Angela E. Lin

16.3k total citations · 1 hit paper
190 papers, 8.6k citations indexed

About

Angela E. Lin is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Angela E. Lin has authored 190 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Genetics, 69 papers in Molecular Biology and 51 papers in Surgery. Recurrent topics in Angela E. Lin's work include Congenital Heart Disease Studies (36 papers), Congenital heart defects research (27 papers) and Tracheal and airway disorders (22 papers). Angela E. Lin is often cited by papers focused on Congenital Heart Disease Studies (36 papers), Congenital heart defects research (27 papers) and Tracheal and airway disorders (22 papers). Angela E. Lin collaborates with scholars based in United States, Italy and Canada. Angela E. Lin's co-authors include Lewis B. Holmes, Allen A. Mitchell, Sonja A. Rasmussen, Karen W. Gripp, Tiffany Riehle‐Colarusso, John M. Graham, Lorenzo D. Botto, Martha M. Werler, Richard S. Olney and Kim M. Keppler‐Noreuil and has published in prestigious journals such as New England Journal of Medicine, Journal of the American Chemical Society and JAMA.

In The Last Decade

Angela E. Lin

182 papers receiving 8.4k citations

Hit Papers

Clinical practice guidelines for the care of girls and wo... 2017 2026 2020 2023 2017 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting
    2017 663 citations Angela E. Lin et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Angela E. Lin United States 48 3.0k 2.7k 2.1k 1.9k 1.6k 190 8.6k
David Chitayat Canada 55 4.8k 1.6× 3.3k 1.2× 1.9k 0.9× 867 0.5× 823 0.5× 403 11.6k
Stephen M. Shalet United Kingdom 66 3.0k 1.0× 1.7k 0.6× 1.7k 0.8× 788 0.4× 844 0.5× 268 13.7k
Cynthia J. Curry United States 54 4.4k 1.5× 2.5k 0.9× 2.2k 1.1× 625 0.3× 416 0.3× 126 9.8k
Claude Férec France 55 3.9k 1.3× 2.8k 1.1× 2.2k 1.1× 2.7k 1.5× 620 0.4× 445 11.8k
Outi Mäkitie Finland 51 3.0k 1.0× 3.2k 1.2× 1.2k 0.6× 651 0.3× 1.4k 0.9× 383 9.8k
Nancy B. Spinner United States 53 4.9k 1.6× 4.0k 1.5× 4.0k 1.9× 2.4k 1.3× 928 0.6× 186 11.2k
Jan M. Wit Netherlands 59 4.0k 1.3× 3.6k 1.3× 992 0.5× 1.0k 0.6× 484 0.3× 316 12.8k
David L. Rimoin United States 60 5.0k 1.7× 6.6k 2.5× 2.0k 1.0× 791 0.4× 944 0.6× 292 13.2k
Claude Stoll France 45 1.2k 0.4× 1.8k 0.7× 2.7k 1.3× 909 0.5× 965 0.6× 209 6.1k
Drucilla J. Roberts United States 49 4.2k 1.4× 1.3k 0.5× 1.6k 0.8× 846 0.5× 875 0.6× 177 10.6k

Countries citing papers authored by Angela E. Lin

Since Specialization
Citations

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

Fields of papers citing papers by Angela E. Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Angela E. Lin. 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 Angela E. Lin. The network helps show where Angela E. Lin may publish in the future.

