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Epigenomic impacts of meditative practices

Epigenomics, 2022-12, Vol.14 (24), p.1593-1608

Zahir, Farah R

2022

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Understanding environmental epigenomics in autism spectrum disorder: an interview with Farah R Zahir

Epigenomics, 2021-09, Vol.13 (17), p.1341-1345

Zahir, Farah R

2021

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Editorial on the Paper “The Epidemiology and Genetics of Hyperuricemia and Gout across Major Racial Groups: A Literature Review and Population Genetics Secondary Database Analysis” by Butler, Alghoubayshi and Roman

Journal of personalized medicine, 2022-08, Vol.12 (8), p.1331

Zahir, Farah R.

2022

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The Need for Precision Therapies as Determined by Genetic Signature for Cystic Fibrosis

Journal of personalized medicine, 2021-12, Vol.11 (12), p.1353

Zahir, Farah R

2021

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Recent Major Transcriptomics and Epitranscriptomics Contributions toward Personalized and Precision Medicine

Journal of personalized medicine, 2022-02, Vol.12 (2), p.199

2022

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ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder

American journal of human genetics, 2017-12, Vol.101 (6), p.1021-1033

2017

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A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8

Journal of human genetics, 2019-04, Vol.64 (4), p.271-280

2019

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Epigenetic impacts on neurodevelopment: pathophysiological mechanisms and genetic modes of action

Pediatric research, 2011-05, Vol.69 (5 Pt 2), p.92R-100R

2011

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Maternal Prenatal Exposures in Pregnancy and Autism Spectrum Disorder: An Insight into the Epigenetics of Drugs and Diet as Key Environmental Influences

Advances in neurobiology, 2020, Vol.24, p.143-162

2020

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Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes

European journal of human genetics : EJHG, 2014-06, Vol.22 (6), p.792-800

2014

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A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation

Journal of genetic counseling, 2023-12, Vol.32 (6), p.1280-1287

2023

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Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Genetics in medicine, 2022-08, Vol.24 (8), p.1753-1760

2022

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Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

BMC genomics, 2017-05, Vol.18 (1), p.403-403, Article 403

2017

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First Whole Transcriptome RNAseq on CHD8 Haploinsufficient Patient and Meta-Analyses Across Cellular Models Uncovers Likely Key Pathophysiological Target Genes

Curēus (Palo Alto, CA), 2020-11

2020

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Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changes

American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2916-2926

2016

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Outcomes for Indigenous Children in Care Presenting at a Specialist Child and Youth Mental Health Service

Australian social work, 2022-01, Vol.75 (1), p.48-61

2022

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Direct oral anticoagulants for cancer‐associated venous thromboembolisms: a systematic review and network meta‐analysis

Internal medicine journal, 2022-02, Vol.52 (2), p.272-281

2022

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A retrospective analysis of the investigative practices of acute limb ischaemia presenting with an unknown aetiology

ANZ journal of surgery, 2022-03, Vol.92 (3), p.453-460

2022

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Environmental pathways affecting gene expression (E.PAGE) as an R package to predict gene-environment associations

Scientific reports, 2022-11, Vol.12 (1), p.18710-19, Article 18710

2022

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Protect peripheral intravenous catheters: a study protocol for a randomised controlled trial of a novel antimicrobial dressing for peripheral intravenous catheters (ProP trial)

BMJ open, 2024-07, Vol.14 (7), p.e084313

2024

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Prospective cohort study to evaluate the accuracy of sleep measurement by consumer-grade smart devices compared with polysomnography in a sleep disorders population

BMJ open, 2021-11, Vol.11 (11), p.e044015-e044015

2021

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De novo pathogenic DNM1L variant in a patient diagnosed with atypical hereditary sensory and autonomic neuropathy

Molecular genetics & genomic medicine, 2019-10, Vol.7 (10), p.e00961-n/a

2019

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Use of Affymetrix Arrays in the Diagnosis of Gene Copy‐Number Variation

Current Protocols in Human Genetics, 2015-04, Vol.85 (1), p.8.13.1-8.13.13

2015

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Epigenomic impacts of meditative practices

Understanding environmental epigenomics in autism spectrum disorder: an interview with Farah R Zahir

Editorial on the Paper “The Epidemiology and Genetics of Hyperuricemia and Gout across Major Racial Groups: A Literature Review and Population Genetics Secondary Database Analysis” by Butler, Alghoubayshi and Roman

The Need for Precision Therapies as Determined by Genetic Signature for Cystic Fibrosis

Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway

Recent Major Transcriptomics and Epitranscriptomics Contributions toward Personalized and Precision Medicine

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder

A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8

Epigenetic impacts on neurodevelopment: pathophysiological mechanisms and genetic modes of action

Maternal Prenatal Exposures in Pregnancy and Autism Spectrum Disorder: An Insight into the Epigenetics of Drugs and Diet as Key Environmental Influences

Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes

A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

First Whole Transcriptome RNAseq on CHD8 Haploinsufficient Patient and Meta-Analyses Across Cellular Models Uncovers Likely Key Pathophysiological Target Genes

Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changes

Outcomes for Indigenous Children in Care Presenting at a Specialist Child and Youth Mental Health Service

Direct oral anticoagulants for cancer‐associated venous thromboembolisms: a systematic review and network meta‐analysis

A retrospective analysis of the investigative practices of acute limb ischaemia presenting with an unknown aetiology

Environmental pathways affecting gene expression (E.PAGE) as an R package to predict gene-environment associations

Protect peripheral intravenous catheters: a study protocol for a randomised controlled trial of a novel antimicrobial dressing for peripheral intravenous catheters (ProP trial)

Prospective cohort study to evaluate the accuracy of sleep measurement by consumer-grade smart devices compared with polysomnography in a sleep disorders population

De novo pathogenic DNM1L variant in a patient diagnosed with atypical hereditary sensory and autonomic neuropathy

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization

Use of Affymetrix Arrays in the Diagnosis of Gene Copy‐Number Variation

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