Judy Correa

1.9k total citations · 1 hit paper
16 papers, 1.5k citations indexed

About

Judy Correa is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Judy Correa has authored 16 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Pulmonary and Respiratory Medicine and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Judy Correa's work include Muscle Physiology and Disorders (8 papers), Mitochondrial Function and Pathology (3 papers) and Childhood Cancer Survivors' Quality of Life (2 papers). Judy Correa is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Mitochondrial Function and Pathology (3 papers) and Childhood Cancer Survivors' Quality of Life (2 papers). Judy Correa collaborates with scholars based in Canada, United Kingdom and United States. Judy Correa's co-authors include Daniela Rotin, Takahiro Ishikawa, Jane McGlade, Olivier Staub, Sascha E. Dho, P Henry, Jane Batt, Pamela Plant, James R. Bain and A. D. Bain and has published in prestigious journals such as Journal of Biological Chemistry, The EMBO Journal and PLoS ONE.

In The Last Decade

Judy Correa

16 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

WW domains of Nedd4 bind to the proline-rich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome.

1996 697 citations Olivier Staub, Sascha E. Dho et al. The EMBO Journal profile →

Peers

Judy Correa

MB

PRM

PHYSI

CB

CCM

Ying Tian Japan

Jonas Rutishauser Switzerland

Michael P. Wiggs United States

Mahroo Mofarrahi Canada

Andréia Z. Chignalia United States

P. Purkiss United Kingdom

Guangming Yang China

Kumiko Tanabe Japan

Richard Godin Canada

Donald Fisher United States

Ying Tian Japan

Judy Correa

615 ×0.6

MB

532 ×1.7

PRM

120 ×0.5

PHYSI

33 ×0.2

CB

168 ×1.2

CCM

Citations per year, relative to Judy Correa Judy Correa (= 1×) peers Ying Tian

Countries citing papers authored by Judy Correa

Since Specialization

Citations

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

Fields of papers citing papers by Judy Correa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judy Correa. 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 Judy Correa. The network helps show where Judy Correa may publish in the future.

Co-authorship network of co-authors of Judy Correa

This figure shows the co-authorship network connecting the top 25 collaborators of Judy Correa. A scholar is included among the top collaborators of Judy Correa based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Judy Correa. Judy Correa is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

1.

Lodyga, Monika, et al.. (2024). Utilization of the Rat Tibial Nerve Transection Model to Evaluate Cellular and Molecular Mechanisms Underpinning Denervation-Mediated Muscle Injury. International Journal of Molecular Sciences. 25(3). 1847–1847. 4 indexed citations

2.

Walsh, Christopher J., Muskan Gupta, Pamela Plant, et al.. (2022). MicroRNA regulatory networks associated with abnormal muscle repair in survivors of critical illness. Journal of Cachexia Sarcopenia and Muscle. 13(2). 1262–1276. 10 indexed citations

3.

Correa, Judy, et al.. (2021). Identification, Isolation, and Characterization of Fibro-Adipogenic Progenitors (FAPs) and Myogenic Progenitors (MPs) in Skeletal Muscle in the Rat. Journal of Visualized Experiments. 5 indexed citations

4.

Correa, Judy, et al.. (2021). Identification, Isolation, and Characterization of Fibro-Adipogenic Progenitors (FAPs) and Myogenic Progenitors (MPs) in Skeletal Muscle in the Rat. Journal of Visualized Experiments. 4 indexed citations

5.

Santos, Claúdia C. dos, Sabah N. A. Hussain, Sunita Mathur, et al.. (2016). Mechanisms of Chronic Muscle Wasting and Dysfunction after an Intensive Care Unit Stay. A Pilot Study. American Journal of Respiratory and Critical Care Medicine. 194(7). 821–830. 175 indexed citations

6.

Plant, Pamela, et al.. (2015). PDLIM7 is a novel target of the ubiquitin ligase Nedd4-1 in skeletal muscle. Biochemical Journal. 473(3). 267–276. 21 indexed citations

7.

Batt, Jane, et al.. (2013). Skeletal Muscle Dysfunction in Idiopathic Pulmonary Arterial Hypertension. American Journal of Respiratory Cell and Molecular Biology. 50(1). 74–86. 109 indexed citations

8.

Plant, Pamela, Judy Correa, A. D. Bain, et al.. (2012). The Ubiquitin Ligase Nedd4-1 Participates in Denervation-Induced Skeletal Muscle Atrophy in Mice. PLoS ONE. 7(10). e46427–e46427. 60 indexed citations

9.

Plant, Pamela, Michelle L. North, Andrew Ward, et al.. (2011). Hypertrophic Airway Smooth Muscle Mass Correlates with Increased Airway Responsiveness in a Murine Model of Asthma. American Journal of Respiratory Cell and Molecular Biology. 46(4). 532–540. 26 indexed citations

10.

Plant, Pamela, James R. Bain, Judy Correa, Minna Woo, & Jane Batt. (2009). Absence of caspase-3 protects against denervation-induced skeletal muscle atrophy. Journal of Applied Physiology. 107(1). 224–234. 66 indexed citations

11.

Plant, Pamela, Dina Brooks, Marie E. Faughnan, et al.. (2009). Cellular Markers of Muscle Atrophy in Chronic Obstructive Pulmonary Disease. American Journal of Respiratory Cell and Molecular Biology. 42(4). 461–471. 150 indexed citations

12.

Plant, Pamela, Judy Correa, Neil M. Goldenberg, James R. Bain, & Jane Batt. (2009). The inositol phosphatase MTMR4 is a novel target of the ubiquitin ligase Nedd4. Biochemical Journal. 419(1). 57–63. 22 indexed citations

13.

Landolt-Marticorena, Carolina, Kelly M. Williams, Judy Correa, Weimin Chen, & Morris F. Manolson. (2000). Evidence That the NH2 Terminus of Vph1p, an Integral Subunit of the V0 Sector of the Yeast V-ATPase, Interacts Directly with the Vma1p and Vma13p Subunits of the V1Sector. Journal of Biological Chemistry. 275(20). 15449–15457. 88 indexed citations

14.

Landolt-Marticorena, Carolina, et al.. (1999). Substrate- and Inhibitor-induced Conformational Changes in the Yeast V-ATPase Provide Evidence for Communication between the Catalytic and Proton-translocating Sectors. Journal of Biological Chemistry. 274(37). 26057–26064. 22 indexed citations

15.

Staub, Olivier, Sascha E. Dho, P Henry, et al.. (1996). WW domains of Nedd4 bind to the proline-rich PY motifs in the epithelial Na+ channel deleted in Liddle's syndrome.. The EMBO Journal. 15(10). 2371–2380. 697 indexed citations breakdown →

16.

OʼBrodovich, Hugh, et al.. (1993). Novobiocin forms cation-permeable ion channels in rat fetal distal lung epithelium. American Journal of Physiology-Cell Physiology. 264(6). C1532–C1537. 4 indexed citations

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.

Explore authors with similar magnitude of impact