Nancy Carson

2.3k total citations
46 papers, 1.2k citations indexed

About

Nancy Carson is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Nancy Carson has authored 46 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Surgery. Recurrent topics in Nancy Carson's work include Blood Coagulation and Thrombosis Mechanisms (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Vascular anomalies and interventions (3 papers). Nancy Carson is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Vascular anomalies and interventions (3 papers). Nancy Carson collaborates with scholars based in Canada, United States and France. Nancy Carson's co-authors include Cecilia Meagher, Marc B. Lande, Jason Roy, David L. Nelson, Andrea Peier, Vikram S. Dogra, Nancy E. Simpson, Marc Rodger, Philip S. Wells and Marvin M. Doyley and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Blood.

In The Last Decade

Nancy Carson

43 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nancy Carson Canada	19	342	313	309	138	131	46	1.2k
Susanna Ranta Finland	20	199 0.6×	335 1.1×	183 0.6×	178 1.3×	293 2.2×	93	1.6k
Masaharu Ito Japan	20	161 0.5×	302 1.0×	116 0.4×	190 1.4×	64 0.5×	74	1.3k
R John United Kingdom	24	78 0.2×	313 1.0×	201 0.7×	159 1.2×	142 1.1×	49	1.6k
C. E. Fiore Italy	19	94 0.3×	267 0.9×	97 0.3×	182 1.3×	53 0.4×	48	1.2k
Michelle Harrison Australia	23	227 0.7×	255 0.8×	67 0.2×	164 1.2×	54 0.4×	88	1.4k
Manfred Stuhrmann Germany	24	118 0.3×	527 1.7×	384 1.2×	300 2.2×	97 0.7×	94	1.9k
Neil Friedman United States	20	102 0.3×	242 0.8×	121 0.4×	126 0.9×	307 2.3×	59	1.2k
Louisa Ho Canada	22	59 0.2×	438 1.4×	158 0.5×	222 1.6×	63 0.5×	52	1.7k
Annette Schneider Germany	19	156 0.5×	364 1.2×	184 0.6×	162 1.2×	37 0.3×	36	1.1k
Maurizio Delvecchio Italy	26	79 0.2×	437 1.4×	665 2.2×	419 3.0×	56 0.4×	104	1.7k

Countries citing papers authored by Nancy Carson

Since Specialization

Citations

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

Fields of papers citing papers by Nancy Carson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Carson

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

All Works

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20 of 20 papers shown

Snetsinger, Brooke, Xiao Zhang, Guillaume Richard‐Carpentier, et al.. (2021). Validation, Implementation, and Clinical Impact of the Oncomine Myeloid Targeted-Amplicon DNA and RNA Ion Semiconductor Sequencing Assay. Journal of Molecular Diagnostics. 23(10). 1292–1305. 7 indexed citations

Ohayon, Jacques, et al.. (2017). Principal Strain Vascular Elastography: Simulation and Preliminary Clinical Evaluation. Ultrasound in Medicine & Biology. 43(3). 682–699. 27 indexed citations

Richer, Julie, Hussein Daoud, Pavel Geier, et al.. (2015). Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE. American Journal of Medical Genetics Part A. 167(7). 1654–1658. 12 indexed citations

Rodger, Marc, Mark Walker, Graeme N. Smith, et al.. (2014). Is thrombophilia associated with placenta‐mediated pregnancy complications? A prospective cohort study. Journal of Thrombosis and Haemostasis. 12(4). 469–478. 61 indexed citations

Gándara, Esteban, Michael J. Kovacs, Susan R. Kahn, et al.. (2013). Non-OO blood type influences the risk of recurrent venous thromboembolism. Thrombosis and Haemostasis. 110(12). 1172–1179. 39 indexed citations

Carson, Nancy, et al.. (2013). Noninvasive vascular elastography using plane-wave and sparse-array imaging. IEEE Transactions on Ultrasonics Ferroelectrics and Frequency Control. 60(2). 332–342. 45 indexed citations

Al‐Thihli, Khalid, et al.. (2008). Compound heterozygous deletions of PMP22 causing severe Charcot‐Marie‐Tooth disease of the Dejerine‐Sottas disease phenotype. American Journal of Medical Genetics Part A. 146A(18). 2412–2416. 20 indexed citations

Lande, Marc B., Nancy Carson, Jason Roy, & Cecilia Meagher. (2006). Effects of Childhood Primary Hypertension on Carotid Intima Media Thickness. Hypertension. 48(1). 40–44. 237 indexed citations

Wells, Philip S., Josdalyne Anderson, Marc Rodger, et al.. (2006). The factor XIII Val34Leu polymorphism: is it protective against idiopathic venous thromboembolism?. Blood Coagulation & Fibrinolysis. 17(7). 533–538. 10 indexed citations

10.

Drouin, Jeanne, Nancy Carson, & Odette Laneuville. (2004). Compound heterozygosity for a novel nine-nucleotide deletion and the Asn45Ser missense mutation in the glycoprotein IX gene in a patient with Bernard-Soulier syndrome. American Journal of Hematology. 78(1). 41–48. 11 indexed citations

11.

Rodger, Marc, Melissa A. Forgie, Nicole Langlois, et al.. (2003). The ACE D/D genotype is protective against the development of idiopathic deep vein thrombosis and pulmonary embolism. Thrombosis and Haemostasis. 90(11). 829–834. 16 indexed citations

12.

Carson, Nancy, et al.. (2003). Treated Needles. Journal of Ultrasound in Medicine. 22(11). 1233–1237. 26 indexed citations

13.

Carson, Nancy, et al.. (2000). A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center. Clinical Genetics. 58(4). 299–308. 84 indexed citations

14.

Gottlieb, Ronald H., et al.. (1996). Preliminary assessment of captopril sonography in screening for renal artery stenosis. Academic Radiology. 3(1). 57–62. 3 indexed citations

15.

Peier, Andrea, et al.. (1995). Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome. Nature Genetics. 10(4). 483–485. 111 indexed citations

16.

Nelson, David L., et al.. (1994). Absence of FMR1 protein in two mentally retarded fragile X males without CGG repeat expansion. The American Journal of Human Genetics. 55. 2 indexed citations

17.

Carson, Nancy & Nancy E. Simpson. (1991). A physical map of human chromosome 10 and a comparison with an existing genetic map. Genomics. 11(2). 379–388. 11 indexed citations

18.

Marino, Thomas A., Michael Cassidy, Deborah R. Marino, Nancy Carson, & Steven R. Houser. (1991). Norepinephrine‐induced cardiac hypertrophy of the cat heart. The Anatomical Record. 229(4). 505–510. 10 indexed citations

19.

Myers, Shirley M., Nancy Carson, Judith R. Kidd, et al.. (1990). A refined linkage map for DNA markers around the pericentromeric region of chromosome 10. Genomics. 8(3). 461–468. 14 indexed citations

20.

Wu, Jia Qian, Vijaya Ramesh, J.R. Kidd, et al.. (1988). The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10. Cytogenetic and Genome Research. 48(2). 126–127. 9 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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