David Arthur Stroud (David A Stroud)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 37

Top Venues

Nature communications

International journal of molecular sciences

Proceedings of the National Academy of Sciences of the United States of America

Human mutation

The University of Melbourne

La Trobe University (BSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

The University of Melbourne Jan 08 2018

Australia

NHMRC CDF :: Department of Biochemistry and Molecular Biology

Monash University Oct 06 2014 - Dec 31 2017

Australia

NHMRC Peter Doherty Research Fellow :: Department of Biochemistry and Molecular Biology

La Trobe University Jan 20 2014 - Oct 03 2014

Australia

NHMRC Peter Doherty Research Fellow :: Department of Biochemistry and Genetics

La Trobe University Feb 20 2012 - Jan 17 2014

Australia

Research Officer :: Department of Biochemistry and Genetics

Education History

La Trobe University Mar 01 2004 - Mar 14 2014

Australia

BSC :: Department of Biochemistry and Genetics

Albert-Ludwigs University of Freiburg Mar 17 2008 - Dec 02 2011

Germany

PHD :: Institute of for Biochemistry and Molecular Biology

Publications

Elizabeth G Reisman, Javier Botella, Cheng Huang, Ralf Bernd Schittenhelm, David Arthur Stroud, Cesare Granata, Owala S Chandrasiri, Georg Ramm, Viola Oorschot, Nikeisha J Caruana, David J Bishop
Fibre-specific mitochondrial protein abundance is linked to resting and post-training mitochondrial content in the muscle of men. Nature communications 15 (1) (2024)
Elizabeth G Reisman, Javier Botella, Cheng Huang, Ralf Bernd Schittenhelm, David Arthur Stroud, Cesare Granata, Owala S Chandrasiri, Georg Ramm, Viola Oorschot, Nikeisha J Caruana, David J Bishop
Fibre-specific mitochondrial protein abundance is linked to resting and post-training mitochondrial content in the muscle of men. Nature communications 15 (1) (2024)
Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella Helena Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha Saad Zaki, Alban Ziegler, David R Thorburn, David Arthur Stroud, Reza Maroofian, John Chrisodoulou, Claes M Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature communications 14 (1) (2023)
Nicole J Van Bergen, Karen Gunanayagam, Adam M Bournazos, Adhish S Walvekar, Marc O Warmoes, Liana N Semcesen, Sebastian Lunke, Shobhana Bommireddipalli, Tim Sikora, Myrto Patraskaki, Dean L Jones, Denisse Garza, Dale Sebire, Samuel Gooley, Catriona A Mclean, Parm Naidoo, Mugil Rajasekaran, David Arthur Stroud, Carole L Linster, Mathew Wallis, Sandra T Cooper, John Chrisodoulou
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma. International journal of molecular sciences 24 (4) (2023)
Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella Helena Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha Saad Zaki, Alban Ziegler, David R Thorburn, David Arthur Stroud, Reza Maroofian, John Chrisodoulou, Claes M Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature communications 14 (1) (2023)
Nicole J Van Bergen, Karen Gunanayagam, Adam M Bournazos, Adhish S Walvekar, Marc O Warmoes, Liana N Semcesen, Sebastian Lunke, Shobhana Bommireddipalli, Tim Sikora, Myrto Patraskaki, Dean L Jones, Denisse Garza, Dale Sebire, Samuel Gooley, Catriona A Mclean, Parm Naidoo, Mugil Rajasekaran, David Arthur Stroud, Carole L Linster, Mathew Wallis, Sandra T Cooper, John Chrisodoulou
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma. International journal of molecular sciences 24 (4) (2023)
Nicole J Van Bergen, Karen Gunanayagam, Adam M Bournazos, Adhish S Walvekar, Marc O Warmoes, Liana N Semcesen, Sebastian Lunke, Shobhana Bommireddipalli, Tim Sikora, Myrto Patraskaki, Dean L Jones, Denisse Garza, Dale Sebire, Samuel Gooley, Catriona A Mclean, Parm Naidoo, Mugil Rajasekaran, David Arthur Stroud, Carole L Linster, Mathew Wallis, Sandra T Cooper, John Chrisodoulou
