WilliamSBrooksIIIMD

PubMed

• 6 citations
  The surgical anatomy of the dorsal scapular nerve: a triple-tendon transfer perspective.
  Martim Pinto, John L. Johnson, Harshadkumar A Patel, Eva J. Lehtonen, Amit M. Momaya, William S. Brooks, Eugene W. Brabston, Brent A. Ponce> ;Journal of Shoulder and Elbow Surgery. 2019 Jan 1
• 32 citations
  A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.
  Ming Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, Julia Keith, Ezequiel Surace, Uri Wolf, Christine Sato, Mark Grinberg, Yan Liang, Zhengrui Xi, Kyle Dupont, Phil...> ;Brain. 2018 Oct 1
• A Case of Pancreatic Cancer: Abdominal Anatomy Team-Based Learning Module for Medical Students.
  Bass, R. Z.,Morgan, D. E.,Brooks, W. S.> ;MedEdPORTAL. 2019 Feb 26
• Long-Term Results of Stenting versus Endarterectomy for Carotid-Artery Stenosis.
  Brott, T. G.,Howard, G.,Roubin, G. S.,Meschia, J. F.,Mackey, A.,Brooks, W.,Moore, W. S.,Hill, M. D.,Mantese, V. A.,Clark, W. M.,Timaran, C. H.,Heck, D.,Leimgruber, P. ...> ;N. Engl. J. Med.. 2016 Feb 19
• Characteristics of participants consenting versus declining follow-up for up to 10 years in a randomized clinical trial.
  Sheffet, A. J.,Voeks, J. H.,Mackey, A.,Brooks, W.,Clark, W. M.,Hill, M. D.,Howard, V. J.,Hughes, S. E.,Tom, M.,Longbottom, M. E.,Brott, T. G.> ;Clin Trials. 2015 Jul 01
• 54 citations
  Factors Associated With the Onset and Persistence of Post–Lumbar Puncture Headache
  Andrés E Monserrate, Davis C. Ryman, Shengmei Ma, Chengjie Xiong, James M. Noble, John M. Ringman, John C. Morris, Adrian Danek, Felix Müller-Sarnowski, David B. Cliff...> ;JAMA Neurology. 2015 Mar 1
• Frontotemporal dementia and its subtypes: a genome-wide association study.
  Ferrari, R.,Hernandez, D. G.,Nalls, M. A.,Rohrer, J. D.,Ramasamy, A.,Kwok, J. B.,Dobson-Stone, C.,Brooks, W. S.,Schofield, P. R.,Halliday, G. M.,Hodges, J. R.,Piguet, ...> ;Lancet Neurol. 2014 Jun 20
• TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
  Gallagher, M. D.,Suh, E.,Grossman, M.,Elman, L.,McCluskey, L.,Van Swieten, J. C.,Al-Sarraj, S.,Neumann, M.,Gelpi, E.,Ghetti, B.,Rohrer, J. D.,Halliday, G.,Van Broeckho...> ;Acta Neuropathol.. 2014 Jan 21
• 110 citations
  Preclinical trials in autosomal dominant AD: implementation of the DIAN-TU trial.
  Sarah M. Mills, J. Mallmann, Anna Santacruz, A. Fuqua, M. Carril, Paul S. Aisen, M. C. Althage, S. Belyew, Tammie L.S. Benzinger, William S. Brooks, Virginia Buckles, ...> ;Revue Neurologique. 2013 Oct 1
• 52 citations
  C9ORF72 Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients
  Carol Dobson-Stone, Marianne Hallupp, Clement T. Loy, Elizabeth Thompson, Eric Haan, Carolyn M. Sue, Peter K. Panegyres, Cristina Razquin, Manuel Seijo-Martínez, Ramón...> ;Plos One. 2013 Feb 20
• 20 citations
  Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: Genetic, clinical and neuropathological analysis
  Carol Dobson-Stone, Agnes Luty, Elizabeth Thompson, Peter C. Blumbergs, William S. Brooks, Cathy L. Short, Colin D. Field, Peter K. Panegyres, Jane Hecker, Jennifer A....> ;Acta Neuropathologica. 2013 Jan 22
• 85 citations
  Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
  Alice Chen-Plotkin, Maria Martinez-Lage, Patrick M. A. Sleiman, William T. Hu, Robert W. Greene, Elisabeth M. Wood, Shaoxu Bing, Murray Grossman, Gerard D. Schellenber...> ;Archives of Neurology. 2011 Apr 11
• 159 citations
  Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease.
