Steven A. Moore - Publications, H-index & Citations

Steven A. Moore

Carver College of Medicine

62H指数

433论文数

1.9W被引数

收录论文 110

发表时间

Regenerative Index: a method to assess muscle regeneration in patients with Duchenne muscular dystrophy 再生指数：一种评估杜氏肌营养不良症患者肌肉再生的方法

Skeletal Muscle

IF4.4

2026-07-01

OAAI

Johnathan K. Smid; Charis A. McPherson; Jacob G. Monast; Shanti S. S. Rayagiri; Steven A. Moore; Michael A. Rudnicki

Pathologic Variability Associated With Phenotypic Differences in Siblings With ACTA1 Myopathy 与ACTA1肌病同胞表型差异相关的病理学变异性

MUSCLE & NERVE

IF3.1

2026-02-01

PREAI

Kiss, Robert; Moore, Steven A.; Stefans, Vikki; Gokden, Murat; Veerapandiyan, Aravindhan

Spatial proteomics reveals recombinant human laminin-111 restores adhesion signaling to laminin-α2-deficient muscle 空间蛋白质组学揭示重组人层粘连蛋白-111恢复层粘连蛋白-α2缺乏的肌肉的粘附信号。

JCI INSIGHT

IF6.1

2025-11-24

OAAI

Hermann, Hailey J.; Wuebbles, Ryan D.; Dagda, Marisela; Munoz, Axel; Parker, Lauren L.; Guzman, Paula C.; Byrne, Lola T.; Moore, Steven A.; Burkin, Dean J.

Establishment of normal myofiber size distribution in children and young adults

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

IF3

2025-11-01

PREAI

Lawlor, Michael W.; Margeta, Marta; Jones, Karra A.; Schoser, Benedikt; Cotter, Jennifer A.; Rajaram, Veena; Moore, Steven A.; Prom, Mariah J.; Beatka, Margaret; Ott, Emily; Slick, Rebecca A.; Collins, Michael P.; Esselman, Ann; Shahnoor, Nazima; Danielson, Susan; Meng, Hui; Varfaj, Fatbardha; Prasad, Suyash; Rico, Salvador; Lee, Jun; Kumar, Suresh N.; Dressman, Heather Gordish

A genetic variant in SMAD7 acts as a modifier of LMNA-associated muscular dystrophy, implicating SMAD signaling as a therapeutic target SMAD7基因变异在LMNA相关肌营养不良中起修饰作用，表明SMAD信号通路可作为治疗靶点。

SCIENCE ADVANCES

IF12.5

2025-04-18

OAAI

Mohar, Nathaniel P.; Langland, Christopher J.; Darr, Zachary; Viles, Jill; Moore, Steven A.; Darbro, Benjamin W.; Wallrath, Lori L.

UDP-glucose dehydrogenase variants cause dystroglycanopathy

ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY

IF3.9

2025-04-01

OAAI

Reelfs, Anna M.; Stephan, Carrie M.; Czech, Theresa M.; Cox, Mary O.; Joseph, Soumya; Darbro, Benjamin W.; Moore, Steven A.; Campbell, Kevin P.; Mathews, Katherine D.

A pineal region mass in a 55-year-old female

BRAIN PATHOLOGY

IF6.2

2024-11-03

OAAI

McConeghey, Aaron; Abdullaev, Zied; Aldape, Kenneth; Moore, Steven A.; Neto, Osorio Lopes Abath

Expedited Exome Reanalysis Following Deep Phenotyping and Muscle Biopsy in Suspected Mitochondrial Disorder

PEDIATRIC NEUROLOGY

IF2.1

2024-07-01

PREAI

Pickup, Elizabeth; Moore, Steven A.; Suwannarat, Pim; Grant, Christina; Mew, Nicholas Ah; Gropman, Andrea; Sen, Kuntal

Elevated aminotransferases ina 62-year-old woman

CLEVELAND CLINIC JOURNAL OF MEDICINE

IF4.1

2023-11-01

OAAI

Prakash, Shahana; Moore, Steven; Snow, Anthony; Brown, Kyle E.

High-throughput method to analyze the cytotoxicity of CAR T cells in a 3D tumor spheroid model using image cytometry

CANCER RESEARCH

IF16.6

2023-04-04

PREAI

Patel, Samir; Zurowski, David; Hui, Daniel; Ka, Mignane; Hernandez, Charles; Love, Andrea; Lin, Bo; Moore, Andrea; Chan, Leo Li-Ying

A De Novo Sequence Variant in Barrier-to-Autointegration Factor Is Associated with Dominant Motor Neuronopathy

CELLS

IF5.2

2023-03-09

OAAI

Marcelot, Agathe; Rodriguez-Tirado, Felipe; Cuniasse, Philippe; Joiner, Mei-ling; Miron, Simona; Soshnev, Alexey A.; Fang, Mimi; Pufall, Miles A.; Mathews, Katherine D.; Moore, Steven A.; Zinn-Justin, Sophie; Geyer, Pamela K.

