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The Canadian Journal of Cardiology|June 16, 2022
Development and Internal Validation of a Risk Prediction Model for Acute Cardiovascular Morbidity in PreeclampsiaIsabelle Malhamé, Christina A Raker, Erica J Hardy, et al.
JAMA Network Open|August 21, 2024
Assessing Psychosocial Risk and Resilience to Support Readiness for Gene Therapy in Sickle Cell Disease: A Consensus StatementSteven J Hardy, Lori E Crosby, Jerlym S Porter, et al.
Frontiers in Oncology|July 3, 2023
Stroke death in patients receiving radiation for head and neck cancer in the modern eraSara J Hardy, Sanjukta Bandyopadhyay, Hongmei Yang, et al.
The New Phytologist|October 31, 2019
Large-scale genomic sequence data resolve the deepest divergences in the legume phylogeny and support a near-simultaneous evolutionary origin of all six subfamiliesErik J M Koenen, Dario I Ojeda, Royce Steeves, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 14, 2006
Prevalence and course of strabismus in the first year of life for infants with prethreshold retinopathy of prematurity: findings from the Early Treatment for Retinopathy of Prematurity studyDeborah K VanderVeen, David K Coats, Velma Dobson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 12, 2007
Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosisP Hollingworth, M L Hamshere, P A Holmans, et al.
Human Molecular Genetics|July 8, 2005
The H1c haplotype at the MAPT locus is associated with Alzheimer's diseaseA J Myers, M Kaleem, L Marlowe, et al.
Magnetic Resonance in Medicine|June 7, 2006
Toward single breath-hold whole-heart coverage coronary MRA using highly accelerated parallel imaging with a 32-channel MR systemThoralf Niendorf, Christopher J Hardy, Randy O Giaquinto, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genesA B West, A Zimprich, P J Lockhart, et al.
Brain : a Journal of Neurology|March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factorN C Fox, A M Kennedy, R J Harvey, et al.
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