Alisha Daniels

ORCID: 0009-0001-1464-6465
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Alzheimer's disease research and treatments
  • Dementia and Cognitive Impairment Research
  • Functional Brain Connectivity Studies
  • Bioinformatics and Genomic Networks
  • Advanced Neuroimaging Techniques and Applications
  • Parkinson's Disease Mechanisms and Treatments
  • Resilience and Mental Health
  • Ubiquitin and proteasome pathways
  • Optimism, Hope, and Well-being
  • Prion Diseases and Protein Misfolding
  • Down syndrome and intellectual disability research
  • Genetic Associations and Epidemiology
  • Attention Deficit Hyperactivity Disorder
  • Cancer Genomics and Diagnostics
  • Neurological Disease Mechanisms and Treatments
  • Renal cell carcinoma treatment
  • Endoplasmic Reticulum Stress and Disease
  • Amyotrophic Lateral Sclerosis Research
  • Bipolar Disorder and Treatment
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Frailty in Older Adults
  • Tryptophan and brain disorders
  • Mitochondrial Function and Pathology
  • Pancreatic and Hepatic Oncology Research
  • Genetics and Neurodevelopmental Disorders

Washington University in St. Louis
2022-2025

University of Ulsan
2024

Asan Medical Center
2024

Dankook University
2024

Ulsan College
2024

Alzheimer’s Disease Neuroimaging Initiative
2023

University of Florida
2019

Willemijn J. Jansen Olin Janssen Betty M. Tijms Stephanie J. B. Vos Rik Ossenkoppele and 95 more Pieter Jelle Visser Dag Aarsland Daniel Alcolea Daniele Altomare Christine A. F. Von Arnim Simone Baiardi Inês Baldeiras Henryk Barthel Randall J. Bateman Bart van Berckel Alexa Pichet Binette Kaj Blennow Merçé Boada Henning Boecker Michel Bottlaender Anouk den Braber David J. Brooks Mark A. van Buchem Vincent Camus Jose Manuel Carill Jiří Cerman Kewei Chen Gaël Chételat Elena Chipi Ann D. Cohen Alisha Daniels Marion Delarue Mira Didic Alexander Drzezga Bruno Dubois Marie Eckerström Laura L. Ekblad Sebastiaan Engelborghs Stéphane Epelbaum Anne M. Fagan Yong Fan Tormod Fladby Adam Fleisher Wiesje M. van der Flier Stefan Förster Juan Fortea Kristian Steen Frederiksen Yvonne Freund‐Levi Lars Frings Giovanni B. Frisoni Lutz Fröhlich Tomasz Gabryelewicz Hermann‐Josef Gertz Kiran Dip Gill Olymbia Gkatzima Estrella Gómez‐Tortosa Timo Grimmer Eric Guedj Christian Habeck Harald Hampel Ron Handels Oskar Hansson Lucrezia Hausner Sabine Hellwig Michael T. Heneka Sanna‐Kaisa Herukka Helmut Hildebrandt John R. Hodges Jakub Hort Chin‐Chang Huang Ane Iriondo Yoshiaki Itoh Adrian Ivanoiu William J. Jagust Frank Jessen Peter Johannsen Keith A. Johnson Ramesh Kandimalla Elisabeth Kapaki Silke Kern Lena Kilander Aleksandra Klimkowicz‐Mrowiec William E. Klunk Norman Koglin Johannes Kornhuber Milica G. Kramberger Hung‐Chou Kuo Koen Van Laere Susan Landau Brigitte Landeau Dong Young Lee Mony J. de Leon Cristian E. Leyton Kun‐Ju Lin Alberto Lleó Malin Löwenmark Karine Madsen Wolfgang Maier Jan Marcusson Marta Marquié

One characteristic histopathological event in Alzheimer disease (AD) is cerebral amyloid aggregation, which can be detected by biomarkers cerebrospinal fluid (CSF) and on positron emission tomography (PET) scans. Prevalence estimates of pathology are important for health care planning clinical trial design. To estimate the prevalence abnormality persons with normal cognition, subjective cognitive decline, mild impairment, or AD dementia to examine potential implications cutoff methods,...

