JoAnne S. Richards

24.3k total citations · 5 hit papers
225 papers, 19.9k citations indexed

About

JoAnne S. Richards is a scholar working on Public Health, Environmental and Occupational Health, Genetics and Reproductive Medicine. According to data from OpenAlex, JoAnne S. Richards has authored 225 papers receiving a total of 19.9k indexed citations (citations by other indexed papers that have themselves been cited), including 115 papers in Public Health, Environmental and Occupational Health, 81 papers in Genetics and 73 papers in Reproductive Medicine. Recurrent topics in JoAnne S. Richards's work include Reproductive Biology and Fertility (114 papers), Estrogen and related hormone effects (64 papers) and Reproductive System and Pregnancy (56 papers). JoAnne S. Richards is often cited by papers focused on Reproductive Biology and Fertility (114 papers), Estrogen and related hormone effects (64 papers) and Reproductive System and Pregnancy (56 papers). JoAnne S. Richards collaborates with scholars based in United States, Japan and Canada. JoAnne S. Richards's co-authors include Masayuki Shimada, Darryl L. Russell, Rebecca L. Robker, Jean Sirois, Lawrence L. Espey, Heng‐Yu Fan, Lars O. Hedin, A. REES MIDGLEY, Scott A. Ochsner and Zhilin Liu and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

JoAnne S. Richards

221 papers receiving 19.5k citations

Hit Papers

Hormonal Control of Gene ... 1976 2026 1992 2009 1994 1980 1996 2009 1976 200 400 600

Author Peers

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

Author Last Decade Papers Cites
JoAnne S. Richards 9.4k 6.8k 6.7k 6.5k 4.1k 225 19.9k
Philippa T. K. Saunders 4.2k 0.5× 9.8k 1.5× 7.0k 1.0× 6.1k 0.9× 3.7k 0.9× 293 19.3k
Francesco J. DeMayo 4.5k 0.5× 7.8k 1.2× 8.5k 1.3× 14.7k 2.2× 10.0k 2.5× 401 32.3k
John P. Lydon 2.8k 0.3× 6.6k 1.0× 6.2k 0.9× 5.0k 0.8× 7.7k 1.9× 270 17.3k
Jonathan L. Tilly 9.0k 1.0× 5.4k 0.8× 2.1k 0.3× 7.7k 1.2× 2.1k 0.5× 161 15.8k
Nigel P. Groome 5.4k 0.6× 5.1k 0.7× 2.4k 0.4× 6.0k 0.9× 1.2k 0.3× 226 13.8k
Edwin Milgröm 1.8k 0.2× 5.6k 0.8× 6.8k 1.0× 7.1k 1.1× 2.6k 0.6× 233 16.6k
Dennis B. Lubahn 2.1k 0.2× 5.1k 0.8× 12.1k 1.8× 9.0k 1.4× 3.0k 0.7× 189 24.6k
David T. Armstrong 7.5k 0.8× 5.8k 0.9× 3.4k 0.5× 2.9k 0.4× 1.4k 0.3× 323 13.3k
Bibhash C. Paria 3.2k 0.3× 4.3k 0.6× 2.4k 0.4× 2.8k 0.4× 6.7k 1.6× 116 11.8k
Marco Conti 6.1k 0.7× 4.3k 0.6× 1.7k 0.3× 14.5k 2.2× 2.3k 0.6× 238 21.0k

Countries citing papers authored by JoAnne S. Richards

Since Specialization
Citations

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

Fields of papers citing papers by JoAnne S. Richards

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by JoAnne S. Richards. 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 JoAnne S. Richards. The network helps show where JoAnne S. Richards may publish in the future.

