Charles A. Williams

9.3k total citations
117 papers, 4.6k citations indexed

About

Charles A. Williams is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Charles A. Williams has authored 117 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Genetics, 46 papers in Molecular Biology and 21 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Charles A. Williams's work include Genetic Syndromes and Imprinting (36 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Epigenetics and DNA Methylation (18 papers). Charles A. Williams is often cited by papers focused on Genetic Syndromes and Imprinting (36 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Epigenetics and DNA Methylation (18 papers). Charles A. Williams collaborates with scholars based in United States, United Kingdom and Germany. Charles A. Williams's co-authors include Karin Buiting, Daniel J. Driscoll, Bernhard Horsthemke, Roberto T. Zori, Margaret R. Wallace, Aditi I Dagli, Joseph Wagstaff, Suzanne B. Cassidy, Jill Clayton‐Smith and Brian A. Gray and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Charles A. Williams

114 papers receiving 4.4k citations

Peers

Charles A. Williams

GENET

PPCH

NEURO

Karen Brøndum‐Nielsen Denmark

J. P. Fryns Belgium

David J. Amor Australia

Markku Ryynänen Finland

John M. Optiz United States

Albert E. Chudley Canada

Ankita Patel United States

Lisenka E.L.M. Vissers Netherlands

Michael L. Frigge Iceland

Sau Wai Cheung United States

Karen Brøndum‐Nielsen Denmark

Charles A. Williams

2.0k ×0.6

GENET

2.3k ×0.9

485 ×0.5

PPCH

514 ×1.2

83 ×0.3

NEURO

Citations per year, relative to Charles A. Williams Charles A. Williams (= 1×) peers Karen Brøndum‐Nielsen

Countries citing papers authored by Charles A. Williams

Since Specialization

Citations

This map shows the geographic impact of Charles A. Williams'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 Charles A. Williams with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles A. Williams more than expected).

Fields of papers citing papers by Charles A. Williams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles A. Williams. 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 Charles A. Williams. The network helps show where Charles A. Williams may publish in the future.

Co-authorship network of co-authors of Charles A. Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Charles A. Williams. A scholar is included among the top collaborators of Charles A. Williams 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 Charles A. Williams. Charles A. Williams 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

Mishra, Swati, Allison Knupp, C. Kinoshita, et al.. (2023). Pharmacologic enhancement of retromer rescues endosomal pathology induced by defects in the Alzheimer’s gene SORL1. Stem Cell Reports. 18(12). 2434–2450. 9 indexed citations

Sparago, Angela, Andrea Freschi, Saskia M. Maas, et al.. (2019). Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus. Genetics in Medicine. 21(8). 1808–1820. 32 indexed citations

Buiting, Karin, Charles A. Williams, & Bernhard Horsthemke. (2016). Angelman syndrome — insights into a rare neurogenetic disorder. Nature Reviews Neurology. 12(10). 584–593. 242 indexed citations

Fort, John, et al.. (2015). Optic nerve pilomyxoid astrocytoma in a patient with Noonan syndrome. Pediatric Blood & Cancer. 62(6). 1084–1086. 7 indexed citations

Tan, Wen‐Hann, Lynne M. Bird, Ronald L. Thibert, & Charles A. Williams. (2014). If not Angelman, what is it? a review of Angelman‐like syndromes. American Journal of Medical Genetics Part A. 164(4). 975–992. 79 indexed citations

Williams, Charles A., et al.. (2012). Neonatal diabetes mellitus and congenital diaphragmatic hernia: coincidence or concurrent etiology?. International Journal of Pediatric Endocrinology. 2012(1). 21–21. 6 indexed citations

Williams, Charles A. & Agatino Battaglia. (2011). Molecular biology of epilepsy genes. Experimental Neurology. 244. 51–58. 18 indexed citations

Dagli, Aditi I, Heather J. Stalker, & Charles A. Williams. (2007). A patient with the syndrome of megalencephaly, mega corpus callosum and complete lack of motor development. American Journal of Medical Genetics Part A. 146A(2). 204–207. 10 indexed citations

Williams, Charles A., Arthur L. Beaudet, Jill Clayton‐Smith, et al.. (2006). Angelman syndrome 2005: Updated consensus for diagnostic criteria. American Journal of Medical Genetics Part A. 140A(5). 413–418. 420 indexed citations

10.

Williams, Charles A., Jaime L. Frías, Mary Kay McCormick, Stylianos E. Antonarakis, & Eduardo S. Cantú. (2005). Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype. American Journal of Medical Genetics. 37(S7). 110–114. 5 indexed citations

11.

Williams, Charles A., et al.. (2003). Treatment of oralfacial clefts by state‐affiliated craniofacial centers and cleft palate clinics. Birth Defects Research Part A Clinical and Molecular Teratology. 67(9). 643–646. 13 indexed citations

12.

Keller, Kory, Charles A. Williams, Brian A. Gray, et al.. (2002). Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders. American Journal of Medical Genetics Part A. 117A(2). 105–111. 19 indexed citations

13.

Cassidy, Suzanne B., Elisabeth M. Dykens, & Charles A. Williams. (2000). Prader-Willi and Angelman syndromes: Sister imprinted disorders. American Journal of Medical Genetics. 97(2). 136–146. 196 indexed citations

14.

Zhang, Jun, Anil Kumar, Kyle J. Roux, Charles A. Williams, & Margaret R. Wallace. (1999). Elastin Region Deletions in Williams Syndrome. Genetic Testing. 3(4). 357–359. 3 indexed citations

15.

Malzac, Perrine, Hayley Webber, A. Moncla, et al.. (1998). Mutation Analysis of UBE3A in Angelman Syndrome Patients. The American Journal of Human Genetics. 62(6). 1353–1360. 121 indexed citations

16.

Donoghue, Susan, et al.. (1994). Diet as a Risk Factor for Feline External Odontoclastic Resorption. Journal of Nutrition. 124(12 Suppl). 2693S–2694S. 8 indexed citations

17.

Williams, Charles A., et al.. (1993). Communication, cognition, and social interaction in the Angelman syndrome. American Journal of Medical Genetics. 46(1). 34–39. 60 indexed citations

18.

Zackowski, Joleen L., Robert D. Nicholls, Brian A. Gray, et al.. (1993). Cytogenetic and molecular analysis in Angelman syndrome. American Journal of Medical Genetics. 46(1). 7–11. 28 indexed citations

19.

Williams, Charles A., et al.. (1992). Gingivitis/Stomatitis in Cats. Veterinary Clinics of North America Small Animal Practice. 22(6). 1361–1383. 24 indexed citations

20.

Bancroft, K., Charles A. Williams, & Max Elstein. (1989). Minimal/mild endometriosis and infertility. A review. BJOG An International Journal of Obstetrics & Gynaecology. 96(4). 454–460. 37 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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