D. Ross McLeod

3.4k total citations
41 papers, 1.3k citations indexed

About

D. Ross McLeod is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, D. Ross McLeod has authored 41 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in D. Ross McLeod's work include Genomic variations and chromosomal abnormalities (4 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). D. Ross McLeod is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). D. Ross McLeod collaborates with scholars based in Canada, United States and United Kingdom. D. Ross McLeod's co-authors include Alan H. Fielding, D. Philip Whitfield, Paul F. Haworth, Kym M. Boycott, Jillian S. Parboosingh, Stephen R. Williams, Sarah H. Elsea, Fahed Halal, R. Ellen Magenis and Vazken M. Der Kaloustian and has published in prestigious journals such as The American Journal of Human Genetics, Biological Conservation and Investigative Ophthalmology & Visual Science.

In The Last Decade

D. Ross McLeod

40 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. Ross McLeod Canada 17 502 462 208 172 171 41 1.3k
Jodie N. Painter Australia 22 606 1.2× 664 1.4× 274 1.3× 140 0.8× 30 0.2× 50 1.8k
Maria Denaro Italy 20 655 1.3× 430 0.9× 192 0.9× 40 0.2× 39 0.2× 52 1.8k
Brian A. Gray United States 20 517 1.0× 567 1.2× 51 0.2× 164 1.0× 42 0.2× 38 1.1k
Roelof‐Jan Oostra Netherlands 27 857 1.7× 466 1.0× 55 0.3× 194 1.1× 61 0.4× 118 2.0k
Lisa M. Davis United States 21 479 1.0× 234 0.5× 67 0.3× 49 0.3× 83 0.5× 38 1.2k
Yoshihiro Hayashi Japan 22 493 1.0× 186 0.4× 41 0.2× 125 0.7× 140 0.8× 121 1.5k
Matthías Kormáksson United States 12 1.4k 2.9× 410 0.9× 49 0.2× 136 0.8× 138 0.8× 21 2.0k
J. W. Kuiper Netherlands 23 555 1.1× 183 0.4× 101 0.5× 38 0.2× 40 0.2× 48 1.6k
Norman J. Wilsman United States 27 865 1.7× 536 1.2× 34 0.2× 63 0.4× 65 0.4× 53 2.1k
Klaudia Walter United Kingdom 18 1.1k 2.1× 578 1.3× 97 0.5× 45 0.3× 75 0.4× 29 1.7k

Countries citing papers authored by D. Ross McLeod

Since Specialization
Citations

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

Fields of papers citing papers by D. Ross McLeod

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. Ross McLeod. 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 D. Ross McLeod. The network helps show where D. Ross McLeod may publish in the future.

