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Aging Cell|February 21, 2012
Human longevity and common variations in the LMNA gene: a meta-analysisKaren N Conneely, Brian C Capell, Michael R Erdos, et al.
Plos One|January 27, 2012
Genetic signatures of exceptional longevity in humansPaola Sebastiani, Nadia Solovieff, Andrew T Dewan, et al.
Archives of Neurology|December 14, 2011
A comprehensive genetic association study of Alzheimer disease in African AmericansMark W Logue, Matthew Schu, Badri N Vardarajan, et al.
Blood Cells, Molecules & Diseases|August 12, 2008
BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathiesAmanda E Sedgewick, Nadia Timofeev, Paola Sebastiani, et al.
Nature|May 7, 2004
Differential modulation of endotoxin responsiveness by human caspase-12 polymorphismsMaya Saleh, John P Vaillancourt, Rona K Graham, et al.
Blood|December 19, 2009
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene clusterNadia Solovieff, Jacqueline N Milton, Stephen W Hartley, et al.
Molecular Neurodegeneration|February 19, 2013
Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohortsBadri Vardarajan, David Vergote, Fadel Tissir, et al.
Circulation|February 12, 2014
Hypoxic response contributes to altered gene expression and precapillary pulmonary hypertension in patients with sickle cell diseaseXu Zhang, Wei Zhang, Shwu-Fan Ma, et al.
British Journal of Haematology|February 15, 2013
Genetic determinants of haemolysis in sickle cell anaemiaJacqueline N Milton, Helen Rooks, Emma Drasar, et al.
Blood Cells, Molecules & Diseases|March 8, 2013
Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotypeDuyen Ngo, Harold Bae, Martin H Steinberg, et al.
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