Author details

Full Name

Melanie E Garrett

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37533140	Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait.	Clin J Am Soc Nephrol	2023
36226494	Variation and impact of polygenic hematologic traits in monogenic sickle cell disease.	Haematologica	2023
36399516	Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy.	Blood Adv	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
37886496	Genomic Structural Equation Modeling Reveals Latent Phenotypes in the Human Cortex with Distinct Genetic Architecture.	Res Sq	2023
38077122	Gene-metabolite annotation with shortest reactional distance enhances metabolite genome-wide association studies results.		2023
37789374	Integrative single-nucleus multi-omics analysis prioritizes candidate cis and trans regulatory networks and their target genes in Alzheimer's disease brains.	Cell Biosci	2023
37967379	Characterizing epigenetic aging in an adult sickle cell disease cohort.		2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
36940203	Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veteran Program.	PLoS Genet	2023
36546431	Sex differences in progression of kidney disease in sickle cell disease.	Haematologica	2023
36542982	Impact of traumatic life events and polygenic risk scores for major depression and posttraumatic stress disorder on Iraq/Afghanistan Veterans.		2023
36993312	Genetic regulation of fetal hemoglobin across global populations.	medRxiv	2023
36993181	Gene-metabolite annotation with shortest reactional distance enhances metabolite genome-wide association studies results.		2023
35347246	A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci.	Mol Psychiatry	2022
35696734	Longitudinal study of glomerular hyperfiltration in adults with sickle cell anemia: a multicenter pooled analysis.	Blood Adv	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
34990411	Clonal hematopoiesis in sickle cell disease.	J Clin Invest	2022
34429139	Sex dependent glial-specific changes in the chromatin accessibility landscape in late-onset Alzheimer's disease brains.	Mol Neurodegener	2021
33860118	Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD.	Hepatology Communications	2021
33545031	Rare and de novo coding variants in chromodomain genes in Chiari I malformation.	American Journal of Human Genetics	2021
34017130	Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation.	Nat Neurosci	2021
33667397	Rare and de novo coding variants in chromodomain genes in Chiari I malformation.	American Journal of Human Genetics	2021
34248484	Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis.	Front Neurosci	2021
33974636	Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1.	PLoS One	2021
33352116	Rare and de novo coding variants in chromodomain genes in Chiari I malformation.	American Journal of Human Genetics	2021
33179474	Rapid decline in estimated glomerular filtration rate in sickle cell anemia: results of a multicenter pooled analysis.	Haematologica	2021
32949984	Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.	Blood Cells Mol Dis	2021
34916497	Trauma and posttraumatic stress disorder modulate polygenic predictors of hippocampal and amygdala volume.	Transl Psychiatry	2021
33214552	PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia.	Nat Commun	2020
32641180	Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.	International Psychogeriatrics	2020
33029326	Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls.	Eur J Psychotraumatol	2020
33235198	Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR.	Nat Commun	2020
32776978	Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts.	PLoS One	2020
30663090	A multi-institutional comparison of younger and older adults with sickle cell disease.	American Journal of Hematology	2019
31594949	International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.	Nat Commun	2019
31158233	RNA sequencing of isolated cell populations expressing human APOL1 G2 risk variant reveals molecular correlates of sickle cell nephropathy in zebrafish podocytes.	PLoS ONE	2019
29452766	Traumatic stress and accelerated DNA methylation age: A meta-analysis.	Psychoneuroendocrinology	2018
28439101	Largest GWAS of PTSD (N=20â¿¿070) yields genetic overlap with schizophrenia and sex differences in heritability.	Mol Psychiatry	2018
30105803	A common functional PIEZO1 deletion allele associates with red blood cell density in sickle cell disease patients.	American Journal of Hematology	2018
30145303	A genome-wide association study of suicide attempts and suicidal ideation in U.S. military veterans.	Psychiatry Research	2018
30144150	Clinical and metabolomic risk factors associated with rapid renal function decline in sickle cell disease.	Am J Hematol	2018
30087329	Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia.	Nat Commun	2018
28033687	Thrombospondin-1 gene polymorphism is associated with estimated pulmonary artery pressure in patients with sickle cell anemia.	Am J Hematol	2017
28691784	Epigenome-wide association of PTSD from heterogeneous cohorts with a common multi-site analysis pipeline.	Am J Med Genet B Neuropsychiatr Genet	2017
28526450	The association of single-nucleotide polymorphisms in theÂ oxytocin receptor and G protein-coupled receptor kinase 6 (GRK6) genes with oxytocin dosing requirements and labor outcomes.	American Journal of Obstetrics and Gynecology	2017
29187748	Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	Translational Psychiatry	2017
28282489	Systematic Functional Testing of Rare Variants: Contributions of CFI to Age-Related Macular Degeneration.	Invest Ophthalmol Vis Sci	2017
27701011	Further evidence for a role of the ADRB2 gene in risk for posttraumatic stress disorder.	J Psychiatr Res	2017