10.1001/jamaneurol.2021.5216 article EN JAMA Neurology 2022-01-31
Jorge J. Llibre‐Guerra María Victoria Fernández Nelly Joseph‐Mathurin Shijia Bian Kathleen Carter and 95 more Yan Li Andrew J. Aschenbrenner Cyril Pottier Wendy Sigurdson Eric McDade Brian A. Gordon Alan E. Renton Tammie L.S. Benzinger Laura Ibáñez Nicole Barthélémy Matthew P. Johnson Jason Hassenstab Guoqiao Wang Alison Goate Daniel Western Ciyang Wang Diana A. Hobbs Alisha Daniels Celeste M. Karch John C. Morris Carlos Cruchaga Erik C. B. Johnson Randall J. Bateman David Aguillón Ricardo Allegri Ana Baena Bryce Baker Jessica Banks Nicolas R. Barthélemy Jamie Bartzel Randall J. Bateman Jacob Bechara Sarah Berman Yamile Bocanegra William S. Brooks David M. Cash Allison Chen Charles Chen Jasmeer P. Chhatwal Patricio Chrem Méndez Laura Courtney Alisha Daniels Gregory S. Day Emma Devenney Anne M. Fagan Martin R. Farlow Shaney Flores Nick C. Fox Erin Franklin Brian Fulton‐Howard Manu S. Goyal Susanne Gräber‐Sultan Neill R. Graff‐Radford Emily Gremminger Cortaiga Hellm David M. Holtzman Russ C. Hornbeck Edward D. Huey Laura Ibáñez Takeshi Ikeuchi Snežana Ikonomović Takanobu Ishiguro Kenji Ishii Kelley Jackson Gina Jerome Mathias Jucker Celeste M. Karch Kensaku Kasuga Sarah Keefe Deborah Koudelis Elke Kuder-Buletta Christian la Fougère Christoph Laske Jae Hong Lee Allan I. Levey Johannes Levin Yudy Milena Leon Francisco Lopera Ruijin Lu Courtney Maa Jacob Marsh Mariana Martin Ralph N. Martins Parinaz Massoumzadeh Colin L. Masters Austin McCullough Nicole S. McKay Matthew Minton Hiroshi Mori Joyce Nicklaus Yu-zheng Nie Yoshiki Niimi James M. Noble Ulrike Obermueller Richard J. Perrin

10.1038/s41591-025-03494-0 article EN Nature Medicine 2025-02-10

Abstract The Dominantly Inherited Alzheimer Network (DIAN) is an international collaboration studying autosomal dominant disease (ADAD). ADAD arises from mutations occurring in three genes. Offspring families have a 50% chance of inheriting their familial mutation, so non-carrier siblings can be recruited for comparisons case–control studies. age onset highly predictable within families, allowing researchers to estimate individual’s point the trajectory. These characteristics allow candidate...

10.1038/s41593-023-01359-8 article EN cc-by Nature Neuroscience 2023-07-10
Julie K. Wisch Nicole S. McKay Anna H. Boerwinkle James L. Kennedy Shaney Flores and 95 more Benjamin L. Handen Bradley T. Christian Elizabeth Head Mark Mapstone Michael S. Rafii Sid E. O’Bryant Julie C. Price Charles M. Laymon Sharon J. Krinsky‐McHale Florence Lai H. Diana Rosas Sigan L. Hartley Shahid Zaman Ira T. Lott Dana Tudorascu Matthew Zammit Adam M. Brickman Joseph H. Lee Thomas D. Bird Annie Cohen Patricio Chrem Alisha Daniels Jasmeer P. Chhatwal Carlos Cruchaga Laura Ibáñez Mathias Jucker Celeste M. Karch Gregory S. Day Jae‐Hong Lee Johannes Levin Jorge J. Llibre‐Guerra Yan Li Francisco Lopera Jee Hoon Roh John M. Ringman Charlene Supnet Christopher H. van Dyck Chengjie Xiong Guoqiao Wang John C. Morris Eric McDade Randall J. Bateman Tammie L.S. Benzinger Brian A. Gordon Beau M. Ances Howard Aizenstein Howard Andrews Karen L. Bell Rasmus M. Birn Peter Bulova Amrita K. Cheema Kewei Chen I. C. H. Clare Lorraine N. Clark Ann D. Cohen John N. Constantino Eric Doran Eleanor Feingold Tatiana Foroud Sigan L. Hartley Christy Hom Lawrence S. Honig Miloš D. Ikonomović Sterling C. Johnson Courtney Jordan M. Ilyas Kamboh David B. Keator William E. Klunk Julia Kofler William Charles Kreisl Sharon J. Krinsky‐McHale Patrick J. Lao Charles M. Laymon Ira T. Lott Victoria Lupson Chester A. Mathis Davneet S. Minhas Neelesh Nadkarni Deborah Pang Melissa Petersen Julie C. Price Margaret B. Pulsifer Eric M. Reiman Batool Rizvi Marwan N. Sabbagh Nicole Schupf Dana Tudorascu Rameshwari V. Tumuluru Benjamin Tycko Badri Varadarajan Desirée A. White Michael A. Yassa Shahid Zaman Fan Zhang Randall J. Bateman

