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Distinguishing post‐translational modifications in dominantly inherited frontotemporal dementias: FTLD‐TDP Type A (GRN) vs Type B (C9orf72)

Neuropathology and applied neurobiology, 2022-10, Vol.48 (6), p.e12836-n/a

2022

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Phagosomal and mitochondrial alterations in RPE may contribute to KCNJ13 retinopathy

Scientific reports, 2019-03, Vol.9 (1), p.3793-3793, Article 3793

2019

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p63 exerts spatio-temporal control of palatal epithelial cell fate to prevent cleft palate

PLoS genetics, 2017-06, Vol.13 (6), p.e1006828

2017

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REP1 deficiency causes systemic dysfunction of lipid metabolism and oxidative stress in choroideremia

JCI insight, 2021-05, Vol.6 (9)

2021

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NEURONAL INTRACYTOPLASMIC PRP DEPOSITS IN DOMINANTLY INHERITED CREUTZFELDT-JAKOB DISEASE ASSOCIATED WITH THE PRNP E200K-129V HAPLOTYPE

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P1116-P1117

2016

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Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [ 18 F]Flortaucipir PET

Acta neuropathologica communications, 2018-10, Vol.6 (1), p.114-114, Article 114

2018

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CONTRIBUTION OF THE NEUROPATHOLOGY LABORATORY AT INDIANA UNIVERSITY TO THE DECIPHERING OF DOMINANTLY INHERITED DEMENTIAS: 1976-2016

Alzheimer's & dementia, 2016-07, Vol.12 (7), p.P744-P745

2016

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Multiple proteinopathies underlying atypical dementia

Alzheimer's & dementia, 2015-07, Vol.11 (7), p.P372-P372

2015

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Mechanism and evidence of nonsense suppression therapy for genetic eye disorders

Experimental eye research, 2017-02, Vol.155, p.24-37

2017

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Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina

The Journal of pathology, 2023-04, Vol.259 (4), p.441-454

2023

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Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches

European journal of human genetics : EJHG, 2017-04, Vol.25 (4), p.512-512

2017

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The genomic basis of temporal niche evolution in a diurnal rodent

Current biology, 2023-08, Vol.33 (15), p.3289-3298.e6

2023

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Clinical utility gene card for: Aniridia

European journal of human genetics : EJHG, 2016-11, Vol.24 (11), p.4-4

2016

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Evolution of neuronal cell classes and types in the vertebrate retina

Nature (London), 2023-12, Vol.624 (7991), p.415-424

2023

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Diffuse Lewy Body Disease and Alzheimer Disease: Neuropathologic Phenotype Associated With the PSEN1 p.A396T Mutation

Journal of neuropathology and experimental neurology, 2019-07, Vol.78 (7), p.585-594

2019

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Exome Sequence Identifies RIPK4 as the Bartsocas- Papas Syndrome Locus

American journal of human genetics, 2012-01, Vol.90 (1), p.69-75

2012

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P4‐228: Neuronal Intracytoplasmic PrP Deposits in Dominantly Inherited Creutzfeldt‐Jakob Disease Associated With the PRNP E200K‐129V Haplotype

Alzheimer's & dementia, 2016-07, Vol.12 (7S_Part_23), p.P1116-P1117

2016

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Falling in Love

The North American review, 2021-10, Vol.306 (3), p.49-49

RICHARD, NATALIE ROSE

2021

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P3‐008: EARLY ONSET AND RAPID COURSE OF ALZHEIMER DISEASE ASSOCIATED WITH THE I143T PSEN1 MUTATION

Alzheimer's & dementia, 2014-07, Vol.10 (4S_Part_17), p.P629-P629

2014

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P1‐086: Multiple proteinopathies underlying atypical dementia

Alzheimer's & dementia, 2015-07, Vol.11 (7S_Part_8), p.P372-P372

2015

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P2‐293: Contribution of the Neuropathology Laboratory at Indiana University to the Deciphering of Dominantly Inherited Dementias: 1976‐2016

