Eileen P. Treacy

4.1k citations

102 papers · 2.6k indexed · h-index 31

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Biochemistry top 1%
- Amino Acid Enzymes and Metabolism

Papers in

Clinical Biochemistry 73
- Metabolism and Genetic Disorders 73
Biochemistry 20
- Amino Acid Enzymes and Metabolism 17

Co-authors: Orval Mamer C. R. Scriver Charles R. Scriver Susan Byck Deborah M. Lambert Paula J. Waters Ina Knerr Karen P. Coss
Journals: Journal of Inherited Metabolic Disease (12 papers)Molecular Genetics and Metabolism (7 papers)Orphanet Journal of Rare Diseases (6 papers)European Journal of Human Genetics (6 papers)The Journal of Pediatrics (5 papers)
Partner nations: Ireland Canada United Kingdom

In The Last Decade

Eileen P. Treacy

98 papers receiving 2.6k citations

Peers

Countries citing papers authored by Eileen P. Treacy

Since Specialization

Citations

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

Fields of papers citing papers by Eileen P. Treacy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eileen P. Treacy. 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 Eileen P. Treacy. The network helps show where Eileen P. Treacy may publish in the future.

Co-authors

The 25 scholars most cited alongside Eileen P. Treacy, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eileen P. Treacy Line = papers co-authored together Eileen P. Treacy links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Clinical and Developmental Outcomes After 50 Years of Newborn Bloodspot Screening for Classical Galactosaemia in the Republic of Ireland JIMD Reports ·D. Pereira, Elizabeth F. Loftus, Charlotte Thompson, Fiona Boyle, Jennifer McNulty, Ritma Boruah, Ellen Crushell, C. B. Howard, Joanne Hughes, Ahmad Monavari, Eileen P. Treacy, Aidan Beegan, Norah Jordan, Y. Rogers, A. Collins, Jennifer J. Brady, Mohamed Elsammak, Philip Mayne, Ina Knerr	2025	0
2	The role of primary care in management of rare diseases in Ireland Irish Journal of Medical Science (1971 -) ·Niall Byrne, Jacqueline A. Turner, Rita Marron, Deborah M. Lambert, Daniel N. Murphy, Grace O‘Sullivan, Maureen Mason, F. W. Broderick, Mary Burke, Sheila C. Casey, Marguerite Doyle, David Gibney, Fergus Mason, David Molony, Deirdre Ormond, Colm O’ Sé, Conor O’Shea, Eileen P. Treacy	2020	18
3	Long‐term outcomes in a 25‐year‐old female affected with lipin‐1 deficiency JIMD Reports ·Karolina M. Stępień, Wolfgang M. Schmidt, Reginald E. Bittner, Orna O’Toole, Brian McNamara, Eileen P. Treacy	2019	15
4	Profiling of intracellular metabolites produced from galactose and its potential for galactosemia research Orphanet Journal of Rare Diseases ·Michel van Weeghel, Lindsey Welling, Eileen P. Treacy, Ronald J. A. Wanders, Sacha Ferdinandusse, Annet M. Bosch	2018	3
5	Fertility in classical galactosaemia, a study of N-glycan, hormonal and inflammatory gene interactions Orphanet Journal of Rare Diseases ·Hugh-Owen Colhoun, M. Estela Rubio‐Gozalbo, Annet M. Bosch, Ina Knerr, Charlotte Dawson, Jennifer J. Brady, Marie Galligan, Karolina M. Stępień, Róisín O’Flaherty, Chloe Moss, Peter Barker, Maria Fitzgibbon, Peter Doran, Eileen P. Treacy	2018	16
6	Two Uneventful Pregnancies in a Woman with Glutaric Aciduria Type 1 JIMD Reports ·Karolina M. Stępień, Gregory M. Pastores, Una Hendroff, Ciara McCormick, Patricia Fitzimons, Naveed Khawaja, Ingrid Borovickova, Eileen P. Treacy	2018	6
7	Classical Galactosaemia and CDG, the N-Glycosylation Interface. A Review JIMD Reports ·Ashwini Maratha, Hugh-Owen Colhoun, Ina Knerr, Karen P. Coss, Peter Doran, Eileen P. Treacy	2016	21
8	Clinical utility gene card for: Trimethylaminuria European Journal of Human Genetics ·Elizabeth A. Shephard, Eileen P. Treacy, Ian Phillips	2011	15
9	IgG N-glycans as potential biomarkers for determining galactose tolerance in Classical Galactosaemia Molecular Genetics and Metabolism ·Karen P. Coss, Jennifer C. Byrne, David Coman, B Adamczyk, Jodie L. Abrahams, Radka Saldova, Andrew Brown, Olivia Walsh, Una Hendroff, C. Carolan, Pauline M. Rudd, Eileen P. Treacy	2011	52
