Sandra L. Marles

532 total citations
25 papers, 298 citations indexed

About

Sandra L. Marles is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Sandra L. Marles has authored 25 papers receiving a total of 298 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 7 papers in Molecular Biology. Recurrent topics in Sandra L. Marles's work include Prenatal Screening and Diagnostics (4 papers), Congenital limb and hand anomalies (3 papers) and Metabolism and Genetic Disorders (3 papers). Sandra L. Marles is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Congenital limb and hand anomalies (3 papers) and Metabolism and Genetic Disorders (3 papers). Sandra L. Marles collaborates with scholars based in Canada, United States and Netherlands. Sandra L. Marles's co-authors include Albert E. Chudley, Cheryl R. Greenberg, Bernard N. Chodirker, Shannon D. Scott, Karen Chalmers, Douglas J. Tataryn, Oscar Casiro, Angelika J. Dawson, Aizeddin A. Mhanni and Alison M. Elliott and has published in prestigious journals such as Frontiers in Immunology, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Sandra L. Marles

24 papers receiving 288 citations

Peers

Sandra L. Marles
Victor Evangelista de Faria Ferraz Brazil
Ryan Noss United States
Özgül M. Alper Türkiye
Elizabeth Hoodfar United States
Carol Chu United Kingdom
M. Y. El‐Khalifa Kuwait
Marcial Francis Galera Brazil
D.A. Driscoll United States
Jay S. Schinfeld United States
Whitney Neufeld‐Kaiser United States
Victor Evangelista de Faria Ferraz Brazil
Sandra L. Marles
Citations per year, relative to Sandra L. Marles Sandra L. Marles (= 1×) peers Victor Evangelista de Faria Ferraz

Countries citing papers authored by Sandra L. Marles

Since Specialization
Citations

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

Fields of papers citing papers by Sandra L. Marles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra L. Marles. 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 Sandra L. Marles. The network helps show where Sandra L. Marles may publish in the future.

Co-authorship network of co-authors of Sandra L. Marles

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra L. Marles. A scholar is included among the top collaborators of Sandra L. Marles 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 Sandra L. Marles. Sandra L. Marles 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.
Rubin, Tamar, Lum Peng Lim, Michael S. Salman, et al.. (2025). Two rare mutations in homozygosity synergize to silence TREX1 in Aicardi-Goutières syndrome. Frontiers in Immunology. 16. 1557632–1557632.
2.
Hanlon‐Dearman, Ana, et al.. (2020). Ten years of evidence for the diagnostic assessment of preschoolers with prenatal alcohol exposure. 27(3). e49–e68. 6 indexed citations
3.
Dawson, Angelika J., Karine Hovanes, Jing Liu, et al.. (2020). Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly. Clinical Dysmorphology. 30(2). 83–88. 3 indexed citations
4.
Hack, Thomas F., et al.. (2016). Parental Decision Making Regarding the Disclosure or Nondisclosure of a Mutation-Positive BRCA1/2 Test Result to Minors. Oncology nursing forum. 43(3). 330–341. 5 indexed citations
5.
Vanan, Magimairajan, et al.. (2016). RARE-22. MEDULLOBLASTOMA IN A CHILD WITH NEUROFIBROMATOSIS-1: CASE REPORT AND REVIEW. Neuro-Oncology. 18(suppl_6). vi164–vi164. 1 indexed citations
6.
Harvard, Chansonette, Eloi Mercier, Rita Colnaghi, et al.. (2011). Understanding the impact of 1q21.1 copy number variant. Orphanet Journal of Rare Diseases. 6(1). 54–54. 43 indexed citations
7.
Salman, Michael S., Sandra L. Marles, Frances Booth, & Marc R. Del Bigio. (2009). Early-Onset Neurodegenerative Disease of the Cerebellum and Motor Axons. Pediatric Neurology. 40(5). 365–370. 3 indexed citations
8.
Chudley, Albert E., et al.. (2008). Increased Nuchal Translucency Thickness: A Potential Indicator for Ritscher-Schinzel Syndrome. Fetal Diagnosis and Therapy. 24(4). 395–399. 4 indexed citations
9.
Li, Chumei, Sandra L. Marles, Cheryl R. Greenberg, et al.. (2007). Manitoba oculotrichoanal (MOTA) syndrome: Report of eight new cases. American Journal of Medical Genetics Part A. 143A(8). 853–857. 16 indexed citations
10.
Chalmers, Karen, et al.. (2003). Reports of information and support needs of daughters and sisters of women with breast cancer. European Journal of Cancer Care. 12(1). 81–90. 36 indexed citations
11.
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
12.
Prasad, Chitra, Sandra L. Marles, Asuri N. Prasad, et al.. (2002). Smith‐Lemli‐Opitz syndrome: New mutation with a mild phenotype. American Journal of Medical Genetics. 108(1). 64–68. 15 indexed citations
13.
Bowman, Natalie M., et al.. (2002). Telemedicine diagnosis for fetal alcohol syndrome – The Manitoba experience. Paediatrics & Child Health. 7(3). 147–151. 14 indexed citations
14.
Marles, Sandra L., Martin H. Reed, & Jane Evans. (2002). Humeroradial synostosis, ulnar aplasia and oligodactyly, with contralateral amelia, in a child with prenatal cocaine exposure. American Journal of Medical Genetics Part A. 116A(1). 85–89. 7 indexed citations
15.
Marles, Sandra L. & Oscar Casiro. (1998). Persistent neonatal hypoglycemia: Diagnosis and management. Paediatrics & Child Health. 3(1). 16–19. 11 indexed citations
16.
Marles, Sandra L., et al.. (1995). Evidence for Ritscher‐Schinzel syndrome in Canadian native Indians. American Journal of Medical Genetics. 56(4). 343–350. 30 indexed citations
17.
Marles, Sandra L., et al.. (1993). Identification of an uncommon haptoglobin type using DNA and protein analysis. Human Genetics. 92(4). 364–366. 5 indexed citations
18.
Marles, Sandra L., et al.. (1992). New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians. American Journal of Medical Genetics. 42(6). 793–799. 23 indexed citations
19.
Marles, Sandra L. & Albert E. Chudley. (1990). Another case of microcephaly, facial clefting, and preaxial polydactyly.. Journal of Medical Genetics. 27(9). 593–594. 1 indexed citations
20.
Marles, Sandra L. & Albert E. Chudley. (1990). Ulnar agenesis and endocardial fibroelastosis. American Journal of Medical Genetics. 37(2). 258–260. 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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