Mary E. Brunkow

11.5k total citations · 5 hit papers
28 papers, 8.6k citations indexed

About

Mary E. Brunkow is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Mary E. Brunkow has authored 28 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 11 papers in Immunology. Recurrent topics in Mary E. Brunkow's work include T-cell and B-cell Immunology (7 papers), Pancreatic function and diabetes (4 papers) and Genomics and Rare Diseases (3 papers). Mary E. Brunkow is often cited by papers focused on T-cell and B-cell Immunology (7 papers), Pancreatic function and diabetes (4 papers) and Genomics and Rare Diseases (3 papers). Mary E. Brunkow collaborates with scholars based in United States, Canada and Netherlands. Mary E. Brunkow's co-authors include Fred Ramsdell, Hans D. Ochs, Craig L. Bennett, Phillip F. Chance, Bryan Paeper, Steven F. Ziegler, David J. Galas, Frank T. Saulsbury, Thaddeus E. Kelly and Polly J. Ferguson and has published in prestigious journals such as Nature Genetics, The Journal of Experimental Medicine and Genes & Development.

In The Last Decade

Mary E. Brunkow

28 papers receiving 8.4k citations

Hit Papers

5 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.

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

2001 2.5k citations Craig L. Bennett, Fred Ramsdell et al. Nature Genetics profile →
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

2001 2.0k citations Mary E. Brunkow, Eric W. Jeffery et al. Nature Genetics profile →
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

2001 1.4k citations Robert S. Wildin, Fred Ramsdell et al. Nature Genetics profile →
Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein

2001 751 citations Mary E. Brunkow, Jessica C. Gardner et al. The American Journal of Human Genetics profile →
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene.

1993 408 citations Marisa S. Bartolomei, Andrea L. Webber et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mary E. Brunkow United States	19	5.7k	2.3k	2.0k	1.2k	418	28	8.6k
Tessa Crompton United Kingdom	35	1.7k 0.3×	4.2k 1.8×	675 0.3×	1.6k 1.3×	207 0.5×	85	6.4k
Ansgar Schulz Germany	33	1.7k 0.3×	1.7k 0.8×	872 0.4×	986 0.8×	131 0.3×	122	4.5k
Stephen G. Emerson United States	46	4.0k 0.7×	2.1k 0.9×	632 0.3×	1.7k 1.4×	66 0.2×	117	8.2k
Andrew G. Geiser United States	32	1.0k 0.2×	3.1k 1.3×	772 0.4×	1.3k 1.1×	135 0.3×	47	5.3k
Kay L. Medina United States	34	2.6k 0.5×	1.9k 0.8×	546 0.3×	745 0.6×	80 0.2×	72	5.1k
John Koreth United States	51	3.6k 0.6×	1.4k 0.6×	412 0.2×	2.0k 1.6×	73 0.2×	199	9.3k
Paula S. Henthorn United States	35	694 0.1×	2.2k 1.0×	1.1k 0.6×	423 0.3×	302 0.7×	105	5.0k
T. M. Dexter United Kingdom	36	1.8k 0.3×	2.3k 1.0×	847 0.4×	1.5k 1.2×	67 0.2×	101	6.3k
Polly J. Ferguson United States	34	3.1k 0.5×	1.7k 0.7×	677 0.3×	429 0.3×	101 0.2×	95	6.2k
Esmail D. Zanjani United States	47	1.6k 0.3×	3.1k 1.3×	1.2k 0.6×	1.5k 1.2×	36 0.1×	186	8.7k

Countries citing papers authored by Mary E. Brunkow

Since Specialization

Citations

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

Fields of papers citing papers by Mary E. Brunkow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary E. Brunkow. 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 Mary E. Brunkow. The network helps show where Mary E. Brunkow may publish in the future.

Co-authorship network of co-authors of Mary E. Brunkow

This figure shows the co-authorship network connecting the top 25 collaborators of Mary E. Brunkow. A scholar is included among the top collaborators of Mary E. Brunkow 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 Mary E. Brunkow. Mary E. Brunkow 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

Kornilov, Sergey A., Nathan D. Price, Richard Gelinas, et al.. (2024). Multi-Omic characterization of the effects of Ocrelizumab in patients with relapsing-remitting multiple sclerosis. Journal of the Neurological Sciences. 467. 123303–123303. 4 indexed citations

