Maurice Godfrey

5.5k total citations · 3 hit papers
63 papers, 4.3k citations indexed

About

Maurice Godfrey is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, Maurice Godfrey has authored 63 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 14 papers in Pulmonary and Respiratory Medicine and 13 papers in Cancer Research. Recurrent topics in Maurice Godfrey's work include Connective tissue disorders research (39 papers), Protease and Inhibitor Mechanisms (12 papers) and Aortic Disease and Treatment Approaches (9 papers). Maurice Godfrey is often cited by papers focused on Connective tissue disorders research (39 papers), Protease and Inhibitor Mechanisms (12 papers) and Aortic Disease and Treatment Approaches (9 papers). Maurice Godfrey collaborates with scholars based in United States, France and Germany. Maurice Godfrey's co-authors include David W. Hollister, Leonard Chess, Richard Axel, Paul J. Maddon, Dan R. Littman, Francesco Ramirez, Reed E. Pyeritz, Lynn Y. Sakai, Petros Tsipouras and Emilia Vitale and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Maurice Godfrey

62 papers receiving 4.1k citations

Hit Papers

align trajectories sort by overperformance

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.

The isolation and nucleotide sequence of a cDNA encoding the T cell surface protein T4: a new member of the immunoglobulin gene family

1985 595 citations Maurice Godfrey et al. profile →
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

1991 515 citations Brendan Lee, Maurice Godfrey et al. Nature profile →
Functional interaction between human T-cell protein CD4 and the major histocompatibility complex HLA-DR antigen

1987 306 citations Maurice Godfrey et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maurice Godfrey United States	29	2.3k	968	921	867	740	63	4.3k
Anne Moon United States	45	2.0k 0.9×	4.4k 4.6×	430 0.5×	508 0.6×	392 0.5×	96	6.1k
Thomas C. Reynolds United States	18	1.8k 0.8×	2.8k 2.9×	339 0.4×	573 0.7×	159 0.2×	23	4.5k
John H. McVey United Kingdom	45	2.0k 0.9×	2.8k 2.9×	464 0.5×	621 0.7×	214 0.3×	144	6.0k
Laure Coulombel France	43	777 0.3×	1.9k 1.9×	424 0.5×	1.5k 1.7×	200 0.3×	127	5.3k
Stacie M. Anderson United States	39	1.3k 0.6×	3.8k 3.9×	262 0.3×	2.3k 2.6×	528 0.7×	83	9.8k
David M. Bodine United States	38	1.9k 0.8×	3.9k 4.0×	249 0.3×	557 0.6×	223 0.3×	97	6.3k
Catherine Y. Ng United States	31	2.0k 0.9×	2.2k 2.2×	252 0.3×	1.8k 2.0×	641 0.9×	60	6.4k
Carol J. Gallione United States	27	710 0.3×	1.5k 1.6×	1.9k 2.1×	163 0.2×	207 0.3×	45	6.1k
Leslie D. Stratford-Perricaudet France	15	3.2k 1.4×	3.1k 3.2×	543 0.6×	307 0.4×	153 0.2×	18	4.8k
Joseph T.C. Shieh United States	24	689 0.3×	911 0.9×	152 0.2×	309 0.4×	202 0.3×	61	2.2k

Countries citing papers authored by Maurice Godfrey

Since Specialization

Citations

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

Fields of papers citing papers by Maurice Godfrey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maurice Godfrey

This figure shows the co-authorship network connecting the top 25 collaborators of Maurice Godfrey. A scholar is included among the top collaborators of Maurice Godfrey 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 Maurice Godfrey. Maurice Godfrey 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

Godfrey, Maurice, et al.. (2021). Respiratory manifestations of Marfan syndrome: a narrative review. Journal of Thoracic Disease. 13(10). 6012–6025. 7 indexed citations

Warzak, William J., et al.. (2011). Developing a Culturally Sensitive Curriculum: Teaching Native American Children about Psychological and Behavioral Health.. US-China education review. 1(7). 127–133. 2 indexed citations