Alzheimer's & dementia, 2016-07, Vol.12 (7S_Part_15), p.P744-P745

2016

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EARLY ONSET AND RAPID COURSE OF ALZHEIMER DISEASE ASSOCIATED WITH THE I143T PSEN1 MUTATION

Alzheimer's & dementia, 2014-07, Vol.10 (4), p.P629-P629

2014

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IC‐P‐032: COMPARATIVE ANALYSIS OF PIB IN VIVO WITH 6‐CN‐PIB AND Aβ‐IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION

Alzheimer's & dementia, 2014-07, Vol.10 (4S_Part_6), p.P20-P21

2014

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O1‐01‐03: COMPARATIVE ANALYSIS OF PIB IN VIVO WITH 6‐CN‐PIB AND AB‐IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER'S DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION

Alzheimer's & dementia, 2014-07, Vol.10 (4S_Part_1), p.P129-P129

2014

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COMPARATIVE ANALYSIS OF PIB IN VIVO WITH 6-CN-PIB AND AB-IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER'S DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION

Alzheimer's & dementia, 2014-07, Vol.10 (4), p.P129-P129

2014

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Distinguishing post‐translational modifications in dominantly inherited frontotemporal dementias: FTLD‐TDP Type A (GRN) vs Type B (C9orf72)

Phagosomal and mitochondrial alterations in RPE may contribute to KCNJ13 retinopathy

p63 exerts spatio-temporal control of palatal epithelial cell fate to prevent cleft palate

REP1 deficiency causes systemic dysfunction of lipid metabolism and oxidative stress in choroideremia

NEURONAL INTRACYTOPLASMIC PRP DEPOSITS IN DOMINANTLY INHERITED CREUTZFELDT-JAKOB DISEASE ASSOCIATED WITH THE PRNP E200K-129V HAPLOTYPE

Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [ 18 F]Flortaucipir PET

CONTRIBUTION OF THE NEUROPATHOLOGY LABORATORY AT INDIANA UNIVERSITY TO THE DECIPHERING OF DOMINANTLY INHERITED DEMENTIAS: 1976-2016

Multiple proteinopathies underlying atypical dementia

Mechanism and evidence of nonsense suppression therapy for genetic eye disorders

Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina

Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches

The genomic basis of temporal niche evolution in a diurnal rodent

Clinical utility gene card for: Aniridia

Evolution of neuronal cell classes and types in the vertebrate retina

Diffuse Lewy Body Disease and Alzheimer Disease: Neuropathologic Phenotype Associated With the PSEN1 p.A396T Mutation

Exome Sequence Identifies RIPK4 as the Bartsocas- Papas Syndrome Locus

P4‐228: Neuronal Intracytoplasmic PrP Deposits in Dominantly Inherited Creutzfeldt‐Jakob Disease Associated With the PRNP E200K‐129V Haplotype

Falling in Love

P3‐008: EARLY ONSET AND RAPID COURSE OF ALZHEIMER DISEASE ASSOCIATED WITH THE I143T PSEN1 MUTATION

P1‐086: Multiple proteinopathies underlying atypical dementia

P2‐293: Contribution of the Neuropathology Laboratory at Indiana University to the Deciphering of Dominantly Inherited Dementias: 1976‐2016

EARLY ONSET AND RAPID COURSE OF ALZHEIMER DISEASE ASSOCIATED WITH THE I143T PSEN1 MUTATION

IC‐P‐032: COMPARATIVE ANALYSIS OF PIB IN VIVO WITH 6‐CN‐PIB AND Aβ‐IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION

O1‐01‐03: COMPARATIVE ANALYSIS OF PIB IN VIVO WITH 6‐CN‐PIB AND AB‐IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER'S DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION

COMPARATIVE ANALYSIS OF PIB IN VIVO WITH 6-CN-PIB AND AB-IMMUNOHISTOCHEMISTRY POSTMORTEM IN FAMILIAL ALZHEIMER'S DISEASE ASSOCIATED WITH THE PSEN1 I229F MUTATION

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