Patrick Ferreira

2.1k total citations
31 papers, 896 citations indexed

About

Patrick Ferreira is a scholar working on Molecular Biology, Physiology and Surgery. According to data from OpenAlex, Patrick Ferreira has authored 31 papers receiving a total of 896 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Physiology and 5 papers in Surgery. Recurrent topics in Patrick Ferreira's work include Metabolism and Genetic Disorders (5 papers), Lysosomal Storage Disorders Research (5 papers) and Glycosylation and Glycoproteins Research (4 papers). Patrick Ferreira is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Lysosomal Storage Disorders Research (5 papers) and Glycosylation and Glycoproteins Research (4 papers). Patrick Ferreira collaborates with scholars based in Canada, United States and United Kingdom. Patrick Ferreira's co-authors include William R. de Araújo, Vanessa N. Ataide, Lúcio Angnes, Wendell K. T. Coltro, C Chagas, Thiago R. L. C. Paixão, Moira Chan‐Yeung, Jiří Fröhlich, Michael Schulzer and Francis Y.M. Choy and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and Annals of Surgery.

In The Last Decade

Patrick Ferreira

30 papers receiving 861 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick Ferreira Canada 18 386 200 146 143 127 31 896
Eizo Marutani United States 20 662 1.7× 278 1.4× 134 0.9× 38 0.3× 87 0.7× 40 1.6k
Manuel Melo Pires Portugal 25 956 2.5× 233 1.2× 137 0.9× 172 1.2× 110 0.9× 86 2.0k
Daniel Winnica United States 15 409 1.1× 319 1.6× 47 0.3× 27 0.2× 64 0.5× 21 1.0k
Naoki Mizutani Japan 17 272 0.7× 119 0.6× 142 1.0× 19 0.1× 83 0.7× 65 790
Fereshteh Moradi Canada 15 575 1.5× 163 0.8× 45 0.3× 57 0.4× 72 0.6× 32 1.0k
Holly C. Williams United States 16 642 1.7× 154 0.8× 24 0.2× 101 0.7× 65 0.5× 25 1.4k
Dan L. Li United States 15 545 1.4× 130 0.7× 28 0.2× 64 0.4× 217 1.7× 26 1.3k
Naoko Fujita Japan 20 277 0.7× 83 0.4× 64 0.4× 24 0.2× 40 0.3× 56 933
Iraida Sharina United States 20 595 1.5× 609 3.0× 29 0.2× 47 0.3× 134 1.1× 40 1.6k
Toshio Kaneko Japan 20 310 0.8× 249 1.2× 54 0.4× 39 0.3× 91 0.7× 80 1.5k

Countries citing papers authored by Patrick Ferreira

Since Specialization
Citations

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

Fields of papers citing papers by Patrick Ferreira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick Ferreira. 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 Patrick Ferreira. The network helps show where Patrick Ferreira may publish in the future.

