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Perturbation of the insomnia WDR90 genome-wide association studies locus pinpoints rs3752495 as a causal variant influencing distal expression of neighboring gene, PIG-Q

Sleep (New York, N.Y.), 2024-07, Vol.47 (7), p.1

2024

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Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3′ UTR of FAIM2

Cell genomics, 2024-05, Vol.4 (5), p.100556-100556, Article 100556

2024

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Osteoporosis GWAS-implicated DNM3 locus contextually regulates osteoblastic and chondrogenic fate of mesenchymal stem/progenitor cells through oscillating miR-199a-5p levels

JBMR plus, 2024-05, Vol.8 (5), p.ziae051-ziae051

2024

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Variant to gene mapping for carpal tunnel syndrome risk loci implicates skeletal muscle regulatory elements

EBioMedicine, 2024-03, Vol.101, p.105038-105038, Article 105038

2024

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Variant to gene mapping for carpal tunnel syndrome risk loci implicates skeletal muscle regulatory elementsResearch in context

EBioMedicine, 2024-03, Vol.101, p.105038

2024

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Metabolic links among milk, genes and gut

Nature metabolism, 2024-01, Vol.6 (1), p.12-13

2024

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Integrative Genomic Analyses Identify LncRNA Regulatory Networks across Pediatric Leukemias and Solid Tumors

Cancer research (Chicago, Ill.), 2023-10, Vol.83 (20), p.3462-3477

2023

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Reference ranges for body composition indices by dual energy X-ray absorptiometry from the Bone Mineral Density in Childhood Study Cohort

The American journal of clinical nutrition, 2023-10, Vol.118 (4), p.792-803

2023

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Genetics and epigenetics in the obesity phenotyping scenario

Reviews in endocrine & metabolic disorders, 2023-10, Vol.24 (5), p.775-793

2023

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Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms

Nature communications, 2023-09, Vol.14 (1), p.5562-18, Article 5562

2023

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Utility of genetic risk scores in type 1 diabetes

Diabetologia, 2023-09, Vol.66 (9), p.1589-1600

2023

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Keeping It in the Family: Consanguinity Reveals P4HTM as a Novel Syndromic Obesity Gene

Diabetes (New York, N.Y.), 2023-09, Vol.72 (9), p.1184-1186

2023

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Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts

Communications biology, 2023-08, Vol.6 (1), p.852-15, Article 852

2023

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Technologies, strategies, and cautions when deconvoluting genome‐wide association signals: FTO in focus

Obesity reviews, 2023-05, Vol.24 (5), p.e13558-n/a

2023

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Pleiotropic effects of a high confidence Autism Spectrum Disorder gene, arid1b, on zebrafish sleep

Neurobiology of sleep and circadian rhythms, 2023-05, Vol.14, p.100096-100096, Article 100096

2023

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Awakening new sleep biology with machine learning

Sleep (New York, N.Y.), 2023-02, Vol.46 (2), p.1

2023

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Human height: a model common complex trait

Annals of human biology, 2023-02, Vol.50 (1), p.258-266

2023

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Variant-to-gene mapping followed by cross-species genetic screening identifies GPI-anchor biosynthesis as a regulator of sleep

Science advances, 2023-01, Vol.9 (1), p.eabq0844-eabq0844

2023

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Patient-derived Colonoids From Disease-spared Tissue Retain Inflammatory Bowel Disease-specific Transcriptomic Signatures

Gastro hep advances, 2023, Vol.2 (6), p.830-842

2023

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Intragenic loci within TOMM40 enhances APOE expression in human microglia

Alzheimer's & dementia, 2022-12, Vol.18 (S3), p.n/a

2022

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Strategies to identify causal common genetic variants and corresponding effector genes for paediatric obesity

Pediatric obesity, 2022-12, Vol.17 (12), p.e12968-n/a

2022

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Leveraging genetic discoveries for sleep to determine causal relationships with common complex traits

Sleep (New York, N.Y.), 2022-10, Vol.45 (10), p.1

2022

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Identifying differential regulatory control of APOE ɛ4 on African versus European haplotypes as potential therapeutic targets

Alzheimer's & dementia, 2022-10, Vol.18 (10), p.1930-1942

2022

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3D chromatin maps of the human pancreas reveal lineage-specific regulatory architecture of T2D risk

Cell metabolism, 2022-09, Vol.34 (9), p.1394-1409.e4

2022

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Variant-to-gene-mapping analyses reveal a role for pancreatic islet cells in conferring genetic susceptibility to sleep-related traits

Sleep (New York, N.Y.), 2022-08, Vol.45 (8), p.1

2022

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Perturbation of the insomnia WDR90 genome-wide association studies locus pinpoints rs3752495 as a causal variant influencing distal expression of neighboring gene, PIG-Q

Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3′ UTR of FAIM2

Osteoporosis GWAS-implicated DNM3 locus contextually regulates osteoblastic and chondrogenic fate of mesenchymal stem/progenitor cells through oscillating miR-199a-5p levels

Variant to gene mapping for carpal tunnel syndrome risk loci implicates skeletal muscle regulatory elements

Variant to gene mapping for carpal tunnel syndrome risk loci implicates skeletal muscle regulatory elementsResearch in context

Metabolic links among milk, genes and gut

Integrative Genomic Analyses Identify LncRNA Regulatory Networks across Pediatric Leukemias and Solid Tumors

Reference ranges for body composition indices by dual energy X-ray absorptiometry from the Bone Mineral Density in Childhood Study Cohort

Genetics and epigenetics in the obesity phenotyping scenario

Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms

Utility of genetic risk scores in type 1 diabetes

Keeping It in the Family: Consanguinity Reveals P4HTM as a Novel Syndromic Obesity Gene

Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts

Technologies, strategies, and cautions when deconvoluting genome‐wide association signals: FTO in focus

Pleiotropic effects of a high confidence Autism Spectrum Disorder gene, arid1b, on zebrafish sleep

Awakening new sleep biology with machine learning

Human height: a model common complex trait

Variant-to-gene mapping followed by cross-species genetic screening identifies GPI-anchor biosynthesis as a regulator of sleep

Patient-derived Colonoids From Disease-spared Tissue Retain Inflammatory Bowel Disease-specific Transcriptomic Signatures

Intragenic loci within TOMM40 enhances APOE expression in human microglia

Strategies to identify causal common genetic variants and corresponding effector genes for paediatric obesity

Leveraging genetic discoveries for sleep to determine causal relationships with common complex traits

Identifying differential regulatory control of APOE ɛ4 on African versus European haplotypes as potential therapeutic targets

3D chromatin maps of the human pancreas reveal lineage-specific regulatory architecture of T2D risk

Variant-to-gene-mapping analyses reveal a role for pancreatic islet cells in conferring genetic susceptibility to sleep-related traits

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