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Author Details
Full Name
Clifton L Dalgard
Affiliation
Uniformed Services University of the Health Sciences
ORCID
Career Start Year
1997
Papers
130
H Index
30
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36797998
Unexpected frequency of the pathogenic AR CAG repeat expansion in the general population.
Brain
2023
37488248
Transmission disequilibrium analysis of whole genome data in childhood-onset systemic lupus erythematosus.
Genes Immun
2023
37515136
Lack of Evidence for a Role of ACE-2 Polymorphisms as a Bedside Clinical Prognostic Marker of COVID-19.
Viruses
2023
37639904
Metronomic dosing of ovarian cancer cells with the ATR inhibitor AZD6738 leads to loss of CDC25A expression and resistance to ATRi treatment.
Gynecol Oncol
2023
37390458
The Early-Onset Alzheimer's Disease Whole-Genome Sequencing Project: Study design and methodology.
Alzheimers Dement
2023
36950378
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism.
Cell Genom
2023
37214860
A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats.
bioRxiv
2023
37202167
Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis.
Neurology
2023
36695634
Genome-Wide Analysis of Structural Variants in Parkinson Disease.
Ann Neurol
2023
36543879
Recurrent germline variant in ATM associated with familial myeloproliferative neoplasms.
Leukemia
2023
36805500
Lymphocyte antigen 6K signaling to aurora kinase promotes advancement of the cell cycle and the growth of cancer cells, which is inhibited by LY6K-NSC243928 interaction.
Cancer Lett
2023
36829800
Transcriptomic Profiling and Pathway Analysis of Mesenchymal Stem Cells Following Low Dose-Rate Radiation Exposure.
Antioxidants (Basel)
2023
36900259
NSC243928 Treatment Induces Anti-Tumor Immune Response in Mouse Mammary Tumor Models.
Cancers (Basel)
2023
34664540
Rare variant association study of veteran twin whole-genomes links severe depression with a nonsynonymous change in the neuronal gene <i>BHLHE22</i>.
World J Biol Psychiatry
2022
35708626
Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia.
J Exp Med
2022
35510647
CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy-like Phenotype.
Mov Disord
2022
35835913
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries.
Nat Genet
2022
35373853
Survival motor neuron protein deficiency alters microglia reactivity.
Glia
2022
35500221
IFNγ regulates NAD+ metabolism to promote the respiratory burst in human monocytes.
Blood Adv
2022
35788729
A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry.
PLoS Genet
2022
35852866
Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19.
JCI Insight
2022
35625955
Whole-Genome Sequencing Identifies <i>PPARGC1A</i> as a Putative Modifier of Cancer Risk in <i>BRCA1/2</i> Mutation Carriers.
Cancers (Basel)
2022
35521889
ATXN2 intermediate expansions in amyotrophic lateral sclerosis.
Brain
2022
35810449
GRN Mutations Are Associated with Lewy Body Dementia.
Mov Disord
2022
36544903
Cell type-specific changes in Wnt signaling and neuronal differentiation in the developing mouse cortex after prenatal alcohol exposure during neurogenesis.
Front Cell Dev Biol
2022
36528667
Integrated multi-omic analysis of low-grade ovarian serous carcinoma collected from short and long-term survivors.
J Transl Med
2022
35911887
<i>APOE</i> Is Associated With Serum Tau Following Uncomplicated Mild Traumatic Brain Injury.
Front Neurol
2022
36313067
Clinical and Metabolic Signature of <i>UNC13A</i> rs12608932 Variant in Amyotrophic Lateral Sclerosis.
Neurol Genet
2022
35866887
Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population.
Mov Disord
2022
35896380
Systematic evaluation of genetic mutations in ALS: a population-based study.
J Neurol Neurosurg Psychiatry
2022
36384096
Proteogenomic analysis of lung adenocarcinoma reveals tumor heterogeneity, survival determinants, and therapeutically relevant pathways.
Cell Rep Med
2022
36265467
ImmunoTyper-SR: A computational approach for genotyping immunoglobulin heavy chain variable genes using short-read data.
