lupski, Pentao Liu, Lowell L. Williams, Pragna I. Patel	26
18	Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia 1993 ·Schizophrenia Research ·Alan R. Sanders, Diego E. Rincón-Limas, Ranajit Chakraborty, Bernard Grandchamp, Joseph D. Hamilton, William E. Fann, Pragna I. Patel	21
19	Identification of Disease Genes and Somatic Gene Therapy: An Overview and Prospects for the Aged 1993 ·Journal of Gerontology ·Pragna I. Patel	6
20	Molecular characterization of a patient with del(1)(q23–q25) 1991 ·Human Genetics ·Brunella Franco, Li-Wen Lai, David Patterson, David H. Ledbetter, Barbara J. Trask, Ger van den Engh, Susan T. Iannaccone, (unknown), Pragna I. Patel, James R. Lupski	24

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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