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Ali Crawford
Ali Crawford
Other namesAli Fenstermaker
Verified email at illumina.com
Title
Cited by
Cited by
Year
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders
G Novarino, AG Fenstermaker, MS Zaki, M Hofree, JL Silhavy, ...
science 343 (6170), 506-511, 2014
5602014
Exome Sequencing Can Improve Diagnosis and Alter Patient Management
TJ Dixon-Salazar, JL Silhavy, N Udpa, J Schroth, S Bielas, AE Schaffer, ...
Science Translational Medicine 4 (138), 138ra78-138ra78, 2012
2962012
Wnt/planar cell polarity signaling controls the anterior–posterior organization of monoaminergic axons in the brainstem
AG Fenstermaker, AA Prasad, A Bechara, Y Adolfs, F Tissir, A Goffinet, ...
Journal of Neuroscience 30 (47), 16053-16064, 2010
1932010
Oligodendrocyte-specific activation of PERK signaling protects mice against experimental autoimmune encephalomyelitis
W Lin, Y Lin, J Li, AG Fenstermaker, SW Way, B Clayton, S Jamison, ...
Journal of Neuroscience 33 (14), 5980-5991, 2013
1202013
Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model
J Fortun, J Li, J Go, A Fenstermaker, BS Fletcher, L Notterpek
Journal of neurochemistry 92 (6), 1531-1541, 2005
1172005
Phosphatidylinositol-3-kinase–atypical protein kinase C signaling is required for Wnt attraction and anterior–posterior axon guidance
AM Wolf, AI Lyuksyutova, AG Fenstermaker, B Shafer, CG Lo, Y Zou
Journal of Neuroscience 28 (13), 3456-3467, 2008
1162008
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder
N Akizu, V Cantagrel, J Schroth, N Cai, K Vaux, D McCloskey, ...
Cell 154 (3), 505-517, 2013
1142013
Off-target effect of doublecortin family shRNA on neuronal migration associated with endogenous microRNA dysregulation
ST Baek, G Kerjan, SL Bielas, JE Lee, AG Fenstermaker, G Novarino, ...
Neuron 82 (6), 1255-1262, 2014
1102014
Mutations in CSPP1 lead to classical Joubert syndrome
N Akizu, JL Silhavy, RO Rosti, E Scott, AG Fenstermaker, J Schroth, ...
The American Journal of Human Genetics 94 (1), 80-86, 2014
932014
Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.
MS Zaki, L Selim, L Mansour, IG Mahmoud, AG Fenstermaker, SB Gabriel, ...
Clinical Genetics 88 (1), 95-97, 2014
162014
Cross-platform transcriptomic profiling of the response to recombinant human erythropoietin
G Wang, T Kitaoka, A Crawford, Q Mao, A Hesketh, FM Guppy, GI Ash, ...
Scientific Reports 11 (1), 21705, 2021
92021
Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome
MN Bainbridge, A Mazumder, D Ogasawara, R Abou Jamra, G Bernard, ...
Brain 145 (10), 3383-3390, 2022
32022
Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt
JL Shepherdson, K Hutchison, DW Don, G McGillivray, TI Choi, CA Allan, ...
The American Journal of Human Genetics, 2024
2024
A validated PCR-free clinical whole genome sequencing system for the detection of germline variants
C Glidewell-Kenney, V Onuchic, K Sabourov, N Dukler, M Mehan, J Lee, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 640-641, 2024
2024
The impact of clinical genome sequencing in a global population of patients with suspected rare genetic disease
R Taft, E Thorpe, T Williams, C Shaw, E Chekalin, J Ortega, K Robinson, ...
2023
Methods and systems for monitoring organ health and disease
Y Li, R Taft, AG Crawford, N Kim
US Patent App. 17/922,930, 2023
2023
Endocannabinoid Dysfunction in Human Disease: Neuro-Ocular DAGLA-related Syndrome (NODrS), a unique pediatric condition
J Friedman, A Mazumder, D Ogasawara, R Abou Jamra, G Bernard, ...
MOVEMENT DISORDERS 37, S294-S295, 2022
2022
OR28 Validation of 2070 common, rare, and novel HLA alleles using Illumina TruSight® HLA ultra-high-resolution sequencing
F Yamamoto, A Lindell, B Baas, A Crawford, M Won, N Baird, ...
Human Immunology 76, 12, 2015
2015
Improved HLA typing by next-generation DNA sequencing
S Conklin, B Yang, N Baird, B Baas, A Crawford, M Won, N Kim, ...
Human Immunology 76, 63, 2015
2015
OR22 Towards clinical NGS HLA-typing: A performance comparison of next-generation sequencing technologies for DNA HLA typing in a clinical diagnostic environment
K Sherwood, J Beckrud, L Allan, A Lindell, A Crawford, N Baird, B Baas, ...
Human Immunology 76, 7, 2015
2015
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Articles 1–20