Co-authorship network of co-authors of JoAnne S. Richards

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

All Works

20 of 20 papers shown
1.
Candelaria, Nicholes R. & JoAnne S. Richards. (2024). Targeted deletion of NR2F2 and VCAM1 in theca cells impacts ovarian follicular development: insights into polycystic ovary syndrome?. Biology of Reproduction. 110(4). 782–797. 3 indexed citations
2.
Combs, C. Andrew, et al.. (2020). Enhanced recovery after cesarean: impact on postoperative opioid use and length of stay. American Journal of Obstetrics and Gynecology. 224(2). 237–239. 3 indexed citations
3.
Richards, JoAnne S.. (2018). From Follicular Development and Ovulation to Ovarian Cancers: An Unexpected Journey. Vitamins and hormones. 107. 453–472. 19 indexed citations
4.
Kawashima, Ikko, Takashi Umehara, Noritaka Noma, et al.. (2014). Targeted Disruption of Nrg1 in Granulosa Cells Alters the Temporal Progression of Oocyte Maturation. Molecular Endocrinology. 28(5). 706–721. 27 indexed citations
5.
Pierce, Angela, Mei Xu, Zhilin Liu, et al.. (2011). Hypothalamic but not pituitary or ovarian defects underlie the reproductive abnormalities in Axl/Tyro3 null mice. Molecular and Cellular Endocrinology. 339(1-2). 151–158. 19 indexed citations
6.
Noma, Noritaka, Ikko Kawashima, Heng‐Yu Fan, et al.. (2010). LH-Induced Neuregulin 1 (NRG1) Type III Transcripts Control Granulosa Cell Differentiation and Oocyte Maturation. Molecular Endocrinology. 25(1). 104–116. 55 indexed citations
7.
Liu, Zhilin, Heng‐Yu Fan, Yibin Wang, & JoAnne S. Richards. (2010). Targeted Disruption of Mapk14 (p38MAPKα) in Granulosa Cells and Cumulus Cells Causes Cell-Specific Changes in Gene Expression Profiles that Rescue COC Expansion and Maintain Fertility. Molecular Endocrinology. 24(9). 1794–1804. 48 indexed citations
8.
Richards, JoAnne S. & Stephanie A. Pangas. (2010). New Insights into Ovarian Function. Handbook of experimental pharmacology. 3–27. 32 indexed citations
9.
Fan, Heng‐Yu, Zhilin Liu, Masayuki Shimada, et al.. (2009). MAPK3/1 (ERK1/2) in Ovarian Granulosa Cells Are Essential for Female Fertility. Science. 324(5929). 938–941. 517 indexed citations breakdown →
10.
Fan, Heng‐Yu, Zhilin Liu, Marilène Paquet, et al.. (2009). Cell Type–Specific Targeted Mutations of Kras and Pten Document Proliferation Arrest in Granulosa Cells versus Oncogenic Insult to Ovarian Surface Epithelial Cells. Cancer Research. 69(16). 6463–6472. 67 indexed citations
11.
Sriraman, Venkataraman, Ursula Eichenlaub-Ritter, Jörg W. Bartsch, et al.. (2008). Regulated Expression of ADAM8 (a Disintegrin and Metalloprotease Domain 8) in the Mouse Ovary: Evidence for a Regulatory Role of Luteinizing Hormone, Progesterone Receptor, and Epidermal Growth Factor-Like Growth Factors1. Biology of Reproduction. 78(6). 1038–1048. 39 indexed citations
12.
Boerboom, Derek, Marilène Paquet, Minnie Hsieh, et al.. (2005). Misregulated Wnt/β-Catenin Signaling Leads to Ovarian Granulosa Cell Tumor Development. Cancer Research. 65(20). 9206–9215. 135 indexed citations
13.
Shimada, Masayuki, et al.. (2005). TAF4b, a TBP associated factor, is required for oocyte development and function. Developmental Biology. 288(2). 405–419. 45 indexed citations
15.
Robker, Rebecca L. & JoAnne S. Richards. (1998). Hormone-Induced Proliferation and Differentiation of Granulosa Cells: A Coordinated Balance of the Cell Cycle Regulators Cyclin D2 and p27Kip1. Molecular Endocrinology. 12(7). 924–940. 379 indexed citations
18.
Richards, JoAnne S.. (1986). Molecular loci for potential drug toxicity in ovaries.. Environmental Health Perspectives. 70. 159–161. 8 indexed citations
19.
Knudson, M. Margaret, et al.. (1976). Progesterone Metabolism by the Ovary of the Pregnant Rat: Discrepancies in the Catabolic Regulation Model112. Endocrinology. 99(4). 929–934. 21 indexed citations
20.
Richards, JoAnne S.. (1973). Changes in fish species composition in the Au Sable River, Michigan, from the 1920's to 1972 (Fisheries research report: 1800). Deep Blue (University of Michigan). 2 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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