Yolanda Lillquist

478 total citations
17 papers, 250 citations indexed

About

Yolanda Lillquist is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yolanda Lillquist has authored 17 papers receiving a total of 250 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Clinical Biochemistry, 7 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yolanda Lillquist's work include Metabolism and Genetic Disorders (11 papers), Neonatal Health and Biochemistry (5 papers) and Amino Acid Enzymes and Metabolism (4 papers). Yolanda Lillquist is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Neonatal Health and Biochemistry (5 papers) and Amino Acid Enzymes and Metabolism (4 papers). Yolanda Lillquist collaborates with scholars based in Canada, United States and Switzerland. Yolanda Lillquist's co-authors include Paula J. Waters, Hilary Vallance, A. George F. Davidson, Sylvia Stöckler‐Ipsiroglu, Majid Alfadhel, Graham Sinclair, Gabriella Horváth, Ramona Salvarinova, S. E. Olpin and Cheryl R. Greenberg and has published in prestigious journals such as Annals of Neurology, Molecular Genetics and Metabolism and Journal of Inherited Metabolic Disease.

In The Last Decade

Yolanda Lillquist

16 papers receiving 239 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yolanda Lillquist Canada 10 146 121 52 46 40 17 250
James R. Bonham United Kingdom 9 180 1.2× 171 1.4× 34 0.7× 44 1.0× 36 0.9× 20 302
Catherine Lynn T. Silao Philippines 9 124 0.8× 79 0.7× 61 1.2× 43 0.9× 85 2.1× 33 287
Mary Anne D. Chiong Philippines 10 142 1.0× 168 1.4× 55 1.1× 54 1.2× 41 1.0× 31 295
Brian J. Shayota United States 10 109 0.7× 127 1.0× 35 0.7× 43 0.9× 29 0.7× 23 321
Satoko Hirano Japan 10 149 1.0× 222 1.8× 38 0.7× 32 0.7× 75 1.9× 19 358
Viola Prietsch Germany 9 104 0.7× 139 1.1× 36 0.7× 33 0.7× 54 1.4× 11 256
G. Sabetta Italy 11 145 1.0× 103 0.9× 66 1.3× 43 0.9× 41 1.0× 29 279
Stephanie J. DeWard United States 8 152 1.0× 210 1.7× 32 0.6× 98 2.1× 35 0.9× 11 372
Mika Ishige Japan 8 155 1.1× 148 1.2× 29 0.6× 23 0.5× 16 0.4× 24 264
Asif Paker United States 5 58 0.4× 116 1.0× 19 0.4× 46 1.0× 23 0.6× 9 193

Countries citing papers authored by Yolanda Lillquist

Since Specialization
Citations

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

Fields of papers citing papers by Yolanda Lillquist

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yolanda Lillquist

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

All Works

17 of 17 papers shown
1.
Stöckler‐Ipsiroglu, Sylvia, Nataliya Yuskiv, Ramona Salvarinova, et al.. (2014). Individualized long-term outcomes in blood phenylalanine concentrations and dietary phenylalanine tolerance in 11 patients with primary phenylalanine hydroxylase (PAH) deficiency treated with Sapropterin-dihydrochloride. Molecular Genetics and Metabolism. 114(3). 409–414. 6 indexed citations
2.
Salvarinova, Ramona, et al.. (2013). Long-term outcomes of blood phenylalanine concentrations in children with classical phenylketonuria. Molecular Genetics and Metabolism. 108(4). 255–258. 10 indexed citations
3.
Davidson, A. George F., Mark Chilvers, & Yolanda Lillquist. (2012). Effects of a Pseudomonas aeruginosa eradication policy in a cystic fibrosis clinic. Current Opinion in Pulmonary Medicine. 18(6). 615–621. 10 indexed citations
4.
Salvarinova, Ramona, Graham Sinclair, David Dix, et al.. (2012). The use of parenteral nutrition for the management of PKU patient undergoing chemotherapy for lymphoma: A case report. Molecular Genetics and Metabolism. 105(4). 571–574. 6 indexed citations
5.
Lillquist, Yolanda, et al.. (2011). Economic effects of an eradication protocol for first appearance of Pseudomonas aeruginosa in cystic fibrosis patients: 1995 vs. 2009. Journal of Cystic Fibrosis. 10(3). 175–180. 21 indexed citations
6.
Alfadhel, Majid, Yolanda Lillquist, Paula J. Waters, et al.. (2011). Infantile cardioencephalopathy due to a COX15 gene defect: Report and review. American Journal of Medical Genetics Part A. 155(4). 840–844. 26 indexed citations
7.
Alfadhel, Majid, Yolanda Lillquist, Cynthia J. Davis, Anne Junker, & Sylvia Stöckler‐Ipsiroglu. (2011). Eighteen‐year follow‐up of a patient with cobalamin F disease (cblF): Report and review. American Journal of Medical Genetics Part A. 155(10). 2571–2577. 16 indexed citations
8.
Alfadhel, Majid, Siu Li Yong, Yolanda Lillquist, & Sylvie Langlois. (2011). Precocious Puberty in Two Girls With PEHO Syndrome: A Clinical Feature Not Previously Described. Journal of Child Neurology. 26(7). 851–857. 9 indexed citations
9.
Greenberg, Cheryl R., Louise A. Dilling, Gilbert R. Thompson, et al.. (2009). The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations. Molecular Genetics and Metabolism. 96(4). 201–207. 59 indexed citations
10.
Scholl‐Bürgi, Sabine, Stanley H. Korman, Derek A. Applegarth, et al.. (2008). The relation of cerebrospinal fluid and plasma glycine levels in propionic acidaemia, a ‘ketotic hyperglycinaemia’. Journal of Inherited Metabolic Disease. 31(3). 395–398. 7 indexed citations
11.
Horváth, Gabriella, Sylvia Stöckler‐Ipsiroglu, Ramona Salvarinova, et al.. (2008). Autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia: Evidence of a phenotypic continuum between dominant and recessive forms. Molecular Genetics and Metabolism. 94(1). 127–131. 30 indexed citations
12.
Horváth, Gabriella, A. George F. Davidson, Sylvia Stöckler‐Ipsiroglu, et al.. (2008). Newborn Screening for MCAD Deficiency. Canadian Journal of Public Health. 99(4). 276–280. 17 indexed citations
13.
Davidson, A. George F., et al.. (2007). 250* Can physiological parameters determine the optimal method of airway clearance for the individual patient with cystic fibosis?. Journal of Cystic Fibrosis. 6. S62–S62. 1 indexed citations
14.
Waters, Paula J., Minesh Khashu, Yolanda Lillquist, et al.. (2005). Neonatal hyperphenylalaninemia, perinatal hemochromatosis, and renal tubulopathy: A unique patient or a novel metabolic disorder?. Molecular Genetics and Metabolism. 86. 148–152. 4 indexed citations
15.
Demos, Michelle, Paula J. Waters, Hilary Vallance, et al.. (2005). 6‐Pyruvoyl‐tetrahydropterin synthase deficiency with mild hyperphenylalaninemia. Annals of Neurology. 58(1). 164–167. 9 indexed citations
16.
Makhseed, Nawal, Hilary Vallance, Murray Potter, et al.. (2004). Carnitine transporter defect due to a novel mutation in the SLC22A5 gene presenting with peripheral neuropathy. Journal of Inherited Metabolic Disease. 27(6). 778–780. 19 indexed citations
17.
Sirrs, Sandra, et al.. (2003). Orthotopic liver transplantation in a patient with carbamyl phosphate synthetase deficiency and cystic fibrosis. Paediatrics & Child Health. 8(8). 497–498.

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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