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, Abha Chauhan, Ved 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

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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 Randi J. Hagerman, Elizabeth Berry‐Kravis et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
W. Ted Brown	5.5k	4.8k	3.7k	821	787	217	10.9k
Nathalie Boddaert	4.4k 0.8×	2.7k 0.6×	2.2k 0.6×	1.3k 1.5×	539 0.7×	389	12.7k
Alan K. Percy	3.9k 0.7×	7.9k 1.6×	5.6k 1.5×	638 0.8×	567 0.7×	237	10.8k
T. Conrad Gilliam	5.4k 1.0×	4.8k 1.0×	1.6k 0.4×	1.4k 1.7×	563 0.7×	122	11.3k
Charles E. Schwartz	7.6k 1.4×	6.3k 1.3×	1.7k 0.5×	851 1.0×	446 0.6×	319	13.0k
Laura Almasy	4.9k 0.9×	6.3k 1.3×	2.5k 0.7×	1.7k 2.1×	2.1k 2.7×	373	18.3k
Glenn D. Rosen	3.4k 0.6×	1.2k 0.3×	3.6k 1.0×	1.1k 1.3×	590 0.7×	200	12.3k
Nigel Williams	2.9k 0.5×	2.9k 0.6×	1.2k 0.3×	1.4k 1.7×	533 0.7×	246	8.3k
Kazuhiko Nakamura	2.2k 0.4×	1.9k 0.4×	2.0k 0.5×	1.3k 1.6×	682 0.9×	376	11.5k
S. Hossein Fatemi	2.7k 0.5×	2.8k 0.6×	3.1k 0.8×	2.1k 2.6×	435 0.6×	117	9.2k
Julie R. Korenberg	5.5k 1.0×	2.5k 0.5×	919 0.3×	1.4k 1.7×	625 0.8×	167	10.5k

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

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20 of 20 papers shown

He, Xue‐Ying, et al.. (2023). Involvement of Type 10 17β-Hydroxysteroid Dehydrogenase in the Pathogenesis of Infantile Neurodegeneration and Alzheimer’s Disease. International Journal of Molecular Sciences. 24(24). 17604–17604. 6 indexed citations

Adayev, Tatyana, Giuseppe LaFauci, Weimin Xu, et al.. (2021). Development of a Quantitative FMRP Assay for Mouse Tissue Applications. Genes. 12(10). 1516–1516. 2 indexed citations

Kaufmann, Walter E., Sharon A. Kidd, Howard Andrews, et al.. (2017). Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment. PEDIATRICS. 139(Supplement_3). S194–S206. 186 indexed citations

Węgiel, Jerzy, Izabela Kuchna, Krzysztof Nowicki, et al.. (2013). Contribution of olivofloccular circuitry developmental defects to atypical gaze in autism. Brain Research. 1512. 106–122. 38 indexed citations

Kover, Sara T., et al.. (2013). A Neurodevelopmental Perspective on the Acquisition of Nonverbal Cognitive Skills in Adolescents With Fragile X Syndrome. Developmental Neuropsychology. 38(7). 445–460. 30 indexed citations

LaFauci, Giuseppe, Tatyana Adayev, Richard J. Kascsak, et al.. (2013). Fragile X Screening by Quantification of FMRP in Dried Blood Spots by a Luminex Immunoassay. Journal of Molecular Diagnostics. 15(4). 508–517. 43 indexed citations

Luo, Xiucui, Yang Gu, Jing Pan, et al.. (2013). LncRNA Pathway Involved in Premature Preterm Rupture of Membrane (PPROM): An Epigenomic Approach to Study the Pathogenesis of Reproductive Disorders. PLoS ONE. 8(11). e79897–e79897. 40 indexed citations

Velinov, Milen, Natalia Dolzhanskaya, Michael Gonzalez, et al.. (2012). 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. PLoS ONE. 7(9). 7 indexed citations

Jenkins, Edmund C., Flora Tassone, Lingling Ye, et al.. (2012). Reduced telomere length in individuals with FMR1 premutations and full mutations. American Journal of Medical Genetics Part A. 158A(5). 1060–1065. 6 indexed citations

10.

Wei, Hongen, Carl Dobkin, Ashfaq M. Sheikh, et al.. (2012). The Therapeutic effect of Memantine through the Stimulation of Synapse Formation and Dendritic Spine Maturation in Autism and Fragile X Syndrome. PLoS ONE. 7(5). e36981–e36981. 47 indexed citations

11.

Yang, Song‐Yu, Carl Dobkin, Xue‐Ying He, Manfred Philipp, & W. Ted Brown. (2012). A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutation. Gene. 515(2). 380–384. 10 indexed citations

12.

Chauhan, Abha, Gu Feng, Musthafa Mohamed Essa, et al.. (2011). Brain region‐specific deficit in mitochondrial electron transport chain complexes in children with autism. Journal of Neurochemistry. 117(2). 209–220. 189 indexed citations

13.

Idrissi, Abdeslem El, Xin Yan, William L’Amoreaux, W. Ted Brown, & Carl Dobkin. (2011). Neuroendocrine Alterations in the Fragile X Mouse. Results and problems in cell differentiation. 54. 201–221. 7 indexed citations

14.

Brown, W. Ted. (2011). Clinical Aspects of the Fragile X Syndrome. Results and problems in cell differentiation. 54. 273–279. 2 indexed citations

15.

Brown, W. Ted, et al.. (2006). Strategic Plan Outline for the Army Utilities Modernization Program: Fiscal Years 2008-2013. US Army Corps of Engineers: Engineer Research and Development Center (Knowledge Core).

16.

Tsiouris, John A. & W. Ted Brown. (2004). Neuropsychiatric Symptoms of Fragile X Syndrome. CNS Drugs. 18(11). 687–703. 92 indexed citations

17.

Zhong, Nanbert, Krystyna E. Wisniewski, Weina Ju, et al.. (2000). Molecular Diagnosis of and Carrier Screening for the Neuronal Ceroid Lipofuscinoses. Genetic Testing. 4(3). 243–248. 9 indexed citations

18.

Brown, W. Ted & Sarah L. Nolin. (2000). Invited Commentary: Apparent FMR1 Allele Instability in Non-Fragile X Males. Genetic Testing. 4(3). 241–242. 1 indexed citations

19.

Poon, Priscilla M.K., et al.. (1999). FRAXAC1 and DXS548 polymorphisms in the Chinese population. American Journal of Medical Genetics. 84(3). 208–213. 10 indexed citations

20.

Brown, W. Ted, et al.. (1996). Hernia of the Lung Repaired by VATS: A Case Report. Journal of Laparoendoscopic Surgery. 6(6). 427–430. 9 indexed citations

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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