DUX4 double whammy: The transcription factor that causes a rare muscular dystrophy also kills the precursors of the human nose

SCIENCE ADVANCES

IF12.5

2023-02-17

OAAI

Inoue, Kaoru; Bostan, Hamed; Browne, MaKenna R.; Bevis, Owen F.; Bortner, Carl D.; Moore, Steven A.; Stence, Aaron A.; Martin, Negin P.; Chen, Shih-Heng; Burkholder, Adam B.; Li, Jian-Liang; Shaw, Natalie D.

Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle Biopsies Western Blot方法的开发和验证，以量化人骨骼肌活检中的小肌营养不良蛋白

AAPS JOURNAL

IF3.7

2022-12-20

OAAI

Soderstrom, Catherine I.; Larsen, Jennifer; Owen, Carolina; Gifondorwa, David; Beidler, David; Yong, Florence H.; Conrad, Patricia; Neubert, Hendrik; Moore, Steven A.; Hassanein, Mohamed

Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With SMCHD1 Variants

NEUROLOGY

IF8.5

2022-03-29

OAAI

Mohassel, Payam; Chang, Ning; Inoue, Kaoru; Delaney, Angela; Hu, Ying; Donkervoort, Sandra; Saade, Dimah; Billioux, B. Jeanne; Meader, Brooke; Volochayev, Rita; Konersman, Chamindra G.; Kaindl, Angela M.; Cho, Chie-Hee; Russell, Bianca; Rodriguez, Adrian; Foster, K. Wade; Foley, A. Reghan; Moore, Steven A.; Jones, Peter L.; Bonnemann, Carsten G.; Jones, Takako; Shaw, Natalie D.

Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy 杜氏和贝克尔肌营养不良症的内含子突变和早期转录终止

HUMAN MUTATION

IF3.7

2022-03-07

OAAI

Waldrop, Megan A.; Moore, Steven A.; Mathews, Katherine D.; Darbro, Benjamin W.; Medne, Livja; Finkel, Richard; Connolly, Anne M.; Crawford, Thomas O.; Drachman, Daniel; Wein, Nicolas; Habib, Ali A.; Krzesniak-Swinarska, Monika A.; Zaidman, Craig M.; Collins, James J.; Jokela, Manu; Udd, Bjarne; Day, John W.; Ortiz-Guerrero, Gloria; Statland, Jeff; Butterfield, Russell J.; Dunn, Diane M.; Weiss, Robert B.; Flanigan, Kevin M.

The inflammatory pathology of dysferlinopathy is distinct from calpainopathy, Becker muscular dystrophy, and inflammatory myopathies

ACTA NEUROPATHOLOGICA COMMUNICATIONS

IF5.7

2022-02-08

OAAI

Becker, Nicole; Moore, Steven A.; Jones, Karra A.

Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy

JOURNAL OF MOLECULAR DIAGNOSTICS

IF3.4

2021-11-01

OAAI

Stence, Aaron A.; Thomason, Jon G.; Pruessner, Jonathan A.; Sompallae, Ramakrishna R.; Snow, Anthony N.; Ma, Deqin; Moore, Steven A.; Bossler, Aaron D.

Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophy

HUMAN MOLECULAR GENETICS

IF3.2

2021-09-25

OAAI

Smith, Sarah J.; Fabian, Lacramioara; Sheikh, Adeel; Noche, Ramil; Cui, Xiucheng; Moore, Steven A.; Dowling, James J.

Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium

JOURNAL OF CLINICAL INVESTIGATION

IF13.6

2021-05-03

OAAI

van de Locht, Martijn; Donkervoort, Sandra; de Winter, Josine M.; Conijn, Stefan; Begthel, Leon; Kusters, Benno; Mohassel, Payam; Hu, Ying; Medne, Livija; Quinn, Colin; Moore, Steven A.; Foley, A. Reghan; Seo, Gwimoon; Hwee, Darren T.; Malik, Fady, I; Irving, Thomas; Ma, Weikang; Granzier, Henk L.; Kamsteeg, Erik-Jan; Immadisetty, Kalyan; Kekenes-Huskey, Peter; Pinto, Jose R.; Voermans, Nicol; Bonnemann, Carsten G.; Ottenheijm, Coen A. C.

CLIA Laboratory Testing for Facioscapulohumeral Dystrophy A Retrospective Analysis

NEUROLOGY

IF8.5

2021-02-16

OAAI

Rieken, Autumn; Bossler, Aaron D.; Mathews, Katherine D.; Moore, Steven A.

研究方向