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Author Details
Full Name
Tengfei Li
Affiliation
University of North Carolina at Chapel Hill
ORCID
Career Start Year
2010
Papers
31
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37693466
The pivotal role of the X-chromosome in the genetic architecture of the human brain.
medRxiv
2024
36205584
Asynchronous functional linear regression models for longitudinal data in reproducing kernel Hilbert space.
Biometrics
2023
37457984
Interactions between <i>Bifidobacterium</i> and <i>Bacteroides</i> and human milk oligosaccharides and their associations with infant cognition.
Front Nutr
2023
37262162
Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images.
Science
2023
37127052
Statistical Learning Methods for Neuroimaging Data Analysis with Applications.
Annu Rev Biomed Data Sci
2023
36824893
Eye-brain connections revealed by multimodal retinal and brain imaging genetics in the UK Biobank.
medRxiv
2023
32948880
Bayesian sparse heritability analysis with high-dimensional neuroimaging phenotypes.
Biostatistics
2022
35393594
Common variants contribute to intrinsic human brain functional networks.
Nat Genet
2022
35869272
Altered neural flexibility in children with attention-deficit/hyperactivity disorder.
Mol Psychiatry
2022
36091236
Joint analyses of human milk fatty acids, phospholipids, and choline in association with cognition and temperament traits during the first 6 months of life.
Front Nutr
2022
35026528
DADP: Dynamic abnormality detection and progression for longitudinal knee magnetic resonance images from the Osteoarthritis Initiative.
Med Image Anal
2022
31666681
Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (nâ¿¿=â¿¿17,706).
Mol Psychiatry
2021
34296751
Corrigendum to: Heritability of regional brain volumes in large-scale neuroimaging and genetic studies.
Cereb Cortex
2021
34140357
Common genetic variation influencing human white matter microstructure.
Science
2021
34001886
Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits.
Nat Commun
2021
31544963
Analysis of secondary phenotypes in multigroup association studies.
Biometrics
2020
33627920
Bayesian Scalar on Image Regression With Nonignorable Nonresponse.
J Am Stat Assoc
2020
31710172
Patterns of protein expression in human head and neck cancer cell lines differ after proton vs photon radiotherapy.
Head Neck
2020
32931941
(TS)<sup>2</sup>WM: Tumor Segmentation and Tract Statistics for Assessing White Matter Integrity with Applications to Glioblastoma Patients.
Neuroimage
2020
30941828
Common genetic variants have associations with human cortical brain regions and risk of schizophrenia.
Genet Epidemiol
2019
31676860
Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits.
Nat Genet
2019
30010813
Heritability of Regional Brain Volumes in Large-Scale Neuroimaging and Genetic Studies.
Cereb Cortex
2019
31485381
A Powerful Global Test Statistic for Functional Statistical Inference.
Proc AAAI Conf Artif Intell
2019
30555624
A Label-fusion-aided Convolutional Neural Network for Isointense Infant Brain Tissue Segmentation.
Proc IEEE Int Symp Biomed Imaging
2018
30175071
Machine Learning Applications in Head and Neck Radiation Oncology: Lessons From Open-Source Radiomics Challenges.
Front Oncol
2018
30344426
Functional Linear Regression Models for Nonignorable Missing Scalar Responses.
Stat Sin
2018
28544218
Genome-wide mediation analysis of psychiatric and cognitive traits through imaging phenotypes.
Hum Brain Mapp
2017
29594229
Radiomic analysis in prediction of Human Papilloma Virus status.
Clin Transl Radiat Oncol
2017
28763065
Genome-wide association analysis identifies common variants influencing infant brain volumes.
Transl Psychiatry
2017
26309201
MAFsnp: A Multi-Sample Accurate and Flexible SNP Caller Using Next-Generation Sequencing Data.
PLoS One
2015
20529080
Influence of population stratification on population-based marker-disease association analysis.
Ann Hum Genet
2010
1 - 31 of 31
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