Gregory A. Cox

7.8k citations

82 papers · 4.4k indexed · h-index 38

Genetics top 1%
- Neurogenetic and Muscular Disorders Research 17
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders 9
Molecular Biology top 2%
- Muscle Physiology and Disorders 32
- Mitochondrial Function and Pathology 10
- RNA Research and Splicing 9
Neurology top 2%
- Amyotrophic Lateral Sclerosis Research 12
- Neurological diseases and metabolism 7
Cell Biology top 2%
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 9

Co-authors: Jeffrey S. Chamberlain Kevin L. Seburn Kevin P. Campbell Roger B. Sher Wayne N. Frankel Stephanie F. Phelps Connie L. Mahaffey Robert W. Burgess
Cited by: Genetics Cellular and Molecular Neuroscience Molecular Biology
Journals: Human Molecular Genetics (13 papers)Journal of Biological Chemistry (4 papers)PLoS ONE (4 papers)
Partner nations: United States Italy Germany

In The Last Decade

Gregory A. Cox

79 papers receiving 4.4k citations

Peers

Countries citing papers authored by Gregory A. Cox

Since Specialization

Citations

This map shows the geographic impact of Gregory A. Cox'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 Gregory A. Cox with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gregory A. Cox more than expected).

Fields of papers citing papers by Gregory A. Cox

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory A. Cox. 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 Gregory A. Cox. The network helps show where Gregory A. Cox may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1 Human Molecular Genetics ·AK Njiru,Amy N. Hicks,Paige Martin,Kelly Chien,Maya Pencheva,Gregory A. Cox	2024	0
2	Mouse models of NADK2 deficiency analyzed for metabolic and gene expression changes to elucidate pathophysiology Human Molecular Genetics ·George Murray,Preeti Bais,Zhizhuo Zhang,Abigail L. D. Tadenev,Brian Hoffmann,Timothy J. Stodola,Kathryn H. Morelli,J�rg Arndt,David G. Schroeder,민지영,Oliver Fiehn,Simon W. M. John,Carol J. Bult,Gregory A. Cox,Robert W. Burgess	2022	5
3	Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease PLoS ONE ·Guillermo M. Alexander,Terry Heiman‐Patterson,T Sharp,Roger B. Sher,Márcio Gonçalves da Silva Brandão,James H. Feldmann,M. Richter,Gregory A. Cox,Vivek M. Philip,Elizabeth Blankenhorn	2022	1
4	Clinically relevant mouse models of Charcot–Marie–Tooth type 2S Human Molecular Genetics ·Paige Martin,AK Njiru,Amy N. Hicks,Kelly Chien,Laurent Bogdanik,Robert W. Burgess,Gregory A. Cox	2022	8
5	Analysis of BMAA enantiomers in cycads, cyanobacteria, and mammals: in vivo formation and toxicity of d-BMAA Amino Acids ·James S. Metcalf,Doug Lobner,Sandra Anne Banack,Gregory A. Cox,Peter B. Nunn,Peter B. Wyatt,Paul Alan Cox	2017	24
6	Genetic Background Effects on Disease Onset and Lifespan of the Mutant Dynactin p150Glued Mouse Model of Motor Neuron Disease PLoS ONE ·Terry Heiman‐Patterson,Elizabeth P. Blankenhorn,Roger B. Sher,Ida Pari Purnawan,Teresa Krämer,Ugo Longobardo,Sin-Ae Jang,Philip C. Wong,Gregory A. Cox,Guillermo M. Alexander	2015	13
7	Ankyrin Repeat Domain Protein 2 and Inhibitor of DNA Binding 3 Cooperatively Inhibit Myoblast Differentiation by Physical Interaction Journal of Biological Chemistry ·Junaith S. Mohamed,Michael A. Lopez,Gregory A. Cox,Aladin M. Boriek	2013	19
8	Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1 (Tal1) Gene Is Associated with Severe Renal Disease and Patchy Alopecia in Hairpatches (Hpt) Mice PLoS ONE ·Vishnu Hosur,Melissa L. Cox,Lisa Burzenski,Rebecca L. Riding,Ed Basart,Bonnie Lyons,Anoop Kavirayani,Kimberly Martin,Gregory A. Cox,Kenneth R. Johnson,Leonard D. Shultz	2013	5
9	A Direct HDAC4-MAP Kinase Crosstalk Activates Muscle Atrophy Program Molecular Cell ·Dasabala,Todd J. Cohen,Tomasa Barrientos,Bin Wang,Ming Li,Bryan J. Simmons,Jeong Soo Yang,Gregory A. Cox,Yingming Zhao,M.T. Khubetsova	2012	56
