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Abigail R. Moye
Observed names:
Abigail Hayes,
Abigail Moye,
Abigail R Moye,
Abigail Ruth Moye,
Moye AR,
Moye, Abigail,
Moye, Abigail R.
show all 7
Institutions:
University of Basel,
Institute of Molecular and Clinical Ophthalmology Basel
Observed institutions:
West Virginia University,
Baylor College of Medicine,
University of Basel,
University Hospital of Basel,
Institute of Molecular and Clinical Ophthalmology Basel
ORCID:
0000-0002-3698-7156
Observed ORCID:
0000-0002-3698-7156
OpenAlex ID:
A5077948240
Bardet–Biedl syndrome-8 (BBS8) protein is crucial for the development of outer segments in photoreceptor neurons
2017
·
Tanya L Dilan
, Ratnesh K Singh
, et al.
·
Human Molecular Genetics
·
66
PDF
ARL13B, a Joubert Syndrome-Associated Protein, Is Critical for Retinogenesis and Elaboration of Mouse Photoreceptor Outer Segments
2018
·
Tanya L. Dilan
, Abigail R. Moye
, et al.
·
Journal of Neuroscience
·
55
Structure and dynamics of photoreceptor sensory cilia
2021
·
Theodore G. Wensel
, Valencia L. Potter
, et al.
·
Pflügers Archiv - European Journal of Physiology
·
45
Dnmt1, Dnmt3a and Dnmt3b cooperate in photoreceptor and outer plexiform layer development in the mammalian retina
2016
·
Ratnesh K. Singh
, Ramya K. Mallela
, et al.
·
Experimental Eye Research
·
42
Knockout of mouse receptor accessory protein 6 leads to sperm function and morphology defects†
2020
·
Darius J Devlin
, Smriti Agrawal Zaneveld
, et al.
·
Biology of Reproduction
·
31
Super-resolution microscopy reveals photoreceptor-specific subciliary location and function of ciliopathy-associated protein CEP290
2021
·
Valencia L. Potter
, Abigail R. Moye
, et al.
·
JCI Insight
·
30
PDF
Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice
2019
·
Abigail R. Moye
, Nicola Bedoni
, et al.
·
PLoS Genetics
·
26
PDF
Ciliary tip actin dynamics regulate photoreceptor outer segment integrity
2024
·
Roly Megaw
, Abigail Moye
, et al.
·
Nature Communications
·
23
PDF
Centriole and transition zone structures in photoreceptor cilia revealed by cryo-electron tomography
2024
·
Zhixian Zhang
, Abigail Moye
, et al.
·
Life Science Alliance
·
20
PDF
ARL2BP, a protein linked to retinitis pigmentosa, is needed for normal photoreceptor cilia doublets and outer segment structure
2018
·
Abigail R. Moye
, Ratnesh Singh
, et al.
·
Molecular Biology of the Cell
·
20
Viral-mediated vision rescue of a novel AIPL1 cone-rod dystrophy model
2014
·
Cristy A. Ku
, Vince A. Chiodo
, et al.
·
Human Molecular Genetics
·
14
PDF
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction
2024
·
Miriam Bauwens
, Elifnaz Celik
, et al.
·
The American Journal of Human Genetics
·
9
PDF
Sub-ciliary localization of CEP290 and effects of its loss in mouse photoreceptors during development
2025
·
Abigail R. Moye
, Michael A. Robichaux
, et al.
·
Journal of Cell Science
·
7
Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy
2025
·
Karolina Kaminska
, Francesca Cancellieri
, et al.
·
The American Journal of Human Genetics
·
7
Expansion Microscopy of Mouse Photoreceptor Cilia
2023
·
Abigail R. Moye
, Michael A. Robichaux
, et al.
·
Advances in experimental medicine and biology
·
7
PDF
Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy
2025
·
Miriam Ehrenberg
, Maayan Avraham
, et al.
·
Genetics in Medicine
·
4
PDF
Loss-of-function variants in SAXO6, encoding a microtubule inner protein of photoreceptor cilia, cause a late-onset retinal dystrophy
2026
·
Abigail R. Moye
, Caitlyn L. McCafferty
, et al.
·
The American Journal of Human Genetics
·
2
Biallelic germline variants in the hematologic malignancy predisposition gene DDX41 cause retinal dystrophy through dysregulation of retinal homeostasis
2026
·
Zoéline Mars
, Andrea Zanetti
, et al.
·
medRxiv
·
1
Ciliopathy-associated protein, CEP290, is required for ciliary necklace and outer segment membrane formation in retinal photoreceptors
2025
·
Abigail R. Moye
, Michael A. Robichaux
, et al.
·
bioRxiv (Cold Spring Harbor Laboratory)
·
1
ARL2BP, a novel ciliopathy protein, is required for cilia microtubule formation
2018
·
Abigail Ruth Moye
·
1
Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy
2026
·
Carlo Rivolta
, Karolina Kaminska
, et al.
·
Research Square
PDF
Bi-allelic variants in FSD1L cause retinitis pigmentosa with or without neurological involvement
2026
·
Siying Lin
, Francesca Cancellieri
, et al.
·
The American Journal of Human Genetics
Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy
2025
·
Kaminska K
, Cancellieri F
, et al.
·
Newcastle University ePrints (Newcastle Univesity)
PDF
Novel genetic cause of specific macular dystrophy due to biallelic variants in three genes encoding subunits of the AP-5 complex
2025
·
Kaminska, Karolina
, Cancellieri, Francesca
, et al.
·
Ghent University Academic Bibliography (Ghent University)
Lysosomal macular dystrophy is a novel ocular phenotype associated with biallelic variants affecting AP-5/ SPG11/SPG15 complex
2025
·
Santos, Cristina Moreira
, Kaminska, Karolina
, et al.
·
Ghent University Academic Bibliography (Ghent University)
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Works count:
27
Citation count:
411
H-index:
11
I10-index:
11
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