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Several phylogenetic analyses place it as the sister taxon or closest relative of Aetosauria.
Several phylogenetic analyses have been published, with the most detailed being those by Alexander Averianov and colleagues in 2006, Hai-Lu You and colleagues in 2008, and Paul Sereno in 2010.
Several phylogenetic analyses recover Monolophosaurus in an unresolved polytomy, or as the most basal member of Allosauroidea (Figure 33) [19], [26], [36], [39], [39].
According to several phylogenetic analyses the virus is grouped either a novel group IV or an early split-off of group II coronaviruses [5], [6].
The relationships of Waimanu manneringi, and its slightly younger sister taxon Waimanu tuatahi, have also been evaluated in several phylogenetic analyses of morphological, and combined molecular and morphological datasets, and are consistently recovered as the basal-most members of Sphenisciformes [85], [111], [112].
Several phylogenetic analyses were performed with the Myotragus sequences.
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Several molecular phylogenetic analyses show that L. deterrimus, L. sanguifluus, Lactarius vinosus and L. fennoscandicus form a group of related species, which might include the North American species L. paradoxus and L. miniatosporus.
Several related phylogenetic analyses based on mitochondrial data support this basal dichotomy [2], [16], [18], [34].
This basic pattern is consistent with several previous phylogenetic analyses of molecular and combined data (see discussion in [1]).
Several recent phylogenetic analyses of CHIKV have grouped the Ag41855 and LR2006 OPY1 strains into the East/Central/South African phylogroup [34], [35] suggesting a close evolutionary relationship.
For several years, phylogenetic analyses have identified high-risk lineages, grouping strains more frequently implicated in neonatal diseases, regardless of the genetic typing method used [3], [4], [5], [6], [7].
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