Steven Mumm

7.6k citations

126 papers · 5.2k indexed · 1 hit paper · h-index 35

Orthopedics and Sports Medicine top 0.5%
- Bone health and osteoporosis research 10
Rheumatology top 0.5%
- Heterotopic Ossification and Related Conditions 15
Endocrinology, Diabetes and Metabolism top 1%
- Alkaline Phosphatase Research Studies 31
Genetics top 1%
- Connective tissue disorders research 22
- Dermatological and Skeletal Disorders 11
Neurology top 2%
Oncology
- Bone health and treatments 34
Molecular Biology
- Bone Metabolism and Diseases 20
Pathology and Forensic Medicine
- Vitamin D Research Studies 11

Co-authors: Michael P. Whyte William H. McAlister Deborah Wenkert Giles D. Watts Sarju Mehta Virginia Kimonis Daniel Darvish Margaret J. Kovach
Cited by: Orthopedics and Sports Medicine Rheumatology Endocrinology, Diabetes and Metabolism
Journals: Journal of Bone and Mineral Research (32 papers)Bone (26 papers)The Journal of Clinical Endocrinology & Metabolism (9 papers)
Partner nations: United States Italy Canada

In The Last Decade

Steven Mumm

120 papers receiving 5.1k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside Steven Mumm, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Steven Mumm Line = papers co-authored together Steven Mumm links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Duplications within exon 1 of TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK) are associated with tendon avulsion Bone ·Jill H. Simmons,Edna E. Mancilla,Steven Mumm,Kathryn Dahir,Shenghui Duan,Kristie Aamodt,J. Todd R. Lawrence,Lynn Peterson,Michael P. Whyte	2025	0
2	Transforming growth factor, beta-2 gene mutation causes autosomal dominant Camurati-Engelmann disease, type 2 (OMIM % 606631) Bone ·Steven Mumm,Yuanchao Shu,Philippe M. Campeau,Wijaya Vincent Ongko,Jonathan C. Baker,Torrance J. Eberhart,Shenghui Duan,William H. McAlister,Michael P. Whyte	2025	0
3	LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low‐Density Lipoprotein Receptor‐Related Protein 6 JBMR Plus ·Michael P. Whyte,Steven Mumm,Jonathan C. Baker,Fan Zhang,Rory Scrace,Shenghui Duan,Tim Cundy	2023	7
4	Early identification of a 12-bp tandem duplication in TNFRSF11A encoding receptor activator of nuclear factor-kappa B (RANK): Clinical characterization and response to bisphosphonate therapy Bone ·大久保憲一,Mary Ellen Vajravelu,Karuna Shekdar,Michael A. Levine,Steven Mumm,Michael P. Whyte,Edna E. Mancilla	2023	2
5	Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia Bone ·Michael P. Whyte,Fan Zhang,Deborah Wenkert,Steven Mumm,Theresa J. Berndt,Rajiv Kumar	2020	18
6	Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANK Bone ·Sean J. Iwamoto,Micol S. Rothman,Shenghui Duan,Jonathan C. Baker,Steven Mumm,Michael P. Whyte	2020	7
7	Auricular ossification: A newly recognized feature of osteoprotegerin‐deficiency juvenile Paget disease American Journal of Medical Genetics Part A ·Gary S. Gottesman,Katherine L. Madson,William H. McAlister,Wensheng Zhao,Deborah Wenkert,Steven Mumm,Michael P. Whyte	2016	8
8	Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9 Bone ·Hessa AlAmeemi,Steven Mumm,William H. McAlister,Deborah V. Novack,Deborah Wenkert,P. VanLeeuwen,Michael P. Whyte	2015	45
9	Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK Bone ·Michael P. Whyte,Cristina Tau,William H. McAlister,Xiafang Zhang,Deborah V. Novack,Juan Manuel Silvero Arévalos,Xuan-Li Zheng,Steven Mumm	2014	30
10	Acute Severe Hypercalcemia After Traumatic Fractures and Immobilization in Hypophosphatasia Complicated by Chronic Renal Failure The Journal of Clinical Endocrinology & Metabolism ·Michael P. Whyte,Rattana Leelawattana,William R. Reinus,Ranjeev Kumar Mishra,Steven Mumm,Deborah V. Novack	2013	21