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma. International journal of molecular sciences 24 (4) (2023)
Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella Helena Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha Saad Zaki, Alban Ziegler, David R Thorburn, David Arthur Stroud, Reza Maroofian, John Chrisodoulou, Claes M Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature communications 14 (1) (2023)
Cecilia Patitucci, Juan Diego Hernández-Camacho, Elodie Vimont, Sonny Yde, Thomas Cokelaer, Thibault Chaze, Quentin Giai Gianetto, Mariette Matondo, Anastasia D Gazi, Ivan Nemazanyy, David Arthur Stroud, Daniella H Hock, Erminia Donnarumma, Timothy Wai
Mtfp1 ablation enhances mitochondrial respiration and protects against hepatic steatosis. Nature communications 14 (1) (2023)
Cecilia Patitucci, Juan Diego Hernández-Camacho, Elodie Vimont, Sonny Yde, Thomas Cokelaer, Thibault Chaze, Quentin Giai Gianetto, Mariette Matondo, Anastasia D Gazi, Ivan Nemazanyy, David Arthur Stroud, Daniella H Hock, Erminia Donnarumma, Timothy Wai
Mtfp1 ablation enhances mitochondrial respiration and protects against hepatic steatosis. Nature communications 14 (1) (2023)
Bogusz Kulawiak, Monika Zochowska, Piotr Bednarczyk, Andrzej Galuba, David Arthur Stroud, Adam Szewczyk
Loss of the large conductance calcium-activated potassium channel causes an increase in mitochondrial reactive oxygen species in glioblastoma cells. Pflugers Archiv : European journal of physiology (2023)
Nicole J Van Bergen, Karen Gunanayagam, Adam M Bournazos, Adhish S Walvekar, Marc O Warmoes, Liana N Semcesen, Sebastian Lunke, Shobhana Bommireddipalli, Tim Sikora, Myrto Patraskaki, Dean L Jones, Denisse Garza, Dale Sebire, Samuel Gooley, Catriona A Mclean, Parm Naidoo, Mugil Rajasekaran, David Arthur Stroud, Carole L Linster, Mathew Wallis, Sandra T Cooper, John Chrisodoulou
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma. International journal of molecular sciences 24 (4) (2023)
Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella Helena Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha Saad Zaki, Alban Ziegler, David R Thorburn, David Arthur Stroud, Reza Maroofian, John Chrisodoulou, Claes M Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature communications 14 (1) (2023)
Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella Helena Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha Saad Zaki, Alban Ziegler, David R Thorburn, David Arthur Stroud, Reza Maroofian, John Chrisodoulou, Claes M Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature communications 14 (1) (2023)
Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella Helena Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha Saad Zaki, Alban Ziegler, David R Thorburn, David Arthur Stroud, Reza Maroofian, John Chrisodoulou, Claes M Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature communications 14 (1) (2023)
Lindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella Helena Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha Saad Zaki, Alban Ziegler, David R Thorburn, David Arthur Stroud, Reza Maroofian, John Chrisodoulou, Claes M Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature communications 14 (1) (2023)
Cecilia Patitucci, Juan Diego Hernández-Camacho, Elodie Vimont, Sonny Yde, Thomas Cokelaer, Thibault Chaze, Quentin Giai Gianetto, Mariette Matondo, Anastasia D Gazi, Ivan Nemazanyy, David Arthur Stroud, Daniella H Hock, Erminia Donnarumma, Timothy Wai
Mtfp1 ablation enhances mitochondrial respiration and protects against hepatic steatosis. Nature communications 14 (1) (2023)
Nicole J Van Bergen, Karen Gunanayagam, Adam M Bournazos, Adhish S Walvekar, Marc O Warmoes, Liana N Semcesen, Sebastian Lunke, Shobhana Bommireddipalli, Tim Sikora, Myrto Patraskaki, Dean L Jones, Denisse Garza, Dale Sebire, Samuel Gooley, Catriona A Mclean, Parm Naidoo, Mugil Rajasekaran, David Arthur Stroud, Carole L Linster, Mathew Wallis, Sandra T Cooper, John Chrisodoulou
