Rachel Susman

1.5k total citations
7 papers, 91 citations indexed

About

Rachel Susman is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Rachel Susman has authored 7 papers receiving a total of 91 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Genetics. Recurrent topics in Rachel Susman's work include Craniofacial Disorders and Treatments (2 papers), Fibroblast Growth Factor Research (2 papers) and Tuberous Sclerosis Complex Research (1 paper). Rachel Susman is often cited by papers focused on Craniofacial Disorders and Treatments (2 papers), Fibroblast Growth Factor Research (2 papers) and Tuberous Sclerosis Complex Research (1 paper). Rachel Susman collaborates with scholars based in Australia and United States. Rachel Susman's co-authors include George Elakis, Tony Roscioli, Michael F. Buckley, Julie McGaughran, Timothy C. Cox, Michael F. Buckley, Glenn Gardener, Andreas Zankl, Kathy Tucker and Gregory Y. Lauwers and has published in prestigious journals such as Modern Pathology, Frontiers in Oncology and European Journal of Human Genetics.

In The Last Decade

Rachel Susman

7 papers receiving 90 citations

Peers

Countries citing papers authored by Rachel Susman

Since Specialization

Citations

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

Fields of papers citing papers by Rachel Susman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel Susman

This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Susman. A scholar is included among the top collaborators of Rachel Susman 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 Rachel Susman. Rachel Susman 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	Birt-Hogg-Dubé Syndrome and Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome: An Effective Multidisciplinary Approach to Hereditary Renal Cancer Predisposing Syndromes 2021 ·Frontiers in Oncology ·(unknown), (unknown), Rachel Susman, (unknown), (unknown), Simon Wood, Andrew J. Mallett	10
2	Spectrum of gastrointestinal tract pathology in a multicenter cohort of 43 Cowden syndrome patients 2019 ·Modern Pathology ·Jennifer Borowsky, Namrata Setia, Christophe Rosty, (unknown), Rachel Susman, Joseph Misdraji, John Hart, Gregory Y. Lauwers, Ian Brown	12
3	Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history 2018 ·European Journal of Human Genetics ·(unknown), Bettina Meiser, Veronica Quinn, Gillian Mitchell, Kathy Tucker, Kaaren Watts, Belinda Rahman, Michelle Peate, Christobel Saunders, Elizabeth Geelhoed, Margaret Gleeson, Kristine Barlow‐Stewart, Michael Field, Marion Harris, Yoland Antill, Rachel Susman, Michael T. Bowen, (unknown), Judy Kirk	12
4	Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X‐inactivation utilizing case‐parent trio SNP microarray analysis 2018 ·Molecular Genetics & Genomic Medicine ·Jane Mason, Hnin Thanda Aung, (unknown), (unknown), David J. Fairbairn, John A. Rowell, David Young, Rachel Susman, Simon Brown, V.J. Hyland, Jeremy Robertson	4
5	Novel SOX2 partner-factor domain mutation in a four-generation family 2009 ·European Journal of Human Genetics ·(unknown), (unknown), Kate Gibson, (unknown), Rachel Susman, (unknown), Yongjuan Chen, Jennifer A. Donald, Patrick Tam, John Grigg, Maree Flaherty, Glen A. Gole, Robyn V. Jamieson	19
6	Prenatal and postnatal presentation of severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN) due to the FGFR3 Lys650Met mutation 2007 ·American Journal of Medical Genetics Part A ·Andreas Zankl, George Elakis, Rachel Susman, (unknown), Glenn Gardener, Michael F. Buckley, Tony Roscioli	16
7	A case of Beare–Stevenson syndrome with a broad spectrum of features and a review of the FGFR2 Y375C mutation phenotype 2006 ·Clinical Dysmorphology ·Julie McGaughran, (unknown), Rachel Susman, Michael F. Buckley, George Elakis, Timothy C. Cox, Tony Roscioli	18

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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