William Ted Brown

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Nanbert ZhongNew York State Institute for Basic Research, Peking University Center of Medical GeneticsE-mail confirmado em opwdd.ny.gov
Ira CohenNew York State Institute for Basic ResearchE-mail confirmado em opwdd.ny.gov
Stephanie L. ShermanProfessor of Human Genetics, Emory University School of MedicineE-mail confirmado em emory.edu
Thomas WisniewskiProfessor of Neurology, Pathology and Psychiatry, New York University School of MedicineE-mail confirmado em nyulangone.org
Milen Velinov, MD, PhDAssociate Professor, Director of Division of Genetics, Rutgers Robert Wood Johnson Medical SchoolE-mail confirmado em rwjms.rutgers.edu
Kathryn ChadmanResearch Scientist, NYS Institute for Basic Research in Developmental DisabilitiesE-mail confirmado em opwdd.ny.gov
Francois RousseauProfesseur, Faculté de médecine, Université LavalE-mail confirmado em fmed.ulaval.ca
Abdeslem El IdrissiProfessor, Biology, College of Staten Island, City University of New YorkE-mail confirmado em csi.cuny.edu
Antonei Benjamin CsokaDepartment of Anatomy, Howard UniversityE-mail confirmado em howard.edu
Charles SchwartzDirector of Research, Greenwood Genetic CenterE-mail confirmado em ggc.org
Sebastien JacquemontCHU Sainte Justine Research Center, University of MontrealE-mail confirmado em umontreal.ca
Veronica HintonAssociate Professor, Columbia UniversityE-mail confirmado em cumc.columbia.edu
Sara T. KoverUniversity of WashingtonE-mail confirmado em uw.edu
Peter VietzeMontclair State UniversityE-mail confirmado em mail.montclair.edu
Laura J ScottDepartment of Biostatistics, Center for Statistical Genetics, University of MichiganE-mail confirmado em umich.edu
Michael BoehnkeProfessor of Biostatistics, University of MichiganE-mail confirmado em umich.edu
Gary J. LathamChief Technology Officer, Bio-TechneE-mail confirmado em bio-techne.com
Dejan B. Budimirovic, MDKennedy Krieger InstituteE-mail confirmado em kennedykrieger.org
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUE-mail confirmado em igbmc.fr
Frank KooyProfessor in Cognitive GeneticsE-mail confirmado em uantwerpen.be

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William Ted Brown

Institute for Basic Research

E-mail confirmado em sydney.edu.au

genetics


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Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome M Eriksson, WT Brown, LB Gordon, MW Glynn, J Singer, L Scott, ... Nature 423 (6937), 293-298, 2003	2582	2003
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1646	2007
Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates S Jacquemont, RJ Hagerman, M Leehey, J Grigsby, L Zhang, ... The American Journal of Human Genetics 72 (4), 869-878, 2003	885	2003
Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases. AM Saunders, K Schmader, JC Breitner, MD Benson, WT Brown, ... Lancet (London, England) 342 (8873), 710-711, 1993	673	1993
The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes J Wegiel, I Kuchna, K Nowicki, H Imaki, J Wegiel, E Marchi, SY Ma, ... Acta neuropathologica 119, 755-770, 2010	671	2010
Analysis of neocortex in three males with the fragile X syndrome VJ Hinton, WT Brown, K Wisniewski, RD Rudelli American journal of medical genetics 41 (3), 289-294, 1991	645	1991
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study—preliminary data DJ Allingham‐Hawkins, R Babul‐Hirji, D Chitayat, JJA Holden, KT Yang, ... American journal of medical genetics 83 (4), 322-325, 1999	585	1999
Oxidative stress in autism: Increased lipid peroxidation and reduced serum levels of ceruloplasmin and transferrin-the antioxidant proteins A Chauhan, V Chauhan, WT Brown, I Cohen Life sciences 75 (21), 2539-2549, 2004	563	2004
Adult fragile X syndrome: clinico-neuropathologic findings RD Rudelli, WT Brown, K Wisniewski, EC Jenkins, M Laure-Kamionowska, ... Acta neuropathologica 67, 289-295, 1985	488	1985
Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles SL Nolin, WT Brown, A Glicksman, GE Houck Jr, AD Gargano, A Sullivan, ... The American Journal of Human Genetics 72 (2), 454-464, 2003	473	2003
Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction JA Brunberg, S Jacquemont, RJ Hagerman, EM Berry-Kravis, J Grigsby, ... American Journal of Neuroradiology 23 (10), 1757-1766, 2002	435	2002
Brain IL-6 elevation causes neuronal circuitry imbalances and mediates autism-like behaviors H Wei, KK Chadman, DP McCloskey, AM Sheikh, M Malik, WT Brown, X Li Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1822 (6), 831-842, 2012	386	2012
Chromosome 21q21 sublocalisation of gene encoding beta-amyloid peptide in cerebral vessels and neuritic (senile) plaques of people with Alzheimer disease and Down syndrome NK Robakis, HM Wisniewski, EC Jenkins, EA Devine-Gage, GE Houck, ... The Lancet 329 (8529), 384-385, 1987	377	1987
IL-6 is increased in the cerebellum of autistic brain and alters neural cell adhesion, migration and synaptic formation H Wei, H Zou, AM Sheikh, M Malik, C Dobkin, WT Brown, X Li Journal of neuroinflammation 8, 1-10, 2011	373	2011
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome D Goldgaber, LG Goldfarb, P Brown, DM Asher, WT Brown, S Lin, ... Experimental Neurology 106 (2), 204-206, 1989	340	1989
Inheritance of mitral valve prolapse: effect of age and sex on gene expression RB DEVEREUX, WTED BROWN, R KRAMER-FOX, I SACHS Annals of internal medicine 97 (6), 826-832, 1982	331	1982
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test WT Brown, GE Houck, A Jeziorowska, FN Levinson, X Ding, C Dobkin, ... Jama 270 (13), 1569-1575, 1993	326	1993
Autism is associated with the fragile-X syndrome. WT Brown, EC Jenkins, E Friedman, J Brooks, K Wisniewski, S Raguthu, ... Journal of autism and developmental disorders, 1982	304	1982
Autism spectrum disorder in fragile X syndrome: cooccurring conditions and current treatment WE Kaufmann, SA Kidd, HF Andrews, DB Budimirovic, A Esler, ... Pediatrics 139 (Supplement_3), S194-S206, 2017	302	2017
Foetal thymic transplant in a case of DiGeorge's syndrome WW Cleveland, BJ Fogel, WT Brown, HEM Kay The Lancet 292 (7580), 1211-1214, 1968	299	1968

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