Danielle Nolan

594 total citations
10 papers, 129 citations indexed

About

Danielle Nolan is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Danielle Nolan has authored 10 papers receiving a total of 129 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Clinical Biochemistry. Recurrent topics in Danielle Nolan's work include Genomics and Rare Diseases (4 papers), Epilepsy research and treatment (3 papers) and Metabolism and Genetic Disorders (3 papers). Danielle Nolan is often cited by papers focused on Genomics and Rare Diseases (4 papers), Epilepsy research and treatment (3 papers) and Metabolism and Genetic Disorders (3 papers). Danielle Nolan collaborates with scholars based in United States, Poland and Pakistan. Danielle Nolan's co-authors include Martha Carlson, John K. Fink, Daniel H. Arndt, Renée A. Shellhaas, S Lester, Baibing Chen, Anant Krishnan, Sara Caylor, Cristian Meghea and Vinod K. Misra and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Journal of Child Neurology.

In The Last Decade

Danielle Nolan

9 papers receiving 128 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Danielle Nolan United States	6	75	46	33	23	18	10	129
Ashley P.L. Marsh Australia	6	44 0.6×	65 1.4×	27 0.8×	40 1.7×	5 0.3×	9	150
Radoslava Vazharova Bulgaria	7	103 1.4×	106 2.3×	46 1.4×	22 1.0×	27 1.5×	26	235
Clara D. van Karnebeek Netherlands	9	60 0.8×	97 2.1×	15 0.5×	12 0.5×	11 0.6×	23	174
Meghan Candee United States	6	71 0.9×	31 0.7×	40 1.2×	17 0.7×	19 1.1×	10	123
Thibaud Jouan France	5	57 0.8×	66 1.4×	11 0.3×	9 0.4×	6 0.3×	7	111
Christelle Rougeot France	6	61 0.8×	81 1.8×	20 0.6×	50 2.2×	4 0.2×	12	183
Ilya Kanivets Russia	7	61 0.8×	91 2.0×	12 0.4×	26 1.1×	4 0.2×	39	162
Philip Holmgren Belgium	5	88 1.2×	66 1.4×	48 1.5×	20 0.9×	2 0.1×	5	174
Timo Roser Germany	7	18 0.2×	30 0.7×	63 1.9×	19 0.8×	10 0.6×	11	113
Stephanie Karch Germany	8	50 0.7×	101 2.2×	9 0.3×	11 0.5×	3 0.2×	8	146

Countries citing papers authored by Danielle Nolan

Since Specialization

Citations

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

Fields of papers citing papers by Danielle Nolan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danielle Nolan

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

1.

Samanta, Debopam, Sonal Bhatia, Cemal Karakas, et al.. (2025). Current and Emerging Precision Therapies for Developmental and Epileptic Encephalopathies. Pediatric Neurology. 168. 67–81. 9 indexed citations

2.

Bupp, Caleb, Danielle Nolan, John J. O’Shea, et al.. (2025). Implementation of Rapid Whole Genome Sequencing in Pediatric Acute Care is Associated with Positive Shifts in Health Care Professionals’ Perspectives Toward Testing. The Journal of Pediatrics. 282. 114571–114571.

3.

Keeley, Jacob, et al.. (2024). Electroencephalographic Patterns on Follow-Up Visits in Extremely Premature Infants With Periventricular Leukomalacia: An Observational Study. Pediatric Neurology. 157. 127–133. 1 indexed citations

4.

Bupp, Caleb, Elizabeth G. Ames, Sara Caylor, et al.. (2023). Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan’s Project Baby Deer. Children. 10(1). 106–106. 17 indexed citations

5.

Nolan, Danielle, et al.. (2020). Unusual case of biotin-thiamine responsive encephalopathy without basal ganglia involvement. Pediatric Radiology. 51(3). 485–488. 2 indexed citations

6.

Nolan, Danielle, et al.. (2019). A Rasmussen encephalitis, autoimmune encephalitis, and mitochondrial disease mimicker: expanding the DNM1L‐associated intractable epilepsy and encephalopathy phenotype. Epileptic Disorders. 21(1). 112–116. 11 indexed citations

7.

Nolan, Danielle & John K. Fink. (2018). Genetics of epilepsy. Handbook of clinical neurology. 148. 467–491. 29 indexed citations

8.

Nolan, Danielle, et al.. (2018). Clinical Use and Efficacy of Levetiracetam for Absence Epilepsies. Journal of Child Neurology. 34(2). 94–98. 7 indexed citations

9.

Nolan, Danielle & Martha Carlson. (2016). Whole Exome Sequencing in Pediatric Neurology Patients. Journal of Child Neurology. 31(7). 887–894. 52 indexed citations

10.

Kawai, Yu, et al.. (2016). A Previously Healthy Adolescent With Acute Encephalopathy and Decorticate Posturing. PEDIATRICS. 139(1). 1 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.

Explore authors with similar magnitude of impact