Jeffrey Boone Miller, PhD
Boston University School of Medicine
Dept of Neurology

PhD, University of California, Berkeley

Boston University School of Medicine
Physiology & Biophysics

Boston University
Whitaker Cardiovascular Institute

2013 University of Maryland, School of Medicine: Robert Wade Memorial Lecturer
2009 Conference on "Myogenesis: Making Muscle in the Embryo and Adult", New York, NY: Silver Medal Poster Prize (out of 262 presentations)
2009 Cure CMD: Invited Member, Animal Model Assessment Group
1993 Montreal Neurological Institute: Invited Lecturer in Killam Series
1989 Harvard University: Invited member, Board of Biochemical Tutors
1973 Washington State University: Phi Lambda Upsilon Scholar
1973 Washington State University: Graduation with Highest Honors, Phi Beta Kappa, Phi Kappa Phi
1972 Washington State University: Outstanding Junior in Chemistry

Pathogenesis and therapeutic targets in FSHD
02/01/2019 - 01/31/2022 (PI)
Muscular Dystrophy Association

Mechanisms of DUX4-mediated FSHD Patholgy
01/01/2017 - 06/30/2019 (Subcontract PI)
Nevada System Of Higher Education, dba University of Nevada, Reno NIH NIAMS

Pathogenesis of Muscular Dystrophies
05/01/2016 - 04/30/2018 (PI)
NIH/National Institute of Arthritis & Musculoskeletal & Skin Diseases

Pathogenesis of congenital muscular dystrophy Type 1A(laminin-alpha2-deficiency)
08/15/2016 - 02/14/2018 (PI)
Association Francaise Contre les Myopathies

Mechanisms of DUX4-Mediated FSHD Pathology
07/01/2016 - 12/31/2016 (Subcontract PI)
University of Massachusetts, Worcester NIH NIAMS

Mechanisms of DUX4-Mediated FSHD Pathology
07/03/2013 - 06/30/2016 (Subcontract PI)
University of Massachusetts, Worcester NIH NIAMS

Pathogenesis of Congenital Muscular Dystrophy Type 1A (laminin-alpha2-deficiency)
02/03/2015 - 06/19/2016 (PI)
Association Francaise Contre les Myopathies

Pathogenesis of Muscular Dystrophies
02/12/2013 - 04/30/2016 (PI)
NIH/National Institute of Arthritis & Musculoskeletal & Skin Diseases

DUX4, epigenetics, and pathogenesis of facioscapulohumeral muscular dystrophy
05/23/2014 - 11/22/2015 (PI)
Association Francaise Contre les Myopathies

CMD and LGMD Therapeutics Targets: Studies with patients myogenic cells (MDA216422)
02/01/2013 - 07/31/2015 (PI)
Muscular Dystrophy Association

Showing 10 of 12 results. Show All Results


Yr Title Project-Sub Proj Pubs
2016 Pathogenesis of Muscular Dystrophies 4R01AR060328-06 8
2015 Pathogenesis of Muscular Dystrophies 5R01AR060328-05 8
2014 Pathogenesis of Muscular Dystrophies 5R01AR060328-04 8
2013 Pathogenesis of Muscular Dystrophies 5R01AR060328-03 8
2012 Pathogenesis of Muscular Dystrophies 1R01AR060328-01A1 8
2012 Pathogenesis of Muscular Dystrophies 7R01AR060328-02 8
2012 Model Studies for FSHD Biomarkers 5U54HD060848-05-4 42
2011 Model Studies for FSHD Biomarkers 5U54HD060848-04-4 42
2010 Molecular physiology of respiratory muscles 5R01HL064641-11 11
2010 Model Studies for FSHD Biomarkers 5U54HD060848-03-4 42
Showing 10 of 58 results. Show All Results

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

iCite Analysis       Copy PMIDs To Clipboard

  1. Mitsuhashi H, Homma S, Beermann ML, Ishimaru S, Takeda H, Yu BK, Liu K, Duraiswamy S, Boyce FM, Miller JB. Efficient system for upstream mRNA trans-splicing to generate covalent, head-to-tail, protein multimers. Sci Rep. 2019 02 19; 9(1):2274.View Related Profiles. PMID: 30783185; PMCID: PMC6381186; DOI: 10.1038/s41598-018-36684-7;
  2. Mitsuhashi H, Ishimaru S, Homma S, Yu B, Honma Y, Beermann ML, Miller JB. Functional domains of the FSHD-associated DUX4 protein. Biol Open. 2018 Apr 26; 7(4).View Related Profiles. PMID: 29618456; PMCID: PMC5936065; DOI: 10.1242/bio.033977;
  3. Yoon S, Beermann ML, Yu B, Shao D, Bachschmid M, Miller JB. Aberrant Caspase Activation in Laminin-a2-Deficient Human Myogenic Cells is Mediated by p53 and Sirtuin Activity. J Neuromuscul Dis. 2018; 5(1):59-73.View Related Profiles. PMID: 29278895; PMCID: PMC5836413; DOI: 10.3233/JND-170262;
  4. Homma S, Beermann ML, Yu B, Boyce FM, Miller JB. Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4. Skelet Muscle. 2016 Dec 01; 6(1):42.View Related Profiles. PMID: 27906075; PMCID: PMC5134237; DOI: 10.1186/s13395-016-0113-7;
  5. Jones TI, King OD, Himeda CL, Homma S, Chen JC, Beermann ML, Yan C, Emerson CP, Miller JB, Wagner KR, Jones PL. Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy. Clin Epigenetics. 2015; 7(1):37.View Related Profiles. PMID: 25904990; PMCID: PMC4405830; DOI: 10.1186/s13148-015-0072-6;
  6. Homma S, Beermann ML, Boyce FM, Miller JB. Expression of FSHD-related DUX4-FL alters proteostasis and induces TDP-43 aggregation. Ann Clin Transl Neurol. 2015 Feb; 2(2):151-66.View Related Profiles. PMID: 25750920; PMCID: PMC4338956; DOI: 10.1002/acn3.158;
  7. Himeda CL, Debarnot C, Homma S, Beermann ML, Miller JB, Jones PL, Jones TI. Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene. Mol Cell Biol. 2014 Jun; 34(11):1942-55.View Related Profiles. PMID: 24636994; PMCID: PMC4019064; DOI: 10.1128/MCB.00149-14;
  8. Yoon S, Stadler G, Beermann ML, Schmidt EV, Windelborn JA, Schneiderat P, Wright WE, Miller JB. Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research. Skelet Muscle. 2013; 3(1):28. PMID: 24314268; PMCID: PMC3906772; DOI: 10.1186/2044-5040-3-28;
  9. Jones TI, Chen JC, Rahimov F, Homma S, Arashiro P, Beermann ML, King OD, Miller JB, Kunkel LM, Emerson CP, Wagner KR, Jones PL. Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis. Hum Mol Genet. 2012 Oct 15; 21(20):4419-30.View Related Profiles. PMID: 22798623; PMCID: PMC3459465; DOI: 10.1093/hmg/dds284;
  10. Homma S, Chen JC, Rahimov F, Beermann ML, Hanger K, Bibat GM, Wagner KR, Kunkel LM, Emerson CP, Miller JB. A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function. Eur J Hum Genet. 2012 Apr; 20(4):404-10.View Related Profiles. PMID: 22108603; PMCID: PMC3306860; DOI: 10.1038/ejhg.2011.213;
Showing 10 of 81 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 76 publications over 35 distinct years, with a maximum of 6 publications in 1996


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700 Albany St Ctr for Adv Biomed Res
Boston MA 02118
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