Co-authorship network of co-authors of D. Ross McLeod

This figure shows the co-authorship network connecting the top 25 collaborators of D. Ross McLeod. A scholar is included among the top collaborators of D. Ross McLeod 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 D. Ross McLeod. D. Ross McLeod 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.
Loucks, Catrina M., Jillian S. Parboosingh, Jessica X. Chong, et al.. (2012). A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch‐German) Mennonite and Hutterite patients in North America. American Journal of Medical Genetics Part A. 158A(5). 1229–1232. 8 indexed citations
2.
Williams, Stephen R., Micheala A. Aldred, Vazken M. Der Kaloustian, et al.. (2010). Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems. The American Journal of Human Genetics. 87(2). 219–228. 216 indexed citations
3.
Thompson, Matthew, Rafael Perera, Richard Mayon‐White, et al.. (2008). Deriving temperature and age appropriate heart rate centiles for children with acute infections. Archives of Disease in Childhood. 94(5). 361–365. 47 indexed citations
4.
Boycott, Kym M., Jillian S. Parboosingh, R. Brian Lowry, et al.. (2008). Clinical genetics and the Hutterite population: A review of Mendelian disorders. American Journal of Medical Genetics Part A. 146A(8). 1088–1098. 33 indexed citations
5.
Leung, Alexander K. C., et al.. (2007). Dominantly‐inherited lop ears. American Journal of Medical Genetics Part A. 143A(19). 2330–2333. 4 indexed citations
6.
Boycott, Kym M., Jillian S. Parboosingh, James N. Scott, et al.. (2007). Meckel syndrome in the Hutterite population is actually a Joubert‐related cerebello‐oculo‐renal syndrome. American Journal of Medical Genetics Part A. 143A(15). 1715–1725. 16 indexed citations
7.
Glass, Hannah C., Kym M. Boycott, Coleen Adams, et al.. (2005). Autosomal recessive cerebellar hypoplasia in the Hutterite population. Developmental Medicine & Child Neurology. 47(10). 691–691. 28 indexed citations
8.
Boycott, Kym M., Alexandre Bureau, Hannah C. Glass, et al.. (2005). Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification. The American Journal of Human Genetics. 77(3). 477–483. 151 indexed citations
9.
Aretz, Stefan, Dietlinde Stienen, Siegfried Uhlhaas, et al.. (2005). High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. Human Mutation. 26(6). 513–519. 174 indexed citations
10.
Lowry, R. Brian, A. Micheil Innes, François P. Bernier, et al.. (2003). Bowen–Conradi syndrome: A clinical and genetic study. American Journal of Medical Genetics Part A. 120A(3). 423–428. 21 indexed citations
11.
Whitfield, D. Philip, Alan H. Fielding, D. Ross McLeod, & Paul F. Haworth. (2003). The effects of persecution on age of breeding and territory occupation in golden eagles in Scotland. Biological Conservation. 118(2). 249–259. 85 indexed citations
12.
Biswas, Susmito, et al.. (2002). Two Forms of Corneal Endothelial Dystrophy Caused by Mutations in COL8A2: The Gene Encoding the Alpha-2 Chain of Type VIII Collagen. Investigative Ophthalmology & Visual Science. 43(13). 2874–2874. 2 indexed citations
13.
McLeod, D. Ross, Floyd F. Snyder, Peter J. Bridge, & Alfredo Pinto. (2002). Acute hemorrhagic leukoencephalitis in male sibs. American Journal of Medical Genetics. 107(4). 325–329.
14.
McLeod, D. Ross, Albert Akierman, & C Trevenen. (2001). Combination of renal agenesis with respiratory and alimentary tract atresia results in normal lung development. American Journal of Medical Genetics. 102(4). 327–329. 2 indexed citations
15.
Pitkänen, Sari, et al.. (1996). Familial Cardiomyopathy with Cataracts and Lactic Acidosis: A Defect in Complex I (NADH-Dehydrogenase) of the Mitochondria Respiratory Chain. Pediatric Research. 39(3). 513–521. 55 indexed citations
16.
McLeod, D. Ross & Stuart G. Coupland. (1992). Asymmetry quantification utilizing hand radiographs. American Journal of Medical Genetics. 44(3). 321–325. 7 indexed citations
17.
Fung, Ernest, et al.. (1991). Dihydropyrimidine Dehydrogenase Deficiency in a Hutterite Newborn. Advances in experimental medicine and biology. 309B. 311–314. 2 indexed citations
18.
McLeod, D. Ross, et al.. (1989). Autosomal dominant hypoparathyroidism with intracranial calcification outside the basal ganglia. American Journal of Medical Genetics. 32(1). 32–35. 8 indexed citations
19.
McLeod, D. Ross, et al.. (1989). A pseudoisochromosome 18q and an isodicentric chromosome 18*. Clinical Genetics. 35(6). 450–454. 7 indexed citations
20.
Butler, Merlin G., Mark A. Fletcher, F. John Meaney, et al.. (1988). Metacarpophalangeal pattern profile analysis in fragile X syndrome. American Journal of Medical Genetics. 31(4). 767–773. 11 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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