G.M. Glenn

17.9k total citations · 2 hit papers
90 papers, 8.5k citations indexed

About

G.M. Glenn is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, G.M. Glenn has authored 90 papers receiving a total of 8.5k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 35 papers in Pulmonary and Respiratory Medicine and 26 papers in Cancer Research. Recurrent topics in G.M. Glenn's work include Renal cell carcinoma treatment (32 papers), Renal and related cancers (27 papers) and Cancer, Hypoxia, and Metabolism (20 papers). G.M. Glenn is often cited by papers focused on Renal cell carcinoma treatment (32 papers), Renal and related cancers (27 papers) and Cancer, Hypoxia, and Metabolism (20 papers). G.M. Glenn collaborates with scholars based in United States, Canada and Cameroon. G.M. Glenn's co-authors include McClellan M. Walther, Peter L. Choyke, W. Marston Linehan, Berton Zbar, W. Marston Linehan, Edward H. Oldfield, Jorge R. Toro, Russell R. Lonser, Maria J. Merino and Steven K. Libutti and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and JAMA.

In The Last Decade

G.M. Glenn

90 papers receiving 8.2k citations

Hit Papers

align trajectories

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.

von Hippel-Lindau disease

2003 1.1k citations Russell R. Lonser, G.M. Glenn et al. The Lancet profile →
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome

2002 638 citations Michael L. Nickerson, Michelle B. Warren et al. Cancer Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G.M. Glenn United States	43	4.7k	4.6k	3.2k	1.4k	1.3k	90	8.5k
Hartmut P.H. Neumann Germany	61	1.5k 0.3×	3.0k 0.7×	5.4k 1.7×	641 0.5×	1.4k 1.1×	217	12.3k
Jonathan A. Fletcher United States	57	5.6k 1.2×	2.4k 0.5×	909 0.3×	293 0.2×	1.7k 1.3×	129	9.5k
Barbara Dockhorn‐Dworniczak Germany	39	1.8k 0.4×	1.9k 0.4×	1.0k 0.3×	358 0.3×	1.4k 1.1×	112	5.0k
Sakari Knuutila Finland	54	3.2k 0.7×	4.0k 0.9×	2.5k 0.8×	161 0.1×	2.1k 1.6×	249	9.5k
Maria Dêbiec‐Rychter Belgium	59	7.5k 1.6×	2.4k 0.5×	1.1k 0.3×	350 0.3×	2.7k 2.0×	318	12.3k
Masahiro Yao Japan	43	2.9k 0.6×	2.9k 0.6×	1.3k 0.4×	409 0.3×	1.1k 0.8×	269	5.8k
Jesse K. McKenney United States	49	4.0k 0.9×	2.3k 0.5×	965 0.3×	447 0.3×	1.4k 1.0×	183	7.4k
Brett S. Carver United States	38	3.8k 0.8×	4.6k 1.0×	2.9k 0.9×	125 0.1×	1.1k 0.9×	141	8.6k
Ivo Leuschner Germany	46	3.1k 0.7×	4.0k 0.9×	830 0.3×	196 0.1×	1.3k 1.0×	220	7.1k
Heinrich Kovar Austria	47	4.5k 1.0×	4.0k 0.9×	1.2k 0.4×	168 0.1×	2.0k 1.5×	135	8.3k

Countries citing papers authored by G.M. Glenn

Since Specialization

Citations

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

Fields of papers citing papers by G.M. Glenn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G.M. Glenn

This figure shows the co-authorship network connecting the top 25 collaborators of G.M. Glenn. A scholar is included among the top collaborators of G.M. Glenn 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 G.M. Glenn. G.M. Glenn 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

Peters, June A., Regina H. Kenen, Lindsey Hoskins, et al.. (2012). Close ties: an exploratory Colored Eco-Genetic Relationship Map (CEGRM) study of social connections of men in Familial Testicular Cancer (FTC) families. Hereditary Cancer in Clinical Practice. 10(1). 2–2. 7 indexed citations

Toro, Jorge R., G.M. Glenn, Michael Weinreich, et al.. (2008). BHD mutations, clinical and molecular genetic investigations of Birt–Hogg–Dubé syndrome: a new series of 50 families and a review of published reports. Journal of Medical Genetics. 45(6). 321–331. 333 indexed citations

Stewart, Laveta, G.M. Glenn, Pamela Stratton, et al.. (2008). Association of Germline Mutations in the Fumarate Hydratase Gene and Uterine Fibroids in Women With Hereditary Leiomyomatosis and Renal Cell Cancer. Archives of Dermatology. 144(12). 1584–92. 70 indexed citations

