Michael B. Bober

5.8k citations

99 papers · 2.0k · h-index 27

Impact in

Rheumatology top 2%
- Moyamoya disease diagnosis and treatment
Genetics top 2%
- Connective tissue disorders research
- Neurogenetic and Muscular Disorders Research

Papers in

Genetics 51
- Connective tissue disorders research 46
- Neurogenetic and Muscular Disorders Research 6
Molecular Biology 31
- RNA modifications and cancer 6

Co-authors: Andrew P. Jackson (10 shared papers)William G. Mackenzie (18 shared papers)Carol A. Wise (6 shared papers)William G. Mackenzie (12 shared papers)Kenneth J. Rogers (12 shared papers)Angela L. Duker (22 shared papers)Julie Hoover‐Fong (18 shared papers)Shunji Tomatsu (7 shared papers)
Journals: Orphanet Journal of Rare Diseases (7 papers)Journal of Pediatric Orthopaedics (7 papers)Genetics in Medicine (4 papers)Molecular Genetics and Metabolism (4 papers)Journal of Neurosurgery Pediatrics (3 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Michael B. Bober

94 papers receiving 1.9k citations

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 99 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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 Touraine, Emmanuel Tubacher, Faiza Senni, Michael B. Bober, Sheela Nampoothiri, Pierre‐Simon Jouk, Elisabeth Steichen, Siren Berland, Annick Toutain, Carol A. Wise, Damien Sanlaville, Francis Rousseau, Françoise Clerget‐Darpoux, Anne‐Louise Leutenegger	2011	159
2	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 Walker, Anna Klingseisen, Tom Stiff, Andrea Leitch, Claudia Kerzendorfer, Carol-Anne Martin, Patricia L. Yeyati, Nouriya Al Sanna, Michael B. Bober, Diana Johnson, Carol A. Wise, Andrew P. Jackson, Mark O’Driscoll, Penny A. Jeggo	2011	148
3	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 Samtani, Agata Jurczyk, Schahram Akbarian, Carol A. Wise, Andrew P. Jackson, Michael B. Bober, Yin Guo, Cecilia Lo, Stephen Doxsey	2014	72
4	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 Lewis, Jeffrey A. Feinstein, Charles I. Scott, Gary K. Steinberg	2010	63
5	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, Yasutsugu Chinen, Robert W. Mason, William G. Mackenzie, Michael B. Bober, Tadao Orii, Hiromasa Yabe, Tsutomu Shimada, Ángela J. Espejo, Alexander Rodríguez‐López, Oscar F. Sánchez	2015	57
6	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 Cuthbertson, Philippe M. Campeau, J. Krischer, Jay R. Shapiro, Robert D. Steiner, Peter A. Smith, Michael B. Bober, Peter H. Byers, Melanie Pepin, Michaela Durigova, Francis H. Glorieux, Frank Rauch, B.H. Lee, Tracy Hart, V. Reid Sutton	2014	57
7	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 G. Mackenzie, Michael B. Bober, Christian Pizarro, Christopher J. Goff, Li Xie, Tadao Orii, Mary C. Theroux	2015	56
8	Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene The American Journal of Human Genetics ·Stuart W. Tompson, Carlos A. Bacino, Nicole P. Safina, Michael B. Bober, Virginia K. Proud, Tara Funari, Michael F. Wangler, Lisette Nevarez, Leena Ala‐Kokko, William R. Wilcox, David R. Eyre, Deborah Krakow, Daniel H. Cohn	2010	54
9	Mucopolysaccharidosis IVA: Correlation between genotype, phenotype and keratan sulfate levels Molecular Genetics and Metabolism ·Vũ Chí Dũng, Shunji Tomatsu, Adriana M. Montaño, Gary S. Gottesman, Michael B. Bober, William G. Mackenzie, Miho Maeda, Grant A. Mitchell, Yasuyuki Suzuki, Tadao Orii	2013	53
10	Enzyme replacement therapy for treating mucopolysaccharidosis type IVA (Morquio A syndrome): effect and limitations Expert Opinion on Orphan Drugs ·Shunji Tomatsu, Kazuki Sawamoto, Tsutomu Shimada, Michael B. Bober, Francyne Kubaski, Eriko Yasuda, Robert W. Mason, Shaukat Khan, Carlos Javier Alméciga-Díaz, Luis A. Barrera, William G. Mackenzie, Tadao Orii	2015	52
11	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 Hoover‐Fong, William G. Mackenzie, Shawn E. Parnell, Cathleen Raggio, David M. Rapoport, Samantha A. Spencer, Ravi Savarirayan	2015	51
12	Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes Diabetes ·Isabel Huang‐Doran, Louise S. Bicknell, Francis Finucane, Nuno Rocha, Keith Porter, Y.C. Loraine Tung, Ferenc Szekeres, Anna Krook, John J. Nolan, Mark O’Driscoll, Michael B. Bober, Stephen O’Rahilly, Andrew P. Jackson, Robert K. Semple, (unknown)	2011	51
