Peter D Galer Profile
Peter D Galer

@PeterDGaler

Followers
57
Following
84
Media
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Statuses
23

Bioengineering PhD student at UPenn. Researching epilepsy through a multimodal approach.

Philadelphia, PA
Joined December 2021
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@GreenJournal
Neurology Journal
5 months
Study results suggest that some #genetic epilepsies and associated functional outcome measures have distinct quantitative EEG signatures: https://t.co/ge8hT8yPwh
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@GreenJournal
Neurology Journal
11 months
This study provides a longitudinal perspective on SCN8A-related disorders, paving the way for future precision medicine approaches. https://t.co/4ATySH3mhl #NeuroX #NeuroTwitter
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@pennbioeng
Penn Bioengineering
2 years
The Department of #PennBioengineering along with Drs. @BrianLitt2 and Ingo Helbig proudly announce the Doctoral Dissertation Defense of @PeterDGaler. "Quantitative Informatics Approaches to Characterize and Predict Childhood Genetic Epilepsies" 9/18 1:00pm https://t.co/mtBX98XwoQ
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@GIMJournal
Genetics in Medicine
2 years
Machinelearning models using EMR data identify clinical features predictive of #genetic #epilepsies leading to earlier molecular diagnosis and treatment #precisionmedicine #diagnosticodyssey https://t.co/QPaEGtRPGn @PeterDGaler @IngoHelbig
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@EpilepsiaJourn
Epilepsia
2 years
Key point: Individuals with prior seizures or a later age at onset of epileptic spasms have a higher risk of developing refractory epileptic spasms https://t.co/eU6s1UBqjR #epilepsy #DEE #ILAE #epilepticspasms #neonatalseizures #STXBP1 @IlaeWeb @epilepsiajourn @WileyNeuro
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@JulieXXian
Julie Xian
3 years
...we identified optimal age windows through #virtual #clinical #trials using real-world data ...implications for clinical trial-readiness in STXBP1 and other genetic epilepsies ...to be presented next week at the STXBP1 Summit in Milan, and more on #STXBP1 to come...
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@IngoHelbig
Ingo Helbig
3 years
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticus ⁦@ddecampo⁩ ⁦@JulieXXian⁩ ⁦@KRSullivanGC⁩ ⁦@AlexGonzalezPHL⁩ ⁦@SarahRuggieroGC⁩ ⁦@PeterDGaler
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@IngoHelbig
Ingo Helbig
3 years
Enriching representation learning using 53 million patient notes through human phenotype ontology embedding ⁦@hp_ontology
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@PeterDGaler
Peter D Galer
3 years
Honored to have won best poster at the #AIinMedicine conference. Our work showed that through the electronic medical records, we can predict genetic epilepsy diagnoses years prior to a clinician. #Epilepsy, #Genetics, #HelbigLab, #CHOP, #ENGIN, #PennBioengineering
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@JulieXXian
Julie Xian
3 years
Here, a thread on @IngoHelbig's live talk on "Disease trajectories using #genetics and ML" at the first annual #AIinEpilepsy Meeting ...presented at Breckenridge, CO at an altitude of 9,603′ #EMRGenomics #RareDisease #ENDD
@JulieXXian
Julie Xian
3 years
@JillianLMcKee @IngoHelbig @ciitizen @cureSYNGAP1 @Prosser_Lab @lab_davidson @EAHellerPhD @SarahRuggieroGC …I’m even later but allow me to join the #SYNGAP1 swag party please? Breckenridge, CO in the background, where we’ll be presenting #NHS data from lab windows above… This will be at the first annual #AIinEpilepsy meeting @IngoHelbig @JillianLMcKee @PeterDGaler @cureSYNGAP1
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@JulieXXian
Julie Xian
3 years
....see thread below commenting on our recent preprint on the genetics of #FIRES and status epileptics more broadly https://t.co/qSHyPwHXmc
@IngoHelbig
Ingo Helbig
3 years
...new preprint online from our team at @ChildrensPhila The genetic spectrum of febrile infection-related epilepsy syndrome (#FIRES) and refractory status epilepticus by @ddecampo @JulieXXian @SarahRuggieroGC @PeterDGaler @AlexGonzalezPHL https://t.co/nWBs80v6B4
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@IngoHelbig
Ingo Helbig
3 years
…the same gene that allows hummingbirds to hover when absent …leads to a remitting #leukodystrophy in humans #FBP2 fructose 1,6-bisphosphatase https://t.co/IMZmTP1QXx
Tweet card summary image
pubmed.ncbi.nlm.nih.gov
Leukodystrophies are genetic disorders of cerebral white matter that almost exclusively have a progressive disease course. We became aware of three members of a family with a disorder characterized...
@ScienceMagazine
Science Magazine
3 years
The loss of a gene in hummingbirds was likely a key step in the evolution of metabolic muscle adaptations required for true hovering flight, a new Science study suggests. https://t.co/d5UjCRssI9
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@PeterDGaler
Peter D Galer
3 years
Great to see that our work is reaching more ears and will hopefully make a positive clinical impact! #epilepsy #genetics @IngoHelbig @JulieXXian @shridparth @SarahRuggieroGC
@NeurologyToday
Neurology Today
3 years
Via @AES: Researchers who took data from electronic medical records identified clinical features associated with genetic epilepsies and hope it may lead to earlier diagnoses: https://t.co/ozzmZX4vHt #neurotwitter @PeterDGaler @DellMedSchool @harvardmed @nationwidekids @AANMember
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@NeurologyToday
Neurology Today
3 years
Via @AES: Researchers who took data from electronic medical records identified clinical features associated with genetic epilepsies and hope it may lead to earlier diagnoses: https://t.co/ozzmZX4vHt #neurotwitter @PeterDGaler @DellMedSchool @harvardmed @nationwidekids @AANMember
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@AkashRPattnaik
Akash Pattnaik
3 years
🚨🚨new preprint!!🚨🚨: A quantitative tool for seizure severity: diagnostic and therapeutic applications https://t.co/PRKdmcbcOY We combine iEEG and semiology + clinical validation! w/ @ojemannw @bscheid @bernabei_john @katedavis12341 @_Nishant_Sinha @BrianLitt2 & others!
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@IngoHelbig
Ingo Helbig
4 years
...preprint alert Enriching Representation Learning Using 53 Million Patient Notes through Human Phenotype Ontology Embedding https://t.co/CGPs2nasnk @shridparth @CHOPDBHi @CHOP_Research @DLSneurocyclist
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@IngoHelbig
Ingo Helbig
4 years
Our STXBP1 paper is finally on PubMed | here is one of our figures with seizure history reconstruction that we hope to expand further in the near future @JulieXXian @curestxbp1
@LalDennis
Dennis Lal
4 years
Assessing the landscape of STXBP1-related disorders in 534 individuals https://t.co/02glXYVW4A
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