Publications by authors named "Paras Garg"

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A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank.
Celine A Manigbas, Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee

Nat Commun· December 2024

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A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability.
Bharati Jadhav, Paras Garg, Joke J F A van Vugt, Kristina Ibanez, Delia Gagliardi

Nat Genet· November 2024

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Increased frequency of repeat expansion mutations across different populations.
Kristina Ibañez, Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Paras Garg

Nat Med· November 2024

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Increased frequency of repeat expansion mutations across different populations.
Kristina Ibañez, Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Paras Garg

medRxiv· July 2024

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A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank.
Celine A Manigbas, Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee

medRxiv· January 2024

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A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in as a significant cause of intellectual disability.
Bharati Jadhav, Paras Garg, Joke J F A van Vugt, Kristina Ibanez, Delia Gagliardi

medRxiv· December 2023

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Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylation.
Alejandro Martin-Trujillo, Paras Garg, Nihir Patel, Bharati Jadhav, Andrew J Sharp

Genome Res· February 2023

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Incident portal vein thrombosis in liver transplant recipients in New Zealand: Predictors of risk and validation of portal vein thrombosis risk index calculator.
Paras Garg, Barry Harrison, Edward J Gane

Front Transplant· December 2022

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Automated Bone Marrow Cell Classification for Haematological Disease Diagnosis Using Siamese Neural Network.
Balasundaram Ananthakrishnan, Ayesha Shaik, Shivam Akhouri, Paras Garg, Vaibhav Gadag

Diagnostics (Basel)· December 2022

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A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits.
Paras Garg, Bharati Jadhav, William Lee, Oscar L Rodriguez, Alejandro Martin-Trujillo

Am J Hum Genet· June 2022

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A comparison of intravenous methylprednisolone and hydrocortisone for the treatment of acute inflammatory bowel disease.
Cameron Schauer, Victoria Avery, Sam Seleq, Paras Garg, Michael T M Wang

J Gastroenterol Hepatol· October 2021

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Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression.
Paras Garg, Alejandro Martin-Trujillo, Oscar L Rodriguez, Scott J Gies, Elina Hadelia

Am J Hum Genet· May 2021

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Is evaluation of non-HDL-C better than calculated LDL-C in CAD patients? MMIMSR experiences.
Gobardhan Kathariya, Jyoti Aggarwal, Paras Garg, Sonu Singh, Sajaad Manzoor

Indian Heart J· March 2021

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Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles.
Alejandro Martin-Trujillo, Nihir Patel, Felix Richter, Bharati Jadhav, Paras Garg

PLoS Genet· November 2020

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A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.
Paras Garg, Bharati Jadhav, Oscar L Rodriguez, Nihir Patel, Alejandro Martin-Trujillo

Am J Hum Genet· October 2020

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Virtual Reality Use for Symptom Management in Palliative Care: A Pilot Study to Assess User Perceptions.
Tracy Johnson, Laura Bauler, Duncan Vos, Alan Hifko, Paras Garg

J Palliat Med· September 2020

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Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype.
Michael S Breen, Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy

Am J Hum Genet· September 2020

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Screening for rare epigenetic variations in autism and schizophrenia.
Paras Garg, Andrew J Sharp

Hum Mutat· July 2019

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Predictors of non-attendance at outpatient endoscopy: a five-year multi-centre observational study from New Zealand.
Mehul Lamba, Yassar Alamri, Paras Garg, Chris Frampton, David Rowbotham

N Z Med J· June 2019

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A survey of inter-individual variation in DNA methylation identifies environmentally responsive co-regulated networks of epigenetic variation in the human genome.
Paras Garg, Ricky S Joshi, Corey Watson, Andrew J Sharp

PLoS Genet· October 2018

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Identification of rare de novo epigenetic variations in congenital disorders.
Mafalda Barbosa, Ricky S Joshi, Paras Garg, Alejandro Martin-Trujillo, Nihir Patel

Nat Commun· May 2018

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DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition.
Cyril J Peter, Laura K Fischer, Marija Kundakovic, Paras Garg, Mira Jakovcevski

Biol Psychiatry· November 2016

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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.
Ricky S Joshi, Paras Garg, Noah Zaitlen, Tuuli Lappalainen, Corey T Watson

Am J Hum Genet· September 2016

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Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans.
Javier Quilez, Audrey Guilmatre, Paras Garg, Gareth Highnam, Melissa Gymrek

Nucleic Acids Res· May 2016

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Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer's disease.
Corey T Watson, Panos Roussos, Paras Garg, Daniel J Ho, Nidha Azam

Genome Med· January 2016

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