Danielle M Andrade

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 27

Top Topics

Carbon Nanotubes

Temporal Lobe Epilepsy

Top Venues

Epilepsy currents

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

This page only lists publications with an associated author ORCID identifier.

Publications

Satoshi Tanikawa, Danielle M Andrade, Ekaterina A Rogaeva, Maria Carmela Tartaglia, Gábor G Kovács
Novel neuropathological findings in a long-term survivor of D-2-hydroxyglutaric aciduria type 1. Virchows Archiv : an international journal of pathology (2024)
Christine Van Winssen, Andrea V Andrade, Danielle M Andrade, Jorge G Burneo, Sandrine de Ribaupierre, Elizabeth J Donner, Ayman Hassan, George Ibrahim, Kevin C Jones, Lysa Boissé Lomax, Katherine Muir, Maryam N Nouri, Nikki Porter, Rajesh Ramachandrannair, Paul Raymond, James Rutka, Michelle J Shapiro, David A Steven, Darryl Swain, Taufik A Valiante, Sharon Whiting, Robyn Whitney, Ivanna Yau, Tadeu A Fantaneanu
Evaluating the Current State of Epilepsy Care in the Province of Ontario. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2024)
Danielle M Andrade
Are We Doing Enough to Prevent SUDEP? Epilepsy currents 24 (4) (2024)
Christine Van Winssen, Andrea V Andrade, Danielle M Andrade, Jorge G Burneo, Sandrine de Ribaupierre, Elizabeth J Donner, Ayman Hassan, George Ibrahim, Kevin C Jones, Lysa Boissé Lomax, Katherine Muir, Maryam N Nouri, Nikki Porter, Rajesh Ramachandrannair, Paul Raymond, James Rutka, Michelle J Shapiro, David A Steven, Darryl Swain, Taufik A Valiante, Sharon Whiting, Robyn Whitney, Ivanna Yau, Tadeu A Fantaneanu
Evaluating the Current State of Epilepsy Care in the Province of Ontario. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2024)
Danielle M Andrade
Is There a Continuum Between Acute Symptomatic Seizures Secondary to Autoimmune Encephalitis and Autoimmune-Associated Epilepsy? Epilepsy currents 23 (5) (2023)
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, Danielle M Andrade, Yoshiko Murakami, Taroh Kinoshita, Thomas O Carpenter
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3). Genes 14 (2) (2023)
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, Danielle M Andrade, Yoshiko Murakami, Taroh Kinoshita, Thomas O Carpenter
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3). Genes 14 (2) (2023)
Gregory Costain, Danielle M Andrade
Third-generation computational approaches for genetic variant interpretation. Brain : a journal of neurology 146 (2) (2023)
Marlene Rong, Tim Benke, Quratulain Zulfiqar Ali, Angel Aledo-Serrano, Carolina Alvarez, Alessandra Rossi, Orrin Devinsky, Farah Qaiser, Anum Sadruddin Pidani, Alfonso Fasano, Anne S Bassett, Danielle M Andrade
Adult Phenotype of SYNGAP1 -DEE. Neurology. Genetics 9 (6) (2023)
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, Danielle M Andrade, Yoshiko Murakami, Taroh Kinoshita, Thomas O Carpenter
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3). Genes 14 (2) (2023)
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, Danielle M Andrade, Yoshiko Murakami, Taroh Kinoshita, Thomas O Carpenter
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3). Genes 14 (2) (2023)
Gregory Costain, Danielle M Andrade
Third-generation computational approaches for genetic variant interpretation. Brain : a journal of neurology 146 (2) (2023)
Katherine M Sawicka, Lindsey M Logan, Danielle M Andrade, Hans D Katzberg, Steven P Miller, Mahendranath Moharir, David F Tang-Wai, Anna Marissa Lagman-Bartolome
Building the bridge from pediatric to adult neurological care. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2023)
Danielle M Andrade
Somatic Variants and Surgical Epilepsies: Search and You Will Find. Epilepsy currents 23 (3) (2023)
Gregory Costain, Danielle M Andrade
Third-generation computational approaches for genetic variant interpretation. Brain : a journal of neurology (2023)
Miles D Thompson, Xueying Li, Michele Spencer-Manzon, Danielle M Andrade, Yoshiko Murakami, Taroh Kinoshita, Thomas O Carpenter
Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with PGAP2 Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3). Genes 14 (2) (2023)
Arunan Selvarajah, Carolina Gorodetsky, Paula Teixeira Marques, Quratulain Zulfiqar Ali, Anne T Berg, Alfonso Fasano, Danielle M Andrade
Progressive Worsening of Gait and Motor Abnormalities in Older Adults With Dravet Syndrome. Neurology 98 (22) (2022)
Danielle M Andrade
Time Is Brain: The Importance of an Accurate SCN1A Prediction Score in the Era of Precision Medicine. Epilepsy currents 22 (4) (2022)
Paula Teixeira Marques, Richard A Wennberg, Danielle M Andrade
Teaching NeuroImage: Ictal Pouting Associated With Focal Cortical Dysplasia and Frontal Seizures on Stereotactic Depth Electrode EEG. Neurology (2022)
Danielle M Andrade
Genetic Mechanisms Behind Severe Psychotic Reactions to Levetiracetam. Epilepsy currents 23 (1) (2022)
Veronica Hood, Anne T Berg, Kelly G Knupp, Sookyong Koh, Linda Laux, Mary Anne Meskis, Quratulain Zulfiqar Ali, Michael Scott Perry, Ingrid Eileen Scheffer, Joseph Sullivan, Elaine C Wirrell, Danielle M Andrade
COVID-19 vaccine in patients with Dravet syndrome: Observations and real-world experiences. Epilepsia 63 (7) (2022)
Farah Qaiser, Tara Sadoway, Yue Yin, Quratulain Zulfiqar Ali, Charlotte M Nguyen, Natalie Shum, Ian Backstrom, Paula Teixeira Marques, Sepideh Tabarestani, Renato P Munhoz, Timo Krings, Christopher E Pearson, Ryan K C Yuen, Danielle M Andrade
Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndrome. Brain communications 3 (3) (2021)
Danielle M Andrade
Precision medicine for epilepsies: are we there yet? Journal of neurology, neurosurgery, and psychiatry 92 (10) (2021)
Felippe Borlot, Danielle M Andrade
Epilepsy gene panel yield and impact on outcomes for adults with unexplained seizures. Epilepsia 61 (8) (2020)
Farah Qaiser, Ryan K C Yuen, Danielle M Andrade
Genetics of Epileptic Networks: from Focal to Generalized Genetic Epilepsies. Current neurology and neuroscience reports 20 (10) (2020)
Quratulain Zulfiqar Ali, Paula Teixeira Marques, Arunan Selvarajah, Sepideh Tabarestani, Tara Sadoway, Danielle M Andrade
Starting stiripentol in adults with Dravet syndrome? Watch for ammonia and carnitine. Epilepsia 61 (11) (2020)
Paula Teixeira Marques, Quratulain Zulfiqar Ali, Arunan Selvarajah, Hanna Faghfoury, Richard A Wennberg, Danielle M Andrade
Hyperammonemic Encephalopathy Associated with Perampanel: Case Report and Discussion. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 48 (3) (2020)