Joseph S. Reddy

1.8k total citations
22 papers, 359 citations indexed

About

Joseph S. Reddy is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Joseph S. Reddy has authored 22 papers receiving a total of 359 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Physiology and 8 papers in Genetics. Recurrent topics in Joseph S. Reddy's work include Alzheimer's disease research and treatments (7 papers), Genetic Associations and Epidemiology (6 papers) and Genomics and Rare Diseases (4 papers). Joseph S. Reddy is often cited by papers focused on Alzheimer's disease research and treatments (7 papers), Genetic Associations and Epidemiology (6 papers) and Genomics and Rare Diseases (4 papers). Joseph S. Reddy collaborates with scholars based in United States, Belgium and South Korea. Joseph S. Reddy's co-authors include Nilüfer Ertekin‐Taner, Minerva M. Carrasquillo, Yan W. Asmann, Mariet Allen, Rosa Rademakers, Mark L. Lawrence, Dennis W. Dickson, Paul K. Crane, Thuy Nguyen and Owen A. Ross and has published in prestigious journals such as PLoS ONE, Genome biology and Frontiers in Microbiology.

In The Last Decade

Joseph S. Reddy

21 papers receiving 352 citations

Peers

Countries citing papers authored by Joseph S. Reddy

Since Specialization

Citations

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

Fields of papers citing papers by Joseph S. Reddy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph S. Reddy. 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 Joseph S. Reddy. The network helps show where Joseph S. Reddy may publish in the future.

