Martínez Abadías, Neus, 1978-
Neus Martínez-Abadías researcher
Martínez-Abadías, Neus
VIAF ID: 8607152140008111100003 (Personal)
Permalink: http://viaf.org/viaf/8607152140008111100003
Preferred Forms
4xx's: Alternate Name Forms (8)
Works
| Title | Sources |
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| Beyond the closed suture in apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth |
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| Comparison between Inbreeding Analyses Methodologies |
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| Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice |
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| Cultural diversification promotes rapid phenotypic evolution in Xavánte Indians |
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| Detection of a population replacement at the Classic-Postclassic transition in Mexico. |
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| Drosophila wing modularity revisited through a quantitative genetic approach. |
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| Evolutionary patterns of the human skull a quantitative genetic analysis of craniofacial phenotypic variation = Patrons evolutius del crani humà, anàlisi geneticoquantitativa de la variació fenotípica craniofacial |
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| FGFR1 signaling is associated with the magnitude of morphological integration in human head shape. |
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| From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome |
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| Functional-cranial approach to the influence of economic strategy on skull morphology |
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| Geometric Morphometrics on Gene Expression Patterns Within Phenotypes: A Case Example on Limb Development |
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| Heritability of human cranial dimensions: comparing the evolvability of different cranial regions |
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| Lack of support for the association between facial shape and aggression: a reappraisal based on a worldwide population genetics perspective |
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| Measuring fitness heritability: Life history traits versus morphological traits in humans. |
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| Phenotypic evolution of human craniofacial morphology after admixture: a geometric morphometrics approach. |
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| Postnatal brain and skull growth in an Apert syndrome mouse model. |
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| Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes. |
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| Quantification of gene expression patterns to reveal the origins of abnormal morphogenesis |
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| Tissue-specific responses to aberrant FGF signaling in complex head phenotypes |
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| Unilateral and bilateral expression of a quantitative trait: asymmetry and symmetry in coronal craniosynostosis. |
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