R. Sean Hill

6.5k total citations
17 papers, 1.7k citations indexed

About

R. Sean Hill is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, R. Sean Hill has authored 17 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in R. Sean Hill's work include Microtubule and mitosis dynamics (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). R. Sean Hill is often cited by papers focused on Microtubule and mitosis dynamics (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). R. Sean Hill collaborates with scholars based in United States, New Zealand and Australia. R. Sean Hill's co-authors include Christopher A. Walsh, A. James Barkovich, Adria Bodell, Generoso G. Gascon, Brenda J. Barry, Xuyu Cai, Rachel Straussberg, Bernard S. Chang, Thomas Voit and Jacques L. Michaud and has published in prestigious journals such as Science, Neuron and Nature Genetics.

In The Last Decade

R. Sean Hill

17 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R. Sean Hill United States	13	956	624	286	267	199	17	1.7k
Pascale Saugier-Véber France	28	1.1k 1.2×	672 1.1×	437 1.5×	267 1.0×	156 0.8×	82	2.3k
Martin J. Somerville Canada	23	767 0.8×	640 1.0×	167 0.6×	208 0.8×	92 0.5×	45	1.8k
Victoria Mok Siu Canada	25	1.3k 1.3×	868 1.4×	150 0.5×	138 0.5×	149 0.7×	73	1.9k
Cornelia Kraus Germany	25	1.0k 1.1×	967 1.5×	106 0.4×	212 0.8×	164 0.8×	75	2.0k
Elena Parrini Italy	22	899 0.9×	1.0k 1.6×	549 1.9×	596 2.2×	227 1.1×	61	2.2k
Agathe Roubertie France	28	769 0.8×	359 0.6×	618 2.2×	173 0.6×	230 1.2×	114	2.1k
Bert van der Zwaag Netherlands	23	1.2k 1.3×	704 1.1×	372 1.3×	138 0.5×	316 1.6×	44	2.2k
Keiko Shimojima Japan	25	1.0k 1.1×	1.2k 1.9×	190 0.7×	218 0.8×	190 1.0×	125	1.9k
Ginevra Zanni Italy	25	968 1.0×	489 0.8×	442 1.5×	193 0.7×	213 1.1×	82	1.6k
Kan Ding United States	19	1.0k 1.1×	310 0.5×	364 1.3×	157 0.6×	219 1.1×	60	2.3k

Countries citing papers authored by R. Sean Hill

Since Specialization

Citations

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

Fields of papers citing papers by R. Sean Hill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. Sean Hill. 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 R. Sean Hill. The network helps show where R. Sean Hill may publish in the future.

Co-authorship network of co-authors of R. Sean Hill

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

All Works

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17 of 17 papers shown

1.

Schmitz‐Abe, Klaus, Guzman Sánchez‐Schmitz, Ryan N. Doan, et al.. (2020). Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10(1). 14045–14045. 13 indexed citations

2.

Jacobsen, Jessie C., Juliet Taylor, Donald R. Love, et al.. (2017). Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q10 Deficiency in a Female Sib-Pair. JIMD Reports. 42. 31–36. 16 indexed citations

3.

Glamuzina, Emma, Andrew Marshall, Fern Ashton, et al.. (2017). Compound heterozygous SLC19A3 mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia disease. Molecular Case Studies. 3(6). a001909–a001909. 13 indexed citations

4.

Virúes‐Ortega, Javier, Klaus Lehnert, Michael W. Taylor, et al.. (2017). The New Zealand minds for minds autism spectrum disorder self-reported cohort. Research in autism spectrum disorders. 36. 1–7. 2 indexed citations

5.

Hume, Patria, Alice Theadom, Gwyn N. Lewis, et al.. (2017). COGNITION IN FORMER RUGBY UNION PLAYERS AND IMPACT OF CONCUSSION HISTORY. British Journal of Sports Medicine. 51(4). 333.1–333. 2 indexed citations

6.

Hume, Patria, Alice Theadom, Gwyn N. Lewis, et al.. (2016). A Comparison of Cognitive Function in Former Rugby Union Players Compared with Former Non-Contact-Sport Players and the Impact of Concussion History. Sports Medicine. 47(6). 1209–1220. 96 indexed citations

7.

Jacobsen, Jessie C., Callum Wilson, Emma Glamuzina, et al.. (2015). Brain dopamine‐serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorder. Journal of Inherited Metabolic Disease. 39(2). 305–308. 31 indexed citations

8.

Jacobsen, Jessie C., Emma Glamuzina, Juliet Taylor, et al.. (2015). Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1. SHILAP Revista de lepidopterología. 2015. 1–4. 2 indexed citations

9.

Poduri, Annapurna, Gilad D. Evrony, Xuyu Cai, et al.. (2012). Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations. Neuron. 74(1). 41–48. 319 indexed citations

10.

Alkuraya, Fowzan S., Xuyu Cai, Ganeshwaran H. Mochida, et al.. (2011). Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly. The American Journal of Human Genetics. 88(5). 677–677. 2 indexed citations

11.

Alkuraya, Fowzan S., Xuyu Cai, Ganeshwaran H. Mochida, et al.. (2011). Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly. The American Journal of Human Genetics. 88(5). 536–547. 151 indexed citations

12.

Mochida, Ganeshwaran H., Vijay Ganesh, Jillian M. Felie, et al.. (2010). A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts. The American Journal of Human Genetics. 87(6). 882–889. 64 indexed citations

13.

Manzini, M. Chiara, Anna Rajab, Thomas M. Maynard, et al.. (2009). Developmental and degenerative features in a complicated spastic paraplegia. Annals of Neurology. 67(4). 516–525. 27 indexed citations

14.

Poduri, Annapurna, Derek Gordon, Christie Barker‐Cummings, et al.. (2009). Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+. Neurology. 73(16). 1264–1272. 16 indexed citations

15.

Kantarci, Sibel, Lihadh Al‐Gazali, R. Sean Hill, et al.. (2007). Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes. Nature Genetics. 39(8). 957–959. 238 indexed citations

16.

Piao, Xianhua, R. Sean Hill, Adria Bodell, et al.. (2004). G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex. Science. 303(5666). 2033–2036. 405 indexed citations

17.

Ferland, Russell J., Wafaa Eyaid, Randall V. Collura, et al.. (2004). Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome. Nature Genetics. 36(9). 1008–1013. 286 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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