Michael T. Geraghty

8.7k total citations
121 papers, 3.6k citations indexed

About

Michael T. Geraghty is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Michael T. Geraghty has authored 121 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 38 papers in Clinical Biochemistry and 33 papers in Genetics. Recurrent topics in Michael T. Geraghty's work include Metabolism and Genetic Disorders (38 papers), Mitochondrial Function and Pathology (14 papers) and Genomics and Rare Diseases (12 papers). Michael T. Geraghty is often cited by papers focused on Metabolism and Genetic Disorders (38 papers), Mitochondrial Function and Pathology (14 papers) and Genomics and Rare Diseases (12 papers). Michael T. Geraghty collaborates with scholars based in United States, Canada and Netherlands. Michael T. Geraghty's co-authors include Barbara K. Goodman, Peter C. Rowe, Stephen J. Gould, Julie Rutberg, Irene H. Maumenee, Kym M. Boycott, Ethylin Wang Jabs, Patrick Tong, John Kinsella and Mohamed Amin and has published in prestigious journals such as Journal of Biological Chemistry, Blood and Brain.

In The Last Decade

Michael T. Geraghty

114 papers receiving 3.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Michael T. Geraghty United States	36	1.9k	913	896	422	402	121	3.6k
George A. Díaz United States	34	1.6k 0.8×	801 0.9×	769 0.9×	622 1.5×	278 0.7×	101	3.6k
Paul M. Fernhoff United States	32	1.9k 1.0×	658 0.7×	978 1.1×	377 0.9×	932 2.3×	66	4.0k
Han‐Wook Yoo South Korea	33	1.8k 1.0×	426 0.5×	971 1.1×	650 1.5×	398 1.0×	300	4.0k
Clara van Karnebeek Canada	34	1.5k 0.8×	1.2k 1.3×	1.4k 1.5×	310 0.7×	528 1.3×	118	3.5k
John J. Mitchell United States	33	1.7k 0.9×	1.0k 1.1×	590 0.7×	1.2k 2.7×	374 0.9×	131	4.2k
Michèl A.A.P. Willemsen Netherlands	41	2.8k 1.5×	1.2k 1.3×	1.3k 1.4×	734 1.7×	583 1.5×	199	5.7k
Allan M. Lund Denmark	32	1.1k 0.6×	941 1.0×	876 1.0×	1.1k 2.7×	324 0.8×	171	3.3k
David Dimmock United States	33	1.7k 0.9×	1000 1.1×	1.8k 2.0×	466 1.1×	499 1.2×	116	3.9k
Pietro Strisciuglio Italy	30	1.1k 0.6×	597 0.7×	356 0.4×	532 1.3×	214 0.5×	131	2.9k
Neil R.M. Buist United States	35	2.0k 1.1×	1.6k 1.8×	767 0.9×	731 1.7×	497 1.2×	111	5.4k

Countries citing papers authored by Michael T. Geraghty

Since Specialization

Citations

This map shows the geographic impact of Michael T. Geraghty'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 Michael T. Geraghty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael T. Geraghty more than expected).

Fields of papers citing papers by Michael T. Geraghty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael T. Geraghty. 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 Michael T. Geraghty. The network helps show where Michael T. Geraghty may publish in the future.

Co-authorship network of co-authors of Michael T. Geraghty

This figure shows the co-authorship network connecting the top 25 collaborators of Michael T. Geraghty. A scholar is included among the top collaborators of Michael T. Geraghty 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 Michael T. Geraghty. Michael T. Geraghty 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

Royo, C., et al.. (2025). Low-level direct currents eradicate multi-drug-resistant Candidozyma auris through physiological stress and antifungal permeation. Chemical Engineering Journal. 520. 166070–166070. 1 indexed citations

Geraghty, Michael T., et al.. (2024). Raman amplifier based on stimulated Raman scattering in a methane-filled hollow core fiber. Optics Express. 32(15). 26279–26279.

