Hillary Lipe

2.5k total citations
40 papers, 1.5k citations indexed

About

Hillary Lipe is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Hillary Lipe has authored 40 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Cellular and Molecular Neuroscience, 14 papers in Neurology and 12 papers in Molecular Biology. Recurrent topics in Hillary Lipe's work include Genetic Neurodegenerative Diseases (21 papers), Hereditary Neurological Disorders (13 papers) and Neurological diseases and metabolism (8 papers). Hillary Lipe is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Hereditary Neurological Disorders (13 papers) and Neurological diseases and metabolism (8 papers). Hillary Lipe collaborates with scholars based in United States, Iran and Russia. Hillary Lipe's co-authors include Thomas D. Bird, Wendy H. Raskind, John Wolff, Mark Matsushita, Thomas D. Bird, Dong-Hui Chen, Phillip F. Chance, Magali Fernandez, M. William Lensch and Pamela H. Mitchell and has published in prestigious journals such as American Journal of Psychiatry, Neurology and Cancer.

In The Last Decade

Hillary Lipe

38 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hillary Lipe United States 24 945 600 593 210 123 40 1.5k
Javier Arpa Spain 20 798 0.8× 791 1.3× 583 1.0× 163 0.8× 105 0.9× 83 1.7k
Pedro Mancías United States 15 809 0.9× 380 0.6× 750 1.3× 280 1.3× 228 1.9× 37 1.7k
Alessandro Filla Italy 24 1.0k 1.1× 498 0.8× 949 1.6× 191 0.9× 145 1.2× 45 1.6k
Riadh Gouider Tunisia 20 803 0.8× 554 0.9× 321 0.5× 383 1.8× 225 1.8× 127 1.5k
Velina Guergueltcheva Bulgaria 23 561 0.6× 408 0.7× 899 1.5× 213 1.0× 308 2.5× 52 1.6k
H.-M. Meinck Germany 13 553 0.6× 952 1.6× 362 0.6× 113 0.5× 146 1.2× 18 1.4k
Maria Luiza Saraiva Pereira Brazil 24 981 1.0× 521 0.9× 977 1.6× 114 0.5× 100 0.8× 126 1.7k
N. Rizzuto Italy 20 502 0.5× 418 0.7× 289 0.5× 220 1.0× 147 1.2× 62 1.1k
A.A.W.M. Gabreëls‐Festen Netherlands 26 1.3k 1.4× 743 1.2× 439 0.7× 564 2.7× 271 2.2× 54 2.0k
Yoshihisa Takiyama Japan 30 1.6k 1.7× 693 1.2× 1.7k 2.9× 524 2.5× 106 0.9× 139 2.4k

Countries citing papers authored by Hillary Lipe

Since Specialization
Citations

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

Fields of papers citing papers by Hillary Lipe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hillary Lipe

This figure shows the co-authorship network connecting the top 25 collaborators of Hillary Lipe. A scholar is included among the top collaborators of Hillary Lipe 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 Hillary Lipe. Hillary Lipe 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.
Chen, Dong-Hui, Wendy H. Raskind, William W. Parson, et al.. (2010). A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations. Journal of the Neurological Sciences. 296(1-2). 22–29. 32 indexed citations
2.
Lipe, Hillary & Thomas D. Bird. (2008). Late onset Huntington Disease: Clinical and genetic characteristics of 34 cases. Journal of the Neurological Sciences. 276(1-2). 159–162. 52 indexed citations
3.
Bird, Thomas D., Hillary Lipe, & Ellen J. Steinbart. (2008). Geriatric Neurogenetics. Archives of Neurology. 65(4). 537–537. 9 indexed citations
4.
Carter, Gregory T., et al.. (2006). Double Trouble in Hereditary Neuropathy. Archives of Neurology. 63(1). 112–112. 42 indexed citations
5.
Jayadev, Suman, et al.. (2006). Cambodian founder effect for spinocerebellar ataxia type 3 (Machado–Joseph disease). Journal of the Neurological Sciences. 250(1-2). 110–113. 6 indexed citations
6.
Chen, Dong-Hui, Mark Matsushita, Shirley Rainier, et al.. (2005). Presence of Alanine-to-Valine Substitutions in Myofibrillogenesis Regulator 1 in Paroxysmal Nonkinesigenic Dyskinesia. Archives of Neurology. 62(4). 597–597. 34 indexed citations
7.
Lipe, Hillary, et al.. (2004). Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders. Archives of Neurology. 61(6). 875–875. 34 indexed citations
8.
Chen, Dong-Hui, Zoran Brkanac, Christophe L. M. J. Verlinde, et al.. (2003). Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia. The American Journal of Human Genetics. 72(4). 839–849. 174 indexed citations
9.
Brkanac, Zoran, Magali Fernandez, Mark Matsushita, et al.. (2002). A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qter. Archives of Neurology. 59(8). 1291–1291. 53 indexed citations
10.
Meekins, Gregg, et al.. (2002). Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes. Neuromuscular Disorders. 12(7-8). 643–650. 37 indexed citations
11.
Chen, Dong-Hui, Hillary Lipe, Zhen Qin, & Thomas D. Bird. (2002). Cerebral cavernous malformation: novel mutation in a Chinese family and evidence for heterogeneity. Journal of the Neurological Sciences. 196(1-2). 91–96. 39 indexed citations
12.
Tsuang, Debby W., E. Almqvist, Hillary Lipe, et al.. (2000). Familial Aggregation of Psychotic Symptoms in Huntington’s Disease. American Journal of Psychiatry. 157(12). 1955–1959. 45 indexed citations
13.
Raskind, Wendy H., John Wolff, John K. Fink, et al.. (1998). Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34. Human Genetics. 102(1). 93–97. 22 indexed citations
14.
Tsuang, Debby W., et al.. (1998). Familial aggregation of schizophrenia‐like symptoms in huntington's disease. American Journal of Medical Genetics. 81(4). 323–327. 3 indexed citations
15.
Bird, Thomas D., George H. Kraft, Hillary Lipe, Kimbra Kenney, & S. M. Sumi. (1997). Clinical and pathological phenotype of the original family with Charcot‐Marie‐Tooth type 1B: A 20‐year study. Annals of Neurology. 41(4). 463–469. 44 indexed citations
16.
Raskind, Wendy H., Margaret A. Pericak‐Vance, Felicia Lennon, et al.. (1997). Familial spastic paraparesis: Evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2. American Journal of Medical Genetics. 74(1). 26–36. 21 indexed citations
17.
Bird, Thomas D., et al.. (1994). Impotence Associated with the Charcot-Marie-Tooth Syndrome. European Neurology. 34(3). 155–157. 12 indexed citations
18.
Lipe, Hillary, et al.. (1993). Risk factors for suicide in huntingtons disease: A retrospective case controlled study. American Journal of Medical Genetics. 48(4). 231–233. 45 indexed citations
19.
Lipe, Hillary. (1985). Prevention of Nervous System Trauma From Travel in Motor Vehicles. Journal of Neuroscience Nursing. 17(2). 77–82. 2 indexed citations
20.
Mitchell, Pamela H., et al.. (1981). Moving the patient in bed: effects on intracranial pressure.. PubMed. 30(4). 212–8. 36 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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