W. Ted Brown

15.9k total citations · 2 hit papers
217 papers, 10.9k citations indexed

About

W. Ted Brown is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, W. Ted Brown has authored 217 papers receiving a total of 10.9k indexed citations (citations by other indexed papers that have themselves been cited), including 105 papers in Genetics, 98 papers in Molecular Biology and 69 papers in Cognitive Neuroscience. Recurrent topics in W. Ted Brown's work include Genetics and Neurodevelopmental Disorders (88 papers), Autism Spectrum Disorder Research (67 papers) and Genomic variations and chromosomal abnormalities (32 papers). W. Ted Brown is often cited by papers focused on Genetics and Neurodevelopmental Disorders (88 papers), Autism Spectrum Disorder Research (67 papers) and Genomic variations and chromosomal abnormalities (32 papers). W. Ted Brown collaborates with scholars based in United States, China and Australia. W. Ted Brown's co-authors include Ira L. Cohen, Ved Chauhan, Abha Chauhan, Carl Dobkin, Ashfaq M. Sheikh, Leslie B. Gordon, Mazhar N. Malik, Paul H. Holinger, John A. Tsiouris and Edmund C. Jenkins and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

W. Ted Brown

214 papers receiving 10.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

2003 1.6k citations W. Ted Brown et al. profile →
Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates

2003 556 citations Sébastien Jacquemont, Randi J. Hagerman et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by W. Ted Brown

Since Specialization

Citations

This map shows the geographic impact of W. Ted Brown's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by W. Ted Brown with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W. Ted Brown more than expected).

Fields of papers citing papers by W. Ted Brown

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by W. Ted Brown. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by W. Ted Brown. The network helps show where W. Ted Brown may publish in the future.

