Michael B. Bober

6.1k citations

148 papers · 4.2k · 1 hit paper · h-index 36

Impact in

Genetics top 1%
- Connective tissue disorders research
Rheumatology top 1%
- Heterotopic Ossification and Related Conditions

Papers in

Genetics 78
- Connective tissue disorders research 68
Rheumatology 26
- Moyamoya disease diagnosis and treatment 10
- Bone and Dental Protein Studies 7

Co-authors: Andrew P. Jackson (10 shared papers)Angela L. Duker (28 shared papers)William G. Mackenzie (20 shared papers)Kenneth J. Rogers (14 shared papers)William Giles Stuart Mackenzie (13 shared papers)Carol A. Wise (6 shared papers)Julie Elizabeth Hoover-Fong (19 shared papers)Shunji Tomatsu (8 shared papers)
Journals: Genetics in Medicine (12 papers)Orphanet Journal of Rare Diseases (8 papers)Journal of Pediatric Orthopaedics (7 papers)The American Journal of Human Genetics (5 papers)Nature Genetics (4 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Michael B. Bober

145 papers receiving 4.1k citations

Michael B. Bober's Hit Papers

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Enzyme-Replacement Therapy in Life-Threatening Hypophosphatasia 2012 · 452 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2012 New England Journal of Medicine

Peers

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-authors

The 25 scholars most cited alongside Michael B. Bober, 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 Michael B. Bober Line = papers co-authored together Michael B. Bober links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 148 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Enzyme-Replacement Therapy in Life-Threatening Hypophosphatasia New England Journal of Medicine ·Michael P. Whyte, Cheryl R. Greenberg, Nada Salman, Michael B. Bober, William Howard McAlister, Deborah Wenkert, Bradley J. Van Sickle, Jill H. Simmons Hit paper breakdown →	2012	452
2	Mutations in the pre-replication complex cause Meier-Gorlin syndrome Nature Genetics ·Louise S. Bicknell, Ernie M.H.F. Bongers, Andrea Leitch, Stephen Brown, Jeroen Schoots, Margaret E Harley, Salim F. Aftimos, Jumana Yousuf Al-Aama	2011	194
3	Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA Science ·Patrick Edery, Charles Marcaillou, Mourad Sahbatou, Audrey Labalme, Joëlle Chastang, Renaud L. Touraine, Emmanuel Tubacher, Faiza Senni	2011	181
4	Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome Nature Genetics ·Louise S. Bicknell, Sarah K. Walker, Anna Klingseisen, Tom Stiff, Andrea Leitch, Claudia Kerzendorfer, Carol-Anne Martin, Patricia Levy Yeyati	2011	158
5	Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial The Lancet ·Ravi Savarirayan, Louise Tofts, Melita D. Irving, William Ross Wilcox, Carlos A. Bacino, Julie Elizabeth Hoover-Fong, Rosendo Ullot Font, Paul Harmatz	2020	140
6	International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia Nature Reviews Endocrinology ·Ravi Savarirayan, Penny Ireland, Melita D. Irving, Dominic N. P. Thompson, Inês Alves, Wagner Antonio da Rosa Baratela, James A. Betts, Michael B. Bober	2021	100
7	Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism Nature Genetics ·John J. Reynolds, Louise S. Bicknell, Paula Carroll, Martin R. Higgs, Ranad Shaheen, Jennie Murray, Dimitrios K. Papadopoulos, Andrea Leitch	2017	84
8	Meier–Gorlin syndrome genotype–phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis European Journal of Human Genetics ·Sonja A. de Munnik, Louise S. Bicknell, Salim F. Aftimos, Jumana Yousuf Al-Aama, Yolande van Bever, Michael B. Bober, Jill Clayton‐Smith, Alaa Y. Edrees	2012	80
9	TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism Nature Genetics ·Margaret E Harley, Olga Murina, Andrea Leitch, Martin R. Higgs, Louise S. Bicknell, Gökhan Yigit, Andrew N. Blackford, Anastasia Zlatanou	2015	77
10	Extreme Growth Failure is a Common Presentation of Ligase IV Deficiency Human Mutation ·Jennie Murray, Louise S. Bicknell, Gökhan Yigit, Angela L. Duker, Margriet van Kogelenberg, Sara Haghayegh, Dagmar Wieczorek, Hülya Kayserili	2013	75
11	A Unique Set of Centrosome Proteins Requires Pericentrin for Spindle-Pole Localization and Spindle Orientation Current Biology ·Chun‐Ting Chen, Heidi Hehnly, YU Qing, Debby Farkas, Guoqiang Zheng, Sambra D. Redick, Hui-Fang Hung, Rajeev R. Samtani	2014	74
12	GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome The American Journal of Human Genetics ·Amy J. LaCroix, Deborah L. Stabley, Rebecca Sahraoui, Margaret P Adam, Michele G. Mehaffey, Kelly A. Kernan, Candace T. Myers, Carrie Fagerstrom	2018	74
13	Majewski Osteodysplastic Primordial Dwarfism Type II (MOPD II): Expanding the vascular phenotype American Journal of Medical Genetics Part A ·Michael B. Bober, Nadia Khan, Jennifer A. Kaplan, Kristi L. Lewis, Jeffrey A. Feinstein, Charles I. Scott, Gary Kenneth Steinberg	2010	70
14	DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency The American Journal of Human Genetics ·Clare V. Logan, Jennie Murray, David A.D. Parry, Andrea Robertson, Roberto Bellelli, Žygimantė Tarnauskaitė, Rachel C. Challis, Louise Cleal	2018	70
15	Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene The American Journal of Human Genetics ·Stuart W. J. Tompson, Carlos A. Bacino, Nicole P. Safina, Michael B. Bober, Virginia K. Proud, Tara L. Funari, Michael F. Wangler, Lisette Nevarez	2010	69
16	Impact of enzyme replacement therapy and hematopoietic stem cell transplantation in patients with Morquio A syndrome Drug Design Development and Therapy ·Shunji Tomatsu, Roberto Giugliani, Francyne Kubaski, Sawamoto Kazuki, Carlos Javier Alméciga-Díaz, Luis A. Barrera, Adriana M. Montaño, Eriko Yasuda	2015	67
17	Safe and persistent growth-promoting effects of vosoritide in children with achondroplasia: 2-year results from an open-label, phase 3 extension study Genetics in Medicine ·Ravi Savarirayan, Louise Tofts, Melita D. Irving, William Ross Wilcox, Carlos A. Bacino, Julie Elizabeth Hoover-Fong, Rosendo Ullot Font, Paul Harmatz	2021	65
18	A cross‐sectional multicenter study of osteogenesis imperfecta in North America – results from the linked clinical research centers Clinical Genetics ·Ruchita Patel, Sandesh C.S. Nagamani, David D Cuthbertson, Philippe M. Campeau, Jeff Krischer, Jay Robert Shapiro, Robert D. Steiner, Peter Andrey Smith	2014	64
19	Best practices in the evaluation and treatment of foramen magnum stenosis in achondroplasia during infancy American Journal of Medical Genetics Part A ·Klane K. White, Viviana Bompadre, Michael J. Goldberg, Michael B. Bober, Jeffrey W. Campbell, Tae‐Joon Cho, Julie Elizabeth Hoover-Fong, William G. Mackenzie	2015	60
20	Obstructive airway in Morquio A syndrome, the past, the present and the future Molecular Genetics and Metabolism ·Shunji Tomatsu, Lauren W. Averill, Kazuki Sawamoto, William Giles Stuart Mackenzie, Michael B. Bober, Christian Pizarro, Christopher J. Goff, Li Xie	2015	60

