Tyler Mark Pierson

3.2k total citations
42 papers, 1.3k citations indexed

About

Tyler Mark Pierson is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Tyler Mark Pierson has authored 42 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Tyler Mark Pierson's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Lysosomal Storage Disorders Research (6 papers). Tyler Mark Pierson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Lysosomal Storage Disorders Research (6 papers). Tyler Mark Pierson collaborates with scholars based in United States, Canada and Mexico. Tyler Mark Pierson's co-authors include William A. Gahl, Cornelius F. Boerkoel, David R. Adams, Gretchen Golas, Thomas C. Markello, Camilo Toro, Hongjie Yuan, Stephen F. Traynelis, Cynthia J. Tifft and Conisha Holloman and has published in prestigious journals such as Nature Communications, Brain and Neurology.

In The Last Decade

Tyler Mark Pierson

42 papers receiving 1.3k citations

Peers

Tyler Mark Pierson

GENET

CMN

PMH

Chihiro Ohba Japan

Barry A. Chioza United Kingdom

Gökhan Uyanık Germany

Charles Marques Lourenço Brazil

Dora Angelicheva Australia

F. Lucy Raymond United Kingdom

Marianna Baybis United States

Laura A. Jansen United States

Tracy Dixon‐Salazar United States

Velina Guergueltcheva Bulgaria

Chihiro Ohba Japan

Tyler Mark Pierson

563 ×0.8

341 ×0.8

GENET

252 ×0.6

CMN

108 ×0.6

PMH

102 ×0.7

Citations per year, relative to Tyler Mark Pierson Tyler Mark Pierson (= 1×) peers Chihiro Ohba

Countries citing papers authored by Tyler Mark Pierson

Since Specialization

Citations

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

Fields of papers citing papers by Tyler Mark Pierson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tyler Mark Pierson. 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 Tyler Mark Pierson. The network helps show where Tyler Mark Pierson may publish in the future.

Co-authorship network of co-authors of Tyler Mark Pierson

This figure shows the co-authorship network connecting the top 25 collaborators of Tyler Mark Pierson. A scholar is included among the top collaborators of Tyler Mark Pierson 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 Tyler Mark Pierson. Tyler Mark Pierson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Abad, Clemer, María Gabriela Otero, Anthony J. Griswold, et al.. (2024). Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning. Translational Psychiatry. 14(1). 33–33. 3 indexed citations

Macnamara, Ellen F., Yvonne L. Latour, Precilla D’Souza, et al.. (2023). Risks and benefits of anesthesia for combined pediatric procedures in the NIH undiagnosed diseases program. Molecular Genetics and Metabolism. 140(3). 107707–107707. 1 indexed citations

Wagner, Matias, Jorge L. Granadillo, Amanda V. Tyndall, et al.. (2023). De novo variants in GATAD2A in individuals with a neurodevelopmental disorder: GATAD2A-related neurodevelopmental disorder. Human Genetics and Genomics Advances. 4(3). 100198–100198. 2 indexed citations

Xie, Lingling, Miranda J. McDaniel, Riley E. Perszyk, et al.. (2023). Functional effects of disease-associated variants reveal that the S1–M1 linker of the NMDA receptor critically controls channel opening. Cellular and Molecular Life Sciences. 80(4). 110–110. 6 indexed citations

Jiang, Xiao, Nazzareno D’Avanzo, Mathieu Lachance, et al.. (2019). Both gain‐of‐function and loss‐of‐function de novo CACNA 1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome. Epilepsia. 60(9). 1881–1894. 62 indexed citations

Mazza, Davide, Franca Codazzi, Tyler Mark Pierson, et al.. (2019). Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation. Journal of Medical Genetics. 56(8). 499–511. 19 indexed citations

Souza, Ivana A., María A. Gandini, Fang‐Xiong Zhang, et al.. (2019). Pathogenic Cav3.2 channel mutation in a child with primary generalized epilepsy. Molecular Brain. 12(1). 86–86. 9 indexed citations

Curiel, Julian, Guillermo Rodríguez Bey, Asako Takanohashi, et al.. (2017). TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. Human Molecular Genetics. 26(22). 4506–4518. 53 indexed citations

Chen, Wenjuan, Christine Shieh, Sharon A. Swanger, et al.. (2017). GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function. Journal of Human Genetics. 62(6). 589–597. 59 indexed citations

10.

Yuan, Hongjie, Kasper B. Hansen, Jing Zhang, et al.. (2014). Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy. Nature Communications. 5(1). 3251–3251. 103 indexed citations

11.

Zhu, Peng-Peng, Kyle Denton, Tyler Mark Pierson, Xue Jun Li, & Craig Blackstone. (2014). Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A. Human Molecular Genetics. 23(21). 5638–5648. 51 indexed citations

12.

Totonchy, Mariam, Deborah Tamura, Matthew S. Pantell, et al.. (2013). Auditory analysis of xeroderma pigmentosum 1971–2012: hearing function, sun sensitivity and DNA repair predict neurological degeneration. Brain. 136(1). 194–208. 34 indexed citations

13.

Pierson, Tyler Mark, Paola Torres, Allan M. Glanzman, et al.. (2012). Juvenile-onset motor neuron disease caused by novel mutations in β-hexosaminidase. Molecular Genetics and Metabolism. 108(1). 65–69. 3 indexed citations

14.

Sincan, Murat, Dimitre R. Simeonov, David R. Adams, et al.. (2012). VAR-MD: A tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance. Human Mutation. 33(4). 593–598. 25 indexed citations

15.

Donsante, Anthony, et al.. (2011). Increased frequency of congenital heart defects in Menkes disease. Clinical Dysmorphology. 21(2). 59–63. 24 indexed citations

16.

Pierson, Tyler Mark, Dimitre R. Simeonov, Murat Sincan, et al.. (2011). Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration. European Journal of Human Genetics. 20(4). 476–479. 44 indexed citations

17.

Pierson, Tyler Mark, Carsten G. Bönnemann, Richard S. Finkel, Nancy Bunin, & Gihan Tennekoon. (2008). Umbilical cord blood transplantation for juvenile metachromatic leukodystrophy. Annals of Neurology. 64(5). 583–587. 28 indexed citations

18.

Perrien, Daniel S., Nisreen Akel, Paul Edwards, et al.. (2006). Inhibin A Is an Endocrine Stimulator of Bone Mass and Strength. Endocrinology. 148(4). 1654–1665. 83 indexed citations

19.

Pierson, Tyler Mark, Yaolin Wang, Francesco J. DeMayo, et al.. (2000). Regulable Expression of Inhibin A in Wild-Type and Inhibinα Null Mice. Molecular Endocrinology. 14(7). 1075–1085. 62 indexed citations

20.

Pierson, Tyler Mark & Paul D. Heideman. (1994). Acceleration and deceleration of sexual maturation by social cues in a tropical rodent Zygodontomys brevicauda. Reproduction. 102(2). 459–462. 1 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.

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