Madeline Couse

520 total citations
16 papers, 187 citations indexed

About

Madeline Couse is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Madeline Couse has authored 16 papers receiving a total of 187 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Madeline Couse's work include Genomics and Rare Diseases (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Madeline Couse is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Madeline Couse collaborates with scholars based in Canada, United States and United Kingdom. Madeline Couse's co-authors include Melissa A. Wilson, Bruno M. Grande, Tanya N. Phung, Phillip A. Richmond, Timothy H. Webster, Eric Karlins, Jan M. Friedman, Clara van Karnebeek, Andrew S. Medeiros and Derek J. Taylor and has published in prestigious journals such as Journal of Chromatography A, PLoS Genetics and BMC Genomics.

In The Last Decade

Madeline Couse

14 papers receiving 185 citations

Peers

Countries citing papers authored by Madeline Couse

Since Specialization

Citations

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

Fields of papers citing papers by Madeline Couse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Madeline Couse

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants 2025 ·PLoS Genetics ·(unknown), (unknown), (unknown), Meredith Curtis, Thomas Nalpathamkalam, (unknown), (unknown), Bhooma Thiruvahindrapuram, (unknown), Madeline Couse, Taila Hartley, Michelle M. Morrow, (unknown), Susan Walker, David Malkin, Frederick P. Roth, Gregory Costain	0
2	FGF14 GAA Intronic Expansion in Unsolved Adult‐Onset Ataxia in the Care4Rare Canada Consortium 2025 ·Annals of Clinical and Translational Neurology ·Alexanne Cuillerier, Giulia Gobbo, (unknown), Erika Wall, Madeline Couse, Laura M. McDonell, M. Cloutier, Matt C. Danzi, Jodi Warman‐Chardon, Pierre R. Bourque, (unknown), Alan J. Mears, (unknown), Wendy Mears, (unknown), (unknown), Gerald Pfeffer, Dennis E. Bulman, David A. Dyment, Kym M. Boycott	1
3	Biallelic SOX8 Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction 2023 ·Neurology Genetics ·Jodi Warman‐Chardon, Taila Hartley, Aren E. Marshall, Arran McBride, Madeline Couse, William MacDonald, Mellissa R.W. Mann, Pierre R. Bourque, Ari Breiner, Hanns Lochmüller, John Woulfe, (unknown), Gerd Melkus, Bernard Brais, David A. Dyment, Kym M. Boycott, Kristin D. Kernohan	2
4	RNA sequencing reveals deep intronic CEP120 variant: A report of the diagnostic odyssey for two siblings with Joubert syndrome type 31 2023 ·American Journal of Medical Genetics Part A ·Aren E. Marshall, Gabrielle Lemire, (unknown), Jorge Dávila, Madeline Couse, Kym M. Boycott, Kristin D. Kernohan	1
5	Long‐read genome sequencing reveals a novel intronic retroelement insertion in NR5A1 associated with 46,XY differences of sexual development 2023 ·American Journal of Medical Genetics Part A ·Giulia Gobbo, Xueqi Wang, Madeline Couse, (unknown), (unknown), Aren E. Marshall, (unknown), Christine Lambert, Siyuan Zhang, (unknown), (unknown), William J. Rowell, Christian R. Marshall, Kristin D. Kernohan, Kym M. Boycott	6
6	RNA sequencing resolves novel DYNC2H1 variants causing short‐rib thoracic dysplasia type 3: Case report 2023 ·Molecular Genetics & Genomic Medicine ·Aren E. Marshall, (unknown), (unknown), Madeline Couse, Kym M. Boycott, Julie Richer, Kristin D. Kernohan	3
7	Genome-Wide Sequencing Identified Rare Genetic Variants for Childhood-Onset Monogenic Lupus 2022 ·The Journal of Rheumatology ·(unknown), (unknown), Madeline Couse, Jingjing Cao, (unknown), Lynette Lau, Christian R. Marshall, Sergey Naumenko, Andrea Knight, Deborah M. Levy, Linda T. Hiraki	13
8	Hemophagocytic Lymphohistiocytosis Gene Variants in Childhood-Onset Systemic Lupus Erythematosus With Macrophage Activation Syndrome 2022 ·The Journal of Rheumatology ·Piya Lahiry, Sergey Naumenko, Madeline Couse, (unknown), (unknown), Andrea Knight, Deborah M. Levy, (unknown), (unknown), Linda T. Hiraki	1
9	Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions 2021 ·Genome Medicine ·Indhu‐Shree Rajan‐Babu, (unknown), Readman Chiu, (unknown), Patricia Birch, Madeline Couse, Colleen Guimond, Anna Lehman, Jill Mwenifumbo, Clara van Karnebeek, Jan M. Friedman, (unknown), Shelin Adam, Christèle du Souich, Alison M. Elliott, Tanya N. Nelson, Chenkai Li, Arezoo Mohajeri, Egor Dolzhenko, Michael A. Eberle, İnanç Birol	33
10	Identifying, understanding, and correcting technical artifacts on the sex chromosomes in next-generation sequencing data 2019 ·GigaScience ·Timothy H. Webster, Madeline Couse, Bruno M. Grande, Eric Karlins, Tanya N. Phung, Phillip A. Richmond, (unknown), Melissa A. Wilson	48
11	Aspartylglycosamine is a biomarker for NGLY1-CDDG, a congenital disorder of deglycosylation 2019 ·Molecular Genetics and Metabolism ·Hanneke A. Haijes, Monique G.M. de Sain–van der Velden, Hubertus C.M.T. Prinsen, (unknown), Maria van der Ham, Johan Gerrits, Madeline Couse, Jan M. Friedman, Clara van Karnebeek, Kathryn Selby, Peter M. van Hasselt, Nanda M. Verhoeven‐Duif, Judith Jans	36
12	XYalign: Version 1.1.6 2019 ·Zenodo (CERN European Organization for Nuclear Research) ·Timothy H. Webster, Madeline Couse, Bruno M. Grande, Eric Karlins, Tanya N. Phung, Phillip A. Richmond, (unknown), Melissa A. Wilson	1
13	Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability 2017 ·BMC Genomics ·Farah Zahir, Jill Mwenifumbo, Hye-Jung E. Chun, Emilia L. Lim, Clara van Karnebeek, Madeline Couse, Karen Mungall, (unknown), (unknown), Linlea Armstrong, Cornelius F. Boerkoel, Sylvie Langlois, (unknown), Steven J.M. Jones, Jan M. Friedman, Marco A. Marra	15
14	An optical relay approach to very low cost hybrid polymer-complementary metal-oxide semiconductor electrophoresis instrumentation 2014 ·Journal of Chromatography A ·(unknown), (unknown), Tianchi Ma, Madeline Couse, (unknown), D.G. Elliott, D. Moira Glerum, C. Backhouse	6
15	An automated hand-held CMOS-based instrument for hand-held mutation detection via electrophoresis 2014 ·(unknown), Tianchi Ma, Madeline Couse, Stacey Hume, (unknown), D.G. Elliott, D. Moira Glerum, C. Backhouse	0
16	Biological and nutrient responses to catchment disturbance and warming in small lakes near the Alaskan tundra–taiga boundary 2014 ·The Holocene ·Andrew S. Medeiros, Derek J. Taylor, Madeline Couse, Roland I. Hall, Roberto Quinlan, Brent B. Wolfe	21

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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