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Author Details
Full Name
Murray H Brilliant
Affiliation
Marshfield Clinic Research Institute
ORCID
Career Start Year
1983
Papers
167
H Index
44
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36548377
FMR1 CGG Repeats and Stress Influence Self-Reported Cognitive Functioning in Mothers.
Am J Intellect Dev Disabil
2023
38020121
Estimating the efficacy of pharmacogenomics over a lifetime.
Front Med (Lausanne)
2023
36982708
Heritable Risk and Protective Genetic Components of Glaucoma Medication Non-Adherence.
Int J Mol Sci
2023
34906516
Response to Timothé Ménard.
Genet Med
2022
35689224
Advancing artificial intelligence-assisted pre-screening for fragile X syndrome.
BMC Med Inform Decis Mak
2022
36238818
The effect of college degree attainment on neurodegenerative symptoms in genetically at-risk women.
SSM Popul Health
2022
34086673
Novel EDGE encoding method enhances ability to identify genetic interactions.
PLoS Genet
2021
36246950
Assessing Foveal Structure in Individuals with <i>TYR</i> R402Q and S192Y Hypomorphic Alleles.
Ophthalmol Sci
2021
33850243
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
NPJ Digit Med
2021
33772223
Artificial intelligence-assisted phenotype discovery of fragile X syndrome in a population-based sample.
Genet Med
2021
34967885
Prevalence of Underdiagnosed Fragile X Syndrome in 2 Health Systems.
JAMA Netw Open
2021
34213066
Health profiles of adults with autism spectrum disorder: Differences between women and men.
Autism Res
2021
34117786
Mild Neurological Signs in FMR1 Premutation Women in an Unselected Community-Based Cohort.
Mov Disord
2021
31386280
Development of an Integrated Platform Using Multidisciplinary Real-World Data to Facilitate Biomarker Discovery for Medical Products.
Clin Transl Sci
2020
32478017
<i>FMR1</i> Low Zone CGG Repeats: Phenotypic Associations in the Context of Parenting Stress.
Front Pediatr
2020
30414857
Novel locus for atopic dermatitis in African Americans and replication in European Americans.
J Allergy Clin Immunol
2019
31415684
Preliminary outcomes of preemptive warfarin pharmacogenetic testing at a large rural healthcare center.
Am J Health Syst Pharm
2019
31436842
Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis.
JAMA Ophthalmol
2019
31457090
Data-driven phenotype discovery of <i>FMR1</i> premutation carriers in a population-based sample.
Sci Adv
2019
30988330
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.
Sci Rep
2019
31160809
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2019
29273807
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
30240342
Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.
AJOB Empir Bioeth
2018
30166544
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.
Nat Commun
2018
29868121
Health Profiles of Mosaic Versus Non-mosaic <i>FMR1</i> Premutation Carrier Mothers of Children With Fragile X Syndrome.
Front Genet
2018
30398625
The Henle Fiber Layer in Albinism: Comparison to Normal and Relationship to Outer Nuclear Layer Thickness and Foveal Cone Density.
Invest Ophthalmol Vis Sci
2018
29392307
Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets.
Invest Ophthalmol Vis Sci
2018
29549330
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29549329
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29734508
Using machine learning to identify patterns of lifetime health problems in decedents with autism spectrum disorder.
Autism Res
2018
29590070
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.
Science
2018
28968884
Applying family analyses to electronic health records to facilitate genetic research.
Bioinformatics
2018
29053189
Pilot screening study of targeted genetic polymorphisms for association with seasonal influenza hospital admission.
J Med Virol
2018
27760082
Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample.
Menopause
2017
28190457
Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
Am J Hum Genet
2017
28146470
Rare and low-frequency coding variants alter human adult height.
Nature
2017
28416512
Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes.
Circ Cardiovasc Genet
2017
28490672
Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants.
Sci Transl Med
2017
29079728
PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.
Nat Commun
2017
28853718
Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis.
Eur J Hum Genet
2017
28667565
Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records.
J Genet Couns
2017
28903894
Prototype Development: Context-Driven Dynamic XML Ophthalmologic Data Capture Application.
JMIR Med Inform
2017
27908689
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.
Lancet Diabetes Endocrinol
2017
27611488
Identification of Four Novel Loci in Asthma in European American and African American Populations.
Am J Respir Crit Care Med
2017
26169577
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.
Pharmacogenomics J
2016
26587656
CYP2C19 and CES1 polymorphisms and efficacy of clopidogrel and aspirin dual antiplatelet therapy in patients with symptomatic intracranial atherosclerotic disease.
J Neurosurg
2016
26524704
Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration.
Am J Med
2016
27881091
Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.
BMC Med Res Methodol
2016
27661856
Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses.
Invest Ophthalmol Vis Sci
2016
27780847
Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical Data.
Circ Cardiovasc Genet
2016
1 - 50 of 167
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Erwin P Bottinger
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Gerard Tromp
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Jessica N Cooke Bailey
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14
Marc S Williams
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Hakon Hakonarson
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Margaret A Pericak-Vance
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Donald J Zack
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