Christopher Stoddard

420 total citations
11 papers, 258 citations indexed

About

Christopher Stoddard is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christopher Stoddard has authored 11 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christopher Stoddard's work include Genetic Syndromes and Imprinting (5 papers), Epigenetics and DNA Methylation (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Christopher Stoddard is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Epigenetics and DNA Methylation (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Christopher Stoddard collaborates with scholars based in United States, Germany and Poland. Christopher Stoddard's co-authors include Caiying Guo, Marco Brotto, Jinhua Shen, Wen-Mei Yu, Thomas M. Nosek, Cheng‐Kui Qu, Héctor H. Valdivia, Christina Grant, Leslie A. Caromile and Stormy J. Chamberlain and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Christopher Stoddard

10 papers receiving 257 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christopher Stoddard United States	7	167	91	41	33	28	11	258
Tiffany Busa France	11	174 1.0×	163 1.8×	27 0.7×	13 0.4×	26 0.9×	27	312
Frederike L. Harms Germany	11	188 1.1×	83 0.9×	60 1.5×	11 0.3×	15 0.5×	29	280
Ken Matsuura Japan	8	257 1.5×	45 0.5×	72 1.8×	39 1.2×	13 0.5×	11	383
Anne Gläser Germany	9	212 1.3×	75 0.8×	34 0.8×	17 0.5×	16 0.6×	15	332
Melanie Jäger Germany	11	147 0.9×	45 0.5×	44 1.1×	28 0.8×	39 1.4×	19	347
Ilse J. Anderson United States	7	164 1.0×	165 1.8×	34 0.8×	9 0.3×	11 0.4×	11	304
Kelly E. Jackson United States	8	204 1.2×	211 2.3×	26 0.6×	11 0.3×	13 0.5×	15	375
Dingge Ying Hong Kong	9	156 0.9×	147 1.6×	14 0.3×	27 0.8×	10 0.4×	16	313
Shinobu Fukumura Japan	11	149 0.9×	55 0.6×	43 1.0×	12 0.4×	12 0.4×	29	272
Hande Kaymakçalan Türkiye	9	187 1.1×	133 1.5×	114 2.8×	20 0.6×	5 0.2×	14	337

Countries citing papers authored by Christopher Stoddard

Since Specialization

Citations

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

Fields of papers citing papers by Christopher Stoddard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Stoddard

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Stoddard. A scholar is included among the top collaborators of Christopher Stoddard 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 Christopher Stoddard. Christopher Stoddard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Stoddard, Christopher, et al.. (2024). Generation of isogenic models of Angelman syndrome and Prader-Willi syndrome in CRISPR/Cas9-engineered human embryonic stem cells. PLoS ONE. 19(11). e0311565–e0311565.

Glatt-Deeley, Heather R., Christopher Stoddard, Jeremy W. Linsley, et al.. (2024). A dynamic in vitro model of Down syndrome neurogenesis with trisomy 21 gene dosage correction. Science Advances. 10(23). eadj0385–eadj0385. 3 indexed citations

Liu, Yaling, et al.. (2024). Identifying key underlying regulatory networks and predicting targets of orphan C/D box SNORD116 snoRNAs in Prader–Willi syndrome. Nucleic Acids Research. 52(22). 13757–13774. 1 indexed citations

Elamin, Marwa, et al.. (2023). The role of UBE3A in the autism and epilepsy-related Dup15q syndrome using patient-derived, CRISPR-corrected neurons. Stem Cell Reports. 18(4). 884–898. 10 indexed citations

Stutz, Bernardo, Feng Li, Haining Lv, et al.. (2022). TET3 epigenetically controls feeding and stress response behaviors via AGRP neurons. Journal of Clinical Investigation. 132(19). 23 indexed citations

Langouët, Maéva, Michael Chung, Heather R. Glatt-Deeley, et al.. (2020). Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics. 29(19). 3285–3295. 12 indexed citations

Hsiao, Jack S., Noélle D. Germain, Andrea Wilderman, et al.. (2019). A bipartite boundary element restricts UBE3A imprinting to mature neurons. Proceedings of the National Academy of Sciences. 116(6). 2181–2186. 46 indexed citations

Becker, Sandy, Martin Schicht, Christopher Stoddard, et al.. (2018). Examining the role of the surfactant family member SFTA3 in interneuron specification. PLoS ONE. 13(11). e0198703–e0198703. 2 indexed citations

Caromile, Leslie A., Mamunur Rahman, Christina Grant, et al.. (2017). PSMA redirects cell survival signaling from the MAPK to the PI3K-AKT pathways to promote the progression of prostate cancer. Science Signaling. 10(470). 47 indexed citations

10.

Langouët, Maéva, Heather R. Glatt-Deeley, Michael Chung, et al.. (2017). Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons. Human Molecular Genetics. 27(3). 505–515. 30 indexed citations

11.

Shen, Jinhua, Wen-Mei Yu, Marco Brotto, et al.. (2009). Deficiency of MIP/MTMR14 phosphatase induces a muscle disorder by disrupting Ca2+ homeostasis. Nature Cell Biology. 11(6). 769–776. 84 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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