Donald T. Whelan

1.4k total citations
42 papers, 917 citations indexed

About

Donald T. Whelan is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Donald T. Whelan has authored 42 papers receiving a total of 917 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 15 papers in Clinical Biochemistry and 10 papers in Rheumatology. Recurrent topics in Donald T. Whelan's work include Metabolism and Genetic Disorders (15 papers), Amino Acid Enzymes and Metabolism (9 papers) and Folate and B Vitamins Research (8 papers). Donald T. Whelan is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Amino Acid Enzymes and Metabolism (9 papers) and Folate and B Vitamins Research (8 papers). Donald T. Whelan collaborates with scholars based in Canada, United States and United Kingdom. Donald T. Whelan's co-authors include Charles R. Scriver, Robert E. Hill, F Mohyuddin, Małgorzata J.M. Nowaczyk, C. R. Scriver, Susan Zeesman, Gerald Lancaster, W. M. Feldman, Irene A. Uchida and John S. Waye and has published in prestigious journals such as Nature, New England Journal of Medicine and PEDIATRICS.

In The Last Decade

Donald T. Whelan

41 papers receiving 847 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Donald T. Whelan Canada 20 488 243 224 166 141 42 917
N. J. Brandt Denmark 24 729 1.5× 147 0.6× 773 3.5× 216 1.3× 152 1.1× 66 1.4k
Brendan C. Lanpher United States 17 581 1.2× 465 1.9× 259 1.2× 120 0.7× 85 0.6× 41 1.2k
Alice Masurel‐Paulet France 15 344 0.7× 386 1.6× 164 0.7× 105 0.6× 79 0.6× 26 800
S. Lane Rutledge United States 19 844 1.7× 252 1.0× 519 2.3× 152 0.9× 66 0.5× 31 1.3k
David S. Sinasac Canada 20 665 1.4× 290 1.2× 572 2.6× 181 1.1× 155 1.1× 31 1.3k
Jennifer R. Toone Canada 17 600 1.2× 99 0.4× 627 2.8× 157 0.9× 306 2.2× 39 1.2k
V. Barash Israel 22 483 1.0× 172 0.7× 229 1.0× 163 1.0× 98 0.7× 49 1.1k
K. Tada Japan 24 889 1.8× 145 0.6× 939 4.2× 224 1.3× 339 2.4× 102 1.6k
Luísa Diogo Portugal 20 790 1.6× 304 1.3× 622 2.8× 143 0.9× 138 1.0× 71 1.4k
Shlomo Almashanu Israel 16 390 0.8× 136 0.6× 271 1.2× 134 0.8× 88 0.6× 45 838

Countries citing papers authored by Donald T. Whelan

Since Specialization
Citations

This map shows the geographic impact of Donald T. Whelan'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 Donald T. Whelan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Donald T. Whelan more than expected).

Fields of papers citing papers by Donald T. Whelan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Donald T. Whelan. 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 Donald T. Whelan. The network helps show where Donald T. Whelan may publish in the future.

