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Molecular Psychiatry|October 14, 2005
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locusX Liang, N Schnetz-Boutaud, S J Kenealy, et al.
Science (New York, N.Y.)|March 12, 2005
Complement factor H variant increases the risk of age-related macular degenerationJonathan L Haines, Michael A Hauser, Silke Schmidt, et al.
Molecular Genetics & Genomic Medicine|April 11, 2025
COG6-related prenatal phenotype (CDG2L): Clinico-pathological report and review of the literatureSarah Guterman, Agnese Feresin, Lucile Boutaud, et al.
Chemical Research in Toxicology|September 12, 2014
Protein modification by adenine propenalSarah C Shuck, Orrette R Wauchope, Kristie L Rose, et al.
ACS Medicinal Chemistry Letters|August 14, 2024
Discovery of VU6008677: A Structurally Distinct Tricyclic M4 Positive Allosteric Modulator with Improved CYP450 ProfileRory A Capstick, Sean R Bollinger, Julie L Engers, et al.
Hypertension (Dallas, Tex. : 1979)|October 5, 2020
Mitochondrial Isolevuglandins Contribute to Vascular Oxidative Stress and Mitochondria-Targeted Scavenger of Isolevuglandins Reduces Mitochondrial Dysfunction and HypertensionAnna Dikalova, Vladimir Mayorov, Liang Xiao, et al.
Plos One|March 18, 2016
Harmonization of the Volume of Interest Delineation among All Eleven Radiotherapy Centers in the North of FranceDavid Pasquier, Laurence Boutaud de la Combe-Chossiere, Damien Carlier, et al.
Plos Genetics|December 5, 2014
Detection of pleiotropy through a Phenome-wide association study (PheWAS) of epidemiologic data as part of the Environmental Architecture for Genes Linked to Environment (EAGLE) studyMolly A Hall, Anurag Verma, Kristin D Brown-Gentry, et al.
Circulation. Cardiovascular Genetics|November 4, 2014
Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment StudyDana C Crawford, Logan Dumitrescu, Robert Goodloe, et al.
Birth Defects Research|September 7, 2021
Prenatal-onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutationSuzanne Chartier, Lucile Boutaud, Edouard Le Guillou, et al.
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