Laura Robb

552 total citations
17 papers, 373 citations indexed

About

Laura Robb is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Laura Robb has authored 17 papers receiving a total of 373 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Laura Robb's work include Cardiac electrophysiology and arrhythmias (3 papers), Congenital limb and hand anomalies (2 papers) and Pharmacogenetics and Drug Metabolism (2 papers). Laura Robb is often cited by papers focused on Cardiac electrophysiology and arrhythmias (3 papers), Congenital limb and hand anomalies (2 papers) and Pharmacogenetics and Drug Metabolism (2 papers). Laura Robb collaborates with scholars based in Canada, United States and France. Laura Robb's co-authors include Vazken M. Der Kaloustian, François Rousseau, Mario Talajic, Jacques Turgeon, Nancy L. Sheehan, Thierry Hurlimann, Jean‐Philippe Lambert, Nathalie Letarte, Simon de Denus and David Chitayat and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Human Genetics.

In The Last Decade

Laura Robb

16 papers receiving 362 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laura Robb Canada	11	158	134	77	60	57	17	373
Megan E. Grove United States	11	209 1.3×	344 2.6×	60 0.8×	10 0.2×	38 0.7×	17	523
В. Н. Максимов Russia	10	145 0.9×	71 0.5×	91 1.2×	4 0.1×	31 0.5×	158	461
Mel Maranian United Kingdom	8	107 0.7×	111 0.8×	20 0.3×	68 1.1×	15 0.3×	12	389
Ken Livak United States	4	193 1.2×	175 1.3×	19 0.2×	7 0.1×	10 0.2×	5	409
Manish Pungliya United States	7	275 1.7×	131 1.0×	238 3.1×	8 0.1×	8 0.1×	11	472
Ji Yoon Han South Korea	13	139 0.9×	145 1.1×	12 0.2×	3 0.1×	86 1.5×	58	420
Mitchel Pariani United States	9	77 0.5×	167 1.2×	52 0.7×	3 0.1×	16 0.3×	13	349
Sawona Biswas United States	10	110 0.7×	374 2.8×	10 0.1×	6 0.1×	88 1.5×	13	513
Angela Zeng United States	5	183 1.2×	25 0.2×	15 0.2×	12 0.2×	28 0.5×	8	309
Keitaro Yamada Japan	11	189 1.2×	57 0.4×	9 0.1×	4 0.1×	25 0.4×	31	347

Countries citing papers authored by Laura Robb

Since Specialization

Citations

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

Fields of papers citing papers by Laura Robb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Robb

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

All Works

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17 of 17 papers shown

Jordà, Paloma, Laura Robb, Julie Amyot, et al.. (2020). Missense variants in the spectrin repeat domain of DSP are associated with arrhythmogenic cardiomyopathy: A family report and systematic review. American Journal of Medical Genetics Part A. 182(10). 2359–2368. 3 indexed citations

Robb, Laura, et al.. (2017). Understanding the Gaps in Postsecondary Education Participation Based on Income and Place of Birth: The role of high school course selection and performance. 2 indexed citations

Gélinas, Roselle, Nabil Khoury, Marie Chaix, et al.. (2017). Characterization of a Human Induced Pluripotent Stem Cell–Derived Cardiomyocyte Model for the Study of Variant Pathogenicity. Circulation Cardiovascular Genetics. 10(5). 14 indexed citations

Chami, Nathalie, Rafik Tadros, Ken Sin Lo, et al.. (2014). Nonsense Mutations in BAG3 are Associated With Early-Onset Dilated Cardiomyopathy in French Canadians. Canadian Journal of Cardiology. 30(12). 1655–1661. 49 indexed citations

Denus, Simon de, Nathalie Letarte, Thierry Hurlimann, et al.. (2013). An Evaluation of Pharmacists‘ Expectations Towards Pharmacogenomics. Pharmacogenomics. 14(2). 165–175. 70 indexed citations

Fitzpatrick, Jennifer, et al.. (2013). The Establishment of Core Competencies for Canadian Genetic Counsellors: Validation of Practice Based Competencies. Journal of Genetic Counseling. 22(6). 690–706. 14 indexed citations

Letarte, Nathalie, Nancy L. Sheehan, Thierry Hurlimann, et al.. (2013). La pharmacothérapie personnalisée et la pharmacogénétique. 46(4). 2 indexed citations

Benito, Begoña, Óscar Campuzano, Anna Iglesias, et al.. (2009). Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia. Clinical Genetics. 77(1). 37–48. 32 indexed citations

Robb, Laura. (2006). Erthe upon Erthe.

10.

Feldman, George, Dolores Saavedra, Nathaniel H. Robin, et al.. (1997). A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22. Human Molecular Genetics. 6(11). 1937–1941. 28 indexed citations

11.

Toutain, Annick, Nathalie Ronce, Laura Robb, et al.. (1997). Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region. Human Genetics. 99(2). 256–261. 25 indexed citations

12.

Ronce, Nathalie, Marie‐Pierre Moizard, Laura Robb, et al.. (1997). A C2055T Transition in Exon 8 of the ATP7A Gene Is Associated with Exon Skipping in an Occipital Horn Syndrome Family. The American Journal of Human Genetics. 61(1). 233–238. 4 indexed citations

13.

Rozen, Rima, et al.. (1995). L206W mutation of the cystic fibrosis gene, relatively frequent in French Canadians, is associated with atypical presentations of cystic fibrosis. American Journal of Medical Genetics. 57(3). 437–439. 18 indexed citations

14.

Rousseau, François, et al.. (1994). No mental retardation in a man with 40% abnormal methylation at the FMR-1 locus and transmission of sperm cell mutations as premutations. Human Molecular Genetics. 3(6). 927–930. 60 indexed citations

15.

Chitayat, David, et al.. (1992). Acrania: A manifestation of the Adams‐Oliver syndrome. American Journal of Medical Genetics. 44(5). 562–566. 31 indexed citations

16.

Kieran, Mark W., et al.. (1992). Portohepatic shunt in a down syndrome patient with an interchange trisomy 47,XY,−2,+der(2),+der(21)t(2;21)(p13;q22.1)mat. American Journal of Medical Genetics. 44(3). 288–292. 13 indexed citations

17.

Thomson, David M., et al.. (1987). Extraction of human organ-specific cancer neoantigens from cancer cells and plasma membranes with 1-butanol.. PubMed. 47(4). 1058–64. 8 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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