Neurotransmitters and Sodium Channelopathies; Possible Link? by Michael F. Hammer, Alejandra D.C. Encinas

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Machine learning models reveal distinct disease subgroups and improve diagnostic and prognostic accuracy for individuals with pathogenic SCN8A gain-of-function variants by Joshua B. Hack, Joseph C. Watkins, Michael F. Hammer

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Variable patterns of mutation density among NaV1.1, NaV1.2 and NaV1.6 point to channel-specific functional differences associated with childhood epilepsy. by Alejandra C Encinas, Joseph C Watkins, Iris Arenas Longoria, J P Johnson, Michael F Hammer

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Machine-learning approaches for classifying haplogroup from Y chromosome STR data. by Joseph Schlecht, Matthew E Kaplan, Kobus Barnard, Tatiana Karafet, Michael F Hammer, Nirav C Merchant

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Sex-biased evolutionary forces shape genomic patterns of human diversity. by Michael F Hammer, Fernando L Mendez, Murray P Cox, August E Woerner, Jeffrey D Wall

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Autosomal resequence data reveal Late Stone Age signals of population expansion in sub-Saharan African foraging and farming populations. by Murray P Cox, David A Morales, August E Woerner, Jesse Sozanski, Jeffrey D Wall, Michael F Hammer

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A novel de novo mutation of SCN8A (Nav1.6) with enhanced channel activation in a child with epileptic encephalopathy by Mark Estacion, Janelle E. O'Brien, Allison Conravey, Michael F. Hammer, Stephen G. Waxman, Sulayman D. Dib-Hajj, Miriam H. Meisler

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