Lisa Emrick

4.7k total citations
43 papers, 736 citations indexed

About

Lisa Emrick is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Lisa Emrick has authored 43 papers receiving a total of 736 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 19 papers in Clinical Biochemistry and 11 papers in Genetics. Recurrent topics in Lisa Emrick's work include Metabolism and Genetic Disorders (19 papers), Mitochondrial Function and Pathology (16 papers) and Genomics and Rare Diseases (6 papers). Lisa Emrick is often cited by papers focused on Metabolism and Genetic Disorders (19 papers), Mitochondrial Function and Pathology (16 papers) and Genomics and Rare Diseases (6 papers). Lisa Emrick collaborates with scholars based in United States, Hong Kong and United Kingdom. Lisa Emrick's co-authors include Fernando Scaglia, Ayman W. El‐Hattab, William J. Craigen, Farook Jahoor, Jean W. Hsu, William J. Craigen, Sirisak Chanprasert, Lee‐Jun C. Wong, V. Reid Sutton and Sarah H. Elsea and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and The American Journal of Human Genetics.

In The Last Decade

Lisa Emrick

35 papers receiving 726 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lisa Emrick United States 15 486 290 134 105 53 43 736
Pascale Delonlay France 11 304 0.6× 255 0.9× 100 0.7× 42 0.4× 48 0.9× 13 530
László Wenchich Czechia 14 542 1.1× 226 0.8× 123 0.9× 42 0.4× 29 0.5× 33 707
Atsushi Shima Japan 14 358 0.7× 239 0.8× 217 1.6× 37 0.4× 64 1.2× 38 782
A. A. M. Morris United Kingdom 17 613 1.3× 529 1.8× 254 1.9× 126 1.2× 50 0.9× 27 1.0k
Karen L. Madsen Denmark 15 364 0.7× 168 0.6× 260 1.9× 83 0.8× 111 2.1× 41 725
María Antònia Vilaseca Spain 20 639 1.3× 652 2.2× 269 2.0× 138 1.3× 49 0.9× 45 1.1k
Tamara Ramadan Switzerland 10 361 0.7× 132 0.5× 101 0.8× 60 0.6× 86 1.6× 11 832
Alecia Willis United States 14 373 0.8× 132 0.5× 77 0.6× 195 1.9× 42 0.8× 17 643
Noman Kadhom France 10 1.0k 2.1× 453 1.6× 79 0.6× 149 1.4× 42 0.8× 10 1.2k
Arno van Cruchten Netherlands 14 646 1.3× 297 1.0× 173 1.3× 45 0.4× 46 0.9× 16 894

Countries citing papers authored by Lisa Emrick

Since Specialization
Citations

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

Fields of papers citing papers by Lisa Emrick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa Emrick

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa Emrick. A scholar is included among the top collaborators of Lisa Emrick 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 Lisa Emrick. Lisa Emrick 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.
Zhao, Sen, Shenglan Li, Jill A. Rosenfeld, et al.. (2025). The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics. The American Journal of Human Genetics. 112(11). 2578–2590.
2.
Calame, Daniel G., et al.. (2024). ATP1A3 Disease Spectrum Includes Paroxysmal Weakness and Encephalopathy Not Triggered by Fever. Neurology Genetics. 10(3). e200150–e200150.
3.
Gijavanekar, Charul, Yue Wang, Keren Machol, et al.. (2024). Untargeted metabolomics analysis as a potential screening tool for 3-methylglutaconic aciduria syndromes. Molecular Genetics and Metabolism. 144(3). 109009–109009.
4.
Calame, Daniel G. & Lisa Emrick. (2024). Functional genomics and small molecules in mitochondrial neurodevelopmental disorders. Neurotherapeutics. 21(1). e00316–e00316. 1 indexed citations
5.
Machol, Keren, Stephen F. Kralik, Mir Reza Bekheirnia, et al.. (2024). Expanded clinical phenotype and untargeted metabolomics analysis in RARS2-related mitochondrial disorder: a case report. BMC Neurology. 24(1). 2 indexed citations
6.
Ward, Scott, Paul J. Benke, Lisa Emrick, et al.. (2023). De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities. American Journal of Medical Genetics Part A. 194(1). 17–30.
7.
Tarui, Tomo, Charu Venkatesan, Dawn Gano, et al.. (2023). Fetal Neurology Practice Survey: Current Practice and the Future Directions. Pediatric Neurology. 145. 74–79. 15 indexed citations
8.
Wang, Julia, Wenmiao Zhu, Hongzheng Dai, et al.. (2021). PPP3CA truncating variants clustered in the regulatory domain cause early‐onset refractory epilepsy. Clinical Genetics. 100(2). 227–233. 11 indexed citations
9.
Wilson, Jenny L., Allison Gregory, Manju A. Kurian, et al.. (2021). Consensus clinical management guideline for beta‐propeller protein‐associated neurodegeneration. Developmental Medicine & Child Neurology. 63(12). 1402–1409. 23 indexed citations
10.
Calame, Daniel G., et al.. (2021). A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients. European Journal of Paediatric Neurology. 31. 21–26. 5 indexed citations
11.
Jiang, Ming‐Ming, Xiaohui Li, Ronit Marom, et al.. (2021). A novel de novo intronic variant in ITPR1 causes Gillespie syndrome. American Journal of Medical Genetics Part A. 185(8). 2315–2324. 5 indexed citations
12.
13.
Kennedy, Adam D., Kirk L. Pappan, Taraka Donti, et al.. (2019). 2-Pyrrolidinone and Succinimide as Clinical Screening Biomarkers for GABA-Transaminase Deficiency: Anti-seizure Medications Impact Accurate Diagnosis. Frontiers in Neuroscience. 13. 1344–1344. 29 indexed citations
14.
Ng, Bobby G., Jill A. Rosenfeld, Lisa Emrick, et al.. (2018). Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation. The American Journal of Human Genetics. 103(6). 1030–1037. 25 indexed citations
15.
Donti, Taraka, Gerarda Cappuccio, Leroy Hubert, et al.. (2016). Diagnosis of adenylosuccinate lyase deficiency by metabolomic profiling in plasma reveals a phenotypic spectrum. Molecular Genetics and Metabolism Reports. 8. 61–66. 49 indexed citations
16.
Agarwal, Sonika & Lisa Emrick. (2015). De Novo Mutations in Patients with Ataxic CP. SHILAP Revista de lepidopterología. 29(8). 62–62. 1 indexed citations
17.
Atwal, Paldeep S., Taraka Donti, Aaron L. Cardon, et al.. (2015). Aromatic l-amino acid decarboxylase deficiency diagnosed by clinical metabolomic profiling of plasma. Molecular Genetics and Metabolism. 115(2-3). 91–94. 48 indexed citations
18.
Emrick, Lisa, Lauren Murphy, Alireza A. Shamshirsaz, et al.. (2014). Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes. American Journal of Medical Genetics Part A. 164(10). 2633–2637. 25 indexed citations
19.
El‐Hattab, Ayman W., Lisa Emrick, William J. Craigen, & Fernando Scaglia. (2012). Citrulline and arginine utility in treating nitric oxide deficiency in mitochondrial disorders. Molecular Genetics and Metabolism. 107(3). 247–252. 82 indexed citations
20.
Aweeka, Francesca, John G. Gambertoglio, Françoise Kramer, et al.. (1995). Foscarnet and ganciclovir pharmacokinetics during concomitant or alternating maintenance therapy for AIDS-related cytomegalovirus retinitis*. Clinical Pharmacology & Therapeutics. 57(4). 403–412. 12 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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