Michael B. Bober

5.8k total citations
99 papers, 2.0k citations indexed

About

Michael B. Bober is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Michael B. Bober has authored 99 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 31 papers in Molecular Biology and 28 papers in Rheumatology. Recurrent topics in Michael B. Bober's work include Connective tissue disorders research (46 papers), Lysosomal Storage Disorders Research (10 papers) and Hip disorders and treatments (9 papers). Michael B. Bober is often cited by papers focused on Connective tissue disorders research (46 papers), Lysosomal Storage Disorders Research (10 papers) and Hip disorders and treatments (9 papers). Michael B. Bober collaborates with scholars based in United States, United Kingdom and Canada. Michael B. Bober's co-authors include Andrew P. Jackson, William G. Mackenzie, Carol A. Wise, Kenneth J. Rogers, William G. Mackenzie, Angela L. Duker, Julie Hoover‐Fong, Shunji Tomatsu, Tadao Orii and Louise S. Bicknell and has published in prestigious journals such as Science, Nature Communications and Nature Genetics.

In The Last Decade

Michael B. Bober

94 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael B. Bober United States 27 834 761 455 291 268 99 2.0k
Gary S. Gottesman United States 20 394 0.5× 542 0.7× 451 1.0× 369 1.3× 132 0.5× 55 1.6k
Maria Hoeltzenbein Germany 23 794 1.0× 899 1.2× 420 0.9× 98 0.3× 272 1.0× 54 2.8k
Marianne Rohrbach Switzerland 26 1.0k 1.2× 631 0.8× 638 1.4× 897 3.1× 143 0.5× 81 2.4k
Katta M. Girisha India 24 866 1.0× 977 1.3× 218 0.5× 221 0.8× 123 0.5× 196 1.9k
Emily L. Germain‐Lee United States 24 905 1.1× 1.1k 1.5× 195 0.4× 216 0.7× 236 0.9× 56 1.8k
Donald A. Glass United States 16 552 0.7× 2.3k 3.1× 256 0.6× 121 0.4× 225 0.8× 38 3.3k
Jung Min Ko South Korea 22 677 0.8× 767 1.0× 123 0.3× 120 0.4× 167 0.6× 156 1.6k
Sheela Nampoothiri India 21 763 0.9× 917 1.2× 172 0.4× 183 0.6× 124 0.5× 125 1.7k
Marina Colombi Italy 31 1.8k 2.2× 1.1k 1.4× 489 1.1× 125 0.4× 477 1.8× 181 3.7k
Yangli Xie China 25 342 0.4× 1.1k 1.5× 468 1.0× 118 0.4× 257 1.0× 53 2.0k

Countries citing papers authored by Michael B. Bober

Since Specialization
Citations

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

Fields of papers citing papers by Michael B. Bober

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael B. Bober. 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 Michael B. Bober. The network helps show where Michael B. Bober may publish in the future.

