Tom Glaser

9.6k total citations · 4 hit papers
51 papers, 7.7k citations indexed

About

Tom Glaser is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Tom Glaser has authored 51 papers receiving a total of 7.7k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Cell Biology. Recurrent topics in Tom Glaser's work include Retinal Development and Disorders (24 papers), Renal and related cancers (12 papers) and Developmental Biology and Gene Regulation (11 papers). Tom Glaser is often cited by papers focused on Retinal Development and Disorders (24 papers), Renal and related cancers (12 papers) and Developmental Biology and Gene Regulation (11 papers). Tom Glaser collaborates with scholars based in United States, Canada and Finland. Tom Glaser's co-authors include David E. Housman, Barbara Handelin, Cary Weinberger, Jeffrey L. Arriza, Ronald M. Evans, Katherine M. Call, David S. Walton, Daniel A. Haber, Alan Buckler and Jerry Pelletier and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Tom Glaser

50 papers receiving 7.5k 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.

Cloning of Human Mineralocorticoid Receptor Complementary DNA: Structural and Functional Kinship with the Glucocorticoid Receptor

1987 1.6k citations Tom Glaser, David E. Housman et al. profile →
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1990 1.6k citations Katherine M. Call, Tom Glaser et al. Cell profile →
Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

1992 540 citations Tom Glaser, David S. Walton et al. profile →
An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

1990 478 citations Daniel A. Haber, Alan Buckler et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tom Glaser United States	31	5.9k	1.8k	1.3k	825	716	51	7.7k
Michael Karl United States	40	3.2k 0.5×	1.1k 0.6×	1.6k 1.2×	339 0.4×	1.0k 1.4×	109	6.1k
Juan Pedro Martı́nez-Barberá United Kingdom	46	4.1k 0.7×	1.6k 0.9×	2.0k 1.5×	191 0.2×	544 0.8×	107	7.0k
M. Graziella Persico Italy	41	4.4k 0.7×	949 0.5×	227 0.2×	478 0.6×	418 0.6×	69	6.4k
Mireille Claustres France	46	4.3k 0.7×	1.8k 1.1×	188 0.1×	1.7k 2.0×	744 1.0×	221	8.2k
Tania Attié‐Bitach France	42	3.6k 0.6×	2.4k 1.4×	217 0.2×	716 0.9×	333 0.5×	156	6.7k
Naoya Asai Japan	45	4.2k 0.7×	823 0.5×	612 0.5×	390 0.5×	1.4k 1.9×	121	6.8k
Anna B. Auerbach United States	19	4.0k 0.7×	976 0.6×	513 0.4×	218 0.3×	1.2k 1.6×	22	5.6k
Aimee K. Ryan Canada	22	4.0k 0.7×	1.9k 1.1×	985 0.7×	145 0.2×	556 0.8×	48	5.7k
Chyuan‐Sheng Lin United States	31	4.3k 0.7×	1.3k 0.7×	114 0.1×	297 0.4×	778 1.1×	70	6.5k
Vijak Mahdavi United States	34	6.6k 1.1×	1.6k 0.9×	762 0.6×	178 0.2×	525 0.7×	46	8.5k

Countries citing papers authored by Tom Glaser

Since Specialization

Citations

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

Fields of papers citing papers by Tom Glaser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tom Glaser

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Reis, Linda M., Donald Basel, Pierre Bitoun, et al.. (2024). Novel Intragenic and Genomic Variants Highlight the Phenotypic Variability in HCCS-Related Disease. Genes. 15(12). 1636–1636. 1 indexed citations

Capasso, Jenina, et al.. (2023). Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis. American Journal of Medical Genetics Part A. 191(4). 1007–1012.

Clark, Brian S., Qing Shi, Fion Shiau, et al.. (2021). Atoh7-independent specification of retinal ganglion cell identity. Science Advances. 7(11). 37 indexed citations

Miesfeld, Joel B., Noor M. Ghiasvand, Nicholas Marsh‐Armstrong, et al.. (2020). TheAtoh7remote enhancer provides transcriptional robustness during retinal ganglion cell development. Proceedings of the National Academy of Sciences. 117(35). 21690–21700. 30 indexed citations

Kaukonen, Maria, Saija Ahonen, Maarit Hellman, et al.. (2018). Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease. Cell Reports. 23(9). 2643–2652. 12 indexed citations

Miesfeld, Joel B., Tom Glaser, & Nadean L. Brown. (2017). The dynamics of native Atoh7 protein expression during mouse retinal histogenesis, revealed with a new antibody. Gene Expression Patterns. 27. 114–121. 21 indexed citations

Hufnagel, Robert B., Amy N. Riesenberg, Malgorzata E. Quinn, et al.. (2013). Heterochronic misexpression of Ascl1 in the Atoh7 retinal cell lineage blocks cell cycle exit. Molecular and Cellular Neuroscience. 54. 108–120. 18 indexed citations

Prasov, Lev & Tom Glaser. (2012). Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle. Molecular and Cellular Neuroscience. 50(2). 160–168. 28 indexed citations

Prasov, Lev, Tehmina Masud, Shagufta Khaliq, et al.. (2012). ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Human Molecular Genetics. 21(16). 3681–3694. 51 indexed citations

10.

Prasov, Lev, et al.. (2012). Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis. Neuroreport. 23(10). 631–634. 22 indexed citations

11.

Ghiasvand, Noor M., et al.. (2011). Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. Nature Neuroscience. 14(5). 578–586. 110 indexed citations

12.

Prasov, Lev, Nadean L. Brown, & Tom Glaser. (2010). A Critical Analysis of Atoh7 (Math5) mRNA Splicing in the Developing Mouse Retina. PLoS ONE. 5(8). e12315–e12315. 14 indexed citations

13.

Brzezinski, Joseph A., Nadean L. Brown, Atsuhiro Tanikawa, et al.. (2005). Loss of Circadian Photoentrainment and Abnormal Retinal Electrophysiology inMath5Mutant Mice. Investigative Ophthalmology & Visual Science. 46(7). 2540–2540. 50 indexed citations

14.

Sun, Yan, Shami Kanekar, Monica L. Vetter, et al.. (2003). Conserved and divergent functions of Drosophila atonal, amphibian, and mammalian Ath5 genes. Evolution & Development. 5(5). 532–541. 15 indexed citations

15.

Brown, Nadean L., et al.. (2002). Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development. Mammalian Genome. 13(2). 95–101. 29 indexed citations

16.

Brown, Nadean L., Sima Patel, Joseph A. Brzezinski, & Tom Glaser. (2001). Math5is required for retinal ganglion cell and optic nerve formation. Development. 128(13). 2497–2508. 397 indexed citations

17.

Brown, Nadean L., et al.. (1998). Math5 encodes a murine basic helix-loop-helix transcription factor expressed during early stages of retinal neurogenesis. Development. 125(23). 4821–4833. 272 indexed citations

18.

Buckler, Alan, Jerry Pelletier, Daniel A. Haber, Tom Glaser, & David E. Housman. (1991). Isolation, Characterization, and Expression of the Murine Wilms’ Tumor Gene (WT1) During Kidney Development. Molecular and Cellular Biology. 11(3). 1707–1712. 54 indexed citations

19.

Rose, Elise, Tom Glaser, Carol Jones, et al.. (1990). Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene. Cell. 60(3). 495–508. 214 indexed citations

20.

Haber, Daniel A., Alan Buckler, Tom Glaser, et al.. (1990). An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell. 61(7). 1257–1269. 478 indexed citations breakdown →

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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