Hillary B. Heins

1.1k total citations
19 papers, 347 citations indexed

About

Hillary B. Heins is a scholar working on Pulmonary and Respiratory Medicine, Endocrine and Autonomic Systems and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hillary B. Heins has authored 19 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pulmonary and Respiratory Medicine, 8 papers in Endocrine and Autonomic Systems and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hillary B. Heins's work include Neonatal Respiratory Health Research (16 papers), Neuroscience of respiration and sleep (8 papers) and Neonatal Health and Biochemistry (5 papers). Hillary B. Heins is often cited by papers focused on Neonatal Respiratory Health Research (16 papers), Neuroscience of respiration and sleep (8 papers) and Neonatal Health and Biochemistry (5 papers). Hillary B. Heins collaborates with scholars based in United States, Ireland and South Africa. Hillary B. Heins's co-authors include F. Sessions Cole, Daniel Wegner, Aaron Hamvas, Jennifer Wambach, Lawrence M. Nogee, Ping An, Ping Yang, Francis White, Todd E. Druley and Michelle Trusgnich and has published in prestigious journals such as Journal of Clinical Investigation, Analytical Chemistry and PEDIATRICS.

In The Last Decade

Hillary B. Heins

18 papers receiving 339 citations

Peers

Hillary B. Heins
Marilyn L. Scott United States
J. Egberts Netherlands
Marye H. Godinez United States
Marianne Anderson United States
Benjamin C Planer United States
Matthew Harrison United Kingdom
Bonnie G. Landrum United States
Marilyn L. Scott United States
Hillary B. Heins
Citations per year, relative to Hillary B. Heins Hillary B. Heins (= 1×) peers Marilyn L. Scott

Countries citing papers authored by Hillary B. Heins

Since Specialization
Citations

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

Fields of papers citing papers by Hillary B. Heins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hillary B. Heins

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

All Works

19 of 19 papers shown
1.
Heins, Hillary B., et al.. (2025). Proteome-wide assessment of differential missense variant clustering in neurodevelopmental disorders and cancer. Cell Genomics. 5(4). 100807–100807. 1 indexed citations
2.
Sun, Yuliang, Erin Hennessey, Hillary B. Heins, et al.. (2024). Human pluripotent stem cell modeling of alveolar type 2 cell dysfunction caused by ABCA3 mutations. Journal of Clinical Investigation. 134(2). 7 indexed citations
3.
Wegner, Daniel, Hillary B. Heins, Ping Yang, et al.. (2022). Biologic characterization of ABCA3 variants in lung tissue from infants and children with ABCA3 deficiency. Pediatric Pulmonology. 57(5). 1325–1330. 4 indexed citations
4.
Wambach, Jennifer, Ping Yang, Daniel Wegner, et al.. (2020). Functional Genomics of ABCA3 Variants. American Journal of Respiratory Cell and Molecular Biology. 63(4). 436–443. 17 indexed citations
5.
Yang, Ping, Daniel Wegner, Hillary B. Heins, et al.. (2020). Functional characterization of four ATP‐binding cassette transporter A3 gene (ABCA3) variants. Human Mutation. 41(7). 1298–1307. 15 indexed citations
6.
Wambach, Jennifer, Ping Yang, Daniel Wegner, et al.. (2016). Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome. American Journal of Respiratory Cell and Molecular Biology. 55(5). 716–721. 46 indexed citations
7.
Wambach, Jennifer, et al.. (2015). Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort. World Journal of Pediatrics. 12(2). 190–195. 7 indexed citations
8.
Wambach, Jennifer, Daniel Wegner, Hillary B. Heins, et al.. (2014). Synonymous ABCA3 Variants Do Not Increase Risk for Neonatal Respiratory Distress Syndrome. The Journal of Pediatrics. 164(6). 1316–1321.e3. 7 indexed citations
9.
Bereman, Michael S., Daniela M. Tomazela, Hillary B. Heins, et al.. (2012). A method to determine the kinetics of multiple proteins in human infants with respiratory distress syndrome. Analytical and Bioanalytical Chemistry. 403(8). 2397–2402. 4 indexed citations
10.
Wambach, Jennifer, Daniel Wegner, Hillary B. Heins, et al.. (2012). Single ABCA3 Mutations Increase Risk for Neonatal Respiratory Distress Syndrome. PEDIATRICS. 130(6). e1575–e1582. 65 indexed citations
11.
Morrison, Lake, Hillary B. Heins, Daniel Wegner, et al.. (2011). Rare Damaging Variants In The Surfactant Protein-C And ABCA3 Genes In Adult Patients With Idiopathic Pulmonary Fibrosis. A6003–A6003.
12.
Tomazela, Daniela M., Bruce W. Patterson, David H. Salinger, et al.. (2010). Measurement of Human Surfactant Protein-B Turnover in Vivo from Tracheal Aspirates Using Targeted Proteomics. Analytical Chemistry. 82(6). 2561–2567. 18 indexed citations
13.
Hamvas, Aaron, Hillary B. Heins, Susan H. Guttentag, et al.. (2008). Developmental and Genetic Regulation of Human Surfactant Protein B in vivo. Neonatology. 95(2). 117–124. 18 indexed citations
14.
Wegner, Daniel, Christopher S. Carlson, Jennifer Wambach, et al.. (2008). Recombination as a mechanism for sporadic mutation in the surfactant protein‐C gene. Pediatric Pulmonology. 43(5). 443–450. 8 indexed citations
15.
Wambach, Jennifer, Hillary B. Heins, Daniel Wegner, et al.. (2008). Population and Disease-Based Prevalence of the Common Mutations Associated With Surfactant Deficiency. Pediatric Research. 63(6). 645–649. 71 indexed citations
16.
Wegner, Daniel, Torbjörn Hertzberg, Hillary B. Heins, et al.. (2007). A major deletion in the surfactant protein‐B gene causing lethal respiratory distress. Acta Paediatrica. 96(4). 516–520. 19 indexed citations
17.
Hamvas, Aaron, Daniel Wegner, Michelle Trusgnich, et al.. (2005). Genetic variant characterization in intron 4 of the surfactant protein B gene. Human Mutation. 26(5). 494–495. 11 indexed citations
18.
Hamvas, Aaron, Lawrence M. Nogee, Michelle Trusgnich, et al.. (2004). Informed Consent for Genetic Research. Archives of Pediatrics and Adolescent Medicine. 158(6). 551–551. 27 indexed citations
19.
Kangarloo, Hooshang, et al.. (1981). Ultrasonography of mucocutaneous lymph node syndrome.. Radiology. 139(1). 166–166. 2 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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