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Author Details
Full Name
Xiaolan Hu
Affiliation
ORCID
Career Start Year
2004
Papers
15
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
26194313
Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans.
Alzheimers Dement
2015
24092460
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers.
Brain Imaging Behav
2014
24126932
A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing.
Molecular Psychiatry
2014
23237317
Contribution of common genetic variants to antidepressant response.
Biol Psychiatry
2013
23091423
Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis.
PLoS Med
2012
21390209
Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.
PLoS ONE
2011
22833209
Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment.
Transl Psychiatry
2011
20732625
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.
J Am Acad Child Adolesc Psychiatry
2010
20732626
Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.
J Am Acad Child Adolesc Psychiatry
2010
19662163
Evolutionary processes acting on candidate cis-regulatory regions in humans inferred from patterns of polymorphism and divergence.
PLoS Genet
2009
17135225
The 620W allele is the PTPN22 genetic variant conferring susceptibility to RA in a Dutch population.
Rheumatology (Oxford)
2007
16508985
The functional -169T-->C single-nucleotide polymorphism in FCRL3 is not associated with rheumatoid arthritis in white North Americans.
Arthritis Rheum
2006
16697732
Identification of two gene variants associated with risk of advanced fibrosis in patients with chronic hepatitis C.
Gastroenterology
2006
16175503
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
Am J Hum Genet
2005
15297809
Selecting tagging SNPs for association studies using power calculations from genotype data.
Hum Hered
2004
1 - 15 of 15
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