Emily G Allen Selected Research

5' Untranslated Regions (5' UTR)

1/2021	Ectopic expression of CGG-repeats alters ovarian response to gonadotropins and leads to infertility in a murine FMR1 premutation model.
1/2021	Therapeutic Development for CGG Repeat Expansion-Associated Neurodegeneration.
1/2020	Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima.
1/2020	Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy.
11/2017	Women who carry a fragile X premutation are biologically older than noncarriers as measured by telomere length.
1/2014	Approaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary study.
7/2010	Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.
4/2004	A study of the distributional characteristics of FMR1 transcript levels in 238 individuals.

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Emily G Allen Research Topics

Disease

7	Neurodegenerative Diseases (Neurodegenerative Disease) 01/2021 - 10/2019
6	Fragile X Tremor Ataxia Syndrome 01/2022 - 01/2019
4	Fragile X Syndrome (Martin Bell Syndrome) 10/2021 - 04/2004
4	Intellectual Disability (Idiocy) 01/2021 - 04/2004
3	Primary Ovarian Insufficiency 01/2021 - 01/2014
3	Congenital Abnormalities (Deformity) 03/2013 - 09/2010
3	Down Syndrome (Down's Syndrome) 03/2013 - 09/2010
2	Alzheimer Disease (Alzheimer's Disease) 01/2021 - 01/2020
2	Congenital Heart Defects (Congenital Heart Defect) 10/2011 - 09/2010
1	Brain Diseases (Brain Disorder) 01/2022
1	Allergic Rhinitis 10/2021
1	Inflammation (Inflammations) 10/2021
1	Cerebellar Neoplasms 01/2021
1	Ataxia (Dyssynergia) 01/2021
1	Tremor (Tremors) 01/2021
1	Essential Tremor (Essential Tremors) 01/2021
1	Neuronal intranuclear inclusion disease 01/2021
1	Infertility (Sterility) 01/2021
1	Medulloblastoma 01/2021
1	Ovarian Cysts (Ovarian Cyst) 01/2021
1	Hypoxia (Hypoxemia) 01/2020
1	Neoplasms (Cancer) 12/2019
1	Adenocarcinoma 12/2019
1	Nervous System Diseases (Neurological Disorders) 11/2019
1	Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease) 10/2019
1	Frontotemporal Dementia (Semantic Dementia) 10/2019
1	Amenorrhea 01/2018
1	Atrial Heart Septal Defects (Atrial Septal Defect) 10/2011
1	Neural Tube Defects (Exencephaly) 10/2011
1	Atrioventricular Septal Defect 09/2010

Drug/Important Bio-Agent (IBA)

8	5' Untranslated Regions (5' UTR)IBA 01/2021 - 04/2004
4	Proteins (Proteins, Gene)FDA Link 01/2021 - 11/2019
3	Biomarkers (Surrogate Marker)IBA 01/2022 - 01/2019
3	RNA (Ribonucleic Acid)IBA 01/2022 - 01/2021
3	Folic Acid (Vitamin M)FDA LinkGeneric 03/2013 - 09/2010
2	5-hydroxymethylcytosineIBA 10/2021 - 12/2019
2	6-methyladenineIBA 01/2021 - 01/2020
1	Cell-Free Nucleic AcidsIBA 01/2022
1	AllergensIBA 10/2021
1	Immunoglobulin E (IgE)IBA 10/2021
1	RNA-Binding Proteins (RNA-Binding Protein)IBA 10/2021
1	Fragile X Mental Retardation ProteinIBA 10/2021
1	EnzymesIBA 01/2021
1	GonadotropinsIBA 01/2021
1	CholesterolIBA 01/2021
1	N-methyladenosineIBA 01/2021
1	CytosineIBA 01/2020
1	Transcription Factors (Transcription Factor)IBA 01/2020
1	Hypoxia-Inducible Factor 1IBA 12/2019
1	ChromatinIBA 11/2019
1	Microtubule-Associated Proteins (Microtubule-Associated Protein 2)IBA 10/2019
1	purineIBA 01/2019
1	SphingolipidsIBA 01/2019
1	Oxidoreductases (Dehydrogenase)IBA 09/2010
1	5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase (Methyltetrahydrofolate Homocysteine Methyltransferase)IBA 09/2010
1	methionine synthase reductaseIBA 09/2010
1	Reduced Folate Carrier ProteinIBA 09/2010
1	Cystathionine beta-Synthase (Serine Sulfhydrase)IBA 09/2010

Therapy/Procedure

1	Hysterectomy 01/2018