Nicholas Nagykery

1.1k total citations
19 papers, 775 citations indexed

About

Nicholas Nagykery is a scholar working on Molecular Biology, Pharmacology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Nicholas Nagykery has authored 19 papers receiving a total of 775 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Pharmacology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Nicholas Nagykery's work include Reproductive Biology and Fertility (5 papers), Cholinesterase and Neurodegenerative Diseases (5 papers) and Memory and Neural Mechanisms (5 papers). Nicholas Nagykery is often cited by papers focused on Reproductive Biology and Fertility (5 papers), Cholinesterase and Neurodegenerative Diseases (5 papers) and Memory and Neural Mechanisms (5 papers). Nicholas Nagykery collaborates with scholars based in United States and Australia. Nicholas Nagykery's co-authors include Changiz Geula, Chuang-Kuo Wu, Alexander Nicholas, Patricia K. Donahoe, David Pépin, Motohiro Kano, Hatice D. Saatcioglu, Chuang‐Kuo Wu, Guangping Gao and Dan Wang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and The Journal of Comparative Neurology.

In The Last Decade

Nicholas Nagykery

16 papers receiving 767 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicholas Nagykery United States 12 258 232 216 173 159 19 775
Bertalan Dudás United States 18 110 0.4× 178 0.8× 37 0.2× 190 1.1× 55 0.3× 47 774
L. A. Martin United States 17 99 0.4× 418 1.8× 71 0.3× 76 0.4× 108 0.7× 34 876
Armando Arroyo United States 9 215 0.8× 266 1.1× 78 0.4× 116 0.7× 20 0.1× 9 825
Sandrine De Seranno France 10 183 0.7× 241 1.0× 16 0.1× 153 0.9× 52 0.3× 10 686
Csaba Vastagh Hungary 14 86 0.3× 163 0.7× 27 0.1× 162 0.9× 32 0.2× 26 545
Gang Pei China 20 233 0.9× 590 2.5× 28 0.1× 104 0.6× 46 0.3× 31 1.1k
Timothy J. Sendera United States 14 147 0.6× 500 2.2× 43 0.2× 38 0.2× 33 0.2× 17 1.2k
Martine El‐Etr France 15 70 0.3× 286 1.2× 129 0.6× 144 0.8× 13 0.1× 19 1.1k
Liisa Eränkö Finland 17 154 0.6× 297 1.3× 107 0.5× 43 0.2× 51 0.3× 31 832
Sonia Canterini Italy 17 244 0.9× 258 1.1× 36 0.2× 15 0.1× 28 0.2× 32 671

