Sarah Bowdin

5.3k total citations · 1 hit paper
40 papers, 2.3k citations indexed

About

Sarah Bowdin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sarah Bowdin has authored 40 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 16 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sarah Bowdin's work include Genomics and Rare Diseases (14 papers), Prenatal Screening and Diagnostics (7 papers) and Genetic Syndromes and Imprinting (6 papers). Sarah Bowdin is often cited by papers focused on Genomics and Rare Diseases (14 papers), Prenatal Screening and Diagnostics (7 papers) and Genetic Syndromes and Imprinting (6 papers). Sarah Bowdin collaborates with scholars based in Canada, United Kingdom and United States. Sarah Bowdin's co-authors include Eamonn R. Maher, M. Stephen Meyn, Bart Loeys, Gail Kirby, Ismaı̈l El-Hamamsy, Paul D. Sponseller, James H. Black, Anthony L. Guerrerio, Gretchen MacCarrick and Harry C. Dietz and has published in prestigious journals such as Circulation, Annals of Neurology and Human Reproduction.

In The Last Decade

Sarah Bowdin

40 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Loeys–Dietz syndrome: a primer for diagnosis and management

2014 338 citations Sarah Bowdin, Bart Loeys et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sarah Bowdin Canada	23	1.4k	954	712	392	345	40	2.3k
Birgit Sikkema‐Raddatz Netherlands	26	1.4k 1.0×	972 1.0×	1.1k 1.5×	112 0.3×	202 0.6×	69	2.6k
Christopher N. Vlangos United States	19	1.5k 1.1×	1.1k 1.1×	246 0.3×	135 0.3×	149 0.4×	24	2.8k
Victoria Murday United Kingdom	20	805 0.6×	566 0.6×	253 0.4×	203 0.5×	104 0.3×	35	1.9k
Florence Fellmann Switzerland	18	691 0.5×	417 0.4×	188 0.3×	193 0.5×	56 0.2×	54	1.4k
Christine Francannet France	23	737 0.5×	751 0.8×	241 0.3×	104 0.3×	440 1.3×	77	2.0k
Marita Lipsanen‐Nyman Finland	23	575 0.4×	755 0.8×	337 0.5×	105 0.3×	70 0.2×	46	1.4k
Dianne Abuelo United States	23	768 0.5×	757 0.8×	298 0.4×	80 0.2×	199 0.6×	52	1.9k
Carmen Morales Spain	23	337 0.2×	284 0.3×	449 0.6×	127 0.3×	130 0.4×	69	1.4k
Sheri A. Brandenburg United States	11	1.1k 0.8×	2.0k 2.1×	510 0.7×	112 0.3×	88 0.3×	11	2.3k
Tom H. Lindner Germany	21	694 0.5×	1.1k 1.1×	409 0.6×	113 0.3×	92 0.3×	49	2.2k

Countries citing papers authored by Sarah Bowdin

Since Specialization

Citations

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

Fields of papers citing papers by Sarah Bowdin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Bowdin

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Bowdin. A scholar is included among the top collaborators of Sarah Bowdin 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 Sarah Bowdin. Sarah Bowdin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Rayment, Jonathan H., Rebekah Jobling, Sarah Bowdin, Ernest Cutz, & Sharon Dell. (2019). Prolidase deficiency diagnosed by whole exome sequencing in a child with pulmonary capillaritis. ERJ Open Research. 5(2). 205–2018. 5 indexed citations

French, Courtney E., Isabelle Delon, Helen Dolling, et al.. (2019). Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children. Intensive Care Medicine. 45(5). 627–636. 149 indexed citations

Hosseini, S. Mohsen, Raymond H. Kim, Sharmila Udupa, et al.. (2018). Reappraisal of Reported Genes for Sudden Arrhythmic Death. Circulation. 138(12). 1195–1205. 210 indexed citations