Hamroun, Dalil, Laurence Faivre, Guillaume Jondeau, et al.. (2008). TheFBN2gene: new mutations, locus-specific database (Universal Mutation DatabaseFBN2), and genotype-phenotype correlations. Human Mutation. 30(2). 181–190. 46 indexed citations

Robinson, Peter N., Emilio Arteaga‐Solis, Clair Baldock, et al.. (2006). The molecular genetics of Marfan syndrome and related disorders. Journal of Medical Genetics. 43(10). 769–787. 304 indexed citations

Li, Aihua, et al.. (2005). Autocrine Role of Interleukin-8 in Induction of Endothelial Cell Proliferation, Survival, Migration and MMP-2 Production and Angiogenesis. Angiogenesis. 8(1). 63–71. 239 indexed citations

Robinson, Peter N. & Maurice Godfrey. (2004). Marfan Syndrome: A Primer for Clinicians and Scientists. 24 indexed citations

Schrijver, Iris, Wouter I. Schievink, Maurice Godfrey, Fredric B. Meyer, & Uta Francke. (2002). Spontaneous spinal cerebrospinal fluid leaks and minor skeletal features of Marfan syndrome: a microfibrillopathy. Journal of neurosurgery. 96(3). 483–489. 88 indexed citations

Booms, Patrick, Maurice Godfrey, Frank Tiecke, et al.. (1999). Novel exon skipping mutation in the fibrillin‐1 gene: Two ‘hot spots’ for the neonatal Marfan syndrome. Clinical Genetics. 55(2). 110–117. 72 indexed citations

Collod‐Béroud, Gwenaëlle, Christophe Béroud, Lesley C. Adès, et al.. (1997). Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene. Nucleic Acids Research. 25(1). 147–150. 25 indexed citations

10.

Allanson, Judith, et al.. (1997). Prenatal Diagnosis in Congenital Contractural Arachnodactyly. Genetic Testing. 1(4). 293–296. 2 indexed citations

11.

Wang, Mei, Kiyoshi Imaizumi, Barbara K. Burton, et al.. (1997). Three novel fibrillin mutations in exons 25 and 27: Classic versus neonatal Marfan syndrome. Human Mutation. 9(4). 359–362. 21 indexed citations

12.

Wang, Menglin, et al.. (1996). Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome.. Journal of Medical Genetics. 33(9). 760–763. 19 indexed citations

13.

Wang, Mei, Carol L. Clericuzio, & Maurice Godfrey. (1996). Familial occurrence of typical and severe lethal congenital contractural arachnodactyly caused by missplicing of exon 34 of fibrillin-2.. PubMed. 59(5). 1027–34. 59 indexed citations

14.

Godfrey, Maurice, et al.. (1995). Fibrillin immunofluorescence in pseudoxanthoma elasticum. Journal of the American Academy of Dermatology. 32(4). 589–594. 3 indexed citations

15.

Godfrey, Maurice, et al.. (1993). Elastin and Fibrillin Mrna and Protein Levels in the Ontogeny of Normal Human Aorta. Connective Tissue Research. 29(1). 61–69. 24 indexed citations

16.

Lee, Brendan, Maurice Godfrey, Emilia Vitale, et al.. (1991). Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. Nature. 352(6333). 330–334. 515 indexed citations breakdown →

17.

Hollister, David W., Maurice Godfrey, Lynn Y. Sakai, & Reed E. Pyeritz. (1990). Immunohistologic Abnormalities of the Microfibrillar-Fiber System in the Marfan Syndrome. New England Journal of Medicine. 323(3). 152–159. 300 indexed citations

18.

Godfrey, Maurice, Victor Menashe, Richard G. Weleber, et al.. (1990). Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families.. PubMed. 46(4). 652–60. 71 indexed citations

19.

Suciu‐Foca, Nicole, et al.. (1981). Expression of HLA-D and DR gene products on in vitro and in vivo primed human T cells.. PubMed. 13(1 Pt 2). 1020–5. 4 indexed citations

20.

Suciu‐Foca, Nicole, et al.. (1979). Evidence that HLA-D is different from DR and that two different HLA loci code for B-cell antigens.. PubMed. 11(4). 1781–7. 11 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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