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Gillian Morven Belbin
Gillian Morven Belbin
gencove inc.
在 gencove.com 的电子邮件经过验证
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引用次数
年份
Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations
NJ Lennon, LC Kottyan, C Kachulis, NS Abul-Husn, J Arias, G Belbin, ...
Nature Medicine, 1-8, 2024
132024
Life is pain: Fibromyalgia as a nexus of multiple liability distributions
A Moscati, AB Faucon, C Arnaiz‐Yépez, SL Lönn, J Sundquist, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 192 …, 2023
2023
Association of HSD17B13 and PNPLA3 with liver enzymes and fibrosis in Hispanic/Latino individuals of diverse genetic ancestries
SM Rutledge, ER Soper, N Ma, V Pejaver, SL Friedman, AD Branch, ...
Clinical Gastroenterology and Hepatology 21 (10), 2578-2587. e11, 2023
32023
The effects of reference panel perturbations on the accuracy of genotype imputation
JH Li, A Liu, CA Buerkle, W Palmer, GM Belbin, M Ahangari, MJS Gibson, ...
bioRxiv, 2023.08. 10.552684, 2023
2023
Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35
S Cullina, GL Wojcik, R Shemirani, D Klarin, BR Gorman, EP Sorokin, ...
Frontiers in Genetics 14, 1181167, 2023
22023
Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region
C Caggiano, A Boudaie, R Shemirani, J Mefford, E Petter, A Chiu, ...
Nature Medicine 29 (7), 1845-1856, 2023
2023
Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals
K Hou, Y Ding, Z Xu, Y Wu, A Bhattacharya, R Mester, GM Belbin, ...
Nature genetics 55 (4), 549-558, 2023
452023
Returning integrated genomic risk and clinical recommendations: The eMERGE study
JE Linder, A Allworth, HT Bland, PJ Caraballo, RL Chisholm, EW Clayton, ...
Genetics in Medicine 25 (4), 100006, 2023
422023
Abstract P5-02-54: Application of low-pass whole genome sequencing for the detection of Homologous Recombination Deficiency in breast cancer
G Belbin, J An, C Mazur, J Pickrell, J Li, D Metzger, S Gao, E Van Roey, ...
Cancer Research 83 (5_Supplement), P5-02-54-P5-02-54, 2023
2023
Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations
B Noyvert, AM Erzurumluoglu, D Drichel, S Omland, TFM Andlauer, ...
medRxiv, 2023.12. 20.23300308, 2023
22023
Combined Low-pass Whole Genome and Targeted Sequencing Identifies Causative Mutations and Associated Genomic Scarring Indicative of Homologous Recombination Deficiency
J An, GM Belbin, C Mazur, J Li, J Pickrell, D Metzger, S Gao, E Van Roey, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 24 (10), S109-S110, 2022
2022
Comparing Methods to Adjust for Fine-Scale Population Structure in Rare Variant Analyses
KM Marker, R Shemirani, M Lin, EE Kenny, GM Belbin, CR Gignoux
GENETIC EPIDEMIOLOGY 46 (7), 515-515, 2022
2022
Evaluating the Biomedical Relevance of Identity by Descent Genetic Communities in The Biobank at The Colorado Center for Personalized Medicine
JA Shortt, M Lin, NM Rafaels, C Caggiano, R Shemirani, GM Belbin, ...
GENETIC EPIDEMIOLOGY 46 (7), 532-533, 2022
2022
Causal effects on complex traits are similar across segments of different continental ancestries within admixed individuals
K Hou, Y Ding, Z Xu, Y Wu, A Bhattacharya, R Mester, G Belbin, D Conti, ...
MedRxiv, 2022.08. 16.22278868, 2022
82022
Health care utilization of fine-scale identity by descent clusters in a Los Angeles biobank
C Caggiano, A Boudaie, R Shemirani, E Petter, A Chiu, R Johnson, ...
medRxiv, 2022.07. 12.22277520, 2022
22022
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
2302022
Hunter-gatherer genomes reveal diverse demographic trajectories during the rise of farming in Eastern Africa
S Gopalan, REW Berl, JW Myrick, ZH Garfield, AW Reynolds, BK Bafens, ...
Current Biology 32 (8), 1852-1860. e5, 2022
212022
Current Status and Future Challenges of Biobank Data Analysis
TP Lu, Y Kamatani, G Belbin, T Park, CK Hsiao
Frontiers in Genetics 13, 882611, 2022
12022
CDH1 pathogenic variants and cancer risk in an unselected patient population
A Bar-Mashiah, ER Soper, S Cullina, GM Belbin, EE Kenny, AL Lucas, ...
Familial cancer 21 (2), 235-239, 2022
62022
eP113: Prevalence and clinical consequences of genetic variants associated with familial hypercholesterolemia and LDL-C lowering in a diverse patient population
B Dubois, E Soper, M Turchin, G Belbin, E Kenny, N Abul-Husn
Genetics in Medicine 24 (3), S71, 2022
2022
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