Molly B. Sheridan

842 total citations
11 papers, 281 citations indexed

About

Molly B. Sheridan is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Molly B. Sheridan has authored 11 papers receiving a total of 281 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Molly B. Sheridan's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Molly B. Sheridan is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Molly B. Sheridan collaborates with scholars based in United States, Switzerland and Japan. Molly B. Sheridan's co-authors include Garry R. Cutting, Elizabeth Wohler, Denise Batista, Julie Hoover‐Fong, Carolyn Applegate, Joshua D. Groman, Lindsay B. Henderson, Rubén Díaz, Christopher Harris and C. Conrad and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Molly B. Sheridan

11 papers receiving 265 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Molly B. Sheridan United States	8	137	118	98	34	30	11	281
Margaret N. Berry United States	9	109 0.8×	182 1.5×	64 0.7×	23 0.7×	37 1.2×	15	275
Koen Devriendt Belgium	9	137 1.0×	205 1.7×	31 0.3×	20 0.6×	61 2.0×	13	290
Jostein Westvik Norway	9	172 1.3×	246 2.1×	23 0.2×	21 0.6×	35 1.2×	14	364
Konstantina Kosma Greece	10	137 1.0×	130 1.1×	18 0.2×	17 0.5×	37 1.2×	30	288
Jillene Kogan United States	9	94 0.7×	105 0.9×	20 0.2×	25 0.7×	34 1.1×	13	217
Fernando Santos Spain	9	228 1.7×	193 1.6×	20 0.2×	21 0.6×	84 2.8×	13	325
Mengmeng Shi China	10	81 0.6×	99 0.8×	25 0.3×	11 0.3×	74 2.5×	20	289
Alison Yeung Australia	11	283 2.1×	130 1.1×	22 0.2×	16 0.5×	69 2.3×	19	385
Cindy Pham Lorentz United States	8	294 2.1×	287 2.4×	50 0.5×	77 2.3×	64 2.1×	9	438
Alice Bailey United States	6	74 0.5×	115 1.0×	35 0.4×	11 0.3×	14 0.5×	10	163

Countries citing papers authored by Molly B. Sheridan

Since Specialization

Citations

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

Fields of papers citing papers by Molly B. Sheridan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Molly B. Sheridan. 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 Molly B. Sheridan. The network helps show where Molly B. Sheridan may publish in the future.

Co-authorship network of co-authors of Molly B. Sheridan

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

All Works

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11 of 11 papers shown

Li, Dong, Suzanne M. Jan de Beur, Cuiping Hou, et al.. (2024). Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1B. JCI Insight. 9(24). 1 indexed citations

Sheridan, Molly B., Melis A. Aksit, Kymberleigh A. Pagel, et al.. (2024). The clinical utility of sequencing the entirety of CFTR. Journal of Cystic Fibrosis. 23(4). 707–715. 1 indexed citations

Collaco, Joseph M., Karen S. Raraigh, Joshua Betz, et al.. (2021). Accurate assignment of disease liability to genetic variants using only population data. Genetics in Medicine. 24(1). 87–99. 1 indexed citations

Raraigh, Karen S., Sangwoo T. Han, Emily F. Davis-Marcisak, et al.. (2018). Functional Assays Are Essential for Interpretation of Missense Variants Associated with Variable Expressivity. The American Journal of Human Genetics. 102(6). 1062–1077. 51 indexed citations

Sheridan, Molly B., Elizabeth Wohler, Denise Batista, Carolyn Applegate, & Julie Hoover‐Fong. (2015). The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome. SHILAP Revista de lepidopterología. 2015. 1–6. 8 indexed citations

Kato, Takema, Molly B. Sheridan, April M. Hacker, et al.. (2014). Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation. Cancer Genetics. 207(4). 133–140. 18 indexed citations

Henderson, Lindsay B., Carolyn Applegate, Elizabeth Wohler, et al.. (2014). The impact of chromosomal microarray on clinical management: a retrospective analysis. Genetics in Medicine. 16(9). 657–664. 56 indexed citations

Widdershoven, Josine, Mark Bowser, Molly B. Sheridan, et al.. (2012). A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients. International Journal of Pediatric Otorhinolaryngology. 77(1). 123–127. 16 indexed citations

Sheridan, Molly B., Takema Kato, Chad Haldeman‐Englert, et al.. (2010). A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic Nondisjunction: The t(8;22)(q24.13;q11.21). The American Journal of Human Genetics. 87(2). 209–218. 48 indexed citations

10.

Groman, Joshua D., Barbara Karczeski, Molly B. Sheridan, et al.. (2005). Phenotypic and genetic characterization of patients with features of “nonclassic” forms of cystic fibrosis. The Journal of Pediatrics. 146(5). 675–680. 21 indexed citations

11.

Sheridan, Molly B., Peying Fong, Joshua D. Groman, et al.. (2005). Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. Human Molecular Genetics. 14(22). 3493–3498. 60 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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