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Xueqiu Jian

The University of Texas at San Antonio Health Science Center · US
Area of research
Genetics · Physiology
Research interest
Research interests include Genetic Associations and Epidemiology, Alzheimer's disease research and treatments, Genomics and Rare Diseases, and Dementia and Cognitive Impairment Research.
h-index
32
citations
15,870
works
97
NIH funding
primary concept
email

Recent publications

Genetic variants for head size share genes and pathways with cancer
Cell Reports Medicine 2024cited by 10position: middledoi
Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function
Neurology 2023cited by 34position: middledoi
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Brain 2021cited by 32position: middledoi
Multiomics integrative analysis identifies APOE allele-specific blood biomarkers associated to Alzheimer’s disease etiopathogenesis
Aging 2021cited by 29position: middledoi
Cerebral small vessel disease genomics and its implications across the lifespan
Nature Communications 2020cited by 207position: middledoi
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults
Nature Communications 2020cited by 107position: middledoi
Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes
Cerebral Cortex 2020cited by 24position: middledoi
Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos
Translational Psychiatry 2020cited by 18position: firstdoi
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Nature Genetics 2019cited by 3,176position: middledoi
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature Genetics 2019cited by 285position: middledoi
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Nature Genetics 2019cited by 90position: middledoi
Serum magnesium and calcium levels in relation to ischemic stroke
Neurology 2019cited by 85position: middledoi
Association of variants in<i>HTRA1</i>and<i>NOTCH3</i>with MRI-defined extremes of cerebral small vessel disease in older subjects
Brain 2019cited by 58position: middledoi
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Nature Genetics 2019cited by 32position: middledoi
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
Nature Genetics 2018cited by 1,709position: middledoi
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
Molecular Psychiatry 2018cited by 266position: middledoi
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Nature Communications 2018cited by 55position: middledoi
Apolipoprotein E genotypes among diverse middle-aged and older Latinos: Study of Latinos-Investigation of Neurocognitive Aging results (HCHS/SOL)
Scientific Reports 2018cited by 43position: middledoi
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in <i>MRPL38</i> for White Matter Hyperintensities on Brain Magnetic Resonance Imaging
Stroke 2018cited by 25position: firstdoi
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Nature Genetics 2017cited by 1,094position: middledoi
Whole genome sequence analyses of brain imaging measures in the Framingham Study
Neurology 2017cited by 46position: middledoi
<i>In silico</i> prediction of splice-altering single nucleotide variants in the human genome
Nucleic Acids Research 2014cited by 568position: firstdoi
In silico tools for splicing defect prediction: a survey from the viewpoint of end users
Genetics in Medicine 2013cited by 146position: firstdoi

Grants

No grants ingested yet.

Frequent collaborators

Eric Boerwinkle · Training Programs in Epidemiology and Public Health Interventions Network2 papers (2013–2014)Donglin Zeng · University of North Carolina at Chapel Hill2 papers (2018–2020)Wassim Tarraf · Wayne State University2 papers (2018–2020)Héctor M. González · University of San Diego2 papers (2018–2020)Xiaoming Liu · Beijing Institute of Technology2 papers (2013–2014)Myriam Fornage · The University of Texas Health Science Center2 papers (2018–2020)Melissa Lamar · University of Illinois Chicago2 papers (2018–2020)Lenore J. Launer · University of Washington1 papers (2020–2020)Tamar Sofer · Beth Israel Deaconess Medical Center1 papers (2020–2020)Clinton B. Wright · National Institute of Neurological Disorders and Stroke1 papers (2020–2020)Cathy C. Laurie · University of Washington1 papers (2020–2020)Scott M. Ratliff · University of Michigan1 papers (2020–2020)Kristine Yaffe · Icahn School of Medicine at Mount Sinai1 papers (2020–2020)David R. Weir · Irish Hospice Foundation1 papers (2020–2020)Jennifer A. Smith · Central Queensland University1 papers (2020–2020)Priscilla M. Vásquez · Charles R. Drew University of Medicine and Science1 papers (2018–2018)Bharat Thyagarajan · University of Minnesota1 papers (2018–2018)Charles DeCarli · Resonance Research (United States)1 papers (2020–2020)Thomas H. Mosley · University of Mississippi Medical Center1 papers (2020–2020)Wei Zhao · The University of Texas Health Science Center1 papers (2020–2020)