William Ted Brown

Cited by

	All	Since 2019
Citations	29210	6313
h-index	83	39
i10-index	299	117

1400

700

350

1050

1985198619871988198919901991199219931994199519961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024198 279 323 387 314 260 471 354 264 424 383 443 359 396 457 478 466 474 496 604 699 623 699 835 781 803 1014 1193 1259 1342 1183 1216 1205 1177 1220 1280 1302 1159 1048 297

Public access

View all

43 articles

1 article

available

not available

Based on funding mandates

Co-authors

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

William Ted Brown

Institute for Basic Research

Verified email at sydney.edu.au

genetics


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
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	2463	2003
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1649	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	850	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	662	1993
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	636	1991
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	610	2010
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	581	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	530	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	483	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	467	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	427	2002
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	374	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	345	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	337	1989
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	334	2012
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	331	1993
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	328	1982
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	301	1982
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	300	1968
Familial transmission of the FMR1 CGG repeat. SL Nolin, FA Lewis 3rd, LL Ye, GE Houck Jr, AE Glicksman, P Limprasert, ... American journal of human genetics 59 (6), 1252, 1996	258	1996

The system can't perform the operation now. Try again later.

Articles 1–20

Citations per year

Duplicate citations

Merged citations

Add co-authorsCo-authors

Follow

Cited by

Co-authors