Toro, Jorge R., Stephen E. Pautler, Laveta Stewart, et al.. (2007). Lung Cysts, Spontaneous Pneumothorax, and Genetic Associations in 89 Families with Birt-Hogg-Dubé Syndrome. American Journal of Respiratory and Critical Care Medicine. 175(10). 1044–1053. 232 indexed citations

Schmidt, Laura S., Michael L. Nickerson, Debora Angeloni, et al.. (2004). EARLY ONSET HEREDITARY PAPILLARY RENAL CARCINOMA: GERMLINE MISSENSE MUTATIONS IN THE TYROSINE KINASE DOMAIN OF THE MET PROTO-ONCOGENE. The Journal of Urology. 172(4 Part 1). 1256–1261. 75 indexed citations

Lonser, Russell R., G.M. Glenn, McClellan M. Walther, et al.. (2003). von Hippel-Lindau disease. The Lancet. 361(9374). 2059–2067. 1079 indexed citations breakdown →

Toro, Jorge R., Michael L. Nickerson, Ming-Hui Wei, et al.. (2003). Mutations in the Fumarate Hydratase Gene Cause Hereditary Leiomyomatosis and Renal Cell Cancer in Families in North America. The American Journal of Human Genetics. 73(1). 95–106. 407 indexed citations

Nickerson, Michael L., Michelle B. Warren, Jorge R. Toro, et al.. (2002). Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome. Cancer Cell. 2(2). 157–164. 638 indexed citations breakdown →

Marcos, Hani B., Steven K. Libutti, H. Richard Alexander, et al.. (2002). Neuroendocrine Tumors of the Pancreas in von Hippel–Lindau Disease: Spectrum of Appearances at CT and MR Imaging with Histopathologic Comparison. Radiology. 225(3). 751–758. 73 indexed citations

10.

McNeil, D. Elizabeth, W. Marston Linehan, & G.M. Glenn. (2001). Comorbid genetic diseases, von Hippel-Lindau disease and spinocerebellar ataxia type 2, confounding the diagnosis of cerebellar dysfunction in an adolescent. Clinical Neurology and Neurosurgery. 103(4). 216–219. 1 indexed citations

11.

Sgambati, Maria, Catherine A. Stolle, Peter L. Choyke, et al.. (2000). Mosaicism in von Hippel–Lindau Disease: Lessons from Kindreds with Germline Mutations Identified in Offspring with Mosaic Parents. The American Journal of Human Genetics. 66(1). 84–91. 122 indexed citations

12.

Pack, Svetlana, Berton Zbar, Evgenia Pak, et al.. (1999). Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization.. PubMed. 59(21). 5560–4. 47 indexed citations

13.

Stolle, Catherine A., G.M. Glenn, Berton Zbar, et al.. (1998). Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene. Human Mutation. 12(6). 417–423. 346 indexed citations

14.

Choyke, Peter L., G.M. Glenn, M Walther, et al.. (1995). von Hippel-Lindau disease: genetic, clinical, and imaging features.. Radiology. 194(3). 629–642. 353 indexed citations

15.

Ortaldo, John R., et al.. (1992). Natural Killer (NK) Cell Lytic Dysfunction and Putative NK Cell Receptor Expression Abnormality in Members of a Family With Chromosome 3p-Linked von Hippel-Lindau Disease. JNCI Journal of the National Cancer Institute. 84(24). 1897–1903. 7 indexed citations

16.

Latif, Farida, et al.. (1991). A new polymorphic probe on chromosome 3p: λLIB24–12′ (D3S727). Nucleic Acids Research. 19(4). 962–962. 1 indexed citations

17.

Latif, Farida, G.M. Glenn, Meicun Yao, et al.. (1991). A new polymorphic probe on chromosome 3p: λLIB46–27′ (D3S635). Nucleic Acids Research. 19(16). 4564–4564. 1 indexed citations

18.

Latif, Farida, G.M. Glenn, L.N. Daniel, et al.. (1990). A new polymorphic probe on chromosome 3p: λLIB31-57′ (D3S213). Nucleic Acids Research. 18(4). 1089–1089. 1 indexed citations

19.

Brauch, Hiltrud, Farida Latif, Stephen B. Baylin, et al.. (1990). Mspl and Dral Polymorphisms at the ERBA beta locus on chromosome 3p. Nucleic Acids Research. 18(9). 2833–2833. 1 indexed citations

20.

Glenn, G.M., Béla Szende, Takahiko Yano, Berton Zbar, & Tibor Borsos. (1988). Serotherapy of cancer: Cellular changes in primary rat mammary carcinomas after infusion of syngeneic sera absorbed with protein a‐sepharose. International Journal of Cancer. 42(1). 76–83. 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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