Joseph Wagstaff

4.4k total citations · 1 hit paper
27 papers, 3.0k citations indexed

About

Joseph Wagstaff is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Joseph Wagstaff has authored 27 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 18 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Joseph Wagstaff's work include Genetic Syndromes and Imprinting (18 papers), Epigenetics and DNA Methylation (13 papers) and Prenatal Screening and Diagnostics (9 papers). Joseph Wagstaff is often cited by papers focused on Genetic Syndromes and Imprinting (18 papers), Epigenetics and DNA Methylation (13 papers) and Prenatal Screening and Diagnostics (9 papers). Joseph Wagstaff collaborates with scholars based in United States, Japan and France. Joseph Wagstaff's co-authors include Tatsuya Kishino, Marc Lalande, Bernhard Horsthemke, Charles A. Williams, Joan H.M. Knoll, R. Ellen Magenis, Albert Schinzel, Jill Clayton‐Smith, Hayley Webber and Laura Laan and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Joseph Wagstaff

27 papers receiving 2.9k citations

Hit Papers

align trajectories sort by overperformance

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.

UBE3A/E6-AP mutations cause Angelman syndrome

1997 969 citations Tatsuya Kishino, Marc Lalande et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Joseph Wagstaff United States	20	2.3k	2.3k	642	262	153	27	3.0k
Fiorella Gurrieri Italy	27	1.3k 0.5×	1.4k 0.6×	345 0.5×	290 1.1×	131 0.9×	88	2.4k
Stormy J. Chamberlain United States	25	1.3k 0.6×	2.1k 0.9×	327 0.5×	270 1.0×	103 0.7×	44	2.5k
Anne Moncla France	24	1.3k 0.6×	1.1k 0.5×	185 0.3×	343 1.3×	89 0.6×	38	1.9k
R.E. Magenis United States	28	1.5k 0.7×	1.5k 0.6×	495 0.8×	109 0.4×	385 2.5×	55	2.7k
Sylvain Briault France	23	1.6k 0.7×	1.8k 0.8×	248 0.4×	610 2.3×	426 2.8×	64	3.1k
Lionel Willatt United Kingdom	22	1.3k 0.5×	909 0.4×	328 0.5×	129 0.5×	95 0.6×	30	1.8k
Carlos Cardoso France	24	871 0.4×	1.2k 0.5×	282 0.4×	211 0.8×	302 2.0×	37	2.0k
Ragnheiður Fossdal Iceland	15	1.5k 0.6×	987 0.4×	211 0.3×	580 2.2×	77 0.5×	21	2.2k
Svetlana G. Vorsanova Russia	31	2.1k 0.9×	1.5k 0.6×	452 0.7×	315 1.2×	162 1.1×	175	3.1k
Keiko Shimojima Japan	25	1.2k 0.5×	1.0k 0.5×	218 0.3×	99 0.4×	190 1.2×	125	1.9k

Countries citing papers authored by Joseph Wagstaff

Since Specialization

Citations

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

Fields of papers citing papers by Joseph Wagstaff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph Wagstaff. 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 Joseph Wagstaff. The network helps show where Joseph Wagstaff may publish in the future.

Co-authorship network of co-authors of Joseph Wagstaff

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

Horsthemke, Bernhard & Joseph Wagstaff. (2008). Mechanisms of imprinting of the Prader–Willi/Angelman region. American Journal of Medical Genetics Part A. 146A(16). 2041–2052. 204 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

Miura, Kiyonori, Koh‐ichiro Yoshiura, Shoko Miura, et al.. (2006). Clinical outcome of infants with confined placental mosaicism and intrauterine growth restriction of unknown cause. American Journal of Medical Genetics Part A. 140A(17). 1827–1833. 23 indexed citations

Soejima, Hidenobu & Joseph Wagstaff. (2005). Imprinting centers, chromatin structure, and disease. Journal of Cellular Biochemistry. 95(2). 226–233. 26 indexed citations

Cooper, Eric M., Amy W. Hudson, Joseph Amos, Joseph Wagstaff, & Peter M. Howley. (2004). Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein. Journal of Biological Chemistry. 279(39). 41208–41217. 87 indexed citations

Dan, Bernard, Laurent Servais, Stewart Boyd, Joseph Wagstaff, & Guy Chéron. (2004). From Electrophysiology to Chromatin: A Bottom‐Up Approach to Angelman Syndrome. Annals of the New York Academy of Sciences. 1030(1). 599–611. 11 indexed citations

Tachibana, Makoto, et al.. (2003). Role of Histone Methyltransferase G9a in CpG Methylation of the Prader-Willi Syndrome Imprinting Center. Journal of Biological Chemistry. 278(17). 14996–15000. 135 indexed citations

Miura, Kiyonori, Tatsuya Kishino, En Li, et al.. (2002). Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice. Neurobiology of Disease. 9(2). 149–159. 196 indexed citations

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

10.

Kishino, Tatsuya & Joseph Wagstaff. (1998). Genomic Organization of theUBE3A/E6-AP Gene and Related Pseudogenes. Genomics. 47(1). 101–107. 43 indexed citations

11.

Repetto, Gabriela M., Joseph Wagstaff, Bruce R. Korf, & Joan H.M. Knoll. (1998). Complex familial rearrangement of chromosome 9p24.3 detected by FISH. American Journal of Medical Genetics. 76(4). 306–309. 1 indexed citations

12.

Kishino, Tatsuya, Marc Lalande, & Joseph Wagstaff. (1997). UBE3A/E6-AP mutations cause Angelman syndrome. Nature Genetics. 15(1). 70–73. 969 indexed citations breakdown →

13.

Saitoh, Shinji, Naoki Harada, Yoshihiro Jinno, et al.. (1994). Molecular and clinical study of 61 Angelman syndrome patients. American Journal of Medical Genetics. 52(2). 158–163. 67 indexed citations

14.

Schnur, Rhonda E., L. Charles Bailey, Timothy R. Rebbeck, et al.. (1994). Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypes.. PubMed. 55(3). 484–96. 19 indexed citations

15.

Nakatsu, Yoshimichi, Rachel F. Tyndale, Timothy M. DeLorey, et al.. (1993). A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus. Nature. 364(6436). 448–450. 83 indexed citations

16.

Knoll, Joan H.M., Daniel Sinnett, Joseph Wagstaff, et al.. (1993). FISH ordering of reference markers and of the gene for the α5 subunit of the γ-aminobutyric acid receptor (GABRA5) within the Angelman and Prader–Willi syndrome chromosomal regions. Human Molecular Genetics. 2(2). 183–189. 73 indexed citations

17.

Koch, Thomas, et al.. (1992). Neurologic complications in galactosemia. Pediatric Neurology. 8(3). 217–220. 25 indexed citations

18.

Wagstaff, Joseph, Mark Korson, Jan P. Kraus, & Harvey L. Levy. (1991). Severe folate deficiency and pancytopenia in a nutritionally deprived infant with homocystinuria caused by cystathionine beta-synthase deficiency. The Journal of Pediatrics. 118(4). 569–572. 6 indexed citations

19.

Wagstaff, Joseph, Sue Klapholz, & Rochelle Easton Esposito. (1982). Meiosis in haploid yeast. Proceedings of the National Academy of Sciences. 79(9). 2986–2990. 58 indexed citations

20.

Esposito, Michael S. & Joseph Wagstaff. (1981). Mechanisms of Mitotic Recombination. Cold Spring Harbor Monograph Archive. 341–370. 47 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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