Co-authorship network of co-authors of W. Ted Brown

This figure shows the co-authorship network connecting the top 25 collaborators of W. Ted Brown. A scholar is included among the top collaborators of W. Ted Brown based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with W. Ted Brown. W. Ted Brown is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Involvement of Type 10 17β-Hydroxysteroid Dehydrogenase in the Pathogenesis of Infantile Neurodegeneration and Alzheimer’s Disease 2023 ·International Journal of Molecular Sciences ·Xue‐Ying He, (unknown), Carl Dobkin, W. Ted Brown, Song‐Yu Yang	6
2	Development of a Quantitative FMRP Assay for Mouse Tissue Applications 2021 ·Genes ·Tatyana Adayev, Giuseppe LaFauci, Weimin Xu, Carl Dobkin, Richard J. Kascsak, W. Ted Brown, Jeffrey H. Goodman	2
3	Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment 2017 ·PEDIATRICS ·Walter E. Kaufmann, Sharon A. Kidd, Howard Andrews, Dejan B. Budimirovic, Amy Esler, Barbara Haas‐Givler, Tracy Stackhouse, Catharine Riley, Georgina Peacock, Stephanie L. Sherman, W. Ted Brown, Elizabeth Berry‐Kravis	186
4	Hypermethylation of the enolase gene (ENO2) in autism 2014 ·European Journal of Pediatrics ·(unknown), (unknown), Fengling Zhang, Miao Xu, Jingzhi Zhang, Jingbin Yan, Weina Ju, W. Ted Brown, Nanbert Zhong	27
5	Contribution of olivofloccular circuitry developmental defects to atypical gaze in autism 2013 ·Brain Research ·Jerzy Węgiel, (unknown), Izabela Kuchna, Krzysztof Nowicki, Humi Imaki, Jarek Wegiel, Shuang Yong, Efrain C. Azmitia, Probal Banerjee, Michael Flory, Ira L. Cohen, Eric London, W. Ted Brown, (unknown), Thomas Wısnıewskı	38
6	A Neurodevelopmental Perspective on the Acquisition of Nonverbal Cognitive Skills in Adolescents With Fragile X Syndrome 2013 ·Developmental Neuropsychology ·Sara T. Kover, Elizabeth I. Pierpont, (unknown), W. Ted Brown, Leonard Abbeduto	30
7	Correction: Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families 2012 ·PLoS ONE ·Milen Velinov, Natalia Dolzhanskaya, Michael Gonzalez, Eric Powell, Ioanna Konidari, William Hulme, John F. Staropoli, Winnie Xin, G. Y. Wen, (unknown), (unknown), Katherine B. Sims, W. Ted Brown, (unknown)	7
8	Reduced telomere length in individuals with FMR1 premutations and full mutations 2012 ·American Journal of Medical Genetics Part A ·Edmund C. Jenkins, Flora Tassone, Lingling Ye, A. T. Hoogeveen, W. Ted Brown, Randi J. Hagerman, Paul J. Hagerman	6
9	The Therapeutic effect of Memantine through the Stimulation of Synapse Formation and Dendritic Spine Maturation in Autism and Fragile X Syndrome 2012 ·PLoS ONE ·Hongen Wei, Carl Dobkin, Ashfaq M. Sheikh, Mazhar N. Malik, W. Ted Brown, Xiaohong Li	47
10	A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutation 2012 ·Gene ·Song‐Yu Yang, Carl Dobkin, Xue‐Ying He, Manfred Philipp, W. Ted Brown	10
11	Brain IL-6 elevation causes neuronal circuitry imbalances and mediates autism-like behaviors 2012 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Hongen Wei, Kathryn K. Chadman, Daniel P. McCloskey, Ashfaq M. Sheikh, Mazhar N. Malik, W. Ted Brown, Xiaohong Li	205
12	Neuroendocrine Alterations in the Fragile X Mouse 2011 ·Results and problems in cell differentiation ·Abdeslem El Idrissi, Xin Yan, William L’Amoreaux, W. Ted Brown, Carl Dobkin	7
13	Brain region‐specific deficit in mitochondrial electron transport chain complexes in children with autism 2011 ·Journal of Neurochemistry ·Abha Chauhan, Gu Feng, Musthafa Mohamed Essa, Jerzy Węgiel, Kulbir Kaur, W. Ted Brown, Ved Chauhan	189
14	Sera from Children with Autism Alter Proliferation of Human Neuronal Progenitor Cells Exposed to Oxidation 2009 ·Neurotoxicity Research ·Bozena Mazur‐Kolecka, Ira L. Cohen, Edmund C. Jenkins, Michael Flory, George Merz, W. Ted Brown, Janusz Frackowiak	11
15	Strategic Plan Outline for the Army Utilities Modernization Program: Fiscal Years 2008-2013 2006 ·US Army Corps of Engineers: Engineer Research and Development Center (Knowledge Core) ·W. Ted Brown, (unknown), (unknown), Charles P. Marsh, (unknown), (unknown), (unknown), Christophe Sohn, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	0
16	Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates breakdown → 2003 ·The American Journal of Human Genetics ·Sébastien Jacquemont, Randi J. Hagerman, Maureen A. Leehey, Jim Grigsby, Lin Zhang, James A. Brunberg, Claudia Greco, Vincent des Portes, (unknown), Richard A. Levine, Elizabeth Berry‐Kravis, W. Ted Brown, S. Schaeffer, John T. Kissel, Flora Tassone, Paul J. Hagerman	556
17	Molecular Diagnosis of and Carrier Screening for the Neuronal Ceroid Lipofuscinoses 2000 ·Genetic Testing ·Nanbert Zhong, Krystyna E. Wisniewski, Weina Ju, Dorota Moroziewicz, Anna Jurkiewicz, (unknown), Edmund C. Jenkins, W. Ted Brown	9
18	Invited Commentary: Apparent FMR1 Allele Instability in Non-Fragile X Males 2000 ·Genetic Testing ·W. Ted Brown, Sarah L. Nolin	1
19	FRAXAC1 and DXS548 polymorphisms in the Chinese population 1999 ·American Journal of Medical Genetics ·Priscilla M.K. Poon, Chi‐Pui Pang, (unknown), Nan Zhong, Kelly Y. C. Lai, (unknown), (unknown), W. Ted Brown	10
20	Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation 1999 ·American Journal of Medical Genetics ·Nan Zhong, Weina Ju, David L. Nelson, Carl Dobkin, W. Ted Brown	16

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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