Dementia assessment and management in primary care settings: a survey of current provider practices in the United States
Bernstein, Alissa, Rogers, Kirsten M, Possin, Katherine L, Steele, Natasha Z R, Ritchie, Christine S, Kramer, Joel H, Geschwind, Michael, Higgins, Joseph J, Wohlgemuth, Jay, Pesano, Rick, Miller, Bruce L, Rankin, Katherine P
Published in BMC health services research (29.11.2019)
Published in BMC health services research (29.11.2019)
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Markers of Celiac Disease and Gluten Sensitivity in Children with Autism
Lau, Nga M, Green, Peter H R, Taylor, Annette K, Hellberg, Dan, Ajamian, Mary, Tan, Caroline Z, Kosofsky, Barry E, Higgins, Joseph J, Rajadhyaksha, Anjali M, Alaedini, Armin
Published in PloS one (18.06.2013)
Published in PloS one (18.06.2013)
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VLDL receptor gene therapy for reducing atherogenic lipoproteins
Krauss, Ronald M., Lu, Jonathan T., Higgins, Joseph J., Clary, Cathryn M., Tabibiazar, Ray
Published in Molecular metabolism (Germany) (01.03.2023)
Published in Molecular metabolism (Germany) (01.03.2023)
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Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase-mTORC1 Translational Pathway
Bavley, Charlotte C, Rice, Richard C, Fischer, Delaney K, Fakira, Amanda K, Byrne, Maureen, Kosovsky, Maria, Rizzo, Bryant K, Del Prete, Dolores, Alaedini, Armin, Morón, Jose A, Higgins, Joseph J, D'Adamio, Luciano, Rajadhyaksha, Anjali M
Published in The Journal of neuroscience (14.03.2018)
Published in The Journal of neuroscience (14.03.2018)
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Mechanism, Prevalence, and More Severe Neuropathy Phenotype of the Charcot-Marie-Tooth Type 1A Triplication
Liu, Pengfei, Gelowani, Violet, Zhang, Feng, Drory, Vivian E., Ben-Shachar, Shay, Roney, Erin, Medeiros, Adam C., Moore, Rebecca J., DiVincenzo, Christina, Burnette, William B., Higgins, Joseph J., Li, Jun, Orr-Urtreger, Avi, Lupski, James R.
Published in American journal of human genetics (06.03.2014)
Published in American journal of human genetics (06.03.2014)
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Mutations in FLVCR1 Cause Posterior Column Ataxia and Retinitis Pigmentosa
Rajadhyaksha, Anjali M., Elemento, Olivier, Puffenberger, Erik G., Schierberl, Kathryn C., Xiang, Jenny Z., Putorti, Maria L., Berciano, José, Poulin, Chantal, Brais, Bernard, Michaelides, Michel, Weleber, Richard G., Higgins, Joseph J.
Published in American journal of human genetics (12.11.2010)
Published in American journal of human genetics (12.11.2010)
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Behavioral characterization of cereblon forebrain-specific conditional null mice: A model for human non-syndromic intellectual disability
Rajadhyaksha, Anjali M., Ra, Stephen, Kishinevsky, Sarah, Lee, Anni S., Romanienko, Peter, DuBoff, Mariel, Yang, Chingwen, Zupan, Bojana, Byrne, Maureen, Daruwalla, Zeeba R., Mark, Willie, Kosofsky, Barry E., Toth, Miklos, Higgins, Joseph J.
Published in Behavioural brain research (15.01.2012)
Published in Behavioural brain research (15.01.2012)
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A brief review of recent Charcot-Marie-Tooth research and priorities
Ekins, Sean, Litterman, Nadia K, Arnold, Renée J G, Burgess, Robert W, Freundlich, Joel S, Gray, Steven J, Higgins, Joseph J, Langley, Brett, Willis, Dianna E, Notterpek, Lucia, Pleasure, David, Sereda, Michael W, Moore, Allison
Published in F1000 research (26.02.2015)
Published in F1000 research (26.02.2015)
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Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23
Polymeropoulos, Mihael H., Higgins, Joseph J., Golbe, Lawrence I., Johnson, William G., Ide, Susan E., Di Iorio, Giuseppe, Sanges, Giuseppe, Stenroos, Edward S., Pho, Lana T., Schaffer, Alejandro A., Lazzarini, Alice M., Nussbaum, Robert L., Duvoisin, Roger C.