10.1016/s1474-4422(24)00084-x article EN publisher-specific-oa The Lancet Neurology 2024-04-15

Abstract We present a comprehensive global analysis of genetic variants associated with autosomal-dominant Alzheimer's disease (ADAD). A total 550 in the APP, PSEN1, and PSEN2 genes were identified, which 279 classified as pathogenic or likely based on ACMG-AMP criteria, utilizing data from Dominantly Inherited Alzheimer Network (DIAN), literature, public databases. Symptomatic age at onset (AAO) was estimated for 227 these variants, allowing detailed characterization their frequency,...

10.1093/brain/awaf038 article EN cc-by-nc Brain 2025-02-04

Abstract INTRODUCTION Studies suggest distinct differences in the development, presentation, progression, and response to treatment of Alzheimer's disease (AD) between females males. We investigated sex cognition, neuroimaging, fluid biomarkers dominantly inherited AD (DIAD). METHODS Three hundred twenty‐five mutation carriers (55% female) one eighty‐six non‐carriers (58% Dominantly Inherited Alzheimer Network Observational Study were analyzed. Linear mixed models Spearman's correlation...

10.1002/alz.13460 article EN cc-by-nc-nd Alzheimer s & Dementia 2023-09-23
Stephanie Doering Austin McCullough Brian A. Gordon Charles D. Chen Nicole S. McKay and 95 more Diana A. Hobbs Sarah Keefe Shaney Flores Jalen Scott Hunter Smith Stephen Jarman Kelley Jackson Russ C. Hornbeck Beau M. Ances Chengjie Xiong Andrew J. Aschenbrenner Jason Hassenstab Carlos Cruchaga Alisha Daniels Randall J. Bateman James M. Noble Gregory S. Day Neill R. Graff‐Radford Jonathan Vöglein Johannes Levin Ricardo Allegri Patricio Chrem Méndez Ezequiel Surace Sarah Berman Snežana Ikonomović Neelesh K. Nadkarni Francisco Lopera Laura Ramírez David Aguillón Yudy Milena Leon Cláudia Ramos Diana Alzate Ana Baena Natalia Padilla Sonia Moreno Mathias Jucker Christoph Laske Elke Kuder-Buletta Susanne Gräber‐Sultan Oliver Preische Anna Hofmann Takeshi Ikeuchi Kensaku Kasuga Yoshiki Niimi Kenji Ishii Michio Senda Raquel Sánchez‐Valle Pedro Rosa‐Neto Nick C. Fox David M. Cash Jae‐Hong Lee Jee Hoon Roh Stephen Salloway Meghan C. Riddle William Menard Courtney Bodge Mustafa Surti Leonel Tadao Takada Martin R. Farlow Jasmeer P. Chhatwal Víctor Javier Sánchez-González Maribel Orozco-Barajas Alison Goate Alan E. Renton Bianca Esposito Celeste M. Karch Jacob Marsh Carlos Cruchaga Victoria Fernanadez Brian A. Gordon Anne M. Fagan Gina Jerome Elizabeth Herries Jorge J. Llibre‐Guerra Allan I. Levey Erik C. B. Johnson Nicholas T. Seyfried Peter R. Schofield William S. Brooks Jacob Bechara Randall J. Bateman Eric McDade Jason Hassenstab Richard J. Perrin Erin Franklin Tammie L.S. Benzinger Allison Chen Charles Chen Shaney Flores Nelly Friedrichsen Brian A. Gordon Nancy Hantler Russ C. Hornbeck Steve Jarman Sarah Keefe

BackgroundNeuroimaging studies often quantify tau burden in standardized brain regions to assess Alzheimer disease (AD) progression. However, this method ignores another key biological process which spreads additional regions. We have developed a metric for calculating the extent pathology has spread throughout and evaluate relationship between across early stages of AD.Methods445 cross-sectional participants (aged ≥ 50) who had MRI, amyloid PET, clinical testing were separated into...

