Sandra A. Farrell

3.4k total citations
57 papers, 1.6k citations indexed

About

Sandra A. Farrell is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sandra A. Farrell has authored 57 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 23 papers in Molecular Biology and 22 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sandra A. Farrell's work include Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Sandra A. Farrell is often cited by papers focused on Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (16 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Sandra A. Farrell collaborates with scholars based in Canada, United States and United Kingdom. Sandra A. Farrell's co-authors include Philip Wyatt, Marsha Speevak, Ronald G. Worton, Masahide Yazaki, Merrill D. Benson, Chris Meier, J. Siegel‐Bartelt, Anne Summers, Pui-Yuen Wong and Joel G. Ray and has published in prestigious journals such as Nature Genetics, The Journal of Immunology and Neurology.

In The Last Decade

Sandra A. Farrell

54 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra A. Farrell Canada 25 635 559 479 181 181 57 1.6k
Barbara F. Crandall United States 25 719 1.1× 704 1.3× 740 1.5× 245 1.4× 104 0.6× 88 2.0k
Orit Reish Israel 25 516 0.8× 880 1.6× 425 0.9× 145 0.8× 74 0.4× 72 1.8k
Marie‐Sylvie Gross France 22 411 0.6× 1.1k 1.9× 409 0.9× 196 1.1× 95 0.5× 43 1.9k
Luis E. Figuera Mexico 23 622 1.0× 637 1.1× 126 0.3× 140 0.8× 188 1.0× 134 1.8k
Boleslaw Goldman Israel 22 575 0.9× 746 1.3× 246 0.5× 161 0.9× 69 0.4× 74 1.7k
W.G. Kearns United States 23 948 1.5× 1.0k 1.8× 663 1.4× 134 0.7× 47 0.3× 97 2.2k
Claude Bendavid France 23 727 1.1× 994 1.8× 384 0.8× 149 0.8× 43 0.2× 81 1.7k
Véronique David France 19 406 0.6× 523 0.9× 173 0.4× 127 0.7× 113 0.6× 40 1.6k
Güven Lüleci Türkiye 21 808 1.3× 750 1.3× 286 0.6× 132 0.7× 38 0.2× 110 1.7k
E. Bottini Italy 18 271 0.4× 495 0.9× 290 0.6× 178 1.0× 69 0.4× 151 1.5k

Countries citing papers authored by Sandra A. Farrell

Since Specialization
Citations

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

Fields of papers citing papers by Sandra A. Farrell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra A. Farrell

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra A. Farrell. A scholar is included among the top collaborators of Sandra A. Farrell 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 A. Farrell. Sandra A. Farrell 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.
Fauth, Christine, Katharina Steindl, Annick Toutain, et al.. (2015). A recurrent germline mutation in the PIGA gene causes Simpson‐Golabi‐Behmel syndrome type 2. American Journal of Medical Genetics Part A. 170(2). 392–402. 30 indexed citations
2.
Qiao, Ying, Eloi Mercier, Barbara McGillivray, et al.. (2014). Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID). BMC Medical Genetics. 15(1). 82–82. 8 indexed citations
3.
Lepage, Nathalie, et al.. (2012). Standardized Procedural Practices of the Ontario Prenatal Screening Program for aneuploidies and open neural tube defects. Clinical Biochemistry. 45(15). 1152–1157. 5 indexed citations
4.
Speevak, Marsha & Sandra A. Farrell. (2011). Non‐syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pair. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(4). 484–489. 33 indexed citations
5.
Yang, Ping, et al.. (2010). A case of 8q22.1 microdeletion without the Nablus mask-like facial syndrome phenotype. European Journal of Medical Genetics. 53(2). 108–110. 14 indexed citations
6.
Carroll, June, Andrea L. Rideout, Brenda J. Wilson, et al.. (2009). Genetic education for primary care providers. Canadian Family Physician. 55(12). 6 indexed citations
7.
Kurth, Ingo, J. Christopher Hennings, Antje K. Huebner, et al.. (2009). Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy. Nature Genetics. 41(11). 1179–1181. 184 indexed citations
8.
Pereira, Lexley M Pinto, et al.. (2009). Health burden of co-morbid asthma and allergic rhinitis in West Indian children. Allergologia et Immunopathologia. 38(3). 129–134. 16 indexed citations
9.
Speevak, Marsha, J.-A. Dolling, Deborah Terespolsky, Andrea Blumenthal, & Sandra A. Farrell. (2008). An algorithm for the prenatal detection of chromosome anomalies by QF‐PCR and G‐banded analysis. Prenatal Diagnosis. 28(13). 1221–1226. 7 indexed citations
10.
Ray, Joel G., Miles D. Thompson, Marian J. Vermeulen, et al.. (2007). Metabolic Syndrome features and risk of neural tube defects. BMC Pregnancy and Childbirth. 7(1). 21–21. 28 indexed citations
11.
Bruyèrè, Hélène, Marsha Speevak, E.J.T. Winsor, et al.. (2006). Isodicentric Yp: prenatal diagnosis and outcome in 12 cases. Prenatal Diagnosis. 26(4). 324–329. 27 indexed citations
12.
Yazaki, Masahide, Sandra A. Farrell, & Merrill D. Benson. (2003). A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis. Kidney International. 63(5). 1652–1657. 89 indexed citations
13.
Chitayat, David, Sandra A. Farrell, Tianhua Huang, et al.. (2002). Double-positive maternal serum screening results for down syndrome and open neural tube defects: An indicator for fetal structural or chromosomal abnormalities and adverse obstetric outcomes. American Journal of Obstetrics and Gynecology. 187(3). 758–763. 32 indexed citations
14.
Tomkins, Darrell J., Helen McDonald, Sandra A. Farrell, & Carolyn J. Brown. (2002). Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay. European Journal of Human Genetics. 10(1). 44–51. 28 indexed citations
15.
Ives, Elizabeth, Maryse Chalifoux, Sandra A. Farrell, et al.. (1996). Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38). American Journal of Medical Genetics. 64(1). 89–96. 15 indexed citations
16.
Farrell, Sandra A. & Yao‐Shan Fan. (1995). Balanced nonacrocentric whole‐arm reciprocal translocations: A de novo case and literature review. American Journal of Medical Genetics. 55(4). 423–426. 19 indexed citations
17.
Terespolsky, Deborah, Sandra A. Farrell, J. Siegel‐Bartelt, & Rosanna Weksberg. (1995). Infantile lethal variant of Simpson‐Golabi‐Behmel syndrome associated with hydrops fetalis. American Journal of Medical Genetics. 59(3). 329–333. 59 indexed citations
18.
Farrell, Sandra A., et al.. (1992). Intrachromosomal insertion of chromosome 7. Clinical Genetics. 41(6). 299–302. 22 indexed citations
19.
Farrell, Sandra A., et al.. (1987). Neonatal manifestations of Schwartz‐Jampel syndrome. American Journal of Medical Genetics. 27(4). 799–805. 16 indexed citations
20.
Kerr, Ian G., et al.. (1987). Phase I and pharmacokinetic study of high volume intraperitoneal aclacinomycin — A (Aclarubicin). Investigational New Drugs. 5(2). 171–176. 2 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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