Natalie Lippa

7.1k total citations · 1 hit paper
14 papers, 5.5k citations indexed

About

Natalie Lippa is a scholar working on Genetics, Psychiatry and Mental health and Physiology. According to data from OpenAlex, Natalie Lippa has authored 14 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Psychiatry and Mental health and 3 papers in Physiology. Recurrent topics in Natalie Lippa's work include Genomics and Rare Diseases (7 papers), Epilepsy research and treatment (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Natalie Lippa is often cited by papers focused on Genomics and Rare Diseases (7 papers), Epilepsy research and treatment (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Natalie Lippa collaborates with scholars based in United States, Belgium and Italy. Natalie Lippa's co-authors include Saskia C. Sanderson, Melissa Wasserstein, Margaret M. McGovern, Emilia Bagiella, Edward H. Schuchman, Robert J. Desnick, Lacey Smith, Beth Rosen Sheidley, Jennifer Malinowski and Nephi Walton and has published in prestigious journals such as Epilepsia, Obesity and Journal of Medical Genetics.

In The Last Decade

Natalie Lippa

12 papers receiving 5.4k citations

Hit Papers

align trajectories

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.

Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study

2013 5.2k citations Natalie Lippa, Saskia C. Sanderson Human Heredity profile →

Peers

Natalie Lippa

CP

PHEOH

PHARM

SP

GHP

Alison E. Field United States

Martin Teufel Germany

Carolyn Black Becker United States

Brenda B. Toner Canada

Sarah J. Shema United States

Helen Truby Australia

Charles W. Lidz United States

Ami D. Sperber Israel

Bernard F. Fuemmeler United States

Pauline W. Jansen Netherlands

Alison E. Field United States

Natalie Lippa

4.3k ×1.8

CP

3.0k ×2.2

PHEOH

1.4k ×1.1

PHARM

924 ×0.9

SP

562 ×0.7

GHP

Citations per year, relative to Natalie Lippa Natalie Lippa (= 1×) peers Alison E. Field

Countries citing papers authored by Natalie Lippa

Since Specialization

Citations

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

Fields of papers citing papers by Natalie Lippa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalie Lippa

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

All Works

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14 of 14 papers shown

1.

Bergner, Amanda L., et al.. (2025). Barriers to the implementation of epilepsy genetic testing and counseling guidelines. Epilepsia Open. 10(5). 1595–1604.

2.

Sands, Tristan T., et al.. (2024). Comparing the frequency of variants of uncertain significance (VUS) between ancestry groups in a paediatric epilepsy cohort. Journal of Medical Genetics. 61(7). 645–651. 3 indexed citations

3.

Lippa, Natalie, et al.. (2023). Clinical utility of exome sequencing in a pediatric epilepsy cohort. Epilepsia. 64(4). 986–997. 10 indexed citations

4.

Smith, Lacey, et al.. (2022). Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors. Journal of Genetic Counseling. 32(2). 266–280. 52 indexed citations

5.

Lippa, Natalie, Louise Bier, Anya Revah‐Politi, et al.. (2022). Diagnostic sequencing to support genetically stratified medicine in a tertiary care setting. Genetics in Medicine. 24(4). 862–869. 3 indexed citations

6.

Motelow, Joshua E., Natalie Lippa, Joseph Hostyk, et al.. (2022). Risk Variants in the Exomes of Children With Critical Illness. JAMA Network Open. 5(10). e2239122–e2239122.

7.

Lippa, Natalie, et al.. (2021). A novel de novo KDM5C variant in a female with global developmental delay and ataxia: a case report. BMC Neurology. 21(1). 358–358. 5 indexed citations

8.

Miceli, Francesco, Vincenzo Barrese, Maria Virginia Soldovieri, et al.. (2020). A Novel Kv7.3 Variant in the Voltage-Sensing S4 Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and in vitro Rescue by β-Hydroxybutyrate. Frontiers in Physiology. 11. 1040–1040. 7 indexed citations

9.

Stong, Nicholas, et al.. (2017). Spasmodic Dysphonia in Hereditary Spastic Paraplegia Type 7. Movement Disorders Clinical Practice. 5(2). 221–222. 5 indexed citations

10.

Wasserstein, Melissa, Simon Jones, Handrean Soran, et al.. (2015). Successful within-patient dose escalation of olipudase alfa in acid sphingomyelinase deficiency. Molecular Genetics and Metabolism. 116(1-2). 88–97. 70 indexed citations

11.

McGovern, Margaret M., Natalie Lippa, Emilia Bagiella, et al.. (2013). Morbidity and mortality in type B Niemann–Pick disease. Genetics in Medicine. 15(8). 618–623. 90 indexed citations

12.

Wasserstein, Melissa, Natalie Lippa, Emilia Bagiella, & Margaret M. McGovern. (2013). Morbidity and mortality in type B Niemann–Pick disease. Molecular Genetics and Metabolism. 108(2). S96–S96. 4 indexed citations

13.

Lippa, Natalie & Saskia C. Sanderson. (2013). Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study. Human Heredity. 75(2-4). 186–203. 5188 indexed citations breakdown →

14.

Lippa, Natalie & Saskia C. Sanderson. (2012). Impact of Information About Obesity Genomics on the Stigmatization of Overweight Individuals: An Experimental Study. Obesity. 20(12). 2367–2376. 29 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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