10.1016/j.ebiom.2024.105080 article EN cc-by EBioMedicine 2024-03-28

Abstract This manuscript describes and summarizes the Dominantly Inherited Alzheimer Network Observational Study (DIAN Obs), highlighting wealth of longitudinal data, samples, results from this human cohort study brain aging a rare monogenic form Alzheimer’s disease (AD). DIAN Obs is an international collaborative initiated in 2008 with support National Institute on Aging (NIA), designed to obtain comprehensive uniform data biology function individuals at risk for autosomal dominant AD...

10.1101/2024.08.08.24311689 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2024-08-09

Abstract INTRODUCTION We investigated longitudinal associations between self‐reported exercise and Alzheimer's disease (AD)‐related biomarkers in individuals with autosomal dominant AD (ADAD) mutations. METHODS Participants were 308 ADAD mutation carriers aged 39.7 ± 10.8 years from the Dominantly Inherited Network. Weekly volume was measured via questionnaire brain (magnetic resonance imaging), cerebrospinal fluid biomarkers, amyloid beta (Aβ) by positron emission tomography investigated....

10.1002/alz.14270 article EN cc-by-nc Alzheimer s & Dementia 2024-09-26

Amyloid-plaque removal by monoclonal antibody therapies slows clinical progression in symptomatic Alzheimer's disease; however, the potential for delaying onset of symptoms asymptomatic people is unknown. The Dominantly Inherited Alzheimer Network Trials Unit (DIAN-TU) an ongoing platform trial assessing safety and efficacy multiple investigational products participants with dominantly inherited disease (DIAD) caused mutations. On basis findings amyloid downstream biological effects from...

10.1101/2024.10.29.24316289 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2024-11-06
Anna Hofmann Lisa M. Häsler Marius Lambert Stephan A. Kaeser Susanne Gräber‐Sultan and 95 more Ulrike Obermüller Elke Kuder-Buletta Christian la Fougère Christoph Laske Jonathan Vöglein Johannes Levin Nick C. Fox Natalie S. Ryan Henrik Zetterberg Jorge J. Llibre‐Guerra Richard J. Perrin Laura Ibáñez Peter R. Schofield William S. Brooks Gregory S. Day Martin R. Farlow Ricardo Allegri Patricio Chrem Méndez Takeshi Ikeuchi Kensaku Kasuga Jae‐Hong Lee Jee Hoon Roh Hiroshi Mori Francisco Lopera Randall J. Bateman Eric McDade Brian A. Gordon Jasmeer P. Chhatwal Mathias Jucker Stephanie A. Schultz David Aguillón Andrew J. Aschenbrenner Bryce Baker Nicolas R. Barthélemy Randall J. Bateman Jacob Bechara Tammie L.S. Benzinger Sarah Berman David M. Cash Allison Chen Charles D. Chen Jasmeer P. Chhatwal Patricio Chrem Méndez Laura Courtney Carlos Cruchaga Alisha Daniels Gregory S. Day Anne M. Fagan Martin R. Farlow Shaney Flores Erin Franklin Alison Goate Susanne Gräber‐Sultan Neill R. Graff‐Radford Emily Gremminger Jason Hassenstab Elizabeth Herries David M. Holtzman Russ C. Hornbeck Edward D. Huey Snežana Ikonomović Kelley Jackson Steve Jarman Gina Jerome Erik C. B. Johnson Nelly Joseph‐Mathurin Celeste M. Karch Sarah Keefe Deborah Koudelis Christoph Laske Yudy Milena Leon Allan I. Levey Yan Li Ruijin Lu Jacob I. Marsh Ralph N. Martins Parinaz Massoumzadeh Colin L. Masters Austin McCullough Eric McDade Nicole S. McKay Matthew Minton John C. Morris Neelesh K. Nadkarni Joyce Nicklaus Yoshiki Niimi James M. Noble Ulrike Obermueller Danielle M. Picarello Christine Pulizos Laura Ramírez Alan E. Renton John M. Ringman Jacqueline Rizzo Yvonne Roedenbeck

Disease-modifying therapies for Alzheimer's disease (AD) are likely to be most beneficial when initiated in the presymptomatic phase. To track benefit of such interventions, fluid biomarkers great importance, with neurofilament light chain protein (NfL) showing promise monitoring neurodegeneration and predicting cognitive outcomes. Here, we update complement previous findings from Dominantly Inherited Alzheimer Network Observational Study by using matched cross-sectional longitudinal...

