Morgan Similuk

2.7k total citations
32 papers, 338 citations indexed

About

Morgan Similuk is a scholar working on Genetics, Immunology and Molecular Biology. According to data from OpenAlex, Morgan Similuk has authored 32 papers receiving a total of 338 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Immunology and 9 papers in Molecular Biology. Recurrent topics in Morgan Similuk's work include BRCA gene mutations in cancer (9 papers), Immunodeficiency and Autoimmune Disorders (9 papers) and Genomics and Rare Diseases (6 papers). Morgan Similuk is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Immunodeficiency and Autoimmune Disorders (9 papers) and Genomics and Rare Diseases (6 papers). Morgan Similuk collaborates with scholars based in United States, Australia and Canada. Morgan Similuk's co-authors include Andrew J. Oler, Michael J. Lenardo, Ivan J. Fuss, Martha Quezado, Warren Strober, Liming Mao, Michael Yao, Judith R. Kelsen, Lindsey Albenberg and Atsushi Kitani and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Morgan Similuk

28 papers receiving 335 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Morgan Similuk United States	10	139	125	89	44	38	32	338
Hannah Wand United States	13	107 0.8×	195 1.6×	30 0.3×	38 0.9×	63 1.7×	23	484
Stephen L. Guthery United States	12	108 0.8×	266 2.1×	86 1.0×	22 0.5×	26 0.7×	20	570
Farha El‐Chennawi Egypt	13	79 0.6×	118 0.9×	111 1.2×	20 0.5×	33 0.9×	24	385
Susan Mahler Zneimer United States	11	175 1.3×	170 1.4×	59 0.7×	65 1.5×	23 0.6×	21	465
Howard Grundy United States	9	103 0.7×	48 0.4×	76 0.9×	61 1.4×	50 1.3×	14	334
Leslie S. Jones United States	9	60 0.4×	70 0.6×	116 1.3×	25 0.6×	65 1.7×	19	524
Thayne Woycinck Kowalski Brazil	11	117 0.8×	59 0.5×	48 0.5×	30 0.7×	32 0.8×	50	307
Estelle Dubruc Switzerland	8	81 0.6×	104 0.8×	54 0.6×	143 3.3×	132 3.5×	18	549
Paula Araya United States	10	77 0.6×	41 0.3×	136 1.5×	14 0.3×	87 2.3×	20	321
Heather L. Mulder United States	11	269 1.9×	69 0.6×	28 0.3×	189 4.3×	81 2.1×	22	630

Countries citing papers authored by Morgan Similuk

Since Specialization

Citations

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

Fields of papers citing papers by Morgan Similuk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morgan Similuk

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

Zainab, Rida, Justin Lack, Morgan Similuk, et al.. (2025). Genetic evaluation of pediatric pituitary adenomas and USP8-related genotype-phenotype correlations in Cushing’s disease. Pituitary. 28(5). 92–92.

Lewis, Katie L., et al.. (2025). “I am sick, but that’s not all that I am”: patient perspectives on psychological adaptation over time to inborn errors of immunity. Journal of Community Genetics. 16(2). 117–130.

Moses, Rachel Gore, Bryce A. Seifert, Siyuan Liu, et al.. (2024). Deep Screening for X Chromosome Parent-of-Origin Effects on Neurobehavioral and Neuroanatomical Phenotypes in 47,XXY Klinefelter Syndrome. SHILAP Revista de lepidopterología. 4(6). 100391–100391. 1 indexed citations

Jamal, Leila, et al.. (2024). Renegotiation, uncertainty, imagination: Assemblage perspectives on reproductive and family planning with an Inborn Error of immunity. Social Science & Medicine. 360. 117303–117303. 1 indexed citations

Lisco, Andrea, Ana M. Ortega‐Villa, Megan Anderson, et al.. (2023). Reappraisal of Idiopathic CD4 Lymphocytopenia at 30 Years. New England Journal of Medicine. 388(18). 1680–1691. 16 indexed citations

Similuk, Morgan & Taco W. Kuijpers. (2023). Nature and nurture: understanding phenotypic variation in inborn errors of immunity. Frontiers in Cellular and Infection Microbiology. 13. 1183142–1183142. 5 indexed citations

Paschall, Justin, Suiyuan Zhang, Morgan Similuk, et al.. (2023). Genotype first: Clinical genomics research through a reverse phenotyping approach. The American Journal of Human Genetics. 110(1). 3–12. 32 indexed citations

Jia, Yan, et al.. (2023). Perceived control is significantly associated with psychological adaptation in individuals with known or suspected inborn errors of immunity. Journal of Community Genetics. 14(6). 639–647. 2 indexed citations

Moses, Rachel Gore, et al.. (2023). Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling. Journal of Community Genetics. 14(1). 17–25. 2 indexed citations

10.

Nghiem, Paul, Jenna Bergerson, Morgan Similuk, et al.. (2022). Early-Onset Merkel Cell Carcinoma is Associated with Germline Defects in DNA Repair Genes and a Rare Immunodeficiency. Journal of Investigative Dermatology. 142(10). 2839–2839. 1 indexed citations

11.

Similuk, Morgan, et al.. (2022). Genomic tools for health: Secondary findings as findings to be shared. Genetics in Medicine. 24(11). 2220–2227. 7 indexed citations

12.

Yan, Shankai, Ling Luo, Po‐Ting Lai, et al.. (2022). PhenoRerank: A re-ranking model for phenotypic concept recognition pre-trained on human phenotype ontology. Journal of Biomedical Informatics. 129. 104059–104059. 4 indexed citations

13.

Ghosh, Rajarshi, Marita Bosticardo, Sunita Singh, et al.. (2022). FOXI3 haploinsufficiency contributes to low T-cell receptor excision circles and T-cell lymphopenia. Journal of Allergy and Clinical Immunology. 150(6). 1556–1562. 10 indexed citations

14.

Price, Susan, Morgan Similuk, Jia Yan, et al.. (2022). The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome. Blood Advances. 6(13). 3974–3978. 3 indexed citations

15.

Luo, Ling, Shankai Yan, Po‐Ting Lai, et al.. (2021). PhenoTagger: a hybrid method for phenotype concept recognition using human phenotype ontology. Bioinformatics. 37(13). 1884–1890. 37 indexed citations

16.

Chauvin, Samuel D., Susan Price, Juan Zou, et al.. (2021). A Double-Blind, Placebo-Controlled, Crossover Study of Magnesium Supplementation in Patients with XMEN Disease. Journal of Clinical Immunology. 42(1). 108–118. 13 indexed citations

17.

Turriff, Amy, Delphine Blain, Morgan Similuk, et al.. (2019). Motivations and Decision Making Processes of Men With X-linked Retinoschisis Considering Participation in an Ocular Gene Therapy Trial. American Journal of Ophthalmology. 204. 90–96. 7 indexed citations

18.

Mao, Liming, Atsushi Kitani, Morgan Similuk, et al.. (2018). Loss-of-function CARD8 mutation causes NLRP3 inflammasome activation and Crohn’s disease. Journal of Clinical Investigation. 128(5). 1793–1806. 75 indexed citations

19.

Jacobs, Aryana, Marc D. Schwartz, Heiðdís Valdimarsdóttir, et al.. (2016). Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer. Familial Cancer. 15(4). 529–539. 25 indexed citations

20.

Peshkin, Beth N., Scott P. Kelly, Rachel Nusbaum, et al.. (2015). Patient Perceptions of Telephone vs. In‐Person BRCA1/BRCA2 Genetic Counseling. Journal of Genetic Counseling. 25(3). 472–482. 46 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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