Joy M. Richman

5.9k total citations · 2 hit papers
86 papers, 4.3k citations indexed

About

Joy M. Richman is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Joy M. Richman has authored 86 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 39 papers in Genetics and 12 papers in Genetics. Recurrent topics in Joy M. Richman's work include dental development and anomalies (36 papers), Cleft Lip and Palate Research (27 papers) and Hedgehog Signaling Pathway Studies (25 papers). Joy M. Richman is often cited by papers focused on dental development and anomalies (36 papers), Cleft Lip and Palate Research (27 papers) and Hedgehog Signaling Pathway Studies (25 papers). Joy M. Richman collaborates with scholars based in Canada, United States and United Kingdom. Joy M. Richman's co-authors include Gregory R. Handrigan, Katherine Fu, Virginia M. Diewert, Cheryll Tickle, Amir M. Ashique, Marcela Buchtová, Peter Koopman, Kallayanee Chawengsaksophak, Deon Knight and Josephine Bowles and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Joy M. Richman

83 papers receiving 4.3k citations

Hit Papers

Retinoid Signaling Determines Germ Cell Fate in Mice 1995 2026 2005 2015 2006 1995 250 500 750
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.

  1. Retinoid Signaling Determines Germ Cell Fate in Mice
    2006 756 citations Josephine Bowles, Deon Knight et al. Science profile →
  2. Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes
    1995 633 citations Virginia M. Diewert, Joy M. Richman et al. profile →

Peers

Joy M. Richman
Robert E. Maxson United States
G Couly France
Shinji Takada Japan
Paul A. Trainor United States
Drew M. Noden United States
Gillian Morriss‐Kay United Kingdom
Chi‐chung Hui Canada
Lisa V. Goodrich United States
David Sassoon United States
Lee Niswander United States
Robert E. Maxson United States
Joy M. Richman
Citations per year, relative to Joy M. Richman Joy M. Richman (= 1×) peers Robert E. Maxson

Countries citing papers authored by Joy M. Richman

Since Specialization
Citations

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

Fields of papers citing papers by Joy M. Richman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joy M. Richman. 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 Joy M. Richman. The network helps show where Joy M. Richman may publish in the future.

Co-authorship network of co-authors of Joy M. Richman

This figure shows the co-authorship network connecting the top 25 collaborators of Joy M. Richman. A scholar is included among the top collaborators of Joy M. Richman 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 Joy M. Richman. Joy M. Richman 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.
Richman, Joy M., et al.. (2024). Bone labeling experiments and intraskeletal growth patterns in captive leopard geckos (Eublepharis macularius). Journal of Anatomy. 247(3-4). 542–555.
2.
Zikmund, Tomáš, Siddharth R. Vora, Brian Metscher, et al.. (2024). 3D atlas of the human fetal chondrocranium in the middle trimester. Scientific Data. 11(1). 626–626. 1 indexed citations
3.
Fu, Katherine, et al.. (2023). Mechanistic studies in Drosophila and chicken give new insights into functions of DVL1 in dominant Robinow syndrome. Disease Models & Mechanisms. 16(4). 5 indexed citations
4.
Rens, Elisabeth G., et al.. (2021). Symmetry and fluctuation of cell movements in neural crest-derived facial mesenchyme. Development. 148(9). 7 indexed citations
5.
Rolfe, Sara, et al.. (2019). Analysis of facial skeletal asymmetry during foetal development using μCT imaging. Orthodontics and Craniofacial Research. 22(S1). 199–206. 8 indexed citations
6.
Abramyan, John & Joy M. Richman. (2018). Craniofacial development: discoveries made in the chicken embryo. The International Journal of Developmental Biology. 62(1-2-3). 97–107. 28 indexed citations
7.
Abramyan, John, et al.. (2013). Divergent palate morphology in turtles and birds correlates with differences in proliferation and BMP2 expression during embryonic development. Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 322(2). 73–85. 18 indexed citations
8.
Geetha‐Loganathan, Poongodi, et al.. (2013). Dual functions for WNT5A during cartilage development and in disease. Matrix Biology. 32(5). 252–264. 52 indexed citations
9.
Town, Liam, Edwina McGlinn, Tara‐Lynne Davidson, et al.. (2011). Tmem26 Is Dynamically Expressed during Palate and Limb Development but Is Not Required for Embryonic Survival. PLoS ONE. 6(9). e25228–e25228. 7 indexed citations
10.
Levinson, Joshua N., Geoffroy Noël, Gregory R. Handrigan, et al.. (2009). Synaptic localization of neuroligin 2 in the rodent retina: Comparative study with the dystroglycan‐containing complex. Journal of Neuroscience Research. 88(4). 837–849. 2 indexed citations
11.
Boughner, Julia C., Marcela Buchtová, Katherine Fu, et al.. (2007). Embryonic development of Python sebae – I: Staging criteria and macroscopic skeletal morphogenesis of the head and limbs. Zoology. 110(3). 212–230. 82 indexed citations
12.
Buchtová, Marcela, et al.. (2007). Gene discovery in craniofacial development and disease – cashing in your chips. Clinical Genetics. 71(2). 109–119. 9 indexed citations
13.
Bowles, Josephine, Deon Knight, Christopher Smith, et al.. (2006). Retinoid Signaling Determines Germ Cell Fate in Mice. Science. 312(5773). 596–600. 756 indexed citations breakdown →
14.
Song, Yiping, et al.. (2004). Control of retinoic acid synthesis and FGF expression in the nasal pit is required to pattern the craniofacial skeleton. Developmental Biology. 276(2). 313–329. 68 indexed citations
15.
Lee, Sang-Hwy, et al.. (2004). A new origin for the maxillary jaw. Developmental Biology. 276(1). 207–224. 80 indexed citations
16.
Richman, Joy M., et al.. (2002). Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development. The International Journal of Developmental Biology. 46(4). 441–448. 20 indexed citations
17.
Grad, Leslie I., et al.. (2000). Locally released retinoic acid repatterns the first branchial arch cartilages in vivo. Developmental Biology. 222(1). 12–26. 30 indexed citations
18.
Richman, Joy M., et al.. (1997). Effect of Fibroblast Growth Factors on Outgrowth of Facial Mesenchyme. Developmental Biology. 189(1). 135–147. 58 indexed citations
19.
Richman, Joy M. & Pamela J. Mitchell. (1996). Craniofacial development: Knockout mice take one on the chin. Current Biology. 6(4). 364–367. 19 indexed citations
20.
Richman, Joy M.. (1995). Head Development: Craniofacial genetics makes headway. Current Biology. 5(4). 345–348. 8 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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