Margot A. Cousin

1.9k total citations
42 papers, 660 citations indexed

About

Margot A. Cousin is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Margot A. Cousin has authored 42 papers receiving a total of 660 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 21 papers in Genetics and 6 papers in Immunology. Recurrent topics in Margot A. Cousin's work include Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and RNA Research and Splicing (5 papers). Margot A. Cousin is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (6 papers) and RNA Research and Splicing (5 papers). Margot A. Cousin collaborates with scholars based in United States, Netherlands and Canada. Margot A. Cousin's co-authors include Eric W. Klee, Patrick R. Blackburn, Nicole J. Boczek, Jon O. Ebbert, Gavin R. Oliver, Stephen C. Ekker, Karl J. Clark, Victor M. Karpyak, H. Schneider and David O. Warner and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Bioinformatics.

In The Last Decade

Margot A. Cousin

42 papers receiving 648 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Margot A. Cousin United States	14	304	223	166	72	65	42	660
Takahito Wada Japan	19	626 2.1×	383 1.7×	166 1.0×	97 1.3×	107 1.6×	77	1.1k
Rachel K. Miller United States	17	632 2.1×	156 0.7×	154 0.9×	35 0.5×	35 0.5×	32	869
Emilie Pallesi‐Pocachard France	10	376 1.2×	125 0.6×	286 1.7×	83 1.2×	41 0.6×	13	628
Nataliya Di Donato Germany	18	463 1.5×	371 1.7×	114 0.7×	54 0.8×	157 2.4×	61	914
Jennifer N. Partlow United States	13	432 1.4×	209 0.9×	186 1.1×	119 1.7×	89 1.4×	14	640
Ruth Simon United States	12	694 2.3×	200 0.9×	65 0.4×	112 1.6×	71 1.1×	16	853
Shanaz Pasha United Kingdom	14	515 1.7×	295 1.3×	141 0.8×	128 1.8×	134 2.1×	14	919
Julien Thévenon France	15	450 1.5×	474 2.1×	78 0.5×	30 0.4×	54 0.8×	51	798
Miriam S. Reuter Germany	15	358 1.2×	335 1.5×	84 0.5×	127 1.8×	62 1.0×	29	786
Kit Doudney United Kingdom	13	500 1.6×	298 1.3×	117 0.7×	123 1.7×	70 1.1×	25	762

Countries citing papers authored by Margot A. Cousin

Since Specialization

Citations

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

Fields of papers citing papers by Margot A. Cousin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Margot A. Cousin

This figure shows the co-authorship network connecting the top 25 collaborators of Margot A. Cousin. A scholar is included among the top collaborators of Margot A. Cousin 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 Margot A. Cousin. Margot A. Cousin 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

Fadra, Numrah, Laura Schultz‐Rogers, Pritha Chanana, et al.. (2024). Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease. BMC Genomics. 25(1). 371–371. 1 indexed citations

Sun, Haixiang, Bo Lei, Kévin Nay, et al.. (2024). Convergence on CaMK4: A Key Modulator of Autism-Associated Signaling Pathways in Neurons. Biological Psychiatry. 97(5). 439–449. 1 indexed citations

Ramazzotti, Giulia, Sara Mongiorgi, Isabella Rusciano, et al.. (2023). Understanding the Ultra-Rare Disease Autosomal Dominant Leukodystrophy: an Updated Review on Morpho-Functional Alterations Found in Experimental Models. Molecular Neurobiology. 60(11). 6362–6372. 5 indexed citations

Morales‐Rosado, Joel A., Erica L. Macke, Margot A. Cousin, et al.. (2020). Interpretation challenges of novel dual‐class missense and splice‐impacting variant in POLR3A‐related late‐onset hereditary spastic ataxia. Molecular Genetics & Genomic Medicine. 8(9). e1341–e1341. 6 indexed citations

Jenkinson, Garrett, et al.. (2020). LeafCutterMD: an algorithm for outlier splicing detection in rare diseases. Bioinformatics. 36(17). 4609–4615. 31 indexed citations

