Michael T. Geraghty

8.7k citations

121 papers · 3.6k indexed · h-index 36

Molecular Biology top 5%
Clinical Biochemistry top 0.2%
Genetics top 2%
Physiology top 5%
Pediatrics, Perinatology and Child Health top 2%

Co-authors: Barbara K. Goodman Peter C. Rowe Stephen J. Gould Julie Rutberg Irene H. Maumenee Kym M. Boycott Ethylin Wang Jabs Patrick Tong
Topics: Metabolism and Genetic Disorders (38 papers)Mitochondrial Function and Pathology (14 papers)Genomics and Rare Diseases (12 papers)
Cited by: Clinical Biochemistry Genetics Molecular Biology
Journals: Journal of Biological Chemistry Blood Brain
Partner nations: United States Canada Netherlands

In The Last Decade

Michael T. Geraghty

114 papers receiving 3.5k citations

Peers

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

#	Work	Indexed citations
1	Low-level direct currents eradicate multi-drug-resistant Candidozyma auris through physiological stress and antifungal permeation 2025 ·Chemical Engineering Journal ·C. Royo,Charles Landis,Michael T. Geraghty,(unknown),Tagbo H. R. Niepa	1
2	Raman amplifier based on stimulated Raman scattering in a methane-filled hollow core fiber 2024 ·Optics Express ·(unknown),Michael T. Geraghty,(unknown),Andrew P. Ongstad,(unknown)	0
3	A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency 2021 ·European Journal of Human Genetics ·Matthew A. Lines,Alexanne Cuillerier,Pranesh Chakraborty,Thierry Naas,(unknown),Jean Michaud,Chantal A. Pileggi,Mary‐Ellen Harper,Yan Burelle,Tomi L. Toler,Neal Sondheimer,Heather P. Crawford,Francisca Millan,Michael T. Geraghty	4
4	Hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome in pregnancy: Considerations for management and review of the literature 2019 ·JIMD Reports ·(unknown),Jennifer MacKenzie,Jagdeep S. Walia,Michael T. Geraghty,Graeme N. Smith,(unknown),Andrea Guerin	4
5	Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment 2017 ·JIMD Reports ·Paula J. Waters,Thomas M. Kitzler,Annette Feigenbaum,Michael T. Geraghty,Osama Y. Al-Dirbashi,Patrick Bhérer,Christiane Auray‐Blais,Serge Gravel,(unknown),Komudi Siriwardena,Yannis Trakadis,Catherine Brunel‐Guitton,Walla Al‐Hertani	12
6	Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) Deficiency 2016 ·JIMD Reports ·(unknown),Amanda Smith,Skye McBride,Julien Marcadier,Jean Michaud,Osama Y. Al-Dirbashi,Jeremy Schwartzentruber,Chandree L. Beaulieu,Sherri L. Katz,Jacek Majewski,Dennis E. Bulman,Michael T. Geraghty,Mary‐Ellen Harper,Pranesh Chakraborty,Matthew A. Lines	16
7	Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome 2015 ·Human Genetics ·Martine Tétreault,Somayyeh Fahiminiya,Hana Antonická,Grant A. Mitchell,Michael T. Geraghty,Matthew A. Lines,Kym M. Boycott,Eric A. Shoubridge,John J. Mitchell,Jacques L. Michaud,Jacek Majewski	44
8	Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease 2014 ·BMC Medical Genetics ·Hugh J. McMillan,Jeremy Schwartzentruber,Amanda Smith,(unknown),Pranesh Chakraborty,Dennis E. Bulman,Chandree L. Beaulieu,Jacek Majewski,Kym M. Boycott,Michael T. Geraghty	33
9	Congenital Visual Impairment and Progressive Microcephaly Due to Lysyl–Transfer Ribonucleic Acid (RNA) Synthetase (KARS) Mutations 2014 ·Journal of Child Neurology ·Hugh J. McMillan,Peter Humphreys,Amanda Smith,Jeremy Schwartzentruber,Pranesh Chakraborty,Dennis E. Bulman,Chandree L. Beaulieu,Jacek Majewski,Kym M. Boycott,Michael T. Geraghty	36
10	A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3 2013 ·Brain ·Sheena Chew,Ravikumar Balasubramanian,Wai‐Man Chan,Peter B. Kang,Caroline Andrews,Bryn D. Webb,Sarah MacKinnon,Darren T. Oystreck,Jessica K. Rankin,Thomas O. Crawford,Michael T. Geraghty,Scott L. Pomeroy,William F. Crowley,Ethylin Wang Jabs,David G. Hunter,P. Ellen Grant,Elizabeth C. Engle	81
