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Jacob N. Miller
Jacob N. Miller
University of Iowa Hospitals and Clinics
Verified email at uiowa.edu
Title
Cited by
Cited by
Year
Bipolar disorder and suicide: a review
JN Miller, DW Black
Current psychiatry reports 22, 1-10, 2020
3272020
Nonsense-mediated decay in genetic disease: friend or foe?
JN Miller, DA Pearce
Mutation Research/Reviews in Mutation Research 762, 52-64, 2014
2082014
Permanent genetic resources added to molecular ecology resources database 1 January 2009–30 April 2009
Molecular Ecology Resources Primer Development Consortium, ...
Molecular ecology resources 9 (5), 1375-1379, 2009
602009
The novel Cln1R151X mouse model of infantile neuronal ceroid lipofuscinosis (INCL) for testing nonsense suppression therapy
JN Miller, AD Kovacs, DA Pearce
Human molecular genetics 24 (1), 185-196, 2015
572015
The role of nonsense-mediated decay in neuronal ceroid lipofuscinosis
JN Miller, CH Chan, DA Pearce
Human molecular genetics 22 (13), 2723-2734, 2013
552013
Schizoaffective disorder: A review.
JN Miller, DW Black
Annals of clinical psychiatry: official journal of the American Academy of …, 2019
422019
Tissue‐specific variation in nonsense mutant transcript level and drug‐induced read‐through efficiency in the Cln1R151X mouse model of INCL
V Thada, JN Miller, AD Kovács, DA Pearce
Journal of cellular and molecular medicine 20 (2), 381-385, 2016
302016
Brain structural features of myotonic dystrophy type 1 and their relationship with CTG repeats
E van der Plas, MJ Hamilton, JN Miller, TR Koscik, JD Long, S Cumming, ...
Journal of neuromuscular diseases 6 (3), 321-332, 2019
292019
Cognitive deficits, apathy, and hypersomnolence represent the core brain symptoms of adult-onset myotonic dystrophy type 1
JN Miller, A Kruger, DJ Moser, L Gutmann, E van der Plas, TR Koscik, ...
Frontiers in neurology 12, 700796, 2021
172021
Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1
JN Miller, E van der Plas, M Hamilton, TR Koscik, L Gutmann, ...
Neurology: Genetics 6 (5), e504, 2020
172020
A Novel c.1135_1138delCTGT Mutation in CLN3 Leads to Juvenile Neuronal Ceroid Lipofuscinosis
AV Drack, JN Miller, DA Pearce
Journal of child neurology 28 (9), 1112-1116, 2013
142013
A Novel c.776_777insA Mutation in CLN1 Leads to Infantile Neuronal Ceroid Lipofuscinosis
JN Miller, DA Pearce
Journal of Child Neurology 28 (9), 1106-1111, 2013
82013
Supra-second interval timing in bipolar disorder: examining the role of disorder sub-type, mood, and medication status
VAM Ewald, NT Trapp, MCE Sarrett, BD Pace, L Wendt, JG Richards, ...
International Journal of Bipolar Disorders 11 (1), 32, 2023
2023
Cerebellar iTBS for Bipolar Disorder: A Randomized, Controlled Trial of Safety, Feasibility, and Preliminary Effects on Mood and Cognition
N Trapp, B Pace, B Penaluna, VM Ewald, L Wendt, J Miller, A Purgianto, ...
Brain Stimulation: Basic, Translational, and Clinical Research in …, 2023
2023
Supra-second interval timing deficits and abnormal frontal theta oscillations in individuals with bipolar disorder
VA Müller Ewald, NT Trapp, MCE Sarrett, BD Pace, JG Richards, IK Gala, ...
medRxiv, 2022.09. 25.22280348, 2022
2022
Schizoaffective Disorder: A Challenging Diagnosis
JN Miller, DW Black
Current Psychiatry 19 (8), 30, 2020
2020
Neural Correlates of Apathy in Myotonic Dystrophy Type 1
J Miller, E van der Plas, T Koscik, V Magnotta, L Gutmann, P Nopoulos
NEUROPSYCHOPHARMACOLOGY 44 (SUPPL 1), 326-327, 2019
2019
Abnormal Amygdala-Striatal Network Relates to Apathy in Myotonic Dystrophy 1
J Miller, E van der Plas, T Koscik, V Magnotta, L Gutmann, P Nopoulos
NEUROPSYCHOPHARMACOLOGY 43, S459-S459, 2018
2018
A Novel c. 776_777insA Mutation in CLN1 Leads to Infantile Neuronal Ceroid Lipofuscinosis (vol 28, pg 1106, 2013)
JN Miller, DA Pearce
JOURNAL OF CHILD NEUROLOGY 29 (5), NP1-NP1, 2014
2014
Nonsense-mediated decay and neuronal ceroid lipofuscinosis: Utilizing nonsense suppression as a therapeutic tool to enhance functional protein activity
JN Miller
University of South Dakota, 2014
2014
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