Steven Mumm

7.6k total citations · 1 hit paper
126 papers, 5.2k citations indexed

About

Steven Mumm is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Steven Mumm has authored 126 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 53 papers in Genetics and 37 papers in Oncology. Recurrent topics in Steven Mumm's work include Bone health and treatments (34 papers), Alkaline Phosphatase Research Studies (31 papers) and Connective tissue disorders research (22 papers). Steven Mumm is often cited by papers focused on Bone health and treatments (34 papers), Alkaline Phosphatase Research Studies (31 papers) and Connective tissue disorders research (22 papers). Steven Mumm collaborates with scholars based in United States, Italy and Canada. Steven Mumm's co-authors include Michael P. Whyte, William H. McAlister, Deborah Wenkert, Sarju Mehta, Giles D. Watts, Virginia Kimonis, Alan Pestronk, Margaret J. Kovach, Daniel Darvish and Duane P. Grandgenett and has published in prestigious journals such as New England Journal of Medicine, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Steven Mumm

120 papers receiving 5.1k citations

Hit Papers

Inclusion body myopathy associated with Paget disease of ... 2004 2026 2011 2018 2004 250 500 750 1000
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.

  1. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
    2004 1.0k citations Steven Mumm, Michael P. Whyte et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven Mumm United States 35 2.2k 1.3k 1.3k 1.2k 1.1k 126 5.2k
Gen Nishimura Japan 41 3.6k 1.7× 1.2k 0.9× 328 0.3× 3.7k 3.0× 828 0.8× 344 7.1k
Michael W. Starbuck United States 19 3.2k 1.5× 498 0.4× 264 0.2× 703 0.6× 1.2k 1.1× 24 4.8k
Uwe Kornak Germany 36 3.3k 1.5× 617 0.5× 160 0.1× 1.2k 0.9× 903 0.8× 136 5.1k
A. J. Kahn United States 30 2.9k 1.3× 699 0.5× 283 0.2× 655 0.5× 1.1k 1.0× 52 5.1k
Harald Jüppner United States 28 3.5k 1.6× 408 0.3× 558 0.4× 2.4k 1.9× 1.6k 1.5× 65 6.4k
Baruch Frenkel United States 41 3.1k 1.4× 371 0.3× 381 0.3× 851 0.7× 1.2k 1.2× 89 4.9k
P. Joseph Mee United Kingdom 15 2.0k 0.9× 203 0.2× 482 0.4× 555 0.4× 808 0.8× 20 4.3k
Andrew H. Crosby United Kingdom 36 3.9k 1.8× 463 0.3× 98 0.1× 862 0.7× 582 0.5× 125 7.1k
F. Richard Bringhurst United States 35 3.4k 1.6× 424 0.3× 350 0.3× 669 0.5× 2.4k 2.2× 75 6.6k
Andrew C. Karaplis Canada 50 6.2k 2.8× 1.6k 1.2× 699 0.6× 2.1k 1.7× 4.3k 4.0× 125 10.3k

