Sampath Arepalli

16.3k total citations · 1 hit paper
23 papers, 1.9k citations indexed

About

Sampath Arepalli is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Sampath Arepalli has authored 23 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Physiology. Recurrent topics in Sampath Arepalli's work include Genetic Associations and Epidemiology (6 papers), Alzheimer's disease research and treatments (6 papers) and Neurological diseases and metabolism (3 papers). Sampath Arepalli is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Alzheimer's disease research and treatments (6 papers) and Neurological diseases and metabolism (3 papers). Sampath Arepalli collaborates with scholars based in United States, United Kingdom and Sweden. Sampath Arepalli's co-authors include J. Raphael Gibbs, Dena Hernández, Andrew Singleton, Mark Cookson, Bryan J. Traynor, Dan L. Longo, Allissa Dillman, John Hardy, Juan C. Troncoso and Michael A. Nalls and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Brain.

In The Last Decade

Sampath Arepalli

22 papers receiving 1.8k 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.

Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain

2010 536 citations J. Raphael Gibbs, Marcel P. van der Brug et al. PLoS Genetics profile →

Peers

Countries citing papers authored by Sampath Arepalli

Since Specialization

Citations

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

Fields of papers citing papers by Sampath Arepalli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sampath Arepalli

This figure shows the co-authorship network connecting the top 25 collaborators of Sampath Arepalli. A scholar is included among the top collaborators of Sampath Arepalli 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 Sampath Arepalli. Sampath Arepalli 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	Ivermectin as a Treatment Modality in COVID-19 Patients: A Systematic Review and Meta-Analysis of Up-To-Date RCTs 2025 ·Indian Journal of Community Medicine ·(unknown), (unknown), (unknown), Sampath Arepalli	0
2	Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging 2017 ·Scientific Reports ·Allissa Dillman, Elisa Majounie, Jinhui Ding, J. Raphael Gibbs, Dena Hernández, Sampath Arepalli, Bryan J. Traynor, Andrew Singleton, Dagmar Galter, Mark Cookson	35
3	Genetics of Hereditary Ataxia in Scottish Terriers 2017 ·Journal of Veterinary Internal Medicine ·(unknown), Dahlia M. Nielsen, Andrew Singleton, Sampath Arepalli, Dena Hernández, Cary S. Agler, Natasha J. Olby	3
4	Genome-wide assessment of Parkinson's disease in a Southern Spanish population 2016 ·Neurobiology of Aging ·Sara Bandrés‐Ciga, (unknown), Francisco Javier Barrero, Francisco Escamilla‐Sevilla, (unknown), Sampath Arepalli, Dena Hernández, Blanca Gutiérrez, Jorge A. Cervilla, Margarita Rivera, Alberto Rivera, (unknown), Francisco Vives, Michael A. Nalls, Andrew Singleton, Raquel Durán	30
5	Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24 2014 ·PLoS Genetics ·(unknown), Dahlia M. Nielsen, (unknown), Andrew Singleton, Noriko Tonomura, Snævar Sigurðsson, Ruqi Tang, Keith E. Linder, Sampath Arepalli, Dena G. Hernandez, Kerstin Lindblad‐Toh, Joyce van de Leemput, Alison A. Motsinger‐Reif, Dennis P. O’Brien, Jerold S. Bell, Tonya Harris, Steven J. Steinberg, Natasha J. Olby	35
6	Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies 2013 ·Nucleic Acids Research ·Adaikalavan Ramasamy, Daniah Trabzuni, J. Raphael Gibbs, Allissa Dillman, Dena Hernández, Sampath Arepalli, Robert Walker, Colin Smith, (unknown), Andrey A. Shabalin, Yun Li, Andrew B. Singleton, Mark Cookson, John Hardy, Mina Ryten, Michael E. Weale	66
7	Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain 2012 ·Neurobiology of Disease ·Dena Hernández, Mike A. Nalls, Matthew Moore, Sean Chong, Allissa Dillman, Daniah Trabzuni, J. Raphael Gibbs, Mina Ryten, Sampath Arepalli, Michael E. Weale, Alan B. Zonderman, Juan C. Troncoso, Richard M. O’Brien, Robert Walker, Colin Smith, Stefania Bandinelli, Bryan J. Traynor, John Hardy, Andrew B. Singleton, Mark Cookson	100
8	Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease 2012 ·Brain ·Janel O. Johnson, J. Raphael Gibbs, André Mégarbané, J. Andoni Urtizberea, Dena Hernández, A. Reghan Foley, Sampath Arepalli, Amelie Pandraud, Javier Simón‐Sánchez, Peter T. Clayton, Mary M. Reilly, Francesco Muntoni, Yevgeniya Abramzon, Henry Houlden, Andrew Singleton	99