Zhou, Yong, Shizhen Qin, Mingjuan Sun, et al.. (2019). Measurement of Organ-Specific and Acute-Phase Blood Protein Levels in Early Lyme Disease. Journal of Proteome Research. 19(1). 346–359. 12 indexed citations

Hu, Hao, Nayia Petousi, Gustavo Glusman, et al.. (2017). Evolutionary history of Tibetans inferred from whole-genome sequencing. PLoS Genetics. 13(4). e1006675–e1006675. 78 indexed citations

Stittrich, Anna, J. R. Ashworth, Mude Shi, et al.. (2016). Genomic architecture of inflammatory bowel disease in five families with multiple affected individuals. Human Genome Variation. 3(1). 15060–15060. 11 indexed citations

Glusman, Gustavo, Varsha Dhankani, Max Robinson, et al.. (2015). Identification of copy number variants in whole-genome data using Reference Coverage Profiles. Frontiers in Genetics. 6. 45–45. 15 indexed citations

Robinson, Martyn K., John Caminis, & Mary E. Brunkow. (2013). Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis. Drug Discovery Today. 18(13-14). 637–643. 8 indexed citations

Park, Heon, Mark Tsang, Mark W. Appleby, et al.. (2012). Disruption of Fnip1 Reveals a Metabolic Checkpoint Controlling B Lymphocyte Development. Immunity. 36(5). 769–781. 61 indexed citations

Park, Heon, Karen Staehling-Hampton, Mark W. Appleby, et al.. (2008). A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic Protein 1 in lymphopoiesis and innate immunity. The Journal of Experimental Medicine. 205(12). 2899–2913. 43 indexed citations

Uitterlinden, André G., Pascal Arp, Bryan Paeper, et al.. (2004). Polymorphisms in the Sclerosteosis/van Buchem Disease Gene (SOST) Region Are Associated with Bone-Mineral Density in Elderly Whites. The American Journal of Human Genetics. 75(6). 1032–1045. 95 indexed citations

10.

Staehling-Hampton, Karen, Sean Proll, Bryan Paeper, et al.. (2002). A 52‐kb deletion in the SOST‐MEOX1 intergenic region on 17q12‐q21 is associated with van Buchem disease in the Dutch population. American Journal of Medical Genetics. 110(2). 144–152. 239 indexed citations

11.

Khattri, Roli, Deborah J. Kasprowicz, Tom Cox, et al.. (2001). The Amount of Scurfin Protein Determines Peripheral T Cell Number and Responsiveness. The Journal of Immunology. 167(11). 6312–6320. 127 indexed citations

12.

Brunkow, Mary E., Eric W. Jeffery, Kathryn A. Hjerrild, et al.. (2001). Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse. Nature Genetics. 27(1). 68–73. 1960 indexed citations breakdown →

13.

Bennett, Craig L., Fred Ramsdell, Mary E. Brunkow, et al.. (2001). The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3. Nature Genetics. 27(1). 20–21. 2547 indexed citations breakdown →

14.

Bennett, Craig L., Mary E. Brunkow, Fred Ramsdell, et al.. (2001). A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome. Immunogenetics. 53(6). 435–439. 190 indexed citations

15.

Wildin, Robert S., Fred Ramsdell, Jane Peake, et al.. (2001). X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy. Nature Genetics. 27(1). 18–20. 1422 indexed citations breakdown →

16.

Brunkow, Mary E., Jessica C. Gardner, Bryan Paeper, et al.. (2001). Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein. The American Journal of Human Genetics. 68(3). 577–589. 751 indexed citations breakdown →

17.

Appleby, Mark W., et al.. (1999). Cellular and molecular characterization of the scurfy mouse mutant.. PubMed. 162(5). 2546–54. 158 indexed citations

18.

Brunkow, Mary E., Deborah L. Nagle, Alan Bernstein, & Maja Bućan. (1995). A 1.8-Mb YAC contig spanning three members of the receptor tyrosine kinase gene family (Pdgfra, Kit, and Flk1) on mouse chromosome 5. Genomics. 25(2). 421–432. 22 indexed citations

19.

Tilghman, S M, Marisa S. Bartolomei, Andrea L. Webber, et al.. (1993). Parental Imprinting of the H19 and Igf2 Genes in the Mouse. Cold Spring Harbor Symposia on Quantitative Biology. 58(0). 287–295. 19 indexed citations

20.

Forrester, Lesley M., Mary E. Brunkow, & Alan Bernstein. (1992). Proto-oncogenes in mammalian development. Current Opinion in Genetics & Development. 2(1). 38–44. 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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