Christopher T. Gordon

4.9k total citations
58 papers, 1.4k citations indexed

About

Christopher T. Gordon is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Christopher T. Gordon has authored 58 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 27 papers in Genetics and 11 papers in Psychiatry and Mental health. Recurrent topics in Christopher T. Gordon's work include Craniofacial Disorders and Treatments (9 papers), Congenital heart defects research (8 papers) and Congenital Ear and Nasal Anomalies (7 papers). Christopher T. Gordon is often cited by papers focused on Craniofacial Disorders and Treatments (9 papers), Congenital heart defects research (8 papers) and Congenital Ear and Nasal Anomalies (7 papers). Christopher T. Gordon collaborates with scholars based in France, Australia and United States. Christopher T. Gordon's co-authors include Stanislas Lyonnet, Glenn B. Mannheim, Judith L. Rapoport, Jeanne Amiel, Peter G. Farlie, Tiong Yang Tan, B. J. Casey, Judith M. Rumsey, Jean A. Frazier and Sabina Benko and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and American Journal of Psychiatry.

In The Last Decade

Christopher T. Gordon

56 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christopher T. Gordon France	20	594	531	363	325	133	58	1.4k
Lorenzo Sinibaldi Italy	20	447 0.8×	509 1.0×	290 0.8×	414 1.3×	80 0.6×	46	1.5k
Siddharth Srivastava United States	21	700 1.2×	1000 1.9×	143 0.4×	392 1.2×	71 0.5×	80	1.7k
Kiran K. Mantripragada United Kingdom	22	773 1.3×	853 1.6×	241 0.7×	274 0.8×	58 0.4×	41	1.8k
Arvid Heiberg Norway	26	671 1.1×	376 0.7×	271 0.7×	183 0.6×	180 1.4×	80	1.9k
Eli Hatchwell United States	24	1.2k 2.0×	984 1.9×	172 0.5×	534 1.6×	128 1.0×	52	2.1k
Hans Matsson Sweden	16	757 1.3×	315 0.6×	107 0.3×	245 0.8×	58 0.4×	24	1.4k
Janine A. Lamb United Kingdom	25	928 1.6×	937 1.8×	124 0.3×	673 2.1×	45 0.3×	56	2.6k
Décio Brunoni Brazil	23	482 0.8×	555 1.0×	99 0.3×	213 0.7×	127 1.0×	98	1.8k
Vandana Shashi United States	27	1.4k 2.4×	1.3k 2.4×	167 0.5×	307 0.9×	79 0.6×	98	2.9k
Edmund C. Jenkins United States	31	1.1k 1.9×	1.7k 3.1×	231 0.6×	822 2.5×	81 0.6×	123	2.9k

Countries citing papers authored by Christopher T. Gordon

Since Specialization

Citations

This map shows the geographic impact of Christopher T. Gordon'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 T. Gordon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher T. Gordon more than expected).

Fields of papers citing papers by Christopher T. Gordon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher T. Gordon

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher T. Gordon. A scholar is included among the top collaborators of Christopher T. Gordon 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 T. Gordon. Christopher T. Gordon 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

1.

Kurihara, Yukiko, Toru Ekimoto, Christopher T. Gordon, et al.. (2023). Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding. Journal of Clinical Investigation. 133(4). 2 indexed citations

2.

Guimier, Anne, Fanny Bajolle, Christian Turner, et al.. (2018). PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy. Archives of Cardiovascular Diseases Supplements. 11(1). 134–134. 1 indexed citations

3.

Guimier, Anne, Fanny Bajolle, Christian Turner, et al.. (2018). PPA2 gene is involved in neonatal fatal acute dilated cardiomyopathy. Archives of Cardiovascular Diseases Supplements. 10(3-4). 282–282. 2 indexed citations

4.

Sreenivasan, Rajini, Christopher T. Gordon, Sabina Benko, et al.. (2016). Altered SOX9 genital tubercle enhancer region in hypospadias. The Journal of Steroid Biochemistry and Molecular Biology. 170. 28–38. 10 indexed citations

5.