Co-authorship network of co-authors of Michael B. Bober

This figure shows the co-authorship network connecting the top 25 collaborators of Michael B. Bober. A scholar is included among the top collaborators of Michael B. Bober 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 Michael B. Bober. Michael B. Bober 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.
Starrett, Jacqueline H., C. Lemoine, Nabil Kaci, et al.. (2025). TYRA-300, an FGFR3-selective inhibitor, promotes bone growth in two FGFR3-driven models of chondrodysplasia. JCI Insight. 10(9). 1 indexed citations
2.
Hori, Yusuke, Patrick Thornley, Petya Yorgova, et al.. (2024). Midterm Outcomes of Multimodal Approach to Treating Severe Scoliosis in Patients With Osteogenesis Imperfecta. Journal of the American Academy of Orthopaedic Surgeons. 32(18). e951–e960. 1 indexed citations
3.
Dorninger, Fabian, Attila Kiss, Theresa König, et al.. (2023). Overlapping and Distinct Features of Cardiac Pathology in Inherited Human and Murine Ether Lipid Deficiency. International Journal of Molecular Sciences. 24(3). 1884–1884. 1 indexed citations
4.
Duker, Angela L., et al.. (2023). Trends in Serum Cytokine Expression in Pediatric Skeletal Dysplasia. JBMR Plus. 7(12). e10816–e10816. 1 indexed citations
5.
Hoover‐Fong, Julie, S. Shahrukh Hashmi, Jacqueline T. Hecht, et al.. (2021). Achondroplasia Natural History Study (CLARITY): a multicenter retrospective cohort study of achondroplasia in the United States. Genetics in Medicine. 23(8). 1498–1505. 36 indexed citations
6.
Franzone, Jeanne M., et al.. (2020). Cervical kyphosis: A predominant feature of patients with osteogenesis imperfecta type 5. Bone Reports. 13. 100735–100735. 3 indexed citations
7.
Tarnauskaitė, Žygimantė, Louise S. Bicknell, Joseph A. Marsh, et al.. (2019). Biallelic variants in DNA2 cause microcephalic primordial dwarfism. Human Mutation. 40(8). 1063–1070. 17 indexed citations
8.
Benoit‐Pilven, Clara, Audrey Putoux, Amandine Campan-Fournier, et al.. (2019). New insights into minor splicing—a transcriptomic analysis of cells derived from TALS patients. RNA. 25(9). 1130–1149. 26 indexed citations
9.
Rogers, Kenneth J., et al.. (2017). Arthroscopic knee anatomy in young achondroplasia patients. Journal of Children s Orthopaedics. 11(3). 169–174. 3 indexed citations
10.
Franzone, Jeanne M., et al.. (2017). Re-alignment and intramedullary rodding of the humerus and forearm in children with osteogenesis imperfecta: Revision rate and effect on fracture rate. Journal of Children s Orthopaedics. 11(3). 185–190. 7 indexed citations
11.
Bayhan, Avni İlhan, et al.. (2017). Valgus Hip Osteotomy in Children With Spondyloepiphyseal Dysplasia Congenita: Midterm Results. Journal of Pediatric Orthopaedics. 39(6). 282–288. 11 indexed citations
12.
Tomatsu, Shunji, Lauren W. Averill, Kazuki Sawamoto, et al.. (2015). Obstructive airway in Morquio A syndrome, the past, the present and the future. Molecular Genetics and Metabolism. 117(2). 150–156. 56 indexed citations
13.
White, Klane K., Viviana Bompadre, Michael J. Goldberg, et al.. (2015). Best practices in the evaluation and treatment of foramen magnum stenosis in achondroplasia during infancy. American Journal of Medical Genetics Part A. 170(1). 42–51. 51 indexed citations
14.
Jain, Mahim, David Cuthbertson, Deborah Krakow, et al.. (2015). Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta. Genetics in Medicine. 18(6). 570–576. 31 indexed citations
15.
Weaver, K. Nicole, Robert J. Hopkin, Kristen L. Sund, et al.. (2014). Keutel syndrome: Report of two novel MGP mutations and discussion of clinical overlap with arylsulfatase E deficiency and relapsing polychondritis. American Journal of Medical Genetics Part A. 164(4). 1062–1068. 15 indexed citations
16.
Dede, Özgür, Kenneth J. Rogers, Colleen Ditro, et al.. (2013). Growth-Sparing Spinal Instrumentation in Skeletal Dysplasia. Spine. 38(24). E1517–E1526. 19 indexed citations
17.
Edery, Patrick, Charles Marcaillou, Mourad Sahbatou, et al.. (2011). Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA. Science. 332(6026). 240–243. 159 indexed citations
18.
Bicknell, Louise S., Sarah Walker, Anna Klingseisen, et al.. (2011). Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome. Nature Genetics. 43(4). 350–355. 148 indexed citations
19.
Bober, Michael B., Nadia Khan, Jennifer A. Kaplan, et al.. (2010). Majewski Osteodysplastic Primordial Dwarfism Type II (MOPD II): Expanding the vascular phenotype. American Journal of Medical Genetics Part A. 152A(4). 960–965. 63 indexed citations
20.
Gripp, Karen W., Charles I. Scott, Linda K. Nicholson, et al.. (2008). Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts. American Journal of Medical Genetics Part A. 146A(4). 468–473. 7 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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