S. Hartley

发表

Hippocampal morphometry in population-based incident Alzheimer's disease and vascular dementia: the HAAS

Arthur W Toga, Philip Scheltens, Paul M Thompson, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Paola Sebastiani, Nadia Solovieff, Annibale Puca, 2019, Definitions.

Severe sickle cell anemia is associated with increased plasma levels of TNF‐R1 and VCAM‐1

Paola Sebastiani, Nadia Solovieff, Stephen W. Hartley, 2011, American journal of hematology.

A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples

Alberto Riva, Paola Sebastiani, Zhenming Zhao, 2008, BMC Genetics.

Genetic signatures of exceptional longevity in humans.

Stephen W. Hartley, P. Sebastiani, C. Baldwin, 2010, Science.

Detection and Visualization of Differential Exon and Splice Junction Usage in RNA-Seq Data with JunctionSeq

Stephen W. Hartley, J. Mullikin, S. Hartley, 2015 .

Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural Regulation

Stephen W. Hartley, J. Mullikin, Morgan Park, 2016, PloS one.

DNA methylome and transcriptome sequencing in human ovarian granulosa cells links age-related changes in gene expression to gene body methylation and 3ʹ-end GC density

Stephen W. Hartley, J. Mullikin, B. Howard, 2015, Oncotarget.

Eric T. Dawson, Stephen W. Hartley, G. Getz, 2021, Science.

A Genome-Wide Association Study of Total Bilirubin and Cholelithiasis Risk in Sickle Cell Anemia

Paola Sebastiani, Nadia Solovieff, Stephen W. Hartley, 2012, PloS one.

Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.

Stephen W. Hartley, P. Sebastiani, L. Farrer, 2010, Blood.

Genetic modifiers of the severity of sickle cell anemia identified through a genome‐wide association study

Stephen W. Hartley, P. Sebastiani, A. Ashley-Koch, 2009, American journal of hematology.

Bayesian Methods for Multivariate Modeling of Pleiotropic SNP Associations and Genetic Risk Prediction

Paola Sebastiani, Stefano Monti, Stephen W. Hartley, 2012, Front. Gene..

The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas

Nancy F. Hansen, Stephen W. Hartley, J. Mullikin, 2017, Oncogene.

Subsequent Neoplasm Risk Associated With Rare Variants in DNA Damage Response and Clinical Radiation Sensitivity Syndrome Genes in the Childhood Cancer Survivor Study.

Stephen W. Hartley, S. Chanock, D. Karyadi, 2020, JCO precision oncology.

QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments

Stephen Hartley, James C. Mullikin, Stephen W. Hartley, 2015, BMC Bioinformatics.

Detection and visualization of differential splicing in RNA-Seq data with JunctionSeq

James C. Mullikin, Stephen W. Hartley, J. Mullikin, 2015, Nucleic acids research.

A GCH1 haplotype confers sex‐specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia

Stephen W. Hartley, K. Channon, D. Goldman, 2014, American journal of hematology.

Genome-Wide Association Study of Stroke in Sickle Cell Anemia.

Stephen W. Hartley, P. Sebastiani, C. Baldwin, 2009 .

Imputation of missing genotypes: an empirical evaluation of IMPUTE

Paola Sebastiani, Stephen W. Hartley, Zhenming Zhao, 2008, BMC Genetics.

Clustering by genetic ancestry using genome-wide SNP data

Paola Sebastiani, Nadia Solovieff, Thomas T Perls, 2010, BMC Genetics.

Hippocampal shape analysis in Alzheimer’s disease: A population-based study

Paul M. Thompson, Arthur W. Toga, Yuan Xu, 2007, NeuroImage.

Neurotranscriptomics: The Effects of Neonatal Stimulus Deprivation on the Rat Pineal Transcriptome

J. Mullikin, D. Klein, S. Hartley, 2015, PloS one.

Ancestry of African Americans with sickle cell disease.

Stephen W. Hartley, M. Gladwin, P. Sebastiani, 2011, Blood cells, molecules & diseases.

Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study.

Stephen W. Hartley, S. Chanock, D. Karyadi, 2021, JNCI cancer spectrum.

PleioGRiP: genetic risk prediction with pleiotropy

Paola Sebastiani, Stephen W. Hartley, P. Sebastiani, 2013, Bioinform..

Inflated expectations: Rare-variant association analysis using public controls

Stephen W. Hartley, S. Chanock, D. Karyadi, 2023, PloS one.

Analysis and validation of automated skull stripping tools: A validation study based on 296 MR images from the Honolulu Asia aging study

Lenore J. Launer, Ann I. Scher, E. S. C. Korf, 2006, NeuroImage.

Genome-Wide Studies in Sickle Cell Anemia Show Associations Between SNPs in the Olfactory Receptor Gene Cluster and Fetal Hemoglobin Concentration.

Stephen W. Hartley, P. Sebastiani, L. Farrer, 2009 .

A GCH1 Haplotype Associated with Susceptibility to Vasoocclusive Pain and Impaired Vascular Function in Sickle Cell Anemia.

Stephen W. Hartley, M. Max, D. Goldman, 2009 .

Genetic Polymorphisms in NEDD4L Are Associated with Pulmonary Hypertension of Sickle Cell Anemia.

Stephen W. Hartley, M. Gladwin, P. Sebastiani, 2009 .

A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples

P. Sebastiani, A. Riva, C. Baldwin, 2008, BMC Genetics.

A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples

María M. Abad-Grau, Stephen W. Hartley, P. Sebastiani, 2008, BMC Genetics.