About Michael B. Bober

Michael B. Bober is a scholar working on Genetics, Rheumatology, Physiology, Molecular Biology and Cancer Research, having authored 148 papers that have together received 4.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (68 papers), Lysosomal Storage Disorders Research (11 papers), Moyamoya disease diagnosis and treatment (10 papers), Bone and Dental Protein Studies (7 papers), RNA modifications and cancer (6 papers), Bone health and treatments (6 papers), Alkaline Phosphatase Research Studies (6 papers) and Peroxisome Proliferator-Activated Receptors (5 papers). The work is most often cited by research in Genetics (1.7k citations), Rheumatology (726 citations), Endocrinology, Diabetes and Metabolism (482 citations), Developmental Biology (54 citations) and Molecular Biology (1.5k citations). Michael B. Bober has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Andrew P. Jackson, Angela L. Duker, William G. Mackenzie, Kenneth J. Rogers, William Giles Stuart Mackenzie, Carol A. Wise, Julie Elizabeth Hoover-Fong, Shunji Tomatsu, Tadao Orii and Louise S. Bicknell. Their work appears in journals such as Genetics in Medicine, Orphanet Journal of Rare Diseases, Journal of Pediatric Orthopaedics, The American Journal of Human Genetics and Nature Genetics.

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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Michael B. Bober

Michael B. Bober's Hit Papers

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