Erika Tavares
Erika Tavares
Lab Research Proj Manager, Sickkids Hospital
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα
Παρατίθεται από
Παρατίθεται από
Single mitochondrial gene barcodes reliably identify sister-species in diverse clades of birds
ES Tavares, AJ Baker
BMC evolutionary biology 8 (1), 1-14, 2008
Phylogenetic relationships and historical biogeography of neotropical parrots (Psittaciformes: Psittacidae: Arini) inferred from mitochondrial and nuclear DNA sequences
ES Tavares, AJ Baker, SL Pereira, CY Miyaki
Systematic Biology 55 (3), 454-470, 2006
Countering criticisms of single mitochondrial DNA gene barcoding in birds
AJ Baker, ES Tavares, RF Elbourne
Molecular Ecology Resources 9, 257-268, 2009
Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21)
E Heon, G Kim, S Qin, JE Garrison, E Tavares, A Vincent, ...
Human Molecular Genetics, 2016
Multiple independent origins of mitochondrial control region duplications in the order Psittaciformes
EE Schirtzinger, ES Tavares, LA Gonzales, JR Eberhard, CY Miyaki, ...
Molecular Phylogenetics and Evolution 64 (2), 342-356, 2012
DNA barcode detects high genetic structure within Neotropical bird species
ES Tavares, P Gonçalves, CY Miyaki, AJ Baker
PLoS One 6 (12), e28543, 2011
A trans-Amazonian screening of mtDNA reveals deep intraspecific divergence in forest birds and suggests a vast underestimation of species diversity
B Milá, ES Tavares, A Muñoz Saldaña, J Karubian, TB Smith, AJ Baker
PLoS One 7 (7), e40541, 2012
Acidic calcium pools in intraerythrocytic malaria parasites.
CR Garcia, SE Ann, ES Tavares, AR Dluzewski, WT Mason, FB Paiva
European journal of cell biology 76 (2), 133, 1998
Multigene phylogeny and DNA barcoding indicate that the Sandwich tern complex (Thalasseus sandvicensis, Laridae, Sternini) comprises two species
MA Efe, ES Tavares, AJ Baker, SL Bonatto
Molecular Phylogenetics and Evolution 52 (1), 263-267, 2009
Phylogenetic relationships among some Neotropical parrot genera (Psittacidae) based on mitochondrial sequences
ES Tavares, C Yamashita, CY Miyaki
The Auk 121 (1), 230-242, 2004
Biallelic mutations in GNB3 cause a unique form of autosomal-recessive congenital stationary night blindness
A Vincent, I Audo, E Tavares, JT Maynes, A Tumber, T Wright, S Li, ...
The American Journal of Human Genetics 98 (5), 1011-1019, 2016
Phylogenetic and coalescent analysis of three loci suggest that the Water Rail is divisible into two species, Rallus aquaticus and R. indicus
ES Tavares, GHJ de Kroon, AJ Baker
BMC Evolutionary Biology 10 (1), 1-12, 2010
Phylogeny and biogeography of Yellow‐headed and Blue‐fronted Parrots (Amazona ochrocephala and Amazona aestiva) with special reference to the South …
CC Ribas, ES Tavares, C Yoshihara, CY Miyaki
Ibis 149 (3), 564-574, 2007
Biallelic mutations in CRB1 underlie autosomal recessive familial foveal retinoschisis
A Vincent, J Ng, C Gerth-Kahlert, E Tavares, JT Maynes, T Wright, ...
Investigative ophthalmology & visual science 57 (6), 2637-2646, 2016
Eight independent nuclear genes support monophyly of the plovers: The role of mutational variance in gene trees
AJ Baker, Y Yatsenko, ES Tavares
Molecular phylogenetics and evolution 65 (2), 631-641, 2012
Characterization of MHC class I in a long-distance migrant shorebird suggests multiple transcribed genes and intergenic recombination
DM Buehler, YI Verkuil, ES Tavares, AJ Baker
Immunogenetics 65 (3), 211-225, 2013
DNA barcoding a unique avifauna: an important tool for evolution, systematics and conservation
J Tizard, S Patel, J Waugh, E Tavares, T Bergmann, B Gill, J Norman, ...
BMC evolutionary biology 19 (1), 1-13, 2019
DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration
A Vig, JA Poulter, D Ottaviani, E Tavares, K Toropova, AM Tracewska, ...
Genetics in Medicine 22 (12), 2041-2051, 2020
Retrotransposon insertion as a novel mutational event in Bardet‐Biedl syndrome
E Tavares, CY Tang, A Vig, S Li, G Billingsley, W Sung, A Vincent, ...
Molecular genetics & genomic medicine 7 (2), e00521, 2019
Unique retinal signaling defect in GNB5-related disease
Z Shao, A Tumber, J Maynes, E Tavares, P Kannu, E Heon, A Vincent
Documenta Ophthalmologica 140 (3), 273-277, 2020
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