11	“Atypical Femoral Fractures” During Bisphosphonate Exposure In Adult Hypophosphatasia Revistes Científiques de la University of Barcelona (University of Barcelona) ·浩他山崎,Steven Mumm,William S. Halsey,Jesús Hans de Jesús,MP Whyte	2012	0
12	Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis Human Molecular Genetics ·Philippe M. Campeau,James T. Lu,Gautam Sule,Ming‐Ming Jiang,Yun‐Ui Bae,C E Danganan,Wolfgang Högler,N. Shaw,Steven Mumm,Richard A. Gibbs,Michael P. Whyte,Dan Fugloe	2012	65
13	Buschke-Ollendorff Syndrome Archives of Dermatology ·Marta Widuch,Michael P. Whyte,Steven Mumm,Robert Phelps,Alan Shanske,William G. Totty,Steven R. Cohen	2010	17
14	Adult Hypophosphatasia Treated with Teriparatide The Journal of Clinical Endocrinology & Metabolism ·Michael P. Whyte,Steven Mumm,Chad Deal	2007	117
15	Pediatric bone and mineral working group abstracts WG7–WG11 Journal of Bone and Mineral Research ·Deborah Wenkert,Steven Mumm,Richard Alvarado,William H. McAlister,Michael P. Whyte,Thomas Kelly,Trisha M. Shattuck,Miguel Reyes‐Múgica,Barbara K. Kinder,Andrew Arnold,Thomas O. Carpenter	2004	3
16	χ/Autosomal Translocations in the χq Critical Region Associated with Premature Ovarian Failure Fall within and outside Genes Genomics ·Steven Mumm,Luisa Herrera,Paul Waeltz,政利塩田,Ramaiah Nagaraja,Teresa Esposito,David Schlessinger,Mariano Rocchi,Antonino Forabosco	2001	33
17	22-Mb integrated physical and genetic map based on YAC/STS content spanning the interval DXS1125–DXS95 in human Xq12–q21.31 Gene ·Steven Mumm,Kalin V. Lazarov,Paul Waeltz,Darin J. Brown,R G Hennes,Fernando Pastor Merchante,Michael T. Shoemaker,Anand Srivastava,Juha Kere,Ramaiah Nagaraja	1998	7
18	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 ·R. Scott Hansen,Theresa K. Canfield,Danny Andrian,Steven Mumm,Charles D. Laird,Stanley M. Gartler	1997	80
19	Expression and Cloning of the Human X-Linked Hypophosphatemia Gene cDNA Biochemical and Biophysical Research Communications ·Marvin Grieff,Steven Mumm,Paul Waeltz,Richard Mazzarella,Michael P. Whyte,Rajesh V. Thakker,David Schlessinger	1997	47
20	YAC/STS Map of 9 Mb of Xq26 at 100-kb Resolution, Localizing 6 ESTs, 6 Genes, and 32 Genetic Markers Genomics ·Giuseppe Pilia,Sandra MacMillan,Ramaiah Nagaraja,Steven Mumm,Jean Weissenbach,David Schlessinger	1996	16

About Steven Mumm

Steven Mumm is a scholar working on Orthopedics and Sports Medicine, Rheumatology and Endocrinology, Diabetes and Metabolism, having authored 126 papers that have together received 5.2k indexed citations. Recurring topics across this work include Bone health and treatments (34 papers), Alkaline Phosphatase Research Studies (31 papers), Connective tissue disorders research (22 papers), Bone Metabolism and Diseases (20 papers), Heterotopic Ossification and Related Conditions (15 papers), Vitamin D Research Studies (11 papers), Dermatological and Skeletal Disorders (11 papers) and Bone health and osteoporosis research (10 papers). The work is most often cited by research in Orthopedics and Sports Medicine (950 citations), Rheumatology (1.3k citations) and Endocrinology, Diabetes and Metabolism (1.3k citations). Steven Mumm has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Michael P. Whyte, William H. McAlister, Deborah Wenkert, Giles D. Watts, Sarju Mehta, Virginia Kimonis, Daniel Darvish, Margaret J. Kovach, Alan Pestronk and Duane P. Grandgenett. Their work appears in journals such as Journal of Bone and Mineral Research, Bone, The Journal of Clinical Endocrinology & Metabolism, Genomics and Journal of Virology.

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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