Cell Syst
2022
36008116
Exploring the phenotype of Italian patients with ALS with intermediate <i>ATXN2</i> polyQ repeats.
J Neurol Neurosurg Psychiatry
2022
35132409
ImmunoTyper-SR: A Novel Computational Approach for Genotyping Immunoglobulin Heavy Chain Variable Genes using Short Read Data.
bioRxiv
2022
35289316
Genetically programmed alternative splicing of NEMO mediates an autoinflammatory disease phenotype.
J Clin Invest
2022
35177862
Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19.
Nat Med
2022
35271708
Genetic variants of PKLR are associated with acute pain in sickle cell disease.
Blood Adv
2022
35262093
Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19.
medRxiv
2022
35292633
Germline mutation landscape of DNA damage repair genes in African Americans with prostate cancer highlights potentially targetable RAD genes.
Nat Commun
2022
32946850
Distinguishing Smoking-Related Lung Disease Phenotypes Via Imaging and Molecular Features.
Chest
2021
33828448
Transcriptomic Analysis of Mouse Brain After Traumatic Brain Injury Reveals That the Angiotensin Receptor Blocker Candesartan Acts Through Novel Pathways.
Front Neurosci
2021
33522086
Increased APOE ε4 expression is associated with the difference in Alzheimer's disease risk from diverse ancestral backgrounds.
Alzheimers Dement
2021
33902942
Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus.
Neurobiol Aging
2021
33589841
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.
Nat Genet
2021
33556144
Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses.
PLoS Pathog
2021
33931688
Proteogenomic landscape of uterine leiomyomas from hereditary leiomyomatosis and renal cell cancer patients.
Sci Rep
2021
33804348
Transcriptomics of Long-Term Meditation Practice: Evidence for Prevention or Reversal of Stress Effects Harmful to Health.
Medicina (Kaunas)
2021
35036869
Recruitment of MLL1 complex is essential for SETBP1 to induce myeloid transformation.
iScience
2021
35036865
Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.
iScience
2021
34966482
Comparative transcriptome analysis between patient and endometrial cancer cell lines to determine common signaling pathways and markers linked to cancer progression.
Oncotarget
2021
1 - 50 of 130
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row(s) 1 - 30 of 30
Collaborators
Matthew D Wilkerson
Uniformed Services University of the Health Sciences
Co-authored papers
17
Andrew B Singleton
National Institute on Aging
Co-authored papers
8
Thomas P Conrads
Women's Health Integrated Research Center, Inova Health System
Co-authored papers
8
Mike A Nalls
Center for Alzheimer's and Related Dementias, National Institutes of Health
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7
George L Maxwell
Women's Health Integrated Research Center, Inova Health System
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7
Sandra D'Alfonso
Co-authored papers
5
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UCL Great Ormond Street Institute of Child Health, University College London
Co-authored papers
5
Brian L Hood
The Henry M. Jackson Foundation for the Advancement of Military Medicine
Co-authored papers
5
Ali Torkamani
Scripps Science Institute
Co-authored papers
5
Yovanni Casablanca
Uniformed Services of the Health Sciences Gynecologic Cancer Center of Excellence
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4
Robert J Ursano
Uniformed Services University
Co-authored papers
4
Kathleen M Darcy
The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc.
Co-authored papers
4
Margaret A Pericak-Vance
Co-authored papers
4
Gyorgy Petrovics
Henry Jackson Foundation for the Advancement of Military Medicine (HJF)
Co-authored papers
3
Jonathan L Haines
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers
3
Christopher S Hourigan
and Blood Institute, National Institutes of Health
Co-authored papers
3
Hai Hu
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Co-authored papers
3
Clesson Turner
National Human Genome Research Institute, National Institutes of Health
Co-authored papers
3
Craig D Shriver
Walter Reed National Military Medical Center
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3
Cihan Oguz
National Institute of Allergy and Infectious Diseases, National Institutes of Health
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Stephen J Chanock
National Cancer Institute, National Institutes of Health
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