Co-authorship network of co-authors of Joseph S. Reddy

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph S. Reddy. A scholar is included among the top collaborators of Joseph S. Reddy 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 Joseph S. Reddy. Joseph S. Reddy 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	CWH43 Variants Are Associated With Disease Risk and Clinical Phenotypic Measures in Patients With Normal Pressure Hydrocephalus 2023 ·Neurology Genetics ·Philip W. Tipton, (unknown), Alexandra I. Soto‐Beasley, Gregory S. Day, Sanjeet S. Grewal, Kaisorn L. Chaichana, (unknown), Colleen T. Ball, Michael G. Heckman, Launia J. White, Zachary Quicksall, Joseph S. Reddy, Vijay K. Ramanan, Prashanthi Vemuri, Benjamin D. Elder, Nilüfer Ertekin‐Taner, Owen A. Ross, Neill R. Graff‐Radford	7
2	Targeted plasma eQTL and pQTL to identify potential novel biomarkers for Alzheimer’s Disease in African Americans 2023 ·Alzheimer s & Dementia ·Joseph S. Reddy, (unknown), (unknown), Sarah Lincoln, Charlotte C.G. Ho, Julia E. Crook, Xue Wang, Kimberly G. Malphrus, Thuy Nguyen, (unknown), (unknown), John A. Lucas, Neill R. Graff‐Radford, Nilüfer Ertekin‐Taner, Minerva M. Carrasquillo	1
3	Serotype-identifying ions in Listeria monocytogenes using matrix-associated laser desorption ionization-time of flight mass spectrometry 2022 ·Heliyon ·Hossam Abdelhamed, Seong Won Nho, Si Won Kim, Joseph S. Reddy, Seong Bin Park, Tae Sung Jung, Mark L. Lawrence	3
4	Transcript levels in plasma contribute substantial predictive value as potential Alzheimer's disease biomarkers in African Americans 2022 ·EBioMedicine ·Joseph S. Reddy, (unknown), Sarah Lincoln, Charlotte C.G. Ho, Julia E. Crook, Xue Wang, Kimberly G. Malphrus, Thuy Nguyen, (unknown), Maria T. Greig‐Custo, John A. Lucas, Neill R. Graff‐Radford, Nilüfer Ertekin‐Taner, Minerva M. Carrasquillo	2
5	Association of DNA methylation from the temporal cortex and cerebellum with AD‐related neuropathology and biochemistry 2022 ·Alzheimer s & Dementia ·(unknown), Mariet Allen, Zachary Quicksall, Joseph S. Reddy, Minerva M. Carrasquillo, Xue Wang, Chia‐Chen Liu, Yu Yamazaki, Thuy Nguyen, Michael G. Heckman, Yuka A. Martens, Na Zhao, Michael DeTure, Melissa E. Murray, Takahisa Kanekiyo, Dennis W. Dickson, Guojun Bu, Nilüfer Ertekin‐Taner	1
6	Whole genome sequencing–based copy number variations reveal novel pathways and targets in Alzheimer's disease 2021 ·Alzheimer s & Dementia ·Ming Chen, Minghui Wang, Qian Wang, Ryan Neff, Erming Wang, Qi Shen, Joseph S. Reddy, Xue Wang, Mariet Allen, Nilüfer Ertekin‐Taner, Philip L. De Jager, David A. Bennett, Vahram Haroutunian, Eric E. Schadt, Bin Zhang	16
7	Latent trait modeling of tau neuropathology in progressive supranuclear palsy 2021 ·Acta Neuropathologica ·Naomi Kouri, Melissa E. Murray, Joseph S. Reddy, Daniel Serie, Alexandra I. Soto‐Beasley, Mariet Allen, Minerva M. Carrasquillo, Xue Wang, (unknown), Matthew Baker, Rosa Rademakers, Ryan J. Uitti, Neill R. Graff‐Radford, Zbigniew K. Wszołek, Gerard D. Schellenberg, Julia E. Crook, Nilüfer Ertekin‐Taner, Owen A. Ross, Dennis W. Dickson	6
8	Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studies 2021 ·PLoS ONE ·Daniel P. Wickland, Yingxue Ren, Jason P. Sinnwell, Joseph S. Reddy, Cyril Pottier, Vivekananda Sarangi, Minerva M. Carrasquillo, Owen A. Ross, Steven G. Younkin, Nilüfer Ertekin‐Taner, Rosa Rademakers, Matthew E. Hudson, Liudmila S. Mainzer, Joanna M. Biernacka, Yan W. Asmann	5
9	Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer’s disease 2021 ·Acta Neuropathologica Communications ·Joseph S. Reddy, Mariet Allen, Charlotte C.G. Ho, (unknown), (unknown), Zachary Quicksall, Xue Wang, (unknown), Tulsi Patel, (unknown), Thuy Nguyen, Kimberly G. Malphrus, Sarah Lincoln, Minerva M. Carrasquillo, Julia E. Crook, Takahisa Kanekiyo, Melissa E. Murray, Guojun Bu, Dennis W. Dickson, Nilüfer Ertekin‐Taner	14
10	Plasma Biomarkers of Alzheimer’s Disease in African Americans 2020 ·Journal of Alzheimer s Disease ·(unknown), Charlotte C.G. Ho, Kimberly G. Malphrus, Joseph S. Reddy, Thuy Nguyen, (unknown), Julia E. Crook, John A. Lucas, Neill R. Graff‐Radford, Minerva M. Carrasquillo, Nilüfer Ertekin‐Taner	18
11	Deciphering cellular transcriptional alterations in Alzheimer’s disease brains 2020 ·Molecular Neurodegeneration ·Xue Wang, Mariet Allen, Shaoyu Li, Zachary Quicksall, Tulsi Patel, (unknown), Joseph S. Reddy, Minerva M. Carrasquillo, Sarah Lincoln, Thuy Nguyen, Kimberly G. Malphrus, Dennis W. Dickson, Julia E. Crook, Yan W. Asmann, Nilüfer Ertekin‐Taner	32
12	MAPT haplotype–stratified GWAS reveals differential association for AD risk variants 2020 ·Alzheimer s & Dementia ·Samantha L. Strickland, Joseph S. Reddy, Mariet Allen, (unknown), Jeremy D. Burgess, (unknown), (unknown), Xue Wang, Minerva M. Carrasquillo, Joanna M. Biernacka, Gregory D. Jenkins, Shubhabrata Mukherjee, Kevin L. Boehme, Paul K. Crane, John S. K. Kauwe, Nilüfer Ertekin‐Taner	21
13	Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight 2019 ·Genome biology ·Mark Ebbert, Tanner Jensen, Karen Jansen‐West, Jonathon Sens, Joseph S. Reddy, Perry G. Ridge, John S. K. Kauwe, Véronique Belzil, Luc Pregent, Minerva M. Carrasquillo, Dirk Keene, Eric B. Larson, Paul K. Crane, Yan W. Asmann, Nilüfer Ertekin‐Taner, Steven G. Younkin, Owen A. Ross, Rosa Rademakers, Leonard Petrucelli, John Denis Fryer	108
14	TMEM106B haplotypes have distinct gene expression patterns in aged brain 2018 ·Molecular Neurodegeneration ·Yingxue Ren, Marka van Blitterswijk, Mariet Allen, Minerva M. Carrasquillo, Joseph S. Reddy, Xue Wang, Thomas G. Beach, Dennis W. Dickson, Nilüfer Ertekin‐Taner, Yan W. Asmann, Rosa Rademakers	25
15	Identification of missing variants by combining multiple analytic pipelines 2018 ·BMC Bioinformatics ·Yingxue Ren, Joseph S. Reddy, Cyril Pottier, Vivekananda Sarangi, Shulan Tian, Jason P. Sinnwell, Shannon K. McDonnell, Joanna M. Biernacka, Minerva M. Carrasquillo, Owen A. Ross, Nilüfer Ertekin‐Taner, Rosa Rademakers, Matthew E. Hudson, Liudmila S. Mainzer, Yan W. Asmann	6
16	Comparative Genomics and Transcriptional Analysis of Flavobacterium columnare Strain ATCC 49512 2017 ·Frontiers in Microbiology ·Hasan C. Tekedar, Attila Karsi, Joseph S. Reddy, Seong Won Nho, (unknown), Mark L. Lawrence	38
17	Comparative Proteomic Analysis of Cotton Fiber Development and Protein Extraction Method Comparison in Late Stage Fibers 2016 ·Proteomes ·Hana Mujahid, Ken Pendarvis, Joseph S. Reddy, Babi Ramesh Reddy Nallamilli, K. Raja Reddy, Bindu Nanduri, Zhaohua Peng	11
18	Transcriptome profile of a bovine respiratory disease pathogen: Mannheimia haemolytica PHL213 2012 ·BMC Bioinformatics ·Joseph S. Reddy, Ranjit Kumar, James Watt, Mark L. Lawrence, Shane C. Burgess, Bindu Nanduri	14
19	Listeria monocytogenes meningitis: case report. 1977 ·PubMed ·Joseph S. Reddy, (unknown), R. A. Leng, (unknown)	2
20	Vitamin A deficiency in calves. 1967 ·PubMed ·Joseph S. Reddy	2

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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