Cohn, Iris, Tara Paton, Christian R. Marshall, et al.. (2017). Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study. npj Genomic Medicine. 2(1). 19–19. 38 indexed citations

Hayeems, Robin Z., Jasmin Bhawra, Kate Tsiplova, et al.. (2017). Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray. European Journal of Human Genetics. 25(12). 1303–1312. 27 indexed citations

Mathew, Jacob, Laura Zahavich, Myriam Lafrenière‐Roula, et al.. (2017). Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy. Clinical Genetics. 93(2). 310–319. 47 indexed citations

Anderson, James A., M. Stephen Meyn, Cheryl Shuman, et al.. (2016). Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?. Journal of Medical Ethics. 43(8). 535–539. 60 indexed citations

Bowdin, Sarah, Anne‐Marie Laberge, Aline Verstraeten, & Bart Loeys. (2015). Genetic Testing in Thoracic Aortic Disease—When, Why, and How?. Canadian Journal of Cardiology. 32(1). 131–134. 10 indexed citations

Bradley, Timothy J., Sarah Bowdin, Chantal F. Morel, & Reed E. Pyeritz. (2015). The Expanding Clinical Spectrum of Extracardiovascular and Cardiovascular Manifestations of Heritable Thoracic Aortic Aneurysm and Dissection. Canadian Journal of Cardiology. 32(1). 86–99. 52 indexed citations

10.

Bradley, Timothy J. & Sarah Bowdin. (2015). Multidisciplinary Aortopathy Clinics Should Now Be the Standard of Care in Canada. Canadian Journal of Cardiology. 32(1). 8–12. 7 indexed citations

11.

Atık, Tahir, Asuman Koparır, Güney Bademci, et al.. (2015). Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. Orphanet Journal of Rare Diseases. 10(1). 128–128. 34 indexed citations

12.

Lines, Matthew A., Stacy Hewson, William Halliday, et al.. (2013). Danon Disease Due to a Novel LAMP2 Microduplication. JIMD Reports. 14. 11–16. 9 indexed citations

13.

Karp, Natalya, Lars Grosse‐Wortmann, & Sarah Bowdin. (2012). Severe aortic stenosis, bicuspid aortic valve and atrial septal defect in a child with Joubert Syndrome and Related Disorders (JSRD) – A case report and review of congenital heart defects reported in the human ciliopathies. European Journal of Medical Genetics. 55(11). 605–610. 22 indexed citations

14.

Fenwick, Aimée L, et al.. (2011). A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome. BMC Medical Genetics. 12(1). 122–122. 14 indexed citations

15.

Patel, Chirag, et al.. (2009). Mosaic trisomy 1q: The longest surviving case. American Journal of Medical Genetics Part A. 149A(8). 1795–1800. 11 indexed citations

16.

Bowdin, Sarah, Louise Tee, Gail Kirby, et al.. (2008). Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies. Human Reproduction. 24(3). 741–747. 160 indexed citations

17.

Kent, Lindsey, Sarah Bowdin, Gail Kirby, Wendy N. Cooper, & Eamonn R. Maher. (2008). Beckwith Weidemann syndrome: A behavioral phenotype–genotype study. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1295–1297. 53 indexed citations

18.

Allen, Cathy, Sarah Bowdin, Robert F. Harrison, et al.. (2008). Pregnancy and perinatal outcomes after assisted reproduction: a comparative study. Irish Journal of Medical Science (1971 -). 177(3). 233–241. 40 indexed citations

19.

Bowdin, Sarah, Cathy Allen, Gail Kirby, et al.. (2007). A survey of assisted reproductive technology births and imprinting disorders. Human Reproduction. 22(12). 3237–3240. 117 indexed citations

20.

Sutcliffe, Alastair, Catherine Peters, Sarah Bowdin, et al.. (2005). Assisted reproductive therapies and imprinting disorders—a preliminary British survey. Human Reproduction. 21(4). 1009–1011. 186 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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