Co-authorship network of co-authors of Donald T. Whelan

This figure shows the co-authorship network connecting the top 25 collaborators of Donald T. Whelan. A scholar is included among the top collaborators of Donald T. Whelan 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 Donald T. Whelan. Donald T. Whelan 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.
Whelan, Donald T., et al.. (2008). Mucolipidosis II. The clinical, radiological and biochemical features in three cases. Clinical Genetics. 24(2). 90–96. 5 indexed citations
2.
Zeesman, Susan, Lonnie Zwaigenbaum, Donald T. Whelan, et al.. (2004). Paternal transmission of fragile X syndrome. American Journal of Medical Genetics Part A. 129A(2). 184–189. 35 indexed citations
3.
Potter, Murray, Susan Zeesman, Keiko Kobayashi, et al.. (2004). Pregnancy in a healthy woman with untreated citrullinemia. American Journal of Medical Genetics Part A. 129A(1). 77–82. 10 indexed citations
4.
Nowaczyk, Małgorzata J.M., Susan Zeesman, Donald T. Whelan, Victoria Wright, & Sally Feather. (2003). Oral‐facial‐digital syndrome VII is oral‐facial‐digital syndrome I: A clarification. American Journal of Medical Genetics Part A. 123A(2). 179–182. 9 indexed citations
5.
Bagshaw, Richard D., Sunqu Zhang, Marie‐Anne Skomorowski, et al.. (2002). Novel mutations (Asn 484 Lys, Thr 500 Ala, Gly 438 Glu) in Morquio B disease. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1588(3). 247–253. 15 indexed citations
6.
Whelan, Donald T., et al.. (2001). Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada. American Journal of Medical Genetics. 102(1). 18–20. 32 indexed citations
7.
McGowan‐Jordan, Jean, Susan Zeesman, Donald T. Whelan, et al.. (2000). Detection of a de novo mutation in a family with SMA Type I: The importance of dosage testing. Genetics in Medicine. 2(1). 106–106.
8.
Nowaczyk, Małgorzata J.M., Donald T. Whelan, & Robert E. Hill. (1998). Smith-Lemli-Opitz syndrome: phenotypic extreme with minimal clinical findings. American Journal of Medical Genetics. 78(5). 419–423. 50 indexed citations
9.
Tomkins, Darrell J., Anne‐Françoise Roux, John S. Waye, et al.. (1996). Maternal Uniparental Isodisomy of Human Chromosome 14 Associated with a Paternal t(13q14q) and Precocious Puberty. European Journal of Human Genetics. 4(3). 153–159. 50 indexed citations
10.
Kaul, Rajinder, Guang Ping Gao, K. Michals, et al.. (1995). Novel (cys152>arg) missense mutation in an Arab patient with Canavan disease. Human Mutation. 5(3). 269–271. 22 indexed citations
11.
Tomkins, Darrell J., John S. Waye, & Donald T. Whelan. (1994). Maternal uniparental disomy of chromosome 14 in a boy with t(14q14q) associated with a paternal t(13q14q). The American Journal of Human Genetics. 55. 4 indexed citations
12.
Kronick, Jonathan B., Donald T. Whelan, & D. J. McCallion. (1987). Experimental hyperphenylalaninemia in the pregnant guinea pig: Possible phenylalanine teratogenesis and p‐chlorophenylalanine embryotoxicity. Teratology. 36(2). 245–258. 7 indexed citations
13.
Whelan, Donald T., et al.. (1983). Fumaric aciduria: a new organic aciduria, associated with mental retardation and speech impairment. Clinica Chimica Acta. 132(3). 301–308. 44 indexed citations
14.
Whelan, Donald T., et al.. (1979). Methylmalonic acidemia: 6 years' clinical experience with two variants unresponsive to vitamin B12 therapy.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 120(10). 1230–5. 19 indexed citations
15.
Whelan, Donald T., et al.. (1976). Citrullinemia: Phenotypic Variations. PEDIATRICS. 57(6). 935–941. 7 indexed citations
16.
Maijer, R., et al.. (1970). VITAMIN D DEPENDENCY: AN INHERITED POSTNATAL SYNDROME WITH SECONDARY HYPERPARATHYROIDISM. PEDIATRICS. 46(6). 871–880. 47 indexed citations
17.
Glorieux, Francis H., F Mohyuddin, Donald T. Whelan, & C. R. Scriver. (1970). Hypersarcosinemia: New Observations. Pediatric Research. 4(5). 450–450. 3 indexed citations
18.
Pashayan, Hermine M., et al.. (1969). Variability of the de Lange syndrome: Report of 3 cases and genetic analysis of 54 families. The Journal of Pediatrics. 75(5). 853–858. 29 indexed citations
19.
Klein, Marina B., Donald T. Whelan, C Clow, & C. R. Scriver. (1969). Urine Screening for Disorders of Mucopolysaccharide Metabolism. PEDIATRICS. 44(5). 768–769. 2 indexed citations
20.
Whelan, Donald T., Charles R. Scriver, & F Mohyuddin. (1969). Glutamic Acid Decarboxylase and Gamma-aminobutyric Acid in Mammalian Kidney. Nature. 224(5222). 916–917. 54 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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