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Author Details
Full Name
Helen Rankin Willsey
Affiliation
University of California san francisco
ORCID
Career Start Year
2016
Papers
18
H Index
11
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37366052
Pleiotropy of autism-associated chromatin regulators.
Development
2023
34531330
Modeling Human Genetic Disorders with CRISPR Technologies in <i>Xenopus</i>.
Cold Spring Harb Protoc
2022
35440779
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.
Nat Rev Neurosci
2022
33369095
Xenopus leads the way: Frogs as a pioneering model to understand the human brain.
Genesis
2021
33827967
Whole-Mount RNA In Situ Hybridization and Immunofluorescence of <i>Xenopus</i> Embryos and Tadpoles.
Cold Spring Harb Protoc
2021
33887193
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Neuron
2021
33497602
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Neuron
2021
34739029
Deep learning is widely applicable to phenotyping embryonic development and disease.
Development
2021
34737378
Picroscope: low-cost system for simultaneous longitudinal biological imaging.
Commun Biol
2021
34411509
A convergent molecular network underlying autism and congenital heart disease.
Cell Syst
2021
32467234
The neurodevelopmental disorder risk gene <i>DYRK1A</i> is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.
Development
2020
31857706
Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.
Genet Med
2020
33288503
Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.
Development
2020
33308296
In Xenopus ependymal cilia drive embryonic CSF circulation and brain development independently of cardiac pulsatile forces.
Fluids Barriers CNS
2020
31263215
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract.
Genet Med
2019
30096282
Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos.
Dev Biol
2018
30053424
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.
Cell
2018
26974344
Localized JNK signaling regulates organ size during development.
Elife
2016
1 - 18 of 18
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