Lettie E. Rawlins

575 total citations
16 papers, 134 citations indexed

About

Lettie E. Rawlins is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lettie E. Rawlins has authored 16 papers receiving a total of 134 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lettie E. Rawlins's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Hereditary Neurological Disorders (3 papers). Lettie E. Rawlins is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Hereditary Neurological Disorders (3 papers). Lettie E. Rawlins collaborates with scholars based in United Kingdom, United States and Pakistan. Lettie E. Rawlins's co-authors include Malcolm Woollard, Julia Williams, Emma L. Baple, Andrew H. Crosby, Gaurav V. Harlalka, Barry A. Chioza, Hannah Jones, James Fasham, Peter O’Meara and Graham Munro and has published in prestigious journals such as Cellular and Molecular Life Sciences, PLoS Genetics and European Journal of Human Genetics.

In The Last Decade

Lettie E. Rawlins

15 papers receiving 131 citations

Peers

Lettie E. Rawlins

GENET

PHYSI

EPIDE

Frauke Czepluch Germany

Freyja H.M. van Lint Netherlands

Yoshinobu Oyazato Japan

Imran Chishti United States

Stephanie Harris United States

Robyn J. Hylind United States

Tafadzwa Machipisa South Africa

M. A. Tejero Spain

Caroline Stuart United States

Aurélie Coussement France

Frauke Czepluch Germany

Lettie E. Rawlins

22 ×0.4

28 ×0.6

GENET

5 ×0.1

61 ×3.4

PHYSI

86 ×5.1

EPIDE

Citations per year, relative to Lettie E. Rawlins Lettie E. Rawlins (= 1×) peers Frauke Czepluch

Countries citing papers authored by Lettie E. Rawlins

Since Specialization

Citations

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

Fields of papers citing papers by Lettie E. Rawlins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lettie E. Rawlins. 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 Lettie E. Rawlins. The network helps show where Lettie E. Rawlins may publish in the future.

Co-authorship network of co-authors of Lettie E. Rawlins

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

All Works

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16 of 16 papers shown

Khan, Niamat, et al.. (2024). Investigating the genetic basis of hereditary spastic paraplegia and cerebellar Ataxia in Pakistani families. BMC Neurology. 24(1). 354–354. 1 indexed citations

Rawlins, Lettie E., Niamat Khan, Saadullah Khan, et al.. (2024). Expanding the genetic spectrum of hereditary motor sensory neuropathies in Pakistan. BMC Neurology. 24(1). 394–394. 1 indexed citations

Khan, Jahangir, Muhammad Arshad, Siying Lin, et al.. (2024). Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families. BMC Ophthalmology. 24(1). 345–345. 2 indexed citations

Fasham, James, Adam C. Gunning, Martina Owens, et al.. (2024). TECPR2‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine. American Journal of Medical Genetics Part A. 194(7). e63579–e63579. 2 indexed citations

Pérez-Villegas, Eva M., José Á. Armengol, Lettie E. Rawlins, et al.. (2024). Autophagy dysregulation via the USP20-ULK1 axis in the HERC2-related neurodevelopmental disorder. Cell Death Discovery. 10(1). 163–163. 1 indexed citations

Low, Karen, Ramya Nair, Francis H. Sansbury, et al.. (2023). Expanding the phenotypic spectrum of Chromosome 16p13.11 microduplication: A multicentric analysis of 206 patients. European Journal of Medical Genetics. 66(4). 104714–104714. 2 indexed citations

Ullah, Mukhtar, Niamat Khan, Lettie E. Rawlins, et al.. (2023). Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families. BMC Ophthalmology. 23(1). 205–205.

Pedrazza, Leonardo, Juanma Ramírez, Lettie E. Rawlins, et al.. (2022). HERC2 deficiency activates C-RAF/MKK3/p38 signalling pathway altering the cellular response to oxidative stress. Cellular and Molecular Life Sciences. 79(11). 548–548. 8 indexed citations

Rawlins, Lettie E., Hannah Jones, Olivia Wenger, et al.. (2021). A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder. PLoS Genetics. 17(9). e1009803–e1009803. 6 indexed citations

10.

Khan, Shazia, Lettie E. Rawlins, Gaurav V. Harlalka, et al.. (2019). Homozygous variants in the HEXB and MBOAT7 genes underlie neurological diseases in consanguineous families. BMC Medical Genetics. 20(1). 199–199. 16 indexed citations

11.

Rawlins, Lettie E., Barry A. Chioza, Claire Salter, et al.. (2019). MNS1 variant associated with situs inversus and male infertility. European Journal of Human Genetics. 28(1). 50–55. 23 indexed citations

12.

Rawlins, Lettie E., Hannah Jones, Olivia Wenger, et al.. (2019). An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia. European Journal of Human Genetics. 27(4). 657–662. 20 indexed citations

13.

Rawlins, Lettie E., et al.. (2016). De novo SETD5 nonsense mutation associated with diaphragmatic hernia and severe cerebral cortical dysplasia. Clinical Dysmorphology. 26(2). 95–97. 6 indexed citations

14.

Woollard, Malcolm, et al.. (2011). Achy breaky makey wakey heart? A randomised crossover trial of musical prompts. Emergency Medicine Journal. 29(4). 290–294. 15 indexed citations

15.

Rawlins, Lettie E., et al.. (2011). 06 Keeping the beat: does music improve the performance of chest compression by lay persons?. Emergency Medicine Journal. 28(3). e1–e1. 1 indexed citations

16.

Rawlins, Lettie E., et al.. (2009). Effect of listening to Nellie the Elephant during CPR training on performance of chest compressions by lay people: randomised crossover trial. BMJ. 339(dec11 2). b4707–b4707. 30 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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