10	Safety and efficacy of 22 weeks of treatment with sapropterin dihydrochloride in patients with phenylketonuria American Journal of Medical Genetics Part A ·Phillip Lee, Eileen P. Treacy, Eric Crombez, Melissa Wasserstein, Lewis Waber, Jon A. Wolff, U. Wendel, Alex Dorenbaum, Judith D. Bebchuk, Heidi Christ‐Schmidt, Margretta R. Seashore, Marcello Giovannini, Barbara K. Burton, Andrew A. M. Morris	2008	79
11	Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutations Journal of Medical Genetics ·Helen Tuppen, Fabiana Fattori, Rosalba Carrozzo, Massimo Zeviani, S. DiMauro, Sara Seneca, Joanne Martindale, S E Olpin, Eileen P. Treacy, Robert McFarland, Filippo M. Santorelli, Rachael W. Taylor	2008	12
12	Long chain fatty acid oxidation defects in children: importance of detection and treatment options Irish Journal of Medical Science (1971 -) ·Breda Hayes, Branden J. Lynch, M O'Keefe, Ahmad Monavari, Eileen P. Treacy	2007	7
13	Fenofibrate raises plasma homocysteine levels in the fasted and fed states Atherosclerosis ·Rachel Bissonnette, Eileen P. Treacy, Rima Rozen, Betsie Boucher, Jeffrey S. Cohn, Jacques Genest	2001	55
14	Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia Genetics in Medicine ·Vibeke Westphal, Sandra M. Peterson, Marc C. Patterson, Anne Tournay, Andrea Blumenthal, Eileen P. Treacy, Hudson H. Freeze	2001	47
15	Short-chain hydroxyacyl–coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study The Journal of Pediatrics ·Eileen P. Treacy, Deborah M. Lambert, R. Bowling Barnes, Richard L. Boriack, Jerry Vockley, Laurie K. O'Brien, Peter M. Jones, Michael J. Bennett	2000	16
16	Trimethylaminuria Is Caused by Mutations of the FMO3 Gene in a North American Cohort Molecular Genetics and Metabolism ·Beverly R. Akerman, H. Lemass, Lionel M.L. Chow, Deborah M. Lambert, Cheryl R. Greenberg, Christine Bibeau, Orval Mamer, Eileen P. Treacy	1999	60
17	Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication Human Molecular Genetics ·Eileen P. Treacy	1998	171
18	Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype Correlations The American Journal of Human Genetics ·Emre Kayaalp, Eileen P. Treacy, Paula J. Waters, Susan Byck, Piotr Nowacki, Charles R. Scriver	1997	154
19	Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) Pediatric Neurology ·Michael Shevell, Patricia Colangelo, Eileen P. Treacy, Robert C. Polomeno, Bernard Rosenblatt	1996	15
20	Neurological complications of balloon angioplasty in children Pediatric Cardiology ·Eileen P. Treacy, W. Jack Duncan, Michael J. Tyrrell, Noel Lowry	1991	18

About Eileen P. Treacy

Eileen P. Treacy is a scholar working on Clinical Biochemistry, Biochemistry, Rheumatology, Pediatrics, Perinatology and Child Health and Physiology, having authored 102 papers that have together received 2.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (73 papers), Neonatal Health and Biochemistry (20 papers), Mitochondrial Function and Pathology (17 papers), Amino Acid Enzymes and Metabolism (17 papers), Folate and B Vitamins Research (16 papers), Diet and metabolism studies (13 papers), Biochemical and Molecular Research (7 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Clinical Biochemistry (1.4k citations), Biochemistry (390 citations), Rheumatology (566 citations), Pharmacology (217 citations) and Physiology (522 citations). Eileen P. Treacy has collaborated with scholars based in Ireland, Canada and United Kingdom. Frequent co-authors include Orval Mamer, C. R. Scriver, Charles R. Scriver, Susan Byck, Deborah M. Lambert, Paula J. Waters, Ina Knerr, Karen P. Coss, Beverly R. Akerman and Peter Doran. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, European Journal of Human Genetics and The Journal of Pediatrics.

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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