Barbara Hallinan

2.2k total citations
14 papers, 199 citations indexed

About

Barbara Hallinan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Barbara Hallinan has authored 14 papers receiving a total of 199 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Neurology. Recurrent topics in Barbara Hallinan's work include Genomics and Rare Diseases (3 papers), Neuroscience and Neuropharmacology Research (3 papers) and Metabolism and Genetic Disorders (3 papers). Barbara Hallinan is often cited by papers focused on Genomics and Rare Diseases (3 papers), Neuroscience and Neuropharmacology Research (3 papers) and Metabolism and Genetic Disorders (3 papers). Barbara Hallinan collaborates with scholars based in United States, India and Israel. Barbara Hallinan's co-authors include Christine G. Spaeth, Katrina W. Lexa, Thomas Andrew Burrow, Luba Blumkin, A. James Barkovich, Esther Leshinsky‐Silver, Donald L. Gilbert, T. Burrow, John Pappas and Sahar Esmaeeli Nieh and has published in prestigious journals such as SHILAP Revista de lepidopterología, Frontiers in Genetics and Journal of Clinical Sleep Medicine.

In The Last Decade

Barbara Hallinan

14 papers receiving 197 citations

Peers

Barbara Hallinan

CMN

GENET

PMH

Bouchra Ouled Amar Bencheikh Canada

Victoria Poillerat France

Elena Alvárez‐Barón Spain

Naoko Asahina Japan

Amy Harper United States

Hirofumi Kashii Japan

Chloe Stutterd Australia

Kunihiko Araki Japan

Ivan Litvinenko Bulgaria

Kazue Kimura Japan

Bouchra Ouled Amar Bencheikh Canada

Barbara Hallinan

105 ×1.5

80 ×1.4

65 ×1.3

CMN

79 ×1.9

GENET

22 ×0.5

PMH

Citations per year, relative to Barbara Hallinan Barbara Hallinan (= 1×) peers Bouchra Ouled Amar Bencheikh

Countries citing papers authored by Barbara Hallinan

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Hallinan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Hallinan

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Hallinan. A scholar is included among the top collaborators of Barbara Hallinan 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 Barbara Hallinan. Barbara Hallinan 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

Sund, Kristen L., Joyce Lee, John Garbe, et al.. (2024). Long‐read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalities. American Journal of Medical Genetics Part A. 194(12). e63818–e63818. 3 indexed citations

Baker, Elizabeth, Jingfen Han, William A. Langley, et al.. (2023). RNA sequencing reveals a complete picture of a homozygous missense variant in a patient with VPS13D movement disorder: a case report and review of the literature. Molecular Genetics and Genomics. 298(5). 1185–1199. 1 indexed citations

Baker, Elizabeth, Barbara Hallinan, Nancy D. Leslie, et al.. (2022). Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center. Frontiers in Genetics. 13. 887698–887698. 1 indexed citations

Hallinan, Barbara, et al.. (2022). Case report: Clinical and magnetic resonance spectroscopy presentation of a female severely affected with X-linked creatine transporter deficiency. SHILAP Revista de lepidopterología. 17(4). 1115–1119. 3 indexed citations

Leino, Daniel, Christine Fuller, Blaise V. Jones, et al.. (2021). Lethal Pediatric Cerebral Vasculitis Triggered by Severe Acute Respiratory Syndrome Coronavirus 2. Pediatric Neurology. 127. 1–5. 20 indexed citations

Lesmana, Harry, Seyed Ali Hosseini, T. Burrow, et al.. (2018). CNTNAP1-Related Congenital Hypomyelinating Neuropathy. Pediatric Neurology. 93. 43–49. 14 indexed citations

Hallinan, Barbara, et al.. (2016). Correlation Among Genotype, Phenotype, and Histology in Neuronal Ceroid Lipofuscinoses: An Individual Patient Data Meta-Analysis. Pediatric Neurology. 60. 42–48.e4. 9 indexed citations

Hallinan, Barbara, et al.. (2015). A Novel Catastrophic Presentation of X-Linked Adrenoleukodystrophy. JIMD Reports. 24. 97–102. 9 indexed citations

Nieh, Sahar Esmaeeli, Minhajuddin Sirajuddin, Brieana Fregeau, et al.. (2015). De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy. Annals of Clinical and Translational Neurology. 2(6). 623–635. 76 indexed citations

10.

Natarajan, Niranjana, et al.. (2013). Narcolepsy-Cataplexy: Is Streptococcal Infection a Trigger?. Journal of Clinical Sleep Medicine. 9(3). 269–270. 10 indexed citations

11.

Peariso, Katrina, Shannon M. Standridge, Barbara Hallinan, et al.. (2013). Presentation, diagnosis and treatment of bilateral Rasmussen's encephalitis in a 12‐year‐old female. Epileptic Disorders. 15(3). 324–332. 14 indexed citations

12.

Greiner, Hansel M., et al.. (2012). Corpus callosotomy for treatment of pediatric refractory status epilepticus. Seizure. 21(4). 307–309. 14 indexed citations

13.

Tenney, Jeffrey R., Carlos E. Prada, Robert J. Hopkin, & Barbara Hallinan. (2012). Early Spinal Cord and Brainstem Involvement in Infantile Leigh Syndrome Possibly Caused by a Novel Variant. Journal of Child Neurology. 28(12). 1681–1685. 9 indexed citations

14.

Holland, Katherine D., et al.. (2011). When Should Clinicians Order Genetic Testing for Dravet Syndrome?. Pediatric Neurology. 45(5). 319–323. 16 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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