Bouvagnet, Patrice, Anne Guimier, Jeanne Amiel, & Christopher T. Gordon. (2016). Un gène codant une métalloprotéase impliqué dans l’hétérotaxie. médecine/sciences. 32(6-7). 551–553. 1 indexed citations

6.

Désir, Julie, Naseebullah Kakar, Thomas D. Mueller, et al.. (2015). A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia. Orphanet Journal of Rare Diseases. 10(1). 84–84. 16 indexed citations

7.

Bhatia, Shipra, Christopher T. Gordon, Véronique Abadie, et al.. (2015). Functional Assessment of Disease-Associated Regulatory Variants In Vivo Using a Versatile Dual Colour Transgenesis Strategy in Zebrafish. PLoS Genetics. 11(6). e1005193–e1005193. 18 indexed citations

8.

Kido, Yasuhiro, Christopher T. Gordon, Satoru Sakazume, et al.. (2013). Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations. American Journal of Medical Genetics Part A. 161(9). 2339–2346. 20 indexed citations

9.

Clouthier, David E., Maria Rita Passos‐Bueno, André L. P. Tavares, et al.. (2013). Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 163(4). 306–317. 45 indexed citations

10.

Rieder, Mark J., Glenn E. Green, Sarah S. Park, et al.. (2012). A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome. The American Journal of Human Genetics. 91(2). 397–397. 6 indexed citations

11.

Benko, Sabina, Christopher T. Gordon, Jeanne Amiel, & Stanislas Lyonnet. (2011). Cis-ruptions d’éléments génomiques hautement conservés non codants à distance du gèneSOX9dans la séquence de Pierre Robin. Biologie Aujourd hui. 205(2). 111–124. 2 indexed citations

12.

Gordon, Christopher T., et al.. (2011). CXCL14 expression during chick embryonic development. The International Journal of Developmental Biology. 55(3). 335–340. 15 indexed citations

13.

Amiel, Jeanne, Sabina Benko, Christopher T. Gordon, & Stanislas Lyonnet. (2010). Disruption of long‐distance highly conserved noncoding elements in neurocristopathies. Annals of the New York Academy of Sciences. 1214(1). 34–46. 13 indexed citations

14.

Gordon, Christopher T., et al.. (2010). Role of Dlx genes in craniofacial morphogenesis: Dlx2 influences skeletal patterning by inducing ectomesenchymal aggregation in ovo. Evolution & Development. 12(5). 459–473. 26 indexed citations

15.

Gordon, Christopher T., et al.. (2009). The RCAS retroviral expression system in the study of skeletal development. Developmental Dynamics. 238(4). 797–811. 20 indexed citations

16.

Farlie, Peter G., et al.. (2009). Barx1 regulates chondrogenesis via a non-canonical Wnt pathway. Developmental Biology. 331(2). 442–442. 1 indexed citations

17.

Gordon, Christopher T., et al.. (2005). C/EBPδ and C/EBPγ bind the CCAAT-box in the human β-globin promoter and modulate the activity of the CACC-box binding protein, EKLF. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1729(1). 74–80. 14 indexed citations

18.

Su, Yunyun, et al.. (2001). Human ERMAP: An Erythroid Adhesion/Receptor Transmembrane Protein. Blood Cells Molecules and Diseases. 27(5). 938–949. 21 indexed citations

19.

Gordon, Christopher T., et al.. (2000). Ermap, a gene coding for a novel erythroid specific adhesion/receptor membrane protein. Gene. 242(1-2). 337–345. 28 indexed citations

20.

Kumra, Sanjiv, Leslie K. Jacobsen, Christopher T. Gordon, et al.. (1996). Childhood-onset schizophrenia. A double-blind clozapine-haloperidol comparison. The Journal of the American Medical Association (JAMA) Network (American Medical Association). 12 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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