Co-authorship network of co-authors of Angela E. Lin

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

All Works

20 of 20 papers shown
1.
Moschovis, Peter P., Leo C. Ginns, Marc S. Cohen, et al.. (2025). Pulmonary, Airway, and Sleep Features in Myhre Syndrome: A Cohort Study. American Journal of Respiratory and Critical Care Medicine. 211(Supplement_1). A5129–A5129.
2.
Downing, Karrie F., Angela E. Lin, Wendy N. Nembhard, et al.. (2024). Survival to Young Adulthood Among Individuals With Congenital Heart Defects and Genetic Syndromes: Congenital Heart Survey to Recognize Outcomes, Needs, and Well‐Being. Journal of the American Heart Association. 13(15). e036049–e036049. 1 indexed citations
3.
Luben, Thomas J., Ibrahim Zaganjor, Anthony Rhoads, et al.. (2024). Maternal Exposure to Tap Water Disinfection By‐Products and Risk of Selected Congenital Heart Defects. Birth Defects Research. 116(9). e2391–e2391. 3 indexed citations
4.
Louis, James D. St., Aarti Bhat, John C. Carey, et al.. (2024). The American Association for Thoracic Surgery (AATS) 2023 Expert Consensus Document: Recommendation for the care of children with trisomy 13 or trisomy 18 and a congenital heart defect. Journal of Thoracic and Cardiovascular Surgery. 167(5). 1519–1532. 8 indexed citations
5.
Benjamin, Renata H., Keila N. Lopez, Brett R. Anderson, et al.. (2024). Enhancing the Classification of Congenital Heart Defects for Outcome Association Studies in Birth Defects Registries. Birth Defects Research. 116(8). e2393–e2393. 2 indexed citations
6.
Pettersson, Maria, Dora Dias‐Santagata, Daniel Nilsson, et al.. (2023). Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome. Frontiers in Genetics. 14. 1174046–1174046. 5 indexed citations
7.
Sangadala, Sreedhara, Eileen M. Shore, Meiqi Xu, et al.. (2023). Multifocal heterotopic ossification in a man with germline variants of LIM Mineralization Protein‐1 (LMP‐1). American Journal of Medical Genetics Part A. 191(8). 2164–2174.
8.
Lin, Angela E., Sonja A. Rasmussen, Russell S. Kirby, et al.. (2023). Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000–2017: A report from the National Birth Defects Prevention Network. American Journal of Medical Genetics Part A. 191(5). 1339–1349. 10 indexed citations
9.
Berrocal, Audina M., Emily Place, Heather Mason‐Suares, et al.. (2022). Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome. Ophthalmic Genetics. 44(2). 198–203. 2 indexed citations
10.
Patel, Nisha, John M. Graham, Michael J. Bamshad, et al.. (2021). Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. American Journal of Medical Genetics Part A. 185(7). 2136–2149. 3 indexed citations
11.
Gripp, Karen W., Marni E. Axelrad, Kathryn C. Chatfield, et al.. (2019). Costello syndrome: Clinical phenotype, genotype, and management guidelines. American Journal of Medical Genetics Part A. 179(9). 1725–1744. 72 indexed citations
12.
Lin, Angela E., Caroline Michot, Valérie Cormier‐Daire, et al.. (2016). Gain‐of‐function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome. American Journal of Medical Genetics Part A. 170(10). 2617–2631. 45 indexed citations
13.
Lin, Angela E., Avram Z. Traum, Inderneel Sahai, et al.. (2013). Sensenbrenner syndrome (Cranioectodermal dysplasia): Clinical and molecular analyses of 39 patients including two new patients. American Journal of Medical Genetics Part A. 161(11). 2762–2776. 49 indexed citations
14.
Lin, Angela E., et al.. (2013). Human Milk Oligosaccharides Protect Bladder Epithelial Cells Against Uropathogenic Escherichia coli Invasion and Cytotoxicity. The Journal of Infectious Diseases. 209(3). 389–398. 68 indexed citations
15.
Hartman, Robert J., Tiffany Riehle‐Colarusso, Angela E. Lin, et al.. (2011). Descriptive study of nonsyndromic atrioventricular septal defects in the National Birth Defects Prevention Study, 1997–2005. American Journal of Medical Genetics Part A. 155(3). 555–564. 15 indexed citations
16.
Botto, Lorenzo D., Angela E. Lin, Tiffany Riehle‐Colarusso, Sarita Malik, & Adolfo Correa. (2007). Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies. Birth Defects Research Part A Clinical and Molecular Teratology. 79(10). 714–727. 375 indexed citations
17.
Lin, Angela E., Barbara R. Pober, & Ian Adatia. (2007). Congenital diaphragmatic hernia and associated cardiovascular malformations: Type, frequency, and impact on management. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(2). 201–216. 64 indexed citations
18.
Huang, Taosheng, Angela E. Lin, Gerald F. Cox, et al.. (2002). Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene. Genetics in Medicine. 4(6). 464–467. 29 indexed citations
19.
Neri, Giovanni, Fiorella Gurrieri, Ginevra Zanni, & Angela E. Lin. (1998). Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome. American Journal of Medical Genetics. 79(4). 279–283. 135 indexed citations
20.
Lin, Angela E., Robert J. Gorlin, Iosif W. Lurie, et al.. (1995). Further delineation of the branchio‐oculo‐facial syndrome. American Journal of Medical Genetics. 56(1). 42–59. 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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