  Agnes Luty, John B.J. Kwok, Carol Dobson-Stone, Clement T. Loy, Kirsten Coupland, Helena Karlström, Tomasz Sobów, Joanna Tchorzewska, Aleksandra Maruszak, Maria Barcik...> ;Annals of Neurology. 2010 Nov 1
• 10 citations
  Very early-onset frontotemporal dementia with no family history predicts underlying fused in sarcoma pathology
  Clement T. Loy, Elizabeth McCusker, Jillian J. Kril, John B.J. Kwok, William S. Brooks, Heather McCann, Adrian M. Isaacs, Glenda M. Halliday> ;Brain. 2010 Aug 7
• High striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types.
  Villemagne, V.L., Ataka, S., Mizuno, T., Brooks, W.S., Wada, Y., Kondo, M., Jones, G., Watanabe, Y., Mulligan, R., Nakagawa, M., Miki, T., Shimada, H., O'Keefe, G...> ;Arch Neurol. 2009 Dec
• 69 citations
  Pedigree with frontotemporal lobar degeneration – motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
  Agnes Luty, John B.J. Kwok, Elizabeth Thompson, Peter C. Blumbergs, William S. Brooks, Clement T. Loy, Carol Dobson-Stone, Peter K. Panegyres, Jane Hecker, Garth A. Ni...> ;BMC Neurology. 2008 Aug 29
• 62 citations
  Association of alleles carried at TNFA -850 and BAT1 -22 with Alzheimer's disease.
  Anastazija Gnjec, Katarzyna J D'Costa, Simon M. Laws, Ross Hedley, Kelvin Balakrishnan, Kevin Taddei, Georgia Martins, Athena Paton, Giuseppe Verdile, Sam Gandy, G. An...> ;Journal of Neuroinflammation. 2008 Aug 20
• G2E3 is a dual function ubiquitin ligase required for early embryonic development.
  Brooks, W.S., Helton, E.S., Banerjee, S., Venable, M., Johnson, L., Schoeb, T.R., Kesterson, R.A., Crawford, D.F.> ;J Biol Chem. 2008 Aug 8
• 55 citations
  Variable phenotype of Alzheimer’s disease with spastic paraparesis
  Helena Karlström, William S. Brooks, John B.J. Kwok, G. Anthony Broe, Jillian J. Kril, Heather McCann, Glenda M. Halliday, Peter R. Schofield> ;Journal of Neurochemistry. 2007 Oct 8
• 166 citations
  Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative
  Rosa Rademakers, Matt Baker, Jennifer Gass, Jennifer Adamson, Edward D. Huey, Parastoo Momeni, Salvatore Spina, Giovanni Coppola, Anna Karydas, Heather Stewart, Nancy ...> ;The Lancet. Neurology. 2007 Oct 1
• G2E3 is a nucleo-cytoplasmic shuttling protein with DNA damage responsive localization.
  Brooks, W.S., Banerjee, S., Crawford, D.F.> ;Exp Cell Res. 2007 Feb 15
• 5 citations
  Anticipation of onset age in familial Parkinson's disease without SCA gene mutations
  Yue Huang, Michael Hayes, Antony J. Harding, William S. Brooks, Victor S.C. Fung, Dominic B. Rowe, Ron Joffe, Denis Crimmins, M. A. Hely, Glenda M. Halliday> ;Parkinsonism & Related Disorders. 2006 Jun 1
• 45 citations
  Pick bodies in a family with presenilin-1 Alzheimer's disease
  Glenda M. Halliday, Yun Ju C. Song, Gila Lepar, William S. Brooks, John B.J. Kwok, Cindy Kersaitis, Gillian C. Gregory, Claire E. Shepherd, Farid Rahimi, Peter R. Scho...> ;Annals of Neurology. 2005 Jan 1
• 22 citations
  Similar early clinical presentations in familial and non-familial frontotemporal dementia
  Olivier Piguet, William S. Brooks, Glenda M. Halliday, Peter R. Schofield, Prudence M Stanford, John B.J. Kwok, Maria Grazia Spillantini, Despina Yancopoulou, Peter J....> ;Journal of Neurology, Neurosurgery, and Psychiatry. 2004 Dec 1
• 41 citations
  Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies.
  Prudence M Stanford, William S. Brooks, Erdahl Teber, Marianne Hallupp, Catriona McLean, Glenda M. Halliday, Ralph N. Martins, John B.J. Kwok, Peter R. Schofield> ;Journal of Neurology. 2004 Sep 1
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