10.1038/s41467-024-52937-8 article EN cc-by Nature Communications 2024-11-18

Abstract Carriers of mutations responsible for dominantly inherited Alzheimer disease provide a unique opportunity to study potential imaging biomarkers. Biomarkers based on routinely acquired clinical MR images, could supplement the extant invasive or logistically challenging) biomarker studies. We used 1104 longitudinal MR, 324 amyloid beta, and 87 tau positron emission tomography sessions from 525 participants enrolled in Dominantly Inherited Network Observational Study extract novel...

10.1002/hbm.26514 article EN cc-by Human Brain Mapping 2023-10-23

Abstract Hub regions in the brain, recognized for their roles ensuring efficient information transfer, are vulnerable to pathological alterations neurodegenerative conditions, including Alzheimer’s disease (AD). Computational simulations and animal experiments have hinted at theory of activity-dependent degeneration as cause this hub vulnerability. However, two critical issues remain unresolved. First, past research has not clearly distinguished between scenarios: facing a higher risk...

10.1162/netn_a_00395 article EN cc-by Network Neuroscience 2024-01-01

It remains unknown whether the associations between protective lifestyles and sporadic dementia risk reported in observational studies also affect age at symptom onset (AAO) autosomal dominant Alzheimer disease (ADAD) with predominant genetic influences. We investigated resilience-related life experiences interindividual AAO variability ADAD.

10.1212/wnl.0000000000209766 article EN Neurology 2024-09-13

Abstract Background Cognitive reserve (CR) has emerged as a critical factor in understanding clinical‐cognitive heterogeneity Alzheimer’s disease (AD). However, there is limited evidence of the effect CR during asymptomatic phases disease, age at symptom onset (AAO) and longitudinal decline. In this study, we elucidate impact on AAO decline rate using Dominantly Inherited Disease (DIAD) progression model. Methods DIAD participants were selected from Alzheimer Network (DIAN) study 1 . Using...

10.1002/alz.086295 article EN cc-by Alzheimer s & Dementia 2024-12-01

Abstract Hub regions in the brain, recognized for their roles ensuring efficient information transfer, are vulnerable to pathological alterations neurodegenerative conditions, including Alzheimer Disease (AD). Given essential role neural communication, disruptions these hubs have profound implications overall brain network integrity and functionality. disruption, or targeted impairment of functional connectivity at hubs, is AD patients. Computational models paired with evidence from animal...

10.1101/2023.10.29.564633 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-11-01

Abstract Background Studies suggest distinct differences in the development, presentation and longitudinal progression of Alzheimer’s Disease (AD) between women men. However, most these sex‐specific have been explored symptomatic stages sporadic AD. We investigated cross‐sectional sex clinical‐cognitive assessments as well fluid imaging biomarkers spectrum dominantly inherited AD (DIAD). Method 319 DIAD mutation carriers Dominantly Inherited Alzheimer Network‐Observational study (DIAN‐OBS)...

10.1002/alz.071752 article EN Alzheimer s & Dementia 2023-12-01

Abstract Background Both sporadic and dominantly inherited Alzheimer’s disease (DIAD) present with similar pathobiology symptoms. A loss of proteostasis in AD has been identified recent studies highlighting the role ubiquitin‐dependent mechanisms brain homeostasis neurodegenerative diseases. The Ubiquitin Proteasome System (UPS) is responsible for degradation misfolded or aggregated proteins via an ATP‐dependent proteolytic mechanism. This process involves a cascade ubiquitin transfer steps...

10.1002/alz.071786 article EN Alzheimer s & Dementia 2023-12-01

Background: It remains unknown whether associations between protective lifestyles and the risk of sporadic dementia in observational studies also affect age at symptom onset (AAO) autosomal dominant Alzheimer’s disease (ADAD), which genetic influences predominate. We investigated resilience-related during preclinical period interindividual variability AAO ADAD.Methods: performed a longitudinal confirmatory analysis data from 320 carriers 209 noncarriers Dominantly Inherited Alzheimer Network...

10.2139/ssrn.4438006 preprint EN 2023-01-01

TPS476 Background: Neoadjuvant treatment for borderline resectable pancreatic cancer (PCa) is increasing in acceptability, but a standard regimen has yet to be established. Multiple studies have demonstrated feasibility and effectiveness of the FOLFIRINOX (5-fluorouracil, leucovorin, oxaliplatin irinotecan) perioperative setting. However, often requires dose modifications, delays growth factor support due excessive toxicity which can complicate care delivery when given neoadjuvantly....

10.1200/jco.2019.37.4_suppl.tps476 article EN Journal of Clinical Oncology 2019-01-29
Coming Soon ...