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Genome Research|February 19, 2016
Whole-genome sequence analyses of Western Central African Pygmy hunter-gatherers reveal a complex demographic history and identify candidate genes under positive natural selectionPingHsun Hsieh, Krishna R Veeramah, Joseph Lachance, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 15, 2011
Telomere attrition and decreased fetuin-A levels indicate accelerated biological aging and are implicated in the pathogenesis of colorectal cancerFraser Maxwell, Liane M McGlynn, Hannah C Muir, et al.
Genetics|September 3, 2004
Heterogeneous patterns of variation among multiple human x-linked Loci: the possible role of diversity-reducing selection in non-africansMichael F Hammer, Daniel Garrigan, Elizabeth Wood, et al.
Forensic Science International|December 13, 2005
Population structure of Y chromosome SNP haplogroups in the United States and forensic implications for constructing Y chromosome STR databasesMichael F Hammer, Veronica F Chamberlain, Veronica F Kearney, et al.
Neurobiology of Disease|May 31, 2014
A novel de novo mutation of SCN8A (Nav1.6) with enhanced channel activation in a child with epileptic encephalopathyMark Estacion, Janelle E O'Brien, Allison Conravey, et al.
Clinical Science (London, England : 1979)|February 13, 2024
Sex differences in physiological response to increased neuronal excitability in a knockin mouse model of pediatric epilepsyMichael F Hammer, Collin T Krzyzaniak, Erfan Bahramnejad, et al.
Journal of Forensic Sciences|May 16, 2006
Genetic structure among 38 populations from the United States based on 11 U.S. core Y chromosome STRsAlan J Redd, Veronica F Chamberlain, Veronica F Kearney, et al.
European Journal of Cancer (Oxford, England : 1990)|July 5, 2011
A comparison of inflammation-based prognostic scores in patients with cancer. A Glasgow Inflammation Outcome StudyMichael J Proctor, David S Morrison, Dinesh Talwar, et al.
Epilepsia|October 20, 2020
Fenfluramine HCl (Fintepla® ) provides long-term clinically meaningful reduction in seizure frequency: Analysis of an ongoing open-label extension studyJoseph Sullivan, Ingrid E Scheffer, Lieven Lagae, et al.
Epilepsia|May 20, 2022
Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plusMichael F Hammer, Yanling Pan, Medhane Cumbay, et al.
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