Published in Science (American Association for the Advancement of Science) (15.11.1996)
Published in Science (American Association for the Advancement of Science) (15.11.1996)
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Stargardt macular dystrophy and therapeutic approaches
Fujinami, Kaoru, Waheed, Nadia, Laich, Yannik, Yang, Paul, Fujinami-Yokokawa, Yu, Higgins, Joseph J, Lu, Jonathan T, Curtiss, Darin, Clary, Cathryn, Michaelides, Michel
Published in British journal of ophthalmology (08.11.2023)
Published in British journal of ophthalmology (08.11.2023)
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The Brain Health Assessment for Detecting and Diagnosing Neurocognitive Disorders
Possin, Katherine L., Moskowitz, Tacie, Erlhoff, Sabrina J., Rogers, Kirsten M., Johnson, Erica T., Steele, Natasha Z. R., Higgins, Joseph J., Stiver, Jordan, Alioto, Andrea G., Farias, Sarah T., Miller, Bruce L., Rankin, Katherine P.
Published in Journal of the American Geriatrics Society (JAGS) (01.01.2018)
Published in Journal of the American Geriatrics Society (JAGS) (01.01.2018)
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Temporal and Spatial Mouse Brain Expression of Cereblon, An Ionic Channel Regulator Involved in Human Intelligence
Higgins, Joseph J., Tal, Adit L., Sun, Xiaowei, Hauck, Stefanie C. R., Hao, Jin, Kosofosky, Barry E., Rajadhyaksha, Anjali M.
Published in Journal of neurogenetics (2010)
Published in Journal of neurogenetics (2010)
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A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders
Karbassi, Izabela, Maston, Glenn A., Love, Angela, DiVincenzo, Christina, Braastad, Corey D., Elzinga, Christopher D., Bright, Alison R., Previte, Domenic, Zhang, Ke, Rowland, Charles M., McCarthy, Michele, Lapierre, Jennifer L., Dubois, Felicita, Medeiros, Katelyn A., Batish, Sat Dev, Jones, Jeffrey, Liaquat, Khalida, Hoffman, Carol A., Jaremko, Malgorzata, Wang, Zhenyuan, Sun, Weimin, Buller-Burckle, Arlene, Strom, Charles M., Keiles, Steven B., Higgins, Joseph J.
Published in Human mutation (01.01.2016)
Published in Human mutation (01.01.2016)
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The allelic spectrum of Charcot–Marie–Tooth disease in over 17,000 individuals with neuropathy
DiVincenzo, Christina, Elzinga, Christopher D., Medeiros, Adam C., Karbassi, Izabela, Jones, Jeremiah R., Evans, Matthew C., Braastad, Corey D., Bishop, Crystal M., Jaremko, Malgorzata, Wang, Zhenyuan, Liaquat, Khalida, Hoffman, Carol A., York, Michelle D., Batish, Sat D., Lupski, James R., Higgins, Joseph J.
Published in Molecular genetics & genomic medicine (01.11.2014)
Published in Molecular genetics & genomic medicine (01.11.2014)
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A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation
Higgins, Joseph J, Pucilowska, Joanna, Lombardi, Roni Q, Rooney, John P
Published in Neurology (23.11.2004)
Published in Neurology (23.11.2004)
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Integrated physical map of the human essential tremor gene region (ETM2) on chromosome 2p24.3-p24.2
Higgins, Joseph. J., Lombardi, Roni Q., Pucilowska, Joanna, Ruszczyk, Melanie U.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.05.2004)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.05.2004)
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