Countries citing papers authored by Steven Mumm

Since Specialization
Citations

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

Fields of papers citing papers by Steven Mumm

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven Mumm

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

All Works

20 of 20 papers shown
1.
Simmons, Jill H., Edna E. Mancilla, Steven Mumm, et al.. (2025). Duplications within exon 1 of TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK) are associated with tendon avulsion. Bone. 197. 117486–117486.
2.
Mumm, Steven, Philippe M. Campeau, Jonathan C. Baker, et al.. (2025). Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631). Bone. 197. 117477–117477.
3.
Whyte, Michael P., Steven Mumm, Jonathan C. Baker, et al.. (2023). LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low‐Density Lipoprotein Receptor‐Related Protein 6. JBMR Plus. 7(4). e10717–e10717. 7 indexed citations
4.
5.
Whyte, Michael P., Fan Zhang, Deborah Wenkert, et al.. (2020). Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia. Bone. 134. 115300–115300. 18 indexed citations
6.
Smith, Pamela S., Gary S. Gottesman, Fan Zhang, et al.. (2020). X-Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3′-UTR Mutation c.*231A>G (A Retrospective Case–Control Study). Journal of Bone and Mineral Research. 35(5). 920–931. 10 indexed citations
7.
Iwamoto, Sean J., Micol S. Rothman, Shenghui Duan, et al.. (2020). Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANK. Bone. 133. 115224–115224. 7 indexed citations
8.
Gottesman, Gary S., Katherine L. Madson, William H. McAlister, et al.. (2016). Auricular ossification: A newly recognized feature of osteoprotegerin‐deficiency juvenile Paget disease. American Journal of Medical Genetics Part A. 170(4). 978–985. 8 indexed citations
9.
Whyte, Michael P., et al.. (2013). Acute Severe Hypercalcemia After Traumatic Fractures and Immobilization in Hypophosphatasia Complicated by Chronic Renal Failure. The Journal of Clinical Endocrinology & Metabolism. 98(12). 4606–4612. 21 indexed citations
10.
Mumm, Steven, et al.. (2012). “Atypical Femoral Fractures” During Bisphosphonate Exposure In Adult Hypophosphatasia. Revistes Científiques de la University of Barcelona (University of Barcelona). 51(1). 14.
11.
12.
Whyte, Michael P., Steven Mumm, Robert Phelps, et al.. (2010). Buschke-Ollendorff Syndrome. Archives of Dermatology. 146(1). 63–8. 17 indexed citations
13.
Whyte, Michael P., Steven Mumm, & Chad Deal. (2007). Adult Hypophosphatasia Treated with Teriparatide. The Journal of Clinical Endocrinology & Metabolism. 92(4). 1203–1208. 117 indexed citations
14.
Mumm, Steven, Deborah Wenkert, Xiafang Zhang, et al.. (2006). Deactivating Germline Mutations in LEMD3 Cause Osteopoikilosis and Buschke-Ollendorff Syndrome, but Not Sporadic Melorheostosis. Journal of Bone and Mineral Research. 22(2). 243–250. 58 indexed citations
15.
Wenkert, Deborah, Steven Mumm, William H. McAlister, et al.. (2004). Pediatric bone and mineral working group abstracts WG7–WG11. Journal of Bone and Mineral Research. 19(S1). S487–S488. 3 indexed citations
16.
Whyte, Michael P., Joanne Kurtzberg, William H. McAlister, et al.. (2003). Marrow Cell Transplantation for Infantile Hypophosphatasia. Journal of Bone and Mineral Research. 18(4). 624–636. 117 indexed citations
17.
Mumm, Steven, Luisa Herrera, Paul Waeltz, et al.. (2001). χ/Autosomal Translocations in the χq Critical Region Associated with Premature Ovarian Failure Fall within and outside Genes. Genomics. 76(1-3). 30–36. 33 indexed citations
18.
Parvari, Ruti, Steven Mumm, A Galil, et al.. (1999). Deletion of 8.5 Mb, including theFMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth. American Journal of Medical Genetics. 83(4). 302–307. 16 indexed citations
19.
Pizzuti, Antonio, Tullio Labella, Maurizio Affer, et al.. (1999). Mapping of the MYCL2 processed gene to Xq22‐23 and identification of an additional L MYC‐related sequence in Xq27.2. FEBS Letters. 446(2-3). 273–277. 8 indexed citations
20.
Hansen, R. Scott, et al.. (1997). A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication. Proceedings of the National Academy of Sciences. 94(9). 4587–4592. 80 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Gen Nishimura Breakdown of academic impact, for papers by Michael W. Starbuck Breakdown of academic impact, for papers by Uwe Kornak Breakdown of academic impact, for papers by A. J. Kahn Breakdown of academic impact, for papers by Harald Jüppner Breakdown of academic impact, for papers by Baruch Frenkel Breakdown of academic impact, for papers by P. Joseph Mee Breakdown of academic impact, for papers by Andrew H. Crosby Breakdown of academic impact, for papers by F. Richard Bringhurst Breakdown of academic impact, for papers by Andrew C. Karaplis
Rankless by CCL
2026