Lines, Matthew A., Alexanne Cuillerier, Pranesh Chakraborty, et al.. (2021). A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency. European Journal of Human Genetics. 29(11). 1719–1724. 4 indexed citations

MacKenzie, Jennifer, et al.. (2019). Hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome in pregnancy: Considerations for management and review of the literature. JIMD Reports. 46(1). 28–34. 4 indexed citations

Waters, Paula J., Thomas M. Kitzler, Annette Feigenbaum, et al.. (2017). Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment. JIMD Reports. 39. 89–96. 12 indexed citations

Smith, Amanda, Skye McBride, Julien Marcadier, et al.. (2016). Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) Deficiency. JIMD Reports. 30. 73–79. 16 indexed citations

Tétreault, Martine, Somayyeh Fahiminiya, Hana Antonická, et al.. (2015). Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome. Human Genetics. 134(9). 981–991. 44 indexed citations

McMillan, Hugh J., Jeremy Schwartzentruber, Amanda Smith, et al.. (2014). Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease. BMC Medical Genetics. 15(1). 36–36. 33 indexed citations

McMillan, Hugh J., Peter Humphreys, Amanda Smith, et al.. (2014). Congenital Visual Impairment and Progressive Microcephaly Due to Lysyl–Transfer Ribonucleic Acid (RNA) Synthetase (KARS) Mutations. Journal of Child Neurology. 30(8). 1037–1043. 36 indexed citations

10.

Chew, Sheena, Ravikumar Balasubramanian, Wai‐Man Chan, et al.. (2013). A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3. Brain. 136(2). 522–535. 81 indexed citations

11.

Yoon, Grace, Berivan Baskin, Mark A. Tarnopolsky, et al.. (2013). Autosomal recessive hereditary spastic paraplegia—clinical and genetic characteristics of a well-defined cohort. Neurogenetics. 14(3-4). 181–188. 26 indexed citations

12.

Marcadier, Julien, Amanda M. Smith, Daniela Pohl, et al.. (2013). Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria. Orphanet Journal of Rare Diseases. 8(1). 98–98. 31 indexed citations

13.

Potter, Beth K., Pranesh Chakraborty, Jonathan B. Kronick, et al.. (2012). Achieving the “triple aim” for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework. Genetics in Medicine. 15(6). 415–422. 21 indexed citations

14.

Wilson, Kumanan, Shelley Kennedy, Beth K. Potter, Michael T. Geraghty, & Pranesh Chakraborty. (2010). Developing a National Newborn Screening Strategy for Canada. uO Research (University of Ottawa). 18(2). 31. 13 indexed citations

15.

Baskin, Berivan, Michael T. Geraghty, & Peter N. Ray. (2010). Paternal isodisomy of chromosome 2 as a cause of long chain 3‐hydroxyacyl‐CoA dehydrogenase (LCHAD) deficiency. American Journal of Medical Genetics Part A. 152A(7). 1808–1811. 12 indexed citations

16.

Li, Madeline, Cheryl Shuman, Eva Maria Cutiongco, et al.. (2001). GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome. American Journal of Medical Genetics. 102(2). 161–168. 87 indexed citations

17.

Hanley, William, et al.. (1999). Undiagnosed maternal phenylketonuria: The need for prenatal selective screening or case finding. American Journal of Obstetrics and Gynecology. 180(4). 986–994. 13 indexed citations

18.

Montgomery, Robert A., et al.. (1998). Multiple Molecular Mechanisms Underlying Subdiagnostic Variants of Marfan Syndrome. The American Journal of Human Genetics. 63(6). 1703–1711. 68 indexed citations

19.

Geisbrecht, Brian V., Kerstin Schulz, Katja Nau, et al.. (1998). Molecular Characterization of Saccharomyces cerevisiae Δ3,Δ2-Enoyl-CoA Isomerase. Journal of Biological Chemistry. 273(50). 33184–33191. 55 indexed citations

20.

Geraghty, Michael T., W.G. Kearns, P. Pearson, & David Valle. (1993). Isolation and Characterization of an Ornithine Aminotransferase-Related Sequence (OATL3) Mapping to 10q26. Genomics. 17(2). 510–513. 3 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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