Co-authorship network of co-authors of Patrick Ferreira

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

All Works

20 of 20 papers shown
1.
2.
Benson, Matthew D., Paul R. Freund, James R. Lewis, et al.. (2020). Severe retinal degeneration in a patient with Canavan disease. Ophthalmic Genetics. 42(1). 75–78. 5 indexed citations
3.
Bashir, Rani A., Abhijit Dixit, Jillian S. Parboosingh, et al.. (2017). Lin‐Gettig syndrome: Craniosynostosis expands the spectrum of the KAT6B related disorders. American Journal of Medical Genetics Part A. 173(10). 2596–2604. 11 indexed citations
4.
Ferreira, Patrick, et al.. (2017). Hypertryptophanemia due to tryptophan 2,3-dioxygenase deficiency. Molecular Genetics and Metabolism. 120(4). 317–324. 25 indexed citations
5.
Ferreira, Patrick, Alicia Chan, & Barry Wolf. (2017). Irreversibility of Symptoms with Biotin Therapy in an Adult with Profound Biotinidase Deficiency. JIMD Reports. 36. 117–120. 19 indexed citations
6.
Webster, Duncan, Chris Smith, David S. Sinasac, et al.. (2017). ALG9-CDG: New clinical case and review of the literature. Molecular Genetics and Metabolism Reports. 13. 55–63. 18 indexed citations
7.
Ferreira, Patrick, Sarah L. Sawyer, Jorge Dávila, et al.. (2015). Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblings. Neurology Genetics. 2(1). e38–e38. 13 indexed citations
8.
Dyment, David A., Martine Tétreault, Chandree L. Beaulieu, et al.. (2014). Whole‐exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study. Clinical Genetics. 88(1). 34–40. 64 indexed citations
9.
Kevelam, Sietske H., Richard J. Rodenburg, Nicole I. Wolf, et al.. (2013). NUBPL mutations in patients with complex I deficiency and a distinct MRI pattern. Neurology. 80(17). 1577–1583. 61 indexed citations
10.
Ferrè, Silvia, Jeroen H. F. de Baaij, Patrick Ferreira, et al.. (2013). Mutations in PCBD1 Cause Hypomagnesemia and Renal Magnesium Wasting. Journal of the American Society of Nephrology. 25(3). 574–586. 54 indexed citations
11.
Choy, Francis Y.M., Weimin Zhang, Huiping Shi, et al.. (2006). Gaucher disease among Chinese patients: Review on genotype/phenotype correlation from 29 patients and identification of novel and rare alleles. Blood Cells Molecules and Diseases. 38(3). 287–293. 49 indexed citations
12.
Sinclair, Graham, Francis Y.M. Choy, & Patrick Ferreira. (2001). Heterologous Expression and Characterization of a Rare Gaucher Disease Mutation (c.481C > T) from a Canadian Aboriginal Population Using Archival Tissue Samples. Molecular Genetics and Metabolism. 74(3). 345–352. 5 indexed citations
13.
Thöny, Beat, L. Kierat, M. Blaskovics, et al.. (1998). Hyperphenylalaninemia with High Levels of 7-Biopterin is Associated with Mutations in the PCBD Gene Encoding the Bifunctional Protein Pterin-4a-Carbinolamine Dehydratase and Transcriptional Coactivator (DCoH). The American Journal of Human Genetics. 62(6). 1302–1311. 40 indexed citations
14.
Tomatsu, Shunji, Seiji Fukuda, Alan Cooper, et al.. (1997). Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene. Human Mutation. 10(5). 368–375. 35 indexed citations
15.
Choy, Francis Y.M., et al.. (1997). Novel insertion mutation in a non-Jewish Caucasian type 1 Gaucher disease patient. American Journal of Medical Genetics. 68(2). 211–215. 15 indexed citations
16.
Bayever, Eliel, Naynesh Kamani, Patrick Ferreira, et al.. (1992). Bone marrow transplantation for Niemann‐Pick Type IA disease. Journal of Inherited Metabolic Disease. 15(6). 919–928. 25 indexed citations
17.
Waterman, Michael R., et al.. (1989). Identification of a common molecular basis for combined 17?-hydroxylase/17,20-lyase deficiency in two Mennonite families. Human Genetics. 82(3). 285–286. 32 indexed citations
18.
Winter, Jeremy S.D., J. Müller, Y. S. PERRY, et al.. (1989). Combined 17-Hydroxylase and 17,20-Desmolase Deficiencies: Evidence for Synthesis of a Defective Cytochrome P450c17*. The Journal of Clinical Endocrinology & Metabolism. 68(2). 309–316. 32 indexed citations
19.
Ferreira, Patrick, et al.. (1980). Assessment of the Amylase-Creatinine Clearance Ratio in Postoperative Patients. Annals of Surgery. 192(2). 195–198. 4 indexed citations
20.
Ferreira, Patrick, et al.. (1979). Clinical laboratory evaluation of the Orion SS‐20 ionized calcium analyser. Journal of Analytical Methods in Chemistry. 1(2). 94–102. 13 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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