Search details
1.
Angiosperm flowers reached their highest morphological diversity early in their evolutionary history.
New Phytol
; 241(3): 1348-1360, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38029781
2.
Integrating Fossil Flowers into the Angiosperm Phylogeny Using Molecular and Morphological Evidence.
Syst Biol
; 72(4): 837-855, 2023 08 07.
Article
in English
| MEDLINE | ID: mdl-36995161
3.
Assessing digital accessible botanical knowledge and priorities for exploration and discovery of plant diversity across Mesoamerica.
New Phytol
; 240(4): 1659-1672, 2023 11.
Article
in English
| MEDLINE | ID: mdl-37571871
4.
The use of Anchored Hybrid Enrichment data to resolve higher-level phylogenetic relationships: A proof-of-concept applied to Asterales (Eudicotyledoneae; Angiosperms).
Mol Phylogenet Evol
; 181: 107714, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36708940
5.
What is the age of flowering plants?
J Exp Bot
; 73(12): 3840-3853, 2022 06 24.
Article
in English
| MEDLINE | ID: mdl-35438718
6.
Role of diversification rates and evolutionary history as a driver of plant naturalization success.
New Phytol
; 229(5): 2998-3008, 2021 03.
Article
in English
| MEDLINE | ID: mdl-33078849
7.
Phylogenetic analysis of fossil flowers using an angiosperm-wide data set: proof-of-concept and challenges ahead.
Am J Bot
; 107(10): 1433-1448, 2020 10.
Article
in English
| MEDLINE | ID: mdl-33026116
8.
Thirty clues to the exceptional diversification of flowering plants.
Ann Bot
; 123(3): 491-503, 2019 02 15.
Article
in English
| MEDLINE | ID: mdl-30376040
9.
Key questions and challenges in angiosperm macroevolution.
New Phytol
; 219(4): 1170-1187, 2018 09.
Article
in English
| MEDLINE | ID: mdl-29577323
10.
Evolution of Trichobaris (Curculionidae) in relation to host plants: Geometric morphometrics, phylogeny and phylogeography.
Mol Phylogenet Evol
; 124: 37-49, 2018 07.
Article
in English
| MEDLINE | ID: mdl-29486237
11.
Recent radiation and dispersal of an ancient lineage: The case of Fouquieria (Fouquiericeae, Ericales) in North American deserts.
Mol Phylogenet Evol
; 126: 92-104, 2018 09.
Article
in English
| MEDLINE | ID: mdl-29574271
12.
Uncovering Higher-Taxon Diversification Dynamics from Clade Age and Species-Richness Data.
Syst Biol
; 66(3): 367-378, 2017 May 01.
Article
in English
| MEDLINE | ID: mdl-28003532
13.
A pilot study applying the plant Anchored Hybrid Enrichment method to New World sages (Salvia subgenus Calosphace; Lamiaceae).
Mol Phylogenet Evol
; 117: 124-134, 2017 12.
Article
in English
| MEDLINE | ID: mdl-28189618
14.
Non-equilibrium dynamics and floral trait interactions shape extant angiosperm diversity.
Proc Biol Sci
; 283(1830)2016 05 11.
Article
in English
| MEDLINE | ID: mdl-27147092
15.
Physalis and physaloids: A recent and complex evolutionary history.
Mol Phylogenet Evol
; 100: 41-50, 2016 07.
Article
in English
| MEDLINE | ID: mdl-27063196
16.
A metacalibrated time-tree documents the early rise of flowering plant phylogenetic diversity.
New Phytol
; 207(2): 437-453, 2015 Jul.
Article
in English
| MEDLINE | ID: mdl-25615647
17.
Fast demographic traits promote high diversification rates of Amazonian trees.
Ecol Lett
; 17(5): 527-36, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24589190
18.
Beyond aridification: multiple explanations for the elevated diversification of cacti in the New World Succulent Biome.
New Phytol
; 202(4): 1382-1397, 2014 Jun.
Article
in English
| MEDLINE | ID: mdl-24611540
19.
The timing of Malvales evolution: Incorporating its extensive fossil record to inform about lineage diversification.
Mol Phylogenet Evol
; 140: 106606, 2019 11.
Article
in English
| MEDLINE | ID: mdl-31472220
20.
Land plant evolutionary timeline: gene effects are secondary to fossil constraints in relaxed clock estimation of age and substitution rates.
Am J Bot
; 100(3): 556-73, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23445823