Michael W. Lawlor

Also affiliated with University of Wisconsin–Milwaukee, Milwaukee School of Engineering

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 17 papers. Top paper: “Aberrations in Energetic Metabolism and Stress-Related Pathways Contribute to Pathophysiology in the Neb Conditional Knockout Mouse Model of Nemaline Myopathy”.

Aberrations in Energetic Metabolism and Stress-Related Pathways Contribute to Pathophysiology in the Neb Conditional Knockout Mouse Model of Nemaline Myopathy

American Journal Of Pathology(2023)10.1016/j.ajpath.2023.06.009

N/A

0.385DataRank · unranked

12 citations

Jennifer A Tinklenberg, J. R. Sutton, Liwen Zhang, Hui Meng, Margaret Beatka +12 more

Cardioprotective effect of nicorandil on isoproterenol induced cardiomyopathy in the Mdx mouse model

BMC Cardiovascular Disorders(2021)10.1186/s12872-021-02112-4

N/A

0.360DataRank · unranked

10 citations

Ngoc Thien Lam, Margaret Haberman, Margaret Beatka, Muhammad Zeeshan Afzal, Michael W. Lawlor +2 more

Establishment of normal myofiber size distribution in children and young adults

Journal of Neuropathology & Experimental Neurology(2025)10.1093/jnen/nlaf123

N/A

0.104DataRank · unranked

1 citations

Marta Margeta, Karra A. Jones, Benedikt Schoser, Jennifer Cotter, Veena Rajaram +17 more

X-linked myotubular myopathy

Neuromuscular Disorders(2021)10.1016/j.nmd.2021.08.003

N/A

0DataRank · unranked

85 citations

James J. Dowling, Michael W. Lawlor

Cardiomyocyte-produced miR-339-5p mediates pathology in Duchenne muscular dystrophy cardiomyopathy

Human Molecular Genetics(2021)10.1093/hmg/ddab199

N/A

0DataRank · unranked

16 citations

Margaret Beatka, Mariah J. Prom, Jennifer L. Strande, Michael W. Lawlor, Melanie Gartz

Clonally Focused Public and Private T Cells in Resected Brain Tissue From Surgeries to Treat Children With Intractable Seizures

Frontiers in Immunology(2021)10.3389/fimmu.2021.664344

N/A

0DataRank · unranked

14 citations

Samuel D. Reyes, Emmanuelle Faure-Kumar, Sandi Lam, Michael W. Lawlor, Richard J. Leventer +10 more

Assessment of systemic AAV-microdystrophin gene therapy in the GRMD model of Duchenne muscular dystrophy

Science Translational Medicine(2023)10.1126/scitranslmed.abo1815

N/A

0DataRank · unranked

68 citations

Michael W. Lawlor, Thomas J. Conlon, Lee‐Jae Guo, Julie M. Crudele, Eleanor C. Hawkins +26 more

Tetraspanin CD82 is necessary for muscle stem cell activation and supports dystrophic muscle function

Skeletal Muscle(2020)10.1186/s13395-020-00252-3

N/A

0DataRank · unranked

20 citations

Tatiana M. Fontelonga, Alec M. Wright, Katlynn Bugda Gwilt, Jeffrey J. Widrick, Alessandra Pasut +8 more

Effects of gene replacement therapy with resamirigene bilparvovec (AT132) on skeletal muscle pathology in X-linked myotubular myopathy: results from a substudy of the ASPIRO open-label clinical trial

EBioMedicine(2023)10.1016/j.ebiom.2023.104894

N/A

0DataRank · unranked

10 citations

Benedikt Schoser, Marta Margeta, Caroline A. Sewry, Karra A. Jones, Perry B. Shieh +34 more

ACTA1 H40Y mutant iPSC-derived skeletal myocytes display mitochondrial defects in an in vitro model of nemaline myopathy

Experimental Cell Research(2023)10.1016/j.yexcr.2023.113507

N/A

0DataRank · unranked

7 citations

Margaret Haberman, J. R. Sutton, Rebecca A. Slick, Shawn M. Luttrell, David L. Mack +2 more

Different Mouse Models of Nemaline Myopathy Harboring Acta1 Mutations Display Differing Abnormalities Related to Mitochondrial Biology

American Journal Of Pathology(2023)10.1016/j.ajpath.2023.06.008

N/A

0DataRank · unranked

11 citations

Rebecca A. Slick, J. R. Sutton, Liwen Zhang, Hui Meng, Margaret Beatka +12 more

High mobility group box 1 (HMGB1) is a potential disease biomarker in cell and mouse models of Duchenne muscular dystrophy

Biology Open(2024)10.1242/bio.060542

N/A

0DataRank · unranked

0 citations

J. R. Sutton, Margaret Haberman, Benjamin S. O’Brien, Jennifer A Tinklenberg, Aashay Mardikar +11 more

Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy

JCI Insight(2025)10.1172/jci.insight.194868

N/A

0DataRank · unranked

3 citations

F. Rostedt, Charlotte Gineste, Robert A. Seaborne, Hannah F. Dugdale, Vladimir Belhac +12 more

The D2.B10-Dmd/J Mouse Model of Duchenne Muscular Dystrophy Exhibits a Severe Mitochondrial Deficiency Not Observed in the C57BL/10ScSn-Dmd/J Mouse

American Journal Of Pathology(2025)10.1016/j.ajpath.2025.09.005

N/A

0DataRank · unranked

0 citations

J. R. Sutton, Rebecca A. Slick, Hui Meng, Margaret Haberman, Mariah J. Prom +7 more

Loss of Mtm1 causes cholestatic liver disease in a model of X-linked myotubular myopathy

Journal of Clinical Investigation(2023)10.1172/jci166275

N/A

0DataRank · unranked

20 citations

Ashish R. Deshwar, Evangelina Aristegui, Binita M. Kamath, Michael W. Lawlor, Gaia Andreoletti +5 more

Conference report on contractures in musculoskeletal and neurological conditions

Muscle & Nerve(2020)10.1002/mus.26845

N/A

0DataRank · unranked

22 citations

Kathi Kinnett, Sudarshan Dayanidhi, Andrea A. Domenighetti, Tina Duong, Yetrib Hathout +18 more

Duchenne muscular dystrophy (DMD) cardiomyocyte-secreted exosomes promote the pathogenesis of DMD-associated cardiomyopathy

Disease Models & Mechanisms(2020)10.1242/dmm.045559

N/A

0DataRank · unranked

30 citations

Chien-Wei Lin, Mark A. Sussman, Michael W. Lawlor, Jennifer L. Strande, Melanie Gartz