10	Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: A window of opportunity in the search for genetic modifiers Amyotrophic Lateral Sclerosis ·Terry Heiman‐Patterson,Roger B. Sher,Elizabeth Blankenhorn,Guillermo M. Alexander,Jeffrey S. Deitch,Catherine B. Kunst,Nicholas J. Maragakis,Gregory A. Cox	2011	87
11	Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice PLoS Genetics ·Yan Yang,Connie L. Mahaffey,Nathalie G. Bérubé,Terry P. Maddatu,Gregory A. Cox,Wayne N. Frankel	2007	50
12	Ocular abnormalities in Largemyd and Largevls mice, spontaneous models for muscle, eye, and brain diseases Molecular and Cellular Neuroscience ·Abhishek Yadav,Shuhei Kameya,Gregory A. Cox,Jennifer L. Hsu,Wanda L. Hicks,Terry P. Maddatu,Richard S. Smith,Jürgen Κ. Naggert,Neal S. Peachey,Patsy M. Nishina	2005	63
13	Adult-Onset Alopecia Areata Is a Complex Polygenic Trait in the C3H/HeJ Mouse Model Journal of Investigative Dermatology ·John P. Sundberg,Kathleen A. Silva,Renhua Li,Gregory A. Cox,Lloyd E. King	2004	43
14	Paralytic Autoimmune Myositis Develops in Nonobese Diabetic Mice Made Th1 Cytokine-Deficient by Expression of an IFN-γ Receptor β-Chain Transgene The Journal of Immunology ·David Serreze,Sonali Mishra,A Adesh Sai,Harold D. Chapman,Vera Varga,Roderick T. Bronson,Paul B. Rothman,Gregory A. Cox	2003	7
15	Major Locus on Mouse Chromosome 17 and Minor Locus on Chromosome 9 are Linked with Alopecia Areata in C3H/HeJ Mice Journal of Investigative Dermatology ·John P. Sundberg,Dawnalyn Boggess,Kathleen A. Silva,Kevin J. McElwee,Lloyd E. King,Renhua Li,Gary A. Churchill,Gregory A. Cox	2003	30
16	Identification and Characterization of Human Rhinovirus-14 3C Protease Deamidation Isoform Journal of Biological Chemistry ·Gregory A. Cox,Robert B. Johnson,James A. Cook,Mark Wakulchik,Melvin G. Johnson,Elcira C. Villarreal,Q. May Wang	1999	5
17	Expression and Purification of Recombinant Rhinovirus 14 3CD Proteinase and Its Comparison to the 3C Proteinase Archives of Biochemistry and Biophysics ·Gerard J. Davis,Christian Alexander Wiik,Gregory A. Cox,Robert B. Johnson,Mark Wakulchik,Sai-Yu Liu,Elcira C. Villarreal	1997	16
18	Myotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulation. Molecular Biology of the Cell ·Karen Stephanie de Souza Mangabeira,F. Woodward Hopf,Gregory A. Cox,Jeffrey S. Chamberlain,Richard A. Steinhardt	1994	23
19	Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity Nature ·Gregory A. Cox,Neil M. Cole,Kiichiro Matsumura,Stephanie F. Phelps,Stephen D. Hauschka,Kevin P. Campbell,John A. Faulkner,Jeffrey S. Chamberlain	1993	231
20	PCR analysis of dystrophin gene mutation and expression Journal of Cellular Biochemistry ·Jeffrey S. Chamberlain,Tristan Slotosch,(unknown),(unknown),Gregory A. Cox,C. Thomas Caskey	1991	23

About Gregory A. Cox

Gregory A. Cox is a scholar working on Genetics, Cell Biology, Cellular and Molecular Neuroscience, Molecular Biology and Neurology, having authored 82 papers that have together received 4.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (32 papers), Neurogenetic and Muscular Disorders Research (17 papers), Amyotrophic Lateral Sclerosis Research (12 papers), Mitochondrial Function and Pathology (10 papers), Hereditary Neurological Disorders (9 papers), Cardiomyopathy and Myosin Studies (9 papers), RNA Research and Splicing (9 papers) and Neurological diseases and metabolism (7 papers). The work is most often cited by research in Genetics (617 citations), Cellular and Molecular Neuroscience (891 citations), Molecular Biology (3.3k citations), Neurology (577 citations) and Cell Biology (497 citations). Gregory A. Cox has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Jeffrey S. Chamberlain, Kevin L. Seburn, Kevin P. Campbell, Roger B. Sher, Wayne N. Frankel, Stephanie F. Phelps, Connie L. Mahaffey, Wayne N. Frankel, Robert W. Burgess and John P. Sundberg. Their work appears in journals such as Human Molecular Genetics, Journal of Biological Chemistry, PLoS ONE, Nature Genetics and Journal of Virology.

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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