Paras Garg

2.1k citations

20 papers · 1.0k indexed · h-index 13

Impact in

Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genetic Associations and Epidemiology
Molecular Biology
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics

Papers in

Genetics 15
- Genetic Associations and Epidemiology 7
- Genomic variations and chromosomal abnormalities 6
- Genetic Syndromes and Imprinting 4
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 2
Molecular Biology 14
- Epigenetics and DNA Methylation 12

Co-authors: Andrew J. Sharp Corey T. Watson Vahram Haroutunian Ricky S. Joshi Henrietta Szutorisz Joseph A. Landry Yasmin L. Hurd Daniel Ho
Journals: PLoS Genetics (3 papers)The American Journal of Human Genetics (3 papers)Biological Psychiatry (1 paper)European Journal of Human Genetics (1 paper)Nature Communications (1 paper)
Partner nations: United States United Kingdom Italy

In The Last Decade

Paras Garg

19 papers receiving 992 citations

Peers

Countries citing papers authored by Paras Garg

Since Specialization

Citations

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

Fields of papers citing papers by Paras Garg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Paras Garg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Paras Garg Line = papers co-authored together Paras Garg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank Nature Communications ·滕威, Bharati Jadhav, Paras Garg, Richard G. Doisneau, William Lee, María Dolores Arjona Carpintero, Alejandro Martin-Trujillo, Andrew J. Sharp	2024	5
2	Comprehensive Analysis of the Genetic Variation in the LPA Gene from Short-Read Sequencing SHILAP Revista de lepidopterología ·J O Hirsh, Людмила Тітомир, Paras Garg, 池内浩基, Massimiliano Rossi, Sebastian Schönherr, Stefan Blankenberg, Raphael Twerenbold, Tanja Zeller, Andreas Ziegler	2024	0
3	A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits The American Journal of Human Genetics ·Paras Garg, Bharati Jadhav, William Lee, Oscar L. Rodriguez, Alejandro Martin-Trujillo, Andrew J. Sharp	2022	12
4	Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylation Genome Research ·Alejandro Martin-Trujillo, Paras Garg, Nihir Patel, Bharati Jadhav, Andrew J. Sharp	2022	13
5	Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression The American Journal of Human Genetics ·Paras Garg, Alejandro Martin-Trujillo, Oscar L. Rodriguez, Rızvan Güven, Catharina Karlsson, Bharati Jadhav, Miten Jain, Benedict Paten, Andrew J. Sharp	2021	21
6	Virtual Reality Use for Symptom Management in Palliative Care: A Pilot Study to Assess User Perceptions Journal of Palliative Medicine ·Muhammad Hanif Aditya, Laura Bauler, Duncan Vos, I Mira, Paras Garg, B Ghanti, Yang Hongchao	2020	49
7	A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions The American Journal of Human Genetics ·Paras Garg, Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain, Bernd Koizar, Hugh E. Olsen, Benedict Paten, Beate Ritz, R. Frank Kooy, Jozef Gécz, Andrew J. Sharp	2020	33
8	Screening for rare epigenetic variations in autism and schizophrenia Human Mutation ·Paras Garg, Andrew J. Sharp	2019	11
9	A survey of inter-individual variation in DNA methylation identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome PLoS Genetics ·Paras Garg, Ricky S. Joshi, Corey T. Watson, Andrew J. Sharp	2018	39
10	DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition Biological Psychiatry ·Cyril Peter, Laura Fischer, Marija Kundaković, Paras Garg, Mira Jakovcevski, Aslihan Dincer, Ana C. Amaral, Edward I. Ginns, Marzena Galdzicka, Cyralene P. Bryce, Mugiyono Mugiyono, Deborah P. Waber, David J. Mokler, Renata Aldaz Portas, Frances A. Champagne, Douglas L. Rosene, Jill McGaughy, Andrew J. Sharp, Janina R. Galler, Schahram Akbarian	2016	101
11	Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans Nucleic Acids Research ·Javier Quilez, Audrey Guilmatre, Paras Garg, Gareth Highnam, Melissa Gymrek, Yaniv Erlich, Ricky S. Joshi, David Mittelman, Andrew J. Sharp	2016	100
12	Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease Genome Medicine ·Corey T. Watson, Panos Roussos, Paras Garg, Daniel Ho, S Keerthanapriya, Pavel Katsel, Vahram Haroutunian, Andrew J. Sharp	2016	146
13	Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure Neuropsychopharmacology ·Corey T. Watson, Henrietta Szutorisz, Paras Garg, H. T. Barker, Joseph A. Landry, Andrew J. Sharp, Yasmin L. Hurd	2015	131
14	The Effects of Childhood Malnutrition on DNA Methylation in Adulthood The FASEB Journal ·Laura Fischer, Cyril Peter, Paras Garg, Andrew J. Sharp, Schahram Akbarian, Janina R. Galler	2015	1
15	Comment on “Genomic Hypomethylation in the Human Germline Associates with Selective Structural Mutability in the Human Genome” PLoS Genetics ·Corey T. Watson, Paras Garg, Andrew J. Sharp	2013	3
16	Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts European Journal of Human Genetics ·Paras Garg, Kerstin U. Ludwig, Anne C. Böhmer, Michele Rubini, Régine P.M. Steegers‐Theunissen, Peter Mossey, Elisabeth Mangold, Andrew J. Sharp	2013	12
17	Dynamics of DNA Methylation in Recent Human and Great Ape Evolution PLoS Genetics ·Irene Hernando-Herraez, Javier Prado-Martinez, Paras Garg, Marcos Fernández-Callejo, Holger Heyn, Christina Hvilsom, Arcadi Navarro, Manel Esteller, Andrew J. Sharp, Tomàs Marquès‐Bonet	2013	93
18	DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation Human Molecular Genetics ·М Мөнхболд, Manisha Brahmachary, Paras Garg, Christelle Borel, 成美池田, Corey T. Watson, N. Simon Thomas, Andrew J. Sharp	2013	37
19	Epigenome-wide differences in pathology-free regions of multiple sclerosis–affected brains Nature Neuroscience ·Jimmy Huynh, Paras Garg, Tin Htwe Thin, Seungyeul Yoo, Ranjan Dutta, Bruce D. Trapp, Vahram Haroutunian, Jun Zhu, Michael Donovan, Andrew J. Sharp, Patrizia Casaccia	2013	187
20	Detection of Parent-of-Origin Specific Expression Quantitative Trait Loci by Cis-Association Analysis of Gene Expression in Trios PLoS ONE ·Paras Garg, Christelle Borel, Andrew J. Sharp	2012	10

About Paras Garg

Paras Garg is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Nutrition and Dietetics and Rheumatology, having authored 20 papers that have together received 1.0k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (12 papers), Genetic Associations and Epidemiology (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetic Syndromes and Imprinting (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers), Child Nutrition and Water Access (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Genetics (349 citations), Molecular Biology (655 citations), Developmental Neuroscience (39 citations), Pediatrics, Perinatology and Child Health (156 citations) and Biological Psychiatry (19 citations). Paras Garg has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Andrew J. Sharp, Corey T. Watson, Vahram Haroutunian, Ricky S. Joshi, Henrietta Szutorisz, Joseph A. Landry, Yasmin L. Hurd, Daniel Ho, Pavel Katsel and Panos Roussos. Their work appears in journals such as PLoS Genetics, The American Journal of Human Genetics, Biological Psychiatry, European Journal of Human Genetics and Nature Communications.

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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