
Brent Fogel
@FogelLab
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Using genomics to study neurodegenerative diseases & neurodevelopmental disorders to improve diagnosis & treatment. Focus on cerebellar ataxia.
Joined January 2012
RT @UCLANeurology: "Vanishing White Matter" (VNM) is a type of #leukodystrophy that affects axons in our nervous system. There are currentl….
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Our latest publication highlighting the need for improving patient access to #exome sequencing @UCLANeurology @NAF_Ataxia @UCLAHealth.
Spinocerebellar #ataxia type 14 (#SCA14) in an #Argentinian family. This case report expands the #global presence of this neurological disorder.@FogelLab .
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RT @UCLANeurology: This @iScience_CP study with Kathie Ngo and Drs. @HinmanLabUCLA and @FogelLab identifies targetable region-specific vuln….
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Read from @fogellab "multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data" #BMCBioInformatics for study of disease-associated gene networks across time or space @TommasiniDario @UCLANeurology @UCLAHealthNews
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"Alterations in oligodendrocyte transcriptional networks reveal region-specific vulnerabilities to neurological disease" in @iScience_CP @TommasiniDario @rachelgiulia @Kathie0309 collaboration with @HinmanLabUCLA @NAF_Ataxia @UCLAHealthNews @UCLANeurology
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Read @FogelLab picks for the Best Advances in Neurogenetics in 2022 in @NeurologyToday .including detection of repeat expansions using genome sequencing and novel genetic interactions between SCA17 & SCA48.@UCLANeurology @AANmember @NAF_Ataxia.
Check out @NeurologyToday's Best Advances! The annual feature highlights the most noteworthy advancements across #neurology subspecialties and areas of practice. #NeuroTwitter
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RT @AJHGNews: New! Rafehi et al. identify an intronic FGF14 repeat expansion in adult-onset ataxia.
cell.com
Pathogenic repeat expansions (RE) cause an array of neurogenetic disorders including cerebellar ataxia. While traditionally difficult to identify, new genomic tools and bioinformatic analyses are...
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Can you guess the diagnosis? Excellent case report by Dr. Molly Fensterwald (with contributions from Drs. Noriko Salamon, Joshua Buyers, Harry Vinters, and @FogelLab ) @UCLANeurology @UCLAHealth @AJNR.
#AJNRcow >> August 4, 2022 >> A 45-year-old woman with a history of focal segmental glomerulosclerosis status post kidney transplant on immunosuppression presents with subacute weakness, paresthesias, & a shaking episode of her left arm. View the case at
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RT @UCLANeurology: Dr. Brent Fogel @FogelLab was quoted in a @NeurologyToday article on how advances in #genetics #research of the past 20….
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@FogelLab discusses how #exome sequencing has advanced care in cerebellar #ataxia @NeurologyToday @NAF_Ataxia @UCLANeurology #RareDisease
journals.lww.com
An abstract is unavailable.
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Think about the future of #ataxia therapies. Read "Paving the Way Toward Meaningful Trials in Ataxias: An Ataxia Global Initiative Perspective" @NAF_Ataxia @UCLANeurology @MDJ_Journal @ataxia_global.
movementdisorders.onlinelibrary.wiley.com
Click on the article title to read more.
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RT @UCLANeurology: To close out #BrainAwarenessWeek, we have a thread by Dr. Brent Fogel @FogelLab on @UCLA and neurogenetics! 🧠🧬 https://t….
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RT @UCLANeurology: The @UCLANeurology Clinical Neurogenomics Research Center helps connect #patients with exciting #research studies such a….
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RT @UCLANeurology: Dr. Brent Fogel in the @UCLA Neurogenetics #Clinic cares for patients with X-linked adrenoleukodystrophy. X-linked adre….
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RT @UCLANeurology: Did you know @UCLANeurology has the largest clinical Ataxia Center in the West?. #UCLA is also a leader in #research and….
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RT @UCLAHealth: At UCLA Health, Dr. Brent Fogel is transforming the future of #Neuroscience by identifying the unique genetics of patients….
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RT @NeurologyToday: Best #Neurogenetics advances of 2021: Thanks to @AANmember @FogelLab @dgsomucla for sharing his picks on the UK 100,000….
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Hadjinicolaou & Ngo #SETX confirmed functionally to cause a rapidly progressive early‑onset #neurogenetic disorder w severe polyneuropathy @Fogellab collab w C Bennett Al La Spada & Grace Yoon #ALS4 @UCLANeurology @UCLAHealthNews @SickKidsNews @NAF_Ataxia
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RT @FogelLab: @UCLANeurology Although dystonia can occur with certain medications, it is often unknown why some people develop this and oth….
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Wong & @Fogellab report a woman & family with acute dystonia to ondansetron, prochlorperazine, and metoclopramide. #Pharmacogenomic testing revealed the CYP2D6 enzyme *41 allele as the likely cause of the medication-induced dystonia. @UCLANeurology
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