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Huang, Alden
201  results:
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1

Reanalysis of RNA sequencing data ends diagnostic odyssey a..:

McNamee, Lucy ; Schoch, Kelly ; Huang, Alden...
American Journal of Medical Genetics Part A.  , 2024
Link: https://doi.org/10.1002/..
 
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2

Whole-Exome Sequencing Identifies Homozygote Nonsense Varia..:

Sono, Reiri ; Larrinaga, Tania M. ; Huang, Alden...
Cells.  12 (2023)  11 - p. 1455 , 2023
Link: https://doi.org/10.3390/..
 
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3

Commonalities across computational workflows for uncovering..:

Kobren, Shilpa Nadimpalli ; Baldridge, Dustin ; Velinder, Matt...
Genetics in Medicine.  23 (2021)  6 - p. 1075-1085 , 2021
Link: https://doi.org/10.1038/..
 
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4

Collaborative Genome-Wide Association and Copy Number Varia..:

Scharf, Jeremiah ; Yu, Dongmei ; Huang, Alden...
European Neuropsychopharmacology.  29 (2019)  - p. S736-S737 , 2019
Link: https://doi.org/10.1016/..
 
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5

Neurodegenerative disease biomarkers Aβ1–40, Aβ1–42, tau, a..:

Chen, Jason A. ; Fears, Scott C. ; Jasinska, Anna J....
Brain and Behavior.  8 (2018)  2 - p. , 2018
Link: https://doi.org/10.1002/..
 
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6

Activity-Dependent Regulation of Alternative Cleavage and P..:

Fontes, Mariana M. ; Guvenek, Aysegul ; Kawaguchi, Riki...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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7

Transcriptome Profiling of Peripheral Blood in 22q11.2 Dele..:

Jalbrzikowski, Maria ; Lazaro, Maria T. ; Gao, Fuying...
PLOS ONE.  10 (2015)  7 - p. e0132542 , 2015
Link: https://doi.org/10.1371/..
 
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8

Mutations in SLC20A2 are a major cause of familial idiopath..:

Hsu, Sandy Chan ; Sears, Renee L. ; Lemos, Roberta R....
neurogenetics.  14 (2013)  1 - p. 11-22 , 2013
Link: https://doi.org/10.1007/..
 
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9

Familial cortical myoclonus with a mutation in NOL3:

Russell, Jonathan F. ; Steckley, Jamie L. ; Coppola, Giovanni...
Annals of Neurology.  72 (2012)  2 - p. 175-183 , 2012
Link: https://doi.org/10.1002/..
 
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10

Mutations in rare ataxia genes are uncommon causes of spora..:

Fogel, Brent L. ; Lee, Ji Yong ; Lane, Jessica...
Movement Disorders.  27 (2012)  3 - p. 442-446 , 2012
Link: https://doi.org/10.1002/..
 
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11

Loss-of-function in RBBP5 results in a syndromic neurodevel..:

Huang, Yue ; Jay, Kristy L. ; Huang, Alden Yen-Wen...
Genetics in Medicine.  , 2024
Link: https://doi.org/10.1016/..
 
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12

Synaptic processes and immune-related pathways implicated i..:

Tsetsos, Fotis ; Yu, Dongmei ; Sul, Jae Hoon...
Translational Psychiatry.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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13

Contribution of common and rare variants to bipolar disorde..:

Sul, Jae Hoon ; Service, Susan K. ; Huang, Alden Y....
Translational Psychiatry.  10 (2020)  1 - p. , 2020
Link: https://doi.org/10.1038/..
 
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14

Genetic and functional analysis of a Pacific hagfish opioid..:

Huang, Alden Y. ; Taylor, Anna M. W. ; Ghogha, Atefeh...
Journal of Neuroscience Research.  100 (2020)  1 - p. 19-34 , 2020
Link: https://doi.org/10.1002/..
 
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15

Correction: GATAD2B-associated neurodevelopmental disorder ..:

Shieh, Christine ; Jones, Natasha ; Vanle, Brigitte...
Genetics in Medicine.  22 (2020)  4 - p. 822 , 2020
Link: https://doi.org/10.1038/..
 
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