Norma Leonard

1.0k total citations
30 papers, 520 citations indexed

About

Norma Leonard is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Norma Leonard has authored 30 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Pulmonary and Respiratory Medicine and 7 papers in Genetics. Recurrent topics in Norma Leonard's work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Neonatal Respiratory Health Research (3 papers). Norma Leonard is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Neonatal Respiratory Health Research (3 papers). Norma Leonard collaborates with scholars based in Canada, United States and Germany. Norma Leonard's co-authors include Darrell J. Tomkins, Alfred Rademaker, Renée H. Martin, Ravi Bhargava, Charlene M.T. Robertson, Cyril Gitiaux, Isabelle Desguerre, M. Kirwan, Tushar D. Bhagat and T. Vulliamy and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Pediatrics and Journal of Thoracic and Cardiovascular Surgery.

In The Last Decade

Norma Leonard

30 papers receiving 500 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Norma Leonard Canada 14 279 103 92 87 78 30 520
M. Gonzalés France 16 244 0.9× 131 1.3× 37 0.4× 47 0.5× 100 1.3× 38 617
Marie‐Claire Malinge France 14 264 0.9× 37 0.4× 113 1.2× 55 0.6× 66 0.8× 20 678
Maria Garofalo Italy 16 285 1.0× 119 1.2× 39 0.4× 73 0.8× 113 1.4× 32 799
Chin‐To Fong United States 11 282 1.0× 197 1.9× 58 0.6× 27 0.3× 35 0.4× 22 738
Chiara Di Bella Italy 13 291 1.0× 171 1.7× 67 0.7× 69 0.8× 139 1.8× 30 668
Michael J. Lyons United States 16 301 1.1× 302 2.9× 67 0.7× 35 0.4× 69 0.9× 41 737
Edmond G. Lemire Canada 14 240 0.9× 202 2.0× 142 1.5× 22 0.3× 67 0.9× 42 616
Carlos A. Saavedra‐Matiz United States 17 362 1.3× 116 1.1× 95 1.0× 146 1.7× 66 0.8× 21 736
Audrey Letourneau Switzerland 14 333 1.2× 171 1.7× 46 0.5× 27 0.3× 55 0.7× 20 622
Margo L. Whiteford United Kingdom 12 238 0.9× 239 2.3× 139 1.5× 28 0.3× 159 2.0× 17 627

Countries citing papers authored by Norma Leonard

Since Specialization
Citations

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

Fields of papers citing papers by Norma Leonard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Norma Leonard

This figure shows the co-authorship network connecting the top 25 collaborators of Norma Leonard. A scholar is included among the top collaborators of Norma Leonard 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 Norma Leonard. Norma Leonard 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.
Banerjee, Mayukh, Denis Arutyunov, Hanna Kolski, et al.. (2019). The novel p.Ser263Phe mutation in the human high‐affinity choline transporter 1 (CHT1/ SLC5A7 ) causes a lethal form of fetal akinesia syndrome. Human Mutation. 40(10). 1676–1683. 14 indexed citations
2.
Leonard, Norma, et al.. (2018). Prevalence of Childhood Permanent Hearing Loss after Early Complex Cardiac Surgery. The Journal of Pediatrics. 198. 104–109. 6 indexed citations
3.
Aziz, Khalid, et al.. (2014). Miller–Dieker Syndrome Associated with Congenital Lobar Emphysema. American Journal of Perinatology Reports. 4(1). 13–16. 4 indexed citations
4.
5.
Bhargava, Ravi, et al.. (2013). Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients. American Journal of Neuroradiology. 35(2). 402–406. 25 indexed citations
6.
Speevak, Marsha, et al.. (2013). Further evidence that a 100 Kb critical region is responsible for developmental delay, seizures, and dysmorphic features in 1q43q44 deletion patients. American Journal of Medical Genetics Part A. 161(4). 913–915. 3 indexed citations
7.
Gripp, Karen W., et al.. (2012). Transmission of the rare HRAS mutation (c. 173C > T; p.T58I) further illustrates its attenuated phenotype. American Journal of Medical Genetics Part A. 158A(5). 1095–1101. 14 indexed citations
8.
Bhagat, Tushar D., M. Kirwan, Cyril Gitiaux, et al.. (2012). Mutations in the telomere capping complex in bone marrow failure and related syndromes. Haematologica. 98(3). 334–338. 73 indexed citations
9.
Joynt, Chloë, Charlene M.T. Robertson, Po‐Yin Cheung, et al.. (2009). Two-year neurodevelopmental outcomes of infants undergoing neonatal cardiac surgery for interrupted aortic arch: A descriptive analysis. Journal of Thoracic and Cardiovascular Surgery. 138(4). 924–932. 11 indexed citations
10.
Gripp, Karen W., A. Micheil Innes, Marni E. Axelrad, et al.. (2008). Costello syndrome associated with novel germline HRAS mutations: An attenuated phenotype?. American Journal of Medical Genetics Part A. 146A(6). 683–690. 54 indexed citations
11.
Leonard, Norma, et al.. (2007). Testicular Mixed Germ Cell Tumor in an Adolescent with Cowden Disease. Oncology. 72(3-4). 194–196. 12 indexed citations
12.
Atallah, Joseph, Ari R. Joffe, Charlene M.T. Robertson, et al.. (2007). Two-year general and neurodevelopmental outcome after neonatal complex cardiac surgery in patients with deletion 22q11.2: A comparative study. Journal of Thoracic and Cardiovascular Surgery. 134(3). 772–779. 38 indexed citations
13.
Leonard, Norma, et al.. (2005). Sensorineural hearing loss, striate palmoplantar hyperkeratosis, and knuckle pads in a patient with a novel connexin 26 (GJB2) mutation. Journal of Medical Genetics. 42(1). e2–e2. 14 indexed citations
14.
Bhargava, Ravi, et al.. (2005). Autosomal dominant inheritance of spondyloenchondrodysplasia. American Journal of Medical Genetics Part A. 135A(3). 282–288. 15 indexed citations
15.
Gupta, Sandeep, Bernadette Earley, S. T. L. Ting, Norma Leonard, & M.A. Crowe. (2004). Technical Note: Effect of corticotropin-releasing hormone on adrenocorticotropic hormone and cortisol in steers. Journal of Animal Science. 82(7). 1952–1956. 17 indexed citations
16.
Leonard, Norma & Darrell J. Tomkins. (2002). Diploid/tetraploid/t(1;6) mosaicism in a 17‐year‐old female with hypomelanosis of Ito, multiple congenital anomalies, and body asymmetry. American Journal of Medical Genetics. 112(1). 86–90. 29 indexed citations
17.
Leonard, Norma, Darrell J. Tomkins, & Nestor Demianczuk. (2000). Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat. Prenatal Diagnosis. 20(12). 947–949. 13 indexed citations
18.
Steuer, A, et al.. (1997). An unusual case of familial Mediterranean fever. Lara D. Veeken. 36(10). 1118–1121. 6 indexed citations
19.
Martin, Renée H., Alfred Rademaker, & Norma Leonard. (1995). Analysis of chromosomal abnormalities in human sperm after chemotherapy by karyotyping and fluorescence in situ hybridization (FISH). Cancer Genetics and Cytogenetics. 80(1). 29–32. 44 indexed citations
20.
Nash, David R., et al.. (1994). The raspberry locus of Drosophila melanogaster includes an inosine monophosphate dehydrogenase like coding sequence. Genome. 37(2). 333–344. 5 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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