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Author Details
Full Name
Min-Tzu Lo
Affiliation
Center for Multimodal Imaging and Genetics, University of California
ORCID
Career Start Year
2003
Papers
30
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36856935
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception.
Breast Cancer Res Treat
2023
37178433
Correction to: Pathogenic variants among females with breast cancer and a nonâ¿¿breast cancer reveal opportunities for cancer interception.
Breast Cancer Res Treat
2023
34875721
Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers evaluated by clinical characteristics.
Cancer
2022
35603838
Clinician-Reported Impact of Germline Multigene Panel Testing on Cancer Risk Management Recommendations.
JNCI Cancer Spectr
2022
34122051
Similar Genetic Architecture of Alzheimer's Disease and Differential <i>APOE</i> Effect Between Sexes.
Front Aging Neurosci
2021
35005200
Causal association of cognitive reserve on Alzheimer's disease with putative sex difference.
Alzheimers Dement (Amst)
2021
33258481
Validation of a prostate cancer polygenic risk score.
Prostate
2020
30859582
Collagen Formation Assessed by N-Terminal Propeptide of Type 3 Procollagen Is a Heritable Trait and Is Associated With Liver Fibrosis Assessed by Magnetic Resonance Elastography.
Hepatology
2019
29931045
GWASinlps: non-local prior based iterative SNP selection tool for genome-wide association studies.
Bioinformatics
2019
30979435
Identification of genetic heterogeneity of Alzheimer's disease across age.
Neurobiol Aging
2019
29572891
Link between gut-microbiome derived metabolite and shared gene-effects with hepatic steatosis and fibrosis in NAFLD.
Hepatology
2018
29522091
Beyond heritability: improving discoverability in imaging genetics.
Hum Mol Genet
2018
29495895
Revisiting Antipsychotic Drug Actions Through Gene Networks Associated With Schizophrenia.
Am J Psychiatry
2018
27380033
Simple obstructive sleep apnea patients without hypertension or diabetes accelerate kidney dysfunction: a population follow-up cohort study from Taiwan.
Sleep Breath
2017
29147026
Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure.
Sci Rep
2017
28973307
Modeling prior information of common genetic variants improves gene discovery for neuroticism.
Hum Mol Genet
2017
28533504
Identification of genetic loci shared between schizophrenia and the Big Five personality traits.
Sci Rep
2017
27918536
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.
Nat Genet
2017
26909100
Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics.
Front Genet
2016
27315352
Shared genetic effects between hepatic steatosis and fibrosis: A prospective twin study.
Hepatology
2016
27459196
Conservation of Distinct Genetically-Mediated Human Cortical Pattern.
PLoS Genet
2016
26166778
Modeling the 3D geometry of the cortical surface with genetic ancestry.
Curr Biol
2015
26189703
Large-scale genomics unveil polygenic architecture of human cortical surface area.
Nat Commun
2015
24866319
Detecting a weak association by testing its multiple perturbations: a data mining approach.
Sci Rep
2014
23041145
Postural stability in patients with knee osteoarthritis: comparison with controls and evaluation of relationships between postural stability scores and International Classification of Functioning, Disability and Health components.
Arch Phys Med Rehabil
2013
22459700
Short-term effects of 890-nanometer radiation on pain, physical activity, and postural stability in patients with knee osteoarthritis: a double-blind, randomized, placebo-controlled study.
Arch Phys Med Rehabil
2012
22960644
Therapeutic effects of short-term monochromatic infrared energy therapy on patients with knee osteoarthritis: a double-blind, randomized, placebo-controlled study.
J Orthop Sports Phys Ther
2012
21934636
Genetic predisposition and nongenetic risk factors of thiazolidinedione-related edema in patients with type 2 diabetes.
Pharmacogenet Genomics
2011
19484507
Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes.
Fam Cancer
2009
14975101
Sibling recurrence risk ratio analysis of the metabolic syndrome and its components over time.
BMC Genet
2003
1 - 30 of 30
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Norwegian Institute of Public Health
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Heze University
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