Colleen M. Donlin‐Smith

960 total citations
7 papers, 209 citations indexed

About

Colleen M. Donlin‐Smith is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Surgery. According to data from OpenAlex, Colleen M. Donlin‐Smith has authored 7 papers receiving a total of 209 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 1 paper in Surgery. Recurrent topics in Colleen M. Donlin‐Smith's work include Muscle Physiology and Disorders (5 papers), RNA modifications and cancer (2 papers) and Congenital limb and hand anomalies (1 paper). Colleen M. Donlin‐Smith is often cited by papers focused on Muscle Physiology and Disorders (5 papers), RNA modifications and cancer (2 papers) and Congenital limb and hand anomalies (1 paper). Colleen M. Donlin‐Smith collaborates with scholars based in United States, Netherlands and Italy. Colleen M. Donlin‐Smith's co-authors include Rabi Tawil, Jeffrey Statland, Silvère M. van der Maarel, Stephen J. Tapscott, Richard J.L.F. Lemmers, Mina Chung, Sabrina Sacconi, Constantine Farmakidis, Katy Eichinger and Patricia Heard and has published in prestigious journals such as Neurology, Journal of Medical Genetics and Muscle & Nerve.

In The Last Decade

Colleen M. Donlin‐Smith

7 papers receiving 203 citations

Peers

Countries citing papers authored by Colleen M. Donlin‐Smith

Since Specialization

Citations

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

Fields of papers citing papers by Colleen M. Donlin‐Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Colleen M. Donlin‐Smith. 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 Colleen M. Donlin‐Smith. The network helps show where Colleen M. Donlin‐Smith may publish in the future.

Co-authorship network of co-authors of Colleen M. Donlin‐Smith

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Monosomy 18p is a risk factor for facioscapulohumeral dystrophy 2018 ·Journal of Medical Genetics ·Judit Balog, (unknown), Richard J.L.F. Lemmers, Kirsten R. Straasheijm, Patrick J. van der Vliet, Anita van den Heuvel, Chiara Cambieri, Nicolas Capet, Léonard Féasson, Véronique Manel, (unknown), Marjolein Kriek, Colleen M. Donlin‐Smith, Claudia Ruivenkamp, Patricia Heard, Stephen J. Tapscott, Jannine D. Cody, Rabi Tawil, Sabrina Sacconi, Silvère M. van der Maarel	12
2	Milder phenotype in facioscapulohumeral dystrophy with 7–10 residual D4Z4 repeats 2015 ·Neurology ·Jeffrey Statland, Colleen M. Donlin‐Smith, Stephen J. Tapscott, Richard J.L.F. Lemmers, Silvère M. van der Maarel, Rabi Tawil	41
3	Hemizygosity forSMCHD1in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion Syndrome 2015 ·Human Mutation ·Richard J.L.F. Lemmers, Marlinde L. van den Boogaard, Patrick J. van der Vliet, Colleen M. Donlin‐Smith, Sharon Nations, Claudia Ruivenkamp, Patricia Heard, Egbert Bakker, Stephen J. Tapscott, Jannine D. Cody, Rabi Tawil, Silvère M. van der Maarel	28
4	The course and outcome of pregnancy in women with nondystrophic myotonias 2015 ·Muscle & Nerve ·(unknown), Colleen M. Donlin‐Smith, Eric M. Snyder, Eva K. Pressman, Emma Ciafaloni	9
5	Multiplex Screen of Serum Biomarkers in Facioscapulohumeral Muscular Dystrophy 2014 ·Journal of Neuromuscular Diseases ·Jeffrey Statland, Colleen M. Donlin‐Smith, Stephen J. Tapscott, Silvère M. van der Maarel, Rabi Tawil	33
6	Restrictive lung involvement in facioscapulohumeral muscular dystrophy 2014 ·Muscle & Nerve ·(unknown), Katy Eichinger, Colleen M. Donlin‐Smith, Rabi Tawil, Jeffrey Statland	28
7	Coats syndrome in facioscapulohumeral dystrophy type 1 2013 ·Neurology ·Jeffrey Statland, Sabrina Sacconi, Constantine Farmakidis, Colleen M. Donlin‐Smith, Mina Chung, Rabi Tawil	58

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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