Lacey Smith

1.4k total citations
20 papers, 393 citations indexed

About

Lacey Smith is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Lacey Smith has authored 20 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Psychiatry and Mental health and 4 papers in Molecular Biology. Recurrent topics in Lacey Smith's work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Epilepsy research and treatment (8 papers). Lacey Smith is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Epilepsy research and treatment (8 papers). Lacey Smith collaborates with scholars based in United States, Germany and Australia. Lacey Smith's co-authors include Beth Rosen Sheidley, Annapurna Poduri, Christelle Moufawad El Achkar, Heather E. Olson, Kathleen J. Haley, Nilika S. Singhal, Joseph Sullivan, McKenna Kelly, Alan Taylor and Sonal Mahida and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Lacey Smith

16 papers receiving 388 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lacey Smith United States	10	207	139	130	65	45	20	393
Haiqing Xu China	8	284 1.4×	243 1.7×	217 1.7×	84 1.3×	30 0.7×	16	588
Ji Yoon Han South Korea	13	145 0.7×	103 0.7×	139 1.1×	86 1.3×	33 0.7×	58	420
In Goo Lee South Korea	12	126 0.6×	156 1.1×	107 0.8×	151 2.3×	49 1.1×	31	411
Anne Rochtus Belgium	10	217 1.0×	98 0.7×	189 1.5×	75 1.2×	8 0.2×	26	379
Takehiko Inui Japan	13	116 0.6×	126 0.9×	194 1.5×	103 1.6×	13 0.3×	48	459
Kiyokuni Miura Japan	12	141 0.7×	100 0.7×	133 1.0×	77 1.2×	15 0.3×	29	444
Wakaba Endo Japan	12	108 0.5×	82 0.6×	151 1.2×	66 1.0×	10 0.2×	38	365
Ewa Jamroz Poland	13	139 0.7×	47 0.3×	241 1.9×	83 1.3×	15 0.3×	52	529
Mutluay Arslan Türkiye	10	78 0.4×	40 0.3×	106 0.8×	50 0.8×	23 0.5×	29	245

Countries citing papers authored by Lacey Smith

Since Specialization

Citations

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

Fields of papers citing papers by Lacey Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lacey Smith

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

All Works

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20 of 20 papers shown

Budnik, Nikita, Siwei Chen, David Báez-Nieto, et al.. (2025). Characterization of the functional and clinical impacts of CACNA1A missense variants found in neurodevelopmental disorders. Science Translational Medicine. 17(828). eadr0024–eadr0024.

Brünger, Tobias, Eduardo Pérez‐Palma, Ludovica Montanucci, et al.. (2025). Conserved missense variant pathogenicity and correlated phenotypes across paralogous genes. Genome biology. 26(1). 197–197.

Smith, Lacey, et al.. (2025). Frugal Innovations in Orthopaedics. Current Reviews in Musculoskeletal Medicine. 18(12). 568–576.

Srivastava, Siddharth, et al.. (2024). Cerebral Palsy Phenotypes in Genetic Epilepsies. Pediatric Neurology. 157. 79–86.

D’Gama, Alissa M., Wanqing Shao, Lacey Smith, et al.. (2024). Genome Sequencing After Exome Sequencing in Pediatric Epilepsy. JAMA Neurology. 81(12). 1316–1316. 2 indexed citations

Singhal, Nilika S., Joseph Sullivan, Tina Shih, et al.. (2023). Epilepsy surgery as a treatment option for select patients with PCDH19-related epilepsy. Epilepsy & Behavior. 149. 109517–109517. 3 indexed citations

Smith, Lacey, Elia Pestana‐Knight, Scott Demarest, et al.. (2023). CDKL5 deficiency disorder and other infantile‐onset genetic epilepsies. Developmental Medicine & Child Neurology. 66(4). 456–468. 5 indexed citations

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

Drew, Jacqueline M., Jamie Love‐Nichols, Lindsay C. Swanson, et al.. (2022). Genetic Diagnosis Impacts Medical Management for Pediatric Epilepsies. Pediatric Neurology. 138. 71–80. 14 indexed citations

10.

Ganesan, Shiva, David Lewis‐Smith, Manuela Pendziwiat, et al.. (2020). Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies. The American Journal of Human Genetics. 107(4). 683–697. 22 indexed citations

11.

Achkar, Christelle Moufawad El, Lacey Smith, McKenna Kelly, et al.. (2020). Characterization of the GABRB2‐Associated Neurodevelopmental Disorders. Annals of Neurology. 89(3). 573–586. 19 indexed citations

12.

Bushlin, Ittai, Lacey Smith, Jurriaan M. Peters, & Christelle Moufawad El Achkar. (2020). Clinical Reasoning: A 6-week-old infant with migrating focal seizures. Neurology. 94(4). 178–183. 1 indexed citations

13.

Rochtus, Anne, Heather E. Olson, Lacey Smith, et al.. (2020). Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort. Epilepsia. 61(2). 249–258. 88 indexed citations

14.

Smith, Lacey, Nilika S. Singhal, Christelle Moufawad El Achkar, et al.. (2018). PCDH19‐related epilepsy is associated with a broad neurodevelopmental spectrum. Epilepsia. 59(3). 679–689. 58 indexed citations

15.

Rodan, Lance H., Kwame Anyane‐Yeboa, Karen Chong, et al.. (2018). Gain‐of‐function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities. American Journal of Medical Genetics Part A. 176(12). 2554–2560. 28 indexed citations

16.

Sheidley, Beth Rosen, Lacey Smith, & Katherine L. Helbig. (2018). Genetics of Epilepsy in the Era of Precision Medicine: Implications for Testing, Treatment, and Genetic Counseling. 6(2). 73–82. 2 indexed citations

17.

Smith, Lacey, Jeremy F.P. Ullmann, Heather E. Olson, et al.. (2017). A Model Program for Translational Medicine in Epilepsy Genetics. Journal of Child Neurology. 32(4). 429–436. 5 indexed citations

18.

Smith, Lacey, Jessica Douglas, Alicia Braxton, & Kate M. Kramer. (2014). Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling. Journal of Genetic Counseling. 24(4). 654–662. 18 indexed citations

19.

Smith, Lacey, Carrie A. Vyhlidal, Chang Hyeok An, et al.. (2012). Maternal smoking and the retinoid pathway in the developing lung. Respiratory Research. 13(1). 42–42. 25 indexed citations

20.

Haley, Kathleen J., Jessica Lasky‐Su, Lacey Smith, et al.. (2011). RUNX transcription factors: association with pediatric asthma and modulated by maternal smoking. American Journal of Physiology-Lung Cellular and Molecular Physiology. 301(5). L693–L701. 51 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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