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma. International journal of molecular sciences 24 (4) (2023)
Cecilia Patitucci, Juan Diego Hernández-Camacho, Elodie Vimont, Sonny Yde, Thomas Cokelaer, Thibault Chaze, Quentin Giai Gianetto, Mariette Matondo, Anastasia D Gazi, Ivan Nemazanyy, David Arthur Stroud, Daniella H Hock, Erminia Donnarumma, Timothy Wai
Mtfp1 ablation enhances mitochondrial respiration and protects against hepatic steatosis. Nature communications 14 (1) (2023)
Nicole J Van Bergen, Daniella Helena Hock, Lucy Spencer, Sean Massey, Tegan Stait, Zornitza Stark, Sebastian Lunke, Ain Roesley, Heidi Peters, Joy Yaplito Lee, Anna Le Fevre, Oliver Heath, Cristina Mignone, Joseph Yuan-Mou Yang, Monique M Ryan, Colleen D'Arcy, Margot Nash, Sile Smith, Nikeisha J Caruana, David R Thorburn, David Arthur Stroud, Susan M White, John Chrisodoulou, Natasha J Brown
Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function. International journal of molecular sciences 23 (2) (2022)
Allan Shuai Huang, Hui San Chin, Boris Reljic, Tirta M Djajawi, Iris K L Tan, Jia-Nan Gong, David Arthur Stroud, David Ching Siang Huang, Mark F van Delft, Grant Dewson
Mitochondrial E3 ubiquitin ligase MARCHF5 controls BAK apoptotic activity independently of BH3-only proteins. Cell death and differentiation (2022)
Thomas D Jackson, Jordan James Crameri, Linden S Muellner-Wong, Ann E Frazier, Catherine S Palmer, Luke E Formosa, Daniella H Hock, Kenji M Fujihara, Tegan Stait, Alice J Sharpe, David R Thorburn, Michael T Ryan, David Arthur Stroud, Diana Stojanovski
Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module. Proceedings of the National Academy of Sciences of the United States of America 119 (13) (2022)
Silja Lucia Salscheider, Sarah Gerlich, Alfredo Cabrera-Orefice, Esra Peker, Robin Alexander Rothemann, Lena Maria Murschall, Yannik Finger, Karolina Szczepanowska, Zeinab Alsadat Ahmadi, Sergio Guerrero-Castillo, Alican Erdogan, Mark Becker, Muna Ali, Markus Habich, Carmelina Petrungaro, Nele Burdina, Guenter Schwarz, Merlin Klußmann, Ines Neundorf, David Arthur Stroud, Michael T Ryan, Aleksandra Trifunovic, Ulrich Brandt, Jan Riemer
AIFM1 is a component of the mitochondrial disulfide relay that drives complex I assembly through efficient import of NDUFS5. The EMBO journal 41 (17) (2022)
Raman Kumar, Mark A Corbett, Nicholas J C Smith, Daniella Helena Hock, Zoya Kikhtyak, Liana N Semcesen, Atsushi Morimoto, Sangmoon Lee, David Arthur Stroud, Joseph G Gleeson, Eric A Haan, Jozef Gecz
Oligonucleotide correction of an intronic TIMMDC1 variant in cells of patients with severe neurodegenerative disorder. NPJ genomic medicine 7 (1) (2022)
Luke E Formosa, Shadi Maghool, Alice J Sharpe, Boris Reljić, Linden S Muellner-Wong, David Arthur Stroud, Michael T Ryan, Megan J Maher
Mitochondrial COA7 is a heme-binding protein with disulfide reductase activity, which acts in the early stages of complex IV assembly. Proceedings of the National Academy of Sciences of the United States of America 119 (9) (2022)
Kai-En Chen, Qian Guo, Timothy A Hill, Yi Cui, Amy K Kendall, Zhe Yang, Ryan J Hall, Michael D Healy, Joanna Sacharz, Suzanne J Norwood, Sachini Fonseka, Boyang Xie, Robert C Reid, Natalya Leneva, Robert G Parton, Rajesh Ghai, David Arthur Stroud, David P Fairlie, Hiroaki Suga, Lauren Parker Jackson, Rohan D Teasdale, Toby Passioura, Brett M Collins
De novo macrocyclic peptides for inhibiting, stabilizing, and probing the function of the retromer endosomal trafficking complex. Science advances 7 (49) (2021)
Luke E Formosa, Boris Reljić, Alice J Sharpe, Daniella Helena Hock, Linden S Muellner-Wong, David Arthur Stroud, Michael T Ryan
Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I. Proceedings of the National Academy of Sciences of the United States of America 118 (17) (2021)
Cesare Granata, Nikeisha J Caruana, Javier Botella, Nicholas A Jamnick, Kevin Huynh, Jujiao Kuang, Hans A Janssen, Boris Reljić, Natalie A Mellett, Adrienne Laskowski, Tegan L Stait, Ann E Frazier, Melinda T Coughlan, Peter J Meikle, David R Thorburn, David Arthur Stroud, David J Bishop
High-intensity training induces non-stoichiometric changes in the mitochondrial proteome of human skeletal muscle without reorganisation of respiratory chain content. Nature communications 12 (1) (2021)
Cheryl Q E Lee, Baptiste Kerouanton, Sonia Chothani, Shan Zhang, Ying Chen, Chinmay Kumar Mantri, Daniella Helena Hock, Radiance Lim, Rhea Nadkarni, Vinh Thang Huynh, Daryl Lim, Wei Leong Chew, Franklin Lei Zhong, David Arthur Stroud, Sebastian Schafer, Vinay Tergaonkar, Ashley Lauren St John, Owen J L Rackham, Lena Ho
Coding and non-coding roles of MOCCI (C15ORF48) coordinate to regulate host inflammation and immunity. Nature communications 12 (1) (2021)
Rachel Thijssen, Sarah T Diepstraten, Donia Moujalled, Edward Chew, Christoffer Flensburg, Melissa X Shi, Michael A Dengler, Veronique Litalien, Sarah MacRaild, Maoshan Chen, Natasha S Anstee, Boris Reljić, Sarah S Gabriel, Tirta M Djajawi, Chris D Riffkin, Brandon J Aubrey, Catherine Chang, Lin Tai, Zhen Xu, Thomas Morley, Giovanna Pomilio, Claudia Bruedigam, Axel Kallies, David Arthur Stroud, Ashish Bajel, Ruth M Kluck, Steven W Lane, Marie Schoumacher, Sébastien Banquet, Ian J Majewski, Andreas Strasser, Andrew W Roberts, David Ching Siang Huang, Fiona C Brown, Gemma L Kelly, Andrew H Wei
Intact TP-53 function is essential for sustaining durable responses to BH3-mimetic drugs in leukemias. Blood 137 (20) (2021)
Guy Helman, Alison G Compton, Daniella Helena Hock, Marzena Walkiewicz, Gemma R Brett, Lynn Pais, Tiong Yang Tan, Ricardo De Paoli-Iseppi, Michael B Clark, John Chrisodoulou, Susan M White, David R Thorburn, David Arthur Stroud, Zornitza Stark, Cas Simons
Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10. Human mutation 42 (1) (2020)
Shan Zhang, Boris Reljić, Chao Liang, Baptiste Kerouanton, Joel Celio Francisco, Jih Hou Peh, Camille Mary, Narendra Suhas Jagannathan, Volodimir Olexiouk, Claire Tang, Gio Fidelito, Srikanth Nama, Ruey-Kuang Cheng, Caroline Lei Wee, Loo Chien Wang, Paula Duek Roggli, Prabha Sampath, Lydie Lane, Enrico Petretto, Radoslaw Mikolaj Sobota, Suresh J Jesuthasan, Lisa Tucker-Kellogg, Bruno Reversade, Gerben Menschaert, Lei Sun, David Arthur Stroud, Lena Ho
Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assembly. Nature communications 11 (1) (2020)
Shadi Maghool, N Dinesha G Cooray, David Arthur Stroud, David Aragão, Michael T Ryan, Megan J Maher
Structural and functional characterization of the mitochondrial complex IV assembly factor Coa6. Life science alliance 2 (5) (2019)
Nicole J Lake, Luke E Formosa, David Arthur Stroud, Michael T Ryan, Sarah E Calvo, Vamsi K Mootha, Bharti Morar, Peter G Procopis, John Chrisodoulou, Alison G Compton, David R Thorburn
A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein-truncating variant. Human mutation 40 (7) (2019)
David Arthur Stroud
ABA/ASB Omics 2018. Biophysical reviews 11 (3) (2019)
Alexandra I C Höhr, Caroline Lindau, Christophe Wirth, Jian Qiu, David Arthur Stroud, Stephan Kutik, Bernard Guiard, Carola Hunte, Thomas Becker, Nikolaus Pfanner, Nils Wiedemann
Membrane protein insertion through a mitochondrial β-barrel gate. Science (New York, N.Y.) 359 (6373) (2018)
Marris G Dibley, Michael T Ryan, David Arthur Stroud
A novel isoform of the human mitochondrial complex I subunit NDUFV3. FEBS letters 591 (1) (2016)

David Arthur Stroud.css-eqlu8i{font-size:small;padding-left:4px;} (David A Stroud)

Publication Activity (10 Years)

Top Topics

Top Venues

David Arthur Stroud (David A Stroud)