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Author Details
Full Name
Rebecca D Burdine
Affiliation
Princeton University
ORCID
Career Start Year
1997
Papers
60
H Index
37
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37039911
Health-related quality of life and medication use among individuals with Angelman syndrome.
Qual Life Res
2023
37126546
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.
Sci Adv
2023
37039911
Health-related quality of life and medication use among individuals with Angelman syndrome.
Qual Life Res
2023
37126546
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.
Sci Adv
2023
36347237
A twist in Pitx2 regulation of gut looping.
Dev Cell
2022
36125045
Promoting validation and cross-phylogenetic integration in model organism research.
Dis Model Mech
2022
36347237
A twist in Pitx2 regulation of gut looping.
Dev Cell
2022
36125045
Promoting validation and cross-phylogenetic integration in model organism research.
Dis Model Mech
2022
32880036
Measuring What Matters to Individuals with Angelman Syndrome and Their Families: Development of a Patient-Centered Disease Concept Model.
Child Psychiatry Hum Dev
2021
33443117
The STARS Phase 2 Study: A Randomized Controlled Trial of Gaboxadol in Angelman Syndrome.
Neurology
2021
32880036
Measuring What Matters to Individuals with Angelman Syndrome and Their Families: Development of a Patient-Centered Disease Concept Model.
Child Psychiatry Hum Dev
2021
34531379
Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5.
Nat Commun
2021
34531379
Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5.
Nat Commun
2021
33443117
The STARS Phase 2 Study: A Randomized Controlled Trial of Gaboxadol in Angelman Syndrome.
Neurology
2021
32506834
Swimming toward solutions: Using fish and frogs as models for understanding RASopathies.
Birth Defects Res
2020
32506834
Swimming toward solutions: Using fish and frogs as models for understanding RASopathies.
Birth Defects Res
2020
31758943
Left-right asymmetric heart jogging increases the robustness of dextral heart looping in zebrafish.
Dev Biol
2020
31758943
Left-right asymmetric heart jogging increases the robustness of dextral heart looping in zebrafish.
Dev Biol
2020
31796593
Optimizing photoswitchable MEK.
Proc Natl Acad Sci U S A
2019
31796593
Optimizing photoswitchable MEK.
Proc Natl Acad Sci U S A
2019
29735715
ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling.
Proc Natl Acad Sci U S A
2018
29735715
ZNRF3 functions in mammalian sex determination by inhibiting canonical WNT signaling.
Proc Natl Acad Sci U S A
2018
28049852
In vivo severity ranking of Ras pathway mutations associated with developmental disorders.
Proc Natl Acad Sci U S A
2017
28720483
Left-Right Patterning: Breaking Symmetry to Asymmetric Morphogenesis.
Trends Genet
2017
28335857
Modeling Syndromic Congenital Heart Defects in Zebrafish.
Curr Top Dev Biol
2017
28166211
Divergent effects of intrinsically active MEK variants on developmental Ras signaling.
Nat Genet
2017
28049852
In vivo severity ranking of Ras pathway mutations associated with developmental disorders.
Proc Natl Acad Sci U S A
2017
29140250
Gdf3 is required for robust Nodal signaling during germ layer formation and left-right patterning.
Elife
2017
29049395
Guidelines for morpholino use in zebrafish.
PLoS Genet
2017
29018093
How activating mutations affect MEK1 regulation and function.
J Biol Chem
2017
28335857
Modeling Syndromic Congenital Heart Defects in Zebrafish.
Curr Top Dev Biol
2017
28166211
Divergent effects of intrinsically active MEK variants on developmental Ras signaling.
Nat Genet
2017
29049395
Guidelines for morpholino use in zebrafish.
PLoS Genet
2017
29140250
Gdf3 is required for robust Nodal signaling during germ layer formation and left-right patterning.
Elife
2017
29018093
How activating mutations affect MEK1 regulation and function.
J Biol Chem
2017
28720483
Left-Right Patterning: Breaking Symmetry to Asymmetric Morphogenesis.
Trends Genet
2017
26904945
c21orf59/kurly Controls Both Cilia Motility and Polarization.
Cell Rep
2016
27821532
Antagonistic interactions in the zebrafish midline prior to the emergence of asymmetric gene expression are important for left-right patterning.
Philos Trans R Soc Lond B Biol Sci
2016
27284198
Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature.
Science
2016
26904945
c21orf59/kurly Controls Both Cilia Motility and Polarization.
Cell Rep
2016
27821532
Antagonistic interactions in the zebrafish midline prior to the emergence of asymmetric gene expression are important for left-right patterning.
Philos Trans R Soc Lond B Biol Sci
2016
27284198
Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature.
Science
2016
26203125
RASopathies: unraveling mechanisms with animal models.
Dis Model Mech
2015
26398161
RASopathies: unraveling mechanisms with animal models.
Dis Model Mech
2015
26203125
RASopathies: unraveling mechanisms with animal models.
Dis Model Mech
2015
26398161
RASopathies: unraveling mechanisms with animal models.
Dis Model Mech
2015
25192045
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.
Am J Hum Genet
2014
25505384
Prolonged, brain-wide expression of nuclear-localized GCaMP3 for functional circuit mapping.
Front Neural Circuits
2014
25192045
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.
Am J Hum Genet
2014
25505384
Prolonged, brain-wide expression of nuclear-localized GCaMP3 for functional circuit mapping.
Front Neural Circuits
2014
1 - 50 of 120
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Children's Hospital of Philadelphia
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