Zepeda‐Mendoza, Cinthya, Margot A. Cousin, Garrett Jenkinson, et al.. (2019). An intragenic duplication of TRPS1 leading to abnormal transcripts and causing trichorhinophalangeal syndrome type I. Molecular Case Studies. 5(6). a004655–a004655. 6 indexed citations

Mangaonkar, Abhishek A., Alejandro Ferrer, Filippo Pinto e Vairo, et al.. (2019). Clinical Applications and Utility of a Precision Medicine Approach for Patients With Unexplained Cytopenias. Mayo Clinic Proceedings. 94(9). 1753–1768. 12 indexed citations

Cousin, Margot A., Matthew J. Smith, Ashley N. Sigafoos, et al.. (2018). Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies. Journal of Clinical Immunology. 38(3). 307–319. 21 indexed citations

Boczek, Nicole J., Katharina Hopp, Daniel Kraft, et al.. (2018). Characterization of three ciliopathy pedigrees expands the phenotype associated with biallelic C2CD3 variants. European Journal of Human Genetics. 26(12). 1797–1809. 17 indexed citations

10.

Zimmermann, Michael T., Raúl Urrutia, Patrick R. Blackburn, et al.. (2017). Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz Syndrome. SHILAP Revista de lepidopterología. 2017. 1–4. 3 indexed citations

11.

Blackburn, Patrick R., Duygu Selcen, Jennifer Gass, et al.. (2017). Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1. Molecular Genetics & Genomic Medicine. 5(3). 295–302. 4 indexed citations

12.

Zimmermann, Michael T., Raúl Urrutia, Gavin R. Oliver, et al.. (2017). Molecular modeling and molecular dynamic simulation of the effects of variants in the TGFBR2 kinase domain as a paradigm for interpretation of variants obtained by next generation sequencing. PLoS ONE. 12(2). e0170822–e0170822. 19 indexed citations

13.

Vairo, Filippo Pinto e, Nicole J. Boczek, Margot A. Cousin, et al.. (2017). The prevalence of diseases caused by lysosome-related genes in a cohort of undiagnosed patients. Molecular Genetics and Metabolism Reports. 13. 46–51. 17 indexed citations

14.

Blackburn, Patrick R., Alexander Tischer, Michael T. Zimmermann, et al.. (2017). A Novel Kleefstra Syndrome-associated Variant That Affects the Conserved TPLX Motif within the Ankyrin Repeat of EHMT1 Leads to Abnormal Protein Folding. Journal of Biological Chemistry. 292(9). 3866–3876. 12 indexed citations

15.

Cousin, Margot A., Alexandra J. Greenberg, Diana Angius, et al.. (2016). The Value of Systematic Reviews in Estimating the Cost and Barriers to Translation in Tissue Engineering. Tissue Engineering Part B Reviews. 22(6). 430–437. 12 indexed citations

16.

Blackburn, Patrick R., Michael T. Zimmermann, Jennifer Gass, et al.. (2016). A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor tics. BMC Medical Genetics. 17(1). 93–93. 10 indexed citations

17.

Morales‐Rosado, Joel A., Margot A. Cousin, Jon O. Ebbert, & Eric W. Klee. (2015). A Critical Review of Repurposing Apomorphine for Smoking Cessation. Assay and Drug Development Technologies. 13(10). 612–622. 6 indexed citations

18.

Cousin, Margot A., et al.. (2012). Reducing the Noise in Behavioral Assays: Sex and Age in Adult Zebrafish Locomotion. Zebrafish. 9(4). 191–194. 29 indexed citations

19.

Klee, Eric W., H. Schneider, Karl J. Clark, et al.. (2011). Zebrafish: a model for the study of addiction genetics. Human Genetics. 131(6). 977–1008. 102 indexed citations

20.

Kipp, Benjamin R., Rhett P. Ketterling, Margot A. Cousin, et al.. (2010). Comparison of Fluorescence In Situ Hybridization, p57 Immunostaining, Flow Cytometry, and Digital Image Analysis for Diagnosing Molar and Nonmolar Products of Conception. American Journal of Clinical Pathology. 133(2). 196–204. 25 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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