Countries citing papers authored by Nicholas Nagykery

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas Nagykery

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicholas Nagykery

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

All Works

19 of 19 papers shown
1.
Howard, J. A., Richard L. Cate, Nicholas Nagykery, et al.. (2025). A divergent two-domain structure of the anti-Müllerian hormone prodomain. Proceedings of the National Academy of Sciences. 122(3). e2418088122–e2418088122.
2.
Chang, Eun Mi, Maëva Chauvin, A Kashiwagi, et al.. (2025). AMH protects the ovary from doxorubicin by regulating cell fate and the response to DNA damage. Proceedings of the National Academy of Sciences. 122(5). e2414734122–e2414734122.
3.
Nagykery, Nicholas, Motohiro Kano, Guangping Gao, et al.. (2025). Gene therapy delivery of anti-Müllerian hormone in prepubertal female domestic cats induces long-term sterilization. Nature Communications. 16(1). 10747–10747.
4.
Chauvin, Maëva, Marie-Charlotte Meinsohn, Santosh K. Dasari, et al.. (2023). Cancer-associated mesothelial cells are regulated by the anti-Müllerian hormone axis. Cell Reports. 42(7). 112730–112730. 11 indexed citations
5.
Li, Yi, Marie-Charlotte Meinsohn, Maëva Chauvin, et al.. (2022). A screen of repurposed drugs identifies AMHR2/MISR2 agonists as potential contraceptives. Proceedings of the National Academy of Sciences. 119(15). e2122512119–e2122512119. 9 indexed citations
6.
Nagykery, Nicholas, Kelly L. Walton, Craig A. Harrison, et al.. (2021). Structure of AMH bound to AMHR2 provides insight into a unique signaling pair in the TGF-β family. Proceedings of the National Academy of Sciences. 118(26). 32 indexed citations
7.
Meinsohn, Marie-Charlotte, Hatice D. Saatcioglu, Yi Li, et al.. (2021). Single-cell sequencing reveals suppressive transcriptional programs regulated by MIS/AMH in neonatal ovaries. Proceedings of the National Academy of Sciences. 118(20). 47 indexed citations
8.
Saatcioglu, Hatice D., Motohiro Kano, Heiko Horn, et al.. (2019). Single-cell sequencing of neonatal uterus reveals an Misr2+ endometrial progenitor indispensable for fertility. eLife. 8. 29 indexed citations
9.
Kano, Motohiro, Hatice D. Saatcioglu, Nicholas Nagykery, et al.. (2019). Neoadjuvant Treatment With Müllerian-Inhibiting Substance Synchronizes Follicles and Enhances Superovulation Yield. Journal of the Endocrine Society. 3(11). 2123–2134. 15 indexed citations
10.
Kano, Motohiro, LiHua Zhang, Hatice D. Saatcioglu, et al.. (2017). AMH/MIS as a contraceptive that protects the ovarian reserve during chemotherapy. Proceedings of the National Academy of Sciences. 114(9). E1688–E1697. 150 indexed citations
11.
Nagykery, Nicholas, Ernest F. Terwilliger, & Changiz Geula. (2012). In vivo AAV-mediated expression of calbindin-D28K in rat basal forebrain cholinergic neurons. Journal of Neuroscience Methods. 212(1). 106–113. 2 indexed citations
12.
Geula, Changiz, Nicholas Nagykery, Alexander Nicholas, & Chuang-Kuo Wu. (2008). Cholinergic Neuronal and Axonal Abnormalities Are Present Early in Aging and in Alzheimer Disease. Journal of Neuropathology & Experimental Neurology. 67(4). 309–318. 156 indexed citations
13.
Geula, Changiz & Nicholas Nagykery. (2006). Butyrylcholinesterase activity in the rat forebrain and upper brainstem: Postnatal development and adult distribution. Experimental Neurology. 204(2). 640–657. 16 indexed citations
14.
Eskander, Mariam F., et al.. (2005). Rivastigmine is a potent inhibitor of acetyl- and butyrylcholinesterase in Alzheimer's plaques and tangles. Brain Research. 1060(1-2). 144–152. 70 indexed citations
15.
Wu, Chuang, Nicholas Nagykery, L.B. Hersh, Leonard F. M. Scinto, & Changiz Geula. (2003). Selective age-related loss of CALBINDIN-D28k from basal forebrain cholinergic neurons in the common marmoset (callithrix jacchus). Neuroscience. 120(1). 249–259. 30 indexed citations
16.
Geula, Changiz, Nicholas Nagykery, Chuang‐Kuo Wu, & Jing Bu. (2003). Loss of Calbindin-D28Kfrom Aging Human Cholinergic Basal Forebrain: Relation to Plaques and Tangles. Journal of Neuropathology & Experimental Neurology. 62(6). 605–616. 32 indexed citations
17.
Geula, Changiz, Jing Bu, Nicholas Nagykery, et al.. (2002). Loss of calbindin‐D28k from aging human cholinergic basal forebrain: Relation to neuronal loss. The Journal of Comparative Neurology. 455(2). 249–259. 78 indexed citations
18.
Geula, Changiz, Nicholas Nagykery, & Chuang-Kuo Wu. (2001). Amyloid-β deposits in the cerebral cortex of the aged common marmoset (Callithrix jacchus): incidence and chemical composition. Acta Neuropathologica. 103(1). 48–58. 94 indexed citations
19.
Wu, Chuang‐Kuo, Nicholas Nagykery, & Changiz Geula. (2000). Age-related loss of calcium binding proteins may predispose basal forebrain cholinergic neurons to degeneration in Alzheimer's disease. Neurobiology of Aging. 21. 121–121. 4 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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