Katy Barwick

728 total citations
9 papers, 207 citations indexed

About

Katy Barwick is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Katy Barwick has authored 9 papers receiving a total of 207 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in Katy Barwick's work include Hereditary Neurological Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Neurological diseases and metabolism (3 papers). Katy Barwick is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Neurological diseases and metabolism (3 papers). Katy Barwick collaborates with scholars based in United Kingdom, United States and Israel. Katy Barwick's co-authors include Manju A. Kurian, Andrew H. Crosby, Barry A. Chioza, Arianna Ferrini, Dora Steel, Matt Hurles, Saeed Al-Turki, Randy Blakely, Jane Wright and Alicia M. Ruggiero and has published in prestigious journals such as Brain, Neurology and The American Journal of Human Genetics.

In The Last Decade

Katy Barwick

9 papers receiving 203 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Katy Barwick United Kingdom	7	89	78	47	42	37	9	207
Keren Yosovich Israel	10	148 1.7×	51 0.7×	40 0.9×	26 0.6×	35 0.9×	24	231
Maartje Pennings Netherlands	10	134 1.5×	112 1.4×	33 0.7×	48 1.1×	76 2.1×	21	272
Hannah E. Steele United Kingdom	9	180 2.0×	77 1.0×	51 1.1×	29 0.7×	30 0.8×	14	275
Dorra H’mida-Ben Brahim Tunisia	6	128 1.4×	78 1.0×	24 0.5×	17 0.4×	26 0.7×	9	258
Fabrizia Stregapede Italy	9	83 0.9×	90 1.2×	22 0.5×	43 1.0×	47 1.3×	17	205
Irene Sambri Italy	7	129 1.4×	30 0.4×	79 1.7×	23 0.5×	27 0.7×	9	285
Saeed Al-Turki United Kingdom	4	114 1.3×	41 0.5×	36 0.8×	19 0.5×	102 2.8×	7	250
Kevin Garofalo United States	4	146 1.6×	60 0.8×	74 1.6×	31 0.7×	15 0.4×	7	245
Nicolas Chrestian Canada	10	195 2.2×	142 1.8×	15 0.3×	43 1.0×	26 0.7×	24	272
Claire Guissart France	12	174 2.0×	76 1.0×	17 0.4×	65 1.5×	73 2.0×	22	301

Countries citing papers authored by Katy Barwick

Since Specialization

Citations

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

Fields of papers citing papers by Katy Barwick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katy Barwick

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

All Works

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9 of 9 papers shown

Steel, Dora, Federica Rachele Danti, Benjamin Kamien, et al.. (2023). Clinical Phenotype in Individuals With Birk-Landau-Perez Syndrome Associated With Biallelic SLC30A9 Pathogenic Variants. Neurology. 100(21). e2214–e2223. 1 indexed citations

Ferrini, Arianna, Dora Steel, Katy Barwick, & Manju A. Kurian. (2021). An Update on the Phenotype, Genotype and Neurobiology of ADCY5‐Related Disease. Movement Disorders. 36(5). 1104–1114. 33 indexed citations

Pope, Simon, Katy Barwick, Joanne Ng, et al.. (2021). Aromatic l-amino acid decarboxylase deficiency: a patient-derived neuronal model for precision therapies. Brain. 144(8). 2443–2456. 20 indexed citations

Sanchis‐Juan, Alba, Amy McTague, Katy Barwick, et al.. (2020). Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gate. Molecular Genetics & Genomic Medicine. 8(7). e1106–e1106. 6 indexed citations

Salter, Claire, Danique Beijer, Katy Barwick, et al.. (2018). Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies. Neurology Genetics. 4(2). e222–e222. 21 indexed citations

Aharoni, Sharon, Katy Barwick, Rachel Straussberg, et al.. (2016). Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel. BMC Medical Genetics. 17(1). 82–82. 14 indexed citations

Ingram, Gillian, Katy Barwick, Louise Hartley, et al.. (2016). Distal hereditary motor neuropathy with vocal cord paresis: from difficulty in choral singing to a molecular genetic diagnosis. Practical Neurology. 16(3). 247–251. 6 indexed citations

Baple, Emma L., Reza Maroofian, Barry A. Chioza, et al.. (2013). Mutations in KPTN Cause Macrocephaly, Neurodevelopmental Delay, and Seizures. The American Journal of Human Genetics. 94(1). 87–94. 35 indexed citations

Barwick, Katy, Jane Wright, Saeed Al-Turki, et al.. (2012). Defective Presynaptic Choline Transport Underlies Hereditary Motor Neuropathy. The American Journal of Human Genetics. 91(6). 1103–1107. 71 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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