11	Autosomal recessive hereditary spastic paraplegia—clinical and genetic characteristics of a well-defined cohort 2013 ·Neurogenetics ·Grace Yoon,Berivan Baskin,Mark A. Tarnopolsky,Kym M. Boycott,Michael T. Geraghty,Erick Sell,Sharan Goobie,Wendy S. Meschino,Brenda Banwell,Peter N. Ray	26
12	Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria 2013 ·Orphanet Journal of Rare Diseases ·Julien Marcadier,Amanda M. Smith,Daniela Pohl,Jeremy Schwartzentruber,Osama Y. Al-Dirbashi,Jacek Majewski,Sacha Ferdinandusse,Ronald J. A. Wanders,Dennis E. Bulman,Kym M. Boycott,Pranesh Chakraborty,Michael T. Geraghty	31
13	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 2012 ·Genetics in Medicine ·Beth K. Potter,Pranesh Chakraborty,Jonathan B. Kronick,Kumanan Wilson,Doug Coyle,Annette Feigenbaum,Michael T. Geraghty,(unknown),Julian Little,(unknown),John J. Mitchell,Komudi Siriwardena,Brenda J. Wilson,Ania Syrowatka	21
14	Developing a National Newborn Screening Strategy for Canada 2010 ·uO Research (University of Ottawa) ·Kumanan Wilson,Shelley Kennedy,Beth K. Potter,Michael T. Geraghty,Pranesh Chakraborty	13
15	Paternal isodisomy of chromosome 2 as a cause of long chain 3‐hydroxyacyl‐CoA dehydrogenase (LCHAD) deficiency 2010 ·American Journal of Medical Genetics Part A ·Berivan Baskin,Michael T. Geraghty,Peter N. Ray	12
16	GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome 2001 ·American Journal of Medical Genetics ·Madeline Li,Cheryl Shuman,(unknown),Eva Maria Cutiongco,Harvey A. Bender,(unknown),Louise Wilkins‐Haug,(unknown),Siu Li Yong,Michael T. Geraghty,Jeremy A. Squire,Rosanna Weksberg	87
17	Undiagnosed maternal phenylketonuria: The need for prenatal selective screening or case finding 1999 ·American Journal of Obstetrics and Gynecology ·William Hanley,(unknown),(unknown),Neil R.M. Buist,Michael T. Geraghty,(unknown),Margaret E. O’Flynn,William J. Rhead,(unknown),(unknown)	13
18	Multiple Molecular Mechanisms Underlying Subdiagnostic Variants of Marfan Syndrome 1998 ·The American Journal of Human Genetics ·Robert A. Montgomery,Michael T. Geraghty,(unknown),(unknown),(unknown),Iain McIntosh,Clair A. Francomano,Harry C. Dietz	68
19	Molecular Characterization of Saccharomyces cerevisiae Δ3,Δ2-Enoyl-CoA Isomerase 1998 ·Journal of Biological Chemistry ·Brian V. Geisbrecht,(unknown),Kerstin Schulz,Katja Nau,James C. Morrell,Michael T. Geraghty,Horst Schulz,Ralf Erdmann,Stephen J. Gould	55
20	Isolation and Characterization of an Ornithine Aminotransferase-Related Sequence (OATL3) Mapping to 10q26 1993 ·Genomics ·Michael T. Geraghty,W.G. Kearns,P. Pearson,David Valle	3

About Michael T. Geraghty

Michael T. Geraghty is a scholar working on Clinical Biochemistry, Genetics and Biochemistry, having authored 121 papers that have together received 3.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (38 papers), Mitochondrial Function and Pathology (14 papers) and Genomics and Rare Diseases (12 papers). The work is most often cited by research in Clinical Biochemistry (913 citations), Genetics (896 citations) and Molecular Biology (1.9k citations). Michael T. Geraghty has collaborated with scholars based in United States, Canada and Netherlands. Frequent 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. Their work appears in journals such as Journal of Biological Chemistry, Blood and Brain.

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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