L. Olson

J. Sutcliffe, S. Folstein, J. Haines, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mechanistic Phenotypes: An Aggregative Phenotyping Strategy to Identify Disease Mechanisms Using GWAS Data

Gerard Tromp, Yan Guo, Marylyn D. Ritchie, 2013, PloS one.

Genetic Susceptibility to Postdiarrheal Hemolytic-Uremic Syndrome After Shiga Toxin–Producing Escherichia coli Infection: A Centers for Disease Control and Prevention FoodNet Study

L. Olson, A. Kallianpur, T. Jones, 2018, The Journal of infectious diseases.

Rare variants in RTEL1 are associated with familial interstitial pneumonia.

Zhongming Zhao, L. Olson, D. Schwartz, 2015, American journal of respiratory and critical care medicine.

Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy

Dana C. Crawford, Erica A. Bowton, Dan M. Roden, 2015, PloS one.

Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma

B. Yaspan, J. Haines, M. Pericak-Vance, 2014, Eye.

A genomewide scan identifies novel early-onset primary open-angle glaucoma loci on 9q22 and 20p12.

J. Haines, L. Olson, J. Wiggs, 2004, American journal of human genetics.

Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia

L. Olson, D. Haas, J. Currier, 2015, Open forum infectious diseases.

Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6.

J. Gilbert, J. Haines, M. Pericak-Vance, 2006, Investigative ophthalmology & visual science.

Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration.

J. Haines, M. Pericak-Vance, W. Scott, 2007, Investigative ophthalmology & visual science.

Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility.

J. Haines, M. Pericak-Vance, D. Weeks, 2011, Investigative ophthalmology & visual science.

Race/ethnicity difference in the pharmacogenetics of bilirubin-related atazanavir discontinuation

L. Olson, D. Haas, Danielle M Richardson, 2017, Pharmacogenetics and genomics.

Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration.

J. Haines, M. Pericak-Vance, W. Scott, 2007, Human molecular genetics.

Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples

J. Haines, Melissa Parkin, L. Pasquale, 2010, Biomarker insights.

Localization of age-related macular degeneration-associated ARMS2 in cytosol, not mitochondria.

J. Haines, M. Pericak-Vance, Gaofeng Wang, 2009, Investigative ophthalmology & visual science.

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Dana C Crawford, Yuki Bradford, Mariza de Andrade, 2011, Genetic epidemiology.

Pharmacogenetics of efavirenz discontinuation for reported central nervous system symptoms appears to differ by race

L. Olson, D. Haas, Danielle M Richardson, 2016, Pharmacogenetics and genomics.

Title Screening for UGT 1 A 1 Genotype in Study A 5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia Permalink

L. Olson, D. Haas, J. Currier, 2015 .

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid‐compulsive subset of autism

J. Sutcliffe, S. Folstein, R. Blakely, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

J. Sutcliffe, S. Folstein, L. Olson, 2005, BMC Medical Genetics.