Work Address:
695 Charles E. Young Drive South, Gonda Room 2309 Los Angeles, CA 90095 UNITED STATES
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My research seeks to understand basic molecular mechanisms underlying human neurodevelopment and neurodegenerative disease. We are currently examining genes which influence the development of two classes of neurogenetic disease: 1) autism and autistic spectrum disorder, and 2) hereditary ataxia. Our goal is to better understand the molecular etiologies behind these diseases in order to improve diagnosis and clinical treatment for patients and their families.
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Hsu Sandy Chan, Sears Renee L, Lemos Roberta R, Quintáns Beatriz, Huang Alden, Spiteri Elizabeth, Nevarez Lisette, Mamah Catherine, Zatz Mayana, Pierce Kerrie D, Fullerton Janice M, Adair John C, Berner Jon E, Bower Matthew, Brodaty Henry, Carmona Olga, Dobrici? Valerija, Fogel Brent L, García-Estevez Daniel, Goldman Jill, Goudreau John L, Hopfer Suellen, Jankovi? Milena, Jaumà Serge, Jen Joanna C, Kirdlarp Suppachok, Klepper Joerg, Kosti? Vladimir, Lang Anthony E, Linglart Agnès, Maisenbacher Melissa K, Manyam Bala V, Mazzoni Pietro, Miedzybrodzka Zofia, Mitarnun Witoon, Mitchell Philip B, Mueller Jennifer, Novakovi? Ivana, Paucar Martin, Paulson Henry, Simpson Sheila A, Svenningsson Per, Tuite Paul, Vitek Jerrold, Wetchaphanphesat Suppachok, Williams Charles, Yang Michele, Schofield Peter R, de Oliveira João R M, Sobrido María-Jesús, Geschwind Daniel H, Coppola Giovanni Mutations in SLC20A2 are a major cause of familial idiopathic basal
ganglia calcification..
Neurogenetics.
2013; 14(1):
11-22.
Fogel Brent L, Baker Cameron, Curnow Andrew, Perlman Susan L, Geschwind Daniel H, Coppola Giovanni Mutations in PDYN are not responsible for multiple system atrophy..
Journal of neurology.
2013; 14(1):
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Mochel Fanny, Schiffmann Raphael, Steenweg Marjan E, Akman Hasan O, Wallace Mary, Sedel Frédéric, Laforêt Pascal, Levy Richard, Powers J Michael, Demeret Sophie, Maisonobe Thierry, Froissart Roseline, Da Nobrega Bruno Barcelos, Fogel Brent L, Natowicz Marvin R, Lubetzki Catherine, Durr Alexandra, Brice Alexis, Rosenmann Hanna, Barash Varda, Kakhlon Or, Gomori J Moshe, van der Knaap Marjo S, Lossos Alexander Adult polyglucosan body disease: Natural History and Key Magnetic
Resonance Imaging Findings..
Annals of neurology.
2012; 72(3):
433-41.
Cho Ellen, Fogel Brent L A Family with Spinocerebellar Ataxia Type 5 Found to Have a Novel
Missense Mutation within a SPTBN2 Spectrin Repeat..
Cerebellum (London, England).
2012; 72(3):
.
Fogel Brent L, Wexler Eric, Wahnich Amanda, Friedrich Tara, Vijayendran Chandran, Gao Fuying, Parikshak Neelroop, Konopka Genevieve, Geschwind Daniel H RBFOX1 Regulates Both Splicing and Transcriptional Networks in Human
Neuronal Development..
Human molecular genetics.
2012;
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Fogel Brent L, Lee Ji Yong, Lane Jessica, Wahnich Amanda, Chan Sandy, Huang Alden, Osborn Greg E, Klein Eric, Mamah Catherine, Perlman Susan, Geschwind Daniel H, Coppola Giovanni Mutations in rare ataxia genes are uncommon causes of sporadic
cerebellar ataxia..
Movement disorders : official journal of the Movement Disorder Society.
2012; 27(3):
442-6.
Becker Esther B E, Fogel Brent L, Rajakulendran Sanjeev, Dulneva Anna, Hanna Michael G, Perlman Susan L, Geschwind Daniel H, Davies Kay E Candidate screening of the TRPC3 gene in cerebellar ataxia..
Cerebellum (London, England).
2011; 10(2):
296-9.
Fogel Brent L Interpretation of genetic testing: variants of unknown significance..
Continuum (Minneapolis, Minn.).
2011; 17(2 Neurogenetics):
347-52.
Fogel Brent L, Lee Ji Yong, Perlman Susan Aberrant splicing of the senataxin gene in a patient with ataxia with
oculomotor apraxia type 2..
Cerebellum (London, England).
2009; 8(4):
448-53.
Fogel Brent L, Young Pari, Thompson Arthur R, Perlman Susan A family with combined mutations of the hemophilia A and X-linked
adrenoleukodystrophy genes..
Neurogenetics.
2008; 9(3):
215-8.
Fogel Brent L, Perlman Susan Clinical features and molecular genetics of autosomal recessive
cerebellar ataxias..
Lancet neurology.
2007; 6(3):
245-57.
Fogel Brent L, Perlman Susan Novel mutations in the senataxin DNA/RNA helicase domain in ataxia
with oculomotor apraxia 2..
Neurology.
2006; 67(11):
2083-4.
Fogel Brent, Cardenas Doris, Ovbiagele Bruce Magnetic resonance imaging abnormalities in the corpus callosum of a
patient with neuropsychiatric lupus..
The neurologist.
2006; 12(5):
271-3.
Fogel Brent L, McNally Lisa M, McNally Mark T Efficient polyadenylation of Rous sarcoma virus RNA requires the
negative regulator of splicing element..
Nucleic acids research.
2002; 30(3):
810-7.
Fogel B L, McNally M T A cellular protein, hnRNP H, binds to the negative regulator of
splicing element from Rous sarcoma virus..
The Journal of biological chemistry.
2000; 275(41):
32371-8.
Fogel B L, McNally M T Trace contamination following reuse of anion-exchange DNA purification
resins..
BioTechniques.
2000; 28(2):
299-302.
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