13	Microcephalic Osteodysplastic Primordial Dwarfism, Type II: a Clinical Review Current Osteoporosis Reports ·Michael B. Bober, Andrew P. Jackson	2017	41
14	The Effect of Intravenous Pamidronate on Bone Mineral Density, Bone Histomorphometry, and Parameters of Bone Turnover in Adults with Type IA Osteogenesis Imperfecta Calcified Tissue International ·Jay R. Shapiro, Edward F. McCarthy, Kevin Rossiter, K Ernest, Rebecca Gelman, Neal S. Fedarko, Helen T. Santiago, Michael B. Bober	2003	37
15	Respiratory mechanics in an infant with perinatal lethal hypophosphatasia treated with human recombinant enzyme replacement therapy Pediatric Pulmonology ·Elena Rodriguez, Michael B. Bober, Lauren Davey, Arlene Zamora, Annelise B. Li Puma, Aaron Chidekel, Thomas H. Shaffer	2012	36
16	Achondroplasia Natural History Study (CLARITY): a multicenter retrospective cohort study of achondroplasia in the United States Genetics in Medicine ·Julie Hoover‐Fong, Adekemi Yewande Alade, S. Shahrukh Hashmi, Jacqueline T. Hecht, Janet M. Legare, Mary Ellen Little, Chengxin Liu, John McGready, Peggy Modaff, Richard M. Pauli, David Rodriguez‐Buritica, Kerry Schulze, Maria E. Serna, Cory J. Smid, Michael B. Bober	2021	36
17	The Lower Extremity in Morquio Syndrome Journal of Pediatric Orthopaedics ·Arjun Dhawale, Mihir M. Thacker, Mohan V. Belthur, Kenneth J. Rogers, Michael B. Bober, William G. Mackenzie	2012	35
18	The expanding phenotype of RNU4ATAC pathogenic variants to Lowry Wood syndrome American Journal of Medical Genetics Part A ·Laura S. Farach, Mary Ellen Little, Angela L. Duker, Clare V. Logan, Andrew P. Jackson, Jaqueline T. Hecht, Michael B. Bober	2017	35
19	Growth in individuals with Majewski osteodysplastic primordial dwarfism type II caused by pericentrin mutations American Journal of Medical Genetics Part A ·Michael B. Bober, Tim Niiler, Angela L. Duker, Jennie Murray, Tara Ketterer, Margaret E Harley, Sabah Alvi, Christina Flora, Cecilie F. Rustad, Ernie M.H.F. Bongers, Louise S. Bicknell, Carol A. Wise, Andrew P. Jackson	2012	33
20	Growth in achondroplasia including stature, weight, weight-for-height and head circumference from CLARITY: achondroplasia natural history study—a multi-center retrospective cohort study of achondroplasia in the US Orphanet Journal of Rare Diseases ·Julie Hoover‐Fong, Kerry Schulze, Adekemi Yewande Alade, Michael B. Bober, Ethan Gough, S. Shahrukh Hashmi, Jacqueline T. Hecht, Janet M. Legare, Mary Ellen Little, Peggy Modaff, Richard M. Pauli, David Rodriguez‐Buritica, Maria E. Serna, Cory J. Smid, Chengxin Liu, John McGready	2021	33

About Michael B. Bober

Michael B. Bober is a scholar working on Genetics, Molecular Biology, Rheumatology, Surgery and Physiology, having authored 99 papers that have together received 2.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (46 papers), Lysosomal Storage Disorders Research (10 papers), Hip disorders and treatments (9 papers), Moyamoya disease diagnosis and treatment (9 papers), Neonatal Respiratory Health Research (9 papers), RNA modifications and cancer (6 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Bone and Dental Protein Studies (6 papers). The work is most often cited by research in Rheumatology (455 citations), Genetics (834 citations), Genetics (132 citations), Physiology (291 citations) and Molecular Biology (761 citations). Michael B. Bober has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Andrew P. Jackson, William G. Mackenzie, Carol A. Wise, William G. Mackenzie, Kenneth J. Rogers, Angela L. Duker, Julie Hoover‐Fong, Shunji Tomatsu, Tadao Orii and Louise S. Bicknell. Their work appears in journals such as Orphanet Journal of Rare Diseases, Journal of Pediatric Orthopaedics, Genetics in Medicine, Molecular Genetics and Metabolism and Journal of Neurosurgery Pediatrics.

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

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Michael B. Bober

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