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Nature|April 21, 1988
A highly polymorphic locus very tightly linked to the Huntington's disease geneJ J Wasmuth, J Hewitt, B Smith, et al.
Neurogenetics|March 29, 2000
Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosisJ L Haines, R M Boustany, J Alroy, et al.
Annals of Human Genetics|January 1, 1995
Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1E P Henske, M P Short, S Jozwiak, et al.
American Journal of Medical Genetics|February 15, 1992
Linkage analysis in juvenile neuronal ceroid lipofuscinosisJ L Haines, W L Yan, R M Boustany, et al.
Psychiatric Genetics|June 5, 2010
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibilityGary W Beecham, Adam C Naj, John R Gilbert, et al.
Genomics|December 12, 2001
Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locusK W Jones, M G Ehm, M A Pericak-Vance, et al.
Molecular Vision|December 30, 2008
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucomaBao Jian Fan, Teresa Chen, Cynthia Grosskreutz, et al.
Annals of Human Genetics|September 5, 2012
Identification and confirmation of an exonic splicing enhancer variation in exon 5 of the Alzheimer disease associated PICALM geneNathalie C Schnetz-Boutaud, Joshua Hoffman, Jared E Coe, et al.
The Journal of Surgical Research|February 11, 2025
Generative Artificial Intelligence in Academic Surgery: Ethical Implications and Transformative PotentialJamie R Robinson, Anne Stey, David F Schneider, et al.
Critical Care Clinics|February 28, 2025
Novel Strategies to Promote Intensive Care Unit Recovery via Personalized Exercise, Nutrition, and Anabolic InterventionsAshley L Artese, Hilary M Winthrop, Megan Beyer, et al.
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