Louise A. Dilling

2.1k total citations
33 papers, 1.1k citations indexed

About

Louise A. Dilling is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Louise A. Dilling has authored 33 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Clinical Biochemistry, 13 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Louise A. Dilling's work include Metabolism and Genetic Disorders (16 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (8 papers) and Mitochondrial Function and Pathology (6 papers). Louise A. Dilling is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (8 papers) and Mitochondrial Function and Pathology (6 papers). Louise A. Dilling collaborates with scholars based in Canada, United States and France. Louise A. Dilling's co-authors include J. C. Haworth, Cheryl R. Greenberg, L.E. Seargeant, J. Edward King, Frances Booth, James C. Haworth, Albert E. Chudley, Paul Thornton, Charles A. Stanley and Betty Y.L. Hsu and has published in prestigious journals such as The Lancet, PEDIATRICS and Human Molecular Genetics.

In The Last Decade

Louise A. Dilling

33 papers receiving 992 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Louise A. Dilling Canada 20 420 394 241 140 134 33 1.1k
James C. Haworth Canada 19 268 0.6× 305 0.8× 156 0.6× 166 1.2× 120 0.9× 28 1.1k
C Kleinknecht France 20 130 0.3× 239 0.6× 287 1.2× 99 0.7× 179 1.3× 75 1.3k
Timos Valaes Greece 25 250 0.6× 661 1.7× 1.2k 4.8× 74 0.5× 212 1.6× 55 1.6k
Keith N. Drummond Canada 21 67 0.2× 264 0.7× 187 0.8× 97 0.7× 96 0.7× 38 1.3k
Dietrich Michalk Germany 21 64 0.2× 184 0.5× 222 0.9× 60 0.4× 173 1.3× 65 1.1k
Michel Tsimaratos France 22 55 0.1× 550 1.4× 349 1.4× 104 0.7× 244 1.8× 67 1.7k
Rachel Becker‐Cohen Israel 18 87 0.2× 417 1.1× 148 0.6× 41 0.3× 46 0.3× 36 1.1k
Piers R. Blackett United States 20 85 0.2× 354 0.9× 106 0.4× 501 3.6× 160 1.2× 59 1.2k
L.C.K. Low Hong Kong 22 70 0.2× 165 0.4× 456 1.9× 502 3.6× 128 1.0× 65 1.5k
A Pruna France 14 45 0.1× 146 0.4× 167 0.7× 156 1.1× 89 0.7× 42 950

Countries citing papers authored by Louise A. Dilling

Since Specialization
Citations

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

Fields of papers citing papers by Louise A. Dilling

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louise A. Dilling. 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 Louise A. Dilling. The network helps show where Louise A. Dilling may publish in the future.

Co-authorship network of co-authors of Louise A. Dilling

This figure shows the co-authorship network connecting the top 25 collaborators of Louise A. Dilling. A scholar is included among the top collaborators of Louise A. Dilling 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 Louise A. Dilling. Louise A. Dilling 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.
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
2.
Innes, A. Micheil, Molly Seshia, Chitra Prasad, et al.. (2002). Congenital rickets caused by maternal vitamin D deficiency. Paediatrics & Child Health. 7(7). 455–458. 32 indexed citations
3.
Prip‐Buus, Carina, Laure Thuillier, Chitra Prasad, et al.. (2001). Molecular and Enzymatic Characterization of a Unique Carnitine Palmitoyltransferase 1A Mutation in the Hutterite Community. Molecular Genetics and Metabolism. 73(1). 46–54. 47 indexed citations
4.
Hsu, Betty Y.L., Andrea Kelly, Paul Thornton, et al.. (2001). Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome. The Journal of Pediatrics. 138(3). 383–389. 100 indexed citations
5.
6.
Greenberg, Cheryl R., David Reimer, Barbara L. Triggs‐Raine, et al.. (1995). A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I. Human Molecular Genetics. 4(3). 493–495. 54 indexed citations
7.
Seargeant, L.E., et al.. (1995). Cardiomyopathy in infancy and postmortem di diagnosis of a fatty acid oxidation defect. Clinical Biochemistry. 28(3). 324–324. 2 indexed citations
8.
9.
Moffatt, Michael, et al.. (1994). Vitamin D deficiency in a Manitoba community.. PubMed. 84(6). 394–6. 54 indexed citations
10.
Haworth, James C., France Demaugre, Frances Booth, et al.. (1992). Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite family. The Journal of Pediatrics. 121(4). 553–557. 28 indexed citations
11.
Seargeant, L.E., et al.. (1991). Primary oxaluria type 2 (l-glyceric aciduria): A rare cause of nephrolithiasis in children. The Journal of Pediatrics. 118(6). 912–914. 19 indexed citations
12.
Haworth, J. C., Frances Booth, Albert E. Chudley, et al.. (1991). Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds. The Journal of Pediatrics. 118(1). 52–58. 99 indexed citations
13.
Greenberg, Cheryl R., et al.. (1989). Newborn Screening for Galactosemia: A New Method Used in Manitoba. PEDIATRICS. 84(2). 331–335. 12 indexed citations
14.
Booth, Frances, J. C. Haworth, Louise A. Dilling, et al.. (1989). Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibship. The Journal of Pediatrics. 115(1). 81–88. 3 indexed citations
15.
Perry, Thomas L., Shirley Hansen, Frances Booth, et al.. (1988). An unusual aminoacidopathy associated with mitochondrial encephalomyopathy. Journal of Inherited Metabolic Disease. 12(1). 23–32. 3 indexed citations
16.
Haworth, J. C. & Louise A. Dilling. (1986). Vitamin-D-deficient rickets in Manitoba, 1972-84.. PubMed. 134(3). 237–41. 43 indexed citations
17.
Haworth, J. C. & Louise A. Dilling. (1976). Relationships between maternal glucose intolerance and neonatal blood glucose. The Journal of Pediatrics. 89(5). 810–813. 7 indexed citations
18.
Haworth, J. C., Louise A. Dilling, & D. Vidyasagar. (1973). Hypoglycemia in infants of diabetic mothers: Effect of epinephrine therapy. The Journal of Pediatrics. 82(1). 94–97. 6 indexed citations
19.
Younoszai, M. K., et al.. (1969). Urinary hydroxyproline: creatinine ratio in normal term, pre-term, and growth-retarded infants.. Archives of Disease in Childhood. 44(236). 517–520. 12 indexed citations
20.
Haworth, J. C., Louise A. Dilling, & M. K. Younoszai. (1967). RELATION OF BLOOD-GLUCOSE TO HÆMATOCRIT, BIRTHWEIGHT, AND OTHER BODY MEASUREMENTS IN NORMAL AND GROWTH-RETARDED NEWBORN INFANTS. The Lancet. 290(7522). 901–905. 23 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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