9	MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies 2012 ·Human Molecular Genetics ·Daniah Trabzuni, Selina Wray, Jana Vandrovcová, Adaikalavan Ramasamy, Robert Walker, Colin Smith, (unknown), J. Raphael Gibbs, Allissa Dillman, Dena Hernández, Sampath Arepalli, Andrew Singleton, Mark Cookson, Alan Pittman, Rohan de Silva, Michael E. Weale, John Hardy, Mina Ryten	169
10	Genome-wide association study confirms extant PD risk loci among the Dutch 2011 ·European Journal of Human Genetics ·Javier Simón‐Sánchez, Jacobus J. van Hilten, (unknown), Bart Post, Henk W. Berendse, Sampath Arepalli, (unknown), Rob M.A. de Bie, Daan C. Velseboer, Hans Scheffer, Bas R. Bloem, (unknown), Fernando Rivadeneira, (unknown), André G. Uitterlinden, Patrizia Rizzu, Zoltán Bochdanovits, Andrew B. Singleton, Peter Heutink	146
11	Distinct DNA methylation changes highly correlated with chronological age in the human brain 2011 ·Human Molecular Genetics ·Dena Hernández, Michael A. Nalls, J. Raphael Gibbs, Sampath Arepalli, Marcel van der Brug, Sean Chong, Matthew Moore, Dan L. Longo, Mark Cookson, Bryan J. Traynor, Andrew Singleton	281
12	Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients 2010 ·Proceedings of the National Academy of Sciences ·Bryan J. Traynor, Michael A. Nalls, (unknown), J. Raphael Gibbs, Jennifer C. Schymick, Sampath Arepalli, Dena Hernandez, Marcel P. van der Brug, Janel O. Johnson, Allissa Dillman, Mark Cookson, Cristina Moglia, Andrea Calvo, Gabriella Restagno, Gabriele Mora, Adriano Chiò	22
13	Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain breakdown → 2010 ·PLoS Genetics ·J. Raphael Gibbs, Marcel P. van der Brug, Dena Hernández, Bryan J. Traynor, Michael A. Nalls, (unknown), Sampath Arepalli, Allissa Dillman, Ian Rafferty, Juan C. Troncoso, Robert Johnson, H. Ronald Zielke, Luigi Ferrucci, Dan L. Longo, Mark Cookson, Andrew Singleton	536
14	Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs 2009 ·BMC Medical Genetics ·E. Blom, Vilmantas Giedraitis, Sampath Arepalli, Marian L. Hamshere, Omanma Adighibe, Alison Goate, Julie Williams, Lars Lannfelt, John Hardy, Fabienne Wavrant‐De Vrièze, Anna Glaser	3
15	Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown), Peter Holmans, Sampath Arepalli, Omanma Adighibe, Marian L. Hamshere, Margaret Gatz, Nancy L. Pedersen, Astrid Liv Mina Bergem, Michael J. Owen, Paul Hollingworth, Alison Goate, Julie Williams, Lars Lannfelt, John Hardy, Fabienne Wavrant‐De Vrièze, Anna Glaser	7
16	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data 2007 ·The Lancet Neurology ·Jennifer C. Schymick, Sonja W. Scholz, Hon‐Chung Fung, Angela Britton, Sampath Arepalli, J. Raphael Gibbs, Federica Lombardo, Mar Matarín, Dalia Kasperavičiūtė, Dena Hernández, Cynthia Crews, Lucie Bruijn, Jeffrey D. Rothstein, Gabriele Mora, Gabriella Restagno, Adriano Chiò, Andrew Singleton, John Hardy, Bryan J. Traynor	153
17	ABCA1 polymorphisms and Alzheimer's disease 2007 ·Neuroscience Letters ·Fabienne Wavrant‐De Vrièze, Danielle Compton, (unknown), Sampath Arepalli, Omanma Adighibe, Ling Li, Jordi Pérez‐Tur, John Hardy	27
18	Association of the dopamine receptor D4 (DRD4) gene 7‐repeat allele with children with attention‐deficit/hyperactivity disorder (ADHD): An update 2006 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Michele C. Gornick, Anjené Addington, Philip Shaw, Andrew J. Bobb, Wendy Sharp, Deanna Greenstein, Sampath Arepalli, F. Xavier Castellanos, Judith L. Rapoport	56
19	Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: A two-stage study 2005 ·Journal of the Neurological Sciences ·Liisa Myllykangas, Fabienne Wavrant‐De Vrièze, Tuomo Polvikoski, Irma‐Leena Notkola, Raimo Sulkava, Leena Niinistö, Steven D. Edland, Sampath Arepalli, Omanma Adighibe, Danielle Compton, John Hardy, Matti Haltia, Pentti J. Tienari	26
20	Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease 2005 ·Neurobiology of Aging ·Omanma Adighibe, Sampath Arepalli, Jaime Duckworth, John Hardy, Fabienne Wavrant‐De Vrièze	31

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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